-- MySQL Script generated by MySQL Workbench
-- vie 25 ago 2017 16:00:53 ART
-- Model: New Model    Version: 1.0
-- MySQL Workbench Forward Engineering

SET @OLD_UNIQUE_CHECKS=@@UNIQUE_CHECKS, UNIQUE_CHECKS=0;
SET @OLD_FOREIGN_KEY_CHECKS=@@FOREIGN_KEY_CHECKS, FOREIGN_KEY_CHECKS=0;
SET @OLD_SQL_MODE=@@SQL_MODE, SQL_MODE='TRADITIONAL,ALLOW_INVALID_DATES';

-- -----------------------------------------------------
-- Schema kindriver_v82
-- -----------------------------------------------------
DROP SCHEMA IF EXISTS `kindriver_v82` ;

-- -----------------------------------------------------
-- Schema kindriver_v82
-- -----------------------------------------------------
-- CREATE SCHEMA IF NOT EXISTS `kindriver_v82` DEFAULT CHARACTER SET latin1 ;
CREATE SCHEMA IF NOT EXISTS `kindriver_v82` DEFAULT CHARACTER SET utf8 COLLATE utf8_general_ci ;

USE `kindriver_v82` ;

-- -----------------------------------------------------
-- Table `kindriver_v82`.`Protein`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Protein` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Protein` (
  `uniprot_id` VARCHAR(100) NOT NULL,
  `ec_number` VARCHAR(100) NULL,
  `uniprot_acc` VARCHAR(100) NULL,
  `gene_names` VARCHAR(1000) NULL,
  `alt_names` VARCHAR(1000) NULL,
  `length` INT NULL,
  `priority` INT NULL,
  PRIMARY KEY (`uniprot_id`))
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Disease`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Disease` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Disease` (
  `disease_id` INT NOT NULL,
  `disease_desc` VARCHAR(100) NULL,
  PRIMARY KEY (`disease_id`))
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Pfam`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Pfam` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Pfam` (
  `pfam_id` VARCHAR(100) NOT NULL,
  `description` VARCHAR(100) NULL,
  `alignment_file` VARCHAR(200) NULL,
  PRIMARY KEY (`pfam_id`))
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Pfam_Domain`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Pfam_Domain` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Pfam_Domain` (
  `pfam_domain_id` VARCHAR(100) NOT NULL,
  `pfam_id` VARCHAR(100) NOT NULL,
  `uniprot_id` VARCHAR(100) NOT NULL,
  `start` INT NULL,
  `end` INT NULL,
  PRIMARY KEY (`pfam_domain_id`),
  INDEX `fk_Pfam_has_Protein_Protein1_idx` (`uniprot_id` ASC),
  INDEX `fk_Pfam_has_Protein_Pfam1_idx` (`pfam_id` ASC),
  CONSTRAINT `fk_Pfam_has_Protein_Pfam1`
    FOREIGN KEY (`pfam_id`)
    REFERENCES `kindriver_v82`.`Pfam` (`pfam_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Pfam_has_Protein_Protein1`
    FOREIGN KEY (`uniprot_id`)
    REFERENCES `kindriver_v82`.`Protein` (`uniprot_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Mutant`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Mutant` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Mutant` (
  `mutant_id` VARCHAR(100) NOT NULL,
  `mutation` VARCHAR(100) NULL,
  `rel_freq` FLOAT NULL,
  `abs_freq` INT NULL,
  `disease_id` INT NULL,
  `uniprot_id` VARCHAR(100) NOT NULL,
  `validation` VARCHAR(100) NULL,
  `pfam_domain_id` VARCHAR(100) NULL,
  `from_res_n` INT NULL,
  `to_res_n` INT NULL,
  `mut_type` VARCHAR(100) NULL,
  `gene_sample_count` INT NULL,
  PRIMARY KEY (`mutant_id`),
  INDEX `fk_Mutant_1_idx` (`disease_id` ASC),
  INDEX `fk_Mutant_3_idx` (`uniprot_id` ASC),
  INDEX `fk_Mutant_2_idx` (`pfam_domain_id` ASC),
  CONSTRAINT `fk_Mutant_1`
    FOREIGN KEY (`disease_id`)
    REFERENCES `kindriver_v82`.`Disease` (`disease_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Mutant_3`
    FOREIGN KEY (`uniprot_id`)
    REFERENCES `kindriver_v82`.`Protein` (`uniprot_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Mutant_2`
    FOREIGN KEY (`pfam_domain_id`)
    REFERENCES `kindriver_v82`.`Pfam_Domain` (`pfam_domain_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Reference`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Reference` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Reference` (
  `pubmed_id` VARCHAR(30) NOT NULL,
  PRIMARY KEY (`pubmed_id`))
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Mutant_has_Reference`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Mutant_has_Reference` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Mutant_has_Reference` (
  `Mutant_has_Reference_id` VARCHAR(100) NOT NULL,
  `mutant_id` VARCHAR(100) NOT NULL,
  `pubmed_id` VARCHAR(30) NOT NULL,
  INDEX `fk_Mutant_has_Reference2_Reference2_idx` (`pubmed_id` ASC),
  INDEX `fk_Mutant_has_Reference2_Mutant2_idx` (`mutant_id` ASC),
  PRIMARY KEY (`Mutant_has_Reference_id`),
  CONSTRAINT `fk_Mutant_has_Reference2_Mutant2`
    FOREIGN KEY (`mutant_id`)
    REFERENCES `kindriver_v82`.`Mutant` (`mutant_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Mutant_has_Reference2_Reference2`
    FOREIGN KEY (`pubmed_id`)
    REFERENCES `kindriver_v82`.`Reference` (`pubmed_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Segment`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Segment` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Segment` (
  `segment_id` VARCHAR(100) NOT NULL,
  `aln_start` INT NULL,
  `aln_end` INT NULL,
  `segment_desc` VARCHAR(100) NULL,
  `segment_name` VARCHAR(100) NULL,
  PRIMARY KEY (`segment_id`))
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`PDB`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`PDB` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`PDB` (
  `pdb_id` VARCHAR(100) CHARACTER SET 'latin1' BINARY NOT NULL,
  `uniprot_id` VARCHAR(100) NOT NULL,
  `chain` VARCHAR(2) NULL,
  `description` VARCHAR(300) NULL,
  `spaci` FLOAT NULL,
  `aerospaci` FLOAT NULL,
  `resolution` FLOAT NULL,
  PRIMARY KEY (`pdb_id`),
  INDEX `fk_PDB_Protein1_idx` (`uniprot_id` ASC),
  CONSTRAINT `fk_PDB_Protein1`
    FOREIGN KEY (`uniprot_id`)
    REFERENCES `kindriver_v82`.`Protein` (`uniprot_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Protein_residue`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Protein_residue` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Protein_residue` (
  `protein_residue_id` VARCHAR(100) NOT NULL,
  `protein_res_number` INT NULL,
  `uniprot_id` VARCHAR(100) NOT NULL,
  `aa_type` VARCHAR(1) NULL,
  `alignment_col` INT NULL,
  `abs_freq` INT NULL,
  `abs_freq_CA` INT NULL,
  `pfam_domain_id` VARCHAR(100) NULL,
  INDEX `fk_Protein_residue_2_idx` (`uniprot_id` ASC),
  PRIMARY KEY (`protein_residue_id`),
  INDEX `fk_Protein_residue_1_idx` (`pfam_domain_id` ASC),
  CONSTRAINT `fk_Protein_residue_2`
    FOREIGN KEY (`uniprot_id`)
    REFERENCES `kindriver_v82`.`Protein` (`uniprot_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Protein_residue_1`
    FOREIGN KEY (`pfam_domain_id`)
    REFERENCES `kindriver_v82`.`Pfam_Domain` (`pfam_domain_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Protein_residue_has_Mutant`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Protein_residue_has_Mutant` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Protein_residue_has_Mutant` (
  `Protein_residue_has_Mutant_id` VARCHAR(100) NOT NULL,
  `protein_residue_id` VARCHAR(100) NOT NULL,
  `mutant_id` VARCHAR(100) NOT NULL,
  `aa_from` VARCHAR(1) NULL,
  `aa_to` VARCHAR(1) NULL,
  INDEX `fk_Protein_residue_has_Mutant_Mutant1_idx` (`mutant_id` ASC),
  INDEX `fk_Protein_residue_has_Mutant_Protein_residue1_idx` (`protein_residue_id` ASC),
  PRIMARY KEY (`Protein_residue_has_Mutant_id`),
  CONSTRAINT `fk_Protein_residue_has_Mutant_Protein_residue1`
    FOREIGN KEY (`protein_residue_id`)
    REFERENCES `kindriver_v82`.`Protein_residue` (`protein_residue_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Protein_residue_has_Mutant_Mutant1`
    FOREIGN KEY (`mutant_id`)
    REFERENCES `kindriver_v82`.`Mutant` (`mutant_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Protein_residue_has_PDB`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Protein_residue_has_PDB` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Protein_residue_has_PDB` (
  `PDB_has_Protein_residue_id` VARCHAR(100) NOT NULL,
  `pdb_id` VARCHAR(100) CHARACTER SET 'latin1' BINARY NOT NULL,
  `protein_residue_id` VARCHAR(100) NOT NULL,
  `protein_res_number` INT NULL,
  `pdb_res_number` VARCHAR(7) NULL,
  `chain` VARCHAR(2) NULL,
  INDEX `fk_PDB_has_Protein_residue_Protein_residue1_idx` (`protein_residue_id` ASC),
  INDEX `fk_PDB_has_Protein_residue_PDB1_idx` (`pdb_id` ASC),
  PRIMARY KEY (`PDB_has_Protein_residue_id`),
  CONSTRAINT `fk_PDB_has_Protein_residue_PDB1`
    FOREIGN KEY (`pdb_id`)
    REFERENCES `kindriver_v82`.`PDB` (`pdb_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_PDB_has_Protein_residue_Protein_residue1`
    FOREIGN KEY (`protein_residue_id`)
    REFERENCES `kindriver_v82`.`Protein_residue` (`protein_residue_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Protein_has_Segment`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Protein_has_Segment` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Protein_has_Segment` (
  `Protein_has_Segment_id` VARCHAR(100) NOT NULL,
  `pfam_domain_id` VARCHAR(100) NOT NULL,
  `segment_id` VARCHAR(100) NULL,
  `start` INT NULL,
  `end` INT NULL,
  `length` INT NULL,
  INDEX `fk_Protein_has_Segment_Segment1_idx` (`segment_id` ASC),
  PRIMARY KEY (`Protein_has_Segment_id`),
  INDEX `fk_Protein_has_Segment_1_idx` (`pfam_domain_id` ASC),
  CONSTRAINT `fk_Protein_has_Segment_Segment1`
    FOREIGN KEY (`segment_id`)
    REFERENCES `kindriver_v82`.`Segment` (`segment_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Protein_has_Segment_1`
    FOREIGN KEY (`pfam_domain_id`)
    REFERENCES `kindriver_v82`.`Pfam_Domain` (`pfam_domain_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Segment_has_Mutant`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Segment_has_Mutant` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Segment_has_Mutant` (
  `Segment_has_Mutant_id` VARCHAR(100) NOT NULL,
  `segment_id` VARCHAR(100) NOT NULL,
  `mutant_id` VARCHAR(100) NOT NULL,
  PRIMARY KEY (`Segment_has_Mutant_id`),
  INDEX `fk_Segment_has_Mutant_Mutant1_idx` (`mutant_id` ASC),
  INDEX `fk_Segment_has_Mutant_Segment1_idx` (`segment_id` ASC),
  CONSTRAINT `fk_Segment_has_Mutant_Segment1`
    FOREIGN KEY (`segment_id`)
    REFERENCES `kindriver_v82`.`Segment` (`segment_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION,
  CONSTRAINT `fk_Segment_has_Mutant_Mutant1`
    FOREIGN KEY (`mutant_id`)
    REFERENCES `kindriver_v82`.`Mutant` (`mutant_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


-- -----------------------------------------------------
-- Table `kindriver_v82`.`Samples`
-- -----------------------------------------------------
DROP TABLE IF EXISTS `kindriver_v82`.`Samples` ;

CREATE TABLE IF NOT EXISTS `kindriver_v82`.`Samples` (
  `sample_id` INT NOT NULL,
  `histology` VARCHAR(200) NULL,
  `site` VARCHAR(100) NULL,
  `mutant_id` VARCHAR(100) NULL,
  `pubmed_id` VARCHAR(30) NULL,
  `cosmic_mut_id` VARCHAR(100) NULL,
  `cosmic_mutation` VARCHAR(100) NULL,
  `cosmic_sample_id` INT NULL,
  INDEX `fk_Samples_1_idx` (`mutant_id` ASC),
  PRIMARY KEY (`sample_id`),
  CONSTRAINT `fk_Samples_1`
    FOREIGN KEY (`mutant_id`)
    REFERENCES `kindriver_v82`.`Mutant` (`mutant_id`)
    ON DELETE NO ACTION
    ON UPDATE NO ACTION)
ENGINE = InnoDB;


SET SQL_MODE=@OLD_SQL_MODE;
SET FOREIGN_KEY_CHECKS=@OLD_FOREIGN_KEY_CHECKS;
SET UNIQUE_CHECKS=@OLD_UNIQUE_CHECKS;
INSERT INTO `kindriver_v82`.`Disease` (`disease_id`,`disease_desc`) VALUES 
('56','Acute myeloid leukemia'),
('58','Retinitis pigmentosa'),
('15','Acute leukemia (myeloid, lymphoblastic)'),
('19','Fahr disease'),
('38','Severe combined immune deficiency'),
('13','Cortical cataract'),
('10','Lung cancer'),
('54','Breast, lung cancer'),
('53','HNPCC'),
('37','Transient myeloproliferative disorder'),
('50','Loeys-Dietz syndrome'),
('45','Oncogene v-mos'),
('11','Myeloid malignancies'),
('43','Rhabdomyosarcoma (RMS)'),
('6','Cardio‐facio‐cutaneous (CFC) syndrome, Costello syndrome '),
('3','Endometrial carcinomas'),
('46','gastrointestinal stromal tumors'),
('41','Infantile myofibromatosis'),
('34','Sporadic malignant melanoma'),
('22','Neuroblastoma'),
('29','Several carcinomas (lung, kidney, head&neck, etc)'),
('40','Artificial'),
('12','Atypical myeloproliferative neoplasm (aMPN)'),
('25','Cutaneomucosal venous malformations (VMCM)'),
('20','Several carcinomas (bladder, cervix, skin, etc)'),
('57','Sporadic venous malformation'),
('42','Colon cancer'),
('14','Acute lymphoblastic leukemia'),
('26','Lung adenocarcinoma'),
('17','Prostate cancer'),
('16','Carcinoma'),
('44','Breast cancer cell line'),
('49','Loeys-Dietz, Marfan syndromes or related'),
('24','Noonan syndrome'),
('30','Several carcinomas (colon and others)'),
('52','Cancer'),
('4','Craniosynostosis'),
('33','Lung squamous cell carcinoma '),
('39','Familial colorectal cancer'),
('21','Familial acanthosis'),
('7','Pancreatic cancer'),
('35','Peutz-Jegher syndrome'),
('27','Ovary adenocarcinoma'),
('5','Apert\'s syndrome. Some carcinomas (rare)'),
('23','Multiple endocrine neoplasia,  medullary thyroid carcinoma '),
('18','Familial breast cancer'),
('48','Crouzon syndrome'),
('47','Brachydactyly type B (BDB)'),
('36','Megakaryoblastic leukemia'),
('9','Acute myeloid leukemia  leukemia (AML)'),
('0','Gastrointestinal stromal tumours (GISTs)'),
('51','Loeys-Dietz syndrome (or related)'),
('31','Colorectal carcinoma, melanoma and many others'),
('55','Human X-linked agammaglobulinemia'),
('28','Stomach adenocarcinoma'),
('1','Hypereosinophilic syndrome'),
('32','Cardio‐facio‐cutaneous (CFC) syndrome'),
('2','Myeloproliferative neoplasms'),
('8','Hematopoietic and lymphoid malignancies');INSERT INTO `kindriver_v82`.`Pfam` (`pfam_id`,`description`,`alignment_file`) VALUES 
('PF07714','Protein tyrosine kinase','alignments/PF07714/PF07714.txt'),
('PF00069','Protein kinase domain','alignments/PF00069/PF00069.txt');INSERT INTO `kindriver_v82`.`Protein` (`uniprot_id`,`alt_names`,`gene_names`,`ec_number`,`uniprot_acc`,`length`,`priority`) VALUES 
('A0JLR0_HUMAN',NULL,'MAST2',NULL,'A0JLR0','792','0'),
('A0JLT6_HUMAN',NULL,'PRKD2',NULL,'A0JLT6','363','0'),
('A0JP11_HUMAN',NULL,'PIK3R4',NULL,'A0JP11','1358','0'),
('A0MZF5_HUMAN',NULL,'PRKAA2',NULL,'A0MZF5','552','0'),
('A0PJ48_HUMAN',NULL,'TAOK2',NULL,'A0PJ48','762','0'),
('A0PJ51_HUMAN',NULL,'STK4',NULL,'A0PJ51','405','0'),
('A0PJ70_HUMAN',NULL,'GSG2',NULL,'A0PJ70','773','0'),
('A0PJF8_HUMAN',NULL,'RPS6KA4',NULL,'A0PJF8','556','0'),
('A0ZT98_HUMAN',NULL,'TSSK1',NULL,'A0ZT98','367','0'),
('A0ZT99_HUMAN',NULL,'TSSK2',NULL,'A0ZT99','358','0'),
('A1A4C4_HUMAN',NULL,'MAPK4',NULL,'A1A4C4','587','0'),
('A1A5A9_HUMAN',NULL,'KIAA0999,SIK3',NULL,'A1A5A9','1102','0'),
('A1L4F5_HUMAN','Tyrosine-protein kinase transmembrane receptor','ROR2','2.7.10.1','A1L4F5','943','0'),
('A1L4K2_HUMAN',NULL,'MAPK8',NULL,'A1L4K2','427','0'),
('A2ABM8_HUMAN',NULL,'DDR1',NULL,'A2ABM8','493','0'),
('A2VCQ3_HUMAN','Tyrosine-protein kinase transmembrane receptor','ROR1','2.7.10.1','A2VCQ3','940','0'),
('A3KFJ0_HUMAN',NULL,'AURKA',NULL,'A3KFJ0','347','0'),
('A3QNQ0_HUMAN',NULL,'TGFBR2',NULL,'A3QNQ0','567','0'),
('A4CYL7_HUMAN',NULL,NULL,NULL,'A4CYL7','472','0'),
('A4D150_HUMAN',NULL,'LOC402468',NULL,'A4D150','427','0'),
('A4D151_HUMAN',NULL,'LOC402468',NULL,'A4D151','413','0'),
('A4D159_HUMAN',NULL,'STK31',NULL,'A4D159','1019','0'),
('A4D160_HUMAN',NULL,'STK31',NULL,'A4D160','996','0'),
('A4D1G0_HUMAN',NULL,'CDK6',NULL,'A4D1G0','326','0'),
('A4D1R9_HUMAN',NULL,'HIPK2',NULL,'A4D1R9','815','0'),
('A4D2J9_HUMAN',NULL,'CAMK2B',NULL,'A4D2J9','666','0'),
('A4QPA9_HUMAN',NULL,'MAP2K1',NULL,'A4QPA9','393','0'),
('A4VCI5_HUMAN',NULL,'CDC2L1',NULL,'A4VCI5','542','0'),
('A5YM46_HUMAN',NULL,'ERN2',NULL,'A5YM46','874','0'),
('A5YM56_HUMAN','cGMP-dependent protein kinase','PRKG1','2.7.11.12','A5YM56','686','0'),
('A5YM65_HUMAN',NULL,'ERN2',NULL,'A5YM65','926','0'),
('A6H8V9_HUMAN',NULL,'LRRK1',NULL,'A6H8V9','1369','0'),
('A6NF29_HUMAN',NULL,'MAPK8',NULL,'A6NF29','218','0'),
('A6NGQ3_HUMAN',NULL,'OBSCN',NULL,'A6NGQ3','5602','0'),
('A6NHV6_HUMAN',NULL,'PKMYT1',NULL,'A6NHV6','447','0'),
('A6NIA0_HUMAN',NULL,'MAP3K5',NULL,'A6NIA0','621','0'),
('A6NJF2_HUMAN',NULL,'NPR2',NULL,'A6NJF2','265','0'),
('A6NK28_HUMAN',NULL,'MAP2K5',NULL,'A6NK28','258','0'),
('A6P4T4_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','A6P4T4','1059','0'),
('A6P4V4_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','A6P4V4','1310','0'),
('A6PVV2_HUMAN',NULL,'WNK2',NULL,'A6PVV2','790','0'),
('A6YR18_HUMAN',NULL,NULL,NULL,'A6YR18','433','0'),
('A8E633_HUMAN',NULL,'FGFR3',NULL,'A8E633','480','0'),
('A8JZZ5_HUMAN',NULL,NULL,NULL,'A8JZZ5','543','0'),
('A8K0J3_HUMAN',NULL,NULL,NULL,'A8K0J3','898','0'),
('A8K0N1_HUMAN',NULL,NULL,NULL,'A8K0N1','367','0'),
('A8K0W0_HUMAN',NULL,NULL,NULL,'A8K0W0','460','0'),
('A8K161_HUMAN',NULL,'CAMK2A',NULL,'A8K161','489','0'),
('A8K245_HUMAN',NULL,NULL,NULL,'A8K245','396','0'),
('A8K297_HUMAN',NULL,NULL,NULL,'A8K297','647','0'),
('A8K2P1_HUMAN',NULL,NULL,NULL,'A8K2P1','986','0'),
('A8K2S4_HUMAN',NULL,NULL,NULL,'A8K2S4','745','0'),
('A8K2T6_HUMAN',NULL,NULL,NULL,'A8K2T6','976','0'),
('A8K2T7_HUMAN',NULL,NULL,NULL,'A8K2T7','1210','0'),
('A8K341_HUMAN',NULL,NULL,NULL,'A8K341','347','0'),
('A8K342_HUMAN',NULL,NULL,NULL,'A8K342','418','0'),
('A8K379_HUMAN',NULL,NULL,NULL,'A8K379','512','0'),
('A8K3B6_HUMAN',NULL,NULL,NULL,'A8K3B6','450','0'),
('A8K3Y2_HUMAN',NULL,'MAP2K6',NULL,'A8K3Y2','334','0'),
('A8K3Z4_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','A8K3Z4','793','0'),
('A8K4G2_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','A8K4G2','635','0'),
('A8K4G3_HUMAN',NULL,'HCK',NULL,'A8K4G3','506','0'),
('A8K4I7_HUMAN',NULL,NULL,NULL,'A8K4I7','562','0'),
('A8K4K4_HUMAN',NULL,NULL,NULL,'A8K4K4','382','0'),
('A8K574_HUMAN',NULL,NULL,NULL,'A8K574','568','0'),
('A8K5A6_HUMAN',NULL,NULL,NULL,'A8K5A6','1085','0'),
('A8K5M4_HUMAN',NULL,NULL,NULL,'A8K5M4','524','0'),
('A8K5P5_HUMAN',NULL,NULL,NULL,'A8K5P5','765','0'),
('A8K5U6_HUMAN',NULL,NULL,NULL,'A8K5U6','983','0'),
('A8K602_HUMAN','Mitogen-activated protein kinase kinase kinase kinase',NULL,'2.7.11.1','A8K602','894','0'),
('A8K6N9_HUMAN',NULL,NULL,NULL,'A8K6N9','518','0'),
('A8K6P8_HUMAN',NULL,'CCRK',NULL,'A8K6P8','167','0'),
('A8K709_HUMAN',NULL,NULL,NULL,'A8K709','675','0'),
('A8K710_HUMAN',NULL,NULL,NULL,'A8K710','455','0'),
('A8K724_HUMAN',NULL,NULL,NULL,'A8K724','591','0'),
('A8K730_HUMAN',NULL,NULL,NULL,'A8K730','364','0'),
('A8K7G8_HUMAN',NULL,NULL,NULL,'A8K7G8','490','0'),
('A8K7I0_HUMAN',NULL,'CLK2',NULL,'A8K7I0','499','0'),
('A8K869_HUMAN',NULL,NULL,NULL,'A8K869','688','0'),
('A8K8B2_HUMAN',NULL,NULL,NULL,'A8K8B2','655','0'),
('A8K8B9_HUMAN',NULL,NULL,NULL,'A8K8B9','343','0'),
('A8K8F7_HUMAN',NULL,NULL,NULL,'A8K8F7','520','0'),
('A8K8I6_HUMAN',NULL,'CDK10',NULL,'A8K8I6','194','0'),
('A8K8J5_HUMAN',NULL,NULL,NULL,'A8K8J5','502','0'),
('A8K8M5_HUMAN',NULL,NULL,NULL,'A8K8M5','578','0'),
('A8K8R5_HUMAN',NULL,NULL,NULL,'A8K8R5','1038','0'),
('A8K8V9_HUMAN',NULL,NULL,NULL,'A8K8V9','1019','0'),
('A8K8Z3_HUMAN',NULL,NULL,NULL,'A8K8Z3','766','0'),
('A8K910_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','A8K910','1132','0'),
('A8K9I1_HUMAN',NULL,NULL,NULL,'A8K9I1','414','0'),
('A8K9K0_HUMAN',NULL,NULL,NULL,'A8K9K0','798','0'),
('A8K9L2_HUMAN',NULL,NULL,NULL,'A8K9L2','396','0'),
('A8KAE3_HUMAN',NULL,NULL,NULL,'A8KAE3','502','0'),
('A8KAM8_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','A8KAM8','1106','0'),
('A8KAN3_HUMAN',NULL,NULL,NULL,'A8KAN3','553','0'),
('A8MPP7_HUMAN',NULL,'SRPK3',NULL,'A8MPP7','492','0'),
('A8MPY5_HUMAN',NULL,'SRPK3,STK23',NULL,'A8MPY5','534','0'),
('A8MT37_HUMAN',NULL,'GSK3A',NULL,'A8MT37','401','0'),
('A8MU99_HUMAN',NULL,'STK36',NULL,'A8MU99','1294','0'),
('A8MWW6_HUMAN',NULL,'MAPK10',NULL,'A8MWW6','319','0'),
('A8MY87_HUMAN',NULL,'KSR1',NULL,'A8MY87','612','0'),
('A9CB80_HUMAN',NULL,NULL,NULL,'A9CB80','1210','0'),
('A9CP04_HUMAN',NULL,'Par1b',NULL,'A9CP04','699','0'),
('A9NIU4_HUMAN',NULL,'OBSCN',NULL,'A9NIU4','1960','0'),
('A9UEZ6_HUMAN',NULL,'BCR/ABL',NULL,'A9UEZ6','1633','0'),
('A9UF02_HUMAN',NULL,'BCR/ABL',NULL,'A9UF02','1644','0'),
('A9UF07_HUMAN',NULL,'BCR/ABL',NULL,'A9UF07','1790','0'),
('A9YLN4_HUMAN','Tyrosine-protein kinase receptor','CD74/ROS,CD74-ROS1_C6','2.7.10.1','A9YLN4','703','0'),
('A9YLN5_HUMAN','Tyrosine-protein kinase receptor','SLC34A2/ROS','2.7.10.1','A9YLN5','724','0'),
('A9YLN6_HUMAN','Tyrosine-protein kinase receptor','SLC34A2/ROS1','2.7.10.1','A9YLN6','621','0'),
('A9YLN7_HUMAN','Tyrosine-protein kinase receptor','EML4/ALK','2.7.10.1','A9YLN7','796','0'),
('AAK1_HUMAN','AP2-associated protein kinase 1,Adaptor-associated kinase 1','AAK1,KIAA1048','2.7.11.1','Q2M2I8','961','1'),
('AAPK1_HUMAN','5\'-AMP-activated protein kinase catalytic subunit alpha-1,AMPK subunit alpha-1,Acetyl-CoA carboxylase kinase,ACACA kinase,Hydroxymethylglutaryl-CoA reductase kinase,HMGCR kinase,Tau-protein kinase PRKAA1','PRKAA1,AMPK1','2.7.11.1,2.7.11.27,2.7.11.31,2.7.11.26','Q13131','559','1'),
('AAPK2_HUMAN','5\'-AMP-activated protein kinase catalytic subunit alpha-2,AMPK subunit alpha-2,Acetyl-CoA carboxylase kinase,ACACA kinase,Hydroxymethylglutaryl-CoA reductase kinase,HMGCR kinase','PRKAA2,AMPK, AMPK2','2.7.11.1,2.7.11.27,2.7.11.31','P54646','552','1'),
('ABL1_HUMAN','Tyrosine-protein kinase ABL1,Abelson murine leukemia viral oncogene homolog 1,Abelson tyrosine-protein kinase 1,Proto-oncogene c-Abl,p150','ABL1,ABL, JTK7','2.7.10.2','P00519','1130','1'),
('ABL2_HUMAN','Abelson tyrosine-protein kinase 2,Abelson murine leukemia viral oncogene homolog 2,Abelson-related gene protein,Tyrosine-protein kinase ARG','ABL2,ABLL, ARG','2.7.10.2','P42684','1182','1'),
('ACK1_HUMAN','Activated CDC42 kinase 1,ACK-1,Tyrosine kinase non-receptor protein 2','TNK2,ACK1','2.7.10.2,2.7.11.1','Q07912','1038','2'),
('ACV1B_HUMAN','Activin receptor type-1B,Activin receptor type IB,ACTR-IB,Activin receptor-like kinase 4,ALK-4,Serine/threonine-protein kinase receptor R2,SKR2','ACVR1B,ACVRLK4, ALK4','2.7.11.30','P36896','505','1'),
('ACV1C_HUMAN','Activin receptor type-1C,Activin receptor type IC,ACTR-IC,Activin receptor-like kinase 7,ALK-7','ACVR1C,ALK7','2.7.11.30','Q8NER5','493','1'),
('ACVL1_HUMAN','Serine/threonine-protein kinase receptor R3,SKR3,Activin receptor-like kinase 1,ALK-1,TGF-B superfamily receptor type I,TSR-I','ACVRL1,ACVRLK1, ALK1','2.7.11.30','P37023','503','1'),
('ACVR1_HUMAN','Activin receptor type-1,Activin receptor type I,ACTR-I,Activin receptor-like kinase 2,ALK-2,Serine/threonine-protein kinase receptor R1,SKR1,TGF-B superfamily receptor type I,TSR-I','ACVR1,ACVRLK2','2.7.11.30','Q04771','509','1'),
('AKT1_HUMAN','RAC-alpha serine/threonine-protein kinase,Protein kinase B,PKB,Protein kinase B alpha,PKB alpha,Proto-oncogene c-Akt,RAC-PK-alpha','AKT1,PKB, RAC','2.7.11.1','P31749','480','1'),
('AKT2_HUMAN','RAC-beta serine/threonine-protein kinase,Protein kinase Akt-2,Protein kinase B beta,PKB beta,RAC-PK-beta','AKT2','2.7.11.1','P31751','481','1'),
('AKT3_HUMAN','RAC-gamma serine/threonine-protein kinase,Protein kinase Akt-3,Protein kinase B gamma,PKB gamma,RAC-PK-gamma,STK-2','AKT3,PKBG','2.7.11.1','Q9Y243','479','1'),
('ALK_HUMAN','ALK tyrosine kinase receptor,Anaplastic lymphoma kinase','ALK','2.7.10.1','Q9UM73','1620','2'),
('AMHR2_HUMAN','Anti-Muellerian hormone type-2 receptor,Anti-Muellerian hormone type II receptor,AMH type II receptor,MIS type II receptor,MISRII,MRII','AMHR2,AMHR, MISR2','2.7.11.30','Q16671','573','1'),
('ANKK1_HUMAN','Ankyrin repeat and protein kinase domain-containing protein 1,Protein kinase PKK2,Sugen kinase 288,SgK288,X-kinase','ANKK1,PKK2, SGK288','2.7.11.1','Q8NFD2','765','1'),
('ANPRA_HUMAN','Atrial natriuretic peptide receptor 1,Atrial natriuretic peptide receptor type A,ANP-A,ANPR-A,NPR-A,Guanylate cyclase A,GC-A','NPR1,ANPRA','4.6.1.2','P16066','1061','1'),
('ANPRB_HUMAN','Atrial natriuretic peptide receptor 2,Atrial natriuretic peptide receptor type B,ANP-B,ANPR-B,NPR-B,Guanylate cyclase B,GC-B','NPR2,ANPRB','4.6.1.2','P20594','1047','1'),
('ARAF_HUMAN','Serine/threonine-protein kinase A-Raf,Proto-oncogene A-Raf,Proto-oncogene A-Raf-1,Proto-oncogene Pks','ARAF,ARAF1, PKS, PKS2','2.7.11.1','P10398','606','1'),
('ARBK1_HUMAN','Beta-adrenergic receptor kinase 1,Beta-ARK-1,G-protein coupled receptor kinase 2','ADRBK1,BARK, BARK1, GRK2','2.7.11.15','P25098','689','1'),
('ARBK2_HUMAN','Beta-adrenergic receptor kinase 2,Beta-ARK-2,G-protein-coupled receptor kinase 3','ADRBK2,BARK2, GRK3','2.7.11.15','P35626','688','1'),
('AURKA_HUMAN','Aurora kinase A,Aurora 2,Aurora/IPL1-related kinase 1,ARK-1,Aurora-related kinase 1,hARK1,Breast tumor-amplified kinase,Serine/threonine-protein kinase 15,Serine/threonine-protein kinase 6,Serine/threonine-protein kinase aurora-A','AURKA,AIK, AIRK1, ARK1, AURA, AYK1, BTAK, IAK1, STK15, STK6','2.7.11.1','O14965','403','1'),
('AURKB_HUMAN','Aurora kinase B,Aurora 1,Aurora- and IPL1-like midbody-associated protein 1,AIM-1,Aurora/IPL1-related kinase 2,ARK-2,Aurora-related kinase 2,STK-1,Serine/threonine-protein kinase 12,Serine/threonine-protein kinase 5,Serine/threonine-protein kinase aurora-B','AURKB,AIK2, AIM1, AIRK2, ARK2, STK1, STK12, STK5','2.7.11.1','Q96GD4','344','1'),
('AURKC_HUMAN','Aurora kinase C,Aurora 3,Aurora/IPL1-related kinase 3,ARK-3,Aurora-related kinase 3,Aurora/IPL1/Eg2 protein 2,Serine/threonine-protein kinase 13,Serine/threonine-protein kinase aurora-C','AURKC,AIE2, AIK3, AIRK3, ARK3, STK13','2.7.11.1','Q9UQB9','309','1'),
('AVR2A_HUMAN','Activin receptor type-2A,Activin receptor type IIA,ACTR-IIA,ACTRIIA','ACVR2A,ACVR2','2.7.11.30','P27037','513','1'),
('AVR2B_HUMAN','Activin receptor type-2B,Activin receptor type IIB,ACTR-IIB','ACVR2B','2.7.11.30','Q13705','512','1'),
('B0AZM9_HUMAN',NULL,NULL,NULL,'B0AZM9','719','0'),
('B0LPE5_HUMAN',NULL,'AKT1',NULL,'B0LPE5','480','0'),
('B0LPI0_HUMAN',NULL,'WNK4',NULL,'B0LPI0','1243','0'),
('B0QY34_HUMAN',NULL,'CSNK1E',NULL,'B0QY34','336','0'),
('B0QY35_HUMAN',NULL,'CSNK1E',NULL,'B0QY35','311','0'),
('B0QY36_HUMAN',NULL,'CSNK1E',NULL,'B0QY36','225','0'),
('B0QYQ2_HUMAN',NULL,'TRIB3',NULL,'B0QYQ2','271','0'),
('B0YIV3_HUMAN',NULL,'ANKK1',NULL,'B0YIV3','765','0'),
('B0YIY3_HUMAN',NULL,'CAMK1',NULL,'B0YIY3','370','0'),
('B1AKC9_HUMAN',NULL,'EPHB2',NULL,'B1AKC9','946','0'),
('B1ANA3_HUMAN',NULL,'MYO3A',NULL,'B1ANA3','197','0'),
('B1APF7_HUMAN',NULL,'PRKACB',NULL,'B1APF7','186','0'),
('B1APF8_HUMAN',NULL,'PRKACB',NULL,'B1APF8','214','0'),
('B1APF9_HUMAN',NULL,'PRKACB',NULL,'B1APF9','245','0'),
('B1APG0_HUMAN',NULL,'PRKACB',NULL,'B1APG0','206','0'),
('B1APG1_HUMAN',NULL,'PRKACB',NULL,'B1APG1','197','0'),
('B1APG2_HUMAN',NULL,'PRKACB',NULL,'B1APG2','209','0'),
('B1APG3_HUMAN',NULL,'PRKACB',NULL,'B1APG3','264','0'),
('B1APY4_HUMAN',NULL,'ROR2',NULL,'B1APY4','704','0'),
('B1AVT0_HUMAN',NULL,'CLK2',NULL,'B1AVT0','497','0'),
('B1AXG1_HUMAN',NULL,'RPS6KA3',NULL,'B1AXG1','227','0'),
('B2R5T1_HUMAN','Protein kinase C',NULL,'2.7.11.13','B2R5T1','697','0'),
('B2R601_HUMAN',NULL,NULL,NULL,'B2R601','986','0'),
('B2R6D7_HUMAN',NULL,NULL,NULL,'B2R6D7','391','0'),
('B2R6F9_HUMAN',NULL,NULL,NULL,'B2R6F9','465','0'),
('B2R6Q4_HUMAN',NULL,'CSK',NULL,'B2R6Q4','450','0'),
('B2R6V2_HUMAN',NULL,NULL,NULL,'B2R6V2','574','0'),
('B2R6Z3_HUMAN',NULL,NULL,NULL,'B2R6Z3','403','0'),
('B2R747_HUMAN',NULL,NULL,NULL,'B2R747','473','0'),
('B2R748_HUMAN',NULL,NULL,NULL,'B2R748','590','0'),
('B2R757_HUMAN',NULL,NULL,NULL,'B2R757','387','0'),
('B2R779_HUMAN','Ribosomal protein S6 kinase',NULL,'2.7.11.1','B2R779','525','0'),
('B2R7K0_HUMAN',NULL,NULL,NULL,'B2R7K0','590','0'),
('B2R841_HUMAN',NULL,NULL,NULL,'B2R841','603','0'),
('B2R859_HUMAN',NULL,NULL,NULL,'B2R859','553','0'),
('B2R8A5_HUMAN',NULL,NULL,NULL,'B2R8A5','467','0'),
('B2R8C2_HUMAN',NULL,NULL,NULL,'B2R8C2','505','0'),
('B2R8K8_HUMAN',NULL,NULL,NULL,'B2R8K8','302','0'),
('B2R8Z2_HUMAN',NULL,NULL,NULL,'B2R8Z2','382','0'),
('B2R8Z4_HUMAN',NULL,NULL,NULL,'B2R8Z4','675','0'),
('B2R928_HUMAN','Mitogen-activated protein kinase kinase kinase kinase',NULL,'2.7.11.1','B2R928','846','0'),
('B2R9A0_HUMAN',NULL,NULL,NULL,'B2R9A0','303','0'),
('B2R9L6_HUMAN',NULL,NULL,NULL,'B2R9L6','372','0'),
('B2R9M7_HUMAN','Protein kinase C epsilon type,nPKC-epsilon',NULL,'2.7.11.13','B2R9M7','737','0'),
('B2R9M8_HUMAN',NULL,NULL,NULL,'B2R9M8','414','0'),
('B2RA25_HUMAN',NULL,NULL,NULL,'B2RA25','552','0'),
('B2RA52_HUMAN',NULL,NULL,NULL,'B2RA52','596','0'),
('B2RA70_HUMAN',NULL,NULL,NULL,'B2RA70','543','0'),
('B2RAJ6_HUMAN',NULL,NULL,NULL,'B2RAJ6','1358','0'),
('B2RAP9_HUMAN',NULL,NULL,NULL,'B2RAP9','460','0'),
('B2RAW9_HUMAN',NULL,NULL,NULL,'B2RAW9','617','0'),
('B2RB89_HUMAN',NULL,'PRKACB',NULL,'B2RB89','351','0'),
('B2RC06_HUMAN',NULL,NULL,NULL,'B2RC06','344','0'),
('B2RCU6_HUMAN',NULL,NULL,NULL,'B2RCU6','544','0'),
('B2RCZ4_HUMAN',NULL,NULL,NULL,'B2RCZ4','587','0'),
('B2RD76_HUMAN',NULL,NULL,NULL,'B2RD76','448','0'),
('B2RDF9_HUMAN',NULL,NULL,NULL,'B2RDF9','501','0'),
('B2RDI6_HUMAN',NULL,NULL,NULL,'B2RDI6','847','0'),
('B2RDR6_HUMAN',NULL,NULL,NULL,'B2RDR6','507','0'),
('B2RE75_HUMAN',NULL,NULL,NULL,'B2RE75','999','0'),
('B3KNJ2_HUMAN',NULL,NULL,NULL,'B3KNJ2','631','0'),
('B3KNJ3_HUMAN',NULL,NULL,NULL,'B3KNJ3','454','0'),
('B3KNX7_HUMAN',NULL,'PAK1',NULL,'B3KNX7','522','0'),
('B3KP36_HUMAN',NULL,NULL,NULL,'B3KP36','415','0'),
('B3KP61_HUMAN',NULL,NULL,NULL,'B3KP61','382','0'),
('B3KPS5_HUMAN',NULL,NULL,NULL,'B3KPS5','559','0'),
('B3KPS6_HUMAN',NULL,NULL,NULL,'B3KPS6','485','0'),
('B3KQ65_HUMAN',NULL,NULL,NULL,'B3KQ65','258','0'),
('B3KQG4_HUMAN',NULL,NULL,NULL,'B3KQG4','632','0'),
('B3KQI0_HUMAN',NULL,NULL,NULL,'B3KQI0','629','0'),
('B3KQJ1_HUMAN',NULL,NULL,NULL,'B3KQJ1','312','0'),
('B3KQM3_HUMAN',NULL,NULL,NULL,'B3KQM3','540','0'),
('B3KR49_HUMAN',NULL,'MAPK3',NULL,'B3KR49','265','0'),
('B3KR53_HUMAN',NULL,NULL,NULL,'B3KR53','217','0'),
('B3KRI8_HUMAN',NULL,NULL,NULL,'B3KRI8','638','0'),
('B3KRS6_HUMAN',NULL,NULL,NULL,'B3KRS6','349','0'),
('B3KRV2_HUMAN',NULL,NULL,NULL,'B3KRV2','416','0'),
('B3KS39_HUMAN',NULL,NULL,NULL,'B3KS39','327','0'),
('B3KS97_HUMAN',NULL,'MAP2K2',NULL,'B3KS97','210','0'),
('B3KSH7_HUMAN',NULL,NULL,NULL,'B3KSH7','392','0'),
('B3KTB2_HUMAN',NULL,'EPHB1',NULL,'B3KTB2','545','0'),
('B3KTH7_HUMAN',NULL,'CAMK2G',NULL,'B3KTH7','362','0'),
('B3KTJ2_HUMAN',NULL,NULL,NULL,'B3KTJ2','580','0'),
('B3KTK0_HUMAN',NULL,NULL,NULL,'B3KTK0','476','0'),
('B3KTV2_HUMAN',NULL,'CLK3',NULL,'B3KTV2','269','0'),
('B3KU24_HUMAN',NULL,NULL,NULL,'B3KU24','266','0'),
('B3KU51_HUMAN',NULL,NULL,NULL,'B3KU51','630','0'),
('B3KUN5_HUMAN',NULL,NULL,'2.7.11.13','B3KUN5','416','0'),
('B3KUS6_HUMAN',NULL,'MAK',NULL,'B3KUS6','288','0'),
('B3KUU7_HUMAN',NULL,NULL,NULL,'B3KUU7','417','0'),
('B3KUV3_HUMAN',NULL,NULL,NULL,'B3KUV3','249','0'),
('B3KUZ9_HUMAN',NULL,NULL,NULL,'B3KUZ9','952','0'),
('B3KV38_HUMAN',NULL,NULL,NULL,'B3KV38','1075','0'),
('B3KVE9_HUMAN',NULL,NULL,NULL,'B3KVE9','614','0'),
('B3KVF3_HUMAN',NULL,NULL,NULL,'B3KVF3','343','0'),
('B3KVH4_HUMAN',NULL,NULL,NULL,'B3KVH4','480','0'),
('B3KVM3_HUMAN',NULL,NULL,NULL,'B3KVM3','576','0'),
('B3KWB3_HUMAN',NULL,NULL,NULL,'B3KWB3','583','0'),
('B3KX76_HUMAN',NULL,NULL,NULL,'B3KX76','157','0'),
('B3KY45_HUMAN',NULL,NULL,NULL,'B3KY45','965','0'),
('B3KY50_HUMAN',NULL,NULL,NULL,'B3KY50','514','0'),
('B3KY86_HUMAN',NULL,NULL,NULL,'B3KY86','575','0'),
('B3KY91_HUMAN',NULL,NULL,NULL,'B3KY91','576','0'),
('B3KYB0_HUMAN',NULL,NULL,NULL,'B3KYB0','636','0'),
('B3KYB1_HUMAN',NULL,NULL,NULL,'B3KYB1','313','0'),
('B3XZL9_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','B3XZL9','785','0'),
('B3XZM0_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','B3XZM0','796','0'),
('B4DDG2_HUMAN',NULL,NULL,NULL,'B4DDG2','355','0'),
('B4DDH2_HUMAN',NULL,'STK33',NULL,'B4DDH2','473','0'),
('B4DDM0_HUMAN','Ribosomal protein S6 kinase',NULL,'2.7.11.1','B4DDM0','481','0'),
('B4DDN2_HUMAN',NULL,'NEK11',NULL,'B4DDN2','461','0'),
('B4DE88_HUMAN',NULL,NULL,NULL,'B4DE88','395','0'),
('B4DEQ4_HUMAN',NULL,'MKNK2',NULL,'B4DEQ4','334','0'),
('B4DER5_HUMAN',NULL,NULL,NULL,'B4DER5','385','0'),
('B4DER9_HUMAN',NULL,NULL,NULL,'B4DER9','276','0'),
('B4DES9_HUMAN',NULL,NULL,NULL,'B4DES9','670','0'),
('B4DF67_HUMAN',NULL,NULL,NULL,'B4DF67','1120','0'),
('B4DFH4_HUMAN',NULL,NULL,NULL,'B4DFH4','210','0'),
('B4DFN2_HUMAN',NULL,NULL,NULL,'B4DFN2','488','0'),
('B4DFP8_HUMAN',NULL,NULL,NULL,'B4DFP8','167','0'),
('B4DFQ0_HUMAN',NULL,NULL,NULL,'B4DFQ0','398','0'),
('B4DFS6_HUMAN',NULL,NULL,NULL,'B4DFS6','380','0'),
('B4DFT0_HUMAN',NULL,'ULK3',NULL,'B4DFT0','483','0'),
('B4DFV1_HUMAN','Protein kinase C',NULL,'2.7.11.13','B4DFV1','603','0'),
('B4DFY5_HUMAN',NULL,'MAP2K1',NULL,'B4DFY5','371','0'),
('B4DG22_HUMAN',NULL,'RPS6KA3',NULL,'B4DG22','711','0'),
('B4DG79_HUMAN',NULL,NULL,NULL,'B4DG79','419','0'),
('B4DGF4_HUMAN',NULL,NULL,NULL,'B4DGF4','899','0'),
('B4DGP5_HUMAN',NULL,NULL,NULL,'B4DGP5','470','0'),
('B4DGQ7_HUMAN',NULL,'ERBB3',NULL,'B4DGQ7','921','0'),
('B4DGW1_HUMAN',NULL,'VRK3',NULL,'B4DGW1','243','0'),
('B4DGX8_HUMAN',NULL,'RET',NULL,'B4DGX8','818','0'),
('B4DH08_HUMAN',NULL,NULL,NULL,'B4DH08','570','0'),
('B4DH13_HUMAN',NULL,NULL,NULL,'B4DH13','750','0'),
('B4DH44_HUMAN',NULL,NULL,NULL,'B4DH44','376','0'),
('B4DHI4_HUMAN',NULL,NULL,NULL,'B4DHI4','1430','0'),
('B4DHN0_HUMAN',NULL,NULL,NULL,'B4DHN0','348','0'),
('B4DHU6_HUMAN',NULL,NULL,NULL,'B4DHU6','374','0'),
('B4DI23_HUMAN',NULL,NULL,NULL,'B4DI23','882','0'),
('B4DIA4_HUMAN',NULL,NULL,NULL,'B4DIA4','368','0'),
('B4DIB3_HUMAN',NULL,'MARK1',NULL,'B4DIB3','780','0'),
('B4DID9_HUMAN',NULL,NULL,NULL,'B4DID9','482','0'),
('B4DIG8_HUMAN',NULL,NULL,NULL,'B4DIG8','427','0'),
('B4DIJ9_HUMAN',NULL,NULL,NULL,'B4DIJ9','298','0'),
('B4DIP4_HUMAN',NULL,'EIF2AK1',NULL,'B4DIP4','577','0'),
('B4DJD8_HUMAN',NULL,NULL,NULL,'B4DJD8','335','0'),
('B4DJG4_HUMAN',NULL,NULL,NULL,'B4DJG4','248','0'),
('B4DJH7_HUMAN',NULL,NULL,NULL,'B4DJH7','305','0'),
('B4DJN5_HUMAN',NULL,'PRKCH',NULL,'B4DJN5','522','0'),
('B4DJP1_HUMAN',NULL,NULL,NULL,'B4DJP1','221','0'),
('B4DJS8_HUMAN',NULL,NULL,NULL,'B4DJS8','441','0'),
('B4DJZ5_HUMAN',NULL,NULL,NULL,'B4DJZ5','181','0'),
('B4DK03_HUMAN',NULL,NULL,NULL,'B4DK03','504','0'),
('B4DK59_HUMAN',NULL,NULL,NULL,'B4DK59','340','0'),
('B4DKT8_HUMAN',NULL,NULL,NULL,'B4DKT8','993','0'),
('B4DKW0_HUMAN',NULL,NULL,NULL,'B4DKW0','783','0'),
('B4DKZ2_HUMAN',NULL,NULL,NULL,'B4DKZ2','710','0'),
('B4DL04_HUMAN',NULL,NULL,NULL,'B4DL04','654','0'),
('B4DL75_HUMAN',NULL,NULL,NULL,'B4DL75','403','0'),
('B4DLF5_HUMAN',NULL,NULL,NULL,'B4DLF5','960','0'),
('B4DLF9_HUMAN',NULL,NULL,NULL,'B4DLF9','342','0'),
('B4DM24_HUMAN',NULL,'CAMKV',NULL,'B4DM24','426','0'),
('B4DM54_HUMAN',NULL,NULL,NULL,'B4DM54','387','0'),
('B4DM55_HUMAN',NULL,NULL,NULL,'B4DM55','541','0'),
('B4DM56_HUMAN',NULL,NULL,NULL,'B4DM56','540','0'),
('B4DMA5_HUMAN',NULL,NULL,NULL,'B4DMA5','332','0'),
('B4DMF2_HUMAN',NULL,NULL,NULL,'B4DMF2','433','0'),
('B4DMM6_HUMAN',NULL,'TRIB1',NULL,'B4DMM6','206','0'),
('B4DMM9_HUMAN',NULL,NULL,NULL,'B4DMM9','385','0'),
('B4DMN4_HUMAN',NULL,NULL,NULL,'B4DMN4','725','0'),
('B4DMR0_HUMAN',NULL,NULL,NULL,'B4DMR0','342','0'),
('B4DMX3_HUMAN','cGMP-dependent protein kinase',NULL,'2.7.11.12','B4DMX3','733','0'),
('B4DMZ0_HUMAN',NULL,NULL,NULL,'B4DMZ0','371','0'),
('B4DNF9_HUMAN',NULL,'CDK4',NULL,'B4DNF9','183','0'),
('B4DNQ3_HUMAN',NULL,NULL,NULL,'B4DNQ3','795','0'),
('B4DP95_HUMAN',NULL,NULL,NULL,'B4DP95','668','0'),
('B4DP99_HUMAN',NULL,NULL,NULL,'B4DP99','399','0'),
('B4DPK7_HUMAN',NULL,NULL,NULL,'B4DPK7','595','0'),
('B4DPS1_HUMAN',NULL,'STK16',NULL,'B4DPS1','187','0'),
('B4DPV1_HUMAN',NULL,NULL,NULL,'B4DPV1','709','0'),
('B4DPY6_HUMAN',NULL,'MET',NULL,'B4DPY6','260','0'),
('B4DQ47_HUMAN',NULL,'ZAK',NULL,'B4DQ47','354','0'),
('B4DQ79_HUMAN',NULL,NULL,NULL,'B4DQ79','423','0'),
('B4DQK5_HUMAN',NULL,NULL,NULL,'B4DQK5','252','0'),
('B4DQN3_HUMAN',NULL,NULL,NULL,'B4DQN3','353','0'),
('B4DQP7_HUMAN',NULL,NULL,NULL,'B4DQP7','545','0'),
('B4DQQ3_HUMAN',NULL,NULL,NULL,'B4DQQ3','544','0'),
('B4DR46_HUMAN',NULL,NULL,NULL,'B4DR46','407','0'),
('B4DR56_HUMAN',NULL,NULL,NULL,'B4DR56','560','0'),
('B4DR80_HUMAN',NULL,'STK24',NULL,'B4DR80','412','0'),
('B4DRK0_HUMAN',NULL,NULL,NULL,'B4DRK0','854','0'),
('B4DS23_HUMAN',NULL,NULL,NULL,'B4DS23','868','0'),
('B4DS37_HUMAN',NULL,NULL,NULL,'B4DS37','1213','0'),
('B4DS61_HUMAN',NULL,'SRPK1',NULL,'B4DS61','639','0'),
('B4DSE0_HUMAN',NULL,NULL,NULL,'B4DSE0','928','0'),
('B4DSE5_HUMAN',NULL,NULL,NULL,'B4DSE5','880','0'),
('B4DSP6_HUMAN',NULL,NULL,NULL,'B4DSP6','549','0'),
('B4DT57_HUMAN',NULL,NULL,NULL,'B4DT57','450','0'),
('B4DT73_HUMAN',NULL,NULL,NULL,'B4DT73','492','0'),
('B4DTB5_HUMAN',NULL,NULL,NULL,'B4DTB5','214','0'),
('B4DTG1_HUMAN','Ribosomal protein S6 kinase',NULL,'2.7.11.1','B4DTG1','502','0'),
('B4DTR1_HUMAN',NULL,'ERBB2',NULL,'B4DTR1','979','0'),
('B4DTS2_HUMAN','Serine/threonine-protein kinase D',NULL,'2.7.11.13','B4DTS2','888','0'),
('B4DTW8_HUMAN',NULL,NULL,NULL,'B4DTW8','1093','0'),
('B4DU06_HUMAN','Guanylate cyclase',NULL,'4.6.1.2','B4DU06','807','0'),
('B4DUB1_HUMAN',NULL,'CDK19',NULL,'B4DUB1','378','0'),
('B4DUC2_HUMAN',NULL,NULL,NULL,'B4DUC2','718','0'),
('B4DUD9_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','B4DUD9','804','0'),
('B4DUF0_HUMAN',NULL,NULL,NULL,'B4DUF0','240','0'),
('B4DUG0_HUMAN',NULL,'PAK4',NULL,'B4DUG0','240','0'),
('B4DV01_HUMAN',NULL,NULL,NULL,'B4DV01','251','0'),
('B4DV02_HUMAN',NULL,NULL,NULL,'B4DV02','524','0'),
('B4DV85_HUMAN',NULL,NULL,NULL,'B4DV85','472','0'),
('B4DV95_HUMAN',NULL,NULL,NULL,'B4DV95','435','0'),
('B4DVN6_HUMAN',NULL,NULL,NULL,'B4DVN6','226','0'),
('B4DVP5_HUMAN','Fibroblast growth factor receptor',NULL,'2.7.10.1','B4DVP5','734','0'),
('B4DVS7_HUMAN',NULL,NULL,NULL,'B4DVS7','352','0'),
('B4DVT5_HUMAN',NULL,NULL,NULL,'B4DVT5','320','0'),
('B4DW31_HUMAN',NULL,NULL,NULL,'B4DW31','515','0'),
('B4DW95_HUMAN',NULL,NULL,NULL,'B4DW95','460','0'),
('B4DWB2_HUMAN',NULL,NULL,NULL,'B4DWB2','485','0'),
('B4DWX2_HUMAN',NULL,NULL,NULL,'B4DWX2','581','0'),
('B4DX02_HUMAN',NULL,NULL,NULL,'B4DX02','535','0'),
('B4DX16_HUMAN',NULL,NULL,NULL,'B4DX16','335','0'),
('B4DX68_HUMAN',NULL,'PBK',NULL,'B4DX68','333','0'),
('B4DXU2_HUMAN',NULL,NULL,NULL,'B4DXU2','374','0'),
('B4DXY6_HUMAN',NULL,NULL,NULL,'B4DXY6','213','0'),
('B4DXZ7_HUMAN',NULL,NULL,NULL,'B4DXZ7','356','0'),
('B4DY26_HUMAN',NULL,'TGFBR1',NULL,'B4DY26','434','0'),
('B4DY49_HUMAN',NULL,'FRK',NULL,'B4DY49','363','0'),
('B4DYG2_HUMAN',NULL,NULL,NULL,'B4DYG2','1065','0'),
('B4DYR0_HUMAN',NULL,NULL,NULL,'B4DYR0','484','0'),
('B4DYV1_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','B4DYV1','983','0'),
('B4DZ33_HUMAN',NULL,NULL,NULL,'B4DZ33','1281','0'),
('B4DZC9_HUMAN',NULL,NULL,NULL,'B4DZC9','1048','0'),
('B4DZE2_HUMAN',NULL,NULL,NULL,'B4DZE2','530','0'),
('B4DZM6_HUMAN',NULL,'PKMYT1',NULL,'B4DZM6','568','0'),
('B4DZQ5_HUMAN',NULL,NULL,NULL,'B4DZQ5','993','0'),
('B4DZS7_HUMAN',NULL,NULL,NULL,'B4DZS7','536','0'),
('B4DZU0_HUMAN',NULL,'NEK2',NULL,'B4DZU0','402','0'),
('B4E058_HUMAN',NULL,NULL,NULL,'B4E058','279','0'),
('B4E083_HUMAN',NULL,NULL,NULL,'B4E083','506','0'),
('B4E0A7_HUMAN',NULL,NULL,NULL,'B4E0A7','503','0'),
('B4E0D4_HUMAN',NULL,NULL,NULL,'B4E0D4','329','0'),
('B4E0G1_HUMAN',NULL,NULL,NULL,'B4E0G1','358','0'),
('B4E0I7_HUMAN',NULL,NULL,NULL,'B4E0I7','405','0'),
('B4E0K5_HUMAN',NULL,'MAPK14',NULL,'B4E0K5','283','0'),
('B4E0X2_HUMAN',NULL,'RAF1',NULL,'B4E0X2','567','0'),
('B4E0Y5_HUMAN',NULL,NULL,NULL,'B4E0Y5','672','0'),
('B4E0Y9_HUMAN',NULL,'MST4',NULL,'B4E0Y9','438','0'),
('B4E104_HUMAN',NULL,NULL,NULL,'B4E104','458','0'),
('B4E110_HUMAN',NULL,NULL,NULL,'B4E110','222','0'),
('B4E123_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','B4E123','934','0'),
('B4E125_HUMAN',NULL,NULL,NULL,'B4E125','497','0'),
('B4E185_HUMAN',NULL,NULL,NULL,'B4E185','332','0'),
('B4E1D9_HUMAN',NULL,NULL,NULL,'B4E1D9','228','0'),
('B4E1N6_HUMAN',NULL,'RAF1',NULL,'B4E1N6','433','0'),
('B4E2L0_HUMAN',NULL,NULL,NULL,'B4E2L0','398','0'),
('B4E2M4_HUMAN',NULL,NULL,NULL,'B4E2M4','1275','0'),
('B4E2S6_HUMAN',NULL,NULL,NULL,'B4E2S6','397','0'),
('B4E359_HUMAN',NULL,NULL,NULL,'B4E359','336','0'),
('B4E3B5_HUMAN',NULL,NULL,NULL,'B4E3B5','347','0'),
('B4E3D9_HUMAN',NULL,NULL,NULL,'B4E3D9','772','0'),
('B4E3J8_HUMAN',NULL,'STK38L',NULL,'B4E3J8','371','0'),
('B5BTY5_HUMAN',NULL,'MAPK13',NULL,'B5BTY5','365','0'),
('B5BU16_HUMAN',NULL,'MAP2K6',NULL,'B5BU16','334','0'),
('B5BU33_HUMAN',NULL,'LIMK2',NULL,'B5BU33','638','0'),
('B5BU41_HUMAN',NULL,'CAMK1',NULL,'B5BU41','370','0'),
('B5BU52_HUMAN',NULL,'CSK',NULL,'B5BU52','450','0'),
('B5BU53_HUMAN',NULL,'CDK9',NULL,'B5BU53','372','0'),
('B5BU64_HUMAN',NULL,'MKNK1',NULL,'B5BU64','424','0'),
('B5BU77_HUMAN','Protein kinase C eta type,PKC-L,nPKC-eta','PRKCH','2.7.11.13','B5BU77','683','0'),
('B5BUB8_HUMAN',NULL,'MAPK8',NULL,'B5BUB8','384','0'),
('B5BUC0_HUMAN',NULL,'GSK3B',NULL,'B5BUC0','420','0'),
('B5BUG9_HUMAN',NULL,'BMPR1A',NULL,'B5BUG9','532','0'),
('B5BUH5_HUMAN',NULL,'CSNK2A1',NULL,'B5BUH5','391','0'),
('B5BUJ6_HUMAN',NULL,'MKNK1',NULL,'B5BUJ6','424','0'),
('B5BUJ7_HUMAN',NULL,'MAPK9',NULL,'B5BUJ7','424','0'),
('B5BUJ8_HUMAN',NULL,'MAPKAPK3',NULL,'B5BUJ8','382','0'),
('B5BUK7_HUMAN',NULL,'PRKCI',NULL,'B5BUK7','587','0'),
('B5MC51_HUMAN',NULL,'LIMK2',NULL,'B5MC51','629','0'),
('B5MCX4_HUMAN',NULL,'TRIB2',NULL,'B5MCX4','252','0'),
('B5MDL5_HUMAN',NULL,'MAPK12',NULL,'B5MDL5','277','0'),
('B5TY32_HUMAN',NULL,'MAPK14',NULL,'B5TY32','256','0'),
('B5TY33_HUMAN',NULL,'MAPK14',NULL,'B5TY33','173','0'),
('B6D4Y1_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y1','1620','0'),
('B6D4Y2_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y2','1620','0'),
('B6D4Y3_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y3','1620','0'),
('B6D4Y5_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y5','1620','0'),
('B6D4Y6_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y6','1620','0'),
('B6D4Y7_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y7','1620','0'),
('B6D4Y8_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','B6D4Y8','1620','0'),
('B6EXY3_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','B6EXY3','1097','0'),
('B6EXY4_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','B6EXY4','632','0'),
('B6EXY5_HUMAN','Tyrosine-protein kinase receptor',NULL,'2.7.10.1','B6EXY5','671','0'),
('B7Z1G1_HUMAN',NULL,NULL,NULL,'B7Z1G1','288','0'),
('B7Z1I0_HUMAN',NULL,'ILK',NULL,'B7Z1I0','318','0'),
('B7Z1Z1_HUMAN',NULL,NULL,NULL,'B7Z1Z1','308','0'),
('B7Z1Z6_HUMAN',NULL,'CAMK2B',NULL,'B7Z1Z6','305','0'),
('B7Z2B0_HUMAN',NULL,NULL,NULL,'B7Z2B0','533','0'),
('B7Z2I3_HUMAN',NULL,NULL,NULL,'B7Z2I3','1157','0'),
('B7Z2K7_HUMAN',NULL,NULL,NULL,'B7Z2K7','594','0'),
('B7Z2T7_HUMAN',NULL,NULL,NULL,'B7Z2T7','619','0'),
('B7Z2X1_HUMAN',NULL,NULL,NULL,'B7Z2X1','291','0'),
('B7Z2Y5_HUMAN','Ribosomal protein S6 kinase','RPS6KA5','2.7.11.1','B7Z2Y5','723','0'),
('B7Z302_HUMAN',NULL,NULL,NULL,'B7Z302','258','0'),
('B7Z325_HUMAN',NULL,NULL,NULL,'B7Z325','387','0'),
('B7Z388_HUMAN',NULL,NULL,NULL,'B7Z388','1279','0'),
('B7Z3B5_HUMAN',NULL,'RPS6KA2',NULL,'B7Z3B5','644','0'),
('B7Z3K0_HUMAN',NULL,NULL,NULL,'B7Z3K0','455','0'),
('B7Z3V5_HUMAN',NULL,NULL,NULL,'B7Z3V5','1235','0'),
('B7Z3V9_HUMAN',NULL,NULL,NULL,'B7Z3V9','512','0'),
('B7Z3W6_HUMAN','Protein kinase C',NULL,'2.7.11.13','B7Z3W6','710','0'),
('B7Z418_HUMAN',NULL,'ILK',NULL,'B7Z418','391','0'),
('B7Z454_HUMAN',NULL,NULL,NULL,'B7Z454','554','0'),
('B7Z474_HUMAN',NULL,NULL,NULL,'B7Z474','1137','0'),
('B7Z4Y7_HUMAN','Guanylate cyclase',NULL,'4.6.1.2','B7Z4Y7','540','0'),
('B7Z537_HUMAN',NULL,NULL,NULL,'B7Z537','386','0'),
('B7Z5H7_HUMAN',NULL,NULL,NULL,'B7Z5H7','546','0'),
('B7Z5K4_HUMAN',NULL,NULL,NULL,'B7Z5K4','433','0'),
('B7Z5R1_HUMAN',NULL,'AKT1',NULL,'B7Z5R1','418','0'),
('B7Z5U3_HUMAN',NULL,'PHKG1',NULL,'B7Z5U3','333','0'),
('B7Z6Q8_HUMAN',NULL,'EPHA4',NULL,'B7Z6Q8','935','0'),
('B7Z6U2_HUMAN',NULL,NULL,NULL,'B7Z6U2','378','0'),
('B7Z6W7_HUMAN',NULL,NULL,NULL,'B7Z6W7','463','0'),
('B7Z708_HUMAN',NULL,NULL,NULL,'B7Z708','230','0'),
('B7Z7D1_HUMAN',NULL,NULL,NULL,'B7Z7D1','378','0'),
('B7Z7J1_HUMAN',NULL,'STK32C',NULL,'B7Z7J1','499','0'),
('B7Z7K5_HUMAN',NULL,NULL,NULL,'B7Z7K5','347','0'),
('B7Z7R6_HUMAN',NULL,NULL,NULL,'B7Z7R6','1288','0'),
('B7Z7U4_HUMAN','Tyrosine-protein kinase receptor','NTRK3','2.7.10.1','B7Z7U4','617','0'),
('B7Z7V7_HUMAN',NULL,'PASK',NULL,'B7Z7V7','1107','0'),
('B7Z7X0_HUMAN',NULL,NULL,NULL,'B7Z7X0','721','0'),
('B7Z8N6_HUMAN',NULL,'CLK2',NULL,'B7Z8N6','271','0'),
('B7Z8Q0_HUMAN',NULL,'PRKCG',NULL,'B7Z8Q0','548','0'),
('B7Z8T0_HUMAN',NULL,NULL,NULL,'B7Z8T0','601','0'),
('B7Z9H7_HUMAN',NULL,'STK32A',NULL,'B7Z9H7','407','0'),
('B7Z9Y5_HUMAN',NULL,NULL,NULL,'B7Z9Y5','281','0'),
('B7ZA00_HUMAN',NULL,NULL,NULL,'B7ZA00','314','0'),
('B7ZA12_HUMAN',NULL,NULL,NULL,'B7ZA12','526','0'),
('B7ZA25_HUMAN',NULL,'PRKG2',NULL,'B7ZA25','342','0'),
('B7ZA62_HUMAN',NULL,NULL,NULL,'B7ZA62','271','0'),
('B7ZAN7_HUMAN',NULL,NULL,NULL,'B7ZAN7','540','0'),
('B7ZAU7_HUMAN',NULL,'RIPK4',NULL,'B7ZAU7','721','0'),
('B7ZB17_HUMAN',NULL,'RPS6KA3',NULL,'B7ZB17','712','0'),
('B7ZBF6_HUMAN',NULL,'CHEK2',NULL,'B7ZBF6','299','0'),
('B7ZKJ3_HUMAN',NULL,'EPHA5',NULL,'B7ZKJ3','1038','0'),
('B7ZKK7_HUMAN',NULL,'EIF2AK2',NULL,'B7ZKK7','546','0'),
('B7ZKW7_HUMAN',NULL,'EPHA5',NULL,'B7ZKW7','1016','0'),
('B7ZKY2_HUMAN',NULL,'CASK',NULL,'B7ZKY2','897','0'),
('B7ZL31_HUMAN',NULL,'CLK4',NULL,'B7ZL31','373','0'),
('B7ZL90_HUMAN','Ribosomal protein S6 kinase','RPS6KA6','2.7.11.1','B7ZL90','745','0'),
('B7ZLC4_HUMAN',NULL,'AAK1',NULL,'B7ZLC4','863','0'),
('B7ZM71_HUMAN',NULL,'MYO3B',NULL,'B7ZM71','1341','0'),
('B7ZMH9_HUMAN',NULL,'YSK4,MAP3K19',NULL,'B7ZMH9','460','0'),
('B7ZVY7_HUMAN',NULL,'CDC2L1',NULL,'B7ZVY7','782','0'),
('B8ZZI5_HUMAN',NULL,'STK16',NULL,'B8ZZI5','273','0'),
('B8ZZN3_HUMAN',NULL,'STK16',NULL,'B8ZZN3','350','0'),
('B8ZZR0_HUMAN',NULL,'CLK1',NULL,'B8ZZR0','307','0'),
('B9A038_HUMAN',NULL,'SPEG',NULL,'B9A038','2475','0'),
('B9EG64_HUMAN',NULL,'CLK4',NULL,'B9EG64','481','0'),
('B9EGA7_HUMAN',NULL,'CDC42BPA',NULL,'B9EGA7','1699','0'),
('B9EIS4_HUMAN',NULL,'GRK1',NULL,'B9EIS4','563','0'),
('BLK_HUMAN','Tyrosine-protein kinase Blk,B lymphocyte kinase,p55-Blk','BLK','2.7.10.2','P51451','505','1'),
('BMP2K_HUMAN','BMP-2-inducible protein kinase,BIKe','BMP2K,BIKE','2.7.11.1','Q9NSY1','1161','1'),
('BMPR2_HUMAN','Bone morphogenetic protein receptor type-2,BMP type-2 receptor,BMPR-2,Bone morphogenetic protein receptor type II,BMP type II receptor,BMPR-II','BMPR2,PPH1','2.7.11.30','Q13873','1038','1'),
('BMR1A_HUMAN','Bone morphogenetic protein receptor type-1A,BMP type-1A receptor,BMPR-1A,Activin receptor-like kinase 3,ALK-3,Serine/threonine-protein kinase receptor R5,SKR5','BMPR1A,ACVRLK3, ALK3','2.7.11.30','P36894','532','1'),
('BMR1B_HUMAN','Bone morphogenetic protein receptor type-1B,BMP type-1B receptor,BMPR-1B','BMPR1B','2.7.11.30','O00238','502','1'),
('BMX_HUMAN','Cytoplasmic tyrosine-protein kinase BMX,Bone marrow tyrosine kinase gene in chromosome X protein,Epithelial and endothelial tyrosine kinase,ETK,NTK38','BMX','2.7.10.2','P51813','675','1'),
('BRAF_HUMAN','Serine/threonine-protein kinase B-raf,Proto-oncogene B-Raf,p94,v-Raf murine sarcoma viral oncogene homolog B1','BRAF,BRAF1, RAFB1','2.7.11.1','P15056','766','2'),
('BRSK1_HUMAN','Serine/threonine-protein kinase BRSK1,Brain-selective kinase 1,Brain-specific serine/threonine-protein kinase 1,BR serine/threonine-protein kinase 1,Serine/threonine-protein kinase SAD-B,Synapses of Amphids Defective homolog 1,SAD1 homolog,hSAD1','BRSK1,KIAA1811, SAD1, SADB','2.7.11.1,2.7.11.26','Q8TDC3','778','1'),
('BRSK2_HUMAN','Serine/threonine-protein kinase BRSK2,Brain-selective kinase 2,Brain-specific serine/threonine-protein kinase 2,BR serine/threonine-protein kinase 2,Serine/threonine-protein kinase 29,Serine/threonine-protein kinase SAD-A','BRSK2,C11orf7, PEN11B, SADA, STK29','2.7.11.1,2.7.11.26','Q8IWQ3','736','1'),
('BTK_HUMAN','Tyrosine-protein kinase BTK,Agammaglobulinemia tyrosine kinase,ATK,B-cell progenitor kinase,BPK,Bruton tyrosine kinase','BTK,AGMX1, ATK, BPK','2.7.10.2','Q06187','659','1'),
('BUB1B_HUMAN','Mitotic checkpoint serine/threonine-protein kinase BUB1 beta,MAD3/BUB1-related protein kinase,hBUBR1,Mitotic checkpoint kinase MAD3L,Protein SSK1','BUB1B,BUBR1, MAD3L, SSK1','2.7.11.1','O60566','1050','1'),
('BUB1_HUMAN','Mitotic checkpoint serine/threonine-protein kinase BUB1,hBUB1,BUB1A','BUB1,BUB1L','2.7.11.1','O43683','1085','1'),
('C0JYZ2_HUMAN',NULL,'TTN',NULL,'C0JYZ2','33423','0'),
('C0LYZ4_HUMAN',NULL,NULL,NULL,'C0LYZ4','215','0'),
('C1PHA0_HUMAN','Tyrosine-protein kinase receptor','EML4-ALK','2.7.10.1','C1PHA0','1082','0'),
('C1PHA1_HUMAN','Tyrosine-protein kinase receptor','EML4-ALK','2.7.10.1','C1PHA1','1105','0'),
('C1PHA2_HUMAN','Tyrosine-protein kinase receptor','KIF5B-ALK','2.7.10.1','C1PHA2','1483','0'),
('C7DUW4_HUMAN',NULL,'MAP2K3',NULL,'C7DUW4','346','0'),
('C7TPG7_HUMAN',NULL,'SRGAP3:RAF1',NULL,'C7TPG7','831','0'),
('C9IYV2_HUMAN',NULL,'CAMK1G',NULL,'C9IYV2','245','0'),
('C9J185_HUMAN',NULL,'EIF2AK3',NULL,'C9J185','956','0'),
('C9J1X3_HUMAN',NULL,'TNK2',NULL,'C9J1X3','1040','0'),
('C9J232_HUMAN',NULL,'STK25',NULL,'C9J232','177','0'),
('C9J319_HUMAN',NULL,'STK33',NULL,'C9J319','215','0'),
('C9J338_HUMAN',NULL,'TNIK',NULL,'C9J338','350','0'),
('C9J5X1_HUMAN','Tyrosine-protein kinase receptor','IGF1R','2.7.10.1','C9J5X1','1366','0'),
('C9J6L2_HUMAN',NULL,'STK25',NULL,'C9J6L2','161','0'),
('C9J840_HUMAN',NULL,'MAP4K4',NULL,'C9J840','1042','0'),
('C9J8E1_HUMAN',NULL,'MAPKAPK3',NULL,'C9J8E1','332','0'),
('C9J8V9_HUMAN',NULL,'PIM2',NULL,'C9J8V9','145','0'),
('C9J9E2_HUMAN',NULL,'CAMKV',NULL,'C9J9E2','434','0'),
('C9JB09_HUMAN',NULL,'PNCK',NULL,'C9JB09','224','0'),
('C9JCC0_HUMAN',NULL,'STK25',NULL,'C9JCC0','163','0'),
('C9JCU6_HUMAN',NULL,'MAP4K2',NULL,'C9JCU6','307','0'),
('C9JDA4_HUMAN',NULL,'STK36',NULL,'C9JDA4','278','0'),
('C9JDH9_HUMAN',NULL,'STK25',NULL,'C9JDH9','148','0'),
('C9JGD6_HUMAN',NULL,'WNK2',NULL,'C9JGD6','779','0'),
('C9JIG9_HUMAN',NULL,'OXSR1',NULL,'C9JIG9','468','0'),
('C9JJ18_HUMAN',NULL,'PNCK',NULL,'C9JJ18','226','0'),
('C9JMC3_HUMAN',NULL,'MYLK4',NULL,'C9JMC3','388','0'),
('C9JQR6_HUMAN',NULL,'PTK7',NULL,'C9JQR6','257','0'),
('C9JSU7_HUMAN',NULL,'STRADB',NULL,'C9JSU7','194','0'),
('C9JUK9_HUMAN',NULL,'MAPK7',NULL,'C9JUK9','241','0'),
('C9JV82_HUMAN',NULL,'STK32A',NULL,'C9JV82','166','0'),
('C9JWR9_HUMAN',NULL,'PDPK1',NULL,'C9JWR9','532','0'),
('C9JXA2_HUMAN',NULL,'EPHA3',NULL,'C9JXA2','918','0'),
('CAMKV_HUMAN','CaM kinase-like vesicle-associated protein','CAMKV',NULL,'Q8NCB2','501','1'),
('CD11A_HUMAN','Cyclin-dependent kinase 11A,Cell division cycle 2-like protein kinase 2,Cell division protein kinase 11A,Galactosyltransferase-associated protein kinase p58/GTA,PITSLRE serine/threonine-protein kinase CDC2L2','CDK11A,CDC2L2, CDC2L3, PITSLREB','2.7.11.22','Q9UQ88','783','1'),
('CD11B_HUMAN','Cyclin-dependent kinase 11B,Cell division cycle 2-like protein kinase 1,CLK-1,Cell division protein kinase 11B,Galactosyltransferase-associated protein kinase p58/GTA,PITSLRE serine/threonine-protein kinase CDC2L1,p58 CLK-1','CDK11B,CDC2L1, CDK11, PITSLREA, PK58','2.7.11.22','P21127','795','1'),
('CDC7_HUMAN','Cell division cycle 7-related protein kinase,CDC7-related kinase,HsCdc7,huCdc7','CDC7,CDC7L1','2.7.11.1','O00311','574','1'),
('CDK10_HUMAN','Cyclin-dependent kinase 10,Cell division protein kinase 10,Serine/threonine-protein kinase PISSLRE','CDK10','2.7.11.22','Q15131','360','1'),
('CDK12_HUMAN','Cyclin-dependent kinase 12,Cdc2-related kinase, arginine/serine-rich,CrkRS,Cell division cycle 2-related protein kinase 7,CDC2-related protein kinase 7,Cell division protein kinase 12,hCDK12','CDK12,CRK7, CRKRS, KIAA0904','2.7.11.22,2.7.11.23','Q9NYV4','1490','1'),
('CDK13_HUMAN','Cyclin-dependent kinase 13,CDC2-related protein kinase 5,Cell division cycle 2-like protein kinase 5,Cell division protein kinase 13,hCDK13,Cholinesterase-related cell division controller','CDK13,CDC2L, CDC2L5, CHED, KIAA1791','2.7.11.22,2.7.11.23','Q14004','1512','1'),
('CDK14_HUMAN','Cyclin-dependent kinase 14,Cell division protein kinase 14,Serine/threonine-protein kinase PFTAIRE-1,hPFTAIRE1','CDK14,KIAA0834, PFTK1','2.7.11.22','O94921','469','1'),
('CDK15_HUMAN','Cyclin-dependent kinase 15,Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 7 protein,Cell division protein kinase 15,Serine/threonine-protein kinase ALS2CR7,Serine/threonine-protein kinase PFTAIRE-2','CDK15,ALS2CR7, PFTK2','2.7.11.22','Q96Q40','435','1'),
('CDK16_HUMAN','Cyclin-dependent kinase 16,Cell division protein kinase 16,PCTAIRE-motif protein kinase 1,Serine/threonine-protein kinase PCTAIRE-1','CDK16,PCTAIRE1, PCTK1','2.7.11.22','Q00536','496','1'),
('CDK17_HUMAN','Cyclin-dependent kinase 17,Cell division protein kinase 17,PCTAIRE-motif protein kinase 2,Serine/threonine-protein kinase PCTAIRE-2','CDK17,PCTAIRE2, PCTK2','2.7.11.22','Q00537','523','1'),
('CDK18_HUMAN','Cyclin-dependent kinase 18,Cell division protein kinase 18,PCTAIRE-motif protein kinase 3,Serine/threonine-protein kinase PCTAIRE-3','CDK18,PCTAIRE3, PCTK3','2.7.11.22','Q07002','472','1'),
('CDK19_HUMAN','Cyclin-dependent kinase 19,CDC2-related protein kinase 6,Cell division cycle 2-like protein kinase 6,Cell division protein kinase 19,Cyclin-dependent kinase 11,Death-preventing kinase','CDK19,CDC2L6, CDK11, KIAA1028','2.7.11.22','Q9BWU1','502','1'),
('CDK1_HUMAN','Cyclin-dependent kinase 1,CDK1,Cell division control protein 2 homolog,Cell division protein kinase 1,p34 protein kinase','CDK1,CDC2, CDC28A, CDKN1, P34CDC2','2.7.11.22,2.7.11.23','P06493','297','1'),
('CDK20_HUMAN','Cyclin-dependent kinase 20,CDK-activating kinase p42,CAK-kinase p42,Cell cycle-related kinase,Cell division protein kinase 20,Cyclin-dependent protein kinase H,Cyclin-kinase-activating kinase p42','CDK20,CCRK, CDCH','2.7.11.22','Q8IZL9','346','1'),
('CDK2_HUMAN','Cyclin-dependent kinase 2,Cell division protein kinase 2,p33 protein kinase','CDK2,CDKN2','2.7.11.22','P24941','298','1'),
('CDK3_HUMAN','Cyclin-dependent kinase 3,Cell division protein kinase 3','CDK3,CDKN3','2.7.11.22','Q00526','305','1'),
('CDK4_HUMAN','Cyclin-dependent kinase 4,Cell division protein kinase 4,PSK-J3','CDK4','2.7.11.22','P11802','303','1'),
('CDK5_HUMAN','Cyclin-dependent kinase 5,Cell division protein kinase 5,Serine/threonine-protein kinase PSSALRE,Tau protein kinase II catalytic subunit,TPKII catalytic subunit','CDK5,CDKN5','2.7.11.22','Q00535','292','1'),
('CDK6_HUMAN','Cyclin-dependent kinase 6,Cell division protein kinase 6,Serine/threonine-protein kinase PLSTIRE','CDK6,CDKN6','2.7.11.22','Q00534','326','1'),
('CDK7_HUMAN','Cyclin-dependent kinase 7,39 kDa protein kinase,p39 Mo15,CDK-activating kinase 1,Cell division protein kinase 7,Serine/threonine-protein kinase 1,TFIIH basal transcription factor complex kinase subunit','CDK7,CAK, CAK1, CDKN7, MO15, STK1','2.7.11.22,2.7.11.23','P50613','346','1'),
('CDK8_HUMAN','Cyclin-dependent kinase 8,Cell division protein kinase 8,Mediator complex subunit CDK8,Mediator of RNA polymerase II transcription subunit CDK8,Protein kinase K35','CDK8','2.7.11.22,2.7.11.23','P49336','464','1'),
('CDK9_HUMAN','Cyclin-dependent kinase 9,C-2K,Cell division cycle 2-like protein kinase 4,Cell division protein kinase 9,Serine/threonine-protein kinase PITALRE,Tat-associated kinase complex catalytic subunit','CDK9,CDC2L4, TAK','2.7.11.22,2.7.11.23','P50750','372','1'),
('CDKL1_HUMAN','Cyclin-dependent kinase-like 1,Protein kinase p42 KKIALRE,Serine/threonine-protein kinase KKIALRE','CDKL1','2.7.11.22','Q00532','357','1'),
('CDKL2_HUMAN','Cyclin-dependent kinase-like 2,Protein kinase p56 KKIAMRE,Serine/threonine-protein kinase KKIAMRE','CDKL2','2.7.11.22','Q92772','493','1'),
('CDKL3_HUMAN','Cyclin-dependent kinase-like 3,Serine/threonine-protein kinase NKIAMRE','CDKL3,NKIAMRE','2.7.11.22','Q8IVW4','592','1'),
('CDKL4_HUMAN','Cyclin-dependent kinase-like 4','CDKL4','2.7.11.22','Q5MAI5','315','1'),
('CDKL5_HUMAN','Cyclin-dependent kinase-like 5,Serine/threonine-protein kinase 9','CDKL5,STK9','2.7.11.22','O76039','1030','1'),
('CHK1_HUMAN','Serine/threonine-protein kinase Chk1,CHK1 checkpoint homolog,Cell cycle checkpoint kinase,Checkpoint kinase-1','CHEK1,CHK1','2.7.11.1','O14757','476','1'),
('CHK2_HUMAN','Serine/threonine-protein kinase Chk2,CHK2 checkpoint homolog,Cds1 homolog,Hucds1,hCds1,Checkpoint kinase 2','CHEK2,CDS1, CHK2, RAD53','2.7.11.1','O96017','543','2'),
('CLK1_HUMAN','Dual specificity protein kinase CLK1,CDC-like kinase 1','CLK1,CLK','2.7.12.1','P49759','484','1'),
('CLK2_HUMAN','Dual specificity protein kinase CLK2,CDC-like kinase 2','CLK2','2.7.12.1','P49760','499','1'),
('CLK3_HUMAN','Dual specificity protein kinase CLK3,CDC-like kinase 3','CLK3','2.7.12.1','P49761','638','1'),
('CLK4_HUMAN','Dual specificity protein kinase CLK4,CDC-like kinase 4','CLK4','2.7.12.1','Q9HAZ1','481','1'),
('CSF1R_HUMAN','Macrophage colony-stimulating factor 1 receptor,CSF-1 receptor,CSF-1-R,CSF-1R,M-CSF-R,Proto-oncogene c-Fms','CSF1R,FMS','2.7.10.1','P07333','972','2'),
('CSK21_HUMAN','Casein kinase II subunit alpha,CK II alpha','CSNK2A1,CK2A1','2.7.11.1','P68400','391','1'),
('CSK22_HUMAN','Casein kinase II subunit alpha\',CK II alpha\'','CSNK2A2,CK2A2','2.7.11.1','P19784','350','1'),
('CSK23_HUMAN','Casein kinase II subunit alpha 3,CK II alpha 3,Casein kinase II alpha 1 polypeptide pseudogene','CSNK2A3,CSNK2A1P','2.7.11.1','Q8NEV1','391','1'),
('CSKP_HUMAN','Peripheral plasma membrane protein CASK,hCASK,Calcium/calmodulin-dependent serine protein kinase,Protein lin-2 homolog','CASK,LIN2','2.7.11.1','O14936','926','1'),
('CSK_HUMAN','Tyrosine-protein kinase CSK,C-Src kinase,Protein-tyrosine kinase CYL','CSK','2.7.10.2','P41240','450','1'),
('CTRO_HUMAN','Citron Rho-interacting kinase,CRIK,Serine/threonine-protein kinase 21','CIT,CRIK, KIAA0949, STK21','2.7.11.1','O14578','2027','1'),
('D1MAM0_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM0','1620','0'),
('D1MAM1_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM1','1620','0'),
('D1MAM2_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM2','1620','0'),
('D1MAM3_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM3','1620','0'),
('D1MAM4_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM4','1620','0'),
('D1MAM5_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','D1MAM5','1620','0'),
('D2CGD1_HUMAN','Fibroblast growth factor receptor',NULL,'2.7.10.1','D2CGD1','732','0'),
('D2JYI1_HUMAN',NULL,'TGFBR2',NULL,'D2JYI1','592','0'),
('D3DNT9_HUMAN',NULL,'EPHB3',NULL,'D3DNT9','956','0'),
('D3DPA4_HUMAN',NULL,'ACVR1',NULL,'D3DPA4','509','0'),
('D3DPF9_HUMAN',NULL,'TTN',NULL,'D3DPF9','26926','0'),
('D3DPG0_HUMAN',NULL,'TTN',NULL,'D3DPG0','34942','0'),
('D3DQU7_HUMAN',NULL,'STK33',NULL,'D3DQU7','514','0'),
('D3DRD3_HUMAN','Fibroblast growth factor receptor','FGFR2','2.7.10.1','D3DRD3','724','0'),
('D3DRD4_HUMAN','Fibroblast growth factor receptor','FGFR2','2.7.10.1','D3DRD4','724','0'),
('D3DRD5_HUMAN','Fibroblast growth factor receptor','FGFR2','2.7.10.1','D3DRD5','838','0'),
('D3DRD6_HUMAN',NULL,'FGFR2',NULL,'D3DRD6','384','0'),
('D3DSB5_HUMAN',NULL,'MAP4K5',NULL,'D3DSB5','584','0'),
('D3DSX2_HUMAN',NULL,'FGFR1',NULL,'D3DSX2','386','0'),
('D3DTD6_HUMAN',NULL,NULL,NULL,'D3DTD6','162','0'),
('D3DU05_HUMAN',NULL,'TLK2',NULL,'D3DU05','750','0'),
('D3DUP1_HUMAN',NULL,'WNK1',NULL,'D3DUP1','2382','0'),
('D3DUP2_HUMAN',NULL,'WNK1',NULL,'D3DUP2','2107','0'),
('D3DUX0_HUMAN',NULL,'NRK',NULL,'D3DUX0','841','0'),
('D3DVK8_HUMAN',NULL,'CAMK2B',NULL,'D3DVK8','537','0'),
('D3DW67_HUMAN',NULL,NULL,NULL,'D3DW67','257','0'),
('D3YTB5_HUMAN',NULL,'IRAK1',NULL,'D3YTB5','708','0'),
('D4Q8H0_HUMAN',NULL,'pk',NULL,'D4Q8H0','455','0'),
('D6R938_HUMAN',NULL,'CAMK2D',NULL,'D6R938','498','0'),
('D6R9G1_HUMAN',NULL,'CDK7',NULL,'D6R9G1','253','0'),
('D6RA14_HUMAN',NULL,'TXK',NULL,'D6RA14','182','0'),
('D6RAD4_HUMAN',NULL,'CDK7',NULL,'D6RAD4','309','0'),
('D6REC6_HUMAN',NULL,'CDK7',NULL,'D6REC6','149','0'),
('D6REE7_HUMAN',NULL,'ROCK2',NULL,'D6REE7','446','0'),
('D6REM4_HUMAN',NULL,'CSNK1A1',NULL,'D6REM4','236','0'),
('D6RHX8_HUMAN',NULL,'GRK6',NULL,'D6RHX8','475','0'),
('D6RJF7_HUMAN',NULL,'NEK11',NULL,'D6RJF7','212','0'),
('D6W5G0_HUMAN',NULL,'AAK1',NULL,'D6W5G0','862','0'),
('D6W660_HUMAN',NULL,'MAP2K7',NULL,'D6W660','294','0'),
('D7PBN3_HUMAN',NULL,NULL,NULL,'D7PBN3','1061','0'),
('D7PBN4_HUMAN',NULL,NULL,NULL,'D7PBN4','329','0'),
('D7R525_HUMAN',NULL,'MAPK9',NULL,'D7R525','214','0'),
('D7R526_HUMAN',NULL,'MAPK9',NULL,'D7R526','378','0'),
('D7R527_HUMAN',NULL,'MAPK9',NULL,'D7R527','378','0'),
('D7RF68_HUMAN',NULL,NULL,NULL,'D7RF68','597','0'),
('D9ZGF8_HUMAN','Rho-associated protein kinase','ROCK1','2.7.11.1','D9ZGF8','1354','0'),
('DAPK1_HUMAN','Death-associated protein kinase 1,DAP kinase 1','DAPK1,DAPK','2.7.11.1','P53355','1430','1'),
('DAPK2_HUMAN','Death-associated protein kinase 2,DAP kinase 2,DAP-kinase-related protein 1,DRP-1','DAPK2','2.7.11.1','Q9UIK4','370','1'),
('DAPK3_HUMAN','Death-associated protein kinase 3,DAP kinase 3,DAP-like kinase,Dlk,MYPT1 kinase,Zipper-interacting protein kinase,ZIP-kinase','DAPK3,ZIPK','2.7.11.1','O43293','454','1'),
('DCLK1_HUMAN','Serine/threonine-protein kinase DCLK1,Doublecortin domain-containing protein 3A,Doublecortin-like and CAM kinase-like 1,Doublecortin-like kinase 1','DCLK1,DCAMKL1, DCDC3A, KIAA0369','2.7.11.1','O15075','740','1'),
('DCLK2_HUMAN','Serine/threonine-protein kinase DCLK2,CaMK-like CREB regulatory kinase 2,CL2,CLICK-II,CLICK2,Doublecortin domain-containing protein 3B,Doublecortin-like and CAM kinase-like 2,Doublecortin-like kinase 2','DCLK2,DCAMKL2, DCDC3B, DCK2','2.7.11.1','Q8N568','766','1'),
('DCLK3_HUMAN','Serine/threonine-protein kinase DCLK3,Doublecortin domain-containing protein 3C,Doublecortin-like and CAM kinase-like 3,Doublecortin-like kinase 3','DCLK3,DCAMKL3, DCDC3C, KIAA1765','2.7.11.1','Q9C098','648','1'),
('DDR1_HUMAN','Epithelial discoidin domain-containing receptor 1,Epithelial discoidin domain receptor 1,CD167 antigen-like family member A,Cell adhesion kinase,Discoidin receptor tyrosine kinase,HGK2,Mammary carcinoma kinase 10,MCK-10,Protein-tyrosine kinase 3A,Protein-tyrosine kinase RTK-6,TRK E,Tyrosine kinase DDR,Tyrosine-protein kinase CAK','DDR1,CAK, EDDR1, NEP, NTRK4, PTK3A, RTK6, TRKE','2.7.10.1','Q08345','913','1'),
('DDR2_HUMAN','Discoidin domain-containing receptor 2,Discoidin domain receptor 2,CD167 antigen-like family member B,Discoidin domain-containing receptor tyrosine kinase 2,Neurotrophic tyrosine kinase, receptor-related 3,Receptor protein-tyrosine kinase TKT,Tyrosine-protein kinase TYRO10','DDR2,NTRKR3, TKT, TYRO10','2.7.10.1','Q16832','855','1'),
('DMPK_HUMAN','Myotonin-protein kinase,MT-PK,DM-kinase,DMK,DM1 protein kinase,DMPK,Myotonic dystrophy protein kinase','DMPK,DM1PK, MDPK','2.7.11.1','Q09013','629','1'),
('DUSTY_HUMAN','Dual serine/threonine and tyrosine protein kinase,Dusty protein kinase,Dusty PK,RIP-homologous kinase,Receptor-interacting serine/threonine-protein kinase 5,Sugen kinase 496,SgK496','DSTYK,KIAA0472, RIP5, RIPK5, SGK496','2.7.12.1','Q6XUX3','929','1'),
('DYR1A_HUMAN','Dual specificity tyrosine-phosphorylation-regulated kinase 1A,Dual specificity YAK1-related kinase,HP86,Protein kinase minibrain homolog,MNBH,hMNB','DYRK1A,DYRK, MNB, MNBH','2.7.12.1','Q13627','763','1'),
('DYR1B_HUMAN','Dual specificity tyrosine-phosphorylation-regulated kinase 1B,Minibrain-related kinase,Mirk protein kinase','DYRK1B,MIRK','2.7.12.1','Q9Y463','629','1'),
('DYRK2_HUMAN','Dual specificity tyrosine-phosphorylation-regulated kinase 2','DYRK2','2.7.12.1','Q92630','601','1'),
('DYRK3_HUMAN','Dual specificity tyrosine-phosphorylation-regulated kinase 3,Regulatory erythroid kinase,REDK','DYRK3','2.7.12.1','O43781','588','1'),
('DYRK4_HUMAN','Dual specificity tyrosine-phosphorylation-regulated kinase 4','DYRK4','2.7.12.1','Q9NR20','520','1'),
('E2AK1_HUMAN','Eukaryotic translation initiation factor 2-alpha kinase 1,Heme-controlled repressor,HCR,Heme-regulated eukaryotic initiation factor eIF-2-alpha kinase,Heme-regulated inhibitor,Hemin-sensitive initiation factor 2-alpha kinase','EIF2AK1,HRI, KIAA1369','2.7.11.1','Q9BQI3','630','1'),
('E2AK2_HUMAN','Interferon-induced, double-stranded RNA-activated protein kinase,Eukaryotic translation initiation factor 2-alpha kinase 2,eIF-2A protein kinase 2,Interferon-inducible RNA-dependent protein kinase,P1/eIF-2A protein kinase,Protein kinase RNA-activated,PKR,Tyrosine-protein kinase EIF2AK2,p68 kinase','EIF2AK2,PKR, PRKR','2.7.11.1,2.7.10.2','P19525','551','1'),
('E2AK3_HUMAN','Eukaryotic translation initiation factor 2-alpha kinase 3,PRKR-like endoplasmic reticulum kinase,Pancreatic eIF2-alpha kinase,HsPEK','EIF2AK3,PEK, PERK','2.7.11.1','Q9NZJ5','1116','1'),
('E2AK4_HUMAN','Eukaryotic translation initiation factor 2-alpha kinase 4,GCN2-like protein','EIF2AK4,GCN2, KIAA1338','2.7.11.1','Q9P2K8','1649','1'),
('E3WH17_HUMAN','Tyrosine-protein kinase receptor','SQSTM1-ALK','2.7.10.1','E3WH17','814','0'),
('E5KR05_HUMAN',NULL,NULL,NULL,'E5KR05','625','0'),
('E5KR06_HUMAN',NULL,NULL,NULL,'E5KR06','629','0'),
('E5KR07_HUMAN',NULL,'DMPK',NULL,'E5KR07','624','0'),
('E5KR08_HUMAN',NULL,'DMPK',NULL,'E5KR08','639','0'),
('E5RGN0_HUMAN',NULL,'CDK16',NULL,'E5RGN0','393','0'),
('E5RGW5_HUMAN',NULL,'IKBKB',NULL,'E5RGW5','375','0'),
('E5RI85_HUMAN',NULL,'MOK',NULL,'E5RI85','151','0'),
('E5RIU6_HUMAN',NULL,'CDK1',NULL,'E5RIU6','189','0'),
('E7BSV0_HUMAN',NULL,'EGFR',NULL,'E7BSV0','1136','0'),
('E7EML7_HUMAN',NULL,'EPHA10',NULL,'E7EML7','543','0'),
('E7EN07_HUMAN',NULL,'ACVRL1',NULL,'E7EN07','329','0'),
('E7EN19_HUMAN',NULL,'MAP4K4',NULL,'E7EN19','1272','0'),
('E7ENM8_HUMAN','Tyrosine-protein kinase','FES','2.7.10.2','E7ENM8','681','0'),
('E7ENQ1_HUMAN',NULL,'MAP4K4',NULL,'E7ENQ1','1154','0'),
('E7EPE6_HUMAN','cGMP-dependent protein kinase','PRKG2','2.7.11.12','E7EPE6','733','0'),
('E7EPP6_HUMAN',NULL,'CHEK1',NULL,'E7EPP6','492','0'),
('E7EQE4_HUMAN',NULL,'CAMK2B',NULL,'E7EQE4','173','0'),
('E7ER02_HUMAN',NULL,'EIF2AK3',NULL,'E7ER02','965','0'),
('E7ERL6_HUMAN',NULL,'MAST2',NULL,'E7ERL6','1608','0'),
('E7ESA6_HUMAN',NULL,'PTK2',NULL,'E7ESA6','1096','0'),
('E7ESS2_HUMAN',NULL,'MAP4K4',NULL,'E7ESS2','1279','0'),
('E7ET86_HUMAN',NULL,'CDKL3',NULL,'E7ET86','590','0'),
('E7ETG2_HUMAN',NULL,'ERN2',NULL,'E7ETG2','874','0'),
('E7ETM0_HUMAN',NULL,'CSNK1A1',NULL,'E7ETM0','264','0'),
('E7ETR1_HUMAN',NULL,'CAMKV',NULL,'E7ETR1','427','0'),
('E7ETV6_HUMAN',NULL,'SRPK3',NULL,'E7ETV6','634','0'),
('E7ETY4_HUMAN',NULL,'MARK2',NULL,'E7ETY4','699','0'),
('E7EU09_HUMAN','Fibroblast growth factor receptor','FGFR1','2.7.10.1','E7EU09','733','0'),
('E7EU96_HUMAN',NULL,'CSNK2A1',NULL,'E7EU96','385','0'),
('E7EUC1_HUMAN',NULL,'LIMK2',NULL,'E7EUC1','392','0'),
('E7EUK8_HUMAN',NULL,'CDK14',NULL,'E7EUK8','340','0'),
('E7EVR7_HUMAN','Fibroblast growth factor receptor','FGFR2','2.7.10.1','E7EVR7','707','0'),
('E7EWI5_HUMAN',NULL,'MAP3K15',NULL,'E7EWI5','1145','0'),
('E7EWQ5_HUMAN',NULL,'MAST4',NULL,'E7EWQ5','2444','0'),
('E7EX48_HUMAN',NULL,'NEK4',NULL,'E7EX48','722','0'),
('E7EX83_HUMAN',NULL,'MAP4K4',NULL,'E7EX83','1038','0'),
('E9PB13_HUMAN',NULL,'KSR2',NULL,'E9PB13','921','0'),
('E9PBE1_HUMAN',NULL,'PRKCZ',NULL,'E9PBE1','347','0'),
('E9PBE8_HUMAN',NULL,'CAMK2B',NULL,'E9PBE8','168','0'),
('E9PBG7_HUMAN',NULL,'CAMK2D',NULL,'E9PBG7','512','0'),
('E9PBI4_HUMAN',NULL,'PTK2B',NULL,'E9PBI4','596','0'),
('E9PBK7_HUMAN',NULL,'MAPK3',NULL,'E9PBK7','311','0'),
('E9PC47_HUMAN',NULL,'LIMK1',NULL,'E9PC47','677','0'),
('E9PC69_HUMAN',NULL,'MARK2',NULL,'E9PC69','778','0'),
('E9PD35_HUMAN',NULL,'FLT4',NULL,'E9PD35','1306','0'),
('E9PD56_HUMAN',NULL,'PXK',NULL,'E9PD56','482','0'),
('E9PEI4_HUMAN',NULL,'PTK2',NULL,'E9PEI4','680','0'),
('E9PER6_HUMAN',NULL,'PDPK1',NULL,'E9PER6','529','0'),
('E9PF82_HUMAN',NULL,'CAMK2D',NULL,'E9PF82','533','0'),
('E9PFD7_HUMAN',NULL,'EGFR',NULL,'E9PFD7','1157','0'),
('E9PG46_HUMAN',NULL,'AAK1',NULL,'E9PG46','674','0'),
('E9PG63_HUMAN',NULL,'TIE1',NULL,'E9PG63','783','0'),
('E9PG71_HUMAN',NULL,'EPHA4',NULL,'E9PG71','949','0'),
('E9PGR2_HUMAN',NULL,'GAK',NULL,'E9PGR2','1232','0'),
('E9PGT3_HUMAN','Ribosomal protein S6 kinase','RPS6KA1','2.7.11.1','E9PGT3','724','0'),
('E9PHI8_HUMAN',NULL,'NEK11',NULL,'E9PHI8','540','0'),
('E9PHX8_HUMAN',NULL,'MERTK',NULL,'E9PHX8','823','0'),
('E9PIX7_HUMAN',NULL,'NEK5',NULL,'E9PIX7','295','0'),
('E9PJF0_HUMAN',NULL,'MAPK3',NULL,'E9PJF0','316','0'),
('E9PJI4_HUMAN',NULL,'CHEK1',NULL,'E9PJI4','170','0'),
('E9PJN1_HUMAN','Ribosomal protein S6 kinase','RPS6KA4','2.7.11.1','E9PJN1','765','0'),
('E9PJX5_HUMAN',NULL,'BLK',NULL,'E9PJX5','434','0'),
('E9PK59_HUMAN',NULL,'SCYL1',NULL,'E9PK59','780','0'),
('E9PKQ3_HUMAN',NULL,'CHEK1',NULL,'E9PKQ3','204','0'),
('E9PLM7_HUMAN',NULL,'BRSK2',NULL,'E9PLM7','614','0'),
('E9PM17_HUMAN',NULL,'PAK1',NULL,'E9PM17','455','0'),
('E9PM19_HUMAN','Tyrosine-protein kinase','TYK2','2.7.10.2','E9PM19','1002','0'),
('E9PPA5_HUMAN',NULL,'CHEK1',NULL,'E9PPA5','192','0'),
('E9PPF2_HUMAN',NULL,'TYK2',NULL,'E9PPF2','921','0'),
('E9PQ51_HUMAN',NULL,'WEE1',NULL,'E9PQ51','162','0'),
('E9PQW4_HUMAN',NULL,'MAPK3',NULL,'E9PQW4','339','0'),
('E9PR11_HUMAN',NULL,'NRBP2',NULL,'E9PR11','232','0'),
('E9PR89_HUMAN',NULL,'SGK1',NULL,'E9PR89','387','0'),
('E9PRI4_HUMAN','Ribosomal protein S6 kinase','RPS6KA1','2.7.11.1','E9PRI4','719','0'),
('E9PRU3_HUMAN',NULL,'WEE1',NULL,'E9PRU3','214','0'),
('E9PRV7_HUMAN',NULL,'ADRBK1',NULL,'E9PRV7','408','0'),
('E9PS17_HUMAN',NULL,'SCYL1',NULL,'E9PS17','775','0'),
('EGFR_HUMAN','Epidermal growth factor receptor,Proto-oncogene c-ErbB-1,Receptor tyrosine-protein kinase erbB-1','EGFR,ERBB, ERBB1, HER1','2.7.10.1','P00533','1210','2'),
('EPHA1_HUMAN','Ephrin type-A receptor 1,hEpha1,EPH tyrosine kinase,EPH tyrosine kinase 1,Erythropoietin-producing hepatoma receptor,Tyrosine-protein kinase receptor EPH','EPHA1,EPH, EPHT, EPHT1','2.7.10.1','P21709','976','1'),
('EPHA2_HUMAN','Ephrin type-A receptor 2,Epithelial cell kinase,Tyrosine-protein kinase receptor ECK','EPHA2,ECK','2.7.10.1','P29317','976','2'),
('EPHA3_HUMAN','Ephrin type-A receptor 3,EPH-like kinase 4,EK4,hEK4,HEK,Human embryo kinase,Tyrosine-protein kinase TYRO4,Tyrosine-protein kinase receptor ETK1,Eph-like tyrosine kinase 1','EPHA3,ETK, ETK1, HEK, TYRO4','2.7.10.1','P29320','983','1'),
('EPHA4_HUMAN','Ephrin type-A receptor 4,EPH-like kinase 8,EK8,hEK8,Tyrosine-protein kinase TYRO1,Tyrosine-protein kinase receptor SEK','EPHA4,HEK8, SEK, TYRO1','2.7.10.1','P54764','986','1'),
('EPHA5_HUMAN','Ephrin type-A receptor 5,Brain-specific kinase,EPH homology kinase 1,EHK-1,EPH-like kinase 7,EK7,hEK7','EPHA5,BSK, EHK1, HEK7, TYRO4','2.7.10.1','P54756','1037','2'),
('EPHA6_HUMAN','Ephrin type-A receptor 6,EPH homology kinase 2,EHK-2,EPH-like kinase 12,EK12','EPHA6,EHK2, HEK12','2.7.10.1','Q9UF33','1036','1'),
('EPHA7_HUMAN','Ephrin type-A receptor 7,EPH homology kinase 3,EHK-3,EPH-like kinase 11,EK11,hEK11','EPHA7,EHK3, HEK11','2.7.10.1','Q15375','998','1'),
('EPHA8_HUMAN','Ephrin type-A receptor 8,EPH- and ELK-related kinase,EPH-like kinase 3,EK3,hEK3,Tyrosine-protein kinase receptor EEK','EPHA8,EEK, HEK3, KIAA1459','2.7.10.1','P29322','1005','1'),
('EPHAA_HUMAN','Ephrin type-A receptor 10','EPHA10','2.7.10.1','Q5JZY3','1008','1'),
('EPHB1_HUMAN','Ephrin type-B receptor 1,ELK,EPH tyrosine kinase 2,EPH-like kinase 6,EK6,hEK6,Neuronally-expressed EPH-related tyrosine kinase,NET,Tyrosine-protein kinase receptor EPH-2','EPHB1,ELK, EPHT2, HEK6, NET','2.7.10.1','P54762','984','1'),
('EPHB2_HUMAN','Ephrin type-B receptor 2,Developmentally-regulated Eph-related tyrosine kinase,ELK-related tyrosine kinase,EPH tyrosine kinase 3,EPH-like kinase 5,EK5,hEK5,Renal carcinoma antigen NY-REN-47,Tyrosine-protein kinase TYRO5,Tyrosine-protein kinase receptor EPH-3','EPHB2,DRT, EPHT3, EPTH3, ERK, HEK5, TYRO5','2.7.10.1','P29323','1055','1'),
('EPHB3_HUMAN','Ephrin type-B receptor 3,EPH-like tyrosine kinase 2,EPH-like kinase 2,Embryonic kinase 2,EK2,hEK2,Tyrosine-protein kinase TYRO6','EPHB3,ETK2, HEK2, TYRO6','2.7.10.1','P54753','998','1'),
('EPHB4_HUMAN','Ephrin type-B receptor 4,Hepatoma transmembrane kinase,Tyrosine-protein kinase TYRO11','EPHB4,HTK, MYK1, TYRO11','2.7.10.1','P54760','987','1'),
('EPHB6_HUMAN','Ephrin type-B receptor 6,HEP,Tyrosine-protein kinase-defective receptor EPH-6','EPHB6',NULL,'O15197','1021','1'),
('ERBB2_HUMAN','Receptor tyrosine-protein kinase erbB-2,Metastatic lymph node gene 19 protein,MLN 19,Proto-oncogene Neu,Proto-oncogene c-ErbB-2,Tyrosine kinase-type cell surface receptor HER2,p185erbB2','ERBB2,HER2, MLN19, NEU, NGL','2.7.10.1','P04626','1255','2'),
('ERBB3_HUMAN','Receptor tyrosine-protein kinase erbB-3,Proto-oncogene-like protein c-ErbB-3,Tyrosine kinase-type cell surface receptor HER3','ERBB3,HER3','2.7.10.1','P21860','1342','1'),
('ERBB4_HUMAN','Receptor tyrosine-protein kinase erbB-4,Proto-oncogene-like protein c-ErbB-4,Tyrosine kinase-type cell surface receptor HER4,p180erbB4,ERBB4 intracellular domain,4ICD,E4ICD,s80HER4','ERBB4,HER4','2.7.10.1','Q15303','1308','1'),
('ERN1_HUMAN','Serine/threonine-protein kinase/endoribonuclease IRE1,Endoplasmic reticulum-to-nucleus signaling 1,Inositol-requiring protein 1,hIRE1p,Ire1-alpha,IRE1a,Serine/threonine-protein kinase,Endoribonuclease','ERN1,IRE1','2.7.11.1,3.1.26.-','O75460','977','1'),
('ERN2_HUMAN','Serine/threonine-protein kinase/endoribonuclease IRE2,Endoplasmic reticulum-to-nucleus signaling 2,Inositol-requiring protein 2,hIRE2p,Ire1-beta,IRE1b,Serine/threonine-protein kinase,Endoribonuclease','ERN2,IRE2','2.7.11.1,3.1.26.-','Q76MJ5','926','1'),
('F0UY65_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','F0UY65','1620','0'),
('F0UY66_HUMAN','Tyrosine-protein kinase receptor','ALK','2.7.10.1','F0UY66','1620','0'),
('F1JU33_HUMAN',NULL,NULL,NULL,'F1JU33','256','0'),
('F1T0G6_HUMAN',NULL,'MATK',NULL,'F1T0G6','507','0'),
('F2YGG7_HUMAN',NULL,NULL,NULL,'F2YGG7','1167','0'),
('F2Z2J1_HUMAN','Ribosomal protein S6 kinase','RPS6KA2','2.7.11.1','F2Z2J1','758','0'),
('F2Z300_HUMAN',NULL,'STK32C',NULL,'F2Z300','381','0'),
('F2Z3C8_HUMAN',NULL,'SGK2',NULL,'F2Z3C8','285','0'),
('F5GWP9_HUMAN',NULL,'TESK2',NULL,'F5GWP9','488','0'),
('F5GWT4_HUMAN',NULL,'WNK1',NULL,'F5GWT4','2134','0'),
('F5GYC4_HUMAN',NULL,'RPS6KA3',NULL,'F5GYC4','710','0'),
('F5GYW7_HUMAN',NULL,'PASK',NULL,'F5GYW7','1137','0'),
('F5GZ00_HUMAN',NULL,'CAMKK2',NULL,'F5GZ00','343','0'),
('F5H049_HUMAN',NULL,'NRK',NULL,'F5H049','1583','0'),
('F5H0K8_HUMAN',NULL,'KSR1',NULL,'F5H0K8','877','0'),
('F5H0U9_HUMAN',NULL,'MYO3A',NULL,'F5H0U9','664','0'),
('F5H1S7_HUMAN',NULL,'ULK1',NULL,'F5H1S7','184','0'),
('F5H277_HUMAN',NULL,'STK38L',NULL,'F5H277','213','0'),
('F5H2J1_HUMAN',NULL,'MYO3B',NULL,'F5H2J1','1105','0'),
('F5H2M7_HUMAN',NULL,'WNK1',NULL,'F5H2M7','2880','0'),
('F5H2U2_HUMAN',NULL,'PRPF4B',NULL,'F5H2U2','993','0'),
('F5H3M4_HUMAN',NULL,'FGR',NULL,'F5H3M4','463','0'),
('F5H4F6_HUMAN',NULL,'MARK2',NULL,'F5H4F6','161','0'),
('F5H538_HUMAN',NULL,'MAP3K4',NULL,'F5H538','1604','0'),
('F5H5A3_HUMAN','Mitogen-activated protein kinase kinase kinase kinase','MAP4K3','2.7.11.1','F5H5A3','810','0'),
('F5H5C4_HUMAN','Protein kinase C','PRKCG','2.7.11.13','F5H5C4','710','0'),
('F5H5M9_HUMAN',NULL,'TNIK',NULL,'F5H5M9','1312','0'),
('F5H5N0_HUMAN',NULL,'CDC42BPA',NULL,'F5H5N0','1699','0'),
('F5H5U8_HUMAN','Tyrosine-protein kinase','JAK2','2.7.10.2','F5H5U8','983','0'),
('F5H6L9_HUMAN',NULL,'DYRK4',NULL,'F5H6L9','545','0'),
('F5H6Z0_HUMAN',NULL,'CDK17',NULL,'F5H6Z0','470','0'),
('F5H7T0_HUMAN',NULL,'RPS6KC1',NULL,'F5H7T0','854','0'),
('F5H865_HUMAN',NULL,'TNIK',NULL,'F5H865','1338','0'),
('F5H8L5_HUMAN',NULL,'RYK',NULL,'F5H8L5','418','0'),
('F6UYG0_HUMAN',NULL,'WNK1',NULL,'F6UYG0','393','0'),
('F6UYM1_HUMAN','Ribosomal protein S6 kinase','RPS6KB1','2.7.11.1','F6UYM1','502','0'),
('F6WCX7_HUMAN',NULL,'MAP2K7',NULL,'F6WCX7','461','0'),
('F8TLS5_HUMAN',NULL,'RET',NULL,'F8TLS5','1114','0'),
('F8TLW0_HUMAN',NULL,'RET',NULL,'F8TLW0','1114','0'),
('F8VP57_HUMAN',NULL,'EPHA5',NULL,'F8VP57','1004','0'),
('F8VSC5_HUMAN',NULL,'SCYL2',NULL,'F8VSC5','681','0'),
('F8VSH4_HUMAN',NULL,'NUAK1',NULL,'F8VSH4','152','0'),
('F8VTV8_HUMAN',NULL,'CDK4',NULL,'F8VTV8','201','0'),
('F8VUG4_HUMAN',NULL,'MAP3K12',NULL,'F8VUG4','393','0'),
('F8VW56_HUMAN',NULL,'ERBB3',NULL,'F8VW56','583','0'),
('F8VWX7_HUMAN',NULL,'CDK4',NULL,'F8VWX7','203','0'),
('F8VYH9_HUMAN',NULL,'CDK4',NULL,'F8VYH9','170','0'),
('F8VZ51_HUMAN',NULL,'CDK4',NULL,'F8VZ51','208','0'),
('F8VZZ0_HUMAN',NULL,'CDK4',NULL,'F8VZZ0','186','0'),
('F8W1R9_HUMAN',NULL,'TGFBR1',NULL,'F8W1R9','383','0'),
('F8W6G1_HUMAN',NULL,'NRBP1',NULL,'F8W6G1','543','0'),
('F8W872_HUMAN',NULL,'CDK10',NULL,'F8W872','313','0'),
('F8W998_HUMAN',NULL,'CASK',NULL,'F8W998','909','0'),
('F8W9F9_HUMAN',NULL,'WNK2',NULL,'F8W9F9','2217','0'),
('F8W9H1_HUMAN',NULL,'CAMKK1',NULL,'F8W9H1','543','0'),
('F8W9I9_HUMAN',NULL,'DYRK1A',NULL,'F8W9I9','541','0'),
('F8W9L4_HUMAN','Fibroblast growth factor receptor','FGFR3','2.7.10.1','F8W9L4','792','0'),
('F8W9W0_HUMAN',NULL,'EPHA5',NULL,'F8W9W0','874','0'),
('F8W9W2_HUMAN',NULL,'GRK6',NULL,'F8W9W2','542','0'),
('F8WA18_HUMAN',NULL,'TRIB2',NULL,'F8WA18','207','0'),
('F8WAK5_HUMAN',NULL,'STK33',NULL,'F8WAK5','327','0'),
('F8WAP0_HUMAN',NULL,'DYRK1A',NULL,'F8WAP0','535','0'),
('F8WAQ9_HUMAN',NULL,'MAST4',NULL,'F8WAQ9','2626','0'),
('F8WBA3_HUMAN','Serine/threonine-protein kinase D','PRKD1','2.7.11.13','F8WBA3','920','0'),
('F8WBF5_HUMAN',NULL,'CLK1',NULL,'F8WBF5','355','0'),
('F8WCQ3_HUMAN',NULL,'DAPK1',NULL,'F8WCQ3','188','0'),
('F8WEA9_HUMAN',NULL,'KSR1',NULL,'F8WEA9','923','0'),
('FAK1_HUMAN','Focal adhesion kinase 1,FADK 1,Focal adhesion kinase-related nonkinase,FRNK,Protein phosphatase 1 regulatory subunit 71,PPP1R71,Protein-tyrosine kinase 2,p125FAK,pp125FAK','PTK2,FAK, FAK1','2.7.10.2','Q05397','1052','1'),
('FAK2_HUMAN','Protein-tyrosine kinase 2-beta,Calcium-dependent tyrosine kinase,CADTK,Calcium-regulated non-receptor proline-rich tyrosine kinase,Cell adhesion kinase beta,CAK-beta,CAKB,Focal adhesion kinase 2,FADK 2,Proline-rich tyrosine kinase 2,Related adhesion focal tyrosine kinase,RAFTK','PTK2B,FAK2, PYK2, RAFTK','2.7.10.2','Q14289','1009','1'),
('FER_HUMAN','Tyrosine-protein kinase Fer,Feline encephalitis virus-related kinase FER,Fujinami poultry sarcoma/Feline sarcoma-related protein Fer,Proto-oncogene c-Fer,Tyrosine kinase 3,p94-Fer','FER,TYK3','2.7.10.2','P16591','822','1'),
('FES_HUMAN','Tyrosine-protein kinase Fes/Fps,Feline sarcoma/Fujinami avian sarcoma oncogene homolog,Proto-oncogene c-Fes,Proto-oncogene c-Fps,p93c-fes','FES,FPS','2.7.10.2','P07332','822','1'),
('FGFR1_HUMAN','Fibroblast growth factor receptor 1,FGFR-1,Basic fibroblast growth factor receptor 1,BFGFR,bFGF-R-1,Fms-like tyrosine kinase 2,FLT-2,N-sam,Proto-oncogene c-Fgr','FGFR1,BFGFR, CEK, FGFBR, FLG, FLT2, HBGFR','2.7.10.1','P11362','822','1'),
('FGFR2_HUMAN','Fibroblast growth factor receptor 2,FGFR-2,K-sam,KGFR,Keratinocyte growth factor receptor','FGFR2,BEK, KGFR, KSAM','2.7.10.1','P21802','821','2'),
('FGFR3_HUMAN','Fibroblast growth factor receptor 3,FGFR-3','FGFR3,JTK4','2.7.10.1','P22607','806','2'),
('FGFR4_HUMAN','Fibroblast growth factor receptor 4,FGFR-4','FGFR4,JTK2, TKF','2.7.10.1','P22455','802','1'),
('FGR_HUMAN','Tyrosine-protein kinase Fgr,Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog,Proto-oncogene c-Fgr,p55-Fgr,p58-Fgr,p58c-Fgr','FGR,SRC2','2.7.10.2','P09769','529','1'),
('FLT3_HUMAN','Receptor-type tyrosine-protein kinase FLT3,FL cytokine receptor,Fetal liver kinase-2,FLK-2,Fms-like tyrosine kinase 3,FLT-3,Stem cell tyrosine kinase 1,STK-1','FLT3,CD135, FLK2, STK1','2.7.10.1','P36888','993','2'),
('FRK_HUMAN','Tyrosine-protein kinase FRK,FYN-related kinase,Nuclear tyrosine protein kinase RAK,Protein-tyrosine kinase 5','FRK,PTK5, RAK','2.7.10.2','P42685','505','1'),
('FYN_HUMAN','Tyrosine-protein kinase Fyn,Proto-oncogene Syn,Proto-oncogene c-Fyn,Src-like kinase,SLK,p59-Fyn','FYN','2.7.10.2','P06241','537','1'),
('G3V105_HUMAN',NULL,'IKBKB',NULL,'G3V105','562','0'),
('G3V1W8_HUMAN',NULL,'ACVRL1',NULL,'G3V1W8','517','0'),
('G3V202_HUMAN',NULL,'NEK3',NULL,'G3V202','299','0'),
('G3V2D1_HUMAN',NULL,'RPS6KA5',NULL,'G3V2D1','219','0'),
('G3V4L3_HUMAN',NULL,'PRKCH',NULL,'G3V4L3','151','0'),
('G3V5T9_HUMAN',NULL,'CDK2',NULL,'G3V5T9','346','0'),
('G3XAA2_HUMAN',NULL,'MAP4K4',NULL,'G3XAA2','1166','0'),
('G3XAA9_HUMAN',NULL,'RPS6KA4',NULL,'G3XAA9','524','0'),
('G5E948_HUMAN',NULL,'MAP4K4',NULL,'G5E948','1320','0'),
('G5E959_HUMAN',NULL,'CLK3',NULL,'G5E959','467','0'),
('G5E9C7_HUMAN',NULL,'MAP2K2',NULL,'G5E9C7','303','0'),
('G5E9L9_HUMAN',NULL,'DCLK2,DCAMKL2',NULL,'G5E9L9','695','0'),
('G5E9R2_HUMAN',NULL,'PAK6',NULL,'G5E9R2','636','0'),
('G5EKE5_HUMAN','Tyrosine-protein kinase receptor','PPFIBP1-ALK','2.7.10.1','G5EKE5','811','0'),
('G8FPZ9_HUMAN',NULL,'BCR/JAK2',NULL,'G8FPZ9','191','0'),
('G8JLE8_HUMAN',NULL,'GRK5',NULL,'G8JLE8','485','0'),
('G9BXQ3_HUMAN',NULL,NULL,NULL,'G9BXQ3','503','0'),
('G9JXB8_HUMAN',NULL,NULL,NULL,'G9JXB8','1294','0'),
('GAK_HUMAN','Cyclin-G-associated kinase','GAK','2.7.11.1','O14976','1311','1'),
('GRK4_HUMAN','G protein-coupled receptor kinase 4,G protein-coupled receptor kinase GRK4,ITI1','GRK4,GPRK2L, GPRK4','2.7.11.16','P32298','578','1'),
('GRK5_HUMAN','G protein-coupled receptor kinase 5,G protein-coupled receptor kinase GRK5','GRK5,GPRK5','2.7.11.16','P34947','590','1'),
('GRK6_HUMAN','G protein-coupled receptor kinase 6,G protein-coupled receptor kinase GRK6','GRK6,GPRK6','2.7.11.16','P43250','576','1'),
('GRK7_HUMAN','G protein-coupled receptor kinase 7,G protein-coupled receptor kinase GRK7','GRK7,GPRK7','2.7.11.14,2.7.11.16','Q8WTQ7','553','1'),
('GSK3A_HUMAN','Glycogen synthase kinase-3 alpha,GSK-3 alpha,Serine/threonine-protein kinase GSK3A','GSK3A','2.7.11.26,2.7.11.1','P49840','483','1'),
('GSK3B_HUMAN','Glycogen synthase kinase-3 beta,GSK-3 beta,Serine/threonine-protein kinase GSK3B','GSK3B','2.7.11.26,2.7.11.1','P49841','420','1'),
('GUC2C_HUMAN','Heat-stable enterotoxin receptor,STA receptor,hSTAR,Guanylyl cyclase C,GC-C,Intestinal guanylate cyclase','GUCY2C,GUC2C, STAR','4.6.1.2','P25092','1073','1'),
('GUC2D_HUMAN','Retinal guanylyl cyclase 1,RETGC-1,Guanylate cyclase 2D, retinal,Rod outer segment membrane guanylate cyclase,ROS-GC','GUCY2D,CORD6, GUC1A4, GUC2D, RETGC, RETGC1','4.6.1.2','Q02846','1103','1'),
('GUC2F_HUMAN','Retinal guanylyl cyclase 2,RETGC-2,Guanylate cyclase 2F, retinal,Guanylate cyclase F,GC-F,Rod outer segment membrane guanylate cyclase 2,ROS-GC2','GUCY2F,GUC2F, RETGC2','4.6.1.2','P51841','1108','1'),
('GWL_HUMAN','Serine/threonine-protein kinase greatwall,GW,GWL,hGWL,Microtubule-associated serine/threonine-protein kinase-like,MAST-L','MASTL,GW, GWL, THC2','2.7.11.1','Q96GX5','879','1'),
('H0Y3C5_HUMAN',NULL,'HCK',NULL,'H0Y3C5','525','0'),
('H0Y411_HUMAN',NULL,'OBSCN',NULL,'H0Y411','2583','0'),
('H0Y494_HUMAN',NULL,'SIK3',NULL,'H0Y494','1261','0'),
('H0Y4E8_HUMAN',NULL,'SIK3',NULL,'H0Y4E8','1363','0'),
('H0Y630_HUMAN',NULL,'STK24',NULL,'H0Y630','369','0'),
('H0Y645_HUMAN',NULL,'CSNK1E',NULL,'H0Y645','270','0'),
('H0Y7T5_HUMAN',NULL,'WNK2',NULL,'H0Y7T5','2220','0'),
('H0Y820_HUMAN',NULL,'CHEK2',NULL,'H0Y820','276','0'),
('H0Y894_HUMAN',NULL,'MAP3K6',NULL,'H0Y894','798','0'),
('H0Y8A4_HUMAN',NULL,'RYK',NULL,'H0Y8A4','587','0'),
('H0Y8F1_HUMAN',NULL,'PTK7',NULL,'H0Y8F1','365','0'),
('H0Y9F4_HUMAN',NULL,'DDR1',NULL,'H0Y9F4','277','0'),
('H0Y9H3_HUMAN',NULL,'MAPK10',NULL,'H0Y9H3','335','0'),
('H0Y9P2_HUMAN',NULL,'FGFR4',NULL,'H0Y9P2','280','0'),
('H0Y9X2_HUMAN',NULL,'CSNK1A1',NULL,'H0Y9X2','167','0'),
('H0YAZ9_HUMAN',NULL,'CDK16',NULL,'H0YAZ9','260','0'),
('H0YB16_HUMAN',NULL,'PTK2',NULL,'H0YB16','724','0'),
('H0YBP1_HUMAN',NULL,'PTK2',NULL,'H0YBP1','1017','0'),
('H0YBZ1_HUMAN',NULL,'PTK2',NULL,'H0YBZ1','753','0'),
('H0YCC9_HUMAN',NULL,'EPHA10',NULL,'H0YCC9','392','0'),
('H0YCG5_HUMAN',NULL,'PAK1',NULL,'H0YCG5','244','0'),
('H0YCS6_HUMAN',NULL,'BRSK2',NULL,'H0YCS6','170','0'),
('H0YD75_HUMAN',NULL,'NLK',NULL,'H0YD75','475','0'),
('H0YDJ3_HUMAN',NULL,'PRPF4B',NULL,'H0YDJ3','587','0'),
('H0YE48_HUMAN',NULL,'TNNI3K',NULL,'H0YE48','188','0'),
('H0YEW1_HUMAN',NULL,'LRRK1',NULL,'H0YEW1','660','0'),
('H0YEZ7_HUMAN',NULL,'STK33',NULL,'H0YEZ7','211','0'),
('H0YF68_HUMAN',NULL,'TAOK3',NULL,'H0YF68','185','0'),
('H0YJ50_HUMAN',NULL,'VRK1',NULL,'H0YJ50','232','0'),
('H0YM36_HUMAN',NULL,'MOK',NULL,'H0YM36','173','0'),
('H0YM90_HUMAN','Tyrosine-protein kinase receptor','NTRK3','2.7.10.1','H0YM90','705','0'),
('H0YME5_HUMAN',NULL,'EIF2AK4',NULL,'H0YME5','1427','0'),
('H0YNK6_HUMAN',NULL,'TYRO3',NULL,'H0YNK6','845','0'),
('H2E272_HUMAN',NULL,NULL,NULL,'H2E272','254','0'),
('H2E273_HUMAN',NULL,NULL,NULL,'H2E273','574','0'),
('H3BLV9_HUMAN',NULL,'SRPK1',NULL,'H3BLV9','671','0'),
('H3BNQ5_HUMAN',NULL,'CLK3',NULL,'H3BNQ5','193','0'),
('H3BP07_HUMAN',NULL,'PHKG2',NULL,'H3BP07','254','0'),
('H3BPI9_HUMAN',NULL,'AMHR2',NULL,'H3BPI9','172','0'),
('H3BPR7_HUMAN',NULL,'TYRO3',NULL,'H3BPR7','286','0'),
('H3BPX2_HUMAN',NULL,'OBSCN',NULL,'H3BPX2','8923','0'),
('H3BRE4_HUMAN',NULL,'CLK3',NULL,'H3BRE4','190','0'),
('H3BRW9_HUMAN',NULL,'MAP2K1',NULL,'H3BRW9','217','0'),
('H3BSA1_HUMAN',NULL,'CSNK2A2',NULL,'H3BSA1','230','0'),
('H3BT74_HUMAN',NULL,'CDK10',NULL,'H3BT74','239','0'),
('H3BTW6_HUMAN',NULL,'PHKG2',NULL,'H3BTW6','266','0'),
('H3BTZ2_HUMAN',NULL,'ACVRL1',NULL,'H3BTZ2','163','0'),
('H3BVG6_HUMAN','Tyrosine-protein kinase receptor','LTK','2.7.10.1','H3BVG6','562','0'),
('H7BXS4_HUMAN',NULL,'CAMK2B',NULL,'H7BXS4','362','0'),
('H7BXU9_HUMAN',NULL,'FGFR2',NULL,'H7BXU9','669','0'),
('H7BXX9_HUMAN',NULL,'HIPK2',NULL,'H7BXX9','918','0'),
('H7BXZ5_HUMAN',NULL,'KALRN',NULL,'H7BXZ5','2955','0'),
('H7BYG4_HUMAN',NULL,'PXK',NULL,'H7BYG4','498','0'),
('H7BYT1_HUMAN',NULL,'CSNK1D',NULL,'H7BYT1','427','0'),
('H7BYU0_HUMAN',NULL,'KSR1',NULL,'H7BYU0','762','0'),
('H7BZ84_HUMAN',NULL,'SBK3',NULL,'H7BZ84','423','0'),
('H7BZZ3_HUMAN',NULL,'TNK2',NULL,'H7BZZ3','290','0'),
('H7C041_HUMAN',NULL,'MAP3K19',NULL,'H7C041','697','0'),
('H7C074_HUMAN',NULL,'MST1R',NULL,'H7C074','285','0'),
('H7C155_HUMAN',NULL,'RAF1',NULL,'H7C155','527','0'),
('H7C175_HUMAN',NULL,'AATK',NULL,'H7C175','1271','0'),
('H7C1M9_HUMAN',NULL,'MYO3B',NULL,'H7C1M9','360','0'),
('H7C1X3_HUMAN',NULL,'PAK2',NULL,'H7C1X3','221','0'),
('H7C224_HUMAN',NULL,'IRAK1',NULL,'H7C224','392','0'),
('H7C265_HUMAN',NULL,'FGFR2',NULL,'H7C265','371','0'),
('H7C279_HUMAN',NULL,'STK25',NULL,'H7C279','247','0'),
('H7C2I6_HUMAN',NULL,'IRAK1',NULL,'H7C2I6','276','0'),
('H7C360_HUMAN',NULL,'MAP4K4',NULL,'H7C360','1170','0'),
('H7C3H0_HUMAN',NULL,'HUNK',NULL,'H7C3H0','162','0'),
('H7C3L8_HUMAN',NULL,'NEK10',NULL,'H7C3L8','166','0'),
('H7C3L9_HUMAN',NULL,'MERTK',NULL,'H7C3L9','257','0'),
('H7C3X8_HUMAN',NULL,'SIK3',NULL,'H7C3X8','506','0'),
('H7C3Z8_HUMAN',NULL,'MST1R',NULL,'H7C3Z8','270','0'),
('H7C459_HUMAN',NULL,'MAP3K13',NULL,'H7C459','246','0'),
('H7C4V0_HUMAN',NULL,'PXK',NULL,'H7C4V0','312','0'),
('H7C521_HUMAN',NULL,'SRPK2',NULL,'H7C521','204','0'),
('H7C560_HUMAN',NULL,'BRAF',NULL,'H7C560','375','0'),
('H7C5L6_HUMAN',NULL,'SRPK2',NULL,'H7C5L6','295','0'),
('H7C5P0_HUMAN',NULL,'WEE2',NULL,'H7C5P0','203','0'),
('H9KV37_HUMAN',NULL,'CASK',NULL,'H9KV37','921','0'),
('H9N1E7_HUMAN',NULL,'FLT1',NULL,'H9N1E7','433','0'),
('HASP_HUMAN','Serine/threonine-protein kinase haspin,Germ cell-specific gene 2 protein,H-haspin,Haploid germ cell-specific nuclear protein kinase','GSG2','2.7.11.1','Q8TF76','798','1'),
('HCK_HUMAN','Tyrosine-protein kinase HCK,Hematopoietic cell kinase,Hemopoietic cell kinase,p59-HCK/p60-HCK,p59Hck,p61Hck','HCK','2.7.10.2','P08631','526','1'),
('HIPK1_HUMAN','Homeodomain-interacting protein kinase 1,Nuclear body-associated kinase 2','HIPK1,KIAA0630, MYAK, NBAK2','2.7.11.1','Q86Z02','1210','1'),
('HIPK2_HUMAN','Homeodomain-interacting protein kinase 2,hHIPk2','HIPK2','2.7.11.1','Q9H2X6','1198','1'),
('HIPK3_HUMAN','Homeodomain-interacting protein kinase 3,Androgen receptor-interacting nuclear protein kinase,ANPK,Fas-interacting serine/threonine-protein kinase,FIST,Homolog of protein kinase YAK1','HIPK3,DYRK6, FIST3, PKY','2.7.11.1','Q9H422','1215','1'),
('HIPK4_HUMAN','Homeodomain-interacting protein kinase 4','HIPK4','2.7.11.1','Q8NE63','616','1'),
('HUNK_HUMAN','Hormonally up-regulated neu tumor-associated kinase,B19,Serine/threonine-protein kinase MAK-V','HUNK,MAKV','2.7.11.1','P57058','714','1'),
('ICK_HUMAN','Serine/threonine-protein kinase ICK,Intestinal cell kinase,hICK,Laryngeal cancer kinase 2,LCK2,MAK-related kinase,MRK','ICK,KIAA0936','2.7.11.22','Q9UPZ9','632','1'),
('IGF1R_HUMAN','Insulin-like growth factor 1 receptor,Insulin-like growth factor I receptor,IGF-I receptor,Insulin-like growth factor 1 receptor alpha chain,Insulin-like growth factor 1 receptor beta chain','IGF1R','2.7.10.1','P08069','1367','1'),
('IKKA_HUMAN','Inhibitor of nuclear factor kappa-B kinase subunit alpha,I-kappa-B kinase alpha,IKK-A,IKK-alpha,IkBKA,IkappaB kinase,Conserved helix-loop-helix ubiquitous kinase,I-kappa-B kinase 1,IKK1,Nuclear factor NF-kappa-B inhibitor kinase alpha,NFKBIKA,Transcription factor 16,TCF-16','CHUK,IKKA, TCF16','2.7.11.10','O15111','745','1'),
('IKKB_HUMAN','Inhibitor of nuclear factor kappa-B kinase subunit beta,I-kappa-B-kinase beta,IKK-B,IKK-beta,IkBKB,I-kappa-B kinase 2,IKK2,Nuclear factor NF-kappa-B inhibitor kinase beta,NFKBIKB','IKBKB,IKKB','2.7.11.10','O14920','756','1'),
('IKKE_HUMAN','Inhibitor of nuclear factor kappa-B kinase subunit epsilon,I-kappa-B kinase epsilon,IKK-E,IKK-epsilon,IkBKE,Inducible I kappa-B kinase,IKK-i','IKBKE,IKKE, IKKI, KIAA0151','2.7.11.10','Q14164','716','1'),
('ILK_HUMAN','Integrin-linked protein kinase,59 kDa serine/threonine-protein kinase,ILK-1,ILK-2,p59ILK','ILK,ILK1, ILK2','2.7.11.1','Q13418','452','1'),
('INSRR_HUMAN','Insulin receptor-related protein,IRR,IR-related receptor,Insulin receptor-related protein alpha chain,Insulin receptor-related protein beta chain','INSRR,IRR','2.7.10.1','P14616','1297','1'),
('INSR_HUMAN','Insulin receptor,IR,Insulin receptor subunit alpha,Insulin receptor subunit beta','INSR','2.7.10.1','P06213','1382','1'),
('IRAK1_HUMAN','Interleukin-1 receptor-associated kinase 1,IRAK-1','IRAK1,IRAK','2.7.11.1','P51617','712','1'),
('IRAK2_HUMAN','Interleukin-1 receptor-associated kinase-like 2,IRAK-2','IRAK2',NULL,'O43187','625','1'),
('IRAK3_HUMAN','Interleukin-1 receptor-associated kinase 3,IRAK-3,IL-1 receptor-associated kinase M,IRAK-M','IRAK3','2.7.11.1','Q9Y616','596','1'),
('IRAK4_HUMAN','Interleukin-1 receptor-associated kinase 4,IRAK-4,Renal carcinoma antigen NY-REN-64','IRAK4','2.7.11.1','Q9NWZ3','460','1'),
('ITK_HUMAN','Tyrosine-protein kinase ITK/TSK,Interleukin-2-inducible T-cell kinase,IL-2-inducible T-cell kinase,Kinase EMT,T-cell-specific kinase,Tyrosine-protein kinase Lyk','ITK,EMT, LYK','2.7.10.2','Q08881','620','1'),
('JAK1_HUMAN','Tyrosine-protein kinase JAK1,Janus kinase 1,JAK-1','JAK1,JAK1A, JAK1B','2.7.10.2','P23458','1154','2'),
('JAK2_HUMAN','Tyrosine-protein kinase JAK2,Janus kinase 2,JAK-2','JAK2','2.7.10.2','O60674','1132','2'),
('JAK3_HUMAN','Tyrosine-protein kinase JAK3,Janus kinase 3,JAK-3,Leukocyte janus kinase,L-JAK','JAK3','2.7.10.2','P52333','1124','2'),
('KALRN_HUMAN','Kalirin,Huntingtin-associated protein-interacting protein,Protein Duo,Serine/threonine-protein kinase with Dbl- and pleckstrin homology domain','KALRN,DUET, DUO, HAPIP, TRAD','2.7.11.1','O60229','2985','1'),
('KAPCA_HUMAN','cAMP-dependent protein kinase catalytic subunit alpha,PKA C-alpha','PRKACA,PKACA','2.7.11.11','P17612','351','1'),
('KAPCB_HUMAN','cAMP-dependent protein kinase catalytic subunit beta,PKA C-beta','PRKACB','2.7.11.11','P22694','351','1'),
('KAPCG_HUMAN','cAMP-dependent protein kinase catalytic subunit gamma,PKA C-gamma','PRKACG','2.7.11.11','P22612','351','1'),
('KC1AL_HUMAN','Casein kinase I isoform alpha-like,CKI-alpha-like,CK1','CSNK1A1L','2.7.11.1','Q8N752','337','1'),
('KC1A_HUMAN','Casein kinase I isoform alpha,CKI-alpha,CK1','CSNK1A1','2.7.11.1','P48729','337','1'),
('KC1D_HUMAN','Casein kinase I isoform delta,CKI-delta,CKId,Tau-protein kinase CSNK1D','CSNK1D,HCKID','2.7.11.1,2.7.11.26','P48730','415','1'),
('KC1E_HUMAN','Casein kinase I isoform epsilon,CKI-epsilon,CKIe','CSNK1E','2.7.11.1','P49674','416','1'),
('KC1G1_HUMAN','Casein kinase I isoform gamma-1,CKI-gamma 1','CSNK1G1','2.7.11.1','Q9HCP0','422','1'),
('KC1G2_HUMAN','Casein kinase I isoform gamma-2,CKI-gamma 2','CSNK1G2,CK1G2','2.7.11.1','P78368','415','1'),
('KC1G3_HUMAN','Casein kinase I isoform gamma-3,CKI-gamma 3','CSNK1G3','2.7.11.1','Q9Y6M4','447','1'),
('KCC1A_HUMAN','Calcium/calmodulin-dependent protein kinase type 1,CaM kinase I,CaM-KI,CaM kinase I alpha,CaMKI-alpha','CAMK1','2.7.11.17','Q14012','370','1'),
('KCC1B_HUMAN','Calcium/calmodulin-dependent protein kinase type 1B,CaM kinase I beta,CaM kinase IB,CaM-KI beta,CaMKI-beta,Pregnancy up-regulated non-ubiquitously-expressed CaM kinase','PNCK','2.7.11.17','Q6P2M8','343','1'),
('KCC1D_HUMAN','Calcium/calmodulin-dependent protein kinase type 1D,CaM kinase I delta,CaM kinase ID,CaM-KI delta,CaMKI delta,CaMKID,CaMKI-like protein kinase,CKLiK','CAMK1D,CAMKID','2.7.11.17','Q8IU85','385','1'),
('KCC1G_HUMAN','Calcium/calmodulin-dependent protein kinase type 1G,CaM kinase I gamma,CaM kinase IG,CaM-KI gamma,CaMKI gamma,CaMKIG,CaMK-like CREB kinase III,CLICK III','CAMK1G,CLICK3, VWS1','2.7.11.17','Q96NX5','476','1'),
('KCC2A_HUMAN','Calcium/calmodulin-dependent protein kinase type II subunit alpha,CaM kinase II subunit alpha,CaMK-II subunit alpha','CAMK2A,CAMKA, KIAA0968','2.7.11.17','Q9UQM7','478','1'),
('KCC2B_HUMAN','Calcium/calmodulin-dependent protein kinase type II subunit beta,CaM kinase II subunit beta,CaMK-II subunit beta','CAMK2B,CAM2, CAMK2, CAMKB','2.7.11.17','Q13554','666','1'),
('KCC2D_HUMAN','Calcium/calmodulin-dependent protein kinase type II subunit delta,CaM kinase II subunit delta,CaMK-II subunit delta','CAMK2D,CAMKD','2.7.11.17','Q13557','499','1'),
('KCC2G_HUMAN','Calcium/calmodulin-dependent protein kinase type II subunit gamma,CaM kinase II subunit gamma,CaMK-II subunit gamma','CAMK2G,CAMK, CAMK-II, CAMKG','2.7.11.17','Q13555','558','1'),
('KCC4_HUMAN','Calcium/calmodulin-dependent protein kinase type IV,CaMK IV,CaM kinase-GR','CAMK4,CAMK, CAMK-GR, CAMKIV','2.7.11.17','Q16566','473','1'),
('KGP1_HUMAN','cGMP-dependent protein kinase 1,cGK 1,cGK1,cGMP-dependent protein kinase I,cGKI','PRKG1,PRKG1B, PRKGR1A, PRKGR1B','2.7.11.12','Q13976','671','1'),
('KGP2_HUMAN','cGMP-dependent protein kinase 2,cGK 2,cGK2,cGMP-dependent protein kinase II,cGKII','PRKG2,PRKGR2','2.7.11.12','Q13237','762','1'),
('KIT_HUMAN','Mast/stem cell growth factor receptor Kit,SCFR,Piebald trait protein,PBT,Proto-oncogene c-Kit,Tyrosine-protein kinase Kit,p145 c-kit,v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog','KIT,SCFR','2.7.10.1','P10721','976','2'),
('KKCC1_HUMAN','Calcium/calmodulin-dependent protein kinase kinase 1,CaM-KK 1,CaM-kinase kinase 1,CaMKK 1,CaM-kinase IV kinase,Calcium/calmodulin-dependent protein kinase kinase alpha,CaM-KK alpha,CaM-kinase kinase alpha,CaMKK alpha','CAMKK1,CAMKKA','2.7.11.17','Q8N5S9','505','1'),
('KKCC2_HUMAN','Calcium/calmodulin-dependent protein kinase kinase 2,CaM-KK 2,CaM-kinase kinase 2,CaMKK 2,Calcium/calmodulin-dependent protein kinase kinase beta,CaM-KK beta,CaM-kinase kinase beta,CaMKK beta','CAMKK2,CAMKKB, KIAA0787','2.7.11.17','Q96RR4','588','1'),
('KPCA_HUMAN','Protein kinase C alpha type,PKC-A,PKC-alpha','PRKCA,PKCA, PRKACA','2.7.11.13','P17252','672','1'),
('KPCB_HUMAN','Protein kinase C beta type,PKC-B,PKC-beta','PRKCB,PKCB, PRKCB1','2.7.11.13','P05771','671','1'),
('KPCD1_HUMAN','Serine/threonine-protein kinase D1,Protein kinase C mu type,Protein kinase D,nPKC-D1,nPKC-mu','PRKD1,PKD, PKD1, PRKCM','2.7.11.13','Q15139','912','1'),
('KPCD2_HUMAN','Serine/threonine-protein kinase D2,nPKC-D2','PRKD2,PKD2','2.7.11.13','Q9BZL6','878','1'),
('KPCD3_HUMAN','Serine/threonine-protein kinase D3,Protein kinase C nu type,Protein kinase EPK2,nPKC-nu','PRKD3,EPK2, PRKCN','2.7.11.13','O94806','890','1'),
('KPCD_HUMAN','Protein kinase C delta type,Tyrosine-protein kinase PRKCD,nPKC-delta,Protein kinase C delta type regulatory subunit,Protein kinase C delta type catalytic subunit,Sphingosine-dependent protein kinase-1,SDK1','PRKCD','2.7.11.13,2.7.10.2','Q05655','676','1'),
('KPCE_HUMAN','Protein kinase C epsilon type,nPKC-epsilon','PRKCE,PKCE','2.7.11.13','Q02156','737','1'),
('KPCG_HUMAN','Protein kinase C gamma type,PKC-gamma','PRKCG,PKCG','2.7.11.13','P05129','697','2'),
('KPCI_HUMAN','Protein kinase C iota type,Atypical protein kinase C-lambda/iota,PRKC-lambda/iota,aPKC-lambda/iota,nPKC-iota','PRKCI,DXS1179E','2.7.11.13','P41743','596','1'),
('KPCL_HUMAN','Protein kinase C eta type,PKC-L,nPKC-eta','PRKCH,PKCL, PRKCL','2.7.11.13','P24723','683','1'),
('KPCT_HUMAN','Protein kinase C theta type,nPKC-theta','PRKCQ,PRKCT','2.7.11.13','Q04759','706','1'),
('KPCZ_HUMAN','Protein kinase C zeta type,nPKC-zeta','PRKCZ,PKC2','2.7.11.13','Q05513','592','1'),
('KPSH1_HUMAN','Serine/threonine-protein kinase H1,Protein serine kinase H1,PSK-H1','PSKH1','2.7.11.1','P11801','424','1'),
('KPSH2_HUMAN','Serine/threonine-protein kinase H2,Protein serine kinase H2,PSK-H2','PSKH2','2.7.11.1','Q96QS6','385','1'),
('KS6A1_HUMAN','Ribosomal protein S6 kinase alpha-1,S6K-alpha-1,90 kDa ribosomal protein S6 kinase 1,p90-RSK 1,p90RSK1,p90S6K,MAP kinase-activated protein kinase 1a,MAPK-activated protein kinase 1a,MAPKAP kinase 1a,MAPKAPK-1a,Ribosomal S6 kinase 1,RSK-1','RPS6KA1,MAPKAPK1A, RSK1','2.7.11.1','Q15418','735','1'),
('KS6A2_HUMAN','Ribosomal protein S6 kinase alpha-2,S6K-alpha-2,90 kDa ribosomal protein S6 kinase 2,p90-RSK 2,p90RSK2,MAP kinase-activated protein kinase 1c,MAPK-activated protein kinase 1c,MAPKAP kinase 1c,MAPKAPK-1c,Ribosomal S6 kinase 3,RSK-3,pp90RSK3','RPS6KA2,MAPKAPK1C, RSK3','2.7.11.1','Q15349','733','1'),
('KS6A3_HUMAN','Ribosomal protein S6 kinase alpha-3,S6K-alpha-3,90 kDa ribosomal protein S6 kinase 3,p90-RSK 3,p90RSK3,Insulin-stimulated protein kinase 1,ISPK-1,MAP kinase-activated protein kinase 1b,MAPK-activated protein kinase 1b,MAPKAP kinase 1b,MAPKAPK-1b,Ribosomal S6 kinase 2,RSK-2,pp90RSK2','RPS6KA3,ISPK1, MAPKAPK1B, RSK2','2.7.11.1','P51812','740','1'),
('KS6A4_HUMAN','Ribosomal protein S6 kinase alpha-4,S6K-alpha-4,90 kDa ribosomal protein S6 kinase 4,Nuclear mitogen- and stress-activated protein kinase 2,Ribosomal protein kinase B,RSKB','RPS6KA4,MSK2','2.7.11.1','O75676','772','1'),
('KS6A5_HUMAN','Ribosomal protein S6 kinase alpha-5,S6K-alpha-5,90 kDa ribosomal protein S6 kinase 5,Nuclear mitogen- and stress-activated protein kinase 1,RSK-like protein kinase,RSKL','RPS6KA5,MSK1','2.7.11.1','O75582','802','1'),
('KS6A6_HUMAN','Ribosomal protein S6 kinase alpha-6,S6K-alpha-6,90 kDa ribosomal protein S6 kinase 6,p90-RSK 6,p90RSK6,Ribosomal S6 kinase 4,RSK-4,pp90RSK4','RPS6KA6,RSK4','2.7.11.1','Q9UK32','745','1'),
('KS6B1_HUMAN','Ribosomal protein S6 kinase beta-1,S6K-beta-1,S6K1,70 kDa ribosomal protein S6 kinase 1,P70S6K1,p70-S6K 1,Ribosomal protein S6 kinase I,Serine/threonine-protein kinase 14A,p70 ribosomal S6 kinase alpha,p70 S6 kinase alpha,p70 S6K-alpha,p70 S6KA','RPS6KB1,STK14A','2.7.11.1','P23443','525','1'),
('KS6B2_HUMAN','Ribosomal protein S6 kinase beta-2,S6K-beta-2,S6K2,70 kDa ribosomal protein S6 kinase 2,P70S6K2,p70-S6K 2,S6 kinase-related kinase,SRK,Serine/threonine-protein kinase 14B,p70 ribosomal S6 kinase beta,S6K-beta,p70 S6 kinase beta,p70 S6K-beta,p70 S6KB,p70-beta','RPS6KB2,STK14B','2.7.11.1','Q9UBS0','482','1'),
('KS6C1_HUMAN','Ribosomal protein S6 kinase delta-1,S6K-delta-1,52 kDa ribosomal protein S6 kinase,Ribosomal S6 kinase-like protein with two PSK domains 118 kDa protein,SPHK1-binding protein','RPS6KC1,RPK118','2.7.11.1','Q96S38','1066','1'),
('KSR1_HUMAN','Kinase suppressor of Ras 1','KSR1,KSR',NULL,'Q8IVT5','921','1'),
('KSR2_HUMAN','Kinase suppressor of Ras 2,hKSR2','KSR2','2.7.11.1','Q6VAB6','950','1'),
('KSYK_HUMAN','Tyrosine-protein kinase SYK,Spleen tyrosine kinase,p72-Syk','SYK','2.7.10.2','P43405','635','1'),
('LATS1_HUMAN','Serine/threonine-protein kinase LATS1,Large tumor suppressor homolog 1,WARTS protein kinase,h-warts','LATS1,WARTS','2.7.11.1','O95835','1130','1'),
('LATS2_HUMAN','Serine/threonine-protein kinase LATS2,Kinase phosphorylated during mitosis protein,Large tumor suppressor homolog 2,Serine/threonine-protein kinase kpm,Warts-like kinase','LATS2,KPM','2.7.11.1','Q9NRM7','1088','1'),
('LCK_HUMAN','Tyrosine-protein kinase Lck,Leukocyte C-terminal Src kinase,LSK,Lymphocyte cell-specific protein-tyrosine kinase,Protein YT16,Proto-oncogene Lck,T cell-specific protein-tyrosine kinase,p56-LCK','LCK','2.7.10.2','P06239','509','1'),
('LIMK1_HUMAN','LIM domain kinase 1,LIMK-1','LIMK1,LIMK','2.7.11.1','P53667','647','1'),
('LIMK2_HUMAN','LIM domain kinase 2,LIMK-2','LIMK2','2.7.11.1','P53671','638','1'),
('LMTK1_HUMAN','Serine/threonine-protein kinase LMTK1,Apoptosis-associated tyrosine kinase,AATYK,Brain apoptosis-associated tyrosine kinase,CDK5-binding protein,Lemur tyrosine kinase 1,p35-binding protein,p35BP','AATK,AATYK, KIAA0641, LMR1, LMTK1','2.7.11.1','Q6ZMQ8','1374','1'),
('LMTK2_HUMAN','Serine/threonine-protein kinase LMTK2,Apoptosis-associated tyrosine kinase 2,Brain-enriched kinase,hBREK,CDK5/p35-regulated kinase,CPRK,Kinase/phosphatase/inhibitor 2,Lemur tyrosine kinase 2,Serine/threonine-protein kinase KPI-2','LMTK2,AATYK2, BREK, KIAA1079, KPI2, LMR2','2.7.11.1','Q8IWU2','1503','1'),
('LMTK3_HUMAN','Serine/threonine-protein kinase LMTK3,Lemur tyrosine kinase 3','LMTK3,KIAA1883, TYKLM3','2.7.11.1','Q96Q04','1460','1'),
('LRRK1_HUMAN','Leucine-rich repeat serine/threonine-protein kinase 1','LRRK1,KIAA1790','2.7.11.1','Q38SD2','2015','1'),
('LRRK2_HUMAN','Leucine-rich repeat serine/threonine-protein kinase 2,Dardarin','LRRK2,PARK8','2.7.11.1','Q5S007','2527','1'),
('LTK_HUMAN','Leukocyte tyrosine kinase receptor,Protein tyrosine kinase 1','LTK,TYK1','2.7.10.1','P29376','864','1'),
('LYN_HUMAN','Tyrosine-protein kinase Lyn,Lck/Yes-related novel protein tyrosine kinase,V-yes-1 Yamaguchi sarcoma viral related oncogene homolog,p53Lyn,p56Lyn','LYN,JTK8','2.7.10.2','P07948','512','1'),
('M3K10_HUMAN','Mitogen-activated protein kinase kinase kinase 10,Mixed lineage kinase 2,Protein kinase MST','MAP3K10,MLK2, MST','2.7.11.25','Q02779','954','1'),
('M3K11_HUMAN','Mitogen-activated protein kinase kinase kinase 11,Mixed lineage kinase 3,Src-homology 3 domain-containing proline-rich kinase','MAP3K11,MLK3, PTK1, SPRK','2.7.11.25','Q16584','847','1'),
('M3K12_HUMAN','Mitogen-activated protein kinase kinase kinase 12,Dual leucine zipper bearing kinase,DLK,Leucine-zipper protein kinase,ZPK,MAPK-upstream kinase,MUK,Mixed lineage kinase','MAP3K12,ZPK','2.7.11.25','Q12852','859','1'),
('M3K13_HUMAN','Mitogen-activated protein kinase kinase kinase 13,Leucine zipper-bearing kinase,Mixed lineage kinase,MLK','MAP3K13,LZK','2.7.11.25','O43283','966','1'),
('M3K14_HUMAN','Mitogen-activated protein kinase kinase kinase 14,NF-kappa-beta-inducing kinase,HsNIK,Serine/threonine-protein kinase NIK','MAP3K14,NIK','2.7.11.25','Q99558','947','1'),
('M3K15_HUMAN','Mitogen-activated protein kinase kinase kinase 15,Apoptosis signal-regulating kinase 3,MAPK/ERK kinase kinase 15,MEK kinase 15,MEKK 15','MAP3K15,ASK3','2.7.11.25','Q6ZN16','1313','1'),
('M3K19_HUMAN','Mitogen-activated protein kinase kinase kinase 19,Regulated in COPD, protein kinase,SPS1/STE20-related protein kinase YSK4','MAP3K19,RCK, YSK4','2.7.11.1','Q56UN5','1328','1'),
('M3K1_HUMAN','Mitogen-activated protein kinase kinase kinase 1,MAPK/ERK kinase kinase 1,MEK kinase 1,MEKK 1','MAP3K1,MAPKKK1, MEKK, MEKK1','2.7.11.25','Q13233','1512','1'),
('M3K2_HUMAN','Mitogen-activated protein kinase kinase kinase 2,MAPK/ERK kinase kinase 2,MEK kinase 2,MEKK 2','MAP3K2,MAPKKK2, MEKK2','2.7.11.25','Q9Y2U5','619','1'),
('M3K3_HUMAN','Mitogen-activated protein kinase kinase kinase 3,MAPK/ERK kinase kinase 3,MEK kinase 3,MEKK 3','MAP3K3,MAPKKK3, MEKK3','2.7.11.25','Q99759','626','1'),
('M3K4_HUMAN','Mitogen-activated protein kinase kinase kinase 4,MAP three kinase 1,MAPK/ERK kinase kinase 4,MEK kinase 4,MEKK 4','MAP3K4,KIAA0213, MAPKKK4, MEKK4, MTK1','2.7.11.25','Q9Y6R4','1608','1'),
('M3K5_HUMAN','Mitogen-activated protein kinase kinase kinase 5,Apoptosis signal-regulating kinase 1,ASK-1,MAPK/ERK kinase kinase 5,MEK kinase 5,MEKK 5','MAP3K5,ASK1, MAPKKK5, MEKK5','2.7.11.25','Q99683','1374','1'),
('M3K6_HUMAN','Mitogen-activated protein kinase kinase kinase 6,Apoptosis signal-regulating kinase 2','MAP3K6,ASK2, MAPKKK6, MEKK6','2.7.11.25','O95382','1288','1'),
('M3K7_HUMAN','Mitogen-activated protein kinase kinase kinase 7,Transforming growth factor-beta-activated kinase 1,TGF-beta-activated kinase 1','MAP3K7,TAK1','2.7.11.25','O43318','606','1'),
('M3K8_HUMAN','Mitogen-activated protein kinase kinase kinase 8,Cancer Osaka thyroid oncogene,Proto-oncogene c-Cot,Serine/threonine-protein kinase cot,Tumor progression locus 2,TPL-2','MAP3K8,COT, ESTF','2.7.11.25','P41279','467','1'),
('M3K9_HUMAN','Mitogen-activated protein kinase kinase kinase 9,Mixed lineage kinase 1','MAP3K9,MLK1, PRKE1','2.7.11.25','P80192','1104','1'),
('M3KL4_HUMAN','Mitogen-activated protein kinase kinase kinase MLK4,Mixed lineage kinase 4','MLK4,KIAA1804','2.7.11.25','Q5TCX8','1036','1'),
('M4K1_HUMAN','Mitogen-activated protein kinase kinase kinase kinase 1,Hematopoietic progenitor kinase,MAPK/ERK kinase kinase kinase 1,MEK kinase kinase 1,MEKKK 1','MAP4K1,HPK1','2.7.11.1','Q92918','833','1'),
('M4K2_HUMAN','Mitogen-activated protein kinase kinase kinase kinase 2,B lymphocyte serine/threonine-protein kinase,Germinal center kinase,GC kinase,MAPK/ERK kinase kinase kinase 2,MEK kinase kinase 2,MEKKK 2,Rab8-interacting protein','MAP4K2,GCK, RAB8IP','2.7.11.1','Q12851','820','1'),
('M4K3_HUMAN','Mitogen-activated protein kinase kinase kinase kinase 3,Germinal center kinase-related protein kinase,GLK,MAPK/ERK kinase kinase kinase 3,MEK kinase kinase 3,MEKKK 3','MAP4K3,RAB8IPL1','2.7.11.1','Q8IVH8','894','1'),
('M4K4_HUMAN','Mitogen-activated protein kinase kinase kinase kinase 4,HPK/GCK-like kinase HGK,MAPK/ERK kinase kinase kinase 4,MEK kinase kinase 4,MEKKK 4,Nck-interacting kinase','MAP4K4,HGK, KIAA0687, NIK','2.7.11.1','O95819','1239','1'),
('M4K5_HUMAN','Mitogen-activated protein kinase kinase kinase kinase 5,Kinase homologous to SPS1/STE20,KHS,MAPK/ERK kinase kinase kinase 5,MEK kinase kinase 5,MEKKK 5','MAP4K5','2.7.11.1','Q9Y4K4','846','1'),
('MAK_HUMAN','Serine/threonine-protein kinase MAK,Male germ cell-associated kinase','MAK','2.7.11.22','P20794','623','1'),
('MAPK2_HUMAN','MAP kinase-activated protein kinase 2,MAPK-activated protein kinase 2,MAPKAP kinase 2,MAPKAP-K2,MAPKAPK-2,MK-2,MK2','MAPKAPK2','2.7.11.1','P49137','400','1'),
('MAPK3_HUMAN','MAP kinase-activated protein kinase 3,MAPK-activated protein kinase 3,MAPKAP kinase 3,MAPKAP-K3,MAPKAPK-3,MK-3,Chromosome 3p kinase,3pK','MAPKAPK3','2.7.11.1','Q16644','382','1'),
('MAPK5_HUMAN','MAP kinase-activated protein kinase 5,MAPK-activated protein kinase 5,MAPKAP kinase 5,MAPKAP-K5,MAPKAPK-5,MK-5,MK5,p38-regulated/activated protein kinase,PRAK','MAPKAPK5,PRAK','2.7.11.1','Q8IW41','473','1'),
('MARK1_HUMAN','Serine/threonine-protein kinase MARK1,MAP/microtubule affinity-regulating kinase 1,PAR1 homolog c,Par-1c,Par1c','MARK1,KIAA1477, MARK','2.7.11.1,2.7.11.26','Q9P0L2','795','1'),
('MARK2_HUMAN','Serine/threonine-protein kinase MARK2,ELKL motif kinase 1,EMK-1,MAP/microtubule affinity-regulating kinase 2,PAR1 homolog,PAR1 homolog b,Par-1b,Par1b','MARK2,EMK1','2.7.11.1,2.7.11.26','Q7KZI7','788','1'),
('MARK3_HUMAN','MAP/microtubule affinity-regulating kinase 3,C-TAK1,cTAK1,Cdc25C-associated protein kinase 1,ELKL motif kinase 2,EMK-2,Protein kinase STK10,Ser/Thr protein kinase PAR-1,Par-1a,Serine/threonine-protein kinase p78','MARK3,CTAK1, EMK2','2.7.11.1','P27448','753','1'),
('MARK4_HUMAN','MAP/microtubule affinity-regulating kinase 4,MAP/microtubule affinity-regulating kinase-like 1','MARK4,KIAA1860, MARKL1','2.7.11.1','Q96L34','752','1'),
('MAST1_HUMAN','Microtubule-associated serine/threonine-protein kinase 1,Syntrophin-associated serine/threonine-protein kinase','MAST1,KIAA0973, SAST','2.7.11.1','Q9Y2H9','1570','1'),
('MAST2_HUMAN','Microtubule-associated serine/threonine-protein kinase 2','MAST2,KIAA0807, MAST205','2.7.11.1','Q6P0Q8','1798','1'),
('MAST3_HUMAN','Microtubule-associated serine/threonine-protein kinase 3','MAST3,KIAA0561','2.7.11.1','O60307','1309','1'),
('MAST4_HUMAN','Microtubule-associated serine/threonine-protein kinase 4','MAST4,KIAA0303','2.7.11.1','O15021','2626','1'),
('MATK_HUMAN','Megakaryocyte-associated tyrosine-protein kinase,CSK homologous kinase,CHK,Hematopoietic consensus tyrosine-lacking kinase,Protein kinase HYL,Tyrosine-protein kinase CTK','MATK,CTK, HYL','2.7.10.2','P42679','507','1'),
('MELK_HUMAN','Maternal embryonic leucine zipper kinase,hMELK,Protein kinase Eg3,pEg3 kinase,Protein kinase PK38,hPK38,Tyrosine-protein kinase MELK','MELK,KIAA0175','2.7.11.1,2.7.10.2','Q14680','651','1'),
('MERTK_HUMAN','Tyrosine-protein kinase Mer,Proto-oncogene c-Mer,Receptor tyrosine kinase MerTK','MERTK,MER','2.7.10.1','Q12866','999','1'),
('MET_HUMAN','Hepatocyte growth factor receptor,HGF receptor,HGF/SF receptor,Proto-oncogene c-Met,Scatter factor receptor,SF receptor,Tyrosine-protein kinase Met','MET','2.7.10.1','P08581','1390','2'),
('MINK1_HUMAN','Misshapen-like kinase 1,GCK family kinase MiNK,MAPK/ERK kinase kinase kinase 6,MEK kinase kinase 6,MEKKK 6,Misshapen/NIK-related kinase,Mitogen-activated protein kinase kinase kinase kinase 6','MINK1,B55, MAP4K6, MINK, YSK2, ZC3','2.7.11.1','Q8N4C8','1332','1'),
('MK01_HUMAN','Mitogen-activated protein kinase 1,MAP kinase 1,MAPK 1,ERT1,Extracellular signal-regulated kinase 2,ERK-2,MAP kinase isoform p42,p42-MAPK,Mitogen-activated protein kinase 2,MAP kinase 2,MAPK 2','MAPK1,ERK2, PRKM1, PRKM2','2.7.11.24','P28482','360','1'),
('MK03_HUMAN','Mitogen-activated protein kinase 3,MAP kinase 3,MAPK 3,ERT2,Extracellular signal-regulated kinase 1,ERK-1,Insulin-stimulated MAP2 kinase,MAP kinase isoform p44,p44-MAPK,Microtubule-associated protein 2 kinase,p44-ERK1','MAPK3,ERK1, PRKM3','2.7.11.24','P27361','379','1'),
('MK04_HUMAN','Mitogen-activated protein kinase 4,MAP kinase 4,MAPK 4,Extracellular signal-regulated kinase 4,ERK-4,MAP kinase isoform p63,p63-MAPK','MAPK4,ERK4, PRKM4','2.7.11.24','P31152','587','1'),
('MK06_HUMAN','Mitogen-activated protein kinase 6,MAP kinase 6,MAPK 6,Extracellular signal-regulated kinase 3,ERK-3,MAP kinase isoform p97,p97-MAPK','MAPK6,ERK3, PRKM6','2.7.11.24','Q16659','721','1'),
('MK07_HUMAN','Mitogen-activated protein kinase 7,MAP kinase 7,MAPK 7,Big MAP kinase 1,BMK-1,Extracellular signal-regulated kinase 5,ERK-5','MAPK7,BMK1, ERK5, PRKM7','2.7.11.24','Q13164','816','1'),
('MK08_HUMAN','Mitogen-activated protein kinase 8,MAP kinase 8,MAPK 8,JNK-46,Stress-activated protein kinase 1c,SAPK1c,Stress-activated protein kinase JNK1,c-Jun N-terminal kinase 1','MAPK8,JNK1, PRKM8, SAPK1, SAPK1C','2.7.11.24','P45983','427','1'),
('MK09_HUMAN','Mitogen-activated protein kinase 9,MAP kinase 9,MAPK 9,JNK-55,Stress-activated protein kinase 1a,SAPK1a,Stress-activated protein kinase JNK2,c-Jun N-terminal kinase 2','MAPK9,JNK2, PRKM9, SAPK1A','2.7.11.24','P45984','424','1'),
('MK10_HUMAN','Mitogen-activated protein kinase 10,MAP kinase 10,MAPK 10,MAP kinase p49 3F12,Stress-activated protein kinase 1b,SAPK1b,Stress-activated protein kinase JNK3,c-Jun N-terminal kinase 3','MAPK10,JNK3, JNK3A, PRKM10, SAPK1B','2.7.11.24','P53779','464','1'),
('MK11_HUMAN','Mitogen-activated protein kinase 11,MAP kinase 11,MAPK 11,Mitogen-activated protein kinase p38 beta,MAP kinase p38 beta,p38b,Stress-activated protein kinase 2b,SAPK2b,p38-2','MAPK11,PRKM11, SAPK2, SAPK2B','2.7.11.24','Q15759','364','1'),
('MK12_HUMAN','Mitogen-activated protein kinase 12,MAP kinase 12,MAPK 12,Extracellular signal-regulated kinase 6,ERK-6,Mitogen-activated protein kinase p38 gamma,MAP kinase p38 gamma,Stress-activated protein kinase 3','MAPK12,ERK6, SAPK3','2.7.11.24','P53778','367','1'),
('MK13_HUMAN','Mitogen-activated protein kinase 13,MAP kinase 13,MAPK 13,Mitogen-activated protein kinase p38 delta,MAP kinase p38 delta,Stress-activated protein kinase 4','MAPK13,PRKM13, SAPK4','2.7.11.24','O15264','365','1'),
('MK14_HUMAN','Mitogen-activated protein kinase 14,MAP kinase 14,MAPK 14,Cytokine suppressive anti-inflammatory drug-binding protein,CSAID-binding protein,CSBP,MAP kinase MXI2,MAX-interacting protein 2,Mitogen-activated protein kinase p38 alpha,MAP kinase p38 alpha,Stress-activated protein kinase 2a,SAPK2a','MAPK14,CSBP, CSBP1, CSBP2, CSPB1, MXI2, SAPK2A','2.7.11.24','Q16539','360','1'),
('MK15_HUMAN','Mitogen-activated protein kinase 15,MAP kinase 15,MAPK 15,Extracellular signal-regulated kinase 7,ERK-7,Extracellular signal-regulated kinase 8,ERK-8','MAPK15,ERK7, ERK8','2.7.11.24','Q8TD08','544','1'),
('MKNK1_HUMAN','MAP kinase-interacting serine/threonine-protein kinase 1,MAP kinase signal-integrating kinase 1,MAPK signal-integrating kinase 1,Mnk1','MKNK1,MNK1','2.7.11.1','Q9BUB5','465','1'),
('MKNK2_HUMAN','MAP kinase-interacting serine/threonine-protein kinase 2,MAP kinase signal-integrating kinase 2,MAPK signal-integrating kinase 2,Mnk2','MKNK2,GPRK7, MNK2','2.7.11.1','Q9HBH9','465','1'),
('MLKL_HUMAN','Mixed lineage kinase domain-like protein,hMLKL','MLKL',NULL,'Q8NB16','471','1'),
('MLTK_HUMAN','Mitogen-activated protein kinase kinase kinase MLT,Human cervical cancer suppressor gene 4 protein,HCCS-4,Leucine zipper- and sterile alpha motif-containing kinase,MLK-like mitogen-activated protein triple kinase,Mixed lineage kinase-related kinase,MLK-related kinase,MRK,Sterile alpha motif- and leucine zipper-containing kinase AZK','ZAK,MLTK','2.7.11.25','Q9NYL2','800','1'),
('MOK_HUMAN','MAPK/MAK/MRK overlapping kinase,MOK protein kinase,Renal tumor antigen 1,RAGE-1','MOK,RAGE, RAGE1','2.7.11.22','Q9UQ07','419','1'),
('MOS_HUMAN','Proto-oncogene serine/threonine-protein kinase mos,Oocyte maturation factor mos,Proto-oncogene c-Mos','MOS','2.7.11.1','P00540','346','1'),
('MP2K1_HUMAN','Dual specificity mitogen-activated protein kinase kinase 1,MAP kinase kinase 1,MAPKK 1,MKK1,ERK activator kinase 1,MAPK/ERK kinase 1,MEK 1','MAP2K1,MEK1, PRKMK1','2.7.12.2','Q02750','393','2'),
('MP2K2_HUMAN','Dual specificity mitogen-activated protein kinase kinase 2,MAP kinase kinase 2,MAPKK 2,ERK activator kinase 2,MAPK/ERK kinase 2,MEK 2','MAP2K2,MEK2, MKK2, PRKMK2','2.7.12.2','P36507','400','2'),
('MP2K3_HUMAN','Dual specificity mitogen-activated protein kinase kinase 3,MAP kinase kinase 3,MAPKK 3,MAPK/ERK kinase 3,MEK 3,Stress-activated protein kinase kinase 2,SAPK kinase 2,SAPKK-2,SAPKK2','MAP2K3,MEK3, MKK3, PRKMK3, SKK2','2.7.12.2','P46734','347','1'),
('MP2K4_HUMAN','Dual specificity mitogen-activated protein kinase kinase 4,MAP kinase kinase 4,MAPKK 4,JNK-activating kinase 1,MAPK/ERK kinase 4,MEK 4,SAPK/ERK kinase 1,SEK1,Stress-activated protein kinase kinase 1,SAPK kinase 1,SAPKK-1,SAPKK1,c-Jun N-terminal kinase kinase 1,JNKK','MAP2K4,JNKK1, MEK4, MKK4, PRKMK4, SEK1, SERK1, SKK1','2.7.12.2','P45985','399','1'),
('MP2K5_HUMAN','Dual specificity mitogen-activated protein kinase kinase 5,MAP kinase kinase 5,MAPKK 5,MAPK/ERK kinase 5,MEK 5','MAP2K5,MEK5, MKK5, PRKMK5','2.7.12.2','Q13163','448','1'),
('MP2K6_HUMAN','Dual specificity mitogen-activated protein kinase kinase 6,MAP kinase kinase 6,MAPKK 6,MAPK/ERK kinase 6,MEK 6,Stress-activated protein kinase kinase 3,SAPK kinase 3,SAPKK-3,SAPKK3','MAP2K6,MEK6, MKK6, PRKMK6, SKK3','2.7.12.2','P52564','334','1'),
('MP2K7_HUMAN','Dual specificity mitogen-activated protein kinase kinase 7,MAP kinase kinase 7,MAPKK 7,JNK-activating kinase 2,MAPK/ERK kinase 7,MEK 7,Stress-activated protein kinase kinase 4,SAPK kinase 4,SAPKK-4,SAPKK4,c-Jun N-terminal kinase kinase 2,JNK kinase 2,JNKK 2','MAP2K7,JNKK2, MEK7, MKK7, PRKMK7, SKK4','2.7.12.2','O14733','419','1'),
('MRCKA_HUMAN','Serine/threonine-protein kinase MRCK alpha,CDC42-binding protein kinase alpha,DMPK-like alpha,Myotonic dystrophy kinase-related CDC42-binding kinase alpha,MRCK alpha,Myotonic dystrophy protein kinase-like alpha','CDC42BPA,KIAA0451','2.7.11.1','Q5VT25','1732','1'),
('MRCKB_HUMAN','Serine/threonine-protein kinase MRCK beta,CDC42-binding protein kinase beta,CDC42BP-beta,DMPK-like beta,Myotonic dystrophy kinase-related CDC42-binding kinase beta,MRCK beta,Myotonic dystrophy protein kinase-like beta','CDC42BPB,KIAA1124','2.7.11.1','Q9Y5S2','1711','1'),
('MRCKG_HUMAN','Serine/threonine-protein kinase MRCK gamma,CDC42-binding protein kinase gamma,DMPK-like gamma,Myotonic dystrophy kinase-related CDC42-binding kinase gamma,MRCK gamma,MRCKG,Myotonic dystrophy protein kinase-like gamma,Myotonic dystrophy protein kinase-like alpha','CDC42BPG,DMPK2','2.7.11.1','Q6DT37','1551','1'),
('MST4_HUMAN','Serine/threonine-protein kinase MST4,Mammalian STE20-like protein kinase 4,MST-4,Mst3 and SOK1-related kinase,STE20-like kinase MST4,Serine/threonine-protein kinase MASK','MST4,MASK','2.7.11.1','Q9P289','416','1'),
('MUSK_HUMAN','Muscle, skeletal receptor tyrosine-protein kinase,Muscle-specific tyrosine-protein kinase receptor,MuSK,Muscle-specific kinase receptor','MUSK','2.7.10.1','O15146','869','1'),
('MYLK2_HUMAN','Myosin light chain kinase 2, skeletal/cardiac muscle,MLCK2','MYLK2','2.7.11.18','Q9H1R3','596','1'),
('MYLK3_HUMAN','Myosin light chain kinase 3,Cardiac-MyBP-C-associated Ca/CaM kinase,Cardiac-MLCK','MYLK3,MLCK','2.7.11.18','Q32MK0','819','1'),
('MYLK4_HUMAN','Myosin light chain kinase family member 4,Sugen kinase 85,SgK085','MYLK4,SGK085','2.7.11.1','Q86YV6','388','1'),
('MYLK_HUMAN','Myosin light chain kinase, smooth muscle,MLCK,smMLCK,Kinase-related protein,KRP,Telokin,Myosin light chain kinase, smooth muscle, deglutamylated form','MYLK,MLCK, MLCK1, MYLK1','2.7.11.18','Q15746','1914','1'),
('MYO3A_HUMAN','Myosin-IIIa','MYO3A','2.7.11.1','Q8NEV4','1616','1'),
('MYO3B_HUMAN','Myosin-IIIb','MYO3B','2.7.11.1','Q8WXR4','1341','1'),
('NEK10_HUMAN','Serine/threonine-protein kinase Nek10,Never in mitosis A-related kinase 10,NimA-related protein kinase 10','NEK10','2.7.11.1','Q6ZWH5','1172','1'),
('NEK11_HUMAN','Serine/threonine-protein kinase Nek11,Never in mitosis A-related kinase 11,NimA-related protein kinase 11','NEK11','2.7.11.1','Q8NG66','645','1'),
('NEK1_HUMAN','Serine/threonine-protein kinase Nek1,Never in mitosis A-related kinase 1,NimA-related protein kinase 1,Renal carcinoma antigen NY-REN-55','NEK1,KIAA1901','2.7.11.1','Q96PY6','1258','1'),
('NEK2_HUMAN','Serine/threonine-protein kinase Nek2,HSPK 21,Never in mitosis A-related kinase 2,NimA-related protein kinase 2,NimA-like protein kinase 1','NEK2,NEK2A, NLK1','2.7.11.1','P51955','445','1'),
('NEK3_HUMAN','Serine/threonine-protein kinase Nek3,HSPK 36,Never in mitosis A-related kinase 3,NimA-related protein kinase 3','NEK3','2.7.11.1','P51956','506','1'),
('NEK4_HUMAN','Serine/threonine-protein kinase Nek4,Never in mitosis A-related kinase 4,NimA-related protein kinase 4,Serine/threonine-protein kinase 2,Serine/threonine-protein kinase NRK2','NEK4,STK2','2.7.11.1','P51957','841','1'),
('NEK5_HUMAN','Serine/threonine-protein kinase Nek5,Never in mitosis A-related kinase 5,NimA-related protein kinase 5','NEK5','2.7.11.1','Q6P3R8','708','1'),
('NEK6_HUMAN','Serine/threonine-protein kinase Nek6,Never in mitosis A-related kinase 6,NimA-related protein kinase 6,Protein kinase SID6-1512','NEK6','2.7.11.1','Q9HC98','313','1'),
('NEK7_HUMAN','Serine/threonine-protein kinase Nek7,Never in mitosis A-related kinase 7,NimA-related protein kinase 7','NEK7','2.7.11.1','Q8TDX7','302','1'),
('NEK8_HUMAN','Serine/threonine-protein kinase Nek8,Never in mitosis A-related kinase 8,NimA-related protein kinase 8,Nima-related protein kinase 12a','NEK8,JCK, NEK12A','2.7.11.1','Q86SG6','692','2'),
('NEK9_HUMAN','Serine/threonine-protein kinase Nek9,Nercc1 kinase,Never in mitosis A-related kinase 9,NimA-related protein kinase 9,NimA-related kinase 8,Nek8','NEK9,KIAA1995, NEK8, NERCC','2.7.11.1','Q8TD19','979','1'),
('NIM1_HUMAN','Serine/threonine-protein kinase NIM1,NIM1 serine/threonine-protein kinase','NIM1K,NIM1','2.7.11.1','Q8IY84','436','1'),
('NLK_HUMAN','Serine/threonine-protein kinase NLK,Nemo-like kinase,Protein LAK1','NLK,LAK1','2.7.11.24','Q9UBE8','527','1'),
('NRBP2_HUMAN','Nuclear receptor-binding protein 2,Transformation-related gene 16 protein,TRG-16','NRBP2',NULL,'Q9NSY0','501','1'),
('NRBP_HUMAN','Nuclear receptor-binding protein','NRBP1,BCON3, NRBP',NULL,'Q9UHY1','535','1'),
('NRK_HUMAN','Nik-related protein kinase','NRK','2.7.11.1','Q7Z2Y5','1582','1'),
('NTKL_HUMAN','N-terminal kinase-like protein,Coated vesicle-associated kinase of 90 kDa,SCY1-like protein 1,Telomerase regulation-associated protein,Telomerase transcriptional element-interacting factor,Teratoma-associated tyrosine kinase','SCYL1,CVAK90, GKLP, NTKL, TAPK, TEIF, TRAP',NULL,'Q96KG9','808','1'),
('NTRK1_HUMAN','High affinity nerve growth factor receptor,Neurotrophic tyrosine kinase receptor type 1,TRK1-transforming tyrosine kinase protein,Tropomyosin-related kinase A,Tyrosine kinase receptor,Tyrosine kinase receptor A,Trk-A,gp140trk,p140-TrkA','NTRK1,MTC, TRK, TRKA','2.7.10.1','P04629','796','1'),
('NTRK2_HUMAN','BDNF/NT-3 growth factors receptor,GP145-TrkB,Trk-B,Neurotrophic tyrosine kinase receptor type 2,TrkB tyrosine kinase,Tropomyosin-related kinase B','NTRK2,TRKB','2.7.10.1','Q16620','822','1'),
('NTRK3_HUMAN','NT-3 growth factor receptor,GP145-TrkC,Trk-C,Neurotrophic tyrosine kinase receptor type 3,TrkC tyrosine kinase','NTRK3,TRKC','2.7.10.1','Q16288','839','1'),
('NUAK1_HUMAN','NUAK family SNF1-like kinase 1,AMPK-related protein kinase 5,ARK5,Omphalocele kinase 1','NUAK1,ARK5, KIAA0537, OMPHK1','2.7.11.1','O60285','661','1'),
('NUAK2_HUMAN','NUAK family SNF1-like kinase 2,Omphalocele kinase 2,SNF1/AMP kinase-related kinase,SNARK','NUAK2,OMPHK2, SNARK','2.7.11.1','Q9H093','628','1'),
('O75271_HUMAN',NULL,NULL,NULL,'O75271','462','0'),
('OBSCN_HUMAN','Obscurin,Obscurin-RhoGEF,Obscurin-myosin light chain kinase,Obscurin-MLCK','OBSCN,KIAA1556, KIAA1639','2.7.11.1','Q5VST9','7968','1'),
('OXSR1_HUMAN','Serine/threonine-protein kinase OSR1,Oxidative stress-responsive 1 protein','OXSR1,KIAA1101, OSR1','2.7.11.1','O95747','527','1'),
('PACE1_HUMAN','Protein-associating with the carboxyl-terminal domain of ezrin,Ezrin-binding protein PACE-1,SCY1-like protein 3','SCYL3,PACE1',NULL,'Q8IZE3','742','1'),
('PAK1_HUMAN','Serine/threonine-protein kinase PAK 1,Alpha-PAK,p21-activated kinase 1,PAK-1,p65-PAK','PAK1','2.7.11.1','Q13153','545','1'),
('PAK2_HUMAN','Serine/threonine-protein kinase PAK 2,Gamma-PAK,PAK65,S6/H4 kinase,p21-activated kinase 2,PAK-2,p58,PAK-2p27,p27,PAK-2p34,p34,C-t-PAK2','PAK2','2.7.11.1','Q13177','524','1'),
('PAK3_HUMAN','Serine/threonine-protein kinase PAK 3,Beta-PAK,Oligophrenin-3,p21-activated kinase 3,PAK-3','PAK3,OPHN3','2.7.11.1','O75914','559','1'),
('PAK4_HUMAN','Serine/threonine-protein kinase PAK 4,p21-activated kinase 4,PAK-4','PAK4,KIAA1142','2.7.11.1','O96013','591','1'),
('PAK6_HUMAN','Serine/threonine-protein kinase PAK 6,PAK-5,p21-activated kinase 6,PAK-6','PAK6,PAK5','2.7.11.1','Q9NQU5','681','1'),
('PAK7_HUMAN','Serine/threonine-protein kinase PAK 7,p21-activated kinase 5,PAK-5,p21-activated kinase 7,PAK-7','PAK7,KIAA1264, PAK5','2.7.11.1','Q9P286','719','1'),
('PASK_HUMAN','PAS domain-containing serine/threonine-protein kinase,PAS-kinase,PASKIN,hPASK','PASK,KIAA0135','2.7.11.1','Q96RG2','1323','1'),
('PDK1L_HUMAN','Serine/threonine-protein kinase PDIK1L,PDLIM1-interacting kinase 1-like','PDIK1L,CLIK1L','2.7.11.1','Q8N165','341','1'),
('PDPK1_HUMAN','3-phosphoinositide-dependent protein kinase 1,hPDK1','PDPK1,PDK1','2.7.11.1','O15530','556','1'),
('PDPK2_HUMAN','Putative 3-phosphoinositide-dependent protein kinase 2','PDPK2','2.7.11.1','Q6A1A2','396','1'),
('PEAK1_HUMAN','Pseudopodium-enriched atypical kinase 1,Sugen kinase 269,Tyrosine-protein kinase SgK269','PEAK1,KIAA2002','2.7.10.2','Q9H792','1746','1'),
('PGFRA_HUMAN','Platelet-derived growth factor receptor alpha,PDGF-R-alpha,PDGFR-alpha,Alpha platelet-derived growth factor receptor,Alpha-type platelet-derived growth factor receptor,CD140 antigen-like family member A,CD140a antigen,Platelet-derived growth factor alpha receptor,Platelet-derived growth factor receptor 2,PDGFR-2','PDGFRA,PDGFR2, RHEPDGFRA','2.7.10.1','P16234','1089','2'),
('PGFRB_HUMAN','Platelet-derived growth factor receptor beta,PDGF-R-beta,PDGFR-beta,Beta platelet-derived growth factor receptor,Beta-type platelet-derived growth factor receptor,CD140 antigen-like family member B,Platelet-derived growth factor receptor 1,PDGFR-1','PDGFRB,PDGFR, PDGFR1','2.7.10.1','P09619','1106','2'),
('PHKG1_HUMAN','Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform,PHK-gamma-M,Phosphorylase kinase subunit gamma-1,Serine/threonine-protein kinase PHKG1','PHKG1,PHKG','2.7.11.19,2.7.11.1,2.7.11.26','Q16816','387','1'),
('PHKG2_HUMAN','Phosphorylase b kinase gamma catalytic chain, liver/testis isoform,PHK-gamma-LT,PHK-gamma-T,PSK-C3,Phosphorylase kinase subunit gamma-2','PHKG2','2.7.11.19','P15735','406','1'),
('PI3R4_HUMAN','Phosphoinositide 3-kinase regulatory subunit 4,PI3-kinase regulatory subunit 4,PI3-kinase p150 subunit,Phosphoinositide 3-kinase adaptor protein','PIK3R4','2.7.11.1','Q99570','1358','1'),
('PIM1_HUMAN','Serine/threonine-protein kinase pim-1','PIM1','2.7.11.1','P11309','404','1'),
('PIM2_HUMAN','Serine/threonine-protein kinase pim-2,Pim-2h','PIM2','2.7.11.1','Q9P1W9','311','1'),
('PIM3_HUMAN','Serine/threonine-protein kinase pim-3','PIM3','2.7.11.1','Q86V86','326','1'),
('PINK1_HUMAN','Serine/threonine-protein kinase PINK1, mitochondrial,BRPK,PTEN-induced putative kinase protein 1','PINK1','2.7.11.1','Q9BXM7','581','1'),
('PKN1_HUMAN','Serine/threonine-protein kinase N1,Protease-activated kinase 1,PAK-1,Protein kinase C-like 1,Protein kinase C-like PKN,Protein kinase PKN-alpha,Protein-kinase C-related kinase 1,Serine-threonine protein kinase N','PKN1,PAK1, PKN, PRK1, PRKCL1','2.7.11.13','Q16512','942','1'),
('PKN2_HUMAN','Serine/threonine-protein kinase N2,PKN gamma,Protein kinase C-like 2,Protein-kinase C-related kinase 2','PKN2,PRK2, PRKCL2','2.7.11.13','Q16513','984','1'),
('PKN3_HUMAN','Serine/threonine-protein kinase N3,Protein kinase PKN-beta,Protein-kinase C-related kinase 3','PKN3,PKNBETA','2.7.11.13','Q6P5Z2','889','1'),
('PLK1_HUMAN','Serine/threonine-protein kinase PLK1,Polo-like kinase 1,PLK-1,Serine/threonine-protein kinase 13,STPK13','PLK1,PLK','2.7.11.21','P53350','603','1'),
('PLK2_HUMAN','Serine/threonine-protein kinase PLK2,Polo-like kinase 2,PLK-2,hPlk2,Serine/threonine-protein kinase SNK,hSNK,Serum-inducible kinase','PLK2,SNK','2.7.11.21','Q9NYY3','685','1'),
('PLK3_HUMAN','Serine/threonine-protein kinase PLK3,Cytokine-inducible serine/threonine-protein kinase,FGF-inducible kinase,Polo-like kinase 3,PLK-3,Proliferation-related kinase','PLK3,CNK, FNK, PRK','2.7.11.21','Q9H4B4','646','1'),
('PLK4_HUMAN','Serine/threonine-protein kinase PLK4,Polo-like kinase 4,PLK-4,Serine/threonine-protein kinase 18,Serine/threonine-protein kinase Sak','PLK4,SAK, STK18','2.7.11.21','O00444','970','1'),
('PMYT1_HUMAN','Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase,Myt1 kinase','PKMYT1,MYT1','2.7.11.1','Q99640','499','1'),
('PRKX_HUMAN','cAMP-dependent protein kinase catalytic subunit PRKX,PrKX,Protein kinase X,Protein kinase X-linked,Serine/threonine-protein kinase PRKX,Protein kinase PKX1','PRKX,PKX1','2.7.11.1','P51817','358','1'),
('PRKY_HUMAN','Putative serine/threonine-protein kinase PRKY','PRKY','2.7.11.1','O43930','277','1'),
('PRP4B_HUMAN','Serine/threonine-protein kinase PRP4 homolog,PRP4 kinase,PRP4 pre-mRNA-processing factor 4 homolog','PRPF4B,KIAA0536, PRP4, PRP4H, PRP4K','2.7.11.1','Q13523','1007','1'),
('PTK6_HUMAN','Protein-tyrosine kinase 6,Breast tumor kinase,Tyrosine-protein kinase BRK','PTK6,BRK','2.7.10.2','Q13882','451','1'),
('PTK7_HUMAN','Inactive tyrosine-protein kinase 7,Colon carcinoma kinase 4,CCK-4,Protein-tyrosine kinase 7,Pseudo tyrosine kinase receptor 7,Tyrosine-protein kinase-like 7','PTK7,CCK4',NULL,'Q13308','1070','1'),
('PXK_HUMAN','PX domain-containing protein kinase-like protein,Modulator of Na,K-ATPase,MONaKA','PXK',NULL,'Q7Z7A4','578','1'),
('Q05CR6_HUMAN',NULL,'VRK2',NULL,'Q05CR6','427','0'),
('Q05D26_HUMAN',NULL,'BLK',NULL,'Q05D26','599','0'),
('Q05DF6_HUMAN',NULL,'NEK4',NULL,'Q05DF6','451','0'),
('Q05DL3_HUMAN',NULL,'CSNK1A1',NULL,'Q05DL3','232','0'),
('Q0IJ40_HUMAN',NULL,'KIAA0999',NULL,'Q0IJ40','185','0'),
('Q0IJ44_HUMAN',NULL,'FGFR3',NULL,'Q0IJ44','480','0'),
('Q0IJ49_HUMAN',NULL,'PKMYT1',NULL,'Q0IJ49','485','0'),
('Q0VD65_HUMAN',NULL,'MYO3A',NULL,'Q0VD65','664','0'),
('Q0VG04_HUMAN',NULL,'MAPK4',NULL,'Q0VG04','587','0'),
('Q12787_HUMAN',NULL,NULL,NULL,'Q12787','723','0'),
('Q15136_HUMAN',NULL,'KIN27,PRKACA',NULL,'Q15136','207','0'),
('Q15300_HUMAN',NULL,'RET/PTC2',NULL,'Q15300','596','0'),
('Q15516_HUMAN',NULL,NULL,NULL,'Q15516','600','0'),
('Q15523_HUMAN',NULL,NULL,NULL,'Q15523','479','0'),
('Q15850_HUMAN',NULL,'urf-ret',NULL,'Q15850','435','0'),
('Q16176_HUMAN',NULL,'lsk',NULL,'Q16176','465','0'),
('Q17RV3_HUMAN',NULL,'LRRK2',NULL,'Q17RV3','2527','0'),
('Q1HBJ4_HUMAN',NULL,'MAPK1',NULL,'Q1HBJ4','360','0'),
('Q1KKQ2_HUMAN','Serine/threonine-protein kinase D','PRKD1','2.7.11.13','Q1KKQ2','914','0'),
('Q1PBM3_HUMAN',NULL,'MAP3K3',NULL,'Q1PBM3','622','0'),
('Q1RLL8_HUMAN',NULL,'RNASEL',NULL,'Q1RLL8','741','0'),
('Q1RMG3_HUMAN',NULL,'MERTK',NULL,'Q1RMG3','823','0'),
('Q2I0Y7_HUMAN',NULL,NULL,NULL,'Q2I0Y7','385','0'),
('Q2NME9_HUMAN',NULL,'CDKL4',NULL,'Q2NME9','379','0'),
('Q2TB16_HUMAN',NULL,'RIPK4',NULL,'Q2TB16','784','0'),
('Q2TSD3_HUMAN','Protein kinase C',NULL,'2.7.11.13','Q2TSD3','672','0'),
('Q2TTR7_HUMAN',NULL,NULL,NULL,'Q2TTR7','1210','0'),
('Q2TU65_HUMAN',NULL,NULL,NULL,'Q2TU65','540','0'),
('Q2VJ45_HUMAN',NULL,NULL,NULL,'Q2VJ45','776','0'),
('Q2VXS9_HUMAN','Tyrosine-protein kinase',NULL,'2.7.10.2','Q2VXS9','681','0'),
('Q32MQ5_HUMAN',NULL,'MAP3K6',NULL,'Q32MQ5','441','0'),
('Q32ND9_HUMAN',NULL,'IKBKB',NULL,'Q32ND9','420','0'),
('Q32NE9_HUMAN',NULL,'PXK',NULL,'Q32NE9','377','0'),
('Q3MS92_HUMAN',NULL,'BTK',NULL,'Q3MS92','208','0'),
('Q3MS96_HUMAN',NULL,'BTK',NULL,'Q3MS96','319','0'),
('Q499G7_HUMAN',NULL,'MAPK1',NULL,'Q499G7','360','0'),
('Q499L9_HUMAN',NULL,'MST4',NULL,'Q499L9','416','0'),
('Q499Y8_HUMAN',NULL,'MAPK10',NULL,'Q499Y8','319','0'),
('Q4G0X2_HUMAN',NULL,'MYO3A',NULL,'Q4G0X2','247','0'),
('Q4G1A8_HUMAN',NULL,'CAMK2D',NULL,'Q4G1A8','344','0'),
('Q4JFK8_HUMAN',NULL,'FES',NULL,'Q4JFK8','211','0'),
('Q4LDX3_HUMAN',NULL,'JAK1',NULL,'Q4LDX3','1141','0'),
('Q4LE53_HUMAN',NULL,'EPHB2',NULL,'Q4LE53','1004','0'),
('Q4VAU9_HUMAN',NULL,'ACVR2B',NULL,'Q4VAU9','303','0'),
('Q4VBY6_HUMAN',NULL,'CDC2L2',NULL,'Q4VBY6','475','0'),
('Q4W5L5_HUMAN',NULL,'MGC45428',NULL,'Q4W5L5','443','0'),
('Q504U8_HUMAN',NULL,'EGFR',NULL,'Q504U8','1091','0'),
('Q506Q0_HUMAN','Tyrosine-protein kinase','JAK2','2.7.10.2','Q506Q0','1132','0'),
('Q53EL3_HUMAN',NULL,NULL,NULL,'Q53EL3','449','0'),
('Q53EW6_HUMAN',NULL,NULL,NULL,'Q53EW6','496','0'),
('Q53EZ1_HUMAN',NULL,NULL,NULL,'Q53EZ1','416','0'),
('Q53EZ9_HUMAN',NULL,NULL,NULL,'Q53EZ9','347','0'),
('Q53GK9_HUMAN',NULL,NULL,NULL,'Q53GK9','307','0'),
('Q53GX0_HUMAN',NULL,NULL,NULL,'Q53GX0','651','0'),
('Q53H78_HUMAN',NULL,NULL,NULL,'Q53H78','542','0'),
('Q53HA9_HUMAN',NULL,NULL,NULL,'Q53HA9','822','0'),
('Q53HJ9_HUMAN',NULL,NULL,NULL,'Q53HJ9','556','0'),
('Q53QE7_HUMAN',NULL,'STK17B',NULL,'Q53QE7','372','0'),
('Q53R53_HUMAN',NULL,'MERTK',NULL,'Q53R53','567','0'),
('Q53SF4_HUMAN',NULL,'ACVR1',NULL,'Q53SF4','153','0'),
('Q53SV1_HUMAN',NULL,'ACVR1',NULL,'Q53SV1','355','0'),
('Q53T57_HUMAN',NULL,'ERBB4',NULL,'Q53T57','479','0'),
('Q53TA0_HUMAN',NULL,'EPHA4',NULL,'Q53TA0','711','0'),
('Q53TE4_HUMAN',NULL,'TLK1',NULL,'Q53TE4','376','0'),
('Q53TX8_HUMAN',NULL,'MAP4K4',NULL,'Q53TX8','1260','0'),
('Q541P7_HUMAN',NULL,'EPHB4',NULL,'Q541P7','987','0'),
('Q548C2_HUMAN','Tyrosine-protein kinase receptor','NTRK2','2.7.10.1','Q548C2','822','0'),
('Q562E6_HUMAN',NULL,'CHUK',NULL,'Q562E6','745','0'),
('Q56A86_HUMAN',NULL,'AKT3',NULL,'Q56A86','466','0'),
('Q573B4_HUMAN',NULL,'LCK',NULL,'Q573B4','516','0'),
('Q58A51_HUMAN',NULL,'Plk-1',NULL,'Q58A51','247','0'),
('Q58F15_HUMAN',NULL,'EPHA4',NULL,'Q58F15','949','0'),
('Q59EB0_HUMAN',NULL,NULL,NULL,'Q59EB0','1451','0'),
('Q59EB3_HUMAN',NULL,NULL,NULL,'Q59EB3','712','0'),
('Q59EB4_HUMAN',NULL,NULL,NULL,'Q59EB4','924','0'),
('Q59ED6_HUMAN',NULL,NULL,NULL,'Q59ED6','621','0'),
('Q59F04_HUMAN',NULL,NULL,NULL,'Q59F04','777','0'),
('Q59F17_HUMAN',NULL,NULL,NULL,'Q59F17','986','0'),
('Q59F19_HUMAN',NULL,NULL,NULL,'Q59F19','949','0'),
('Q59F30_HUMAN',NULL,NULL,NULL,'Q59F30','1034','0'),
('Q59F75_HUMAN',NULL,NULL,NULL,'Q59F75','255','0'),
('Q59FA7_HUMAN',NULL,NULL,NULL,'Q59FA7','337','0'),
('Q59FC5_HUMAN',NULL,NULL,NULL,'Q59FC5','565','0'),
('Q59FI5_HUMAN',NULL,NULL,NULL,'Q59FI5','461','0'),
('Q59FJ5_HUMAN',NULL,NULL,NULL,'Q59FJ5','556','0'),
('Q59FJ7_HUMAN',NULL,NULL,NULL,'Q59FJ7','342','0'),
('Q59FK4_HUMAN',NULL,NULL,NULL,'Q59FK4','1167','0'),
('Q59FL1_HUMAN',NULL,NULL,NULL,'Q59FL1','514','0'),
('Q59FL8_HUMAN',NULL,NULL,NULL,'Q59FL8','1081','0'),
('Q59FM9_HUMAN',NULL,NULL,NULL,'Q59FM9','951','0'),
('Q59FN2_HUMAN',NULL,NULL,NULL,'Q59FN2','279','0'),
('Q59FN4_HUMAN',NULL,NULL,NULL,'Q59FN4','830','0'),
('Q59FQ5_HUMAN',NULL,NULL,NULL,'Q59FQ5','232','0'),
('Q59FT4_HUMAN',NULL,NULL,NULL,'Q59FT4','1017','0'),
('Q59FU6_HUMAN',NULL,NULL,NULL,'Q59FU6','672','0'),
('Q59FX1_HUMAN',NULL,NULL,NULL,'Q59FX1','400','0'),
('Q59FX2_HUMAN',NULL,NULL,NULL,'Q59FX2','326','0'),
('Q59FZ4_HUMAN',NULL,NULL,NULL,'Q59FZ4','511','0'),
('Q59G02_HUMAN',NULL,NULL,NULL,'Q59G02','436','0'),
('Q59GD0_HUMAN',NULL,NULL,NULL,'Q59GD0','546','0'),
('Q59GF4_HUMAN',NULL,NULL,NULL,'Q59GF4','699','0'),
('Q59GL6_HUMAN',NULL,NULL,NULL,'Q59GL6','1455','0'),
('Q59GL9_HUMAN',NULL,NULL,NULL,'Q59GL9','483','0'),
('Q59GM4_HUMAN',NULL,NULL,NULL,'Q59GM4','802','0'),
('Q59GM6_HUMAN',NULL,NULL,NULL,'Q59GM6','1007','0'),
('Q59GN5_HUMAN',NULL,NULL,NULL,'Q59GN5','208','0'),
('Q59GN8_HUMAN',NULL,NULL,NULL,'Q59GN8','975','0'),
('Q59GQ4_HUMAN',NULL,NULL,NULL,'Q59GQ4','272','0'),
('Q59GQ9_HUMAN',NULL,NULL,NULL,'Q59GQ9','551','0'),
('Q59GT1_HUMAN',NULL,NULL,NULL,'Q59GT1','726','0'),
('Q59H88_HUMAN',NULL,NULL,NULL,'Q59H88','1433','0'),
('Q59HA5_HUMAN',NULL,NULL,NULL,'Q59HA5','1196','0'),
('Q59HG2_HUMAN',NULL,NULL,NULL,'Q59HG2','1157','0'),
('Q5H8Y1_HUMAN','Tyrosine-protein kinase receptor','ROS1','2.7.10.1','Q5H8Y1','2341','0'),
('Q5H8Y5_HUMAN',NULL,'SGK2',NULL,'Q5H8Y5','198','0'),
('Q5H9N4_HUMAN',NULL,'DKFZp686L20222',NULL,'Q5H9N4','303','0'),
('Q5H9Q5_HUMAN',NULL,'DKFZp781N0293',NULL,'Q5H9Q5','496','0'),
('Q5IBP5_HUMAN',NULL,NULL,NULL,'Q5IBP5','1492','0'),
('Q5JP05_HUMAN',NULL,'PRKG1',NULL,'Q5JP05','389','0'),
('Q5JPA7_HUMAN',NULL,'DKFZp667I0511',NULL,'Q5JPA7','391','0'),
('Q5JPB0_HUMAN',NULL,'DKFZp434B079',NULL,'Q5JPB0','501','0'),
('Q5JPC5_HUMAN',NULL,'DKFZp667E1714',NULL,'Q5JPC5','424','0'),
('Q5JQZ9_HUMAN',NULL,'CDK19',NULL,'Q5JQZ9','251','0'),
('Q5JS74_HUMAN',NULL,'CASK',NULL,'Q5JS74','590','0'),
('Q5JXL9_HUMAN',NULL,'DKFZp564L2416',NULL,'Q5JXL9','142','0'),
('Q5MD60_HUMAN',NULL,'MAP4K4',NULL,'Q5MD60','1042','0'),
('Q5QPD4_HUMAN',NULL,'AURKA',NULL,'Q5QPD4','271','0'),
('Q5QPR3_HUMAN',NULL,'CDK11A',NULL,'Q5QPR3','779','0'),
('Q5QPR4_HUMAN',NULL,'CDK11A',NULL,'Q5QPR4','746','0'),
('Q5R363_HUMAN',NULL,'SRPK1',NULL,'Q5R363','547','0'),
('Q5R3A8_HUMAN',NULL,'FYN',NULL,'Q5R3A8','485','0'),
('Q5R3E4_HUMAN',NULL,'MAPK13',NULL,'Q5R3E4','355','0'),
('Q5SQL3_HUMAN',NULL,'HIPK1',NULL,'Q5SQL3','1165','0'),
('Q5SQQ7_HUMAN',NULL,'CAMK1D',NULL,'Q5SQQ7','357','0'),
('Q5SQU3_HUMAN','cGMP-dependent protein kinase','PRKG1','2.7.11.12','Q5SQU3','659','0'),
('Q5SWX3_HUMAN',NULL,'CAMK2G',NULL,'Q5SWX3','516','0'),
('Q5T7S2_HUMAN',NULL,'TGFBR1',NULL,'Q5T7S2','503','0'),
('Q5T8F1_HUMAN',NULL,'DAPK1',NULL,'Q5T8F1','1455','0'),
('Q5TBG1_HUMAN',NULL,'NEK6',NULL,'Q5TBG1','207','0'),
('Q5TBG7_HUMAN',NULL,'NEK6',NULL,'Q5TBG7','219','0'),
('Q5TBH0_HUMAN',NULL,'NEK6',NULL,'Q5TBH0','200','0'),
('Q5TBH1_HUMAN',NULL,'NEK6',NULL,'Q5TBH1','222','0'),
('Q5TBH2_HUMAN',NULL,'NEK6',NULL,'Q5TBH2','220','0'),
('Q5TI62_HUMAN',NULL,'RPS6KA2',NULL,'Q5TI62','166','0'),
('Q5U045_HUMAN',NULL,'CSNK1E',NULL,'Q5U045','416','0'),
('Q5U0C9_HUMAN',NULL,NULL,NULL,'Q5U0C9','606','0'),
('Q5U0D0_HUMAN',NULL,NULL,NULL,'Q5U0D0','579','0'),
('Q5U0E6_HUMAN',NULL,'STK24,HEL-S-95',NULL,'Q5U0E6','431','0'),
('Q5U4A5_HUMAN',NULL,'MAPK13',NULL,'Q5U4A5','257','0'),
('Q5U5J2_HUMAN',NULL,'CSNK2A1',NULL,'Q5U5J2','397','0'),
('Q5VTU6_HUMAN',NULL,'FLT3',NULL,'Q5VTU6','996','0'),
('Q5Y191_HUMAN',NULL,'AURKC',NULL,'Q5Y191','306','0'),
('Q658W2_HUMAN',NULL,'DKFZp666O0110',NULL,'Q658W2','1074','0'),
('Q68D16_HUMAN',NULL,'DKFZp686D0638',NULL,'Q68D16','388','0'),
('Q68D39_HUMAN',NULL,'DKFZp686J04131',NULL,'Q68D39','433','0'),
('Q68DI6_HUMAN',NULL,'DKFZp781H1925',NULL,'Q68DI6','965','0'),
('Q69FE3_HUMAN',NULL,'IRAK4',NULL,'Q69FE3','460','0'),
('Q6AI46_HUMAN',NULL,'DKFZp781D08126,RNASEL',NULL,'Q6AI46','652','0'),
('Q6E0B2_HUMAN',NULL,NULL,NULL,'Q6E0B2','476','0'),
('Q6FG25_HUMAN',NULL,'MAP3K8',NULL,'Q6FG25','467','0'),
('Q6FG81_HUMAN',NULL,'STK24',NULL,'Q6FG81','431','0'),
('Q6FG83_HUMAN',NULL,'STK17B',NULL,'Q6FG83','372','0'),
('Q6FG98_HUMAN',NULL,'STK17B',NULL,'Q6FG98','372','0'),
('Q6FHG1_HUMAN',NULL,'MAP2K3',NULL,'Q6FHG1','347','0'),
('Q6FHR4_HUMAN',NULL,'MAPK13',NULL,'Q6FHR4','365','0'),
('Q6FHV7_HUMAN',NULL,'SGKL',NULL,'Q6FHV7','429','0'),
('Q6FI23_HUMAN',NULL,'MAP2K3',NULL,'Q6FI23','347','0'),
('Q6FI27_HUMAN',NULL,'GSK3B',NULL,'Q6FI27','420','0'),
('Q6IAW3_HUMAN',NULL,'CDK5',NULL,'Q6IAW3','292','0'),
('Q6IC53_HUMAN',NULL,'MAPK12',NULL,'Q6IC53','357','0'),
('Q6LC83_HUMAN',NULL,'CDK4',NULL,'Q6LC83','229','0'),
('Q6MZT2_HUMAN',NULL,'DKFZp686D1354',NULL,'Q6MZT2','855','0'),
('Q6N076_HUMAN',NULL,'DKFZp686M02159',NULL,'Q6N076','319','0'),
('Q6NSL2_HUMAN',NULL,'WEE1',NULL,'Q6NSL2','646','0'),
('Q6NSZ4_HUMAN',NULL,'PHKG1',NULL,'Q6NSZ4','390','0'),
('Q6NUK7_HUMAN',NULL,'LYN',NULL,'Q6NUK7','582','0'),
('Q6P084_HUMAN',NULL,'MAP3K2',NULL,'Q6P084','234','0'),
('Q6P0Y1_HUMAN',NULL,'STK24',NULL,'Q6P0Y1','431','0'),
('Q6P4R6_HUMAN',NULL,'EPHA3',NULL,'Q6P4R6','983','0'),
('Q6P5Y5_HUMAN',NULL,'CDC2L2',NULL,'Q6P5Y5','475','0'),
('Q6PIN8_HUMAN',NULL,'TAOK2',NULL,'Q6PIN8','560','0'),
('Q6PJ06_HUMAN',NULL,'CSNK1A1',NULL,'Q6PJ06','261','0'),
('Q6ZN64_HUMAN',NULL,'NEK3',NULL,'Q6ZN64','510','0'),
('Q6ZNH1_HUMAN',NULL,NULL,NULL,'Q6ZNH1','543','0'),
('Q6ZNI2_HUMAN',NULL,NULL,'2.7.1.-','Q6ZNI2','706','0'),
('Q6ZNR9_HUMAN',NULL,'DDR1',NULL,'Q6ZNR9','441','0'),
('Q6ZRA8_HUMAN',NULL,NULL,NULL,'Q6ZRA8','596','0'),
('Q71TU5_HUMAN',NULL,'CSNK1A1',NULL,'Q71TU5','325','0'),
('Q75MF2_HUMAN',NULL,'EGFR',NULL,'Q75MF2','387','0'),
('Q75MR0_HUMAN',NULL,'HRI',NULL,'Q75MR0','386','0'),
('Q7LDD5_HUMAN',NULL,'CAMK2A',NULL,'Q7LDD5','478','0'),
('Q7Z319_HUMAN',NULL,'DKFZp686E14208,MKNK1',NULL,'Q7Z319','329','0'),
('Q7Z370_HUMAN',NULL,'DKFZp686L02273',NULL,'Q7Z370','303','0'),
('Q7Z3H5_HUMAN',NULL,'DKFZp686O0215',NULL,'Q7Z3H5','323','0'),
('Q7Z635_HUMAN',NULL,'EPHB4',NULL,'Q7Z635','987','0'),
('Q86UI9_HUMAN',NULL,'STK17A',NULL,'Q86UI9','161','0'),
('Q86V29_HUMAN',NULL,'WEE1',NULL,'Q86V29','646','0'),
('Q86V37_HUMAN',NULL,'TAOK2',NULL,'Q86V37','1426','0'),
('Q86VU2_HUMAN',NULL,NULL,NULL,'Q86VU2','524','0'),
('Q86VY5_HUMAN',NULL,'MYO3A',NULL,'Q86VY5','247','0'),
('Q86XZ8_HUMAN',NULL,'CDC42BPB',NULL,'Q86XZ8','492','0'),
('Q86YC8_HUMAN',NULL,'STRADA',NULL,'Q86YC8','234','0'),
('Q8IW76_HUMAN',NULL,'EIF2AK2',NULL,'Q8IW76','513','0'),
('Q8IWB3_HUMAN',NULL,'PCTK3',NULL,'Q8IWB3','231','0'),
('Q8IWE0_HUMAN',NULL,'CAMK2A',NULL,'Q8IWE0','478','0'),
('Q8IWQ7_HUMAN',NULL,'CDC42BPA',NULL,'Q8IWQ7','1638','0'),
('Q8IWY7_HUMAN',NULL,'TTBK2',NULL,'Q8IWY7','1649','0'),
('Q8IXA3_HUMAN',NULL,NULL,NULL,'Q8IXA3','438','0'),
('Q8IXN4_HUMAN',NULL,'MAK',NULL,'Q8IXN4','457','0'),
('Q8IXP2_HUMAN','Tyrosine-protein kinase','JAK2','2.7.10.2','Q8IXP2','1129','0'),
('Q8IYN9_HUMAN',NULL,'PTK2',NULL,'Q8IYN9','1006','0'),
('Q8IZN1_HUMAN',NULL,'C14orf20,TSSK4',NULL,'Q8IZN1','258','0'),
('Q8N2H2_HUMAN',NULL,NULL,NULL,'Q8N2H2','721','0'),
('Q8N2N5_HUMAN',NULL,NULL,NULL,'Q8N2N5','426','0'),
('Q8N433_HUMAN',NULL,NULL,NULL,'Q8N433','387','0'),
('Q8N6J3_HUMAN',NULL,'TYRO3',NULL,'Q8N6J3','518','0'),
('Q8N774_HUMAN',NULL,'NEK10',NULL,'Q8N774','404','0'),
('Q8N7M6_HUMAN',NULL,NULL,NULL,'Q8N7M6','372','0'),
('Q8N9D7_HUMAN',NULL,'PTK2',NULL,'Q8N9D7','720','0'),
('Q8NBY1_HUMAN',NULL,'MST4',NULL,'Q8NBY1','392','0'),
('Q8NCK8_HUMAN',NULL,NULL,NULL,'Q8NCK8','721','0'),
('Q8NFJ4_HUMAN',NULL,NULL,NULL,'Q8NFJ4','244','0'),
('Q8NHX0_HUMAN',NULL,NULL,NULL,'Q8NHX0','335','0'),
('Q8NI15_HUMAN','Fibroblast growth factor receptor','FGFR3','2.7.10.1','Q8NI15','769','0'),
('Q8NI16_HUMAN','Fibroblast growth factor receptor','FGFR3','2.7.10.1','Q8NI16','771','0'),
('Q8TB93_HUMAN',NULL,'PAK7',NULL,'Q8TB93','719','0'),
('Q8TCG9_HUMAN',NULL,'KIT',NULL,'Q8TCG9','160','0'),
('Q8TDJ5_HUMAN','Tyrosine-protein kinase receptor','TFG/ALK','2.7.10.1','Q8TDJ5','803','0'),
('Q8WTZ8_HUMAN',NULL,'RYK',NULL,'Q8WTZ8','395','0'),
('Q8WU40_HUMAN',NULL,'CAMK2G',NULL,'Q8WU40','453','0'),
('Q96AD6_HUMAN',NULL,'GRK6',NULL,'Q96AD6','589','0'),
('Q96BA2_HUMAN',NULL,NULL,NULL,'Q96BA2','426','0'),
('Q96CA8_HUMAN',NULL,'CDC2L2',NULL,'Q96CA8','464','0'),
('Q96E92_HUMAN',NULL,'PRKAA1',NULL,'Q96E92','207','0'),
('Q96GA5_HUMAN',NULL,'PCTK1',NULL,'Q96GA5','395','0'),
('Q96HF4_HUMAN',NULL,'EPHA2',NULL,'Q96HF4','253','0'),
('Q96HN9_HUMAN',NULL,NULL,NULL,'Q96HN9','594','0'),
('Q96II5_HUMAN',NULL,'ARAF',NULL,'Q96II5','609','0'),
('Q96K88_HUMAN',NULL,NULL,NULL,'Q96K88','142','0'),
('Q96L35_HUMAN',NULL,'EPHB4',NULL,'Q96L35','935','0'),
('Q96T11_HUMAN',NULL,NULL,NULL,'Q96T11','784','0'),
('Q9BRG8_HUMAN',NULL,'CLK2',NULL,'Q9BRG8','338','0'),
('Q9BRL4_HUMAN',NULL,'PCTK1',NULL,'Q9BRL4','448','0'),
('Q9BRS0_HUMAN','Ribosomal protein S6 kinase','RPS6KB2','2.7.11.1','Q9BRS0','482','0'),
('Q9BS11_HUMAN',NULL,'LRRK1',NULL,'Q9BS11','659','0'),
('Q9BUD9_HUMAN',NULL,'AAK1',NULL,'Q9BUD9','474','0'),
('Q9BVE2_HUMAN',NULL,NULL,NULL,'Q9BVE2','324','0'),
('Q9BWF9_HUMAN',NULL,'PCTK3',NULL,'Q9BWF9','283','0'),
('Q9H4D1_HUMAN',NULL,'dik',NULL,'Q9H4D1','784','0'),
('Q9H5M4_HUMAN',NULL,NULL,NULL,'Q9H5M4','280','0'),
('Q9H7V3_HUMAN',NULL,NULL,NULL,'Q9H7V3','251','0'),
('Q9HBS3_HUMAN',NULL,NULL,NULL,'Q9HBS3','433','0'),
('Q9HBS4_HUMAN',NULL,'TIE1',NULL,'Q9HBS4','421','0'),
('Q9NPI2_HUMAN',NULL,NULL,NULL,'Q9NPI2','174','0'),
('Q9NPI3_HUMAN',NULL,NULL,NULL,'Q9NPI3','174','0'),
('Q9NRL6_HUMAN',NULL,NULL,NULL,'Q9NRL6','453','0'),
('Q9NSQ6_HUMAN',NULL,'DKFZp434L0319',NULL,'Q9NSQ6','364','0'),
('Q9NT28_HUMAN',NULL,'DKFZp586A1021',NULL,'Q9NT28','316','0'),
('Q9NWE9_HUMAN',NULL,NULL,NULL,'Q9NWE9','332','0'),
('Q9NWX4_HUMAN',NULL,NULL,NULL,'Q9NWX4','293','0'),
('Q9P0L3_HUMAN',NULL,NULL,NULL,'Q9P0L3','172','0'),
('Q9P0L5_HUMAN',NULL,NULL,NULL,'Q9P0L5','174','0'),
('Q9P0L6_HUMAN',NULL,NULL,NULL,'Q9P0L6','174','0'),
('Q9P0L7_HUMAN',NULL,NULL,NULL,'Q9P0L7','174','0'),
('Q9P0M0_HUMAN',NULL,NULL,NULL,'Q9P0M0','149','0'),
('Q9P1M2_HUMAN',NULL,NULL,NULL,'Q9P1M2','544','0'),
('Q9UFE3_HUMAN',NULL,'DKFZp434M058',NULL,'Q9UFE3','380','0'),
('Q9UMQ4_HUMAN',NULL,'RET',NULL,'Q9UMQ4','1091','0'),
('Q9UPJ8_HUMAN',NULL,'PkB-like',NULL,'Q9UPJ8','367','0'),
('Q9Y6B5_HUMAN',NULL,NULL,NULL,'Q9Y6B5','540','0'),
('RAF1_HUMAN','RAF proto-oncogene serine/threonine-protein kinase,Proto-oncogene c-RAF,cRaf,Raf-1','RAF1,RAF','2.7.11.1','P04049','648','2'),
('RET_HUMAN','Proto-oncogene tyrosine-protein kinase receptor Ret,Cadherin family member 12,Proto-oncogene c-Ret,Soluble RET kinase fragment,Extracellular cell-membrane anchored RET cadherin 120 kDa fragment','RET,CDHF12, CDHR16, PTC, RET51','2.7.10.1','P07949','1114','2'),
('RIPK1_HUMAN','Receptor-interacting serine/threonine-protein kinase 1,Cell death protein RIP,Receptor-interacting protein 1,RIP-1,Serine/threonine-protein kinase RIP','RIPK1,RIP, RIP1','2.7.11.1','Q13546','671','1'),
('RIPK2_HUMAN','Receptor-interacting serine/threonine-protein kinase 2,CARD-containing interleukin-1 beta-converting enzyme-associated kinase,CARD-containing IL-1 beta ICE-kinase,RIP-like-interacting CLARP kinase,Receptor-interacting protein 2,RIP-2,Tyrosine-protein kinase RIPK2','RIPK2,CARDIAK, RICK, RIP2','2.7.11.1,2.7.10.2','O43353','540','1'),
('RIPK3_HUMAN','Receptor-interacting serine/threonine-protein kinase 3,RIP-like protein kinase 3,Receptor-interacting protein 3,RIP-3','RIPK3,RIP3','2.7.11.1','Q9Y572','518','1'),
('RIPK4_HUMAN','Receptor-interacting serine/threonine-protein kinase 4,Ankyrin repeat domain-containing protein 3,PKC-delta-interacting protein kinase','RIPK4,ANKRD3, DIK','2.7.11.1','P57078','832','1'),
('RK_HUMAN','Rhodopsin kinase,RK,G protein-coupled receptor kinase 1','GRK1,RHOK','2.7.11.14','Q15835','563','1'),
('RN5A_HUMAN','2-5A-dependent ribonuclease,2-5A-dependent RNase,Ribonuclease 4,Ribonuclease L,RNase L','RNASEL,RNS4','3.1.26.-','Q05823','741','1'),
('ROCK1_HUMAN','Rho-associated protein kinase 1,Renal carcinoma antigen NY-REN-35,Rho-associated, coiled-coil-containing protein kinase 1,Rho-associated, coiled-coil-containing protein kinase I,ROCK-I,p160 ROCK-1,p160ROCK','ROCK1','2.7.11.1','Q13464','1354','1'),
('ROCK2_HUMAN','Rho-associated protein kinase 2,Rho kinase 2,Rho-associated, coiled-coil-containing protein kinase 2,Rho-associated, coiled-coil-containing protein kinase II,ROCK-II,p164 ROCK-2','ROCK2,KIAA0619','2.7.11.1','O75116','1388','1'),
('RON_HUMAN','Macrophage-stimulating protein receptor,MSP receptor,CDw136,Protein-tyrosine kinase 8,p185-Ron,Macrophage-stimulating protein receptor alpha chain,Macrophage-stimulating protein receptor beta chain','MST1R,PTK8, RON','2.7.10.1','Q04912','1400','1'),
('ROR1_HUMAN','Tyrosine-protein kinase transmembrane receptor ROR1,Neurotrophic tyrosine kinase, receptor-related 1','ROR1,NTRKR1','2.7.10.1','Q01973','937','1'),
('ROR2_HUMAN','Tyrosine-protein kinase transmembrane receptor ROR2,Neurotrophic tyrosine kinase, receptor-related 2','ROR2,NTRKR2','2.7.10.1','Q01974','943','1'),
('ROS1_HUMAN','Proto-oncogene tyrosine-protein kinase ROS,Proto-oncogene c-Ros,Proto-oncogene c-Ros-1,Receptor tyrosine kinase c-ros oncogene 1,c-Ros receptor tyrosine kinase','ROS1,MCF3, ROS','2.7.10.1','P08922','2347','1'),
('RPKL1_HUMAN','Ribosomal protein S6 kinase-like 1','RPS6KL1','2.7.11.1','Q9Y6S9','549','1'),
('RYK_HUMAN','Tyrosine-protein kinase RYK','RYK,JTK5A','2.7.10.1','P34925','604','1'),
('SBK1_HUMAN','Serine/threonine-protein kinase SBK1,SH3-binding kinase 1','SBK1','2.7.11.1','Q52WX2','424','1'),
('SBK2_HUMAN','Serine/threonine-protein kinase SBK2,SH3-binding domain kinase family member 2,Sugen kinase 69,SgK069','SBK2,SGK069','2.7.11.1','P0C263','348','1'),
('SCYL2_HUMAN','SCY1-like protein 2,Coated vesicle-associated kinase of 104 kDa','SCYL2,CVAK104, KIAA1360',NULL,'Q6P3W7','929','1'),
('SG110_HUMAN','Uncharacterized serine/threonine-protein kinase SBK3,SH3-binding domain kinase family member 3,Sugen kinase 110','SBK3,SGK110','2.7.11.1','P0C264','359','1'),
('SG196_HUMAN','Protein O-mannose kinase,POMK,Protein kinase-like protein SgK196,Sugen kinase 196','POMK,SGK196','2.7.1.-','Q9H5K3','350','1'),
('SG223_HUMAN','Tyrosine-protein kinase SgK223,Sugen kinase 223','SGK223','2.7.10.2','Q86YV5','1402','1'),
('SG494_HUMAN','Uncharacterized serine/threonine-protein kinase SgK494,Sugen kinase 494','SGK494','2.7.11.1','Q96LW2','274','1'),
('SGK1_HUMAN','Serine/threonine-protein kinase Sgk1,Serum/glucocorticoid-regulated kinase 1','SGK1,SGK','2.7.11.1','O00141','431','1'),
('SGK2_HUMAN','Serine/threonine-protein kinase Sgk2,Serum/glucocorticoid-regulated kinase 2','SGK2','2.7.11.1','Q9HBY8','427','1'),
('SGK3_HUMAN','Serine/threonine-protein kinase Sgk3,Cytokine-independent survival kinase,Serum/glucocorticoid-regulated kinase 3,Serum/glucocorticoid-regulated kinase-like','SGK3,CISK, SGKL','2.7.11.1','Q96BR1','496','1'),
('SGK71_HUMAN','Probable inactive protein kinase-like protein SgK071,Sugen kinase 071','SGK071,C9orf96',NULL,'Q8NE28','680','1'),
('SIK1_HUMAN','Serine/threonine-protein kinase SIK1,Salt-inducible kinase 1,SIK-1,Serine/threonine-protein kinase SNF1-like kinase 1,Serine/threonine-protein kinase SNF1LK','SIK1,SIK, SNF1LK','2.7.11.1','P57059','783','1'),
('SIK2_HUMAN','Serine/threonine-protein kinase SIK2,Qin-induced kinase,Salt-inducible kinase 2,SIK-2,Serine/threonine-protein kinase SNF1-like kinase 2','SIK2,KIAA0781, QIK, SNF1LK2','2.7.11.1','Q9H0K1','926','1'),
('SIK3_HUMAN','Serine/threonine-protein kinase SIK3,Salt-inducible kinase 3,SIK-3,Serine/threonine-protein kinase QSK','SIK3,KIAA0999, QSK','2.7.11.1','Q9Y2K2','1263','1'),
('SLK_HUMAN','STE20-like serine/threonine-protein kinase,STE20-like kinase,hSLK,CTCL tumor antigen se20-9,STE20-related serine/threonine-protein kinase,STE20-related kinase,Serine/threonine-protein kinase 2','SLK,KIAA0204, STK2','2.7.11.1','Q9H2G2','1235','1'),
('SNRK_HUMAN','SNF-related serine/threonine-protein kinase,SNF1-related kinase','SNRK,KIAA0096, SNFRK','2.7.11.1','Q9NRH2','765','1'),
('SPEG_HUMAN','Striated muscle preferentially expressed protein kinase,Aortic preferentially expressed protein 1,APEG-1','SPEG,APEG1, KIAA1297','2.7.11.1','Q15772','3267','1'),
('SRC_HUMAN','Proto-oncogene tyrosine-protein kinase Src,Proto-oncogene c-Src,pp60c-src,p60-Src','SRC,SRC1','2.7.10.2','P12931','536','1'),
('SRMS_HUMAN','Tyrosine-protein kinase Srms','SRMS,C20orf148','2.7.10.2','Q9H3Y6','488','1'),
('SRPK1_HUMAN','SRSF protein kinase 1,SFRS protein kinase 1,Serine/arginine-rich protein-specific kinase 1,SR-protein-specific kinase 1','SRPK1','2.7.11.1','Q96SB4','655','1'),
('SRPK2_HUMAN','SRSF protein kinase 2,SFRS protein kinase 2,Serine/arginine-rich protein-specific kinase 2,SR-protein-specific kinase 2,SRSF protein kinase 2 N-terminal,SRSF protein kinase 2 C-terminal','SRPK2','2.7.11.1','P78362','688','1'),
('SRPK3_HUMAN','SRSF protein kinase 3,Muscle-specific serine kinase 1,MSSK-1,Serine/arginine-rich protein-specific kinase 3,SR-protein-specific kinase 3,Serine/threonine-protein kinase 23','SRPK3,MSSK1, STK23','2.7.11.1','Q9UPE1','567','1'),
('ST17A_HUMAN','Serine/threonine-protein kinase 17A,DAP kinase-related apoptosis-inducing protein kinase 1','STK17A,DRAK1','2.7.11.1','Q9UEE5','414','1'),
('ST17B_HUMAN','Serine/threonine-protein kinase 17B,DAP kinase-related apoptosis-inducing protein kinase 2','STK17B,DRAK2','2.7.11.1','O94768','372','1'),
('ST32A_HUMAN','Serine/threonine-protein kinase 32A,Yet another novel kinase 1','STK32A,YANK1','2.7.11.1','Q8WU08','396','1'),
('ST32B_HUMAN','Serine/threonine-protein kinase 32B,Yet another novel kinase 2','STK32B,YANK2','2.7.11.1','Q9NY57','414','1'),
('ST32C_HUMAN','Serine/threonine-protein kinase 32C,PKE,Yet another novel kinase 3','STK32C,YANK3','2.7.11.1','Q86UX6','486','1'),
('ST38L_HUMAN','Serine/threonine-protein kinase 38-like,NDR2 protein kinase,Nuclear Dbf2-related kinase 2','STK38L,KIAA0965, NDR2','2.7.11.1','Q9Y2H1','464','1'),
('STK10_HUMAN','Serine/threonine-protein kinase 10,Lymphocyte-oriented kinase','STK10,LOK','2.7.11.1','O94804','968','1'),
('STK11_HUMAN','Serine/threonine-protein kinase STK11,Liver kinase B1,LKB1,hLKB1,Renal carcinoma antigen NY-REN-19','STK11,LKB1, PJS','2.7.11.1','Q15831','433','2'),
('STK16_HUMAN','Serine/threonine-protein kinase 16,Myristoylated and palmitoylated serine/threonine-protein kinase,MPSK,Protein kinase PKL12,TGF-beta-stimulated factor 1,TSF-1,Tyrosine-protein kinase STK16,hPSK','STK16,MPSK1, PKL12, TSF1','2.7.11.1,2.7.10.2','O75716','305','1'),
('STK24_HUMAN','Serine/threonine-protein kinase 24,Mammalian STE20-like protein kinase 3,MST-3,STE20-like kinase MST3,Serine/threonine-protein kinase 24 36 kDa subunit,Mammalian STE20-like protein kinase 3 N-terminal,MST3/N,Serine/threonine-protein kinase 24 12 kDa subunit,Mammalian STE20-like protein kinase 3 C-terminal,MST3/C','STK24,MST3, STK3','2.7.11.1','Q9Y6E0','443','1'),
('STK25_HUMAN','Serine/threonine-protein kinase 25,Ste20-like kinase,Sterile 20/oxidant stress-response kinase 1,SOK-1,Ste20/oxidant stress response kinase 1','STK25,SOK1, YSK1','2.7.11.1','O00506','426','1'),
('STK31_HUMAN','Serine/threonine-protein kinase 31,Serine/threonine-protein kinase NYD-SPK,Sugen kinase 396,SgK396','STK31,SGK396','2.7.11.1','Q9BXU1','1019','1'),
('STK33_HUMAN','Serine/threonine-protein kinase 33','STK33','2.7.11.1','Q9BYT3','514','2'),
('STK35_HUMAN','Serine/threonine-protein kinase 35,CLP-36-interacting kinase 1,CLIK-1,PDLIM1-interacting kinase 1,Serine/threonine-protein kinase 35 L1','STK35,CLIK1, PDIK1, STK35L1','2.7.11.1','Q8TDR2','534','1'),
('STK36_HUMAN','Serine/threonine-protein kinase 36,Fused homolog','STK36,KIAA1278','2.7.11.1','Q9NRP7','1315','1'),
('STK38_HUMAN','Serine/threonine-protein kinase 38,NDR1 protein kinase,Nuclear Dbf2-related kinase 1','STK38,NDR1','2.7.11.1','Q15208','465','1'),
('STK39_HUMAN','STE20/SPS1-related proline-alanine-rich protein kinase,Ste-20-related kinase,DCHT,Serine/threonine-protein kinase 39','STK39,SPAK','2.7.11.1','Q9UEW8','545','1'),
('STK3_HUMAN','Serine/threonine-protein kinase 3,Mammalian STE20-like protein kinase 2,MST-2,STE20-like kinase MST2,Serine/threonine-protein kinase Krs-1,Serine/threonine-protein kinase 3 36kDa subunit,MST2/N,Serine/threonine-protein kinase 3 20kDa subunit,MST2/C','STK3,KRS1, MST2','2.7.11.1','Q13188','491','1'),
('STK40_HUMAN','Serine/threonine-protein kinase 40,SINK-homologous serine/threonine-protein kinase,Sugen kinase 495,SgK495','STK40,SGK495, SHIK','2.7.11.1','Q8N2I9','435','1'),
('STK4_HUMAN','Serine/threonine-protein kinase 4,Mammalian STE20-like protein kinase 1,MST-1,STE20-like kinase MST1,Serine/threonine-protein kinase Krs-2,Serine/threonine-protein kinase 4 37kDa subunit,MST1/N,Serine/threonine-protein kinase 4 18kDa subunit,MST1/C','STK4,KRS2, MST1','2.7.11.1','Q13043','487','1'),
('STRAA_HUMAN','STE20-related kinase adapter protein alpha,STRAD alpha,STE20-related adapter protein,Serologically defined breast cancer antigen NY-BR-96','STRADA,LYK5, STRAD',NULL,'Q7RTN6','431','1'),
('STRAB_HUMAN','STE20-related kinase adapter protein beta,STRAD beta,Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 2 protein,CALS-21,ILP-interacting protein,Pseudokinase ALS2CR2','STRADB,ALS2CR2, ILPIP',NULL,'Q9C0K7','418','1'),
('STYK1_HUMAN','Tyrosine-protein kinase STYK1,Novel oncogene with kinase domain,Protein PK-unique,Serine/threonine/tyrosine kinase 1','STYK1,NOK','2.7.10.2','Q6J9G0','422','1'),
('TAOK1_HUMAN','Serine/threonine-protein kinase TAO1,Kinase from chicken homolog B,hKFC-B,MARK Kinase,MARKK,Prostate-derived sterile 20-like kinase 2,PSK-2,PSK2,Prostate-derived STE20-like kinase 2,Thousand and one amino acid protein kinase 1,TAOK1,hTAOK1','TAOK1,KIAA1361, MAP3K16, MARKK','2.7.11.1','Q7L7X3','1001','1'),
('TAOK2_HUMAN','Serine/threonine-protein kinase TAO2,Kinase from chicken homolog C,hKFC-C,Prostate-derived sterile 20-like kinase 1,PSK-1,PSK1,Prostate-derived STE20-like kinase 1,Thousand and one amino acid protein kinase 2','TAOK2,KIAA0881, MAP3K17, PSK, PSK1','2.7.11.1','Q9UL54','1235','1'),
('TAOK3_HUMAN','Serine/threonine-protein kinase TAO3,Cutaneous T-cell lymphoma-associated antigen HD-CL-09,CTCL-associated antigen HD-CL-09,Dendritic cell-derived protein kinase,JNK/SAPK-inhibitory kinase,Jun kinase-inhibitory kinase,Kinase from chicken homolog A,hKFC-A,Thousand and one amino acid protein 3','TAOK3,DPK, JIK, KDS, MAP3K18','2.7.11.1','Q9H2K8','898','1'),
('TBCK_HUMAN','TBC domain-containing protein kinase-like protein','TBCK,TBCKL',NULL,'Q8TEA7','893','1'),
('TBK1_HUMAN','Serine/threonine-protein kinase TBK1,NF-kappa-B-activating kinase,T2K,TANK-binding kinase 1','TBK1,NAK','2.7.11.1','Q9UHD2','729','1'),
('TEC_HUMAN','Tyrosine-protein kinase Tec','TEC,PSCTK4','2.7.10.2','P42680','631','1'),
('TESK1_HUMAN','Dual specificity testis-specific protein kinase 1,Testicular protein kinase 1','TESK1','2.7.12.1','Q15569','626','1'),
('TESK2_HUMAN','Dual specificity testis-specific protein kinase 2,Testicular protein kinase 2','TESK2','2.7.12.1','Q96S53','571','1'),
('TEX14_HUMAN','Inactive serine/threonine-protein kinase TEX14,Protein kinase-like protein SgK307,Sugen kinase 307,Testis-expressed sequence 14,Testis-expressed sequence 14 protein','TEX14,SGK307',NULL,'Q8IWB6','1497','1'),
('TGFR1_HUMAN','TGF-beta receptor type-1,TGFR-1,Activin A receptor type II-like protein kinase of 53kD,Activin receptor-like kinase 5,ALK-5,ALK5,Serine/threonine-protein kinase receptor R4,SKR4,TGF-beta type I receptor,Transforming growth factor-beta receptor type I,TGF-beta receptor type I,TbetaR-I','TGFBR1,ALK5, SKR4','2.7.11.30','P36897','503','1'),
('TGFR2_HUMAN','TGF-beta receptor type-2,TGFR-2,TGF-beta type II receptor,Transforming growth factor-beta receptor type II,TGF-beta receptor type II,TbetaR-II','TGFBR2','2.7.11.30','P37173','567','1'),
('TIE1_HUMAN','Tyrosine-protein kinase receptor Tie-1','TIE1,TIE','2.7.10.1','P35590','1138','1'),
('TIE2_HUMAN','Angiopoietin-1 receptor,Endothelial tyrosine kinase,Tunica interna endothelial cell kinase,Tyrosine kinase with Ig and EGF homology domains-2,Tyrosine-protein kinase receptor TEK,Tyrosine-protein kinase receptor TIE-2,hTIE2,p140 TEK','TEK,TIE2, VMCM, VMCM1','2.7.10.1','Q02763','1124','2'),
('TITIN_HUMAN','Titin,Connectin,Rhabdomyosarcoma antigen MU-RMS-40.14','TTN','2.7.11.1','Q8WZ42','34350','1'),
('TLK1_HUMAN','Serine/threonine-protein kinase tousled-like 1,PKU-beta,Tousled-like kinase 1','TLK1,KIAA0137','2.7.11.1','Q9UKI8','766','1'),
('TLK2_HUMAN','Serine/threonine-protein kinase tousled-like 2,HsHPK,PKU-alpha,Tousled-like kinase 2','TLK2','2.7.11.1','Q86UE8','772','1'),
('TNI3K_HUMAN','Serine/threonine-protein kinase TNNI3K,Cardiac ankyrin repeat kinase,Cardiac troponin I-interacting kinase,TNNI3-interacting kinase','TNNI3K,CARK','2.7.11.1','Q59H18','835','1'),
('TNIK_HUMAN','TRAF2 and NCK-interacting protein kinase','TNIK,KIAA0551','2.7.11.1','Q9UKE5','1360','1'),
('TNK1_HUMAN','Non-receptor tyrosine-protein kinase TNK1,CD38 negative kinase 1','TNK1','2.7.10.2','Q13470','666','1'),
('TOPK_HUMAN','Lymphokine-activated killer T-cell-originated protein kinase,Cancer/testis antigen 84,CT84,MAPKK-like protein kinase,Nori-3,PDZ-binding kinase,Spermatogenesis-related protein kinase,SPK,T-LAK cell-originated protein kinase','PBK,TOPK','2.7.12.2','Q96KB5','322','1'),
('TRIB1_HUMAN','Tribbles homolog 1,TRB-1,G-protein-coupled receptor-induced gene 2 protein,GIG-2,SKIP1','TRIB1,C8FW, GIG2, TRB1',NULL,'Q96RU8','372','1'),
('TRIB2_HUMAN','Tribbles homolog 2,TRB-2','TRIB2,TRB2',NULL,'Q92519','343','1'),
('TRIB3_HUMAN','Tribbles homolog 3,TRB-3,Neuronal cell death-inducible putative kinase,SINK,p65-interacting inhibitor of NF-kappa-B','TRIB3,C20orf97, NIPK, SKIP3, TRB3',NULL,'Q96RU7','358','1'),
('TRIO_HUMAN','Triple functional domain protein,PTPRF-interacting protein','TRIO','2.7.11.1','O75962','3097','1'),
('TSSK1_HUMAN','Testis-specific serine/threonine-protein kinase 1,TSK-1,TSK1,TSSK-1,Testis-specific kinase 1,Serine/threonine-protein kinase 22A','TSSK1B,SPOGA1, SPOGA4, STK22A, STK22D, TSSK1','2.7.11.1','Q9BXA7','367','1'),
('TSSK2_HUMAN','Testis-specific serine/threonine-protein kinase 2,TSK-2,TSK2,TSSK-2,Testis-specific kinase 2,DiGeorge syndrome protein G,DGS-G,Serine/threonine-protein kinase 22B','TSSK2,DGSG, SPOGA2, STK22B','2.7.11.1','Q96PF2','358','1'),
('TSSK3_HUMAN','Testis-specific serine/threonine-protein kinase 3,TSK-3,TSSK-3,Testis-specific kinase 3,Serine/threonine-protein kinase 22C','TSSK3,SPOGA3, STK22C','2.7.11.1','Q96PN8','268','1'),
('TSSK4_HUMAN','Testis-specific serine/threonine-protein kinase 4,TSK-4,TSSK-4,Testis-specific kinase 4,Serine/threonine-protein kinase 22E','TSSK4,C14orf20, STK22E, TSSK5','2.7.11.1','Q6SA08','328','1'),
('TSSK6_HUMAN','Testis-specific serine/threonine-protein kinase 6,TSK-6,TSSK-6,Testis-specific kinase 6,Cancer/testis antigen 72,CT72,Serine/threonine-protein kinase SSTK,Small serine/threonine kinase','TSSK6,SSTK','2.7.11.1','Q9BXA6','273','1'),
('TTBK1_HUMAN','Tau-tubulin kinase 1,Brain-derived tau kinase','TTBK1,BDTK, KIAA1855','2.7.11.1','Q5TCY1','1321','1'),
('TTBK2_HUMAN','Tau-tubulin kinase 2','TTBK2,KIAA0847','2.7.11.1','Q6IQ55','1244','1'),
('TTK_HUMAN','Dual specificity protein kinase TTK,Phosphotyrosine picked threonine-protein kinase,PYT','TTK,MPS1, MPS1L1','2.7.12.1','P33981','857','2'),
('TXK_HUMAN','Tyrosine-protein kinase TXK,Protein-tyrosine kinase 4,Resting lymphocyte kinase','TXK,PTK4, RLK','2.7.10.2','P42681','527','1'),
('TYK2_HUMAN','Non-receptor tyrosine-protein kinase TYK2','TYK2','2.7.10.2','P29597','1187','1'),
('TYRO3_HUMAN','Tyrosine-protein kinase receptor TYRO3,Tyrosine-protein kinase BYK,Tyrosine-protein kinase DTK,Tyrosine-protein kinase RSE,Tyrosine-protein kinase SKY,Tyrosine-protein kinase TIF','TYRO3,BYK, DTK, RSE, SKY, TIF','2.7.10.1','Q06418','890','1'),
('UFO_HUMAN','Tyrosine-protein kinase receptor UFO,AXL oncogene','AXL,UFO','2.7.10.1','P30530','894','1'),
('UHMK1_HUMAN','Serine/threonine-protein kinase Kist,Kinase interacting with stathmin,PAM COOH-terminal interactor protein 2,P-CIP2,U2AF homology motif kinase 1','UHMK1,KIS, KIST','2.7.11.1','Q8TAS1','419','1'),
('ULK1_HUMAN','Serine/threonine-protein kinase ULK1,Autophagy-related protein 1 homolog,ATG1,hATG1,Unc-51-like kinase 1','ULK1,KIAA0722','2.7.11.1','O75385','1050','1'),
('ULK2_HUMAN','Serine/threonine-protein kinase ULK2,Unc-51-like kinase 2','ULK2,KIAA0623','2.7.11.1','Q8IYT8','1036','1'),
('ULK3_HUMAN','Serine/threonine-protein kinase ULK3,Unc-51-like kinase 3','ULK3','2.7.11.1','Q6PHR2','472','1'),
('ULK4_HUMAN','Serine/threonine-protein kinase ULK4,Unc-51-like kinase 4','ULK4','2.7.11.1','Q96C45','1275','1'),
('VGFR1_HUMAN','Vascular endothelial growth factor receptor 1,VEGFR-1,Fms-like tyrosine kinase 1,FLT-1,Tyrosine-protein kinase FRT,Tyrosine-protein kinase receptor FLT,FLT,Vascular permeability factor receptor','FLT1,FLT, FRT, VEGFR1','2.7.10.1','P17948','1338','1'),
('VGFR2_HUMAN','Vascular endothelial growth factor receptor 2,VEGFR-2,Fetal liver kinase 1,FLK-1,Kinase insert domain receptor,KDR,Protein-tyrosine kinase receptor flk-1','KDR,FLK1, VEGFR2','2.7.10.1','P35968','1356','1'),
('VGFR3_HUMAN','Vascular endothelial growth factor receptor 3,VEGFR-3,Fms-like tyrosine kinase 4,FLT-4,Tyrosine-protein kinase receptor FLT4','FLT4,VEGFR3','2.7.10.1','P35916','1363','1'),
('VRK1_HUMAN','Serine/threonine-protein kinase VRK1,Vaccinia-related kinase 1','VRK1','2.7.11.1','Q99986','396','1'),
('VRK2_HUMAN','Serine/threonine-protein kinase VRK2,Vaccinia-related kinase 2','VRK2','2.7.11.1','Q86Y07','508','1'),
('VRK3_HUMAN','Inactive serine/threonine-protein kinase VRK3,Serine/threonine-protein pseudokinase VRK3,Vaccinia-related kinase 3','VRK3',NULL,'Q8IV63','474','1'),
('WEE1_HUMAN','Wee1-like protein kinase,WEE1hu,Wee1A kinase','WEE1','2.7.10.2','P30291','646','1'),
('WEE2_HUMAN','Wee1-like protein kinase 2,Wee1-like protein kinase 1B,Wee1B kinase','WEE2,WEE1B','2.7.10.2','P0C1S8','567','1'),
('WNK1_HUMAN','Serine/threonine-protein kinase WNK1,Erythrocyte 65 kDa protein,p65,Kinase deficient protein,Protein kinase lysine-deficient 1,Protein kinase with no lysine 1,hWNK1','WNK1,HSN2, KDP, KIAA0344, PRKWNK1','2.7.11.1','Q9H4A3','2382','1'),
('WNK2_HUMAN','Serine/threonine-protein kinase WNK2,Antigen NY-CO-43,Protein kinase lysine-deficient 2,Protein kinase with no lysine 2,Serologically defined colon cancer antigen 43','WNK2,KIAA1760, PRKWNK2, SDCCAG43','2.7.11.1','Q9Y3S1','2297','1'),
('WNK3_HUMAN','Serine/threonine-protein kinase WNK3,Protein kinase lysine-deficient 3,Protein kinase with no lysine 3','WNK3,KIAA1566, PRKWNK3','2.7.11.1','Q9BYP7','1800','1'),
('WNK4_HUMAN','Serine/threonine-protein kinase WNK4,Protein kinase lysine-deficient 4,Protein kinase with no lysine 4','WNK4,PRKWNK4','2.7.11.1','Q96J92','1243','1'),
('YES_HUMAN','Tyrosine-protein kinase Yes,Proto-oncogene c-Yes,p61-Yes','YES1,YES','2.7.10.2','P07947','543','1'),
('ZAP70_HUMAN','Tyrosine-protein kinase ZAP-70,70 kDa zeta-chain associated protein,Syk-related tyrosine kinase','ZAP70,SRK','2.7.10.2','P43403','619','1');INSERT INTO `kindriver_v82`.`Reference` (`pubmed_id`) VALUES 
('19079260'),
('19840437'),
('18682749'),
('17603485'),
('18559588'),
('14737077'),
('10445857'),
('19649315'),
('16150941'),
('1104268'),
('10700182'),
('15625552'),
('12372054'),
('17603487'),
('7713939'),
('15863200'),
('15880580'),
('10208439'),
('21816872'),
('19888299'),
('22259224'),
('18724359'),
('17011030'),
('18339844'),
('16843266'),
('10851026'),
('10918602'),
('21270064'),
('12533788'),
('11526490'),
('17603489'),
('12533789'),
('20360610'),
('18339846'),
('26455322'),
('19006214'),
('17603482'),
('18085035'),
('10417759'),
('12552571'),
('19657110'),
('9857065'),
('16091740'),
('15753357'),
('16928994'),
('17676035'),
('EGFR database'),
('10605028'),
('16371029'),
('18794843'),
('28334876'),
('20167706'),
('15178581'),
('16731599'),
('19603346'),
('11313867'),
('19809159'),
('21242967'),
('15235604'),
('21224473'),
('9837816'),
('9012462'),
('9737679'),
('20110370'),
('20871631'),
('9988270'),
('2124297'),
('1760348'),
('16828200'),
('22114986'),
('21453545'),
('2406720'),
('17525745'),
('10353780'),
('17603486'),
('10362519'),
('20581473'),
('21146537'),
('10490816'),
('22942091'),
('19336958'),
('18000903'),
('19946327'),
('15800014'),
('17875876'),
('17332364'),
('12460923'),
('18248647'),
('19079259'),
('25292412'),
('10783308'),
('16439621'),
('19996017'),
('15611137'),
('18971950'),
('16251899'),
('18762776'),
('15035987'),
('15753368'),
('19340004'),
('10352268'),
('10471491'),
('16213360'),
('16990784'),
('19165726'),
('20140017'),
('18923523'),
('9887330'),
('20585391'),
('16835864'),
('17721994'),
('12533791'),
('19139102'),
('16027248'),
('18397343'),
('15526080'),
('16140923'),
('16410449'),
('15731757'),
('23752188'),
('18456658'),
('8570194'),
('17047083'),
('12447696'),
('15121768'),
('18990089'),
('12533790'),
('12620411'),
('15928335'),
('17603484'),
('9826708'),
('15781101'),
('17803937'),
('11429702'),
('9160884'),
('12009017'),
('16043828'),
('17603488'),
('7862439'),
('17267906'),
('9242375'),
('16573742'),
('16912228');INSERT INTO `kindriver_v82`.`Segment` (`segment_id`,`aln_start`,`aln_end`,`segment_name`,`segment_desc`) VALUES 
('1','41','87','I','P-loop'),
('2','88','111','II',NULL),
('3','112','129','III','αC helix'),
('4','131','148','IV',NULL),
('5','149','279','V','Kinase hinge'),
('6','280','304','VI A',NULL),
('7','308','349','VI B','Catalytic loop'),
('8','350','407','VII','Activation loop'),
('9','408','435','VIII','P+I loop'),
('10','436','498','IX',NULL),
('11','499','542','X',NULL),
('12','543','576','XI',NULL),
('13',NULL,NULL,'JM','Juxtamembrane');INSERT INTO `kindriver_v82`.`PDB` (`uniprot_id`,`pdb_id`,`chain`,`description`,`resolution`,`spaci`,`aerospaci`) VALUES 
('SRC_HUMAN','1a07_A','A','c-src (sh2 domain) complexed with ace-malonyl tyr-glu-(n,n- dipentyl amine)','2.2','0.402478743235931','0.402478743235931'),
('SRC_HUMAN','1a07_B','B','c-src (sh2 domain) complexed with ace-malonyl tyr-glu-(n,n- dipentyl amine)','2.2','0.402478743235931','0.402478743235931'),
('SRC_HUMAN','1a08_A','A','c-src (sh2 domain) complexed with ace-difluoro phosphotyr- glu-(n,n-dipentyl amine)','2.2','0.394458996212121','0.394458996212121'),
('SRC_HUMAN','1a08_B','B','c-src (sh2 domain) complexed with ace-difluoro phosphotyr- glu-(n,n-dipentyl amine)','2.2','0.394458996212121','0.394458996212121'),
('SRC_HUMAN','1a09_A','A','c-src (sh2 domain) complexed with ace-formyl phosphotyr-glu- (n,n-dipentyl amine)','2','0.461532604166667','0.461532604166667'),
('SRC_HUMAN','1a09_B','B','c-src (sh2 domain) complexed with ace-formyl phosphotyr-glu- (n,n-dipentyl amine)','2','0.461532604166667','0.461532604166667'),
('FYN_HUMAN','1a0n_B','B','nmr study of the sh3 domain from fyn proto-oncogene tyrosine kinase complexed with the synthetic peptide p2l corresponding to residues 91-104 of the p85 subunit of pi3- kinase, family of 25 structures',NULL,'0.0246538095238095','0.0246538095238095'),
('SRC_HUMAN','1a1a_A','A','c-src (sh2 domain with c188a mutation) complexed with ace-fo phosphotyr-glu-(n,n-dipentyl amine)','2','0.445241934523809','0.445241934523809'),
('SRC_HUMAN','1a1a_B','B','c-src (sh2 domain with c188a mutation) complexed with ace-fo phosphotyr-glu-(n,n-dipentyl amine)','2','0.445241934523809','0.445241934523809'),
('SRC_HUMAN','1a1b_A','A','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(n,n- dipentyl amine)','2.2','0.419735543831169','0.419735543831169'),
('SRC_HUMAN','1a1b_B','B','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(n,n- dipentyl amine)','2.2','0.419735543831169','0.419735543831169'),
('SRC_HUMAN','1a1c_A','A','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(n-me(- (ch2)3-cyclopentyl))','2.4','0.383343824404762','0.383343824404762'),
('SRC_HUMAN','1a1c_B','B','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(n-me(- (ch2)3-cyclopentyl))','2.4','0.383343824404762','0.383343824404762'),
('SRC_HUMAN','1a1e_A','A','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(3- butylpiperidine)','2.2','0.417997850378788','0.417997850378788'),
('SRC_HUMAN','1a1e_B','B','c-src (sh2 domain) complexed with ace-phosphotyr-glu-(3- butylpiperidine)','2.2','0.417997850378788','0.417997850378788'),
('KSYK_HUMAN','1a81_A','A','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('KSYK_HUMAN','1a81_C','C','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('KSYK_HUMAN','1a81_E','E','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('KSYK_HUMAN','1a81_G','G','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('KSYK_HUMAN','1a81_I','I','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('KSYK_HUMAN','1a81_K','K','crystal structure of the tandem sh2 domain of the syk kinase a dually tyrosine-phosphorylated itam','3','0.129727767857143','0.129727767857143'),
('MK14_HUMAN','1a9u_A','A','the complex structure of the map kinase p38/sb203580','2.5','0.309980446428572','0.309980446428572'),
('ABL1_HUMAN','1ab2_A','A','three-dimensional solution structure of the src homology 2 domain of c-abl',NULL,'0.00965700892857141','0.00965700892857141'),
('HCK_HUMAN','1ad5_A','A','src family kinase hck-amp-pnp complex','2.6','0.25337722985348','0.25337722985348'),
('HCK_HUMAN','1ad5_B','B','src family kinase hck-amp-pnp complex','2.6','0.25337722985348','0.25337722985348'),
('FGFR1_HUMAN','1agw_A','A','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 in complex with su4984 inhibitor','2.4','0.369432946428571','0.369432946428571'),
('FGFR1_HUMAN','1agw_B','B','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 in complex with su4984 inhibitor','2.4','0.369432946428571','0.369432946428571'),
('FYN_HUMAN','1aot_F','F','nmr structure of the fyn sh2 domain complexed with a phosphotyrosyl peptide, minimized average structure',NULL,'0.0103241369047619','0.0103241369047619'),
('FYN_HUMAN','1aou_F','F','nmr structure of the fyn sh2 domain complexed with a phosphotyrosyl peptide, 22 structures',NULL,'0.00810172619047617','0.00810172619047617'),
('CDK2_HUMAN','1aq1_A','A','human cyclin dependent kinase 2 complexed with the inhibitor staurosporine','2','0.401146934523809','0.401146934523809'),
('FYN_HUMAN','1avz_C','C','v-1 nef protein in complex with wild type fyn sh3 domain','3','0.223975148809524','0.223975148809524'),
('ABL1_HUMAN','1awo_A','A','the solution nmr structure of abl sh3 and its relationship to sh2 in the sh(32) construct, 20 structures',NULL,'0.0210097321428571','0.0210097321428571'),
('BTK_HUMAN','1aww_A','A','sh3 domain from bruton\'s tyrosine kinase, nmr, 42 structures',NULL,'0.0212384821428571','0.0212384821428571'),
('BTK_HUMAN','1awx_A','A','sh3 domain from bruton\'s tyrosine kinase, nmr, minimized average structure',NULL,'0.0198799404761905','0.0198799404761905'),
('FYN_HUMAN','1azg_B','B','nmr study of the sh3 domain from fyn proto-oncogene tyrosine kinase kinase complexed with the synthetic peptide p2l corresponding to residues 91-104 of the p85 subunit of pi3-kinase, minimized average (probmap) structure',NULL,'0.0248385863095238','0.0248385863095238'),
('CDK2_HUMAN','1b38_A','A','human cyclin-dependent kinase 2','2','0.440582321428571','0.440582321428571'),
('CDK2_HUMAN','1b39_A','A','human cyclin-dependent kinase 2 phosphorylated on thr 160','2.1','0.391146279761905','0.391146279761905'),
('EPHB2_HUMAN','1b4f_A','A','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_B','B','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_C','C','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_D','D','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_E','E','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_F','F','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_G','G','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('EPHB2_HUMAN','1b4f_H','H','oligomeric structure of the human ephb2 receptor sam domain','1.95','0.426744977106227','0.426744977106227'),
('BTK_HUMAN','1b55_A','A','ph domain from bruton\'s tyrosine kinase in complex with inos 4,5-tetrakisphosphate','2.4','0.211949553571429','0.211949553571429'),
('BTK_HUMAN','1b55_B','B','ph domain from bruton\'s tyrosine kinase in complex with inos 4,5-tetrakisphosphate','2.4','0.211949553571429','0.211949553571429'),
('TGFR1_HUMAN','1b6c_B','B','crystal structure of the cytoplasmic domain of the type i tgf-beta receptor in complex with fkbp12','2.6','0.258256277472527','0.258256277472527'),
('TGFR1_HUMAN','1b6c_D','D','crystal structure of the cytoplasmic domain of the type i tgf-beta receptor in complex with fkbp12','2.6','0.258256277472527','0.258256277472527'),
('TGFR1_HUMAN','1b6c_F','F','crystal structure of the cytoplasmic domain of the type i tgf-beta receptor in complex with fkbp12','2.6','0.258256277472527','0.258256277472527'),
('TGFR1_HUMAN','1b6c_H','H','crystal structure of the cytoplasmic domain of the type i tgf-beta receptor in complex with fkbp12','2.6','0.258256277472527','0.258256277472527'),
('ARBK1_HUMAN','1bak_A','A','signal transduction pleckstrin homology domain of g-protein coupled receptor kinase 2 (beta-adrenergic receptor kinase 1), c-terminal extended, nmr, 20 structures',NULL,'0.00394361607142854','0.00394361607142854'),
('ABL1_HUMAN','1bbz_A','A','crystal structure of the abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions','1.65','0.519067332251082','0.519067332251082'),
('ABL1_HUMAN','1bbz_C','C','crystal structure of the abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions','1.65','0.519067332251082','0.519067332251082'),
('ABL1_HUMAN','1bbz_E','E','crystal structure of the abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions','1.65','0.519067332251082','0.519067332251082'),
('ABL1_HUMAN','1bbz_G','G','crystal structure of the abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions','1.65','0.519067332251082','0.519067332251082'),
('LCK_HUMAN','1bhf_A','A','p56lck sh2 domain inhibitor complex','1.8','0.447065079365079','0.447065079365079'),
('LCK_HUMAN','1bhh_A','A','free p56lck sh2 domain','1.9','0.392642753759398','0.392642753759398'),
('LCK_HUMAN','1bhh_B','B','free p56lck sh2 domain','1.9','0.392642753759398','0.392642753759398'),
('CDK6_HUMAN','1bi7_A','A','mechanism of g1 cyclin dependent kinase inhibition from the structure of the cdk6-p16ink4a tumor suppressor complex','3.4','0.108199209558824','0.108199209558824'),
('CDK6_HUMAN','1bi8_A','A','mechanism of g1 cyclin dependent kinase inhibition from the structures cdk6-p19ink4d inhibitor complex','2.8','0.167356205357143','0.167356205357143'),
('CDK6_HUMAN','1bi8_C','C','mechanism of g1 cyclin dependent kinase inhibition from the structures cdk6-p19ink4d inhibitor complex','2.8','0.167356205357143','0.167356205357143'),
('MK14_HUMAN','1bl6_A','A','the complex structure of the map kinase p38/sb216995','2.5','0.305352470238095','0.305352470238095'),
('MK14_HUMAN','1bl7_A','A','the complex structure of the map kinase p38/sb220025','2.5','0.294763883928571','0.294763883928571'),
('CDK6_HUMAN','1blx_A','A','p19ink4d/cdk6 complex','1.9','0.443484331140351','0.443484331140351'),
('MK14_HUMAN','1bmk_A','A','the complex structure of the map kinase p38/sb218655','2.4','0.318492529761905','0.318492529761905'),
('TITIN_HUMAN','1bpv_A','A','titin module a71 from human cardiac muscle, nmr, 50 structures',NULL,'0.0130145833333333','0.0130145833333333'),
('BTK_HUMAN','1btk_A','A','ph domain and btk motif from bruton\'s tyrosine kinase mutant r28c','1.6','0.513210267857143','0.513210267857143'),
('BTK_HUMAN','1btk_B','B','ph domain and btk motif from bruton\'s tyrosine kinase mutant r28c','1.6','0.513210267857143','0.513210267857143'),
('HCK_HUMAN','1bu1_A','A','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('HCK_HUMAN','1bu1_B','B','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('HCK_HUMAN','1bu1_C','C','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('HCK_HUMAN','1bu1_D','D','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('HCK_HUMAN','1bu1_E','E','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('HCK_HUMAN','1bu1_F','F','src family kinase hck sh3 domain','2.6','0.276922527472527','0.276922527472527'),
('CDK2_HUMAN','1buh_A','A','crystal structure of the human cdk2 kinase complex with cell cycle-regulatory protein ckshs1','2.6','0.306047720924908','0.306047720924908'),
('BTK_HUMAN','1bwn_A','A','ph domain and btk motif from bruton\'s tyrosine kinase mutant complex with ins(1,3,4,5)p4','2.1','0.353908482142857','0.353908482142857'),
('BTK_HUMAN','1bwn_B','B','ph domain and btk motif from bruton\'s tyrosine kinase mutant complex with ins(1,3,4,5)p4','2.1','0.353908482142857','0.353908482142857'),
('CSK_HUMAN','1byg_A','A','kinase domain of human c-terminal src kinase (csk) in complex with inhibitor staurosporine','2.4','0.333115431547619','0.333115431547619'),
('RAF1_HUMAN','1c1y_B','B','crystal structure of rap.gmppnp in complex with the ras- binding-domain of c-raf1 kinase (rafrbd).','1.9','0.442933973997494','0.442933973997494'),
('ACK1_HUMAN','1cf4_B','B','cdc42/ack gtpase-binding domain complex',NULL,'0.00379126488095236','0.00379126488095236'),
('CDK2_HUMAN','1ckp_A','A','human cyclin dependent kinase 2 complexed with the inhibitor purvalanol b',NULL,'-0.3','-0.3'),
('MK12_HUMAN','1cm8_A','A','phosphorylated map kinase p38-gamma','2.4','0.300261979166667','0.300261979166667'),
('MK12_HUMAN','1cm8_B','B','phosphorylated map kinase p38-gamma','2.4','0.300261979166667','0.300261979166667'),
('CSK_HUMAN','1csk_A','A','the crystal structure of human csksh3: structural diversity near the rt-src and n-src loop','2.5','0.292983928571429','0.292983928571429'),
('CSK_HUMAN','1csk_B','B','the crystal structure of human csksh3: structural diversity near the rt-src and n-src loop','2.5','0.292983928571429','0.292983928571429'),
('CSK_HUMAN','1csk_C','C','the crystal structure of human csksh3: structural diversity near the rt-src and n-src loop','2.5','0.292983928571429','0.292983928571429'),
('CSK_HUMAN','1csk_D','D','the crystal structure of human csksh3: structural diversity near the rt-src and n-src loop','2.5','0.292983928571429','0.292983928571429'),
('KSYK_HUMAN','1csy_A','A','syk tyrosine kinase c-terminal sh2 domain complexed with a phosphopeptidefrom the gamma chain of the high affinity imm g receptor, nmr',NULL,'0.0134399702380952','0.0134399702380952'),
('KSYK_HUMAN','1csz_A','A','syk tyrosine kinase c-terminal sh2 domain complexed with a phosphopeptidefrom the gamma chain of the high affinity imm g receptor, nmr',NULL,'0.0145441666666666','0.0145441666666666'),
('FGFR1_HUMAN','1cvs_C','C','crystal structure of a dimeric fgf2-fgfr1 complex','2.8','0.235780863095238','0.235780863095238'),
('FGFR1_HUMAN','1cvs_D','D','crystal structure of a dimeric fgf2-fgfr1 complex','2.8','0.235780863095238','0.235780863095238'),
('LCK_HUMAN','1cwd_L','L','human p56lck tyrosine kinase complexed with phosphopeptide','2.25','0.360364429563492','0.360364429563492'),
('LCK_HUMAN','1cwe_A','A','human p56lck tyrosine kinase complexed with phosphopeptide','2.3','0.345060183100414','0.345060183100414'),
('LCK_HUMAN','1cwe_C','C','human p56lck tyrosine kinase complexed with phosphopeptide','2.3','0.345060183100414','0.345060183100414'),
('PKN1_HUMAN','1cxz_B','B','crystal structure of human rhoa complexed with the effector domain of the protein kinase pkn/prk1','2.2','0.365176481331169','0.365176481331169'),
('CDK2_HUMAN','1di8_A','A','the structure of cyclin-dependent kinase 2 (cdk2) in complex with 4-[3-hydroxyanilino]-6,7-dimethoxyquinazoline','2.2','0.411593043831169','0.411593043831169'),
('MK14_HUMAN','1di9_A','A','the structure of p38 mitogen-activated protein kinase in complex with 4-[3-methylsulfanylanilino]-6,7- dimethoxyquinazoline','2.6','0.312948747710623','0.312948747710623'),
('FGFR2_HUMAN','1djs_A','A','ligand-binding portion of fibroblast growth factor receptor complex with fgf1','2.4','0.287062455357143','0.287062455357143'),
('CDK2_HUMAN','1dm2_A','A','human cyclin-dependent kinase 2 complexed with the inhibitor hymenialdisine','2.1','0.396167827380952','0.396167827380952'),
('FGFR2_HUMAN','1e0o_B','B','crystal structure of a ternary fgf1-fgfr2-heparin complex','2.8','0.176332068452381','0.176332068452381'),
('FGFR2_HUMAN','1e0o_D','D','crystal structure of a ternary fgf1-fgfr2-heparin complex','2.8','0.176332068452381','0.176332068452381'),
('CDK2_HUMAN','1e1v_A','A','human cyclin dependent kinase 2 complexed with the inhibitor nu2058','1.95','0.438663310439561','0.438663310439561'),
('CDK2_HUMAN','1e1x_A','A','human cyclin dependent kinase 2 complexed with the inhibitor nu6027','1.85','0.447746671492921','0.447746671492921'),
('CDK2_HUMAN','1e9h_A','A','thr 160 phosphorylated cdk2 - human cyclin a3 complex with the inhibitor indirubin-5-sulphonate bound','2.5','0.282235357142857','0.282235357142857'),
('CDK2_HUMAN','1e9h_C','C','thr 160 phosphorylated cdk2 - human cyclin a3 complex with the inhibitor indirubin-5-sulphonate bound','2.5','0.282235357142857','0.282235357142857'),
('FYN_HUMAN','1efn_A','A','hiv-1 nef protein in complex with r96i mutant fyn sh3 domain','2.5','0.301071130952381','0.301071130952381'),
('FYN_HUMAN','1efn_C','C','hiv-1 nef protein in complex with r96i mutant fyn sh3 domain','2.5','0.301071130952381','0.301071130952381'),
('BMR1A_HUMAN','1es7_B','B','complex between bmp-2 and two bmp receptor ia ectodomains','2.9','0.263440755849754','0.263440755849754'),
('BMR1A_HUMAN','1es7_D','D','complex between bmp-2 and two bmp receptor ia ectodomains','2.9','0.263440755849754','0.263440755849754'),
('FGFR2_HUMAN','1ev2_E','E','crystal structure of fgf2 in complex with the extracellular ligand binding domain of fgf receptor 2 (fgfr2)','2.2','0.346816183712121','0.346816183712121'),
('FGFR2_HUMAN','1ev2_F','F','crystal structure of fgf2 in complex with the extracellular ligand binding domain of fgf receptor 2 (fgfr2)','2.2','0.346816183712121','0.346816183712121'),
('FGFR2_HUMAN','1ev2_G','G','crystal structure of fgf2 in complex with the extracellular ligand binding domain of fgf receptor 2 (fgfr2)','2.2','0.346816183712121','0.346816183712121'),
('FGFR2_HUMAN','1ev2_H','H','crystal structure of fgf2 in complex with the extracellular ligand binding domain of fgf receptor 2 (fgfr2)','2.2','0.346816183712121','0.346816183712121'),
('FGFR1_HUMAN','1evt_C','C','crystal structure of fgf1 in complex with the extracellular ligand binding domain of fgf receptor 1 (fgfr1)','2.8','0.207056473214286','0.207056473214286'),
('FGFR1_HUMAN','1evt_D','D','crystal structure of fgf1 in complex with the extracellular ligand binding domain of fgf receptor 1 (fgfr1)','2.8','0.207056473214286','0.207056473214286'),
('EPHB2_HUMAN','1f0m_A','A','monomeric structure of the human ephb2 sam (sterile alpha motif) domain','2.2','0.330320127164502','0.330320127164502'),
('PAK1_HUMAN','1f3m_A','A','crystal structure of human serine/threonine kinase pak1','2.3','0.315039736671843','0.315039736671843'),
('PAK1_HUMAN','1f3m_B','B','crystal structure of human serine/threonine kinase pak1','2.3','0.315039736671843','0.315039736671843'),
('PAK1_HUMAN','1f3m_C','C','crystal structure of human serine/threonine kinase pak1','2.3','0.315039736671843','0.315039736671843'),
('PAK1_HUMAN','1f3m_D','D','crystal structure of human serine/threonine kinase pak1','2.3','0.315039736671843','0.315039736671843'),
('CDK2_HUMAN','1f5q_A','A','crystal structure of murine gamma herpesvirus cyclin complexed to human cyclin dependent kinase 2','2.5','0.276195327380952','0.276195327380952'),
('CDK2_HUMAN','1f5q_C','C','crystal structure of murine gamma herpesvirus cyclin complexed to human cyclin dependent kinase 2','2.5','0.276195327380952','0.276195327380952'),
('RAF1_HUMAN','1faq_A','A','raf-1 cysteine rich domain, nmr, 27 structures',NULL,'0.00882663690476188','0.00882663690476188'),
('RAF1_HUMAN','1far_A','A','raf-1 cysteine rich domain, nmr, minimized average structure',NULL,'0.0050850595238095','0.0050850595238095'),
('LCK_HUMAN','1fbz_A','A','structure-based design of a novel, osteoclast-selective, nonpeptide src sh2 inhibitor with in vivo anti-resorptive activity','2.4','0.273712336309524','0.273712336309524'),
('LCK_HUMAN','1fbz_B','B','structure-based design of a novel, osteoclast-selective, nonpeptide src sh2 inhibitor with in vivo anti-resorptive activity','2.4','0.273712336309524','0.273712336309524'),
('FGFR1_HUMAN','1fgi_A','A','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 in complex with su5402 inhibitor','2.5','0.353749404761905','0.353749404761905'),
('FGFR1_HUMAN','1fgi_B','B','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 in complex with su5402 inhibitor','2.5','0.353749404761905','0.353749404761905'),
('FGFR1_HUMAN','1fgk_A','A','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1','2','0.438148467261905','0.438148467261905'),
('FGFR1_HUMAN','1fgk_B','B','crystal structure of the tyrosine kinase domain of fibroblast growth factor receptor 1','2','0.438148467261905','0.438148467261905'),
('CDK2_HUMAN','1fin_A','A','cyclin a-cyclin-dependent kinase 2 complex','2.3','0.333469647386128','0.333469647386128'),
('CDK2_HUMAN','1fin_C','C','cyclin a-cyclin-dependent kinase 2 complex','2.3','0.333469647386128','0.333469647386128'),
('VGFR1_HUMAN','1flt_X','X','vegf in complex with domain 2 of the flt-1 receptor','1.7','0.511003210784314','0.511003210784314'),
('VGFR1_HUMAN','1flt_Y','Y','vegf in complex with domain 2 of the flt-1 receptor','1.7','0.511003210784314','0.511003210784314'),
('SRC_HUMAN','1fmk_A','A','crystal structure of human tyrosine-protein kinase c-src','1.5','0.570229910714286','0.570229910714286'),
('CDK2_HUMAN','1fq1_B','B','crystal structure of kinase associated phosphatase (kap) in complex with phospho-cdk2','3','0.138348839285714','0.138348839285714'),
('FGFR1_HUMAN','1fq9_C','C','crystal structure of a ternary fgf2-fgfr1-heparin complex','3','0.203593958333333','0.203593958333333'),
('FGFR1_HUMAN','1fq9_D','D','crystal structure of a ternary fgf2-fgfr1-heparin complex','3','0.203593958333333','0.203593958333333'),
('TIE2_HUMAN','1fvr_A','A','tie2 kinase domain','2.2','0.372914189664502','0.372914189664502'),
('TIE2_HUMAN','1fvr_B','B','tie2 kinase domain','2.2','0.372914189664502','0.372914189664502'),
('CDK2_HUMAN','1fvt_A','A','the structure of cyclin-dependent kinase 2 (cdk2) in complex with an oxindole inhibitor','2.2','0.36567036525974','0.36567036525974'),
('CDK2_HUMAN','1fvv_A','A','the structure of cdk2/cyclin a in complex with an oxindole inhibitor','2.8','0.211860535714286','0.211860535714286'),
('CDK2_HUMAN','1fvv_C','C','the structure of cdk2/cyclin a in complex with an oxindole inhibitor','2.8','0.211860535714286','0.211860535714286'),
('FYN_HUMAN','1fyn_A','A','phosphotransferase','2.3','0.322281180124224','0.322281180124224'),
('MET_HUMAN','1fyr_I','I','dimer formation through domain swapping in the crystal structure of the grb2-sh2 ac-pyvnv complex','2.4','0.345346547619048','0.345346547619048'),
('MET_HUMAN','1fyr_J','J','dimer formation through domain swapping in the crystal structure of the grb2-sh2 ac-pyvnv complex','2.4','0.345346547619048','0.345346547619048'),
('MET_HUMAN','1fyr_K','K','dimer formation through domain swapping in the crystal structure of the grb2-sh2 ac-pyvnv complex','2.4','0.345346547619048','0.345346547619048'),
('MET_HUMAN','1fyr_L','L','dimer formation through domain swapping in the crystal structure of the grb2-sh2 ac-pyvnv complex','2.4','0.345346547619048','0.345346547619048'),
('TITIN_HUMAN','1g1c_A','A','i1 domain from titin','2.1','0.420248422619048','0.420248422619048'),
('TITIN_HUMAN','1g1c_B','B','i1 domain from titin','2.1','0.420248422619048','0.420248422619048'),
('CDK6_HUMAN','1g3n_A','A','structure of a p18(ink4c)-cdk6-k-cyclin ternary complex','2.9','0.23161836001642','0.23161836001642'),
('CDK6_HUMAN','1g3n_E','E','structure of a p18(ink4c)-cdk6-k-cyclin ternary complex','2.9','0.23161836001642','0.23161836001642'),
('CDK2_HUMAN','1g5s_A','A','crystal structure of human cyclin dependent kinase 2 (cdk2) in complex with the inhibitor h717','2.61','0.296346688047345','0.296346688047345'),
('FYN_HUMAN','1g83_A','A','crystal structure of fyn sh3-sh2','2.6','0.28224123282967','0.28224123282967'),
('FYN_HUMAN','1g83_B','B','crystal structure of fyn sh3-sh2','2.6','0.28224123282967','0.28224123282967'),
('INSR_HUMAN','1gag_A','A','crystal structure of the insulin receptor kinase in complex bisubstrate inhibitor','2.7','0.298480965608466','0.298480965608466'),
('CDK2_HUMAN','1gih_A','A','human cyclin dependent kinase 2 complexed with the cdk4 inhibitor','2.8','0.298748318452381','0.298748318452381'),
('CDK2_HUMAN','1gii_A','A','human cyclin dependent kinase 2 complexed with the cdk4 inhibitor','2','0.418695223214286','0.418695223214286'),
('CDK2_HUMAN','1gij_A','A','human cyclin dependent kinase 2 complexed with the cdk4 inhibitor','2.2','0.344166020021645','0.344166020021645'),
('FGFR2_HUMAN','1gjo_A','A','the fgfr2 tyrosine kinase domain','2.4','0.286915952380952','0.286915952380952'),
('GSK3B_HUMAN','1gng_A','A','glycogen synthase kinase-3 beta (gsk3) complex with frattide peptide','2.6','0.304227839972527','0.304227839972527'),
('GSK3B_HUMAN','1gng_B','B','glycogen synthase kinase-3 beta (gsk3) complex with frattide peptide','2.6','0.304227839972527','0.304227839972527'),
('PGFRB_HUMAN','1gq5_A','A','structural determinants of the nherf interaction with beta2-ar and pdgfr','2.2','0.368230543831169','0.368230543831169'),
('RAF1_HUMAN','1gua_B','B','human rap1a, residues 1-167, double mutant (e30d,k31e) complexed with gppnhp and the ras-binding-domain of human c-raf1, residues 51-131','2','0.401958273809524','0.401958273809524'),
('CHK2_HUMAN','1gxc_A','A','fha domain from human chk2 kinase in complex with a synthetic phosphopeptide','2.7','0.252147721560846','0.252147721560846'),
('CHK2_HUMAN','1gxc_D','D','fha domain from human chk2 kinase in complex with a synthetic phosphopeptide','2.7','0.252147721560846','0.252147721560846'),
('CHK2_HUMAN','1gxc_G','G','fha domain from human chk2 kinase in complex with a synthetic phosphopeptide','2.7','0.252147721560846','0.252147721560846'),
('CHK2_HUMAN','1gxc_J','J','fha domain from human chk2 kinase in complex with a synthetic phosphopeptide','2.7','0.252147721560846','0.252147721560846'),
('CDK2_HUMAN','1gy3_A','A','pcdk2/cyclin a in complex with mgadp, nitrate and peptide su','2.7','0.232855221560846','0.232855221560846'),
('CDK2_HUMAN','1gy3_C','C','pcdk2/cyclin a in complex with mgadp, nitrate and peptide su','2.7','0.232855221560846','0.232855221560846'),
('CDK2_HUMAN','1gz8_A','A','human cyclin dependent kinase 2 complexed with the inhibitor 2-amino-6-(3\'-methyl-2\'-oxo)butoxypurine','1.3','0.762642361492674','0.762642361492674'),
('AKT2_HUMAN','1gzk_A','A','molecular mechanism for the regulation of protein kinase b/ akt by hydrophobic motif phosphorylation','2.3','0.276780793219462','0.276780793219462'),
('AKT2_HUMAN','1gzn_A','A','structure of pkb kinase domain','2.5','0.219881607142857','0.219881607142857'),
('AKT2_HUMAN','1gzo_A','A','structure of protein kinase b unphosphorylated','2.75','0.20279308982684','0.20279308982684'),
('CDK2_HUMAN','1h00_A','A','cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor','1.6','0.562961592261905','0.562961592261905'),
('CDK2_HUMAN','1h01_A','A','cdk2 in complex with a disubstituted 2, 4-bis anilino pyrimidine cdk4 inhibitor','1.79','0.499915080972333','0.499915080972333'),
('CDK2_HUMAN','1h07_A','A','cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor','1.85','0.474474558397683','0.474474558397683'),
('CDK2_HUMAN','1h08_A','A','cdk2 in complex with a disubstituted 2, 4-bis anilino pyrimidine cdk4 inhibitor','1.8','0.486374439484127','0.486374439484127'),
('CDK2_HUMAN','1h0v_A','A','human cyclin dependent protein kinase 2 in complex with the inhibitor 2-amino-6-[(r)-pyrrolidino-5\'-yl]methoxypurine','1.9','0.50802064066416','0.50802064066416'),
('CDK2_HUMAN','1h0w_A','A','human cyclin dependent protein kinase 2 in complex with the inhibitor 2-amino-6-[cyclohex-3-enyl]methoxypurine','2.1','0.381142663690476','0.381142663690476'),
('AKT1_HUMAN','1h10_A','A','high resolution structure of the pleckstrin homology domain of protein kinase b/akt bound to ins(1,3,4,5)-tetrakisphophate','1.4','0.742289494047619','0.742289494047619'),
('CDK2_HUMAN','1h1p_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu2058','2.1','0.370930089285714','0.370930089285714'),
('CDK2_HUMAN','1h1p_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu2058','2.1','0.370930089285714','0.370930089285714'),
('CDK2_HUMAN','1h1q_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6094','2.5','0.230729553571429','0.230729553571429'),
('CDK2_HUMAN','1h1q_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6094','2.5','0.230729553571429','0.230729553571429'),
('CDK2_HUMAN','1h1r_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6086','2','0.377062113095238','0.377062113095238'),
('CDK2_HUMAN','1h1r_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6086','2','0.377062113095238','0.377062113095238'),
('CDK2_HUMAN','1h1s_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6102','2','0.377992678571429','0.377992678571429'),
('CDK2_HUMAN','1h1s_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with the inhibitor nu6102','2','0.377992678571429','0.377992678571429'),
('PDPK1_HUMAN','1h1w_A','A','high resolution crystal structure of the human pdk1 catalytic domain','2','0.455255119047619','0.455255119047619'),
('CDK2_HUMAN','1h24_A','A','cdk2/cyclin a in complex with a 9 residue recruitment peptide from e2f','2.5','0.294791116071429','0.294791116071429'),
('CDK2_HUMAN','1h24_C','C','cdk2/cyclin a in complex with a 9 residue recruitment peptide from e2f','2.5','0.294791116071429','0.294791116071429'),
('CDK2_HUMAN','1h25_A','A','cdk2/cyclin a in complex with an 11-residue recruitment peptide from retinoblastoma-associated protein','2.5','0.255354449404762','0.255354449404762'),
('CDK2_HUMAN','1h25_C','C','cdk2/cyclin a in complex with an 11-residue recruitment peptide from retinoblastoma-associated protein','2.5','0.255354449404762','0.255354449404762'),
('CDK2_HUMAN','1h26_A','A','cdk2/cyclin a in complex with an 11-residue recruitment peptide from p53','2.24','0.340880148809524','0.340880148809524'),
('CDK2_HUMAN','1h26_C','C','cdk2/cyclin a in complex with an 11-residue recruitment peptide from p53','2.24','0.340880148809524','0.340880148809524'),
('CDK2_HUMAN','1h27_A','A','cdk2/cyclin a in complex with an 11-residue recruitment pept p27','2.2','0.359466228354978','0.359466228354978'),
('CDK2_HUMAN','1h27_C','C','cdk2/cyclin a in complex with an 11-residue recruitment pept p27','2.2','0.359466228354978','0.359466228354978'),
('CDK2_HUMAN','1h28_A','A','cdk2/cyclin a in complex with an 11-residue recruitment pept p107','2.8','0.180763095238095','0.180763095238095'),
('CDK2_HUMAN','1h28_C','C','cdk2/cyclin a in complex with an 11-residue recruitment pept p107','2.8','0.180763095238095','0.180763095238095'),
('CDK5_HUMAN','1h4l_A','A','structure and regulation of the cdk5-p25(nck5a) complex','2.65','0.251306898304133','0.251306898304133'),
('CDK5_HUMAN','1h4l_B','B','structure and regulation of the cdk5-p25(nck5a) complex','2.65','0.251306898304133','0.251306898304133'),
('GSK3B_HUMAN','1h8f_A','A','glycogen synthase kinase 3 beta.','2.8','0.252629910714286','0.252629910714286'),
('GSK3B_HUMAN','1h8f_B','B','glycogen synthase kinase 3 beta.','2.8','0.252629910714286','0.252629910714286'),
('LCK_HUMAN','1h92_A','A','sh3 domain of human lck tyrosine kinase',NULL,'0.0567199107142857','0.0567199107142857'),
('PGFRB_HUMAN','1h9o_B','B','phosphatidylinositol 3-kinase, p85-alpha subunit: c-terminal sh2 domain complexed with a tyr751 phosphopeptide from the pdgf receptor, crystal structure at 1.79 a','1.79','0.530369426210428','0.530369426210428'),
('NTRK2_HUMAN','1hcf_X','X','crystal structure of trkb-d5 bound to neurotrophin-4/5','2.7','0.266875474537037','0.266875474537037'),
('NTRK2_HUMAN','1hcf_Y','Y','crystal structure of trkb-d5 bound to neurotrophin-4/5','2.7','0.266875474537037','0.266875474537037'),
('CDK2_HUMAN','1hck_A','A','human cyclin-dependent kinase 2','1.9','0.459441607926065','0.459441607926065'),
('CDK2_HUMAN','1hcl_A','A','human cyclin-dependent kinase 2','1.8','0.49333470734127','0.49333470734127'),
('SRC_HUMAN','1hcs_B','B','nmr structure of the human src sh2 domain complex',NULL,'0.0230785119047619','0.0230785119047619'),
('SRC_HUMAN','1hct_B','B','nmr structure of the human src sh2 domain complex',NULL,'0.0206261011904762','0.0206261011904762'),
('NTRK1_HUMAN','1he7_A','A','human nerve growth factor receptor trka','2','0.386942901785714','0.386942901785714'),
('GSK3B_HUMAN','1i09_A','A','structure of glycogen synthase kinase-3 (gsk3b)','2.7','0.23764261739418','0.23764261739418'),
('GSK3B_HUMAN','1i09_B','B','structure of glycogen synthase kinase-3 (gsk3b)','2.7','0.23764261739418','0.23764261739418'),
('INSR_HUMAN','1i44_A','A','crystallographic studies of an activation loop mutant of the insulin receptor tyrosine kinase','2.4','0.348325863095238','0.348325863095238'),
('CHK1_HUMAN','1ia8_A','A','the 1.7 a crystal structure of human cell cycle checkpoint kinase chk1','1.7','0.490782332808123','0.490782332808123'),
('MK14_HUMAN','1ian_A','A','human p38 map kinase inhibitor complex','2','0.316','0.316'),
('TGFR1_HUMAN','1ias_A','A','cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12','2.9','0.200698627873563','0.200698627873563'),
('TGFR1_HUMAN','1ias_B','B','cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12','2.9','0.200698627873563','0.200698627873563'),
('TGFR1_HUMAN','1ias_C','C','cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12','2.9','0.200698627873563','0.200698627873563'),
('TGFR1_HUMAN','1ias_D','D','cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12','2.9','0.200698627873563','0.200698627873563'),
('TGFR1_HUMAN','1ias_E','E','cytoplasmic domain of unphosphorylated type i tgf-beta receptor crystallized without fkbp12','2.9','0.200698627873563','0.200698627873563'),
('DAPK1_HUMAN','1ig1_A','A','1.8a x-ray structure of ternary complex of a catalytic domain of death-associated protein kinase with atp analogue and mn.','1.8','0.513063010912698','0.513063010912698'),
('IGF1R_HUMAN','1igr_A','A','type 1 insulin-like growth factor receptor (domains 1-3)','2.6','0.219223836996337','0.219223836996337'),
('FGFR2_HUMAN','1ii4_E','E','crystal structure of ser252trp apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.7','0.233235325727513','0.233235325727513'),
('FGFR2_HUMAN','1ii4_F','F','crystal structure of ser252trp apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.7','0.233235325727513','0.233235325727513'),
('FGFR2_HUMAN','1ii4_G','G','crystal structure of ser252trp apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.7','0.233235325727513','0.233235325727513'),
('FGFR2_HUMAN','1ii4_H','H','crystal structure of ser252trp apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.7','0.233235325727513','0.233235325727513'),
('FGFR2_HUMAN','1iil_E','E','crystal structure of pro253arg apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.3','0.32129097179089','0.32129097179089'),
('FGFR2_HUMAN','1iil_F','F','crystal structure of pro253arg apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.3','0.32129097179089','0.32129097179089'),
('FGFR2_HUMAN','1iil_G','G','crystal structure of pro253arg apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.3','0.32129097179089','0.32129097179089'),
('FGFR2_HUMAN','1iil_H','H','crystal structure of pro253arg apert mutant fgf receptor 2 (fgfr2) in complex with fgf2','2.3','0.32129097179089','0.32129097179089'),
('LCK_HUMAN','1ijr_A','A','crystal structure of lck sh2 complexed with nonpeptide phosphotyrosine mimetic','2.2','0.343035841450217','0.343035841450217'),
('INSR_HUMAN','1ir3_A','A','phosphorylated insulin receptor tyrosine kinase in complex with peptide substrate and atp analog','1.9','0.481179003759399','0.481179003759399'),
('INSR_HUMAN','1irk_A','A','crystal structure of the tyrosine kinase domain of the human insulin receptor','2.1','0.421450639880952','0.421450639880952'),
('EGFR_HUMAN','1ivo_A','A','crystal structure of the complex of human epidermal growth f receptor extracellular domains.','3.3','0.11272659767316','0.11272659767316'),
('EGFR_HUMAN','1ivo_B','B','crystal structure of the complex of human epidermal growth f receptor extracellular domains.','3.3','0.11272659767316','0.11272659767316'),
('GSK3B_HUMAN','1j1b_A','A','binary complex structure of human tau protein kinase i with amppnp','1.8','0.45832496031746','0.45832496031746'),
('GSK3B_HUMAN','1j1b_B','B','binary complex structure of human tau protein kinase i with amppnp','1.8','0.45832496031746','0.45832496031746'),
('GSK3B_HUMAN','1j1c_A','A','binary complex structure of human tau protein kinase i with adp','2.1','0.375467574404762','0.375467574404762'),
('GSK3B_HUMAN','1j1c_B','B','binary complex structure of human tau protein kinase i with adp','2.1','0.375467574404762','0.375467574404762'),
('DAPK1_HUMAN','1jkk_A','A','2.4a x-ray structure of ternary complex of a catalytic domain of death-associated protein kinase with atp analogue and mg.','2.4','0.356276889880952','0.356276889880952'),
('DAPK1_HUMAN','1jkl_A','A','1.6a x-ray structure of binary complex of a catalytic domain of death-associated protein kinase with atp analogue','1.62','0.564025438712522','0.564025438712522'),
('DAPK1_HUMAN','1jks_A','A','1.5a x-ray structure of apo form of a catalytic domain of death-associated protein kinase','1.5','0.632638199404762','0.632638199404762'),
('DAPK1_HUMAN','1jkt_A','A','tetragonal crystal form of a catalytic domain of death-assoc protein kinase','3.5','0.0122742113095237','0.0122742113095237'),
('DAPK1_HUMAN','1jkt_B','B','tetragonal crystal form of a catalytic domain of death-assoc protein kinase','3.5','0.0122742113095237','0.0122742113095237'),
('MP2K2_HUMAN','1jky_B','B','crystal structure of the anthrax lethal factor (lf): wild- type lf complexed with the n-terminal sequence of mapkk2','3.9','-0.0711980025183149','-0.0711980025183149'),
('MK10_HUMAN','1jnk_A','A','the c-jun n-terminal kinase (jnk3s) complexed with mgamp-pnp','2.3','0.324576328933747','0.324576328933747'),
('CDK6_HUMAN','1jow_B','B','crystal structure of a complex of human cdk6 and a viral cyclin','3.1','0.134706046947005','0.134706046947005'),
('IGF1R_HUMAN','1jqh_A','A','igf-1 receptor kinase domain','2.1','0.39768','0.39768'),
('IGF1R_HUMAN','1jqh_B','B','igf-1 receptor kinase domain','2.1','0.39768','0.39768'),
('IGF1R_HUMAN','1jqh_C','C','igf-1 receptor kinase domain','2.1','0.39768','0.39768'),
('CDK2_HUMAN','1jst_A','A','phosphorylated cyclin-dependent kinase-2 bound to cyclin a','2.6','0.292281039377289','0.292281039377289'),
('CDK2_HUMAN','1jst_C','C','phosphorylated cyclin-dependent kinase-2 bound to cyclin a','2.6','0.292281039377289','0.292281039377289'),
('CDK2_HUMAN','1jsu_A','A','p27(kip1)/cyclin a/cdk2 complex','2.3','0.360236328933747','0.360236328933747'),
('CDK2_HUMAN','1jsv_A','A','the structure of cyclin-dependent kinase 2 (cdk2) in complex with 4-[(6-amino-4-pyrimidinyl) amino]benzenesulfonamide','1.96','0.439581462585034','0.439581462585034'),
('ABL1_HUMAN','1ju5_C','C','ternary complex of an crk sh2 domain, crk-derived phophopeptide, and abl sh3 domain by nmr spectroscopy',NULL,'0.0185339434523809','0.0185339434523809'),
('CDK2_HUMAN','1jvp_P','P','crystal structure of human cdk2 (unphosphorylated) in complex with pkf049-365','1.53','0.565452687908497','0.565452687908497'),
('CSK21_HUMAN','1jwh_A','A','crystal structure of human protein kinase ck2 holoenzyme','3.1','0.115910243375576','0.115910243375576'),
('CSK21_HUMAN','1jwh_B','B','crystal structure of human protein kinase ck2 holoenzyme','3.1','0.115910243375576','0.115910243375576'),
('MATK_HUMAN','1jwo_A','A','crystal structure analysis of the sh2 domain of the csk homologous kinase chk','2.5','0.236167529761905','0.236167529761905'),
('FAK1_HUMAN','1k04_A','A','crystal structure of the focal adhesion targeting domain of adhesion kinase','1.95','0.409988102106227','0.409988102106227'),
('FAK1_HUMAN','1k05_A','A','crystal structure of the focal adhesion targeting domain of focal adhesion kinase','2.9','0.203304178468801','0.203304178468801'),
('FAK1_HUMAN','1k05_B','B','crystal structure of the focal adhesion targeting domain of focal adhesion kinase','2.9','0.203304178468801','0.203304178468801'),
('FAK1_HUMAN','1k05_C','C','crystal structure of the focal adhesion targeting domain of focal adhesion kinase','2.9','0.203304178468801','0.203304178468801'),
('BTK_HUMAN','1k2p_A','A','crystal structure of bruton\'s tyrosine kinase domain','2.1','0.355656607142857','0.355656607142857'),
('BTK_HUMAN','1k2p_B','B','crystal structure of bruton\'s tyrosine kinase domain','2.1','0.355656607142857','0.355656607142857'),
('IGF1R_HUMAN','1k3a_A','A','structure of the insulin-like growth factor 1 receptor kinase','2.1','0.40920375','0.40920375'),
('CDK2_HUMAN','1ke5_A','A','cdk2 complexed with n-methyl-4-{[(2-oxo-1,2-dihydro-3h- indol-3-ylidene)methyl]amino}benzenesulfonamide','2.2','0.415420856331169','0.415420856331169'),
('CDK2_HUMAN','1ke6_A','A','cyclin-dependent kinase 2 (cdk2) complexed with n-methyl-{4- [2-(7-oxo-6,7-dihydro-8h-[1,3]thiazolo[5,4-e]indol-8- ylidene)hydrazino]phenyl}methanesulfonamide','2','0.456220833333333','0.456220833333333'),
('CDK2_HUMAN','1ke7_A','A','cyclin-dependent kinase 2 (cdk2) complexed with 3-{[(2,2- dioxido-1,3-dihydro-2-benzothien-5-yl)amino]methylene}-5- (1,3-oxazol-5-yl)-1,3-dihydro-2h-indol-2-one','2','0.454717232142857','0.454717232142857'),
('CDK2_HUMAN','1ke8_A','A','cyclin-dependent kinase 2 (cdk2) complexed with 4-{[(2-oxo- 1,2-dihydro-3h-indol-3-ylidene)methyl]amino}-n-(1,3- thiazol-2-yl)benzenesulfonamide','2','0.457577693452381','0.457577693452381'),
('CDK2_HUMAN','1ke9_A','A','cyclin-dependent kinase 2 (cdk2) complexed with 3-{[4- ({[amino(imino)methyl]aminosulfonyl)anilino]methylene}-2- oxo-2,3-dihydro-1h-indole','2','0.437565193452381','0.437565193452381'),
('CSKP_HUMAN','1kgd_A','A','crystal structure of the guanylate kinase-like domain of human cask','1.31','0.733965549459287','0.733965549459287'),
('LCK_HUMAN','1kik_A','A','sh3 domain of lymphocyte specific kinase (lck)',NULL,'0.0244198511904762','0.0244198511904762'),
('SRC_HUMAN','1ksw_A','A','structure of human c-src tyrosine kinase (thr338gly mutant) in complex with n6-benzyl adp','2.8','0.194388258928571','0.194388258928571'),
('TGFR2_HUMAN','1ktz_B','B','crystal structure of the human tgf-beta type ii receptor extracellular domain in complex with tgf-beta3','2.15','0.381926308831672','0.381926308831672'),
('MK14_HUMAN','1kv1_A','A','p38 map kinase in complex with inhibitor 1','2.5','0.292276160714286','0.292276160714286'),
('MK14_HUMAN','1kv2_A','A','human p38 map kinase in complex with birb 796','2.8','0.176165238095238','0.176165238095238'),
('CSKP_HUMAN','1kwa_A','A','human cask/lin-2 pdz domain','1.93','0.407990414430669','0.407990414430669'),
('CSKP_HUMAN','1kwa_B','B','human cask/lin-2 pdz domain','1.93','0.407990414430669','0.407990414430669'),
('MAPK2_HUMAN','1kwp_A','A','crystal structure of mapkap2','2.8','0.164719032738095','0.164719032738095'),
('MAPK2_HUMAN','1kwp_B','B','crystal structure of mapkap2','2.8','0.164719032738095','0.164719032738095'),
('LCK_HUMAN','1lcj_A','A','sh2 (src homology-2) domain of human p56-lck tyrosine kinase complexed with the 11 residue phosphotyrosyl peptide epqpyeeipiyl','1.8','0.461641061507937','0.461641061507937'),
('LCK_HUMAN','1lck_A','A','sh3-sh2 domain fragment of human p56-lck tyrosine kinase complexed with the 10 residue synthetic phosphotyrosyl peptide tegqpyqpqpa','2.5','0.314912857142857','0.314912857142857'),
('LCK_HUMAN','1lkk_A','A','human p56-lck tyrosine kinase sh2 domain in complex with the phosphotyrosyl peptide ac-ptyr-glu-glu-ile (pyeei peptide)','1','1.0009224702381','1.0009224702381'),
('LCK_HUMAN','1lkl_A','A','human p56-lck tyrosine kinase sh2 domain in complex with the phosphotyrosyl peptide ac-ptyr-glu-glu-gly (pyeeg peptide)','1.8','0.510114975198413','0.510114975198413'),
('PASK_HUMAN','1ll8_A','A','structure and interactions of pas kinase n-terminal pas domain: model for intramolecular kinase regulation',NULL,'0.00904385416666664','0.00904385416666664'),
('EGFR_HUMAN','1m14_A','A','tyrosine kinase domain from epidermal growth factor receptor','2.6','0.262526664377289','0.262526664377289'),
('EGFR_HUMAN','1m17_A','A','epidermal growth factor receptor tyrosine kinase domain with 4-anilinoquinazoline inhibitor erlotinib','2.6','0.24962879235348','0.24962879235348'),
('FYN_HUMAN','1m27_C','C','crystal structure of sap/fynsh3/slam ternary complex','2.5','0.310129241071429','0.310129241071429'),
('ZAP70_HUMAN','1m61_A','A','crystal structure of the apo sh2 domains of zap-70','2.5','0.251486949404762','0.251486949404762'),
('ERBB3_HUMAN','1m6b_A','A','structure of the her3 (erbb3) extracellular domain','2.6','0.228903628663004','0.228903628663004'),
('ERBB3_HUMAN','1m6b_B','B','structure of the her3 (erbb3) extracellular domain','2.6','0.228903628663004','0.228903628663004'),
('IGF1R_HUMAN','1m7n_A','A','crystal structure of unactivated apo insulin-like growth factor-1 receptor kinase domain','2.7','0.256967111441799','0.256967111441799'),
('IGF1R_HUMAN','1m7n_B','B','crystal structure of unactivated apo insulin-like growth factor-1 receptor kinase domain','2.7','0.256967111441799','0.256967111441799'),
('MK14_HUMAN','1m7q_A','A','crystal structure of p38 map kinase in complex with a dihydroquinazolinone inhibitor','2.4','0.316313660714286','0.316313660714286'),
('TGFR2_HUMAN','1m9z_A','A','crystal structure of human tgf-beta type ii receptor ligand domain','1.05','0.945295446428571','0.945295446428571'),
('ERBB2_HUMAN','1mfg_B','B','the structure of erbin pdz domain bound to the carboxy- terminal tail of the erbb2 receptor','1.25','0.820967752976191','0.820967752976191'),
('ERBB2_HUMAN','1mfl_A','A','the structure of erbin pdz domain bound to the carboxy- terminal tail of the erbb2 receptor','1.88','0.489293152545593','0.489293152545593'),
('DCLK1_HUMAN','1mfw_A','A','structure of n-terminal doublecortin domain from dclk: selenomethionine labeled protein','1.6','0.628334717261905','0.628334717261905'),
('DCLK1_HUMAN','1mg4_A','A','structure of n-terminal doublecortin domain from dclk: wild type protein','1.5','0.655664166666667','0.655664166666667'),
('EGFR_HUMAN','1mox_A','A','crystal structure of human epidermal growth factor receptor 1-501) in complex with tgf-alpha','2.5','0.235461800595238','0.235461800595238'),
('EGFR_HUMAN','1mox_B','B','crystal structure of human epidermal growth factor receptor 1-501) in complex with tgf-alpha','2.5','0.235461800595238','0.235461800595238'),
('FAK1_HUMAN','1mp8_A','A','crystal structure of focal adhesion kinase (fak)','1.6','0.588071994047619','0.588071994047619'),
('AURKA_HUMAN','1mq4_A','A','crystal structure of aurora-a protein kinase','1.9','0.421142128759398','0.421142128759398'),
('EPHA2_HUMAN','1mqb_A','A','crystal structure of ephrin a2 (epha2) receptor protein kinase','2.3','0.315840078933747','0.315840078933747'),
('EPHA2_HUMAN','1mqb_B','B','crystal structure of ephrin a2 (epha2) receptor protein kinase','2.3','0.315840078933747','0.315840078933747'),
('AKT2_HUMAN','1mrv_A','A','crystal structure of an inactive akt2 kinase domain','2.8','0.216389419642857','0.216389419642857'),
('AKT2_HUMAN','1mry_A','A','crystal structure of an inactive akt2 kinase domain','2.8','0.235595758928571','0.235595758928571'),
('AURKA_HUMAN','1muo_A','A','crystal structure of aurora-2, an oncogenic serine- threonine kinase','2.9','0.123890190373563','0.123890190373563'),
('ERBB2_HUMAN','1mw4_B','B','solution structure of the human grb7-sh2 domain in complex w amino acid peptide py1139',NULL,'0.0137802232142857','0.0137802232142857'),
('ERBB2_HUMAN','1n8z_C','C','crystal structure of extracellular domain of human her2 comp herceptin fab','2.52','0.266450233134921','0.266450233134921'),
('CSK21_HUMAN','1na7_A','A','crystal structure of the catalytic subunit of human protein kinase ck2','2.4','0.320364910714286','0.320364910714286'),
('TITIN_HUMAN','1nct_A','A','titin module m5, n-terminally extended, nmr',NULL,'0.00236035714285711','0.00236035714285711'),
('TITIN_HUMAN','1ncu_A','A','titin module m5, n-terminally extended, nmr',NULL,'0.0058510714285714','0.0058510714285714'),
('EGFR_HUMAN','1nql_A','A','structure of the extracellular domain of human epidermal gro (egf) receptor in an inactive (low ph) complex with egf.','2.8','0.170297693452381','0.170297693452381'),
('TRIO_HUMAN','1nty_A','A','crystal structure of the first dh/ph domain of trio to 1.7 a','1.7','0.544885428046218','0.544885428046218'),
('FGFR2_HUMAN','1nun_B','B','crystal structure analysis of the fgf10-fgfr2b complex','2.9','0.198125577278325','0.198125577278325'),
('CHK1_HUMAN','1nvq_A','A','the complex structure of checkpoint kinase chk1/ucn-01','2','0.436751026785714','0.436751026785714'),
('CHK1_HUMAN','1nvr_A','A','the complex structure of checkpoint kinase chk1/staurosporine','1.8','0.50549996031746','0.50549996031746'),
('CHK1_HUMAN','1nvs_A','A','the complex structure of checkpoint kinase chk1/sb218078','1.8','0.466975689484127','0.466975689484127'),
('MAPK2_HUMAN','1nxk_A','A','crystal structure of staurosporine bound to map kap kinase 2','2.7','0.209979239417989','0.209979239417989'),
('MAPK2_HUMAN','1nxk_B','B','crystal structure of staurosporine bound to map kap kinase 2','2.7','0.209979239417989','0.209979239417989'),
('MAPK2_HUMAN','1nxk_C','C','crystal structure of staurosporine bound to map kap kinase 2','2.7','0.209979239417989','0.209979239417989'),
('MAPK2_HUMAN','1nxk_D','D','crystal structure of staurosporine bound to map kap kinase 2','2.7','0.209979239417989','0.209979239417989'),
('MAPK2_HUMAN','1ny3_A','A','crystal structure of adp bound to map kap kinase 2','3','0.168244553571429','0.168244553571429'),
('FYN_HUMAN','1nyf_A','A','nmr study of the sh3 domain from fyn proto-oncogene tyrosine kinase, minimized average (probmap) structure',NULL,'0.0334710267857143','0.0334710267857143'),
('FYN_HUMAN','1nyg_A','A','nmr study of the sh3 domain from fyn proto-oncogene tyrosine kinase, family of 20 structures',NULL,'0.0307864880952381','0.0307864880952381'),
('AVR2B_HUMAN','1nys_A','A','crystal structure of activin a bound to the ecd of actriib p41','3.05','0.156398153054254','0.156398153054254'),
('SRC_HUMAN','1o41_A','A','crystal structure of sh2 in complex with ru78300.','1.7','0.523200130427171','0.523200130427171'),
('SRC_HUMAN','1o42_A','A','crystal structure of sh2 in complex with ru81843.','1.7','0.517582094712885','0.517582094712885'),
('SRC_HUMAN','1o43_A','A','crystal structure of sh2 in complex with ru82129.','1.5','0.59563912202381','0.59563912202381'),
('SRC_HUMAN','1o44_A','A','crystal structure of sh2 in complex with ru85052','1.7','0.536630933998599','0.536630933998599'),
('SRC_HUMAN','1o45_A','A','crystal structure of sh2 in complex with ru84687.','1.8','0.493500823412698','0.493500823412698'),
('SRC_HUMAN','1o46_A','A','crystal structure of sh2 in complex with ru90395.','2','0.437983645833333','0.437983645833333'),
('SRC_HUMAN','1o47_A','A','crystal structure of sh2 in complex with ru82209.','1.8','0.502895436507936','0.502895436507936'),
('SRC_HUMAN','1o48_A','A','crystal structure of sh2 in complex with ru85053.','1.55','0.594410739727342','0.594410739727342'),
('SRC_HUMAN','1o49_A','A','crystal structure of sh2 in complex with ru85493.','1.7','0.534461886379552','0.534461886379552'),
('SRC_HUMAN','1o4a_A','A','crystal structure of sh2 in complex with ru82197.','1.5','0.5925090625','0.5925090625'),
('SRC_HUMAN','1o4b_A','A','crystal structure of sh2 in complex with ru83876.','1.85','0.488141775659588','0.488141775659588'),
('SRC_HUMAN','1o4c_A','A','crystal structure of sh2 in complex with phosphate.','1.8','0.502759856150794','0.502759856150794'),
('SRC_HUMAN','1o4d_A','A','crystal structure of sh2 in complex with ru78262.','1.85','0.506466924469112','0.506466924469112'),
('SRC_HUMAN','1o4e_A','A','crystal structure of sh2 in complex with ru78299.','2','0.436630357142857','0.436630357142857'),
('SRC_HUMAN','1o4f_A','A','crystal structure of sh2 in complex with ru79073.','2','0.480383452380952','0.480383452380952'),
('SRC_HUMAN','1o4g_A','A','crystal structure of sh2 in complex with dpi59.','1.55','0.589332584965438','0.589332584965438'),
('SRC_HUMAN','1o4h_A','A','crystal structure of sh2 in complex with ru79072.','2.25','0.405089518849206','0.405089518849206'),
('SRC_HUMAN','1o4i_A','A','crystal structure of sh2 in complex with pas219.','1.75','0.505608244047619','0.505608244047619'),
('SRC_HUMAN','1o4j_A','A','crystal structure of sh2 in complex with iso24.','1.7','0.539325770308123','0.539325770308123'),
('SRC_HUMAN','1o4k_A','A','crystal structure of sh2 in complex with pasbn.','1.57','0.588943285278283','0.588943285278283'),
('SRC_HUMAN','1o4l_A','A','crystal structure of sh2 in complex with fragment2.','1.65','0.53058925189394','0.53058925189394'),
('SRC_HUMAN','1o4m_A','A','crystal structure of sh2 in complex with malonicacid.','1.6','0.578991086309524','0.578991086309524'),
('SRC_HUMAN','1o4n_A','A','crystal structure of sh2 in complex with oxalic acid.','1.6','0.553478630952381','0.553478630952381'),
('SRC_HUMAN','1o4o_A','A','crystal structure of sh2 in complex with phenylphosphate.','1.7','0.501686558998599','0.501686558998599'),
('SRC_HUMAN','1o4p_A','A','crystal structure of sh2 in complex with ru78791.','1.9','0.499997619830827','0.499997619830827'),
('SRC_HUMAN','1o4q_A','A','crystal structure of sh2 in complex with ru79256.','1.7','0.548923210784314','0.548923210784314'),
('SRC_HUMAN','1o4r_A','A','crystal structure of sh2 in complex with ru78783.','1.5','0.602249895833333','0.602249895833333'),
('AKT2_HUMAN','1o6k_A','A','structure of activated form of pkb kinase domain s474d with gsk3 peptide and amp-pnp','1.7','0.525671871498599','0.525671871498599'),
('GSK3B_HUMAN','1o6k_C','C','structure of activated form of pkb kinase domain s474d with gsk3 peptide and amp-pnp','1.7','0.525671871498599','0.525671871498599'),
('AKT2_HUMAN','1o6l_A','A','crystal structure of an activated akt/protein kinase b (pkb-pif chimera) ternary complex with amp-pnp and gsk3 peptide','1.6','0.57259537202381','0.57259537202381'),
('GSK3B_HUMAN','1o6l_C','C','crystal structure of an activated akt/protein kinase b (pkb-pif chimera) ternary complex with amp-pnp and gsk3 peptide','1.6','0.57259537202381','0.57259537202381'),
('GSK3B_HUMAN','1o9u_A','A','glycogen synthase kinase 3 beta complexed with axin peptide','2.4','0.323971428571429','0.323971428571429'),
('FGFR2_HUMAN','1oec_A','A','fgfr2 kinase domain','2.4','0.324384553571429','0.324384553571429'),
('CDK2_HUMAN','1ogu_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with a 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitor','2.6','0.296680741758242','0.296680741758242'),
('CDK2_HUMAN','1ogu_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with a 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitor','2.6','0.296680741758242','0.296680741758242'),
('CDK2_HUMAN','1oi9_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2.1','0.357198095238095','0.357198095238095'),
('CDK2_HUMAN','1oi9_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2.1','0.357198095238095','0.357198095238095'),
('CDK2_HUMAN','1oiq_A','A','imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation','2.31','0.323405179924242','0.323405179924242'),
('CDK2_HUMAN','1oir_A','A','imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation','1.91','0.460754896924084','0.460754896924084'),
('CDK2_HUMAN','1oit_A','A','imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation','1.6','0.523861339285714','0.523861339285714'),
('CDK2_HUMAN','1oiu_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2','0.407354464285714','0.407354464285714'),
('CDK2_HUMAN','1oiu_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2','0.407354464285714','0.407354464285714'),
('CDK2_HUMAN','1oiy_A','A','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2.4','0.258621369047619','0.258621369047619'),
('CDK2_HUMAN','1oiy_C','C','structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor','2.4','0.258621369047619','0.258621369047619'),
('CDK2_HUMAN','1okv_A','A','cyclin a binding groove inhibitor h-arg-arg-leu-ile-phe-nh2','2.4','0.330688779761905','0.330688779761905'),
('CDK2_HUMAN','1okv_C','C','cyclin a binding groove inhibitor h-arg-arg-leu-ile-phe-nh2','2.4','0.330688779761905','0.330688779761905'),
('CDK2_HUMAN','1okw_A','A','cyclin a binding groove inhibitor ac-arg-arg-leu-asn-(m-cl-p','2.5','0.337971235119048','0.337971235119048'),
('CDK2_HUMAN','1okw_C','C','cyclin a binding groove inhibitor ac-arg-arg-leu-asn-(m-cl-p','2.5','0.337971235119048','0.337971235119048'),
('PDPK1_HUMAN','1oky_A','A','structure of human pdk1 kinase domain in complex with staurosporine','2.3','0.35292315929089','0.35292315929089'),
('PDPK1_HUMAN','1okz_A','A','structure of human pdk1 kinase domain in complex with ucn-01','2.51','0.346966106644849','0.346966106644849'),
('CDK2_HUMAN','1ol1_A','A','cyclin a binding groove inhibitor h-cit-cit-leu-ile-(p-f-phe','2.9','0.207361589183087','0.207361589183087'),
('CDK2_HUMAN','1ol1_C','C','cyclin a binding groove inhibitor h-cit-cit-leu-ile-(p-f-phe','2.9','0.207361589183087','0.207361589183087'),
('CDK2_HUMAN','1ol2_A','A','cyclin a binding groove inhibitor h-arg-arg-leu-asn-(p-f-phe','2.6','0.299799179258242','0.299799179258242'),
('CDK2_HUMAN','1ol2_C','C','cyclin a binding groove inhibitor h-arg-arg-leu-asn-(p-f-phe','2.6','0.299799179258242','0.299799179258242'),
('AURKA_HUMAN','1ol5_A','A','structure of aurora-a 122-403, phosphorylated on thr287, thr288 and bound to tpx2 1-43','2.5','0.327789494047619','0.327789494047619'),
('AURKA_HUMAN','1ol6_A','A','structure of unphosphorylated d274n mutant of aurora-a','3','0.169664151785714','0.169664151785714'),
('AURKA_HUMAN','1ol7_A','A','structure of human aurora-a 122-403 phosphorylated on thr287, thr288','2.75','0.215143193993506','0.215143193993506'),
('ABL1_HUMAN','1opl_A','A','structural basis for the auto-inhibition of c-abl tyrosine kinase','3.42','0.129140860223475','0.129140860223475'),
('ABL1_HUMAN','1opl_B','B','structural basis for the auto-inhibition of c-abl tyrosine kinase','3.42','0.129140860223475','0.129140860223475'),
('MK14_HUMAN','1ouk_A','A','the structure of p38 alpha in complex with a pyridinylimidazole inhibitor','2.5','0.299630610119048','0.299630610119048'),
('MK14_HUMAN','1ouy_A','A','the structure of p38 alpha in complex with a dihydropyrido- pyrimidine inhibitor','2.5','0.29611880952381','0.29611880952381'),
('MK14_HUMAN','1ove_A','A','the structure of p38 alpha in complex with a dihydroquinolin','2.1','0.43050875','0.43050875'),
('FAK1_HUMAN','1ow6_A','A','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.35','0.291810530965046','0.291810530965046'),
('FAK1_HUMAN','1ow6_B','B','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.35','0.291810530965046','0.291810530965046'),
('FAK1_HUMAN','1ow6_C','C','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.35','0.291810530965046','0.291810530965046'),
('FAK1_HUMAN','1ow7_A','A','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.6','0.258431887591575','0.258431887591575'),
('FAK1_HUMAN','1ow7_B','B','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.6','0.258431887591575','0.258431887591575'),
('FAK1_HUMAN','1ow7_C','C','paxillin ld4 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.6','0.258431887591575','0.258431887591575'),
('FAK1_HUMAN','1ow8_A','A','paxillin ld2 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.85','0.201715972744361','0.201715972744361'),
('FAK1_HUMAN','1ow8_B','B','paxillin ld2 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.85','0.201715972744361','0.201715972744361'),
('FAK1_HUMAN','1ow8_C','C','paxillin ld2 motif bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase','2.85','0.201715972744361','0.201715972744361'),
('MK14_HUMAN','1oz1_A','A','p38 mitogen-activated kinase in complex with 4-azaindole inhibitor','2.1','0.397229672619048','0.397229672619048'),
('INSR_HUMAN','1p14_A','A','crystal structure of a catalytic-loop mutant of the insulin receptor tyrosine kinase','1.9','0.45051163768797','0.45051163768797'),
('CDK2_HUMAN','1p2a_A','A','the structure of cyclin dependent kinase 2 (ckd2) with a trisubstituted naphthostyril inhibitor','2.5','0.310350238095238','0.310350238095238'),
('DAPK1_HUMAN','1p4f_A','A','death associated protein kinase catalytic domain with bound inhibitor fragment','1.9','0.487044732926065','0.487044732926065'),
('IGF1R_HUMAN','1p4o_A','A','structure of apo unactivated igf-1r kinase domain at 1.5a re','1.5','0.614347217261905','0.614347217261905'),
('IGF1R_HUMAN','1p4o_B','B','structure of apo unactivated igf-1r kinase domain at 1.5a re','1.5','0.614347217261905','0.614347217261905'),
('CDK2_HUMAN','1p5e_A','A','the strucure of phospho-cdk2/cyclin a in complex with the inhibitor 4,5,6,7-tetrabromobenzotriazole (tbs)','2.22','0.349845004021879','0.349845004021879'),
('CDK2_HUMAN','1p5e_C','C','the strucure of phospho-cdk2/cyclin a in complex with the inhibitor 4,5,6,7-tetrabromobenzotriazole (tbs)','2.22','0.349845004021879','0.349845004021879'),
('AKT2_HUMAN','1p6s_A','A','solution structure of the pleckstrin homology domain of human protein kinase b beta (pkb/akt)',NULL,'0.0280957142857142','0.0280957142857142'),
('CDK2_HUMAN','1pf8_A','A','crystal structure of human cyclin-dependent kinase 2 complexed with a nucleoside inhibitor','2.51','0.298726850692468','0.298726850692468'),
('CSK21_HUMAN','1pjk_A','A','crystal structure of a c-terminal deletion mutant of human p kinase ck2 catalytic subunit','2.5','0.331570044642857','0.331570044642857'),
('CDK2_HUMAN','1pkd_A','A','the crystal structure of ucn-01 in complex with phospho- cdk2/cyclin a','2.3','0.330565287267081','0.330565287267081'),
('CDK2_HUMAN','1pkd_C','C','the crystal structure of ucn-01 in complex with phospho- cdk2/cyclin a','2.3','0.330565287267081','0.330565287267081'),
('KIT_HUMAN','1pkg_A','A','structure of a c-kit kinase product complex','2.9','0.207141574302135','0.207141574302135'),
('TGFR2_HUMAN','1plo_A','A','transforming growth factor-beta type ii receptor extracellular domain',NULL,'0.0372766369047619','0.0372766369047619'),
('MK01_HUMAN','1pme_A','A','structure of penta mutant human erk2 map kinase complexed with a specific inhibitor of human p38 map kinase','2','0.410427767857143','0.410427767857143'),
('MK10_HUMAN','1pmn_A','A','crystal structure of jnk3 in complex with an imidazole- pyrimidine inhibitor','2.2','0.341798758116883','0.341798758116883'),
('MK10_HUMAN','1pmq_A','A','the structure of jnk3 in complex with an imidazole- pyrimidine inhibitor','2.2','0.346645558712121','0.346645558712121'),
('MK10_HUMAN','1pmu_A','A','the crystal structure of jnk3 in complex with a phenantroline inhibitor','2.7','0.243095102513227','0.243095102513227'),
('MK10_HUMAN','1pmv_A','A','the structure of jnk3 in complex with a dihydroanthrapyrazole inhibitor','2.5','0.291815014880952','0.291815014880952'),
('STK38_HUMAN','1psb_C','C','solution structure of calcium loaded s100b complexed to a peptide from n-terminal regulatory domain of ndr kinase.',NULL,'0.0382858035714286','0.0382858035714286'),
('STK38_HUMAN','1psb_D','D','solution structure of calcium loaded s100b complexed to a peptide from n-terminal regulatory domain of ndr kinase.',NULL,'0.0382858035714286','0.0382858035714286'),
('CDK2_HUMAN','1pw2_A','A','apo structure of human cyclin-dependent kinase 2','1.95','0.423229962225275','0.423229962225275'),
('CDK2_HUMAN','1pxi_A','A','human cyclin dependent kinase 2 complexed with the inhibitor 4-(2,5-dichloro-thiophen-3-yl)-pyrimidin-2- ylamine','1.95','0.433160453296703','0.433160453296703'),
('CDK2_HUMAN','1pxj_A','A','human cyclin dependent kinase 2 complexed with the inhibitor 4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine','2.3','0.343703084886128','0.343703084886128'),
('CDK2_HUMAN','1pxk_A','A','human cyclin dependent kinase 2 complexed with the inhibitor n-[4-(2,4-dimethyl-thiazol-5-yl)pyrimidin-2-yl]- n\'-hydroxyiminoformamide','2.8','0.239437276785714','0.239437276785714'),
('CDK2_HUMAN','1pxl_A','A','human cyclin dependent kinase 2 complexed with the inhibitor [4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-yl]- (4-trifluoromethyl-phenyl)-amine','2.5','0.309853303571429','0.309853303571429'),
('CDK2_HUMAN','1pxm_A','A','human cyclin dependent kinase 2 complexed with the inhibitor 3-[4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2- ylamino]-phenol','2.53','0.288554104496048','0.288554104496048'),
('CDK2_HUMAN','1pxn_A','A','human cyclin dependent kinase 2 complexed with the inhibitor 4-[4-(4-methyl-2-methylamino-thiazol-5-yl)- pyrimidin-2-ylamino]-phenol','2.5','0.279404895833333','0.279404895833333'),
('CDK2_HUMAN','1pxo_A','A','human cyclin dependent kinase 2 complexed with the inhibitor [4-(2-amino-4-methyl-thiazol-5-yl)-pyrimidin-2- yl]-(3-nitro-phenyl)-amine','1.96','0.41315449829932','0.41315449829932'),
('CDK2_HUMAN','1pxp_A','A','human cyclin dependent kinase 2 complexed with the inhibitor n-[4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-yl]- n\',n\'-dimethyl-benzene-1,4-diamine','2.3','0.322220421195652','0.322220421195652'),
('TGFR1_HUMAN','1py5_A','A','crystal structure of tgf-beta receptor i kinase with inhibitor','2.3','0.285866760481366','0.285866760481366'),
('CDK2_HUMAN','1pye_A','A','crystal structure of cdk2 with inhibitor','2','0.403713005952381','0.403713005952381'),
('GSK3B_HUMAN','1pyx_A','A','gsk-3 beta complexed with amp-pnp','2.4','0.333620625','0.333620625'),
('GSK3B_HUMAN','1pyx_B','B','gsk-3 beta complexed with amp-pnp','2.4','0.333620625','0.333620625'),
('GSK3B_HUMAN','1q3d_A','A','gsk-3 beta complexed with staurosporine','2.2','0.364470022997836','0.364470022997836'),
('GSK3B_HUMAN','1q3d_B','B','gsk-3 beta complexed with staurosporine','2.2','0.364470022997836','0.364470022997836'),
('GSK3B_HUMAN','1q3w_A','A','gsk-3 beta complexed with alsterpaullone','2.3','0.333208724767081','0.333208724767081'),
('GSK3B_HUMAN','1q3w_B','B','gsk-3 beta complexed with alsterpaullone','2.3','0.333208724767081','0.333208724767081'),
('GSK3B_HUMAN','1q41_A','A','gsk-3 beta complexed with indirubin-3\'-monoxime','2.1','0.389077514880952','0.389077514880952'),
('GSK3B_HUMAN','1q41_B','B','gsk-3 beta complexed with indirubin-3\'-monoxime','2.1','0.389077514880952','0.389077514880952'),
('PLK1_HUMAN','1q4k_A','A','the polo-box domain of plk1 in complex with a phospho- peptide','2.3','0.303982296195652','0.303982296195652'),
('PLK1_HUMAN','1q4k_B','B','the polo-box domain of plk1 in complex with a phospho- peptide','2.3','0.303982296195652','0.303982296195652'),
('PLK1_HUMAN','1q4k_C','C','the polo-box domain of plk1 in complex with a phospho- peptide','2.3','0.303982296195652','0.303982296195652'),
('GSK3B_HUMAN','1q4l_A','A','gsk-3 beta complexed with inhibitor i-5','2.77','0.265742973182053','0.265742973182053'),
('GSK3B_HUMAN','1q4l_B','B','gsk-3 beta complexed with inhibitor i-5','2.77','0.265742973182053','0.265742973182053'),
('PLK1_HUMAN','1q4o_A','A','the structure of the polo box domain of human plk1','2.2','0.354689695616883','0.354689695616883'),
('PLK1_HUMAN','1q4o_B','B','the structure of the polo box domain of human plk1','2.2','0.354689695616883','0.354689695616883'),
('GSK3B_HUMAN','1q5k_A','A','crystal structure of glycogen synthase kinase 3 in complexed with inhibitor','1.94','0.435199468121011','0.435199468121011'),
('GSK3B_HUMAN','1q5k_B','B','crystal structure of glycogen synthase kinase 3 in complexed with inhibitor','1.94','0.435199468121011','0.435199468121011'),
('LCK_HUMAN','1q68_B','B','solution structure of t-cell surface glycoprotein cd4 and proto-oncogene tyrosine-protein kinase lck fragments',NULL,'0.0110512648809524','0.0110512648809524'),
('LCK_HUMAN','1q69_B','B','solution structure of t-cell surface glycoprotein cd8 alpha chain and proto-oncogene tyrosine-protein kinase lck fragments',NULL,'0.00756186011904759','0.00756186011904759'),
('HCK_HUMAN','1qcf_A','A','crystal structure of hck in complex with a src family- selective tyrosine kinase inhibitor','2','0.4278859375','0.4278859375'),
('BTK_HUMAN','1qly_A','A','nmr study of the sh3 domain from bruton\'s tyrosine kinase, 20 structures',NULL,'0.0115784970238095','0.0115784970238095'),
('CDK2_HUMAN','1qmz_A','A','phosphorylated cdk2-cyclyin a-substrate peptide complex','2.2','0.351930975378788','0.351930975378788'),
('CDK2_HUMAN','1qmz_C','C','phosphorylated cdk2-cyclyin a-substrate peptide complex','2.2','0.351930975378788','0.351930975378788'),
('LCK_HUMAN','1qpc_A','A','structural analysis of the lymphocyte-specific kinase lck in with non-selective and src family selective kinase inhibito','1.6','0.57967212797619','0.57967212797619'),
('LCK_HUMAN','1qpd_A','A','structural analysis of the lymphocyte-specific kinase lck in complex with non-selective and src family selective kinase inhibitors','2','0.451936205357143','0.451936205357143'),
('LCK_HUMAN','1qpe_A','A','structural analysis of the lymphocyte-specific kinase lck in complex with non-selective and src family selective kinase inhibitors','2','0.456327708333333','0.456327708333333'),
('LCK_HUMAN','1qpj_A','A','crystal structure of the lymphocyte-specific kinase lck in complex with staurosporine.','2.2','0.381986347402597','0.381986347402597'),
('ERBB2_HUMAN','1qr1_C','C','poor binding of a her-2/neu epitope (gp2) to hla-a2.1 is due to a lack of interactions in the center of the peptide','2.4','0.302007306547619','0.302007306547619'),
('ERBB2_HUMAN','1qr1_F','F','poor binding of a her-2/neu epitope (gp2) to hla-a2.1 is due to a lack of interactions in the center of the peptide','2.4','0.302007306547619','0.302007306547619'),
('VGFR1_HUMAN','1qsv_A','A','the vegf-binding domain of flt-1, 20 nmr structures',NULL,'0.038336369047619','0.038336369047619'),
('VGFR1_HUMAN','1qsz_A','A','the vegf-binding domain of flt-1 (minimized mean)',NULL,'0.0423366517857142','0.0423366517857142'),
('VGFR1_HUMAN','1qty_T','T','vascular endothelial growth factor in complex with domain 2 of the flt-1 receptor','2.7','0.204432632275132','0.204432632275132'),
('VGFR1_HUMAN','1qty_U','U','vascular endothelial growth factor in complex with domain 2 of the flt-1 receptor','2.7','0.204432632275132','0.204432632275132'),
('VGFR1_HUMAN','1qty_X','X','vascular endothelial growth factor in complex with domain 2 of the flt-1 receptor','2.7','0.204432632275132','0.204432632275132'),
('VGFR1_HUMAN','1qty_Y','Y','vascular endothelial growth factor in complex with domain 2 of the flt-1 receptor','2.7','0.204432632275132','0.204432632275132'),
('E2AK2_HUMAN','1qu6_A','A','structure of the double-stranded rna-binding domain of the protein kinase pkr reveals the molecular basis of its dsrna-mediated activation',NULL,'0.0110122767857143','0.0110122767857143'),
('GSK3B_HUMAN','1r0e_A','A','glycogen synthase kinase-3 beta in complex with 3-indolyl-4- arylmaleimide inhibitor','2.25','0.339791780753968','0.339791780753968'),
('GSK3B_HUMAN','1r0e_B','B','glycogen synthase kinase-3 beta in complex with 3-indolyl-4- arylmaleimide inhibitor','2.25','0.339791780753968','0.339791780753968'),
('MET_HUMAN','1r0p_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with the microbial alkaloid k-252a','1.8','0.531992326388889','0.531992326388889'),
('MET_HUMAN','1r1w_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met','1.8','0.513179216269841','0.513179216269841'),
('MK14_HUMAN','1r39_A','A','the structure of p38alpha','2.3','0.348684587862319','0.348684587862319'),
('MK14_HUMAN','1r3c_A','A','the structure of p38alpha c162s mutant','2','0.442087261904762','0.442087261904762'),
('CDK2_HUMAN','1r78_A','A','cdk2 complex with a 4-alkynyl oxindole inhibitor','2','0.401362797619048','0.401362797619048'),
('BMR1A_HUMAN','1rew_C','C','structural refinement of the complex of bone morphogenetic p and its type ia receptor','1.86','0.445292474078341','0.445292474078341'),
('BMR1A_HUMAN','1rew_D','D','structural refinement of the complex of bone morphogenetic p and its type ia receptor','1.86','0.445292474078341','0.445292474078341'),
('RAF1_HUMAN','1rfa_A','A','nmr solution structure of the ras-binding domain of c-raf-1',NULL,'0.0207470684523809','0.0207470684523809'),
('TYRO3_HUMAN','1rhf_A','A','crystal structure of human tyro3-d1d2','1.96','0.431080286989796','0.431080286989796'),
('TYRO3_HUMAN','1rhf_B','B','crystal structure of human tyro3-d1d2','1.96','0.431080286989796','0.431080286989796'),
('PTK6_HUMAN','1rja_A','A','solution structure and backbone dynamics of the nonreceptor kinase ptk6/brk sh2 domain',NULL,'0.0206681994047619','0.0206681994047619'),
('FLT3_HUMAN','1rjb_A','A','crystal structure of flt3','2.1','0.392827544642857','0.392827544642857'),
('INSR_HUMAN','1rqq_A','A','crystal structure of the insulin receptor kinase in complex with the sh2 domain of aps','2.6','0.275066009615385','0.275066009615385'),
('INSR_HUMAN','1rqq_B','B','crystal structure of the insulin receptor kinase in complex with the sh2 domain of aps','2.6','0.275066009615385','0.275066009615385'),
('VGFR1_HUMAN','1rv6_X','X','crystal structure of plgf in complex with domain 2 of vegfr1','2.45','0.324192268282313','0.324192268282313'),
('VGFR1_HUMAN','1rv6_Y','Y','crystal structure of plgf in complex with domain 2 of vegfr1','2.45','0.324192268282313','0.324192268282313'),
('TGFR1_HUMAN','1rw8_A','A','crystal structure of tgf-beta receptor i kinase with atp site inhibitor','2.4','0.269962693452381','0.269962693452381'),
('FGFR3_HUMAN','1ry7_B','B','crystal structure of the 3 ig form of fgfr3c in complex with fgf1','3.2','0.060086369047619','0.060086369047619'),
('ROCK1_HUMAN','1s1c_X','X','crystal structure of the complex between the human rhoa and rho-binding domain of human rocki','2.6','0.280590399496337','0.280590399496337'),
('ROCK1_HUMAN','1s1c_Y','Y','crystal structure of the complex between the human rhoa and rho-binding domain of human rocki','2.6','0.280590399496337','0.280590399496337'),
('ERBB2_HUMAN','1s78_A','A','insights into erbb signaling from the structure of the erbb2 pertuzumab complex','3.25','-0.0873623500457875','-0.0873623500457875'),
('ERBB2_HUMAN','1s78_B','B','insights into erbb signaling from the structure of the erbb2 pertuzumab complex','3.25','-0.0873623500457875','-0.0873623500457875'),
('MP2K2_HUMAN','1s9i_A','A','x-ray structure of the human mitogen-activated protein kinase kinase 2 (mek2)in a complex with ligand and mgatp','3.2','0.0964717113095238','0.0964717113095238'),
('MP2K2_HUMAN','1s9i_B','B','x-ray structure of the human mitogen-activated protein kinase kinase 2 (mek2)in a complex with ligand and mgatp','3.2','0.0964717113095238','0.0964717113095238'),
('MP2K1_HUMAN','1s9j_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a complex with ligand and mgatp','2.4','0.285632946428571','0.285632946428571'),
('NTRK1_HUMAN','1shc_B','B','shc ptb domain complexed with a trka receptor phosphopeptide, nmr, minimized average structure',NULL,'-0.0038966517857143','-0.0038966517857143'),
('SRC_HUMAN','1shd_A','A','peptide inhibitors of src sh3-sh2-phosphoprotein interaction','2','0.427832663690476','0.427832663690476'),
('FYN_HUMAN','1shf_A','A','crystal structure of the sh3 domain in human fyn; comparison of the three-dimensional structures of sh3 domains in tyrosine kinases and spectrin','1.9','0.474958110902256','0.474958110902256'),
('FYN_HUMAN','1shf_B','B','crystal structure of the sh3 domain in human fyn; comparison of the three-dimensional structures of sh3 domains in tyrosine kinases and spectrin','1.9','0.474958110902256','0.474958110902256'),
('MET_HUMAN','1shy_B','B','the crystal structure of hgf beta-chain in complex with the domain of the met receptor.','3.22','0.165863425854037','0.165863425854037'),
('ITK_HUMAN','1sm2_A','A','crystal structure of the phosphorylated interleukin-2 tyrosine kinase catalytic domain','2.3','0.299745540243271','0.299745540243271'),
('ITK_HUMAN','1sm2_B','B','crystal structure of the phosphorylated interleukin-2 tyrosine kinase catalytic domain','2.3','0.299745540243271','0.299745540243271'),
('ITK_HUMAN','1snu_A','A','crystal structure of the unphosphorylated interleukin-2 tyrosine kinase catalytic domain','2.5','0.242940386904762','0.242940386904762'),
('ITK_HUMAN','1snu_B','B','crystal structure of the unphosphorylated interleukin-2 tyrosine kinase catalytic domain','2.5','0.242940386904762','0.242940386904762'),
('ITK_HUMAN','1snx_A','A','crystal structure of apo interleukin-2 tyrosine kinase catalytic domain','3.2','0.102378511904762','0.102378511904762'),
('ITK_HUMAN','1snx_B','B','crystal structure of apo interleukin-2 tyrosine kinase catalytic domain','3.2','0.102378511904762','0.102378511904762'),
('MET_HUMAN','1ssl_A','A','solution structure of the psi domain from the met receptor',NULL,'0.00416181547619045','0.00416181547619045'),
('KIT_HUMAN','1t45_A','A','structural basis for the autoinhibition and sti-571 inhibiti kit tyrosine kinase','1.9','0.477829107926065','0.477829107926065'),
('KIT_HUMAN','1t46_A','A','structural basis for the autoinhibition and sti-571 inhibition of c-kit tyrosine kinase','1.6','0.579159464285714','0.579159464285714'),
('TITIN_HUMAN','1tit_A','A','titin, ig repeat 27, nmr, minimized average structure',NULL,'0.0149774404761904','0.0149774404761904'),
('TITIN_HUMAN','1tiu_A','A','titin, ig repeat 27, nmr, 24 structures',NULL,'0.0194593601190476','0.0194593601190476'),
('TITIN_HUMAN','1tki_A','A','autoinhibited serine kinase domain of the giant muscle protein titin','2','0.414605148809524','0.414605148809524'),
('TITIN_HUMAN','1tki_B','B','autoinhibited serine kinase domain of the giant muscle protein titin','2','0.414605148809524','0.414605148809524'),
('TITIN_HUMAN','1tnm_A','A','tertiary structure of an immunoglobulin-like domain from the muscle protein titin: a new member of the i set',NULL,'0.00616508928571426','0.00616508928571426'),
('TITIN_HUMAN','1tnn_A','A','tertiary structure of an immunoglobulin-like domain from the muscle protein titin: a new member of the i set',NULL,'0.0054851339285714','0.0054851339285714'),
('MK01_HUMAN','1tvo_A','A','the structure of erk2 in complex with a small molecule inhibitor','2.5','0.245208616071429','0.245208616071429'),
('SPEG_HUMAN','1u2h_A','A','x-ray structure of the n-terminally truncated human apep-1','0.96','1.03158711309524','1.03158711309524'),
('ACK1_HUMAN','1u46_A','A','crystal structure of the unphosphorylated kinase domain of the tyrosine kinase ack1','2','0.440436011904762','0.440436011904762'),
('ACK1_HUMAN','1u46_B','B','crystal structure of the unphosphorylated kinase domain of the tyrosine kinase ack1','2','0.440436011904762','0.440436011904762'),
('ACK1_HUMAN','1u4d_A','A','structure of the ack1 kinase domain bound to debromohymenialdisine','2.1','0.393411071428571','0.393411071428571'),
('ACK1_HUMAN','1u4d_B','B','structure of the ack1 kinase domain bound to debromohymenialdisine','2.1','0.393411071428571','0.393411071428571'),
('ACK1_HUMAN','1u54_A','A','crystal structures of the phosphorylated and unphosphorylate domains of the cdc42-associated tyrosine kinase ack1 bound','2.8','0.244238645833333','0.244238645833333'),
('ACK1_HUMAN','1u54_B','B','crystal structures of the phosphorylated and unphosphorylate domains of the cdc42-associated tyrosine kinase ack1 bound','2.8','0.244238645833333','0.244238645833333'),
('ZAP70_HUMAN','1u59_A','A','crystal structure of the zap-70 kinase domain in complex with staurosporine','2.3','0.353324811076605','0.353324811076605'),
('CDK7_HUMAN','1ua2_A','A','crystal structure of human cdk7','3.02','0.179440232576474','0.179440232576474'),
('CDK7_HUMAN','1ua2_B','B','crystal structure of human cdk7','3.02','0.179440232576474','0.179440232576474'),
('CDK7_HUMAN','1ua2_C','C','crystal structure of human cdk7','3.02','0.179440232576474','0.179440232576474'),
('CDK7_HUMAN','1ua2_D','D','crystal structure of human cdk7','3.02','0.179440232576474','0.179440232576474'),
('EPHA8_HUMAN','1ucv_A','A','sterile alpha motif (sam) domain of ephrin type-a receptor 8',NULL,'0.0191854017857143','0.0191854017857143'),
('DCLK1_HUMAN','1uf0_A','A','solution structure of the n-terminal dcx domain of human doublecortin-like kinase',NULL,'0.0220397619047619','0.0220397619047619'),
('MK08_HUMAN','1ukh_A','A','structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125','2.35','0.311228879179331','0.311228879179331'),
('MK08_HUMAN','1uki_A','A','structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125','2.7','0.252507230489418','0.252507230489418'),
('PLK1_HUMAN','1umw_A','A','structure of a human plk1 polo-box domain/phosphopeptide complex','1.9','0.422761340068922','0.422761340068922'),
('PLK1_HUMAN','1umw_B','B','structure of a human plk1 polo-box domain/phosphopeptide complex','1.9','0.422761340068922','0.422761340068922'),
('CDK5_HUMAN','1ung_A','A','structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin.','2.3','0.332467727743271','0.332467727743271'),
('CDK5_HUMAN','1ung_B','B','structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin.','2.3','0.332467727743271','0.332467727743271'),
('CDK5_HUMAN','1unh_A','A','structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin.','2.35','0.313297629179331','0.313297629179331'),
('CDK5_HUMAN','1unh_B','B','structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin.','2.35','0.313297629179331','0.313297629179331'),
('CDK5_HUMAN','1unl_A','A','structural mechanism for the inhibition of cd5-p25 from the roscovitine, aloisine and indirubin.','2.2','0.354980156926407','0.354980156926407'),
('CDK5_HUMAN','1unl_B','B','structural mechanism for the inhibition of cd5-p25 from the roscovitine, aloisine and indirubin.','2.2','0.354980156926407','0.354980156926407'),
('AKT1_HUMAN','1unp_A','A','crystal structure of the pleckstrin homology domain of pkb alpha','1.65','0.539112421536797','0.539112421536797'),
('AKT1_HUMAN','1unq_A','A','high resolution crystal structure of the pleckstrin homology domain of protein kinase b/akt bound to ins (1,3,4,5)-tetrakisphophate','0.98','1.04264954719388','1.04264954719388'),
('AKT1_HUMAN','1unr_A','A','crystal structure of the ph domain of pkb alpha in complex with a sulfate molecule','1.25','0.800871443452381','0.800871443452381'),
('STRAA_HUMAN','1upk_A','A','crystal structure of mo25 in complex with a c-terminal peptide of strad','1.85','0.48609310006435','0.48609310006435'),
('CDK2_HUMAN','1urc_A','A','cyclin a binding groove inhibitor ace-arg-lys-leu- phe-gly','2.6','0.297667185210623','0.297667185210623'),
('CDK2_HUMAN','1urc_C','C','cyclin a binding groove inhibitor ace-arg-lys-leu- phe-gly','2.6','0.297667185210623','0.297667185210623'),
('PKN1_HUMAN','1urf_A','A','hr1b domain from prk1',NULL,'0.0594886309523809','0.0594886309523809'),
('CDK2_HUMAN','1urw_A','A','cdk2 in complex with an imidazo[1,2-b]pyridazine','1.6','0.549747901785714','0.549747901785714'),
('PDPK1_HUMAN','1uu3_A','A','structure of human pdk1 kinase domain in complex with ly333531','1.7','0.562447362570028','0.562447362570028'),
('PDPK1_HUMAN','1uu7_A','A','structure of human pdk1 kinase domain in complex with bim-2','1.9','0.433564405545113','0.433564405545113'),
('PDPK1_HUMAN','1uu8_A','A','structure of human pdk1 kinase domain in complex with bim-1','2.5','0.355368511904762','0.355368511904762'),
('PDPK1_HUMAN','1uu9_A','A','structure of human pdk1 kinase domain in complex with bim-3','1.95','0.481276628891942','0.481276628891942'),
('GSK3B_HUMAN','1uv5_A','A','glycogen synthase kinase 3 beta complexed with 6-bromoindirubin-3\'-oxime','2.8','0.256925833333333','0.256925833333333'),
('PDPK1_HUMAN','1uvr_A','A','structure of human pdk1 kinase domain in complex with bim-8','2.81','0.315614311716235','0.315614311716235'),
('BRAF_HUMAN','1uwh_A','A','the complex of wild type b-raf and bay439006','2.95','0.237531488347458','0.237531488347458'),
('BRAF_HUMAN','1uwh_B','B','the complex of wild type b-raf and bay439006','2.95','0.237531488347458','0.237531488347458'),
('BRAF_HUMAN','1uwj_A','A','the complex of mutant v599e b-raf and bay439006','3.5','0.0926961309523809','0.0926961309523809'),
('OBSCN_HUMAN','1v1c_A','A','solution structure of the sh3 domain of obscurin',NULL,'0.0409834970238095','0.0409834970238095'),
('CDK2_HUMAN','1v1k_A','A','cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor','2.31','0.337937248376623','0.337937248376623'),
('MAST3_HUMAN','1v9v_A','A','solution structure of putative domain of human kiaa0561 protein',NULL,'0.017268556547619','0.017268556547619'),
('KPCI_HUMAN','1vd2_A','A','solution structure of the pb1 domain of pkciota',NULL,'0.0150200744047619','0.0150200744047619'),
('TGFR1_HUMAN','1vjy_A','A','crystal structure of a naphthyridine inhibitor of human tgf- beta type i receptor','2','0.4222203125','0.4222203125'),
('VGFR2_HUMAN','1vr2_A','A','human vascular endothelial growth factor receptor 2 (kdr) kinase domain','2.4','0.311970386904762','0.311970386904762'),
('CDK2_HUMAN','1vyw_A','A','structure of cdk2/cyclin a with pnu-292137','2.3','0.347087177148033','0.347087177148033'),
('CDK2_HUMAN','1vyw_C','C','structure of cdk2/cyclin a with pnu-292137','2.3','0.347087177148033','0.347087177148033'),
('CDK2_HUMAN','1vyz_A','A','structure of cdk2 complexed with pnu-181227','2.21','0.33726059254471','0.33726059254471'),
('KS6A5_HUMAN','1vzo_A','A','the structure of the n-terminal kinase domain of msk1 reveals a novel autoinhibitory conformation for a dual kinase protein','1.8','0.471382653769841','0.471382653769841'),
('CDK2_HUMAN','1w0x_C','C','crystals structure of human cdk2 in complex with the inhibitor olomoucine.','2.2','0.380467522997836','0.380467522997836'),
('PDPK1_HUMAN','1w1d_A','A','crystal structure of the pdk1 pleckstrin homology (ph) domain bound to inositol (1,3,4,5)-tetrakisphosphate','1.5','0.643439717261905','0.643439717261905'),
('LYN_HUMAN','1w1f_A','A','sh3 domain of human lyn tyrosine kinase',NULL,'0.0296176041666666','0.0296176041666666'),
('PDPK1_HUMAN','1w1g_A','A','crystal structure of the pdk1 pleckstrin homology (ph) domain bound to dic4-phosphatidylinositol (3,4,5)- trisphosphate','1.45','0.627034978961412','0.627034978961412'),
('PDPK1_HUMAN','1w1h_B','B','crystal structure of the pdk1 pleckstrin homology (ph) domain','1.45','0.677610187294745','0.677610187294745'),
('MK14_HUMAN','1w7h_A','A','p38 kinase crystal structure in complex with small molecule inhibitor','2.21','0.408905205639948','0.408905205639948'),
('MK14_HUMAN','1w82_A','A','p38 kinase crystal structure in complex with small molecule inhibitor','2.2','0.407365767045455','0.407365767045455'),
('MK14_HUMAN','1w83_A','A','p38 kinase crystal structure in complex with small molecule inhibitor','2.5','0.260851994047619','0.260851994047619'),
('MK14_HUMAN','1w84_A','A','p38 kinase crystal structure in complex with small molecule inhibitor','2.2','0.41491317775974','0.41491317775974'),
('CDK2_HUMAN','1w8c_A','A','co-crystal structure of 6-cyclohexylmethoxy-8-isopropyl-9h- purin-2-ylamine and monomeric cdk2','2.05','0.41221431257259','0.41221431257259'),
('CDK2_HUMAN','1w98_A','A','the structural basis of cdk2 activation by cyclin e','2.15','0.40232535645072','0.40232535645072'),
('LYN_HUMAN','1wa7_A','A','sh3 domain of human lyn tyrosine kinase in complex with a herpesviral ligand',NULL,'0.0199343005952381','0.0199343005952381'),
('TITIN_HUMAN','1waa_A','A','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('TITIN_HUMAN','1waa_B','B','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('TITIN_HUMAN','1waa_C','C','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('TITIN_HUMAN','1waa_D','D','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('TITIN_HUMAN','1waa_E','E','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('TITIN_HUMAN','1waa_F','F','ig27 protein domain','1.8','0.469770451388889','0.469770451388889'),
('SRPK1_HUMAN','1wak_A','A','x-ray structure of srpk1','1.73','0.526728446961877','0.526728446961877'),
('MK14_HUMAN','1wbn_A','A','fragment based p38 inhibitors','2.4','0.355124092261905','0.355124092261905'),
('MK14_HUMAN','1wbo_A','A','fragment based p38 inhibitors','2.16','0.419068230820106','0.419068230820106'),
('SRPK1_HUMAN','1wbp_A','A','srpk1 bound to 9mer docking motif peptide','2.4','0.296865178571429','0.296865178571429'),
('MK14_HUMAN','1wbs_A','A','identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.','1.8','0.487706775793651','0.487706775793651'),
('MK14_HUMAN','1wbt_A','A','identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.','2','0.388687961309524','0.388687961309524'),
('MK14_HUMAN','1wbv_A','A','identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.','2','0.441798229166667','0.441798229166667'),
('MK14_HUMAN','1wbw_A','A','identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation.','2.41','0.329995497431338','0.329995497431338'),
('CDK2_HUMAN','1wcc_A','A','screening for fragment binding by x-ray crystallography','2.2','0.39919823728355','0.39919823728355'),
('RN5A_HUMAN','1wdy_A','A','crystal structure of ribonuclease','1.8','0.51004558531746','0.51004558531746'),
('MK14_HUMAN','1wfc_A','A','structure of apo, unphosphorylated, p38 mitogen activated protein kinase p38 (p38 map kinase) the mammalian homologue of the yeast hog1 protein','2.3','0.341203040243271','0.341203040243271'),
('KPCI_HUMAN','1wmh_A','A','crystal structure of a pb1 domain complex of protein kinase c iota and par6 alpha','1.5','0.607309523809524','0.607309523809524'),
('DAPK2_HUMAN','1wmk_A','A','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_B','B','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_C','C','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_D','D','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_E','E','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_F','F','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_G','G','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('DAPK2_HUMAN','1wmk_H','H','human death-associated kinase drp-1, mutant s308d d40','3.6','0.110603715277778','0.110603715277778'),
('FES_HUMAN','1wqu_A','A','solution structure of the human fes sh2 domain',NULL,'0.0323174255952381','0.0323174255952381'),
('DAPK2_HUMAN','1wrz_B','B','calmodulin complexed with a peptide from a human death-assoc protein kinase','2','0.399557336309524','0.399557336309524'),
('DMPK_HUMAN','1wt6_A','A','coiled-coil domain of dmpk','1.6','0.573099449404762','0.573099449404762'),
('DMPK_HUMAN','1wt6_B','B','coiled-coil domain of dmpk','1.6','0.573099449404762','0.573099449404762'),
('DMPK_HUMAN','1wt6_D','D','coiled-coil domain of dmpk','1.6','0.573099449404762','0.573099449404762'),
('DAPK1_HUMAN','1wvw_A','A','crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors','2.4','0.303516651785714','0.303516651785714'),
('DAPK1_HUMAN','1wvx_A','A','crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors','2.6','0.278407274496337','0.278407274496337'),
('DAPK1_HUMAN','1wvy_A','A','crystal structures of kinase domain of dap kinase in complex with small molecular inhibitors','2.8','0.276982589285714','0.276982589285714'),
('FGFR2_HUMAN','1wvz_A','A','solution structure of the d2 domain of the fibroblast growth factor',NULL,'0.0172953422619047','0.0172953422619047'),
('NTRK1_HUMAN','1wwa_X','X','ngf binding domain of human trka receptor','2.5','0.279426919642857','0.279426919642857'),
('NTRK1_HUMAN','1wwa_Y','Y','ngf binding domain of human trka receptor','2.5','0.279426919642857','0.279426919642857'),
('NTRK2_HUMAN','1wwb_X','X','ligand binding domain of human trkb receptor','2.1','0.311020848214286','0.311020848214286'),
('NTRK3_HUMAN','1wwc_A','A','nt3 binding domain of human trkc receptor','1.9','0.471184375783208','0.471184375783208'),
('NTRK1_HUMAN','1www_X','X','ngf in complex with domain 5 of the trka receptor','2.2','0.352386109307359','0.352386109307359'),
('NTRK1_HUMAN','1www_Y','Y','ngf in complex with domain 5 of the trka receptor','2.2','0.352386109307359','0.352386109307359'),
('ARAF_HUMAN','1wxm_A','A','solution structure of the n-terminal ras-binding domain (rbd) in human a-raf kinase',NULL,'0.0177676934523809','0.0177676934523809'),
('MK01_HUMAN','1wzy_A','A','crystal structure of human erk2 complexed with a pyrazolopyridazine derivative','2.5','0.250368392857143','0.250368392857143'),
('LCK_HUMAN','1x27_A','A','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('LCK_HUMAN','1x27_B','B','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('LCK_HUMAN','1x27_C','C','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('LCK_HUMAN','1x27_D','D','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('LCK_HUMAN','1x27_E','E','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('LCK_HUMAN','1x27_F','F','crystal structure of lck sh2-sh3 with sh2 binding site of p130cas','2.7','0.235828465608466','0.235828465608466'),
('EPHA8_HUMAN','1x5l_A','A','solution structure of the second fn3 domain of eph receptor a8 protein',NULL,'0.0346368452380952','0.0346368452380952'),
('LIMK2_HUMAN','1x6a_A','A','solution structures of the second lim domain of human lim- kinase 2 (limk2)',NULL,'0.0298240922619047','0.0298240922619047'),
('MATK_HUMAN','1x6g_A','A','solution structures of the sh3 domain of human megakaryocyte-associated tyrosine-protein kinase.',NULL,'0.0195185863095238','0.0195185863095238'),
('WEE1_HUMAN','1x8b_A','A','structure of human wee1a kinase: kinase domain complexed with inhibitor pd0407824','1.81','0.476550949750066','0.476550949750066'),
('KSYK_HUMAN','1xba_A','A','crystal structure of apo syk tyrosine kinase domain','2','0.387862976190476','0.387862976190476'),
('KSYK_HUMAN','1xbb_A','A','crystal structure of the syk tyrosine kinase domain with gleevec','1.57','0.612666782302093','0.612666782302093'),
('KSYK_HUMAN','1xbc_A','A','crystal structure of the syk tyrosine kinase domain with staurosporin','2','0.373044717261905','0.373044717261905'),
('KPCT_HUMAN','1xjd_A','A','crystal structure of pkc-theta complexed with staurosporine at 2a resolution','2','0.440781964285714','0.440781964285714'),
('EGFR_HUMAN','1xkk_A','A','egfr kinase domain complexed with a quinazoline inhibitor- gw572016','2.4','0.349657202380952','0.349657202380952'),
('CDK6_HUMAN','1xo2_B','B','crystal structure of a human cyclin-dependent kinase 6 compl flavonol inhibitor, fisetin','2.9','0.174818865968801','0.174818865968801'),
('PIM1_HUMAN','1xqz_A','A','crystal structure of hpim-1 kinase at 2.1 a resolution','2.1','0.343382366071428','0.343382366071428'),
('FGFR1_HUMAN','1xr0_A','A','structural basis of snt ptb domain interactions with distinct neurotrophic receptors',NULL,'0.00802604166666665','0.00802604166666665'),
('PIM1_HUMAN','1xr1_A','A','crystal structure of hpim-1 kinase in complex with amp-pnp at 2.1 a resolution','2.1','0.322240238095238','0.322240238095238'),
('PIM1_HUMAN','1xws_A','A','crystal structure of the human pim1 kinase domain','1.8','0.522940406746032','0.522940406746032'),
('SRC_HUMAN','1y57_A','A','structure of unphosphorylated c-src in complex with an inhib','1.91','0.485783885019322','0.485783885019322'),
('VGFR2_HUMAN','1y6a_A','A','crystal structure of vegfr2 in complex with a 2-anilino-5-ar inhibitor','2.1','0.431788526785714','0.431788526785714'),
('VGFR2_HUMAN','1y6b_A','A','crystal structure of vegfr2 in complex with a 2-anilino-5-ar inhibitor','2.1','0.416008630952381','0.416008630952381'),
('A9CP04_HUMAN','1y8g_A','A','catalytic and ubiqutin-associated domains of mark2/par-1: inactive double mutant with selenomethionine','2.5','0.314590044642857','0.314590044642857'),
('CDK2_HUMAN','1y8y_A','A','crystal structure of human cdk2 complexed with a pyrazolo[1, 5-a]pyrimidine inhibitor','2','0.419172723214286','0.419172723214286'),
('CDK2_HUMAN','1y91_A','A','crystal structure of human cdk2 complexed with a pyrazolo[1, 5-a]pyrimidine inhibitor','2.15','0.338362737403101','0.338362737403101'),
('TITIN_HUMAN','1ya5_A','A','crystal structure of the titin domains z1z2 in complex with','2.44','0.267223401883294','0.267223401883294'),
('TITIN_HUMAN','1ya5_B','B','crystal structure of the titin domains z1z2 in complex with','2.44','0.267223401883294','0.267223401883294'),
('PIM1_HUMAN','1yhs_A','A','crystal structure of pim-1 bound to staurosporine','2.15','0.384203407045958','0.384203407045958'),
('PAK1_HUMAN','1yhv_A','A','crystal structure of pak1 kinase domain with two point mutations (k299r, t423e)','1.8','0.457926805555556','0.457926805555556'),
('PAK1_HUMAN','1yhw_A','A','crystal structure of pak1 kinase domain with one point mutations (k299r)','1.8','0.467819737103175','0.467819737103175'),
('PIM1_HUMAN','1yi3_A','A','crystal structure of pim-1 bound to ly294002','2.5','0.312158005952381','0.312158005952381'),
('PIM1_HUMAN','1yi4_A','A','structure of pim-1 bound to adenosine','2.4','0.322577738095238','0.322577738095238'),
('SRC_HUMAN','1yi6_A','A','c-term tail segment of human tyrosine kinase (258-533)','2','0.406702872023809','0.406702872023809'),
('SRC_HUMAN','1yi6_B','B','c-term tail segment of human tyrosine kinase (258-533)','2','0.406702872023809','0.406702872023809'),
('CDK2_HUMAN','1ykr_A','A','crystal structure of cdk2 with an aminoimidazo pyridine inhibitor','1.8','0.418230228174603','0.418230228174603'),
('SRC_HUMAN','1yoj_A','A','crystal structure of src kinase domain','1.95','0.437276033653846','0.437276033653846'),
('SRC_HUMAN','1yoj_B','B','crystal structure of src kinase domain','1.95','0.437276033653846','0.437276033653846'),
('SRC_HUMAN','1yol_A','A','crystal structure of src kinase domain in complex with cgp77675','2.3','0.360419453933747','0.360419453933747'),
('SRC_HUMAN','1yol_B','B','crystal structure of src kinase domain in complex with cgp77675','2.3','0.360419453933747','0.360419453933747'),
('SRC_HUMAN','1yom_A','A','crystal structure of src kinase domain in complex with purvalanol a','2.9','0.205580755849754','0.205580755849754'),
('SRC_HUMAN','1yom_B','B','crystal structure of src kinase domain in complex with purvalanol a','2.9','0.205580755849754','0.205580755849754'),
('MK14_HUMAN','1yqj_A','A','crystal structure of p38 alpha in complex with a selective pyridazine inhibitor','2','0.408474791666667','0.408474791666667'),
('DAPK1_HUMAN','1yr5_B','B','1.7-a structure of calmodulin bound to a peptide from dap ki','1.7','0.521534133403361','0.521534133403361'),
('KPCD_HUMAN','1yrk_A','A','the c2 domain of pkc<delta> is a new phospho-tyrosine binding domain','1.7','0.561596112570028','0.561596112570028'),
('DAPK3_HUMAN','1yrp_A','A','catalytic domain of human zip kinase phosphorylated at thr26','3.1','0.196952386232719','0.196952386232719'),
('DAPK3_HUMAN','1yrp_B','B','catalytic domain of human zip kinase phosphorylated at thr26','3.1','0.196952386232719','0.196952386232719'),
('JAK3_HUMAN','1yvj_A','A','crystal structure of the jak3 kinase domain in complex with a staurosporine analogue','2.55','0.295708350840336','0.295708350840336'),
('VGFR2_HUMAN','1ywn_A','A','vegfr2 in complex with a novel 4-amino-furo[2,3-d]pyrimidine','1.71','0.527192003185046','0.527192003185046'),
('PIM1_HUMAN','1ywv_A','A','crystal structures of proto-oncogene kinase pim1: a target o somatic hypermutations in diffuse large cell lymphoma','2','0.433203184523809','0.433203184523809'),
('PIM1_HUMAN','1yxs_A','A','crystal structure of kinase pim1 with p123m mutation','2.2','0.385239264069264','0.385239264069264'),
('PIM1_HUMAN','1yxt_A','A','crystal structure of kinase pim1 in complex with amppnp','2','0.461412619047619','0.461412619047619'),
('PIM1_HUMAN','1yxu_A','A','crystal structure of kinase pim1 in complex with amp','2.24','0.339933526785714','0.339933526785714'),
('PIM1_HUMAN','1yxu_B','B','crystal structure of kinase pim1 in complex with amp','2.24','0.339933526785714','0.339933526785714'),
('PIM1_HUMAN','1yxu_C','C','crystal structure of kinase pim1 in complex with amp','2.24','0.339933526785714','0.339933526785714'),
('PIM1_HUMAN','1yxu_D','D','crystal structure of kinase pim1 in complex with amp','2.24','0.339933526785714','0.339933526785714'),
('PIM1_HUMAN','1yxv_A','A','crystal structure of kinase pim1 in complex with 3,4-dihydro methylquinolin-2(1h)-one','2','0.455550505952381','0.455550505952381'),
('PIM1_HUMAN','1yxx_A','A','crystal structure of kinase pim1 in complex with (3e)-3-[(4- hydroxyphenyl)imino]-1h-indol-2(3h)-one','2','0.404993690476191','0.404993690476191'),
('EGFR_HUMAN','1yy9_A','A','structure of the extracellular domain of the epidermal growt receptor in complex with the fab fragment of cetuximab/erbi c225','2.6','0.24892754235348','0.24892754235348'),
('CLK1_HUMAN','1z57_A','A','crystal structure of human clk1 in complex with 10z-hymenial','1.7','0.601716410189075','0.601716410189075'),
('PDPK1_HUMAN','1z5m_A','A','crystal structure of n1-[3-[[5-bromo-2-[[3-[(1-pyrrolidinylc amino]phenyl]amino]-4-pyrimidinyl]amino]propyl]-2,2- dimethylpropanediamide complexed with human pdk1','2.17','0.365014671658986','0.365014671658986'),
('EGFR_HUMAN','1z9i_A','A','a structural model for the membrane-bound form of the juxtamembrane domain of the epidermal growth factor receptor',NULL,'0.0012238095238095','0.0012238095238095'),
('DAPK2_HUMAN','1z9x_A','A','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3.93','0.0733240571610324','0.0733240571610324'),
('DAPK2_HUMAN','1z9x_B','B','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3.93','0.0733240571610324','0.0733240571610324'),
('DAPK2_HUMAN','1z9x_C','C','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3.93','0.0733240571610324','0.0733240571610324'),
('FYN_HUMAN','1zbj_A','A','inferential structure determination of the fyn sh3 domain using noesy data from a 15n,h2 enriched protein',NULL,'0.0137082291666666','0.0137082291666666'),
('CSKP_HUMAN','1zl8_B','B','nmr structure of l27 heterodimer from c. elegans lin-7 and h lin-2 scaffold proteins',NULL,'0.0135825','0.0135825'),
('CHK1_HUMAN','1zlt_A','A','crystal structure of chk1 complexed with a hymenaldisine analog','1.74','0.469917212130542','0.469917212130542'),
('KPCI_HUMAN','1zrz_A','A','crystal structure of the catalytic domain of atypical protein kinase c-iota','3','0.164337142857143','0.164337142857143'),
('PAK1_HUMAN','1zsg_B','B','beta pix-sh3 complexed with an atypical peptide from alpha- pak',NULL,'0.042424181547619','0.042424181547619'),
('DAPK2_HUMAN','1zuz_B','B','calmodulin in complex with a mutant peptide from human drp-1','1.91','0.465556087400274','0.465556087400274'),
('DAPK2_HUMAN','1zws_A','A','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_B','B','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_C','C','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_D','D','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_E','E','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_F','F','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_G','G','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('DAPK2_HUMAN','1zws_H','H','crystal structure of the catalytic domain of human drp-1 kinase','2.9','0.212616351087849','0.212616351087849'),
('KGP1_HUMAN','1zxa_A','A','solution structure of the coiled-coil domain of cgmp- dependent protein kinase ia',NULL,'0.0737143005952381','0.0737143005952381'),
('KGP1_HUMAN','1zxa_B','B','solution structure of the coiled-coil domain of cgmp- dependent protein kinase ia',NULL,'0.0737143005952381','0.0737143005952381'),
('MK14_HUMAN','1zyj_A','A','human p38 map kinase in complex with inhibitor 1a','2','0.380199017857143','0.380199017857143'),
('CHK1_HUMAN','1zys_A','A','co-crystal structure of checkpoint kinase chk1 with a pyrrolo-pyridine inhibitor','1.7','0.502978612570028','0.502978612570028'),
('MK14_HUMAN','1zz2_A','A','two classes of p38alpha map kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes','2','0.365747291666667','0.365747291666667'),
('MK14_HUMAN','1zzl_A','A','crystal structure of p38 with triazolopyridine','2','0.390854404761905','0.390854404761905'),
('ABL1_HUMAN','1zzp_A','A','solution structure of the f-actin binding domain of bcr- abl/c-abl',NULL,'0.0232160416666666','0.0232160416666666'),
('CDK2_HUMAN','2a0c_X','X','human cdk2 in complex with olomoucine ii, a novel 2,6,9- trisubstituted purine cyclin-dependent kinase inhibitor','1.95','0.43477987293956','0.43477987293956'),
('E2AK2_HUMAN','2a19_B','B','pkr kinase domain- eif2alpha- amp-pnp complex.','2.5','0.278759017857143','0.278759017857143'),
('E2AK2_HUMAN','2a19_C','C','pkr kinase domain- eif2alpha- amp-pnp complex.','2.5','0.278759017857143','0.278759017857143'),
('E2AK2_HUMAN','2a1a_B','B','pkr kinase domain-eif2alpha complex','2.8','0.254732023809524','0.254732023809524'),
('DAPK2_HUMAN','2a27_A','A','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_B','B','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_C','C','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_D','D','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_E','E','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_F','F','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_G','G','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a27_H','H','human drp-1 kinase, w305s s308a d40 mutant, crystal form wit monomers in the asymmetric unit','3','0.239726086309524','0.239726086309524'),
('DAPK2_HUMAN','2a2a_A','A','high-resolution crystallographic analysis of the autoinhibit conformation of a human death-associated protein kinase','1.47','0.681753299319728','0.681753299319728'),
('DAPK2_HUMAN','2a2a_B','B','high-resolution crystallographic analysis of the autoinhibit conformation of a human death-associated protein kinase','1.47','0.681753299319728','0.681753299319728'),
('DAPK2_HUMAN','2a2a_C','C','high-resolution crystallographic analysis of the autoinhibit conformation of a human death-associated protein kinase','1.47','0.681753299319728','0.681753299319728'),
('DAPK2_HUMAN','2a2a_D','D','high-resolution crystallographic analysis of the autoinhibit conformation of a human death-associated protein kinase','1.47','0.681753299319728','0.681753299319728'),
('TITIN_HUMAN','2a38_A','A','crystal structure of the n-terminus of titin','2','0.434216056547619','0.434216056547619'),
('TITIN_HUMAN','2a38_B','B','crystal structure of the n-terminus of titin','2','0.434216056547619','0.434216056547619'),
('TITIN_HUMAN','2a38_C','C','crystal structure of the n-terminus of titin','2','0.434216056547619','0.434216056547619'),
('CDK2_HUMAN','2a4l_A','A','human cyclin-dependent kinase 2 in complex with roscovitine','2.4','0.33320505952381','0.33320505952381'),
('ERBB2_HUMAN','2a91_A','A','crystal structure of erbb2 domains 1-3','2.5','0.307923883928571','0.307923883928571'),
('ABL1_HUMAN','2abl_A','A','sh3-sh2 domain fragment of human bcr-abl tyrosine kinase','2.5','0.332444181547619','0.332444181547619'),
('MKNK2_HUMAN','2ac3_A','A','structure of human mnk2 kinase domain','2.1','0.380926041666667','0.380926041666667'),
('MKNK2_HUMAN','2ac5_A','A','structure of human mnk2 kinase domain mutant d228g','3.2','0.138602961309524','0.138602961309524'),
('GRK6_HUMAN','2acx_A','A','crystal structure of g protein coupled receptor kinase 6 bou amppnp','2.6','0.301726500686813','0.301726500686813'),
('GRK6_HUMAN','2acx_B','B','crystal structure of g protein coupled receptor kinase 6 bou amppnp','2.6','0.301726500686813','0.301726500686813'),
('ERBB4_HUMAN','2ahx_A','A','crystal structure of erbb4/her4 extracellular domain','2.4','0.310070386904762','0.310070386904762'),
('ERBB4_HUMAN','2ahx_B','B','crystal structure of erbb4/her4 extracellular domain','2.4','0.310070386904762','0.310070386904762'),
('INSR_HUMAN','2auh_A','A','crystal structure of the grb14 bps region in complex with the insulin receptor tyrosine kinase','3.2','0.181274300595238','0.181274300595238'),
('CHK1_HUMAN','2ayp_A','A','crystal structure of chk1 with an indol inhibitor','2.9','0.219856068349754','0.219856068349754'),
('MK10_HUMAN','2b1p_A','A','inhibitor complex of jnk3','1.9','0.431480343045113','0.431480343045113'),
('INSR_HUMAN','2b4s_B','B','crystal structure of a complex between ptp1b and the insulin receptor tyrosine kinase','2.3','0.371737459886128','0.371737459886128'),
('INSR_HUMAN','2b4s_D','D','crystal structure of a complex between ptp1b and the insulin receptor tyrosine kinase','2.3','0.371737459886128','0.371737459886128'),
('CDK2_HUMAN','2b52_A','A','human cyclin dependent kinase 2 (cdk2) complexed with dph- 042562','1.88','0.427951976950355','0.427951976950355'),
('CDK2_HUMAN','2b53_A','A','human cyclin dependent kinase 2 (cdk2) complexed with din- 234325','2','0.394030446428571','0.394030446428571'),
('CDK2_HUMAN','2b54_A','A','human cyclin dependent kinase 2 (ckd2)complexed with din- 232305','1.85','0.462597638754826','0.462597638754826'),
('CDK2_HUMAN','2b55_A','A','human cyclin dependent kinase 2 (cdk2) complexed with indenopyraxole din-101312','1.85','0.446968903635779','0.446968903635779'),
('JAK2_HUMAN','2b7a_A','A','the structural basis of janus kinase 2 inhibition by a potent and specific pan-janus kinase inhibitor','2','0.434679657738095','0.434679657738095'),
('JAK2_HUMAN','2b7a_B','B','the structural basis of janus kinase 2 inhibition by a potent and specific pan-janus kinase inhibitor','2','0.434679657738095','0.434679657738095'),
('MK14_HUMAN','2baj_A','A','p38alpha bound to pyrazolourea','2.25','0.334166423611111','0.334166423611111'),
('MK14_HUMAN','2bak_A','A','p38alpha map kinase bound to mpaq','2.2','0.354852508116883','0.354852508116883'),
('MK14_HUMAN','2bal_A','A','p38alpha map kinase bound to pyrazoloamine','2.1','0.377328139880952','0.377328139880952'),
('MK14_HUMAN','2baq_A','A','p38alpha bound to ro3201195','2.8','0.244661860119048','0.244661860119048'),
('EPHB4_HUMAN','2bba_A','A','crystal structure and thermodynamic characterization of the receptor in complex with an ephrin-b2 antagonist peptide re determinants for receptor specificity.','1.65','0.572503016774892','0.572503016774892'),
('SRC_HUMAN','2bdf_A','A','src kinase in complex with inhibitor ap23451','2.1','0.384790729166667','0.384790729166667'),
('SRC_HUMAN','2bdf_B','B','src kinase in complex with inhibitor ap23451','2.1','0.384790729166667','0.384790729166667'),
('SRC_HUMAN','2bdj_A','A','src kinase in complex with inhibitor ap23464','2.5','0.355596383928571','0.355596383928571'),
('CDK2_HUMAN','2bhe_A','A','human cyclin dependent protein kinase 2 in complex with the inhibitor 5-bromo-indirubine','1.9','0.396402545426065','0.396402545426065'),
('CDK2_HUMAN','2bhh_A','A','human cyclin dependent protein kinase 2 in complex with the inhibitor 4-hydroxypiperindinesulfonyl-indirubine','2.6','0.252574179258242','0.252574179258242'),
('PIM1_HUMAN','2bik_B','B','human pim1 phosphorylated on ser261','1.8','0.545706924603174','0.545706924603174'),
('PIM1_HUMAN','2bil_B','B','the human protein kinase pim1 in complex with its consensus peptide pimtide','2.55','0.339297234768908','0.339297234768908'),
('PDPK1_HUMAN','2biy_A','A','structure of pdk1-s241a mutant kinase domain','1.95','0.471823548534799','0.471823548534799'),
('TITIN_HUMAN','2bk8_A','A','m1 domain from titin','1.69','0.52847166085517','0.52847166085517'),
('CDK2_HUMAN','2bkz_A','A','structure of cdk2-cyclin a with pha-404611','2.6','0.296345816163004','0.296345816163004'),
('CDK2_HUMAN','2bkz_C','C','structure of cdk2-cyclin a with pha-404611','2.6','0.296345816163004','0.296345816163004'),
('B4DX16_HUMAN','2bmc_A','A','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('AURKA_HUMAN','2bmc_B','B','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('B4DX16_HUMAN','2bmc_C','C','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('B4DX16_HUMAN','2bmc_D','D','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('B4DX16_HUMAN','2bmc_E','E','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('B4DX16_HUMAN','2bmc_F','F','aurora-2 t287d t288d complexed with pha-680632','2.6','0.298103078067765','0.298103078067765'),
('CDK2_HUMAN','2bpm_A','A','structure of cdk2-cyclin a with pha-630529','2.4','0.328517604166667','0.328517604166667'),
('CDK2_HUMAN','2bpm_C','C','structure of cdk2-cyclin a with pha-630529','2.4','0.328517604166667','0.328517604166667'),
('CHK1_HUMAN','2br1_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2','0.456458735119048','0.456458735119048'),
('CHK1_HUMAN','2brb_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.1','0.343078675595238','0.343078675595238'),
('CHK1_HUMAN','2brg_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.1','0.353753169642857','0.353753169642857'),
('CHK1_HUMAN','2brh_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.1','0.402894747023809','0.402894747023809'),
('CHK1_HUMAN','2brm_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.2','0.336933103354978','0.336933103354978'),
('CHK1_HUMAN','2brn_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.8','0.239639955357143','0.239639955357143'),
('CHK1_HUMAN','2bro_A','A','structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity','2.2','0.36193229978355','0.36193229978355'),
('CDK2_HUMAN','2btr_A','A','structure of cdk2 complexed with pnu-198873','1.85','0.437771388754826','0.437771388754826'),
('CDK2_HUMAN','2bts_A','A','structure of cdk2 complexed with pnu-230032','1.99','0.405999646147404','0.405999646147404'),
('STK16_HUMAN','2buj_A','A','crystal structure of the human serine-threonine kinase 16 in complex with staurosporine','2.6','0.323002110805861','0.323002110805861'),
('STK16_HUMAN','2buj_B','B','crystal structure of the human serine-threonine kinase 16 in complex with staurosporine','2.6','0.323002110805861','0.323002110805861'),
('PAK4_HUMAN','2bva_A','A','crystal structure of the human p21-activated kinase 4','2.3','0.281194424171843','0.281194424171843'),
('PAK4_HUMAN','2bva_B','B','crystal structure of the human p21-activated kinase 4','2.3','0.281194424171843','0.281194424171843'),
('PIM1_HUMAN','2bzh_B','B','crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru1','1.9','0.518359063283208','0.518359063283208'),
('PIM1_HUMAN','2bzi_B','B','crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru2','1.9','0.455686503759398','0.455686503759398'),
('PIM1_HUMAN','2bzj_A','A','crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru3','2.05','0.451469074477352','0.451469074477352'),
('PIM1_HUMAN','2bzk_B','B','crystal structure of the human pim1 in complex with amppnp and pimtide','2.45','0.363025928996599','0.363025928996599'),
('HCK_HUMAN','2c0i_A','A','src family kinase hck with bound inhibitor a-420983','2.3','0.333732504528985','0.333732504528985'),
('HCK_HUMAN','2c0i_B','B','src family kinase hck with bound inhibitor a-420983','2.3','0.333732504528985','0.333732504528985'),
('HCK_HUMAN','2c0o_A','A','src family kinase hck with bound inhibitor a-770041','2.85','0.257335317982456','0.257335317982456'),
('HCK_HUMAN','2c0o_B','B','src family kinase hck with bound inhibitor a-770041','2.85','0.257335317982456','0.257335317982456'),
('HCK_HUMAN','2c0t_A','A','src family kinase hck with bound inhibitor a-641359','2.15','0.389901353474529','0.389901353474529'),
('HCK_HUMAN','2c0t_B','B','src family kinase hck with bound inhibitor a-641359','2.15','0.389901353474529','0.389901353474529'),
('PAK6_HUMAN','2c30_A','A','crystal structure of the human p21-activated kinase 6','1.6','0.577614568452381','0.577614568452381'),
('PIM1_HUMAN','2c3i_B','B','crystal structure of human pim1 in complex with imidazopyridazin i','1.9','0.489031087092732','0.489031087092732'),
('CHK1_HUMAN','2c3j_A','A','identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification','2.1','0.405248199404762','0.405248199404762'),
('CHK1_HUMAN','2c3k_A','A','identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification','2.6','0.272655711996337','0.272655711996337'),
('CHK1_HUMAN','2c3l_A','A','identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification','2.35','0.322999891084093','0.322999891084093'),
('KC1G2_HUMAN','2c47_A','A','structure of casein kinase 1 gamma 2','2.4','0.335369717261905','0.335369717261905'),
('KC1G2_HUMAN','2c47_B','B','structure of casein kinase 1 gamma 2','2.4','0.335369717261905','0.335369717261905'),
('KC1G2_HUMAN','2c47_C','C','structure of casein kinase 1 gamma 2','2.4','0.335369717261905','0.335369717261905'),
('KC1G2_HUMAN','2c47_D','D','structure of casein kinase 1 gamma 2','2.4','0.335369717261905','0.335369717261905'),
('CDK2_HUMAN','2c4g_A','A','structure of cdk2-cyclin a with pha-533514','2.7','0.276615236441799','0.276615236441799'),
('CDK2_HUMAN','2c4g_C','C','structure of cdk2-cyclin a with pha-533514','2.7','0.276615236441799','0.276615236441799'),
('UFO_HUMAN','2c5d_C','C','structure of a minimal gas6-axl complex','3.3','0.132537892316017','0.132537892316017'),
('UFO_HUMAN','2c5d_D','D','structure of a minimal gas6-axl complex','3.3','0.132537892316017','0.132537892316017'),
('CDK2_HUMAN','2c5n_A','A','differential binding of inhibitors to active and  inactive cdk2 provides insights for drug design','2.1','0.414644092261905','0.414644092261905'),
('CDK2_HUMAN','2c5n_C','C','differential binding of inhibitors to active and  inactive cdk2 provides insights for drug design','2.1','0.414644092261905','0.414644092261905'),
('CDK2_HUMAN','2c5o_A','A','differential binding of inhibitors to active and  inactive cdk2 provides insights for drug design','2.1','0.392456979166667','0.392456979166667'),
('CDK2_HUMAN','2c5o_C','C','differential binding of inhibitors to active and  inactive cdk2 provides insights for drug design','2.1','0.392456979166667','0.392456979166667'),
('CDK2_HUMAN','2c5v_A','A','differential binding of inhibitors to active and inactive cdk2 provides insights for drug design','2.9','0.234665190373563','0.234665190373563'),
('CDK2_HUMAN','2c5v_C','C','differential binding of inhibitors to active and inactive cdk2 provides insights for drug design','2.9','0.234665190373563','0.234665190373563'),
('CDK2_HUMAN','2c5x_A','A','differential binding of inhibitors to active and inactive cdk2 provides insights for drug design','2.9','0.199072958230706','0.199072958230706'),
('CDK2_HUMAN','2c5x_C','C','differential binding of inhibitors to active and inactive cdk2 provides insights for drug design','2.9','0.199072958230706','0.199072958230706'),
('CDK2_HUMAN','2c5y_A','A','differential binding of inhibitors to active and inactive cdk2 provides insights for drug design','2.25','0.344832465277778','0.344832465277778'),
('M3K3_HUMAN','2c60_A','A','crystal structure of human mitogen-activated protein kinase kinase kinase 3 isoform 2 phox domain at 1.25 a resolution','1.25','0.799417455357143','0.799417455357143'),
('CDK2_HUMAN','2c68_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','1.95','0.449337090201465','0.449337090201465'),
('CDK2_HUMAN','2c69_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','2.1','0.378229449404762','0.378229449404762'),
('AURKA_HUMAN','2c6d_A','A','aurora a kinase activated mutant (t287d) in complex with adpnp','2.2','0.342062746212121','0.342062746212121'),
('AURKA_HUMAN','2c6e_A','A','aurora a kinase activated mutant (t287d) in complex with a 5-aminopyrimidinyl quinazoline inhibitor','2.1','0.395475788690476','0.395475788690476'),
('AURKA_HUMAN','2c6e_B','B','aurora a kinase activated mutant (t287d) in complex with a 5-aminopyrimidinyl quinazoline inhibitor','2.1','0.395475788690476','0.395475788690476'),
('CDK2_HUMAN','2c6i_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','1.8','0.464723263888889','0.464723263888889'),
('CDK2_HUMAN','2c6k_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','1.9','0.457374598997494','0.457374598997494'),
('CDK2_HUMAN','2c6l_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','2.3','0.361816358695652','0.361816358695652'),
('CDK2_HUMAN','2c6m_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','1.9','0.444290268640351','0.444290268640351'),
('CDK2_HUMAN','2c6o_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','2.1','0.350643526785714','0.350643526785714'),
('CDK2_HUMAN','2c6t_A','A','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','2.61','0.292739336856869','0.292739336856869'),
('CDK2_HUMAN','2c6t_C','C','crystal structure of the human cdk2 complexed with the triazolopyrimidine inhibitor','2.61','0.292739336856869','0.292739336856869'),
('CDK2_HUMAN','2cch_A','A','the crystal structure of cdk2 cyclin a in complex with a substrate peptide derived from cdc modified with a gamma- linked atp analogue','1.7','0.584618582808123','0.584618582808123'),
('CDK2_HUMAN','2cch_C','C','the crystal structure of cdk2 cyclin a in complex with a substrate peptide derived from cdc modified with a gamma- linked atp analogue','1.7','0.584618582808123','0.584618582808123'),
('CDK2_HUMAN','2cci_A','A','crystal structure of phospho-cdk2 cyclin a in complex with a peptide containing both the substrate and recruitment sites of cdc6','2.7','0.224493510251323','0.224493510251323'),
('CDK2_HUMAN','2cci_C','C','crystal structure of phospho-cdk2 cyclin a in complex with a peptide containing both the substrate and recruitment sites of cdc6','2.7','0.224493510251323','0.224493510251323'),
('PAK4_HUMAN','2cdz_A','A','crystal structure of the human p21-activated kinase 4 in complex with cgp74514a','2.3','0.372913248576605','0.372913248576605'),
('CHK1_HUMAN','2cgu_A','A','identification of chemically diverse chk1 inhibitors by receptor-based virtual screening','2.5','0.319354196428572','0.319354196428572'),
('CHK1_HUMAN','2cgv_A','A','identification of chemically diverse chk1 inhibitors by receptor-based virtual screening','2.6','0.291889283424908','0.291889283424908'),
('CHK1_HUMAN','2cgw_A','A','identification of chemically diverse chk1 inhibitors by receptor-based virtual screening','2.2','0.37843786525974','0.37843786525974'),
('CHK1_HUMAN','2cgx_A','A','identification of chemically diverse chk1 inhibitors by receptor-based virtual screening','2.2','0.376973371212121','0.376973371212121'),
('KC1G3_HUMAN','2chl_A','A','structure of casein kinase 1 gamma 3','1.95','0.477699173534799','0.477699173534799'),
('CDK2_HUMAN','2cjm_A','A','mechanism of cdk inhibition by active site phosphorylation: cdk2 y15p t160p in complex with cyclin a structure','2.3','0.347210510481367','0.347210510481367'),
('CDK2_HUMAN','2cjm_C','C','mechanism of cdk inhibition by active site phosphorylation: cdk2 y15p t160p in complex with cyclin a structure','2.3','0.347210510481367','0.347210510481367'),
('DAPK2_HUMAN','2cke_A','A','human death-associated drp-1 kinase in complex with inhibitor','2.8','0.296204583333333','0.296204583333333'),
('DAPK2_HUMAN','2cke_B','B','human death-associated drp-1 kinase in complex with inhibitor','2.8','0.296204583333333','0.296204583333333'),
('DAPK2_HUMAN','2cke_C','C','human death-associated drp-1 kinase in complex with inhibitor','2.8','0.296204583333333','0.296204583333333'),
('DAPK2_HUMAN','2cke_D','D','human death-associated drp-1 kinase in complex with inhibitor','2.8','0.296204583333333','0.296204583333333'),
('M3K5_HUMAN','2clq_A','A','structure of mitogen-activated protein kinase kinase kinase 5','2.3','0.350061328933747','0.350061328933747'),
('M3K5_HUMAN','2clq_B','B','structure of mitogen-activated protein kinase kinase kinase 5','2.3','0.350061328933747','0.350061328933747'),
('CDK2_HUMAN','2clx_A','A','4-arylazo-3,5-diamino-1h-pyrazole cdk inhibitors: sar study, crystal structure in complex with cdk2, selectivity, and cellular effects','1.8','0.492299350198413','0.492299350198413'),
('KC1G1_HUMAN','2cmw_A','A','structure of human casein kinase 1 gamma-1 in complex with 2-(2-hydroxyethylamino)-6-(3-chloroanilino)-9- isopropylpurine (casp target)','1.75','0.539285625','0.539285625'),
('CHK2_HUMAN','2cn5_A','A','crystal structure of human chk2 in complex with adp','2.25','0.367112390873016','0.367112390873016'),
('CHK2_HUMAN','2cn8_A','A','crystal structure of human chk2 in complex with debromohymenialdisine','2.7','0.256057126322751','0.256057126322751'),
('KPCD2_HUMAN','2coa_A','A','solution structure of the ph domain of protein kinase c, d2 type from human',NULL,'0.0247028720238095','0.0247028720238095'),
('MYLK_HUMAN','2cqv_A','A','solution structure of the eighth ig-like domain of human myosin light chain kinase',NULL,'0.0306091220238095','0.0306091220238095'),
('FGFR1_HUMAN','2cr3_A','A','solution structure of the first ig-like domain of human fibroblast growth factor receptor 1',NULL,'0.0341844791666666','0.0341844791666666'),
('OBSCN_HUMAN','2cr6_A','A','solution structure of the ig domain (2998-3100) of human obscurin',NULL,'0.0203778571428571','0.0203778571428571'),
('M3K2_HUMAN','2cu1_A','A','solution structure of the pb1 domain of human protein kinase mekk2b',NULL,'0.0225681845238095','0.0225681845238095'),
('KPCD3_HUMAN','2d9z_A','A','solution structure of the ph domain of protein kinase c, nu type from human',NULL,'0.0234639434523809','0.0234639434523809'),
('MERTK_HUMAN','2dbj_A','A','solution structures of the fn3 domain of human proto- oncogene tyrosine-protein kinase mer precursor',NULL,'0.0272366220238095','0.0272366220238095'),
('FES_HUMAN','2dcr_A','A','fully automated solution structure determination of the fes sh2 domain',NULL,'0.025009181547619','0.025009181547619'),
('EPHB1_HUMAN','2djs_A','A','solution structures of the fn3 domain of human ephrin type- b receptor 1',NULL,'0.0351419494047619','0.0351419494047619'),
('OBSCN_HUMAN','2dku_A','A','solution structure of the third ig-like domain of human kiaa1556 protein',NULL,'0.0272318303571428','0.0272318303571428'),
('TXK_HUMAN','2dm0_A','A','solution structure of the sh2 domain of human tyrosine- protein kinase txk',NULL,'0.0230847321428571','0.0230847321428571'),
('OBSCN_HUMAN','2dm7_A','A','solution structure of the 14th ig-like domain of human kiaa1556 protein',NULL,'0.0318023809523809','0.0318023809523809'),
('FYN_HUMAN','2dq7_X','X','crystal structure of fyn kinase domain complexed with staurosporine','2.8','0.206539047619048','0.206539047619048'),
('CDK2_HUMAN','2ds1_A','A','human cyclin dependent kinase 2 complexed with the cdk4 inhibitor','2','0.396816130952381','0.396816130952381'),
('INSR_HUMAN','2dtg_E','E','insulin receptor (ir) ectodomain in complex with fab\'s','3.8','-0.0103189505012531','-0.0103189505012531'),
('CDK2_HUMAN','2duv_A','A','structure of cdk2 with a 3-hydroxychromones','2.2','0.306009100378788','0.306009100378788'),
('AURKA_HUMAN','2dwb_A','A','aurora-a kinase complexed with amppnp','2.5','0.289217738095238','0.289217738095238'),
('MP2K7_HUMAN','2dyl_A','A','crystal structure of human mitogen-activated protein kinase kinase 7 activated mutant (s287d, t291d)','2.45','0.309925795068027','0.309925795068027'),
('ABL1_HUMAN','2e2b_A','A','crystal structure of the c-abl kinase domain in complex with inno-406','2.2','0.357594770021645','0.357594770021645'),
('ITK_HUMAN','2e6i_A','A','solution structure of the btk motif of tyrosine-protein kinase itk from human',NULL,'0.0147342261904762','0.0147342261904762'),
('KPCG_HUMAN','2e73_A','A','solution structure of the phorbol esters/diacylglycerol binding domain of protein kinase c gamma',NULL,'0.0186770535714285','0.0186770535714285'),
('OBSCN_HUMAN','2e7b_A','A','solution structure of the 6th ig-like domain from human kiaa1556',NULL,'0.027007619047619','0.027007619047619'),
('EPHB4_HUMAN','2e7h_A','A','solution structure of the second fn3 domain from human ephrin type-b receptor 4',NULL,'0.0269663839285714','0.0269663839285714'),
('EPHA2_HUMAN','2e8n_A','A','solution structure of the c-terminal sam-domain of ephaa2: ephrin type-a receptor 2 precursor (ec 2.7.10.1)',NULL,'0.0225083630952381','0.0225083630952381'),
('CHK1_HUMAN','2e9n_A','A','structure of h-chk1 complexed with a767085','2.5','0.270507827380952','0.270507827380952'),
('CHK1_HUMAN','2e9o_A','A','structure of h-chk1 complexed with aa582939','2.1','0.36330275297619','0.36330275297619'),
('CHK1_HUMAN','2e9p_A','A','structure of h-chk1 complexed with a771129','2.6','0.23431717032967','0.23431717032967'),
('CHK1_HUMAN','2e9u_A','A','structure of h-chk1 complexed with a780125','2','0.372769761904762','0.372769761904762'),
('CHK1_HUMAN','2e9v_A','A','structure of h-chk1 complexed with a859017','2','0.337152529761905','0.337152529761905'),
('CHK1_HUMAN','2e9v_B','B','structure of h-chk1 complexed with a859017','2','0.337152529761905','0.337152529761905'),
('KIT_HUMAN','2e9w_A','A','crystal structure of the extracellular domain of kit in comp stem cell factor (scf)','3.5','0.102224523809524','0.102224523809524'),
('KIT_HUMAN','2e9w_B','B','crystal structure of the extracellular domain of kit in comp stem cell factor (scf)','3.5','0.102224523809524','0.102224523809524'),
('EPHB1_HUMAN','2eao_A','A','solution structure of the c-terminal sam-domain of mouse ephrin type-b receptor 1 precursor (ec 2.7.1.112)',NULL,'0.0216383482142857','0.0216383482142857'),
('EGFR_HUMAN','2eb2_A','A','crystal structure of mutated egfr kinase domain (g719s)','2.5','0.326237261904762','0.326237261904762'),
('EGFR_HUMAN','2eb3_A','A','crystal structure of mutated egfr kinase domain (l858r) in c with amppnp','2.84','0.281050830818243','0.281050830818243'),
('KIT_HUMAN','2ec8_A','A','crystal structure of the exctracellular domain of the recept tyrosine kinase, kit','3','0.142370119047619','0.142370119047619'),
('ABL2_HUMAN','2ecd_A','A','solution structure of the human abl2 sh2 domain',NULL,'0.0251711904761905','0.0251711904761905'),
('OBSCN_HUMAN','2edf_A','A','solution structure of the second ig-like domain(2826-2915) from human obscurin',NULL,'0.0296317113095238','0.0296317113095238'),
('OBSCN_HUMAN','2edh_A','A','solution structure of the pdz domain (3614- 3713 ) from huma',NULL,'0.0238135119047619','0.0238135119047619'),
('OBSCN_HUMAN','2edl_A','A','solution structure of the ig-like domain (3801-3897) of human obscurin',NULL,'0.0272040922619048','0.0272040922619048'),
('OBSCN_HUMAN','2edq_A','A','solution structure of the ig-like domain (3713-3806) of human obscurin',NULL,'0.0321615773809523','0.0321615773809523'),
('OBSCN_HUMAN','2edr_A','A','solution structure of the ig-like domain (3361-3449) of human obscurin',NULL,'0.0249769642857142','0.0249769642857142'),
('OBSCN_HUMAN','2edt_A','A','solution structure of the ig-like domain (3449-3537) from human obscurin',NULL,'0.0271463988095238','0.0271463988095238'),
('OBSCN_HUMAN','2edw_A','A','solution structure of the i-set domain (3537-3630) of human obscurin',NULL,'0.0307417261904762','0.0307417261904762'),
('BMX_HUMAN','2ekx_A','A','solution structure of the human bmx sh2 domain',NULL,'0.0234535267857143','0.0234535267857143'),
('KPCA_HUMAN','2eli_A','A','solution structure of the second phorbol esters/diacylglycerol binding domain of human protein kinase c alpha type',NULL,'0.0209766964285714','0.0209766964285714'),
('KPCT_HUMAN','2enj_A','A','solution sturcture of the c2 domain from human protein kinase c theta',NULL,'0.0307805803571428','0.0307805803571428'),
('KPCT_HUMAN','2enn_A','A','solution structure of the first c1 domain from human protein kinase c theta',NULL,'0.0309220386904762','0.0309220386904762'),
('OBSCN_HUMAN','2eny_A','A','solution structure of the ig-like domain (2735-2825) of human obscurin',NULL,'0.0283563244047619','0.0283563244047619'),
('KPCT_HUMAN','2enz_A','A','solution structure of the second c1 domain from human protein kinase c theta',NULL,'0.0237749404761904','0.0237749404761904'),
('OBSCN_HUMAN','2eo1_A','A','solution structure of the ig domain of human obscn protein',NULL,'0.0337225','0.0337225'),
('ROCK1_HUMAN','2esm_A','A','crystal structure of rock 1 bound to fasudil','3.2','0.195875163690476','0.195875163690476'),
('ROCK1_HUMAN','2esm_B','B','crystal structure of rock 1 bound to fasudil','3.2','0.195875163690476','0.195875163690476'),
('ROCK1_HUMAN','2etk_A','A','crystal structure of rock 1 bound to hydroxyfasudil','2.96','0.191587257480695','0.191587257480695'),
('ROCK1_HUMAN','2etk_B','B','crystal structure of rock 1 bound to hydroxyfasudil','2.96','0.191587257480695','0.191587257480695'),
('FAK1_HUMAN','2etm_A','A','crystal structure of focal adhesion kinase domain complexed with 7h-pyrrolo [2,3-d] pyrimidine derivative','2.3','0.341276403338509','0.341276403338509'),
('FAK1_HUMAN','2etm_B','B','crystal structure of focal adhesion kinase domain complexed with 7h-pyrrolo [2,3-d] pyrimidine derivative','2.3','0.341276403338509','0.341276403338509'),
('ROCK1_HUMAN','2etr_A','A','crystal structure of rock i bound to y-27632','2.6','0.266295086996337','0.266295086996337'),
('ROCK1_HUMAN','2etr_B','B','crystal structure of rock i bound to y-27632','2.6','0.266295086996337','0.266295086996337'),
('CLK3_HUMAN','2eu9_A','A','crystal structure of clk3','1.53','0.635043640289449','0.635043640289449'),
('CDK6_HUMAN','2euf_B','B','x-ray structure of human cdk6-vcyclin in complex with the in pd0332991','3','0.208561220238095','0.208561220238095'),
('M3K7_HUMAN','2eva_A','A','structural basis for the interaction of tak1 kinase with its activating protein tab1','2','0.401771145833333','0.401771145833333'),
('MK10_HUMAN','2exc_X','X','inhibitor complex of jnk3','2.75','0.241000485660173','0.241000485660173'),
('CLK3_HUMAN','2exe_A','A','crystal structure of the phosphorylated clk3','2.35','0.324851022036474','0.324851022036474'),
('CDK2_HUMAN','2exm_A','A','human cdk2 in complex with isopentenyladenine','1.8','0.471237177579365','0.471237177579365'),
('CDK6_HUMAN','2f2c_B','B','x-ray structure of human cdk6-vcyclinwith the inhibitor aminopurvalanol','2.8','0.223475416666667','0.223475416666667'),
('ABL1_HUMAN','2f4j_A','A','structure of the kinase domain of an imatinib-resistant abl mutant in complex with the aurora kinase inhibitor vx-680','1.91','0.455392545733608','0.455392545733608'),
('PAK7_HUMAN','2f57_A','A','crystal structure of the human p21-activated kinase 5','1.8','0.552547728174603','0.552547728174603'),
('PAK7_HUMAN','2f57_B','B','crystal structure of the human p21-activated kinase 5','1.8','0.552547728174603','0.552547728174603'),
('TITIN_HUMAN','2f8v_A','A','structure of full length telethonin in complex with the n-te titin','2.75','0.204769548160173','0.204769548160173'),
('TITIN_HUMAN','2f8v_B','B','structure of full length telethonin in complex with the n-te titin','2.75','0.204769548160173','0.204769548160173'),
('TITIN_HUMAN','2f8v_C','C','structure of full length telethonin in complex with the n-te titin','2.75','0.204769548160173','0.204769548160173'),
('TITIN_HUMAN','2f8v_D','D','structure of full length telethonin in complex with the n-te titin','2.75','0.204769548160173','0.204769548160173'),
('BRAF_HUMAN','2fb8_A','A','structure of the b-raf kinase domain bound to sb-590885','2.9','0.207412824302135','0.207412824302135'),
('BRAF_HUMAN','2fb8_B','B','structure of the b-raf kinase domain bound to sb-590885','2.9','0.207412824302135','0.207412824302135'),
('FGFR2_HUMAN','2fdb_P','P','crystal structure of fibroblast growth factor (fgf)8b in complex with fgf receptor (fgfr) 2c','2.28','0.343505003132832','0.343505003132832'),
('FGFR2_HUMAN','2fdb_R','R','crystal structure of fibroblast growth factor (fgf)8b in complex with fgf receptor (fgfr) 2c','2.28','0.343505003132832','0.343505003132832'),
('FGFR1_HUMAN','2fgi_A','A','crystal structure of the tyrosine kinase domain of fgf receptor 1 in complex with inhibitor pd173074','2.5','0.337165863095238','0.337165863095238'),
('FGFR1_HUMAN','2fgi_B','B','crystal structure of the tyrosine kinase domain of fgf receptor 1 in complex with inhibitor pd173074','2.5','0.337165863095238','0.337165863095238'),
('KPCL_HUMAN','2fk9_A','A','human protein kinase c, eta','1.75','0.535163318452381','0.535163318452381'),
('ABL1_HUMAN','2fo0_A','A','organization of the sh3-sh2 unit in active and inactive form c-abl tyrosine kinase','2.27','0.374472592694567','0.374472592694567'),
('MK14_HUMAN','2fsl_X','X','mitogen activated protein kinase p38alpha (d176a+f327s) activating mutant form-a','1.7','0.494397347689076','0.494397347689076'),
('MK14_HUMAN','2fsm_X','X','mitogen activated protein kinase p38alpha (d176a+f327s) activating mutant form-b','1.86','0.437388396697389','0.437388396697389'),
('MK14_HUMAN','2fso_X','X','mitogen activated protein kinase p38alpha (d176a) activating mutant','1.83','0.497338474336456','0.497338474336456'),
('MK14_HUMAN','2fst_X','X','mitogen activated protein kinase p38alpha (d176a+f327l) activating mutant','1.45','0.627350603961412','0.627350603961412'),
('CDK2_HUMAN','2fvd_A','A','cyclin dependent kinase 2 (cdk2) with diaminopyrimidine inhibitor','1.85','0.480263144707207','0.480263144707207'),
('MK08_HUMAN','2g01_A','A','pyrazoloquinolones as novel, selective jnk1 inhibitors','3.5','0.0192586011904762','0.0192586011904762'),
('MK08_HUMAN','2g01_B','B','pyrazoloquinolones as novel, selective jnk1 inhibitors','3.5','0.0192586011904762','0.0192586011904762'),
('MET_HUMAN','2g15_A','A','structural characterization of autoinhibited c-met kinase','2.15','0.351493645141196','0.351493645141196'),
('ABL1_HUMAN','2g1t_B','B','a src-like inactive conformation in the abl tyrosine kinase domain','1.8','0.477586180555556','0.477586180555556'),
('ABL1_HUMAN','2g1t_C','C','a src-like inactive conformation in the abl tyrosine kinase domain','1.8','0.477586180555556','0.477586180555556'),
('ABL1_HUMAN','2g1t_D','D','a src-like inactive conformation in the abl tyrosine kinase domain','1.8','0.477586180555556','0.477586180555556'),
('ABL1_HUMAN','2g2f_A','A','a src-like inactive conformation in the abl tyrosine kinase','2.7','0.260571337632275','0.260571337632275'),
('ABL1_HUMAN','2g2f_B','B','a src-like inactive conformation in the abl tyrosine kinase','2.7','0.260571337632275','0.260571337632275'),
('ABL1_HUMAN','2g2h_A','A','a src-like inactive conformation in the abl tyrosine kinase domain','2','0.452369523809524','0.452369523809524'),
('ABL1_HUMAN','2g2h_B','B','a src-like inactive conformation in the abl tyrosine kinase domain','2','0.452369523809524','0.452369523809524'),
('ABL1_HUMAN','2g2i_A','A','a src-like inactive conformation in the abl tyrosine kinase domain','3.12','0.173826838369963','0.173826838369963'),
('ABL1_HUMAN','2g2i_B','B','a src-like inactive conformation in the abl tyrosine kinase domain','3.12','0.173826838369963','0.173826838369963'),
('CDK2_HUMAN','2g9x_A','A','structure of thr 160 phosphorylated cdk2/cyclin a in complex inhibitor nu6271','2.5','0.301881800595238','0.301881800595238'),
('CDK2_HUMAN','2g9x_C','C','structure of thr 160 phosphorylated cdk2/cyclin a in complex inhibitor nu6271','2.5','0.301881800595238','0.301881800595238'),
('CHK1_HUMAN','2gdo_A','A','4-(aminoalkylamino)-3-benzimidazole-quinolinones as potent chk1 inhibitors','3','0.21551068452381','0.21551068452381'),
('BTK_HUMAN','2ge9_A','A','solution structures of the sh2 domain of bruton\'s tyrosine kinase',NULL,'0.0151920089285714','0.0151920089285714'),
('MK14_HUMAN','2gfs_A','A','p38 kinase crystal structure in complex with ro3201195','1.75','0.513974821428571','0.513974821428571'),
('CHK1_HUMAN','2ghg_A','A','h-chk1 complexed with a431994','3.5','0.106000758928571','0.106000758928571'),
('MK08_HUMAN','2gmx_A','A','selective aminopyridine-based c-jun n-terminal kinase inhibitors with cellular activity','3.5','0.0304101934523809','0.0304101934523809'),
('MK08_HUMAN','2gmx_B','B','selective aminopyridine-based c-jun n-terminal kinase inhibitors with cellular activity','3.5','0.0304101934523809','0.0304101934523809'),
('BMR1A_HUMAN','2goo_B','B','ternary complex of bmp-2 bound to bmpr-ia-ecd and actrii-ecd','2.2','0.343331094426407','0.343331094426407'),
('BMR1A_HUMAN','2goo_E','E','ternary complex of bmp-2 bound to bmpr-ia-ecd and actrii-ecd','2.2','0.343331094426407','0.343331094426407'),
('ABL1_HUMAN','2gqg_A','A','x-ray crystal structure of dasatinib (bms-354825) bound to a abl kinase domain','2.4','0.325782693452381','0.325782693452381'),
('ABL1_HUMAN','2gqg_B','B','x-ray crystal structure of dasatinib (bms-354825) bound to a abl kinase domain','2.4','0.325782693452381','0.325782693452381'),
('OBSCN_HUMAN','2gqh_A','A','solution structure of the 15th ig-like domain of human kiaa1556 protein',NULL,'0.0297841666666666','0.0297841666666666'),
('EGFR_HUMAN','2gs2_A','A','crystal structure of the active egfr kinase domain','2.8','0.267664866071429','0.267664866071429'),
('EGFR_HUMAN','2gs6_A','A','crystal structure of the active egfr kinase domain in complex with an atp analog-peptide conjugate','2.6','0.296067185210623','0.296067185210623'),
('EGFR_HUMAN','2gs7_A','A','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.6','0.265955176282051','0.265955176282051'),
('EGFR_HUMAN','2gs7_B','B','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.6','0.265955176282051','0.265955176282051'),
('EPHA3_HUMAN','2gsf_A','A','the human epha3 receptor tyrosine kinase and juxtamembrane region','1.77','0.55520887938862','0.55520887938862'),
('KAPCA_HUMAN','2gu8_A','A','discovery of 2-pyrimidyl-5-amidothiophenes as novel and potent inhibitors for akt: synthesis and sar studies','2.2','0.367866585497836','0.367866585497836'),
('TIE2_HUMAN','2gy5_A','A','tie2 ligand-binding domain crystal structure','2.9','0.194885175492611','0.194885175492611'),
('TIE2_HUMAN','2gy7_B','B','angiopoietin-2/tie2 complex crystal structure','3.7','0.0761528744369369','0.0761528744369369'),
('BMR1A_HUMAN','2h62_C','C','crystal structure of a ternary ligand-receptor complex of bmp-2','1.85','0.452804409588159','0.452804409588159'),
('AVR2B_HUMAN','2h62_D','D','crystal structure of a ternary ligand-receptor complex of bmp-2','1.85','0.452804409588159','0.452804409588159'),
('BMR1A_HUMAN','2h64_B','B','crystal structure of a ternary ligand-receptor complex of bmp-2','1.92','0.425576904761905','0.425576904761905'),
('AAPK2_HUMAN','2h6d_A','A','protein kinase domain of the human 5\'-amp-activated protein kinase catalytic subunit alpha-2 (ampk alpha-2 chain)','1.85','0.480876954231017','0.480876954231017'),
('SRC_HUMAN','2h8h_A','A','src kinase in complex with a quinazoline inhibitor','2.2','0.370122150974026','0.370122150974026'),
('MK08_HUMAN','2h96_A','A','discovery of potent, highly selective, and orally bioavailab pyridine carboxamide c-jun nh2-terminal kinase inhibitors','3','0.159631681547619','0.159631681547619'),
('MK08_HUMAN','2h96_B','B','discovery of potent, highly selective, and orally bioavailab pyridine carboxamide c-jun nh2-terminal kinase inhibitors','3','0.159631681547619','0.159631681547619'),
('MARK1_HUMAN','2hak_A','A','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_B','B','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_C','C','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_D','D','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_E','E','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_F','F','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_G','G','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('MARK1_HUMAN','2hak_H','H','catalytic and ubiqutin-associated domains of mark1/par-1','2.6','0.261546336996337','0.261546336996337'),
('HCK_HUMAN','2hck_A','A','src family kinase hck-quercetin complex','3','0.187888392857143','0.187888392857143'),
('HCK_HUMAN','2hck_B','B','src family kinase hck-quercetin complex','3','0.187888392857143','0.187888392857143'),
('YES_HUMAN','2hda_A','A','yes sh3 domain','1.9','0.451607128759398','0.451607128759398'),
('ABL1_HUMAN','2hiw_A','A','crystal structure of inactive conformation abl kinase catalytic domain complexed with type ii inhibitor','2.2','0.315439591450216','0.315439591450216'),
('ABL1_HUMAN','2hiw_B','B','crystal structure of inactive conformation abl kinase catalytic domain complexed with type ii inhibitor','2.2','0.315439591450216','0.315439591450216'),
('HCK_HUMAN','2hk5_A','A','hck kinase in complex with lck targetted inhibitor pg- 1009247','2','0.423593586309524','0.423593586309524'),
('EPHB4_HUMAN','2hle_A','A','structural and biophysical characterization of the ephb4-eph protein protein interaction and receptor specificity.','2.05','0.364314134001161','0.364314134001161'),
('BMPR2_HUMAN','2hlq_A','A','crystal structure of the extracellular domain of the type ii bmp receptor','1.45','0.631564473009031','0.631564473009031'),
('CHK1_HUMAN','2hog_A','A','crystal structure of chek1 in complex with inhibitor 20','1.9','0.46351445018797','0.46351445018797'),
('INSR_HUMAN','2hr7_A','A','insulin receptor (domains 1-3)','2.32','0.367372905377668','0.367372905377668'),
('INSR_HUMAN','2hr7_B','B','insulin receptor (domains 1-3)','2.32','0.367372905377668','0.367372905377668'),
('MKNK1_HUMAN','2hw6_A','A','crystal structure of mnk1 catalytic domain','2.5','0.30407','0.30407'),
('MKNK1_HUMAN','2hw6_B','B','crystal structure of mnk1 catalytic domain','2.5','0.30407','0.30407'),
('MKNK2_HUMAN','2hw7_A','A','crystal structure of mnk2-d228g in complex with staurosporin','2.71','0.281227916227377','0.281227916227377'),
('CHK1_HUMAN','2hxl_A','A','crystal structure of chek1 in complex with inhibitor 1','1.8','0.434918918650794','0.434918918650794'),
('CHK1_HUMAN','2hxq_A','A','crystal structure of chek1 in complex with inhibitor 2','2','0.387716369047619','0.387716369047619'),
('CHK1_HUMAN','2hy0_A','A','crystal structure of chek1 in complex with inhibitor 22','1.7','0.504200041141457','0.504200041141457'),
('PAK1_HUMAN','2hy8_1','1','pak1 complex with st2001','2','0.425384151785714','0.425384151785714'),
('ABL1_HUMAN','2hyy_A','A','human abl kinase domain in complex with imatinib (sti571, glivec)','2.4','0.327020639880953','0.327020639880953'),
('ABL1_HUMAN','2hyy_B','B','human abl kinase domain in complex with imatinib (sti571, glivec)','2.4','0.327020639880953','0.327020639880953'),
('ABL1_HUMAN','2hyy_C','C','human abl kinase domain in complex with imatinib (sti571, glivec)','2.4','0.327020639880953','0.327020639880953'),
('ABL1_HUMAN','2hyy_D','D','human abl kinase domain in complex with imatinib (sti571, glivec)','2.4','0.327020639880953','0.327020639880953'),
('ABL1_HUMAN','2hz0_A','A','abl kinase domain in complex with nvp-aeg082','2.1','0.399177842261905','0.399177842261905'),
('Q59F19_HUMAN','2hz0_B','B','abl kinase domain in complex with nvp-aeg082','2.1','0.399177842261905','0.399177842261905'),
('ABL1_HUMAN','2hz4_A','A','abl kinase domain unligated and in complex with tetrahydrostaurosporine','2.8','0.252777321428571','0.252777321428571'),
('ABL1_HUMAN','2hz4_B','B','abl kinase domain unligated and in complex with tetrahydrostaurosporine','2.8','0.252777321428571','0.252777321428571'),
('ABL1_HUMAN','2hz4_C','C','abl kinase domain unligated and in complex with tetrahydrostaurosporine','2.8','0.252777321428571','0.252777321428571'),
('ERN1_HUMAN','2hz6_A','A','the crystal structure of human ire1-alpha luminal domain','3.1','0.138761805875576','0.138761805875576'),
('ABL1_HUMAN','2hzi_A','A','abl kinase domain in complex with pd180970','1.7','0.559661112570028','0.559661112570028'),
('ABL1_HUMAN','2hzi_B','B','abl kinase domain in complex with pd180970','1.7','0.559661112570028','0.559661112570028'),
('KPCB_HUMAN','2i0e_A','A','structure of catalytic domain of human protein kinase c beta ii complexed with a bisindolylmaleimide inhibitor','2.6','0.260082720924908','0.260082720924908'),
('KPCB_HUMAN','2i0e_B','B','structure of catalytic domain of human protein kinase c beta ii complexed with a bisindolylmaleimide inhibitor','2.6','0.260082720924908','0.260082720924908'),
('MK14_HUMAN','2i0h_A','A','the structure of p38alpha in complex with an arylpyridazinon','2','0.464828244047619','0.464828244047619'),
('CSF1R_HUMAN','2i0v_A','A','c-fms tyrosine kinase in complex with a quinolone inhibitor','2.8','0.196532827380952','0.196532827380952'),
('CSF1R_HUMAN','2i0y_A','A','cfms tyrosine kinase (fgf kid) in complex with an arylamide inhibitor','1.9','0.425437292449875','0.425437292449875'),
('CSF1R_HUMAN','2i1m_A','A','cfms tyrosine kinase (tie2 kid) in complex with an arylamide inhibitor','1.8','0.439623963293651','0.439623963293651'),
('CDK2_HUMAN','2i40_A','A','cdk2/cyclin a complexed with a thiophene carboxamide inhibit','2.8','0.307203705357143','0.307203705357143'),
('CDK2_HUMAN','2i40_C','C','cdk2/cyclin a complexed with a thiophene carboxamide inhibit','2.8','0.307203705357143','0.307203705357143'),
('MK06_HUMAN','2i6l_A','A','crystal structure of human mitogen activated protein kinase 6 (mapk6)','2.25','0.364957361111111','0.364957361111111'),
('MK06_HUMAN','2i6l_B','B','crystal structure of human mitogen activated protein kinase 6 (mapk6)','2.25','0.364957361111111','0.364957361111111'),
('NTRK1_HUMAN','2ifg_A','A','structure of the extracellular segment of human trka in comp nerve growth factor','3.4','0.0611813077731093','0.0611813077731093'),
('NTRK1_HUMAN','2ifg_B','B','structure of the extracellular segment of human trka in comp nerve growth factor','3.4','0.0611813077731093','0.0611813077731093'),
('LCK_HUMAN','2iim_A','A','sh3 domain of human lck','1','1.03447772321429','1.03447772321429'),
('E9PEI4_HUMAN','2ijm_A','A','crystal structure of focal adhesion kinase domain with 2 molecules in the asymmetric unit complexed with adp and atp','2.19','0.367990498613829','0.367990498613829'),
('FAK1_HUMAN','2ijm_B','B','crystal structure of focal adhesion kinase domain with 2 molecules in the asymmetric unit complexed with adp and atp','2.19','0.367990498613829','0.367990498613829'),
('TITIN_HUMAN','2ill_A','A','anomalous substructure of titin-a168169','2.2','0.366047939664502','0.366047939664502'),
('WEE1_HUMAN','2in6_A','A','wee1 kinase complex with inhibitor pd311839','1.9','0.399051786497494','0.399051786497494'),
('WEE1_HUMAN','2io6_A','A','wee1 kinase complexed with inhibitor pd330961','2.2','0.340612984307359','0.340612984307359'),
('EGFR_HUMAN','2itn_A','A','crystal structure of egfr kinase domain g719s mutation in complex with amp-pnp','2.47','0.319680591261808','0.319680591261808'),
('EGFR_HUMAN','2ito_A','A','crystal structure of egfr kinase domain g719s mutation in complex with iressa','3.25','0.19362706959707','0.19362706959707'),
('EGFR_HUMAN','2itp_A','A','crystal structure of egfr kinase domain g719s mutation in complex with aee788','2.74','0.270470229840111','0.270470229840111'),
('EGFR_HUMAN','2itq_A','A','crystal structure of egfr kinase domain g719s mutation in complex with afn941','2.68','0.28216696228678','0.28216696228678'),
('EGFR_HUMAN','2itt_A','A','crystal structure of egfr kinase domain l858r mutation in complex with aee788','2.73','0.261026095467033','0.261026095467033'),
('EGFR_HUMAN','2itu_A','A','crystal structure of egfr kinase domain l858r mutation in complex with afn941','2.8','0.25899380952381','0.25899380952381'),
('EGFR_HUMAN','2itv_A','A','crystal structure of egfr kinase domain l858r mutation in complex with amp-pnp','2.47','0.319793835309427','0.319793835309427'),
('EGFR_HUMAN','2itw_A','A','crystal structure of egfr kinase domain in complex with afn941','2.88','0.26427121031746','0.26427121031746'),
('EGFR_HUMAN','2itx_A','A','crystal structure of egfr kinase domain in complex with amp- pnp','2.98','0.249090410274848','0.249090410274848'),
('EGFR_HUMAN','2ity_A','A','crystal structure of egfr kinase domain in complex with iressa','3.42','0.177366053675856','0.177366053675856'),
('EGFR_HUMAN','2itz_A','A','crystal structure of egfr kinase domain l858r mutation in complex with iressa','2.72','0.273453338585434','0.273453338585434'),
('RET_HUMAN','2ivs_A','A','crystal structure of non-phosphorylated ret tyrosine kinase domain','2','0.461389345238095','0.461389345238095'),
('RET_HUMAN','2ivs_B','B','crystal structure of non-phosphorylated ret tyrosine kinase domain','2','0.461389345238095','0.461389345238095'),
('RET_HUMAN','2ivt_A','A','crystal structure of phosphorylated ret tyrosine kinase domain','2.6','0.317571009615385','0.317571009615385'),
('RET_HUMAN','2ivu_A','A','crystal structure of phosphorylated ret tyrosine kinase domain complexed with the inhibitor zd6474','2.5','0.329565074404762','0.329565074404762'),
('RET_HUMAN','2ivv_A','A','crystal structure of phosphorylated ret tyrosine kinase domain complexed with the inhibitor pp1','2.25','0.397016185515873','0.397016185515873'),
('CDK2_HUMAN','2iw6_A','A','structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor','2.3','0.323373754528986','0.323373754528986'),
('CDK2_HUMAN','2iw6_C','C','structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor','2.3','0.323373754528986','0.323373754528986'),
('CDK2_HUMAN','2iw8_A','A','structure of human thr160-phospho cdk2-cyclin a f82h-l83v- h84d mutant with an o6-cyclohexylmethylguanine inhibitor','2.3','0.345609945005176','0.345609945005176'),
('CDK2_HUMAN','2iw8_C','C','structure of human thr160-phospho cdk2-cyclin a f82h-l83v- h84d mutant with an o6-cyclohexylmethylguanine inhibitor','2.3','0.345609945005176','0.345609945005176'),
('CDK2_HUMAN','2iw9_A','A','structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor','2','0.418571056547619','0.418571056547619'),
('CDK2_HUMAN','2iw9_C','C','structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor','2','0.418571056547619','0.418571056547619'),
('PIM2_HUMAN','2iwi_A','A','crystal structure of the human pim2 in complex with a ruthenium organometallic ligand ru1','2.8','0.218404300595238','0.218404300595238'),
('PIM2_HUMAN','2iwi_B','B','crystal structure of the human pim2 in complex with a ruthenium organometallic ligand ru1','2.8','0.218404300595238','0.218404300595238'),
('KC1G3_HUMAN','2izr_A','A','structure of casein kinase gamma 3 in complex with inhibitor','1.3','0.798078016254579','0.798078016254579'),
('KC1G3_HUMAN','2izs_A','A','structure of casein kinase gamma 3 in complex with inhibitor','1.95','0.482215736034799','0.482215736034799'),
('KC1G3_HUMAN','2izt_A','A','structure of casein kinase gamma 3 in complex with inhibitor','2','0.40195087797619','0.40195087797619'),
('KC1G3_HUMAN','2izu_A','A','structure of casein kinase gamma 3 in complex with inhibitor','1.85','0.539219022683398','0.539219022683398'),
('PAK4_HUMAN','2j0i_A','A','crystal structure of the human p21-activated kinase 4','1.6','0.595978511904762','0.595978511904762'),
('E9PEI4_HUMAN','2j0m_B','B','crystal structure a two-chain complex between the ferm and kinase domains of focal adhesion kinase.','2.8','0.246078675595238','0.246078675595238'),
('PIM1_HUMAN','2j2i_B','B','crystal structure of the humab pim1 in complex with ly333531','1.9','0.500372709116541','0.500372709116541'),
('AURKA_HUMAN','2j4z_A','A','structure of aurora-2 in complex with pha-680626','2','0.429872142857143','0.429872142857143'),
('AURKA_HUMAN','2j4z_B','B','structure of aurora-2 in complex with pha-680626','2','0.429872142857143','0.429872142857143'),
('AURKA_HUMAN','2j50_A','A','structure of aurora-2 in complex with pha-739358','3','0.201916056547619','0.201916056547619'),
('AURKA_HUMAN','2j50_B','B','structure of aurora-2 in complex with pha-739358','3','0.201916056547619','0.201916056547619'),
('SLK_HUMAN','2j51_A','A','crystal structure of human ste20-like kinase bound to 5- amino-3-((4-(aminosulfonyl)phenyl)amino)-n-(2,6- difluorophenyl)-1h-1,2,4-triazole-1-carbothioamide','2.1','0.425126428571429','0.425126428571429'),
('EGFR_HUMAN','2j5e_A','A','crystal structure of egfr kinase domain in complex with an irreversible inhibitor 13-jab','3.1','0.216270258256529','0.216270258256529'),
('EGFR_HUMAN','2j5f_A','A','crystal structure of egfr kinase domain in complex with an irreversible inhibitor 34-jab','3','0.242152916666667','0.242152916666667'),
('EGFR_HUMAN','2j6m_A','A','crystal structure of egfr kinase domain in complex with aee788','3.1','0.20957939516129','0.20957939516129'),
('STK10_HUMAN','2j7t_A','A','crystal structure of human serine threonine kinase-10 bound to su11274','2','0.444264241071429','0.444264241071429'),
('TITIN_HUMAN','2j8h_A','A','structure of the immunoglobulin tandem repeat a168-a169 of titin','1.99','0.456189110433118','0.456189110433118'),
('TITIN_HUMAN','2j8o_A','A','structure of the immunoglobulin tandem repeat of titin a168- a169','2.49','0.265312512012335','0.265312512012335'),
('TITIN_HUMAN','2j8o_B','B','structure of the immunoglobulin tandem repeat of titin a168- a169','2.49','0.265312512012335','0.265312512012335'),
('DAPK3_HUMAN','2j90_A','A','crystal structure of human zip kinase in complex with a tetracyclic pyridone inhibitor (pyridone 6)','2','0.466034866071429','0.466034866071429'),
('DAPK3_HUMAN','2j90_B','B','crystal structure of human zip kinase in complex with a tetracyclic pyridone inhibitor (pyridone 6)','2','0.466034866071429','0.466034866071429'),
('CDK2_HUMAN','2j9m_A','A','crystal structure of cdk2 in complex with macrocyclic aminopyrimidine','2.5','0.295757068452381','0.295757068452381'),
('KCC1G_HUMAN','2jam_A','A','crystal structure of human calmodulin-dependent protein kinase i g','1.7','0.577998076855742','0.577998076855742'),
('KCC1G_HUMAN','2jam_B','B','crystal structure of human calmodulin-dependent protein kinase i g','1.7','0.577998076855742','0.577998076855742'),
('NEK2_HUMAN','2jav_A','A','human kinase with pyrrole-indolinone ligand','2.2','0.374922255140693','0.374922255140693'),
('MAPK2_HUMAN','2jbo_A','A','protein kinase mk2 in complex with an inhibitor (crystal form-1, soaking)','3.1','0.180305689804147','0.180305689804147'),
('MAPK2_HUMAN','2jbp_B','B','protein kinase mk2 in complex with an inhibitor (crystal form-2, co-crystallization)','3.31','0.15413200600633','0.15413200600633'),
('MAPK2_HUMAN','2jbp_J','J','protein kinase mk2 in complex with an inhibitor (crystal form-2, co-crystallization)','3.31','0.15413200600633','0.15413200600633'),
('MAPK2_HUMAN','2jbp_K','K','protein kinase mk2 in complex with an inhibitor (crystal form-2, co-crystallization)','3.31','0.15413200600633','0.15413200600633'),
('MAPK2_HUMAN','2jbp_L','L','protein kinase mk2 in complex with an inhibitor (crystal form-2, co-crystallization)','3.31','0.15413200600633','0.15413200600633'),
('KCC1D_HUMAN','2jc6_A','A','crystal structure of human calmodulin-dependent protein kinase 1d','2.3','0.370892950957557','0.370892950957557'),
('KCC1D_HUMAN','2jc6_C','C','crystal structure of human calmodulin-dependent protein kinase 1d','2.3','0.370892950957557','0.370892950957557'),
('AKT2_HUMAN','2jdo_A','A','structure of pkb-beta (akt2) complexed with isoquinoline-5- sulfonic acid (2-(2-(4-chlorobenzyloxy) ethylamino)ethyl) amide','1.8','0.527266225198413','0.527266225198413'),
('GSK3B_HUMAN','2jdo_C','C','structure of pkb-beta (akt2) complexed with isoquinoline-5- sulfonic acid (2-(2-(4-chlorobenzyloxy) ethylamino)ethyl) amide','1.8','0.527266225198413','0.527266225198413'),
('AKT2_HUMAN','2jdr_A','A','structure of pkb-beta (akt2) complexed with the inhibitor a- 443654','2.3','0.368067325957557','0.368067325957557'),
('GSK3B_HUMAN','2jdr_C','C','structure of pkb-beta (akt2) complexed with the inhibitor a- 443654','2.3','0.368067325957557','0.368067325957557'),
('KPCT_HUMAN','2jed_A','A','the crystal structure of the kinase domain of the protein kinase c theta in complex with nvp-xaa228 at 2.32a resolution.','2.32','0.363744705972907','0.363744705972907'),
('SLK_HUMAN','2jfl_A','A','crystal structure of human ste20-like kinase ( diphosphorylated form) bound to 5- amino-3-((4-( aminosulfonyl)phenyl)amino)-n-(2,6- difluorophenyl)-1h-1,2, 4-triazole-1-carbothioamide','2.2','0.396398371212121','0.396398371212121'),
('SLK_HUMAN','2jfm_A','A','crystal structure of human ste20-like kinase (unliganded form)','2.85','0.23879259476817','0.23879259476817'),
('CDK2_HUMAN','2jgz_A','A','crystal structure of phospho-cdk2 in complex with cyclin b','2.9','0.243416708230706','0.243416708230706'),
('VRK3_HUMAN','2jii_A','A','structure of vaccinia related kinase 3','2','0.467335119047619','0.467335119047619'),
('VRK3_HUMAN','2jii_B','B','structure of vaccinia related kinase 3','2','0.467335119047619','0.467335119047619'),
('Q59FL8_HUMAN','2jit_A','A','crystal structure of egfr kinase domain t790m mutation','3.1','0.216522252304147','0.216522252304147'),
('EGFR_HUMAN','2jit_B','B','crystal structure of egfr kinase domain t790m mutation','3.1','0.216522252304147','0.216522252304147'),
('Q59FL8_HUMAN','2jiu_A','A','crystal structure of egfr kinase domain t790m mutation in complex with aee788','3.05','0.198566679839969','0.198566679839969'),
('EGFR_HUMAN','2jiu_B','B','crystal structure of egfr kinase domain t790m mutation in complex with aee788','3.05','0.198566679839969','0.198566679839969'),
('EGFR_HUMAN','2jiv_A','A','crystal structure of egfr kinase domain t790m mutation in compex with hki-272','3.5','0.0126281398809523','0.0126281398809523'),
('EGFR_HUMAN','2jiv_B','B','crystal structure of egfr kinase domain t790m mutation in compex with hki-272','3.5','0.0126281398809523','0.0126281398809523'),
('GSK3B_HUMAN','2jld_A','A','extremely tight binding of ruthenium complex to glycogen synthase kinase 3','2.35','0.380148715488855','0.380148715488855'),
('GSK3B_HUMAN','2jld_B','B','extremely tight binding of ruthenium complex to glycogen synthase kinase 3','2.35','0.380148715488855','0.380148715488855'),
('STK4_HUMAN','2jo8_A','A','solution structure of c-terminal domain of human mammalian sterile 20-like kinase 1 (mst1)',NULL,'0.0375249255952381','0.0375249255952381'),
('STK4_HUMAN','2jo8_B','B','solution structure of c-terminal domain of human mammalian sterile 20-like kinase 1 (mst1)',NULL,'0.0375249255952381','0.0375249255952381'),
('M3K3_HUMAN','2jrh_A','A','solution sturcture of human mekk3 pb1 domain cis isomer',NULL,'0.0282764732142857','0.0282764732142857'),
('ERBB2_HUMAN','2jwa_A','A','erbb2 transmembrane segment dimer spatial structure',NULL,'0.0277550297619047','0.0277550297619047'),
('ERBB2_HUMAN','2jwa_B','B','erbb2 transmembrane segment dimer spatial structure',NULL,'0.0277550297619047','0.0277550297619047'),
('MYLK_HUMAN','2k0f_B','B','calmodulin complexed with calmodulin-binding peptide from smooth muscle myosin light chain kinase',NULL,'-2.77555756156289e-17','-2.77555756156289e-17'),
('EPHA1_HUMAN','2k1k_A','A','nmr structures of dimeric transmembrane domain of the receptor tyrosine kinase epha1 in lipid bicelles at ph 4.3',NULL,'0.0177068303571428','0.0177068303571428'),
('EPHA1_HUMAN','2k1k_B','B','nmr structures of dimeric transmembrane domain of the receptor tyrosine kinase epha1 in lipid bicelles at ph 4.3',NULL,'0.0177068303571428','0.0177068303571428'),
('EPHA1_HUMAN','2k1l_A','A','nmr structures of dimeric transmembrane domain of the receptor tyrosine kinase epha1 in lipid bicelles at ph 6.3',NULL,'0.0122554464285714','0.0122554464285714'),
('EPHA1_HUMAN','2k1l_B','B','nmr structures of dimeric transmembrane domain of the receptor tyrosine kinase epha1 in lipid bicelles at ph 6.3',NULL,'0.0122554464285714','0.0122554464285714'),
('BMR1A_HUMAN','2k3g_A','A','nmr structure analysis of a bmp receptor',NULL,'0.045747738095238','0.045747738095238'),
('EPHA2_HUMAN','2k9y_A','A','epha2 dimeric structure in the lipidic bicelle at ph 5.0',NULL,'0.0240903869047619','0.0240903869047619'),
('EPHA2_HUMAN','2k9y_B','B','epha2 dimeric structure in the lipidic bicelle at ph 5.0',NULL,'0.0240903869047619','0.0240903869047619'),
('ILK_HUMAN','2kbx_A','A','solution structure of ilk-pinch complex',NULL,'0.0130847619047619','0.0130847619047619'),
('PTK6_HUMAN','2kgt_A','A','solution structure of sh3 domain of ptk6',NULL,'0.023434375','0.023434375'),
('ABL2_HUMAN','2kk1_A','A','solution structure of c-terminal domain of tyrosine-protein kinase abl2 from homo sapiens, northeast structural genomics consortium (nesg) target hr5537a',NULL,'0.0457569047619047','0.0457569047619047'),
('FER_HUMAN','2kk6_A','A','solution structure of sh2 domain of proto-oncogene tyrosine- protein kinase fer from homo sapiens, northeast structural genomics consortium (nesg) target hr3461d',NULL,'0.0508784821428571','0.0508784821428571'),
('MAST2_HUMAN','2kqf_A','A','solution structure of mast205-pdz complexed with the c-termi rabies virus g protein',NULL,'0.0224037648809524','0.0224037648809524'),
('ERBB2_HUMAN','2ks1_A','A','heterodimeric association of transmembrane domains of erbb1 receptors enabling kinase activation',NULL,'0.0227987797619047','0.0227987797619047'),
('EGFR_HUMAN','2ks1_B','B','heterodimeric association of transmembrane domains of erbb1 receptors enabling kinase activation',NULL,'0.0227987797619047','0.0227987797619047'),
('EPHA2_HUMAN','2kso_A','A','epha2:ship2 sam:sam complex',NULL,'0.0469311755952381','0.0469311755952381'),
('VRK1_HUMAN','2kty_A','A','solution structure of human vaccinia related kinase-1',NULL,'0.0129598511904762','0.0129598511904762'),
('VRK1_HUMAN','2kul_A','A','solution structure of human vaccinia related kinase 1(vrk1)',NULL,'0.0312904464285714','0.0312904464285714'),
('ALK_HUMAN','2kup_B','B','solution structure of the complex of the ptb domain of snt-2 residue peptide (aa 1571-1589) of halk',NULL,'0.0441487797619047','0.0441487797619047'),
('ALK_HUMAN','2kuq_A','A','solution structure of the chimera of the ptb domain of snt-2 residue peptide (aa 1571-1589) of halk',NULL,'0.0484831101190476','0.0484831101190476'),
('MAST2_HUMAN','2kyl_A','A','solution structure of mast2-pdz complexed with the c-terminu',NULL,'0.0398008630952381','0.0398008630952381'),
('BRAF_HUMAN','2l05_A','A','solution nmr structure of the ras-binding domain of serine/t protein kinase b-raf from homo sapiens, northeast structura consortium target hr4694f',NULL,'0.0523331398809524','0.0523331398809524'),
('ERBB4_HUMAN','2l2t_A','A','solution nmr structure of the erbb4 dimeric membrane domain',NULL,'0.0346598809523809','0.0346598809523809'),
('ERBB4_HUMAN','2l2t_B','B','solution nmr structure of the erbb4 dimeric membrane domain',NULL,'0.0346598809523809','0.0346598809523809'),
('ERBB2_HUMAN','2l4k_B','B','water refined solution structure of the human grb7-sh2 domai complex with the 10 amino acid peptide py1139',NULL,'0.0263504017857143','0.0263504017857143'),
('TGFR1_HUMAN','2l5s_A','A','solution structure of the extracellular domain of the tgf-be receptor',NULL,'0.0219259375','0.0219259375'),
('PGFRB_HUMAN','2l6w_A','A','pdgfr beta-tm',NULL,'0.0655176934523809','0.0655176934523809'),
('PGFRB_HUMAN','2l6w_B','B','pdgfr beta-tm',NULL,'0.0655176934523809','0.0655176934523809'),
('ERBB3_HUMAN','2l9u_A','A','spatial structure of dimeric erbb3 transmembrane domain',NULL,'0.0397591071428571','0.0397591071428571'),
('ERBB3_HUMAN','2l9u_B','B','spatial structure of dimeric erbb3 transmembrane domain',NULL,'0.0397591071428571','0.0397591071428571'),
('BUB1_HUMAN','2lah_A','A','solution nmr structure of mitotic checkpoint serine/threonin kinase bub1 n-terminal domain from homo sapiens, northeast genomics consortium target hr5460a (methods development)',NULL,'0.0649854166666666','0.0649854166666666'),
('VRK1_HUMAN','2lav_A','A','nmr solution structure of human vaccinia-related kinase 1',NULL,'0.0177742261904762','0.0177742261904762'),
('ACVL1_HUMAN','2lcr_A','A','nmr structure of alk1 extracellular domain',NULL,'0.0194345833333333','0.0194345833333333'),
('ERBB4_HUMAN','2lcx_A','A','spatial structure of the erbb4 dimeric tm domain',NULL,'0.0346598809523809','0.0346598809523809'),
('ERBB4_HUMAN','2lcx_B','B','spatial structure of the erbb4 dimeric tm domain',NULL,'0.0346598809523809','0.0346598809523809'),
('MK14_HUMAN','2lgc_A','A','joint nmr and x-ray refinement reveals the structure of a no dibenzo[a,d]cycloheptenone inhibitor/p38 map kinase complex solution',NULL,'0.0514626934523809','0.0514626934523809'),
('FAK2_HUMAN','2lk4_A','A','structural and mechanistic insights into the interaction bet pyk2 and paxillin ld motif',NULL,'0.0330915476190476','0.0330915476190476'),
('ITK_HUMAN','2lmj_A','A',NULL,NULL,NULL,NULL),
('TEC_HUMAN','2lul_A','A','solution nmr structure of ph domain of tyrosine-protein kina from homo sapiens, northeast structural genomics consortium target hr3504c',NULL,'0.0420659970238095','0.0420659970238095'),
('MYLK2_HUMAN','2lv6_B','B',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','2m20_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','2m20_B','B',NULL,NULL,NULL,NULL),
('MK08_HUMAN','2no3_B','B','novel 4-anilinopyrimidines as potent jnk1 inhibitors','3.2','0.144254851190476','0.144254851190476'),
('AURKA_HUMAN','2np8_A','A','structural basis for the inhibition of aurora a kinase by a novel class of high affinity disubstituted pyrimidine inhibitors','2.25','0.320237182539682','0.320237182539682'),
('AURKA_HUMAN','2np8_B','B','structural basis for the inhibition of aurora a kinase by a novel class of high affinity disubstituted pyrimidine inhibitors','2.25','0.320237182539682','0.320237182539682'),
('MK14_HUMAN','2npq_A','A','a novel lipid binding site in the p38 alpha map kinase','1.8','0.477180347222222','0.477180347222222'),
('MP2K5_HUMAN','2npt_A','A','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 2 phox domain (map3k','1.75','0.517865386904762','0.517865386904762'),
('M3K2_HUMAN','2npt_B','B','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 2 phox domain (map3k','1.75','0.517865386904762','0.517865386904762'),
('MP2K5_HUMAN','2npt_C','C','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 2 phox domain (map3k','1.75','0.517865386904762','0.517865386904762'),
('M3K2_HUMAN','2npt_D','D','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 2 phox domain (map3k','1.75','0.517865386904762','0.517865386904762'),
('IRAK4_HUMAN','2nru_A','A','crystal structure of irak-4','2','0.375158184523809','0.375158184523809'),
('IRAK4_HUMAN','2nru_B','B','crystal structure of irak-4','2','0.375158184523809','0.375158184523809'),
('IRAK4_HUMAN','2nru_C','C','crystal structure of irak-4','2','0.375158184523809','0.375158184523809'),
('IRAK4_HUMAN','2nru_D','D','crystal structure of irak-4','2','0.375158184523809','0.375158184523809'),
('IRAK4_HUMAN','2nry_A','A','crystal structure of irak-4','2.15','0.37134342192691','0.37134342192691'),
('IRAK4_HUMAN','2nry_B','B','crystal structure of irak-4','2.15','0.37134342192691','0.37134342192691'),
('IRAK4_HUMAN','2nry_C','C','crystal structure of irak-4','2.15','0.37134342192691','0.37134342192691'),
('IRAK4_HUMAN','2nry_D','D','crystal structure of irak-4','2.15','0.37134342192691','0.37134342192691'),
('TRIO_HUMAN','2nz8_B','B','n-terminal dhph cassette of trio in complex with nucleotide- free rac1','2','0.397532678571429','0.397532678571429'),
('TITIN_HUMAN','2nzi_A','A','crystal structure of domains a168-a170 from titin','2.9','0.222088598111658','0.222088598111658'),
('TITIN_HUMAN','2nzi_B','B','crystal structure of domains a168-a170 from titin','2.9','0.222088598111658','0.222088598111658'),
('MK10_HUMAN','2o0u_A','A','crystal structure of human jnk3 complexed with n-{3-cyano-6- piperidinyl)propanoyl]-4,5,6,7-tetrahydrothieno[2,3-c]pyrid 1-naphthalenecarboxamide','2.1','0.373912485119048','0.373912485119048'),
('MK10_HUMAN','2o2u_A','A','crystal structure of human jnk3 complexed with n-(3-cyano-4, tetrahydro-1-benzothien-2-yl)-2-fluorobenzamide','2.45','0.295780869472789','0.295780869472789'),
('MP2K5_HUMAN','2o2v_A','A','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 3 (map3k3b-phox)','1.83','0.50683018564598','0.50683018564598'),
('M3K3_HUMAN','2o2v_B','B','crystal structure of the complex of human mitogen activated kinase kinase 5 phox domain (map2k5-phox) with human mitoge activated protein kinase kinase kinase 3 (map3k3b-phox)','1.83','0.50683018564598','0.50683018564598'),
('PIM1_HUMAN','2o3p_A','A','crystal structure of pim1 with quercetin','2.24','0.38387150297619','0.38387150297619'),
('GSK3B_HUMAN','2o5k_A','A','crystal structure of gsk3beta in complex with a benzoimidazol inhibitor','3.2','0.131998675595238','0.131998675595238'),
('PIM1_HUMAN','2o63_A','A','crystal structure of pim1 with myricetin','2','0.431618258928571','0.431618258928571'),
('PIM1_HUMAN','2o64_A','A','crystal structure of pim1 with quercetagetin','2.44','0.35778706259758','0.35778706259758'),
('PIM1_HUMAN','2o65_A','A','crystal structure of pim1 with pentahydroxyflavone','2.85','0.24939884476817','0.24939884476817'),
('ABL1_HUMAN','2o88_A','A','crystal structure of the n114a mutant of abl-sh3 domain comp a designed high-affinity peptide ligand: implications for s interactions','1.75','0.528538333333333','0.528538333333333'),
('IRAK4_HUMAN','2o8y_A','A','apo irak4 kinase domain','2.4','0.290200178571429','0.290200178571429'),
('IRAK4_HUMAN','2o8y_B','B','apo irak4 kinase domain','2.4','0.290200178571429','0.290200178571429'),
('PIM1_HUMAN','2obj_A','A','crystal structure of human pim-1 kinase in complex with inhibitor','2.5','0.314636860119048','0.314636860119048'),
('PAK6_HUMAN','2odb_B','B','the crystal structure of human cdc42 in complex with the cri of human p21-activated kinase 6 (pak6)','2.4','0.346132752976191','0.346132752976191'),
('LCK_HUMAN','2of2_A','A','crystal structure of furanopyrimidine 8 bound to lck','2','0.385906175595238','0.385906175595238'),
('LCK_HUMAN','2of4_A','A','crystal structure of furanopyrimidine 1 bound to lck','2.7','0.250783659060846','0.250783659060846'),
('LCK_HUMAN','2ofu_A','A','x-ray crystal structure of 2-aminopyrimidine carbamate 43 bound to lck','2','0.415259717261905','0.415259717261905'),
('LCK_HUMAN','2ofv_A','A','crystal structure of aminoquinazoline 1 bound to lck','2','0.343546145833333','0.343546145833333'),
('LCK_HUMAN','2ofv_B','B','crystal structure of aminoquinazoline 1 bound to lck','2','0.343546145833333','0.343546145833333'),
('LCK_HUMAN','2og8_B','B','crystal structure of aminoquinazoline 36 bound to lck','2.3','0.305658992624224','0.305658992624224'),
('PLK1_HUMAN','2ogq_A','A','molecular and structural basis of plk1 substrate recognition: implications in centrosomal localization','1.95','0.497513608058608','0.497513608058608'),
('CSF1R_HUMAN','2ogv_A','A','crystal structure of the autoinhibited human c-fms kinase domain','2.7','0.271672319775132','0.271672319775132'),
('VGFR2_HUMAN','2oh4_A','A','crystal structure of vegfr2 with a benzimidazole-urea inhibi','2.05','0.447452884001162','0.447452884001162'),
('HCK_HUMAN','2oi3_A','A','nmr structure analysis of the hematopoetic cell kinase sh3 domain complexed with an artificial high affinity ligand (pd1)',NULL,'0.0370116666666666','0.0370116666666666'),
('PIM1_HUMAN','2oi4_X','X','crystal structure of human pim1 in complex with fluorinated ruthenium pyridocarbazole','2.2','0.398226168831169','0.398226168831169'),
('IRAK4_HUMAN','2oib_A','A','crystal structure of irak4 kinase domain apo form','2','0.418260104166667','0.418260104166667'),
('IRAK4_HUMAN','2oib_B','B','crystal structure of irak4 kinase domain apo form','2','0.418260104166667','0.418260104166667'),
('B4E359_HUMAN','2oib_C','C','crystal structure of irak4 kinase domain apo form','2','0.418260104166667','0.418260104166667'),
('IRAK4_HUMAN','2oib_D','D','crystal structure of irak4 kinase domain apo form','2','0.418260104166667','0.418260104166667'),
('IRAK4_HUMAN','2oic_A','A','crystal structure of irak4 kinase domain complexed with staurosporine','2.4','0.309261860119048','0.309261860119048'),
('IRAK4_HUMAN','2oic_B','B','crystal structure of irak4 kinase domain complexed with staurosporine','2.4','0.309261860119048','0.309261860119048'),
('IRAK4_HUMAN','2oic_C','C','crystal structure of irak4 kinase domain complexed with staurosporine','2.4','0.309261860119048','0.309261860119048'),
('IRAK4_HUMAN','2oic_D','D','crystal structure of irak4 kinase domain complexed with staurosporine','2.4','0.309261860119048','0.309261860119048'),
('IRAK4_HUMAN','2oid_A','A','crystal structure of irak4 kinase domain complexed with amppnp','2.3','0.307061552148033','0.307061552148033'),
('B4E359_HUMAN','2oid_B','B','crystal structure of irak4 kinase domain complexed with amppnp','2.3','0.307061552148033','0.307061552148033'),
('IRAK4_HUMAN','2oid_C','C','crystal structure of irak4 kinase domain complexed with amppnp','2.3','0.307061552148033','0.307061552148033'),
('IRAK4_HUMAN','2oid_D','D','crystal structure of irak4 kinase domain complexed with amppnp','2.3','0.307061552148033','0.307061552148033'),
('HCK_HUMAN','2oj2_A','A','nmr structure analysis of the hematopoetic cell kinase sh3 domain complexed with an artificial high affinity ligand (pd1)',NULL,'0.0181974255952381','0.0181974255952381'),
('IGF1R_HUMAN','2oj9_A','A','structure of igf-1r kinase domain complexed with a benzimidazole inhibitor','2','0.398949880952381','0.398949880952381'),
('MK01_HUMAN','2ojg_A','A','crystal structure of erk2 in complex with n,n-dimethyl-4-(4- phenyl-1h-pyrazol-3-yl)-1h-pyrrole-2-carboxamide','2','0.405200193452381','0.405200193452381'),
('MK01_HUMAN','2oji_A','A','crystal structure of erk2 in complex with n-benzyl-4-(4-(3- chlorophenyl)-1h-pyrazol-3-yl)-1h-pyrrole-2-carboxamide','2.6','0.306158866758242','0.306158866758242'),
('MK01_HUMAN','2ojj_A','A','crystal structure of erk2 in complex with (s)-n-(1-(3- chloro-4-fluorophenyl)-2-hydroxyethyl)-4-(4-(3- chlorophenyl)-1h-pyrazol-3-yl)-1h-pyrrole-2-carboxamide','2.4','0.323666264880952','0.323666264880952'),
('PLK1_HUMAN','2ojx_A','A','molecular and structural basis of polo-like kinase 1 substrate recognition: implications in centrosomal localization','2.85','0.224292431077694','0.224292431077694'),
('MK10_HUMAN','2ok1_A','A','crystal structure of jnk3 bound to n-benzyl-4-(4-(3- chlorophenyl)-1h-pyrazol-3-yl)-1h-pyrrole-2-carboxamide','2.4','0.283965773809524','0.283965773809524'),
('MK14_HUMAN','2okr_A','A','crystal structure of the p38a-mapkap kinase 2 heterodimer','2','0.376651220238095','0.376651220238095'),
('MAPK2_HUMAN','2okr_C','C','crystal structure of the p38a-mapkap kinase 2 heterodimer','2','0.376651220238095','0.376651220238095'),
('MK14_HUMAN','2okr_D','D','crystal structure of the p38a-mapkap kinase 2 heterodimer','2','0.376651220238095','0.376651220238095'),
('MAPK2_HUMAN','2okr_F','F','crystal structure of the p38a-mapkap kinase 2 heterodimer','2','0.376651220238095','0.376651220238095'),
('MK14_HUMAN','2onl_A','A','crystal structure of the p38a-mapkap kinase 2 heterodimer','4','-0.00782467261904765','-0.00782467261904765'),
('MK14_HUMAN','2onl_B','B','crystal structure of the p38a-mapkap kinase 2 heterodimer','4','-0.00782467261904765','-0.00782467261904765'),
('MAPK2_HUMAN','2onl_C','C','crystal structure of the p38a-mapkap kinase 2 heterodimer','4','-0.00782467261904765','-0.00782467261904765'),
('MAPK2_HUMAN','2onl_D','D','crystal structure of the p38a-mapkap kinase 2 heterodimer','4','-0.00782467261904765','-0.00782467261904765'),
('TIE2_HUMAN','2oo8_X','X','synthesis, structural analysis, and sar studies of triazine derivatives as potent, selective tie-2 inhibitors','2.2','0.358122136093074','0.358122136093074'),
('ZAP70_HUMAN','2oq1_A','A','tandem sh2 domains of zap-70 with 19-mer zeta1 peptide','1.9','0.440135566259399','0.440135566259399'),
('TIE2_HUMAN','2osc_A','A','synthesis, structural analysis, and sar studies of triazine derivatives as potent, selective tie-2 inhibitors','2.8','0.220105431547619','0.220105431547619'),
('PLK1_HUMAN','2ou7_A','A','structure of the catalytic domain of human polo-like kinase','2.4','0.332209657738095','0.332209657738095'),
('PAK4_HUMAN','2ov2_I','I','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_J','J','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_K','K','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_L','L','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_M','M','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_N','N','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_O','O','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('PAK4_HUMAN','2ov2_P','P','the crystal structure of the human rac3 in complex with the domain of human p21-activated kinase 4 (pak4)','2.1','0.442986235119048','0.442986235119048'),
('GSK3B_HUMAN','2ow3_B','B','glycogen synthase kinase-3 beta in complex with bis- (indole)maleimide pyridinophane inhibitor','2.8','0.21929474702381','0.21929474702381'),
('PLK1_HUMAN','2owb_A','A','structure of the catalytic domain of human polo-like kinase','2.1','0.400433452380952','0.400433452380952'),
('MAPK2_HUMAN','2oza_A','A','structure of p38alpha complex','2.7','0.234343629298942','0.234343629298942'),
('ZAP70_HUMAN','2ozo_A','A','autoinhibited intact human zap-70','2.6','0.271032081043956','0.271032081043956'),
('MERTK_HUMAN','2p0c_A','A','catalytic domain of the proto-oncogene tyrosine-protein kina','2.4','0.332603869047619','0.332603869047619'),
('MERTK_HUMAN','2p0c_B','B','catalytic domain of the proto-oncogene tyrosine-protein kina','2.4','0.332603869047619','0.332603869047619'),
('VGFR2_HUMAN','2p2h_A','A','crystal structure of the vegfr2 kinase domain in complex with a pyridinyl-triazine inhibitor','1.95','0.456714084249084','0.456714084249084'),
('VGFR2_HUMAN','2p2i_A','A','crystal structure of the vegfr2 kinase domain in complex with a nicotinamide inhibitor','2.4','0.314458214285714','0.314458214285714'),
('VGFR2_HUMAN','2p2i_B','B','crystal structure of the vegfr2 kinase domain in complex with a nicotinamide inhibitor','2.4','0.314458214285714','0.314458214285714'),
('MK10_HUMAN','2p33_A','A','synthesis and sar of aminopyrimidines as novel c-jun n- terminal kinase (jnk) inhibitors','2.4','0.273553720238095','0.273553720238095'),
('MAPK2_HUMAN','2p3g_X','X','crystal structure of a pyrrolopyridine inhibitor bound to mapkap kinase-2','3.8','-0.00337217966791978','-0.00337217966791978'),
('TIE2_HUMAN','2p4i_A','A','evolution of a highly selective and potent 2-(pyridin-2-yl)- 1,3,5-triazine tie-2 kinase inhibitor','2.5','0.266100863095238','0.266100863095238'),
('TIE2_HUMAN','2p4i_B','B','evolution of a highly selective and potent 2-(pyridin-2-yl)- 1,3,5-triazine tie-2 kinase inhibitor','2.5','0.266100863095238','0.266100863095238'),
('MP2K1_HUMAN','2p55_A','A','x-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp','2.8','0.243084880952381','0.243084880952381'),
('PDPK1_HUMAN','2pe0_A','A','crystal structure of human phosphoinositide-dependent protei (pdk1) 5-hydroxy-3-[1-(1h-pyrrol-2-yl)-eth-(z)-ylidene]-1,3 indol-2-one complex','2.35','0.350427063703141','0.350427063703141'),
('PDPK1_HUMAN','2pe1_A','A','crystal structure of human phosphoinositide-dependent protei (pdk1) {2-oxo-3-[1-(1h-pyrrol-2-yl)-eth-(z)-ylidene]-2,3-di indol-5-yl}-urea {bx-517} complex','2.14','0.369017740459502','0.369017740459502'),
('PDPK1_HUMAN','2pe2_A','A','crystal structure of human phosphoinositide-dependent protei (pdk1) 3-{5-[2-oxo-5-ureido-1,2-dihydro-indol-(3z)-ylidenem pyrrol-3-yl}-n-(2-piperidin-1-yl-ethyl)-benzamide complex','2.13','0.423145204979879','0.423145204979879'),
('TGFR2_HUMAN','2pjy_B','B','structural basis for cooperative assembly of the tgf-beta si complex','3','0.181652916666667','0.181652916666667'),
('TGFR1_HUMAN','2pjy_C','C','structural basis for cooperative assembly of the tgf-beta si complex','3','0.181652916666667','0.181652916666667'),
('LCK_HUMAN','2pl0_A','A','lck bound to imatinib','2.8','0.260637157738095','0.260637157738095'),
('Q59F04_HUMAN','2pld_B','B','nuclear magnetic resonance structure of an sh2 domain of phospholipase c-gamma1 complexed with a high affinity binding peptide',NULL,'0.00995358630952378','0.00995358630952378'),
('Q59F04_HUMAN','2ple_B','B','nuclear magnetic resonance structure of an sh2 domain of phospholipase c-gamma1 complexed with a high affinity binding peptide',NULL,'0.00494084821428568','0.00494084821428568'),
('M3K3_HUMAN','2pph_A','A','solution structure of human mekk3 pb1 domain',NULL,'0.0297714583333333','0.0297714583333333'),
('FGFR2_HUMAN','2psq_A','A','crystal structure of unphosphorylated unactivated wild type fgf receptor 2 (fgfr2) kinase domain','2.4','0.333286547619048','0.333286547619048'),
('FGFR2_HUMAN','2pvf_A','A','crystal structure of tyrosine phosphorylated activated fgf r (fgfr2) kinase domain in complex with atp analog and substr peptide','1.8','0.452944513888889','0.452944513888889'),
('CSK21_HUMAN','2pvr_A','A','crystal structure of the catalytic subunit of protein kinase terminal deletion mutant 1-335) in complex with two sulfate','1.6','0.587965818452381','0.587965818452381'),
('FGFR2_HUMAN','2pvy_A','A','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k659n mutation responsible for an unclassified craniosynostosis syndrome.','2.2','0.344616034902597','0.344616034902597'),
('FGFR2_HUMAN','2pvy_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k659n mutation responsible for an unclassified craniosynostosis syndrome.','2.2','0.344616034902597','0.344616034902597'),
('FGFR2_HUMAN','2pvy_C','C','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k659n mutation responsible for an unclassified craniosynostosis syndrome.','2.2','0.344616034902597','0.344616034902597'),
('FGFR2_HUMAN','2pvy_D','D','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k659n mutation responsible for an unclassified craniosynostosis syndrome.','2.2','0.344616034902597','0.344616034902597'),
('FGFR2_HUMAN','2pwl_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic n549h mutation responsible for crouzon syndrome.','2.4','0.355942916666667','0.355942916666667'),
('FGFR2_HUMAN','2py3_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic e565g mutation responsible for pfeiffer syndrome','2.3','0.368106120600414','0.368106120600414'),
('D3DRD6_HUMAN','2pz5_A','A','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic n549t mutation responsible for pfeiffer syndrome','2.4','0.336505922619048','0.336505922619048'),
('FGFR2_HUMAN','2pz5_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic n549t mutation responsible for pfeiffer syndrome','2.4','0.336505922619048','0.336505922619048'),
('FGFR2_HUMAN','2pzp_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k526e mutation responsible for crouzon syndrome','2.4','0.348340892857143','0.348340892857143'),
('D3DRD6_HUMAN','2pzr_A','A','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k641r mutation responsible for pfeiffer syndrome','3','0.250773586309524','0.250773586309524'),
('FGFR2_HUMAN','2pzr_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic k641r mutation responsible for pfeiffer syndrome','3','0.250773586309524','0.250773586309524'),
('MAPK2_HUMAN','2pzy_A','A','structure of mk2 complexed with compound 76','2.9','0.202465993944992','0.202465993944992'),
('MAPK2_HUMAN','2pzy_B','B','structure of mk2 complexed with compound 76','2.9','0.202465993944992','0.202465993944992'),
('MAPK2_HUMAN','2pzy_C','C','structure of mk2 complexed with compound 76','2.9','0.202465993944992','0.202465993944992'),
('FGFR2_HUMAN','2q0b_B','B','crystal strucure of fgf receptor 2 (fgfr2) kinase domain har pathogenic e565a mutation responsible for pfeiffer syndrome','2.9','0.261458136802135','0.261458136802135'),
('PAK4_HUMAN','2q0n_A','A','structure of human p21 activating kinase 4 (pak4) in complex consensus peptide','1.75','0.535205267857143','0.535205267857143'),
('EPHB2_HUMAN','2qbx_A','A','ephb2/snew antagonistic peptide complex','2.3','0.335961626552795','0.335961626552795'),
('EPHB2_HUMAN','2qbx_B','B','ephb2/snew antagonistic peptide complex','2.3','0.335961626552795','0.335961626552795'),
('MK14_HUMAN','2qd9_A','A','p38 alpha map kinase inhibitor based on heterobicyclic scaffolds','1.7','0.45541206495098','0.45541206495098'),
('CHK1_HUMAN','2qhm_A','A','crystal structure of chek1 in complex with inhibitor 2a','2','0.418593035714286','0.418593035714286'),
('CHK1_HUMAN','2qhn_A','A','crystal structure of chek1 in complex with inhibitor 1a','1.7','0.504608419117647','0.504608419117647'),
('BMR1A_HUMAN','2qj9_D','D','crystal structure analysis of bmp-2 in complex with bmpr-ia','2.44','0.319930366169009','0.319930366169009'),
('BMR1A_HUMAN','2qja_C','C','crystal structure analysis of bmp-2 in complex with bmpr-ia b12','2.6','0.259376902472527','0.259376902472527'),
('BMR1A_HUMAN','2qja_D','D','crystal structure analysis of bmp-2 in complex with bmpr-ia b12','2.6','0.259376902472527','0.259376902472527'),
('BMR1A_HUMAN','2qjb_C','C','crystal structure analysis of bmp-2 in complex with bmpr-ia ia/ib','2.5','0.283331964285714','0.283331964285714'),
('BMR1A_HUMAN','2qjb_D','D','crystal structure analysis of bmp-2 in complex with bmpr-ia ia/ib','2.5','0.283331964285714','0.283331964285714'),
('EPHB4_HUMAN','2qkq_A','A','structure of the sam domain of human ephrin type-b receptor 4','2.1','0.378669166666667','0.378669166666667'),
('EPHB4_HUMAN','2qkq_B','B','structure of the sam domain of human ephrin type-b receptor 4','2.1','0.378669166666667','0.378669166666667'),
('AVR2B_HUMAN','2qlu_A','A','crystal structure of activin receptor type ii kinase domain from human','2','0.390845729166667','0.390845729166667'),
('PAK1_HUMAN','2qme_I','I','crystal structure of human rac3 in complex with crib domain p21-activated kinase 1 (pak1)','1.75','0.562868005952381','0.562868005952381'),
('MARK3_HUMAN','2qnj_B','B','kinase and ubiquitin-associated domains of mark3/par-1','2.7','0.266082200727513','0.266082200727513'),
('EPHA3_HUMAN','2qo2_A','A','human epha3 kinase and juxtamembrane region, dephosphorylated, apo structure','1.6','0.601485059523809','0.601485059523809'),
('EPHA3_HUMAN','2qo7_A','A','human epha3 kinase and juxtamembrane region, dephosphorylate bound','1.6','0.593351056547619','0.593351056547619'),
('EPHA3_HUMAN','2qo9_A','A','human epha3 kinase and juxtamembrane region, phosphorylated, amp-pnp bound','1.55','0.612398448060676','0.612398448060676'),
('EPHA3_HUMAN','2qob_A','A','human epha3 kinase domain, base structure','1.65','0.589003373917749','0.589003373917749'),
('EPHA3_HUMAN','2qoc_A','A','human epha3 kinase domain, phosphorylated, amp-pnp bound structure','1.25','0.799036324404762','0.799036324404762'),
('EPHA3_HUMAN','2qod_A','A','human epha3 kinase and juxtamembrane region, y602f mutant','1.15','0.831440678700828','0.831440678700828'),
('EPHA3_HUMAN','2qof_A','A','human epha3 kinase and juxtamembrane region, y596f mutant','1.2','0.80440875','0.80440875'),
('EPHA3_HUMAN','2qoi_A','A','human epha3 kinase and juxtamembrane region, y596f:y602f double mutant','1.25','0.769846056547619','0.769846056547619'),
('EPHA3_HUMAN','2qok_A','A','human epha3 kinase and juxtamembrane region, y596f:y602f:s768a triple mutant','1.2','0.795141651785714','0.795141651785714'),
('EPHA3_HUMAN','2qol_A','A','human epha3 kinase and juxtamembrane region, y596:y602:s768g triple mutant','1.07','0.893686224966622','0.893686224966622'),
('EPHA3_HUMAN','2qon_A','A','human epha3 kinase and juxtamembrane region, y596f:y602f:y74 mutant','1.79','0.531403086924714','0.531403086924714'),
('EPHA3_HUMAN','2qoo_A','A','human epha3 kinase and juxtamembrane region, y596f:y602f:y742f triple mutant','1.25','0.765063526785714','0.765063526785714'),
('EPHA3_HUMAN','2qoq_A','A','human epha3 kinase and juxtamembrane region, base, amp-pnp bound structure','1.6','0.584306979166667','0.584306979166667'),
('VGFR2_HUMAN','2qu5_A','A','crystal structure of the vegfr2 kinase domain in complex with a benzimidazole inhibitor','2.95','0.245670550847458','0.245670550847458'),
('VGFR2_HUMAN','2qu6_A','A','crystal structure of the vegfr2 kinase domain in complex with a benzoxazole inhibitor','2.1','0.380163630952381','0.380163630952381'),
('VGFR2_HUMAN','2qu6_B','B','crystal structure of the vegfr2 kinase domain in complex with a benzoxazole inhibitor','2.1','0.380163630952381','0.380163630952381'),
('CHK1_HUMAN','2r0u_A','A','crystal structure of chek1 in complex with inhibitor 54','1.9','0.447621756735589','0.447621756735589'),
('EPHA5_HUMAN','2r2p_A','A','kinase domain of human ephrin type-a receptor 5 (epha5)','2.4','0.339020133928571','0.339020133928571'),
('CDK2_HUMAN','2r3f_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.5','0.587230089285714','0.587230089285714'),
('CDK2_HUMAN','2r3g_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.55','0.589411513536866','0.589411513536866'),
('CDK2_HUMAN','2r3h_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.5','0.595161904761905','0.595161904761905'),
('CDK2_HUMAN','2r3i_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.28','0.730370193452381','0.730370193452381'),
('CDK2_HUMAN','2r3j_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.65','0.527574802489177','0.527574802489177'),
('CDK2_HUMAN','2r3k_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.7','0.519967838760504','0.519967838760504'),
('CDK2_HUMAN','2r3l_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.65','0.534408924512987','0.534408924512987'),
('CDK2_HUMAN','2r3m_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.7','0.525012957808123','0.525012957808123'),
('CDK2_HUMAN','2r3n_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.63','0.541594358110575','0.541594358110575'),
('CDK2_HUMAN','2r3o_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.8','0.490363635912698','0.490363635912698'),
('CDK2_HUMAN','2r3p_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.66','0.538810501649455','0.538810501649455'),
('CDK2_HUMAN','2r3q_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.35','0.685704074074074','0.685704074074074'),
('CDK2_HUMAN','2r3r_A','A','crystal structure of cyclin-dependent kinase 2 with inhibitor','1.47','0.618416885629252','0.618416885629252'),
('ERBB4_HUMAN','2r4b_A','A','erbb4 kinase domain complexed with a thienopyrimidine inhibi','2.4','0.346215297619048','0.346215297619048'),
('ERBB4_HUMAN','2r4b_B','B','erbb4 kinase domain complexed with a thienopyrimidine inhibi','2.4','0.346215297619048','0.346215297619048'),
('SGK1_HUMAN','2r5t_A','A','crystal structure of inactive serum and glucocorticoid- regulated kinase 1 in complex with amp-pnp','1.9','0.461985804354637','0.461985804354637'),
('CDK2_HUMAN','2r64_A','A','crystal structure of a 3-aminoindazole compound with cdk2','2.3','0.334423873576605','0.334423873576605'),
('PDPK1_HUMAN','2r7b_A','A','crystal structure of the phosphoinositide-dependent kinase- 1 (pdk-1)catalytic domain bound to a dibenzonaphthyridine inhibitor','2.7','0.263079879298942','0.263079879298942'),
('MK10_HUMAN','2r9s_A','A','c-jun n-terminal kinase 3 with 3,5-disubstituted quinoline i','2.4','0.328645401785714','0.328645401785714'),
('MK10_HUMAN','2r9s_B','B','c-jun n-terminal kinase 3 with 3,5-disubstituted quinoline i','2.4','0.328645401785714','0.328645401785714'),
('EPHA7_HUMAN','2rei_A','A','kinase domain of human ephrin type-a receptor 7 (epha7)','1.6','0.614691294642857','0.614691294642857'),
('M3K10_HUMAN','2rf0_A','A','crystal structure of human mixed lineage kinase map3k10 sh3','2','0.457859136904762','0.457859136904762'),
('M3K10_HUMAN','2rf0_B','B','crystal structure of human mixed lineage kinase map3k10 sh3','2','0.457859136904762','0.457859136904762'),
('M3K10_HUMAN','2rf0_C','C','crystal structure of human mixed lineage kinase map3k10 sh3','2','0.457859136904762','0.457859136904762'),
('M3K10_HUMAN','2rf0_D','D','crystal structure of human mixed lineage kinase map3k10 sh3','2','0.457859136904762','0.457859136904762'),
('EGFR_HUMAN','2rf9_A','A','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','3.5','0.0714469345238095','0.0714469345238095'),
('EGFR_HUMAN','2rfd_A','A','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','3.6','0.133577465277778','0.133577465277778'),
('EGFR_HUMAN','2rfe_A','A','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','2.9','0.222860398706897','0.222860398706897'),
('Q59FL8_HUMAN','2rfe_B','B','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','2.9','0.222860398706897','0.222860398706897'),
('A8K2T7_HUMAN','2rfe_C','C','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','2.9','0.222860398706897','0.222860398706897'),
('EGFR_HUMAN','2rfe_D','D','crystal structure of the complex between the egfr kinase domain and a mig6 peptide','2.9','0.222860398706897','0.222860398706897'),
('Q59EB3_HUMAN','2rfn_A','A','x-ray structure of c-met with inhibitor.','2.5','0.279749880952381','0.279749880952381'),
('MET_HUMAN','2rfn_B','B','x-ray structure of c-met with inhibitor.','2.5','0.279749880952381','0.279749880952381'),
('MET_HUMAN','2rfs_A','A','x-ray structure of su11274 bound to c-met','2.2','0.370796139069264','0.370796139069264'),
('MK14_HUMAN','2rg5_A','A','phenylalanine pyrrolotriazine p38 alpha map kinase inhibitor compound 11b','2.4','0.265937678571429','0.265937678571429'),
('MK14_HUMAN','2rg6_A','A','phenylalanine pyrrolotriazine p38 alpha map kinase inhibitor compound 11j','1.72','0.506536092884828','0.506536092884828'),
('EGFR_HUMAN','2rgp_A','A','structure of egfr in complex with hydrazone, a potent dual inhibitor','2','0.398807470238095','0.398807470238095'),
('PLK1_HUMAN','2rku_A','A','structure of plk1 in complex with bi2536','1.95','0.451716346153846','0.451716346153846'),
('VGFR2_HUMAN','2rl5_A','A','crystal structure of the vegfr2 kinase domain in complex with a 2,3-dihydro-1,4-benzoxazine inhibitor','2.65','0.321760261399371','0.321760261399371'),
('PKN1_HUMAN','2rmk_B','B','rac1/prk1 complex',NULL,'0.0339218452380952','0.0339218452380952'),
('TITIN_HUMAN','2rq8_A','A','solution nmr structure of titin i27 domain mutant',NULL,'0.0255198511904762','0.0255198511904762'),
('SRC_HUMAN','2src_A','A','crystal structure of human tyrosine-protein kinase c-src, in complex with amp-pnp','1.5','0.531947693452381','0.531947693452381'),
('CDK2_HUMAN','2uue_A','A','replace: a strategy for iterative design of cyclin binding groove inhibitors','2.06','0.408706030108645','0.408706030108645'),
('CDK2_HUMAN','2uue_C','C','replace: a strategy for iterative design of cyclin binding groove inhibitors','2.06','0.408706030108645','0.408706030108645'),
('SLK_HUMAN','2uv2_A','A','crystal structure of human ste20-like kinase bound to 4-(4-( 5-cyclopropyl-1h-pyrazol-3-ylamino)-quinazolin-2-ylamino)- phenyl)-acetonitrile','2.3','0.387611552148033','0.387611552148033'),
('AKT1_HUMAN','2uvm_A','A','structure of pkbalpha ph domain in complex with a novel inositol headgroup surrogate, benzene 1,2,3,4- tetrakisphosphate','1.94','0.386183858001964','0.386183858001964'),
('AKT2_HUMAN','2uw9_A','A','structure of pkb-beta (akt2) complexed with 4-(4-chloro- phenyl)-4-(4-(1h-pyrazol-4-yl)-phenyl)-piperidine','2.1','0.364773110119048','0.364773110119048'),
('GSK3B_HUMAN','2uw9_C','C','structure of pkb-beta (akt2) complexed with 4-(4-chloro- phenyl)-4-(4-(1h-pyrazol-4-yl)-phenyl)-piperidine','2.1','0.364773110119048','0.364773110119048'),
('KCC2G_HUMAN','2ux0_A','A','structure of the oligomerisation domain of calcium- calmodulin dependent protein kinase ii gamma','2.46','0.360709079921603','0.360709079921603'),
('KCC2G_HUMAN','2ux0_C','C','structure of the oligomerisation domain of calcium- calmodulin dependent protein kinase ii gamma','2.46','0.360709079921603','0.360709079921603'),
('KCC2G_HUMAN','2ux0_D','D','structure of the oligomerisation domain of calcium- calmodulin dependent protein kinase ii gamma','2.46','0.360709079921603','0.360709079921603'),
('CDK2_HUMAN','2uzb_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.7','0.271570623346561','0.271570623346561'),
('CDK2_HUMAN','2uzb_C','C','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.7','0.271570623346561','0.271570623346561'),
('CDK2_HUMAN','2uzd_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.72','0.267380258228291','0.267380258228291'),
('CDK2_HUMAN','2uzd_C','C','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.72','0.267380258228291','0.267380258228291'),
('CDK2_HUMAN','2uze_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.4','0.335447232142857','0.335447232142857'),
('CDK2_HUMAN','2uze_C','C','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.4','0.335447232142857','0.335447232142857'),
('CDK2_HUMAN','2uzl_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.4','0.325983556547619','0.325983556547619'),
('CDK2_HUMAN','2uzl_C','C','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.4','0.325983556547619','0.325983556547619'),
('CDK2_HUMAN','2uzn_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.3','0.334112683100414','0.334112683100414'),
('CDK2_HUMAN','2uzo_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.3','0.331513918219462','0.331513918219462'),
('KPCG_HUMAN','2uzp_A','A','crystal structure of the c2 domain of human protein kinase c gamma.','2','0.473733943452381','0.473733943452381'),
('KPCG_HUMAN','2uzp_B','B','crystal structure of the c2 domain of human protein kinase c gamma.','2','0.473733943452381','0.473733943452381'),
('KPCG_HUMAN','2uzp_C','C','crystal structure of the c2 domain of human protein kinase c gamma.','2','0.473733943452381','0.473733943452381'),
('AKT1_HUMAN','2uzr_A','A','a transforming mutation in the pleckstrin homology domain of akt1 in cancer (akt1-ph_e17k)','1.94','0.429341372882916','0.429341372882916'),
('AKT1_HUMAN','2uzs_A','A','a transforming mutation in the pleckstrin homology domain of akt1 in cancer (akt1-ph_e17k)','2.46','0.289396267421603','0.289396267421603'),
('MET_HUMAN','2uzx_B','B','structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: crystal form i','2.8','0.190545729166667','0.190545729166667'),
('MET_HUMAN','2uzx_D','D','structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: crystal form i','2.8','0.190545729166667','0.190545729166667'),
('MET_HUMAN','2uzy_B','B','structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: low resolution, crystal form ii','4','0.0808635714285714','0.0808635714285714'),
('MET_HUMAN','2uzy_D','D','structure of the human receptor tyrosine kinase met in complex with the listeria monocytogenes invasion protein inlb: low resolution, crystal form ii','4','0.0808635714285714','0.0808635714285714'),
('CDK2_HUMAN','2v0d_A','A','crystal structure of human cdk2 complexed with a thiazolidinone inhibitor','2.2','0.371697537878788','0.371697537878788'),
('CDK2_HUMAN','2v22_C','C','replace: a strategy for iterative design of cyclin binding groove inhibitors','2.6','0.319404223901099','0.319404223901099'),
('OXSR1_HUMAN','2v3s_A','A','structural insights into the recognition of substrates and activators by the osr1 kinase','1.7','0.530818463760504','0.530818463760504'),
('OXSR1_HUMAN','2v3s_B','B','structural insights into the recognition of substrates and activators by the osr1 kinase','1.7','0.530818463760504','0.530818463760504'),
('WNK4_HUMAN','2v3s_C','C','structural insights into the recognition of substrates and activators by the osr1 kinase','1.7','0.530818463760504','0.530818463760504'),
('WNK4_HUMAN','2v3s_D','D','structural insights into the recognition of substrates and activators by the osr1 kinase','1.7','0.530818463760504','0.530818463760504'),
('ROCK1_HUMAN','2v55_A','A','mechanism of multi-site phosphorylation from a rock-i:rhoe complex structure','3.7','0.0718611928893179','0.0718611928893179'),
('ROCK1_HUMAN','2v55_C','C','mechanism of multi-site phosphorylation from a rock-i:rhoe complex structure','3.7','0.0718611928893179','0.0718611928893179'),
('PLK1_HUMAN','2v5q_A','A','crystal structure of wild-type plk-1 kinase domain in complex with a selective darpin','2.3','0.399496775362319','0.399496775362319'),
('PLK1_HUMAN','2v5q_B','B','crystal structure of wild-type plk-1 kinase domain in complex with a selective darpin','2.3','0.399496775362319','0.399496775362319'),
('Q05CR6_HUMAN','2v62_A','A','structure of vaccinia-related kinase 2','1.7','0.535360963760504','0.535360963760504'),
('VRK2_HUMAN','2v62_B','B','structure of vaccinia-related kinase 2','1.7','0.535360963760504','0.535360963760504'),
('ABL1_HUMAN','2v7a_A','A','crystal structure of the t315i abl mutant in complex with the inhibitor pha-739358','2.5','0.310248407738095','0.310248407738095'),
('ABL1_HUMAN','2v7a_B','B','crystal structure of the t315i abl mutant in complex with the inhibitor pha-739358','2.5','0.310248407738095','0.310248407738095'),
('KCC2G_HUMAN','2v7o_A','A','crystal structure of human calcium-calmodulin-dependent protein kinase ii gamma','2.25','0.413618462301587','0.413618462301587'),
('CLK1_HUMAN','2vag_A','A','crystal structure of di-phosphorylated human clk1 in complex with a novel substituted indole inhibitor','1.8','0.52365876984127','0.52365876984127'),
('DMPK_HUMAN','2vd5_A','A','structure of human myotonic dystrophy protein kinase in complex with the bisindoylmaleide inhibitor bim viii','2.8','0.276254255952381','0.276254255952381'),
('DMPK_HUMAN','2vd5_B','B','structure of human myotonic dystrophy protein kinase in complex with the bisindoylmaleide inhibitor bim viii','2.8','0.276254255952381','0.276254255952381'),
('KIT_HUMAN','2vif_A','A','crystal structure of socs6 sh2 domain in complex with a c-ki phosphopeptide','1.45','0.70090777658046','0.70090777658046'),
('PDPK1_HUMAN','2vki_A','A','structure of the pdk1 ph domain k465e mutant','1.8','0.522640600198413','0.522640600198413'),
('KCC2D_HUMAN','2vn9_A','A','crystal structure of human calcium calmodulin dependent protein kinase ii delta isoform 1, camkd','2.3','0.36964159679089','0.36964159679089'),
('KCC2D_HUMAN','2vn9_B','B','crystal structure of human calcium calmodulin dependent protein kinase ii delta isoform 1, camkd','2.3','0.36964159679089','0.36964159679089'),
('CDK2_HUMAN','2vta_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design.','2','0.384443050595238','0.384443050595238'),
('CDK2_HUMAN','2vth_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.9','0.447178676378446','0.447178676378446'),
('CDK2_HUMAN','2vti_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2','0.453222008928571','0.453222008928571'),
('CDK2_HUMAN','2vtj_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2.2','0.378584234307359','0.378584234307359'),
('CDK2_HUMAN','2vtl_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2','0.436216279761905','0.436216279761905'),
('CDK2_HUMAN','2vtm_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2.25','0.327720873015873','0.327720873015873'),
('CDK2_HUMAN','2vtn_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2.2','0.34389511228355','0.34389511228355'),
('CDK2_HUMAN','2vto_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design.','2.19','0.392980215875734','0.392980215875734'),
('CDK2_HUMAN','2vtp_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','2.15','0.396007618355482','0.396007618355482'),
('CDK2_HUMAN','2vtq_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.9','0.444516786497494','0.444516786497494'),
('CDK2_HUMAN','2vtr_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.9','0.433232590068922','0.433232590068922'),
('CDK2_HUMAN','2vts_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.9','0.43005320018797','0.43005320018797'),
('CDK2_HUMAN','2vtt_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.68','0.513107708333333','0.513107708333333'),
('CDK2_HUMAN','2vu3_A','A','identification of n-(4-piperidinyl)-4-(2,6- dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (at7519), a novel cyclin dependent kinase inhibitor using fragment- based x-ray crystallography and structure based drug design','1.85','0.455369141731017','0.455369141731017'),
('HASP_HUMAN','2vuw_A','A','structure of human haspin kinase domain','1.8','0.556131984126984','0.556131984126984'),
('CDK2_HUMAN','2vv9_A','A','cdk2 in complex with an imidazole piperazine','1.9','0.462421280545113','0.462421280545113'),
('OXSR1_HUMAN','2vwi_D','D','structure of the osr1 kinase, a hypertension drug target','2.15','0.352471427879291','0.352471427879291'),
('EPHB4_HUMAN','2vwu_A','A','ephb4 kinase domain inhibitor complex','2','0.470731875','0.470731875'),
('EPHB4_HUMAN','2vwv_A','A','ephb4 kinase domain inhibitor complex','1.9','0.43052282816416','0.43052282816416'),
('EPHB4_HUMAN','2vww_A','A','ephb4 kinase domain inhibitor complex','1.9','0.48590382518797','0.48590382518797'),
('EPHB4_HUMAN','2vwx_A','A','ephb4 kinase domain inhibitor complex','1.65','0.588239147727273','0.588239147727273'),
('EPHB4_HUMAN','2vwy_A','A','ephb4 kinase domain inhibitor complex','1.65','0.565567168560606','0.565567168560606'),
('EPHB4_HUMAN','2vwz_A','A','ephb4 kinase domain inhibitor complex','1.65','0.58810194534632','0.58810194534632'),
('EPHB4_HUMAN','2vx0_A','A','ephb4 kinase domain inhibitor complex','2.1','0.436558169642857','0.436558169642857'),
('EPHB4_HUMAN','2vx1_A','A','ephb4 kinase domain inhibitor complex','1.65','0.585050531655844','0.585050531655844'),
('DYR1A_HUMAN','2vx3_A','A','crystal structure of the human dual specificity tyrosine- phosphorylation-regulated kinase 1a','2.4','0.370254017857143','0.370254017857143'),
('KCC2A_HUMAN','2vz6_B','B','structure of human calcium calmodulin dependent protein kinase type ii alpha (camk2a) in complex with indirubin e804','2.3','0.416968769409938','0.416968769409938'),
('CDK2_HUMAN','2w05_A','A','structure of cdk2 in complex with an imidazolyl pyrimidine, compound 5b','1.9','0.43884189066416','0.43884189066416'),
('CDK2_HUMAN','2w06_A','A','structure of cdk2 in complex with an imidazolyl pyrimidine, compound 5c','2.04','0.428256956407563','0.428256956407563'),
('CHK2_HUMAN','2w0j_A','A','crystal structure of chk2 in complex with nsc 109555, a specific inhibitor','2.05','0.416027601263066','0.416027601263066'),
('CDK2_HUMAN','2w17_A','A','cdk2 in complex with the imidazole pyrimidine amide, compound (s)-8b','2.15','0.345271204665006','0.345271204665006'),
('AURKA_HUMAN','2w1c_A','A','structure determination of aurora kinase in complex with inhibitor','3.24','0.152098567570547','0.152098567570547'),
('AURKA_HUMAN','2w1d_A','A','structure determination of aurora kinase in complex with inhibitor','2.97','0.188125783128908','0.188125783128908'),
('AURKA_HUMAN','2w1e_A','A','structure determination of aurora kinase in complex with inhibitor','2.93','0.194926392613359','0.194926392613359'),
('AURKA_HUMAN','2w1f_A','A','structure determination of aurora kinase in complex with inhibitor','2.85','0.213197505482456','0.213197505482456'),
('AURKA_HUMAN','2w1g_A','A','structure determination of aurora kinase in complex with inhibitor','2.71','0.252298035274996','0.252298035274996'),
('CDK2_HUMAN','2w1h_A','A','fragment-based discovery of the pyrazol-4-yl urea (at9283), a multi-targeted kinase inhibitor with potent aurora kinase activity','2.15','0.320764820736434','0.320764820736434'),
('JAK2_HUMAN','2w1i_A','A','structure determination of aurora kinase in complex with inhibitor','2.6','0.288380964972527','0.288380964972527'),
('JAK2_HUMAN','2w1i_B','B','structure determination of aurora kinase in complex with inhibitor','2.6','0.288380964972527','0.288380964972527'),
('KCC2D_HUMAN','2w2c_H','H','structure of the tetradecameric oligomerisation domain of calcium-calmodulin dependent protein kinase ii delta','2.7','0.301953197751323','0.301953197751323'),
('DAPK1_HUMAN','2w4j_A','A','x-ray structure of a dap-kinase 2-277','1.3','0.78865352220696','0.78865352220696'),
('DAPK1_HUMAN','2w4k_A','A','x-ray structure of a dap-kinase 2-302','1.9','0.477324688283208','0.477324688283208'),
('KCC4_HUMAN','2w4o_A','A','crystal structure of human camk4 in complex with 4-amino( sulfamoyl-phenylamino)-triazole-carbothioic acid (2,6- difluoro-phenyl)-amide)','2.17','0.37001825796851','0.37001825796851'),
('NEK2_HUMAN','2w5a_A','A','human nek2 kinase adp-bound','1.55','0.622229192108295','0.622229192108295'),
('NEK2_HUMAN','2w5b_A','A','human nek2 kinase atpgammas-bound','2.4','0.356348020833333','0.356348020833333'),
('NEK2_HUMAN','2w5h_A','A','human nek2 kinase apo','2.33','0.367224742808604','0.367224742808604'),
('MAST4_HUMAN','2w7r_A','A','structure of the pdz domain of human microtubule associated serine-threonine kinase 4','1.6','0.579621651785714','0.579621651785714'),
('MAST4_HUMAN','2w7r_B','B','structure of the pdz domain of human microtubule associated serine-threonine kinase 4','1.6','0.579621651785714','0.579621651785714'),
('CHK2_HUMAN','2w7x_A','A','cellular inhibition of checkpoint kinase 2 and potentiation of cytotoxic drugs by novel chk2 inhibitor pv1019','2.07','0.434540909463423','0.434540909463423'),
('CDK4_HUMAN','2w96_B','B','crystal structure of cdk4 in complex with a d-type cyclin','2.3','0.341215138457557','0.341215138457557'),
('CDK4_HUMAN','2w99_B','B','crystal structure of cdk4 in complex with a d-type cyclin','2.8','0.220734285714286','0.220734285714286'),
('CDK4_HUMAN','2w9f_B','B','crystal structure of cdk4 in complex with a d-type cyclin','2.85','0.208764916196742','0.208764916196742'),
('CDK4_HUMAN','2w9z_B','B','crystal structure of cdk4 in complex with a d-type cyclin','2.45','0.287161509353742','0.287161509353742'),
('MK10_HUMAN','2waj_A','A','crystal structure of human jnk3 complexed with a 1-aryl-3,4- dihydroisoquinoline inhibitor','2.4','0.350414211309524','0.350414211309524'),
('HASP_HUMAN','2wb8_A','A','crystal structure of haspin kinase','2.15','0.347657782045958','0.347657782045958'),
('MET_HUMAN','2wd1_A','A','human c-met kinase in complex with azaindole inhibitor','2','0.429350059523809','0.429350059523809'),
('KCC2D_HUMAN','2wel_A','A','crystal structure of su6656-bound calcium/calmodulin- dependent protein kinase ii delta in complex with calmodulin','1.9','0.519657351973684','0.519657351973684'),
('CDK2_HUMAN','2wev_A','A','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.3','0.368945078933747','0.368945078933747'),
('CDK2_HUMAN','2wev_C','C','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.3','0.368945078933747','0.368945078933747'),
('CDK2_HUMAN','2wfy_A','A','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.53','0.311992512234143','0.311992512234143'),
('CDK2_HUMAN','2wfy_C','C','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.53','0.311992512234143','0.311992512234143'),
('MET_HUMAN','2wgj_A','A','x-ray structure of pf-02341066 bound to the kinase domain of c-met','2','0.403013526785714','0.403013526785714'),
('KPCE_HUMAN','2wh0_Q','Q','recognition of an intrachain tandem 14-3-3 binding site within protein kinase c epsilon','2.25','0.372161111111111','0.372161111111111'),
('KPCE_HUMAN','2wh0_R','R','recognition of an intrachain tandem 14-3-3 binding site within protein kinase c epsilon','2.25','0.372161111111111','0.372161111111111'),
('CDK2_HUMAN','2whb_A','A','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.9','0.249824505849754','0.249824505849754'),
('CDK2_HUMAN','2whb_C','C','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.9','0.249824505849754','0.249824505849754'),
('CDK2_HUMAN','2wih_A','A','structure of cdk2-cyclin a with pha-848125','2.5','0.327463482142857','0.327463482142857'),
('CDK2_HUMAN','2wih_C','C','structure of cdk2-cyclin a with pha-848125','2.5','0.327463482142857','0.327463482142857'),
('CDK2_HUMAN','2wip_A','A','structure of cdk2-cyclin a complexed with 8-anilino-1- methyl-4,5-dihydro-1h-pyrazolo[4,3-h] quinazoline-3- carboxylic acid','2.8','0.279311205357143','0.279311205357143'),
('CDK2_HUMAN','2wip_C','C','structure of cdk2-cyclin a complexed with 8-anilino-1- methyl-4,5-dihydro-1h-pyrazolo[4,3-h] quinazoline-3- carboxylic acid','2.8','0.279311205357143','0.279311205357143'),
('MET_HUMAN','2wkm_A','A','x-ray structure of pha-00665752 bound to the kinase domain of c-met','2.2','0.383446838474026','0.383446838474026'),
('CDK2_HUMAN','2wma_A','A','structural and thermodynamic consequences of cyclization of ligands for the recruitment site of cyclin a','2.8','0.247068303571429','0.247068303571429'),
('CDK2_HUMAN','2wmb_A','A','structural and thermodynamic consequences of cyclization of ligands for the recruitment site of cyclin a','2.6','0.262689625686813','0.262689625686813'),
('CHK1_HUMAN','2wmq_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.48','0.30124497311828','0.30124497311828'),
('CHK1_HUMAN','2wmr_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.43','0.323355074221046','0.323355074221046'),
('CHK1_HUMAN','2wms_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.7','0.269520697751323','0.269520697751323'),
('CHK1_HUMAN','2wmt_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.55','0.299434719887955','0.299434719887955'),
('CHK1_HUMAN','2wmu_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.6','0.277275265567765','0.277275265567765'),
('CHK1_HUMAN','2wmv_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.01','0.425137095549041','0.425137095549041'),
('CHK1_HUMAN','2wmw_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.43','0.305926830173427','0.305926830173427'),
('CHK1_HUMAN','2wmx_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.45','0.307806405187075','0.307806405187075'),
('B7Z2K7_HUMAN','2wnt_A','A','crystal structure of the human ribosomal protein s6 kinase','2.4','0.363918095238095','0.363918095238095'),
('KS6A1_HUMAN','2wnt_B','B','crystal structure of the human ribosomal protein s6 kinase','2.4','0.363918095238095','0.363918095238095'),
('EPHA4_HUMAN','2wo1_B','B','crystal structure of the epha4 ligand binding domain','1.85','0.455768948278636','0.455768948278636'),
('EPHA4_HUMAN','2wo2_A','A','crystal structure of the epha4-ephrinb2 complex','2.45','0.325810824829932','0.325810824829932'),
('EPHA4_HUMAN','2wo3_A','A','crystal structure of the epha4-ephrina2 complex','2.35','0.366250277988855','0.366250277988855'),
('DYR1A_HUMAN','2wo6_A','A','human dual-specificity tyrosine-phosphorylation-regulated kinase 1a in complex with a consensus substrate peptide','2.5','0.359750907738095','0.359750907738095'),
('TGFR1_HUMAN','2wot_A','A','alk5 in complex with 4-((5,6-dimethyl-2-(2-pyridyl)-3- pyridyl)oxy)-n-(3,4,5-trimethoxyphenyl)pyridin-2-amine','1.85','0.511332504826255','0.511332504826255'),
('TGFR1_HUMAN','2wou_A','A','alk5 in complex with 4-((4-((2,6-dimethyl-3-pyridyl)oxy)-2- pyridyl)amino)benzenesulfonamide','2.3','0.350819617624224','0.350819617624224'),
('TITIN_HUMAN','2wp3_T','T','crystal structure of the titin m10-obscurin like 1 ig complex','1.48','0.624129559604247','0.624129559604247'),
('CDK2_HUMAN','2wpa_A','A','optimisation of 6,6-dimethyl pyrrolo 3,4-c pyrazoles: identification of pha-793887, a potent cdk inhibitor suitable for intravenous dosing','2.51','0.294929603668659','0.294929603668659'),
('CDK2_HUMAN','2wpa_C','C','optimisation of 6,6-dimethyl pyrrolo 3,4-c pyrazoles: identification of pha-793887, a potent cdk inhibitor suitable for intravenous dosing','2.51','0.294929603668659','0.294929603668659'),
('TIE2_HUMAN','2wqb_A','A','structure of the tie2 kinase domain in complex with a thiazolopyrimidine inhibitor','2.95','0.245190491323648','0.245190491323648'),
('AURKA_HUMAN','2wqe_A','A','structure of s155r aurora-a somatic mutant','2.5','0.314421071428571','0.314421071428571'),
('NEK7_HUMAN','2wqm_A','A','structure of apo human nek7','2.1','0.443382886904762','0.443382886904762'),
('NEK7_HUMAN','2wqn_A','A','structure of adp-bound human nek7','2.3','0.382909751552795','0.382909751552795'),
('NEK2_HUMAN','2wqo_A','A','structure of nek2 bound to the aminopyridine cct241950','2.17','0.399906888920891','0.399906888920891'),
('CHK2_HUMAN','2wtc_A','A','crystal structure of chk2 in complex with an inhibitor','3','0.260604627976191','0.260604627976191'),
('CHK2_HUMAN','2wtd_A','A','crystal structure of chk2 in complex with an inhibitor','2.75','0.293073818993506','0.293073818993506'),
('CHK2_HUMAN','2wti_A','A','crystal structure of chk2 in complex with an inhibitor','2.5','0.347087901785714','0.347087901785714'),
('CHK2_HUMAN','2wtj_A','A','crystal structure of chk2 in complex with an inhibitor','2.1','0.433291800595238','0.433291800595238'),
('STRAA_HUMAN','2wtk_B','B','structure of the heterotrimeric lkb1-stradalpha-mo25alpha complex','2.65','0.257042597708895','0.257042597708895'),
('STK11_HUMAN','2wtk_C','C','structure of the heterotrimeric lkb1-stradalpha-mo25alpha complex','2.65','0.257042597708895','0.257042597708895'),
('Q59FA7_HUMAN','2wtk_F','F','structure of the heterotrimeric lkb1-stradalpha-mo25alpha complex','2.65','0.257042597708895','0.257042597708895'),
('AURKA_HUMAN','2wtv_A','A','aurora-a inhibitor structure','2.4','0.374770089285714','0.374770089285714'),
('B4DX16_HUMAN','2wtv_B','B','aurora-a inhibitor structure','2.4','0.374770089285714','0.374770089285714'),
('B4DX16_HUMAN','2wtv_C','C','aurora-a inhibitor structure','2.4','0.374770089285714','0.374770089285714'),
('AURKA_HUMAN','2wtv_D','D','aurora-a inhibitor structure','2.4','0.374770089285714','0.374770089285714'),
('AURKA_HUMAN','2wtw_A','A','aurora-a inhibitor structure (2nd crystal form)','3.3','0.154765689935065','0.154765689935065'),
('CLK3_HUMAN','2wu6_A','A','crystal structure of the human clk3 in complex with dki','1.92','0.495409866071429','0.495409866071429'),
('CLK3_HUMAN','2wu7_A','A','crystal structure of the human clk3 in complex with v25','2.25','0.39884310515873','0.39884310515873'),
('DDR2_HUMAN','2wuh_A','A','crystal structure of the ddr2 discoidin domain bound to a triple-helical collagen peptide','1.6','0.540492767857143','0.540492767857143'),
('BUB1B_HUMAN','2wvi_A','A','crystal structure of the n-terminal domain of bubr1','1.8','0.459649796626984','0.459649796626984'),
('TITIN_HUMAN','2wwk_T','T','crystal structure of the titin m10-obscurin like 1 ig f17r mutant complex','1.7','0.51402018995098','0.51402018995098'),
('TITIN_HUMAN','2wwm_D','D','crystal structure of the titin m10-obscurin like 1 ig complex in space group p1','2.3','0.363080302148033','0.363080302148033'),
('TITIN_HUMAN','2wwm_T','T','crystal structure of the titin m10-obscurin like 1 ig complex in space group p1','2.3','0.363080302148033','0.363080302148033'),
('CDK2_HUMAN','2wxv_A','A','structure of cdk2-cyclin a with a pyrazolo(4,3-h) quinazoline-3-carboxamide inhibitor','2.6','0.292219402472527','0.292219402472527'),
('CDK2_HUMAN','2wxv_C','C','structure of cdk2-cyclin a with a pyrazolo(4,3-h) quinazoline-3-carboxamide inhibitor','2.6','0.292219402472527','0.292219402472527'),
('A9CP04_HUMAN','2wzj_A','A','catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant','2.79','0.290222016449053','0.290222016449053'),
('A9CP04_HUMAN','2wzj_B','B','catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant','2.79','0.290222016449053','0.290222016449053'),
('A9CP04_HUMAN','2wzj_C','C','catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant','2.79','0.290222016449053','0.290222016449053'),
('A9CP04_HUMAN','2wzj_E','E','catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant','2.79','0.290222016449053','0.290222016449053'),
('A9CP04_HUMAN','2wzj_F','F','catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant','2.79','0.290222016449053','0.290222016449053'),
('DAPK1_HUMAN','2x0g_A','A','x-ray structure of a dap-kinase calmodulin complex','2.2','0.391519293831169','0.391519293831169'),
('EPHA2_HUMAN','2x10_A','A','crystal structure of the complete epha2 ectodomain',NULL,'-0.3','-0.3'),
('EPHA2_HUMAN','2x11_A','A','crystal structure of the complete epha2 ectodomain in complex with ephrin a5 receptor binding domain','4.83','0.0134422987836439','0.0134422987836439'),
('AKT3_HUMAN','2x18_E','E','the crystal structure of the ph domain of human akt3 protein kinase','1.46','0.659676655658839','0.659676655658839'),
('AKT3_HUMAN','2x18_H','H','the crystal structure of the ph domain of human akt3 protein kinase','1.46','0.659676655658839','0.659676655658839'),
('CDK2_HUMAN','2x1n_A','A','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.75','0.279250619588745','0.279250619588745'),
('CDK2_HUMAN','2x1n_C','C','truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design','2.75','0.279250619588745','0.279250619588745'),
('VGFR2_HUMAN','2x1w_L','L','crystal structure of vegf-c in complex with domains 2 and 3 of vegfr2','2.7','0.257944953703704','0.257944953703704'),
('VGFR2_HUMAN','2x1w_M','M','crystal structure of vegf-c in complex with domains 2 and 3 of vegfr2','2.7','0.257944953703704','0.257944953703704'),
('VGFR2_HUMAN','2x1w_N','N','crystal structure of vegf-c in complex with domains 2 and 3 of vegfr2','2.7','0.257944953703704','0.257944953703704'),
('VGFR2_HUMAN','2x1w_O','O','crystal structure of vegf-c in complex with domains 2 and 3 of vegfr2','2.7','0.257944953703704','0.257944953703704'),
('VGFR2_HUMAN','2x1x_R','R','crystal structure of vegf-c in complex with domains 2 and 3 of vegfr2 in a tetragonal crystal form','3.1','0.154166210637481','0.154166210637481'),
('RET_HUMAN','2x2k_A','A','crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor','2.6','0.307618985805861','0.307618985805861'),
('RET_HUMAN','2x2l_A','A','crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor','2','0.404919270833333','0.404919270833333'),
('RET_HUMAN','2x2m_A','A','crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor','2.5','0.31639974702381','0.31639974702381'),
('RET_HUMAN','2x2m_B','B','crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor','2.5','0.31639974702381','0.31639974702381'),
('RET_HUMAN','2x2u_A','A','first two cadherin-like domains from human ret','2','0.459592648809524','0.459592648809524'),
('AKT2_HUMAN','2x39_A','A','structure of 4-amino-n-(4-chlorobenzyl)-1-(7h-pyrrolo(2,3-d) pyrimidin-4-yl)piperidine-4-carboxamide bound to pkb','1.93','0.498332944192573','0.498332944192573'),
('GSK3B_HUMAN','2x39_C','C','structure of 4-amino-n-(4-chlorobenzyl)-1-(7h-pyrrolo(2,3-d) pyrimidin-4-yl)piperidine-4-carboxamide bound to pkb','1.93','0.498332944192573','0.498332944192573'),
('MYLK4_HUMAN','2x4f_A','A','the crystal structure of the human myosin light chain kinase loc340156.','2.67','0.30112025782504','0.30112025782504'),
('MYLK4_HUMAN','2x4f_B','B','the crystal structure of the human myosin light chain kinase loc340156.','2.67','0.30112025782504','0.30112025782504'),
('PAK4_HUMAN','2x4z_A','A','crystal structure of the human p21-activated kinase 4 in complex with pf-03758309','2.1','0.416479985119048','0.416479985119048'),
('AURKA_HUMAN','2x6d_A','A','aurora-a bound to an inhibitor','2.8','0.233179107142857','0.233179107142857'),
('AURKA_HUMAN','2x6e_A','A','aurora-a bound to an inhibitor','3.35','0.131520900186567','0.131520900186567'),
('TNIK_HUMAN','2x7f_B','B','crystal structure of the kinase domain of human traf2- and nck-interacting kinase with wee1chk1 inhibitor','2.8','0.265310639880952','0.265310639880952'),
('SRPK2_HUMAN','2x7g_A','A','structure of human serine-arginine-rich protein-specific kinase 2 (srpk2) bound to purvalanol b','2.5','0.342247232142857','0.342247232142857'),
('TGFR1_HUMAN','2x7o_A','A','crystal structure of tgfbri complexed with an indolinone inhibitor','3.7','0.0994464607464608','0.0994464607464608'),
('TGFR1_HUMAN','2x7o_B','B','crystal structure of tgfbri complexed with an indolinone inhibitor','3.7','0.0994464607464608','0.0994464607464608'),
('TGFR1_HUMAN','2x7o_C','C','crystal structure of tgfbri complexed with an indolinone inhibitor','3.7','0.0994464607464608','0.0994464607464608'),
('TGFR1_HUMAN','2x7o_D','D','crystal structure of tgfbri complexed with an indolinone inhibitor','3.7','0.0994464607464608','0.0994464607464608'),
('TGFR1_HUMAN','2x7o_E','E','crystal structure of tgfbri complexed with an indolinone inhibitor','3.7','0.0994464607464608','0.0994464607464608'),
('AURKA_HUMAN','2x81_A','A','structure of aurora a in complex with mln8054','2.91','0.238056361683849','0.238056361683849'),
('CHK1_HUMAN','2x8d_A','A','discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration','1.9','0.509457426378446','0.509457426378446'),
('CHK1_HUMAN','2x8e_A','A','discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration','2.5','0.26923837797619','0.26923837797619'),
('CHK1_HUMAN','2x8i_A','A','discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration','1.92','0.4756184375','0.4756184375'),
('TTK_HUMAN','2x9e_A','A','human mps1 in complex with nms-p715','3.1','0.209924023137481','0.209924023137481'),
('EPHB4_HUMAN','2x9f_A','A','ephb4 kinase domain inhibitor complex','1.75','0.56445056547619','0.56445056547619'),
('JAK2_HUMAN','2xa4_A','A','inhibitors of jak2 kinase domain','2.04','0.418940855217087','0.418940855217087'),
('Q8IXP2_HUMAN','2xa4_B','B','inhibitors of jak2 kinase domain','2.04','0.418940855217087','0.418940855217087'),
('VGFR1_HUMAN','2xac_C','C','structural insights into the binding of vegf-b by vegfr-1d2: recognition and specificity','2.71','0.166069925155948','0.166069925155948'),
('VGFR1_HUMAN','2xac_X','X','structural insights into the binding of vegf-b by vegfr-1d2: recognition and specificity','2.71','0.166069925155948','0.166069925155948'),
('ALK_HUMAN','2xb7_A','A','structure of human anaplastic lymphoma kinase in complex wit tae684','2.5','0.338414761904762','0.338414761904762'),
('ALK_HUMAN','2xba_A','A','structure of human anaplastic lymphoma kinase in complex with pha-e429','1.95','0.463845721153846','0.463845721153846'),
('CHK2_HUMAN','2xbj_A','A','crystal structure of chk2 in complex with an inhibitor','2.3','0.363852757505176','0.363852757505176'),
('PDPK1_HUMAN','2xch_A','A','crystal structure of pdk1 in complex with a pyrazoloquinazoline inhibitor','2','0.45352505952381','0.45352505952381'),
('PDPK1_HUMAN','2xck_A','A','crystal structure of pdk1 in complex with a pyrazoloquinazoline inhibitor','2.3','0.377321581909938','0.377321581909938'),
('CHK1_HUMAN','2xey_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.7','0.270525534060847','0.270525534060847'),
('CHK1_HUMAN','2xez_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.25','0.374468908730159','0.374468908730159'),
('CHK1_HUMAN','2xf0_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.4','0.334111681547619','0.334111681547619'),
('AKT2_HUMAN','2xh5_A','A','structure of 4-(4-tert-butylbenzyl)-1-(7h-pyrrolo(2,3-d) pyrimidin-4-yl)piperidin-4-amine bound to pkb','2.72','0.267744975490196','0.267744975490196'),
('GSK3B_HUMAN','2xh5_C','C','structure of 4-(4-tert-butylbenzyl)-1-(7h-pyrrolo(2,3-d) pyrimidin-4-yl)piperidin-4-amine bound to pkb','2.72','0.267744975490196','0.267744975490196'),
('STK25_HUMAN','2xik_A','A','structure of human ysk1 (yeast sps1-ste20-related kinase 1)','1.97','0.461240879864636','0.461240879864636'),
('VGFR2_HUMAN','2xir_A','A','crystal structure of the vegfr2 kinase domain in complex with pf-00337210 (n,2-dimethyl-6-(7-(2-morpholinoethoxy) quinolin-4-yloxy)benzofuran-3-carboxamide)','1.5','0.597524077380952','0.597524077380952'),
('PIM1_HUMAN','2xix_A','A','protein kinase pim-1 in complex with fragment-1 from crystallographic fragment screen','2.4','0.366052991071429','0.366052991071429'),
('PIM1_HUMAN','2xiy_A','A','protein kinase pim-1 in complex with fragment-2 from crystallographic fragment screen','2.2','0.426629323593074','0.426629323593074'),
('PIM1_HUMAN','2xiz_A','A','protein kinase pim-1 in complex with fragment-3 from crystallographic fragment screen','2.21','0.319395041949472','0.319395041949472'),
('PIM1_HUMAN','2xj0_A','A','protein kinase pim-1 in complex with fragment-4 from crystallographic fragment screen','3.1','0.241585808851767','0.241585808851767'),
('PIM1_HUMAN','2xj1_A','A','protein kinase pim-1 in complex with small molecule inibitor','2.13','0.418978106765594','0.418978106765594'),
('PIM1_HUMAN','2xj2_A','A','protein kinase pim-1 in complex with small molecule inhibitor','2.2','0.430309145021645','0.430309145021645'),
('NEK2_HUMAN','2xk3_A','A','structure of nek2 bound to aminopyrazine compound 35','2.2','0.41215724025974','0.41215724025974'),
('NEK2_HUMAN','2xk4_A','A','structure of nek2 bound to aminopyrazine compound 17','2.1','0.454703080357143','0.454703080357143'),
('NEK2_HUMAN','2xk6_A','A','structure of nek2 bound to aminopyrazine compound 36','2.2','0.40597380275974','0.40597380275974'),
('NEK2_HUMAN','2xk7_A','A','structure of nek2 bound to aminopyrazine compound 23','1.99','0.476079616385499','0.476079616385499'),
('NEK2_HUMAN','2xk8_A','A','structure of nek2 bound to aminopyrazine compound 15','2','0.47784400297619','0.47784400297619'),
('CHK2_HUMAN','2xk9_A','A','structural analysis of checkpoint kinase 2 (chk2) in complex inhibitor pv1533','2.35','0.376218655965046','0.376218655965046'),
('NEK2_HUMAN','2xkc_A','A','structure of nek2 bound to aminopyrazine compound 14','2.5','0.357215580357143','0.357215580357143'),
('NEK2_HUMAN','2xkd_A','A','structure of nek2 bound to aminopyrazine compound 12','1.96','0.476650197704082','0.476650197704082'),
('NEK2_HUMAN','2xke_A','A','structure of nek2 bound to aminipyrazine compound 5','2.2','0.410143386093074','0.410143386093074'),
('NEK2_HUMAN','2xkf_A','A','structure of nek2 bound to aminopyrazine compound 2','2.35','0.40086812025076','0.40086812025076'),
('CHK2_HUMAN','2xm8_A','A','co-crystal structure of a small molecule inhibitor bound to kinase domain of chk2','3.4','0.114761307773109','0.114761307773109'),
('CHK2_HUMAN','2xm9_A','A','structure of a small molecule inhibitor with the kinase doma chk2','2.5','0.334455967261905','0.334455967261905'),
('CDK2_HUMAN','2xmy_A','A','discovery and characterisation of 2-anilino-4-(thiazol-5-yl) pyrimidine transcriptional cdk inhibitors as anticancer agents','1.9','0.450614167449875','0.450614167449875'),
('CDK2_HUMAN','2xnb_A','A','discovery and characterisation of 2-anilino-4-(thiazol-5-yl) pyrimidine transcriptional cdk inhibitors as anticancer agents','1.85','0.417144469111969','0.417144469111969'),
('AURKA_HUMAN','2xne_A','A','structure of aurora-a bound to an imidazopyrazine inhibitor','2.8','0.250587693452381','0.250587693452381'),
('AURKA_HUMAN','2xng_A','A','structure of aurora-a bound to a selective imidazopyrazine i','2.6','0.277372720924908','0.277372720924908'),
('NEK2_HUMAN','2xnm_A','A','structure of nek2 bound to cct','1.85','0.521974260778636','0.521974260778636'),
('NEK2_HUMAN','2xnn_A','A','structure of nek2 bound to cct242430','2.5','0.347077008928571','0.347077008928571'),
('NEK2_HUMAN','2xno_A','A','structure of nek2 bound to cct243779','1.98','0.4773301627886','0.4773301627886'),
('NEK2_HUMAN','2xnp_A','A','structure of nek2 bound to cct244858','1.98','0.4911089127886','0.4911089127886'),
('ALK_HUMAN','2xp2_A','A','structure of the human anaplastic lymphoma kinase in complex with crizotinib (pf-02341066)','1.9','0.470043497807017','0.470043497807017'),
('AURKA_HUMAN','2xru_A','A','aurora-a t288e complexed with pha-828300','2.9','0.163752586206897','0.163752586206897'),
('MK08_HUMAN','2xrw_A','A','linear binding motifs for jnk and for calcineurin antagonist control the nuclear shuttling of nfat4','1.33','0.739529223057644','0.739529223057644'),
('MK08_HUMAN','2xs0_A','A','linear binding motifs for jnk and for calcineurin antagonist control the nuclear shuttling of nfat4','2.6','0.312087959020147','0.312087959020147'),
('DAPK1_HUMAN','2xuu_A','A','crystal structure of a dap-kinase 1 mutant','1.8','0.524097862103175','0.524097862103175'),
('EPHB4_HUMAN','2xvd_A','A','ephb4 kinase domain inhibitor complex','1.7','0.566624832808123','0.566624832808123'),
('ABL2_HUMAN','2xyn_A','A','human abl2 in complex with aurora kinase inhibitor vx-680','2.81','0.231491543859092','0.231491543859092'),
('ABL2_HUMAN','2xyn_B','B','human abl2 in complex with aurora kinase inhibitor vx-680','2.81','0.231491543859092','0.231491543859092'),
('DAPK1_HUMAN','2xzs_A','A','death associated protein kinase 1 residues 1-312','2','0.463082946428571','0.463082946428571'),
('DAPK1_HUMAN','2xzs_B','B','death associated protein kinase 1 residues 1-312','2','0.463082946428571','0.463082946428571'),
('DAPK1_HUMAN','2y0a_A','A','structure of dapk1 construct residues 1-304','2.6','0.181255384615385','0.181255384615385'),
('ZAP70_HUMAN','2y1n_B','B','structure of c-cbl-zap-70 peptide complex','2','0.461057321428571','0.461057321428571'),
('ZAP70_HUMAN','2y1n_D','D','structure of c-cbl-zap-70 peptide complex','2','0.461057321428571','0.461057321428571'),
('KSR2_HUMAN','2y4i_B','B','ksr2-mek1 heterodimer','3.46','0.166370168421415','0.166370168421415'),
('DAPK1_HUMAN','2y4p_A','A','dimeric structure of dapk-1 catalytic domain','2.65','0.222918460804133','0.222918460804133'),
('DAPK1_HUMAN','2y4p_B','B','dimeric structure of dapk-1 catalytic domain','2.65','0.222918460804133','0.222918460804133'),
('DAPK1_HUMAN','2y4p_C','C','dimeric structure of dapk-1 catalytic domain','2.65','0.222918460804133','0.222918460804133'),
('DAPK1_HUMAN','2y4p_D','D','dimeric structure of dapk-1 catalytic domain','2.65','0.222918460804133','0.222918460804133'),
('DAPK1_HUMAN','2y4v_B','B','crystal structure of human calmodulin in complex with a dap kinase-1 mutant (w305y) peptide','1.8','0.462401909722222','0.462401909722222'),
('PHKG2_HUMAN','2y7j_A','A','structure of human phosphorylase kinase, gamma 2','2.5','0.362955029761905','0.362955029761905'),
('PHKG2_HUMAN','2y7j_B','B','structure of human phosphorylase kinase, gamma 2','2.5','0.362955029761905','0.362955029761905'),
('PHKG2_HUMAN','2y7j_C','C','structure of human phosphorylase kinase, gamma 2','2.5','0.362955029761905','0.362955029761905'),
('PHKG2_HUMAN','2y7j_D','D','structure of human phosphorylase kinase, gamma 2','2.5','0.362955029761905','0.362955029761905'),
('MK14_HUMAN','2y8o_A','A','crystal structure of human p38alpha complexed with a mapk do peptide','1.95','0.485287477106227','0.485287477106227'),
('MP2K6_HUMAN','2y8o_B','B','crystal structure of human p38alpha complexed with a mapk do peptide','1.95','0.485287477106227','0.485287477106227'),
('MK01_HUMAN','2y9q_A','A','crystal structure of human erk2 complexed with a mapk dockin','1.55','0.644993358774962','0.644993358774962'),
('MKNK1_HUMAN','2y9q_B','B','crystal structure of human erk2 complexed with a mapk dockin','1.55','0.644993358774962','0.644993358774962'),
('TITIN_HUMAN','2y9r_T','T','crystal structure of the m10 domain of titin','1.9','0.479397962092732','0.479397962092732'),
('PLK1_HUMAN','2yac_A','A','crystal structure of polo-like kinase 1 in complex with nms-','2.2','0.366647999188312','0.366647999188312'),
('DAPK1_HUMAN','2yak_A','A','structure of death-associated protein kinase 1 (dapk1) in complex with a ruthenium octasporine ligand (osv)','2.2','0.401251585497836','0.401251585497836'),
('CHK2_HUMAN','2ycf_A','A','crystal structure of checkpoint kinase 2 in complex with inhibitor pv1531','1.77','0.522762391293382','0.522762391293382'),
('CHK2_HUMAN','2ycq_A','A','crystal structure of checkpoint kinase 2 in complex with inh pv1115','2.05','0.4269581220964','0.4269581220964'),
('CHK2_HUMAN','2ycr_A','A','crystal structure of checkpoint kinase 2 in complex with inh pv976','2.2','0.402553936688312','0.402553936688312'),
('CHK2_HUMAN','2ycs_A','A','crystal structure of checkpoint kinase 2 in complex with pv7','2.35','0.354053655965046','0.354053655965046'),
('CHK1_HUMAN','2ydi_A','A','discovery of checkpoint kinase inhibitor azd7762 by structur design and optimization of thiophene carboxamide ureas','1.6','0.605401294642857','0.605401294642857'),
('CHK1_HUMAN','2ydj_A','A','discovery of checkpoint kinase inhibitor azd7762 by structur design and optimization of thiophene carboxamide ureas','1.85','0.454541611969112','0.454541611969112'),
('CHK1_HUMAN','2ydj_B','B','discovery of checkpoint kinase inhibitor azd7762 by structur design and optimization of thiophene carboxamide ureas','1.85','0.454541611969112','0.454541611969112'),
('CHK1_HUMAN','2ydk_A','A','discovery of checkpoint kinase inhibitor azd7762 by structur design and optimization of thiophene carboxamide ureas','1.9','0.48953157816416','0.48953157816416'),
('CHK1_HUMAN','2yer_A','A','synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors','1.83','0.547915245169789','0.547915245169789'),
('CHK1_HUMAN','2yex_A','A','synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors','1.3','0.785797063873626','0.785797063873626'),
('ALK_HUMAN','2yfx_A','A','structure of l1196m mutant anaplastic lymphoma kinase in complex with crizotinib','1.7','0.531997853641457','0.531997853641457'),
('ALK_HUMAN','2yhv_A','A','structure of l1196m mutant anaplastic lymphoma kinase','1.9','0.470950045426065','0.470950045426065'),
('CHK2_HUMAN','2yiq_A','A','structural analysis of checkpoint kinase 2 in complex with inhibitor pv1322','1.89','0.483309353505291','0.483309353505291'),
('CHK2_HUMAN','2yir_A','A','structural analysis of checkpoint kinase 2 in complex with inhibitor pv1352','2.1','0.425873110119048','0.425873110119048'),
('MK14_HUMAN','2yis_A','A','triazolopyridine inhibitors of p38 kinase.','2','0.407830416666667','0.407830416666667'),
('CHK2_HUMAN','2yit_A','A','structural analysis of checkpoint kinase 2 in complex with pv1162, a novel inhibitor','2.2','0.40915886228355','0.40915886228355'),
('MK14_HUMAN','2yiw_A','A','triazolopyridine inhibitors of p38 kinase','2','0.400380625','0.400380625'),
('MK14_HUMAN','2yix_A','A','triazolopyridine inhibitors of p38','2.3','0.363152668219462','0.363152668219462'),
('M3K7_HUMAN','2yiy_A','A','crystal structure of compound 8 bound to tak1-tab','2.49','0.32963716975043','0.32963716975043'),
('ALK_HUMAN','2yjr_A','A','structure of f1174l mutant anaplastic lymphoma kinase','1.9','0.454717753759398','0.454717753759398'),
('ALK_HUMAN','2yjs_A','A','structure of c1156y mutant anaplastic lymphoma kinase','1.9','0.466210179354637','0.466210179354637'),
('CHK1_HUMAN','2ym3_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.01','0.464654104477612','0.464654104477612'),
('CHK1_HUMAN','2ym4_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.35','0.342519027988855','0.342519027988855'),
('CHK1_HUMAN','2ym5_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.03','0.449613054700329','0.449613054700329'),
('CHK1_HUMAN','2ym6_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.01','0.463112586620469','0.463112586620469'),
('CHK1_HUMAN','2ym7_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','1.81','0.527642155107209','0.527642155107209'),
('CHK1_HUMAN','2ym8_A','A','crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors','2.07','0.439555105891995','0.439555105891995'),
('MYLK_HUMAN','2yr3_A','A','solution structure of the fourth ig-like domain from myosin light chain kinase, smooth muscle',NULL,'0.0328839583333333','0.0328839583333333'),
('BMX_HUMAN','2ys2_A','A','solution structure of the btk motif of human cytoplasmic tyrosine-protein kinase bmx',NULL,'0.0191505059523809','0.0191505059523809'),
('ALK_HUMAN','2ys5_B','B','solution structure of the complex of the ptb domain of snt-2 residue peptide (aa 1571-1589) of halk',NULL,'0.0241117559523809','0.0241117559523809'),
('ALK_HUMAN','2yt2_A','A','solution structure of the chimera of the ptb domain of snt-2 residue peptide (aa 1571-1589) of halk',NULL,'0.0281104464285714','0.0281104464285714'),
('ITK_HUMAN','2yuq_A','A','solution structure of the sh3 domain of human tyrosine- protein kinase itk/tsk',NULL,'0.0319101934523809','0.0319101934523809'),
('KPCD_HUMAN','2yuu_A','A','solution structure of the first phorbol esters/diacylglycerol binding domain of human protein kinase c, delta',NULL,'0.0175420833333333','0.0175420833333333'),
('CHK1_HUMAN','2ywp_A','A','crystal structure of chk1 with a urea inhibitor','2.9','0.186948508825944','0.186948508825944'),
('OBSCN_HUMAN','2yz8_A','A','crystal structure of the 32th ig-like domain of human obscur (kiaa1556)','2','0.428398645833333','0.428398645833333'),
('AAPK2_HUMAN','2yza_A','A','crystal structure of kinase domain of human 5\'-amp-activated kinase alpha-2 subunit mutant (t172d)','3.02','0.223042345671712','0.223042345671712'),
('BTK_HUMAN','2z0p_A','A','crystal structure of ph domain of bruton\'s tyrosine kinase','2.58','0.260391378391473','0.260391378391473'),
('BTK_HUMAN','2z0p_C','C','crystal structure of ph domain of bruton\'s tyrosine kinase','2.58','0.260391378391473','0.260391378391473'),
('BTK_HUMAN','2z0p_D','D','crystal structure of ph domain of bruton\'s tyrosine kinase','2.58','0.260391378391473','0.260391378391473'),
('WEE1_HUMAN','2z2w_A','A','humand wee1 kinase complexed with inhibitor pf0335770','2.22','0.356941030807593','0.356941030807593'),
('DDR2_HUMAN','2z4f_A','A','solution structure of the discoidin domain of ddr2',NULL,'0.0209485714285714','0.0209485714285714'),
('KS6A1_HUMAN','2z7q_A','A','crystal structure of the n-terminal kinase domain of human r to amp-pcp','2','0.360153779761905','0.360153779761905'),
('KS6A1_HUMAN','2z7r_A','A','crystal structure of the n-terminal kinase domain of human rsk1 bound to staurosporine','2','0.362581904761905','0.362581904761905'),
('KS6A1_HUMAN','2z7s_A','A','crystal structure of the n-terminal kinase domain of human rsk1 bound to purvalnol a','2.1','0.314956011904762','0.314956011904762'),
('INSR_HUMAN','2z8c_A','A','phosphorylated insulin receptor tyrosine kinase in complex with (4-{[5-carbamoyl-4-(3-methylanilino)pyrimidin-2- yl]amino}phenyl)acetic acid','3.25','0.191444420787546','0.191444420787546'),
('MK14_HUMAN','2zaz_A','A','crystal structure of p38 in complex with 4-anilino quinoline','1.8','0.503709558531746','0.503709558531746'),
('MK14_HUMAN','2zb0_A','A','crystal structure of p38 in complex with biphenyl amide inhi','2.1','0.443461577380952','0.443461577380952'),
('MK14_HUMAN','2zb1_A','A','crystal structure of p38 in complex with biphenyl amide inhi','2.5','0.372356011904762','0.372356011904762'),
('MK10_HUMAN','2zdt_A','A','crystal structure of human jnk3 complexed with an isoquinolo inhibitor','2','0.413724181547619','0.413724181547619'),
('MK10_HUMAN','2zdu_A','A','crystal structure of human jnk3 complexed with an isoquinolone inhibitor','2.5','0.265534181547619','0.265534181547619'),
('Q17RV3_HUMAN','2zej_A','A','structure of the roc domain from the parkinson\'s disease-ass leucine-rich repeat kinase 2 reveals a dimeric gtpase','2','0.411908214285714','0.411908214285714'),
('LRRK2_HUMAN','2zej_B','B','structure of the roc domain from the parkinson\'s disease-ass leucine-rich repeat kinase 2 reveals a dimeric gtpase','2','0.411908214285714','0.411908214285714'),
('CSK21_HUMAN','2zjw_A','A','crystal structure of human ck2 alpha complexed with ellagic acid','2.4','0.328426681547619','0.328426681547619'),
('LCK_HUMAN','2zm1_A','A','crystal structure of imidazo pyrazin 1 bound to the kinase domain of human lck, (auto-phosphorylated on tyr394)','2.1','0.448841919642857','0.448841919642857'),
('IGF1R_HUMAN','2zm3_A','A','complex structure of insulin-like growth factor receptor and isoquinolinedione inhibitor','2.5','0.335243422619048','0.335243422619048'),
('IGF1R_HUMAN','2zm3_D','D','complex structure of insulin-like growth factor receptor and isoquinolinedione inhibitor','2.5','0.335243422619048','0.335243422619048'),
('LCK_HUMAN','2zm4_A','A','crystal structure of imidazo quinoxaline 1 bound to the kinase domain of human lck, activated form (auto- phosphorylated on tyr394)','2.7','0.292972141203704','0.292972141203704'),
('TTK_HUMAN','2zmc_A','A','crystal structure of human mitotic checkpoint kinase mps1 ca domain apo form','3.14','0.206102081627237','0.206102081627237'),
('TTK_HUMAN','2zmd_A','A','crystal structure of human mps1 catalytic domain t686a mutan complex with sp600125 inhibitor','2.88','0.260648353174603','0.260648353174603'),
('MK03_HUMAN','2zoq_A','A','structural dissection of human mitogen-activated kinase erk1','2.39','0.276860666841004','0.276860666841004'),
('MK03_HUMAN','2zoq_B','B','structural dissection of human mitogen-activated kinase erk1','2.39','0.276860666841004','0.276860666841004'),
('KKCC2_HUMAN','2zv2_A','A','crystal structure of human calcium/calmodulin-dependent prot kinase 2, beta, camkk2 kinase domain in complex with sto-60','2.4','0.356489404761905','0.356489404761905'),
('LCK_HUMAN','2zyb_A','A','crystal structure of phenylimidazo pyrazin 2 bound to the kinase domain of human lck, (auto-phosphorylated on tyr394)','2.55','0.317990493697479','0.317990493697479'),
('MAPK2_HUMAN','3a2c_A','A','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_B','B','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_C','C','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_D','D','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_E','E','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_F','F','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_G','G','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_H','H','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_I','I','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_J','J','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_K','K','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('MAPK2_HUMAN','3a2c_L','L','crystal structure of a pyrazolopyrimidine inhibitor complex mapkap kinase-2 (mk2)','2.9','0.16604404454023','0.16604404454023'),
('LYN_HUMAN','3a4o_X','X','lyn kinase domain','3','0.0804388690476191','0.0804388690476191'),
('MET_HUMAN','3a4p_A','A','human c-met kinase domain complexed with 6-benzyloxyquinolin inhibitor','2.54','0.327910460020622','0.327910460020622'),
('KS6B1_HUMAN','3a60_A','A','crystal structure of unphosphorylated p70s6k1 (form i)','2.8','0.251841428571429','0.251841428571429'),
('KS6B1_HUMAN','3a60_B','B','crystal structure of unphosphorylated p70s6k1 (form i)','2.8','0.251841428571429','0.251841428571429'),
('KS6B1_HUMAN','3a61_A','A','crystal structure of unphosphorylated p70s6k1 (form ii)','3.43','0.0924872579567541','0.0924872579567541'),
('KS6B1_HUMAN','3a62_A','A','crystal structure of phosphorylated p70s6k1','2.35','0.314251572631712','0.314251572631712'),
('STK24_HUMAN','3a7f_A','A','human mst3 kinase','1.55','0.602698180203533','0.602698180203533'),
('STK24_HUMAN','3a7g_A','A','human mst3 kinase','2','0.427284836309524','0.427284836309524'),
('STK24_HUMAN','3a7g_B','B','human mst3 kinase','2','0.427284836309524','0.427284836309524'),
('STK24_HUMAN','3a7h_A','A','human mst3 kinase in complex with atp','1.96','0.445816894132653','0.445816894132653'),
('STK24_HUMAN','3a7h_B','B','human mst3 kinase in complex with atp','1.96','0.445816894132653','0.445816894132653'),
('STK24_HUMAN','3a7i_A','A','human mst3 kinase in complex with adenine','1.45','0.654907999794745','0.654907999794745'),
('STK24_HUMAN','3a7j_A','A','human mst3 kinase in complex with mnadp','1.5','0.627292157738095','0.627292157738095'),
('KPCI_HUMAN','3a8w_A','A','crystal structure of pkciota kinase domain','2.1','0.343967797619048','0.343967797619048'),
('KPCI_HUMAN','3a8w_B','B','crystal structure of pkciota kinase domain','2.1','0.343967797619048','0.343967797619048'),
('KPCI_HUMAN','3a8x_A','A','crystal structure of pkciota kinase domain','2','0.398556041666667','0.398556041666667'),
('KPCI_HUMAN','3a8x_B','B','crystal structure of pkciota kinase domain','2','0.398556041666667','0.398556041666667'),
('PIM1_HUMAN','3a99_A','A','structure of pim-1 kinase crystallized in the presence of p2 carboxy-terminal peptide','1.6','0.587057678571428','0.587057678571428'),
('LCK_HUMAN','3ac1_A','A','crystal structure of pyrazin derivative bound to the kinase human lck, (auto-phosphorylated on tyr394)','1.99','0.491195479480737','0.491195479480737'),
('LCK_HUMAN','3ac2_A','A','crystal structure of pyrazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.1','0.458420729166667','0.458420729166667'),
('LCK_HUMAN','3ac3_A','A','crystal structure of pyrazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.55','0.32449949667367','0.32449949667367'),
('LCK_HUMAN','3ac4_A','A','crystal structure of triazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.7','0.298212840608466','0.298212840608466'),
('LCK_HUMAN','3ac5_A','A','crystal structure of triazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.5','0.351013616071429','0.351013616071429'),
('LCK_HUMAN','3ac8_A','A','crystal structure of pyrazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.3','0.344454647386128','0.344454647386128'),
('LCK_HUMAN','3acj_A','A','crystal structure of imidazo pyrimidine derivative bound to domain of human lck, (auto-phosphorylated on tyr394)','2.2','0.420899502164502','0.420899502164502'),
('LCK_HUMAN','3ack_A','A','crystal structure of pyrrolo pyrazine derivative bound to th domain of human lck, (auto-phosphorylated on tyr394)','2.6','0.348255875686813','0.348255875686813'),
('LCK_HUMAN','3ad4_A','A','crystal structure of methoxy benzofuran derivative bound to domain of human lck, (auto-phosphorylated on tyr394)','2.2','0.420000008116883','0.420000008116883'),
('LCK_HUMAN','3ad5_A','A','crystal structure of triazolone derivative bound to the kina of human lck, (auto-phosphorylated on tyr394)','2','0.487587172619048','0.487587172619048'),
('LCK_HUMAN','3ad6_A','A','crystal structure of pyrazolo pyrimidine derivative bound to kinase domain of human lck, (auto-phosphorylated on tyr394)','2.15','0.418502395141196','0.418502395141196'),
('KAPCA_HUMAN','3agl_A','A','complex of pka with the bisubstrate protein kinase inhibitor','2.1','0.424972544642857','0.424972544642857'),
('KAPCA_HUMAN','3agl_B','B','complex of pka with the bisubstrate protein kinase inhibitor','2.1','0.424972544642857','0.424972544642857'),
('KAPCA_HUMAN','3agm_A','A','complex of pka with the bisubstrate protein kinase inhibitor','2','0.422186413690476','0.422186413690476'),
('MP2K4_HUMAN','3aln_A','A','crystal structure of human non-phosphorylated mkk4 kinase do complexed with amp-pnp','2.3','0.202021507505176','0.202021507505176'),
('MP2K4_HUMAN','3alo_A','A','crystal structure of human non-phosphorylated mkk4 kinase do ternary complex with amp-pnp and p38 peptide','2.6','0.28431410485348','0.28431410485348'),
('KAPCA_HUMAN','3ama_A','A','protein kinase a sixfold mutant model of aurora b with inhib 7706621','1.75','0.5267615625','0.5267615625'),
('KAPCA_HUMAN','3amb_A','A','protein kinase a sixfold mutant model of aurora b with inhib 680','2.25','0.360444593253968','0.360444593253968'),
('CSK21_HUMAN','3amy_A','A','crystal structure of human ck2 alpha complexed with apigenin','2.3','0.287688918219462','0.287688918219462'),
('DYR1A_HUMAN','3anq_B','B','human dyrk1a/inhibitor complex','2.6','0.269248703067765','0.269248703067765'),
('DYR1A_HUMAN','3anr_A','A','human dyrk1a/harmine complex','2.6','0.273434149496337','0.273434149496337'),
('ALK_HUMAN','3aox_A','A','x-ray crystal structure of human anaplastic lymphoma kinase with ch5424802','1.75','0.552040699404762','0.552040699404762'),
('AAPK2_HUMAN','3aqv_A','A','human amp-activated protein kinase alpha 2 subunit kinase do (t172d) complexed with compound c','2.08','0.380016388507326','0.380016388507326'),
('CSK21_HUMAN','3at2_A','A','crystal structure of ck2alpha','1.6','0.613051413690476','0.613051413690476'),
('CSK21_HUMAN','3at3_A','A','crystal structure of ck2alpha with pyradine derivative','2.6','0.276669000686813','0.276669000686813'),
('CSK21_HUMAN','3at4_A','A','crystal structure of ck2alpha with pyradine derivertive','2.2','0.336768758116883','0.336768758116883'),
('CSK21_HUMAN','3axw_A','A','crystal structure of human ck2alpha complexed with a potent','2.5','0.252559285714286','0.252559285714286'),
('FGFR2_HUMAN','3b2t_A','A','structure of phosphotransferase','1.8','0.503768933531746','0.503768933531746'),
('EGFR_HUMAN','3b2u_A','A','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_B','B','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_E','E','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_I','I','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_M','M','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_P','P','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_S','S','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2u_V','V','crystal structure of isolated domain iii of the extracellula of the epidermal growth factor receptor in complex with the fragment of imc-11f8','2.58','0.272081884343854','0.272081884343854'),
('EGFR_HUMAN','3b2v_A','A','crystal structure of the extracellular region of the epiderm factor receptor in complex with the fab fragment of imc-11f','3.3','0.00944234172077928','0.00944234172077928'),
('LCK_HUMAN','3b2w_A','A','crystal structure of pyrimidine amide 11 bound to lck','2.3','0.320366046195652','0.320366046195652'),
('TITIN_HUMAN','3b43_A','A','i-band fragment i65-i70 from titin','3.3','0.184506939935065','0.184506939935065'),
('Q8N9D7_HUMAN','3b71_A','A','cd4 endocytosis motif bound to the focal adhesion targeting domain of the focal adhesion kinase','2.82','0.208494943958967','0.208494943958967'),
('FAK1_HUMAN','3b71_B','B','cd4 endocytosis motif bound to the focal adhesion targeting domain of the focal adhesion kinase','2.82','0.208494943958967','0.208494943958967'),
('FAK1_HUMAN','3b71_C','C','cd4 endocytosis motif bound to the focal adhesion targeting domain of the focal adhesion kinase','2.82','0.208494943958967','0.208494943958967'),
('VGFR2_HUMAN','3b8q_A','A','crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor','2.75','0.265557732683983','0.265557732683983'),
('VGFR2_HUMAN','3b8q_B','B','crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor','2.75','0.265557732683983','0.265557732683983'),
('VGFR2_HUMAN','3b8r_A','A','crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor','2.7','0.306168926917989','0.306168926917989'),
('VGFR2_HUMAN','3b8r_B','B','crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor','2.7','0.306168926917989','0.306168926917989'),
('ERBB4_HUMAN','3bbt_B','B','crystal structure of the erbb4 kinase in complex with lapati','2.8','0.2324140625','0.2324140625'),
('ERBB4_HUMAN','3bbt_D','D','crystal structure of the erbb4 kinase in complex with lapati','2.8','0.2324140625','0.2324140625'),
('ERBB4_HUMAN','3bbw_A','A','crystal structure of the erbb4 kinase in its inactive conformation','4','0.0335976339285714','0.0335976339285714'),
('ERBB4_HUMAN','3bbw_B','B','crystal structure of the erbb4 kinase in its inactive conformation','4','0.0335976339285714','0.0335976339285714'),
('ERBB4_HUMAN','3bce_A','A','crystal structure of the erbb4 kinase','2.5','0.329705565476191','0.329705565476191'),
('ERBB4_HUMAN','3bce_B','B','crystal structure of the erbb4 kinase','2.5','0.329705565476191','0.329705565476191'),
('ERBB4_HUMAN','3bce_C','C','crystal structure of the erbb4 kinase','2.5','0.329705565476191','0.329705565476191'),
('ERBB2_HUMAN','3be1_A','A','dual specific bh1 fab in complex with the extracellular doma her2/erbb-2','2.9','0.235708538587849','0.235708538587849'),
('VGFR2_HUMAN','3be2_A','A','crystal structure of the vegfr2 kinase domain in complex with a benzamide inhibitor','1.75','0.519278005952381','0.519278005952381'),
('TIE2_HUMAN','3bea_A','A','cfms tyrosine kinase (tie2 kid) in complex with a pyrimidinopyridone inhibitor','2.02','0.443922302569543','0.443922302569543'),
('SRPK1_HUMAN','3beg_A','A','crystal structure of sr protein kinase 1 complexed to its su asf/sf2','2.9','0.186969788587849','0.186969788587849'),
('EGFR_HUMAN','3bel_A','A','x-ray structure of egfr in complex with oxime inhibitor','2.3','0.334123992624224','0.334123992624224'),
('KPCD2_HUMAN','3bgm_C','C','crystal structure of pkd2 phosphopeptide bound to human class i mhc hla-a2','1.6','0.576683005952381','0.576683005952381'),
('PIM1_HUMAN','3bgp_A','A','human pim-1 complexed with a benzoisoxazole inhibitor vx1','2.8','0.285135729166667','0.285135729166667'),
('PIM1_HUMAN','3bgq_A','A','human pim-1 kinase in complex with an triazolo pyridazine inhibitor vx2','2','0.429980550595238','0.429980550595238'),
('PIM1_HUMAN','3bgz_A','A','human pim-1 kinase in complex with diphenyl indole inhibitor vx3','2.4','0.343544613095238','0.343544613095238'),
('KCC2B_HUMAN','3bhh_A','A','crystal structure of human calcium/calmodulin-dependent prot iib isoform 1 (camk2b)','2.4','0.336263824404762','0.336263824404762'),
('KCC2B_HUMAN','3bhh_B','B','crystal structure of human calcium/calmodulin-dependent prot iib isoform 1 (camk2b)','2.4','0.336263824404762','0.336263824404762'),
('KCC2B_HUMAN','3bhh_C','C','crystal structure of human calcium/calmodulin-dependent prot iib isoform 1 (camk2b)','2.4','0.336263824404762','0.336263824404762'),
('KCC2B_HUMAN','3bhh_D','D','crystal structure of human calcium/calmodulin-dependent prot iib isoform 1 (camk2b)','2.4','0.336263824404762','0.336263824404762'),
('CDK2_HUMAN','3bht_A','A','structure of phosphorylated thr160 cdk2/cyclin a in complex inhibitor meriolin 3','2','0.463741473214286','0.463741473214286'),
('CDK2_HUMAN','3bht_C','C','structure of phosphorylated thr160 cdk2/cyclin a in complex inhibitor meriolin 3','2','0.463741473214286','0.463741473214286'),
('CDK2_HUMAN','3bhu_A','A','structure of phosphorylated thr160 cdk2/cyclin a in complex inhibitor meriolin 5','2.3','0.36123284679089','0.36123284679089'),
('CDK2_HUMAN','3bhu_C','C','structure of phosphorylated thr160 cdk2/cyclin a in complex inhibitor meriolin 5','2.3','0.36123284679089','0.36123284679089'),
('CDK2_HUMAN','3bhv_A','A','structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor variolin b','2.1','0.415881458333333','0.415881458333333'),
('CDK2_HUMAN','3bhv_C','C','structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor variolin b','2.1','0.415881458333333','0.415881458333333'),
('DAPK3_HUMAN','3bhy_A','A','crystal structure of human death associated protein kinase 3 in complex with a beta-carboline ligand','1.24','0.818419157546083','0.818419157546083'),
('WEE1_HUMAN','3bi6_A','A','wee1 kinase complex with inhibitor pd352396','2.2','0.375568088474026','0.375568088474026'),
('WEE1_HUMAN','3biz_A','A','wee1 kinase complex with inhibitor pd331618','2.2','0.390013713474026','0.390013713474026'),
('FES_HUMAN','3bkb_A','A','crystal structure of human feline sarcoma viral oncogene hom fes)','1.78','0.565656294475655','0.565656294475655'),
('CDK9_HUMAN','3blh_A','A','crystal structure of human cdk9/cyclint1','2.48','0.344725791570661','0.344725791570661'),
('CDK9_HUMAN','3blq_A','A','crystal structure of human cdk9/cyclint1 in complex with atp','2.9','0.282817630849754','0.282817630849754'),
('CDK9_HUMAN','3blr_A','A','crystal structure of human cdk9/cyclint1 in complex with flavopiridol','2.8','0.298829404761905','0.298829404761905'),
('MERTK_HUMAN','3bpr_A','A','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with inhibitor c52','2.8','0.194336205357143','0.194336205357143'),
('MERTK_HUMAN','3bpr_B','B','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with inhibitor c52','2.8','0.194336205357143','0.194336205357143'),
('MERTK_HUMAN','3bpr_C','C','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with inhibitor c52','2.8','0.194336205357143','0.194336205357143'),
('MERTK_HUMAN','3bpr_D','D','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with inhibitor c52','2.8','0.194336205357143','0.194336205357143'),
('CSK21_HUMAN','3bqc_A','A','high ph-value crystal structure of emodin in complex with the catalytic subunit of protein kinase ck2','1.5','0.677145431547619','0.677145431547619'),
('DAPK3_HUMAN','3bqr_A','A','crystal structure of human death associated protein kinase 3 in complex with an imidazo-pyridazine ligand','1.75','0.540598571428571','0.540598571428571'),
('B4DFQ0_HUMAN','3brb_A','A','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with adp','1.9','0.457302664473684','0.457302664473684'),
('MERTK_HUMAN','3brb_B','B','crystal structure of catalytic domain of the proto-oncogene protein kinase mer in complex with adp','1.9','0.457302664473684','0.457302664473684'),
('LCK_HUMAN','3brh_B','B','protein tyrosine phosphatase ptpn-22 (lyp) bound to the mono-phosphorylated lck active site peptide','2.2','0.376307984307359','0.376307984307359'),
('IKKB_HUMAN','3brv_A','A','nemo/ikkb association domain structure','2.2','0.379379889069264','0.379379889069264'),
('IKKB_HUMAN','3brv_C','C','nemo/ikkb association domain structure','2.2','0.379379889069264','0.379379889069264'),
('INSR_HUMAN','3bu3_A','A','crystal structure of the insulin receptor kinase in complex with irs2 krlb peptide','1.65','0.552631989989178','0.552631989989178'),
('INSR_HUMAN','3bu5_A','A','crystal structure of the insulin receptor kinase in complex with irs2 krlb peptide and atp','2.1','0.408912544642857','0.408912544642857'),
('INSR_HUMAN','3bu6_A','A','crystal structure of the insulin receptor kinase in complex with irs2 krlb phosphopeptide','1.95','0.458830602106227','0.458830602106227'),
('EGFR_HUMAN','3buo_A','A','crystal structure of c-cbl-tkb domain complexed with its binding motif in egf receptor\'','2.6','0.255009774496337','0.255009774496337'),
('EGFR_HUMAN','3buo_C','C','crystal structure of c-cbl-tkb domain complexed with its binding motif in egf receptor\'','2.6','0.255009774496337','0.255009774496337'),
('KSYK_HUMAN','3buw_A','A','crystal structure of c-cbl-tkb domain complexed with its binding motif in syk','1.45','0.609012836104269','0.609012836104269'),
('KSYK_HUMAN','3buw_C','C','crystal structure of c-cbl-tkb domain complexed with its binding motif in syk','1.45','0.609012836104269','0.609012836104269'),
('MET_HUMAN','3bux_A','A','crystal structure of c-cbl-tkb domain complexed with its binding motif in c-met','1.35','0.658581216931217','0.658581216931217'),
('MET_HUMAN','3bux_C','C','crystal structure of c-cbl-tkb domain complexed with its binding motif in c-met','1.35','0.658581216931217','0.658581216931217'),
('MK14_HUMAN','3bv2_A','A','morpholino pyrrolotriazine p38 alpha map kinase inhibitor compound 30','2.4','0.294597678571429','0.294597678571429'),
('MK14_HUMAN','3bv3_A','A','morpholino pyrrolotriazine p38 alpha map kinase inhibitor compound 2','2.59','0.253006695624196','0.253006695624196'),
('PIM1_HUMAN','3bwf_A','A','crystal structure of the human pim1 in complex with an osmium compound','2.35','0.397701855369808','0.397701855369808'),
('MK14_HUMAN','3bx5_A','A','p38 alpha map kinase complexed with bms-640994','2.4','0.276142961309524','0.276142961309524'),
('LCK_HUMAN','3bym_A','A','x-ray co-crystal structure aminobenzimidazole triazine 1 bound to lck','2','0.419109345238095','0.419109345238095'),
('LCK_HUMAN','3byo_A','A','x-ray co-crystal structure of 2-amino-6-phenylpyrimido[5\', 4\':5,6]pyrimido[1,2-a]benzimidazol-5(6h)-one 25 bound to lck','2','0.420446488095238','0.420446488095238'),
('LCK_HUMAN','3bys_A','A','co-crystal structure of lck and aminopyrimidine amide 10b','2.2','0.348944978354978','0.348944978354978'),
('LCK_HUMAN','3byu_A','A','co-crystal structure of lck and aminopyrimidine reverse amide 23','2.3','0.323495049171843','0.323495049171843'),
('FAK1_HUMAN','3bz3_A','A','crystal structure analysis of focal adhesion kinase with a methanesulfonamide diaminopyrimidine inhibitor','2.2','0.437347880140693','0.437347880140693'),
('PLK1_HUMAN','3bzi_A','A','molecular and structural basis of polo-like kinase 1 substrate recognition: implications in centrosomal localization','2.1','0.421588348214286','0.421588348214286'),
('EGFR_HUMAN','3c09_A','A','crystal structure the fab fragment of matuzumab (fab72000) i with domain iii of the extracellular region of egfr','3.2','0.171606979166667','0.171606979166667'),
('EGFR_HUMAN','3c09_D','D','crystal structure the fab fragment of matuzumab (fab72000) i with domain iii of the extracellular region of egfr','3.2','0.171606979166667','0.171606979166667'),
('Q5JS74_HUMAN','3c0g_A','A','cask cam-kinase domain- 3\'-amp complex, p1 form','2.19','0.365202864685258','0.365202864685258'),
('CSKP_HUMAN','3c0g_B','B','cask cam-kinase domain- 3\'-amp complex, p1 form','2.19','0.365202864685258','0.365202864685258'),
('CSKP_HUMAN','3c0h_A','A','cask cam-kinase domain- amppnp complex, p1 form','2.3','0.373734171195652','0.373734171195652'),
('CSKP_HUMAN','3c0h_B','B','cask cam-kinase domain- amppnp complex, p1 form','2.3','0.373734171195652','0.373734171195652'),
('CSKP_HUMAN','3c0i_A','A','cask cam-kinase domain- 3\'-amp complex, p212121 form','1.85','0.488906894707207','0.488906894707207'),
('CSK21_HUMAN','3c13_A','A','low ph-value crystal structure of emodin in complex with the subunit of protein kinase ck2','1.95','0.469087045558608','0.469087045558608'),
('MET_HUMAN','3c1x_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a pyrrolotriazine based inhibitor','2.17','0.3424572609447','0.3424572609447'),
('BRAF_HUMAN','3c4c_A','A','b-raf kinase in complex with plx4720','2.57','0.204988138722902','0.204988138722902'),
('BRAF_HUMAN','3c4c_B','B','b-raf kinase in complex with plx4720','2.57','0.204988138722902','0.204988138722902'),
('PIM1_HUMAN','3c4e_A','A','pim-1 kinase domain in complex with 3-aminophenyl-7- azaindole','1.98','0.411899671717172','0.411899671717172'),
('PIM1_HUMAN','3c4e_B','B','pim-1 kinase domain in complex with 3-aminophenyl-7- azaindole','1.98','0.411899671717172','0.411899671717172'),
('PIM1_HUMAN','3c4e_C','C','pim-1 kinase domain in complex with 3-aminophenyl-7- azaindole','1.98','0.411899671717172','0.411899671717172'),
('PIM1_HUMAN','3c4e_D','D','pim-1 kinase domain in complex with 3-aminophenyl-7- azaindole','1.98','0.411899671717172','0.411899671717172'),
('FGFR1_HUMAN','3c4f_A','A','fgfr tyrosine kinase domain in complex with 3-(3- methoxybenzyl)-7-azaindole','2.07','0.39440788863009','0.39440788863009'),
('FGFR1_HUMAN','3c4f_B','B','fgfr tyrosine kinase domain in complex with 3-(3- methoxybenzyl)-7-azaindole','2.07','0.39440788863009','0.39440788863009'),
('PLK1_HUMAN','3c5l_A','A','polo-like kinase 1 polo box domain in complex with pphspt peptide','2.33','0.300772629713366','0.300772629713366'),
('MK14_HUMAN','3c5u_A','A','p38 alpha map kinase complexed with a benzothiazole based inhibitor','2.8','0.153634985119048','0.153634985119048'),
('VGFR2_HUMAN','3c7q_A','A','structure of vegfr2 kinase domain in complex with bibf1120','2.1','0.375641145833333','0.375641145833333'),
('EPHA2_HUMAN','3c8x_A','A','crystal structure of the ligand binding domain of human ephr (epha2) receptor protein kinase','1.95','0.47085487293956','0.47085487293956'),
('FGFR2_HUMAN','3caf_A','A','crystal structure of hfgfr2 d2 domain','1.96','0.42919949829932','0.42919949829932'),
('FES_HUMAN','3cbl_A','A','crystal structure of human feline sarcoma viral oncogene hom fes) in complex with staurosporine and a consensus peptide','1.75','0.534965907738095','0.534965907738095'),
('FAK2_HUMAN','3cc6_A','A','crystal structure of kinase domain of protein tyrosine kinas (ptk2b)','1.6','0.588437633928571','0.588437633928571'),
('MET_HUMAN','3ccn_A','A','x-ray structure of c-met with triazolopyridazine inhibitor.','1.9','0.432133914473684','0.432133914473684'),
('FES_HUMAN','3cd3_A','A','crystal structure of phosphorylated human feline sarcoma vir oncogene homologue (v-fes) in complex with staurosporine an consensus peptide','1.98','0.464787424693362','0.464787424693362'),
('MET_HUMAN','3cd8_A','A','x-ray structure of c-met with triazolopyridazine inhibitor.','2','0.404839613095238','0.404839613095238'),
('MET_HUMAN','3ce3_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a pyrrolopyridinepyridone based inhibitor','2.4','0.272801398809524','0.272801398809524'),
('TTK_HUMAN','3cek_A','A','crystal structure of human dual specificity protein kinase (','2.3','0.387567236671843','0.387567236671843'),
('MK10_HUMAN','3cgf_A','A','irak-4 inhibitors (part ii)- a structure based assessment of imidazo[1,2 a]pyridine binding','3','0.215162663690476','0.215162663690476'),
('MK10_HUMAN','3cgo_A','A','irak-4 inhibitors (part ii)- a structure based assessment of imidazo[1,2 a]pyridine binding','3','0.199340595238095','0.199340595238095'),
('ARBK1_HUMAN','3cik_A','A','human grk2 in complex with gbetagamma subunits','2.75','0.276619205898268','0.276619205898268'),
('VGFR2_HUMAN','3cjf_A','A','crystal structure of vegfr2 in complex with a 3,4,5-trimetho containing pyrimidine','2.15','0.382675177879291','0.382675177879291'),
('VGFR2_HUMAN','3cjg_A','A','crystal structure of vegfr2 in complex with a 3,4,5-trimetho containing pyrimidine','2.25','0.361215560515873','0.361215560515873'),
('EPHA4_HUMAN','3ckh_A','A','crystal structure of eph a4 receptor','2.8','0.210953601190476','0.210953601190476'),
('STK24_HUMAN','3ckw_A','A','crystal structure of sterile 20-like kinase 3 (mst3, stk24)','1.96','0.447556953656463','0.447556953656463'),
('STK24_HUMAN','3ckx_A','A','crystal structure of sterile 20-like kinase 3 (mst3, stk24) in complex with staurosporine','2.7','0.275595236441799','0.275595236441799'),
('FGFR2_HUMAN','3cly_A','A','crystal structure of fgf receptor 2 (fgfr2) kinase domains t trans-phosphorylation reaction','2','0.435445758928571','0.435445758928571'),
('AURKA_HUMAN','3coh_A','A','crystal structure of aurora-a in complex with a pentacyclic','2.7','0.245402840608466','0.245402840608466'),
('AURKA_HUMAN','3coh_B','B','crystal structure of aurora-a in complex with a pentacyclic','2.7','0.245402840608466','0.245402840608466'),
('MK13_HUMAN','3coi_A','A','crystal structure of p38delta kinase','2.09','0.395756488807245','0.395756488807245'),
('PLK4_HUMAN','3cok_A','A','crystal structure of plk4 kinase','2.25','0.35637566468254','0.35637566468254'),
('PLK4_HUMAN','3cok_B','B','crystal structure of plk4 kinase','2.25','0.35637566468254','0.35637566468254'),
('A0PJ51_HUMAN','3com_A','A','crystal structure of mst1 kinase','2.2','0.371860156926407','0.371860156926407'),
('STK4_HUMAN','3com_B','B','crystal structure of mst1 kinase','2.2','0.371860156926407','0.371860156926407'),
('VGFR2_HUMAN','3cp9_A','A','crystal structure of the vegfr2 kinase domain in complex with a pyridone inhibitor','2.5','0.331148125','0.331148125'),
('VGFR2_HUMAN','3cpb_A','A','crystal structure of the vegfr2 kinase domain in complex with a bisamide inhibitor','2.7','0.275098614417989','0.275098614417989'),
('VGFR2_HUMAN','3cpc_A','A','crystal structure of the vegfr2 kinase domain in complex wit pyridone inhibitor','2.4','0.347371011904762','0.347371011904762'),
('WEE1_HUMAN','3cqe_A','A','wee1 kinase complex with inhibitor pd074291','2.5','0.306700357142857','0.306700357142857'),
('AKT1_HUMAN','3cqu_A','A','crystal structure of akt-1 complexed with substrate peptide and inhibitor','2.2','0.356043772997836','0.356043772997836'),
('GSK3B_HUMAN','3cqu_C','C','crystal structure of akt-1 complexed with substrate peptide and inhibitor','2.2','0.356043772997836','0.356043772997836'),
('AKT1_HUMAN','3cqw_A','A','crystal structure of akt-1 complexed with substrate peptide and inhibitor','2','0.436686339285714','0.436686339285714'),
('GSK3B_HUMAN','3cqw_C','C','crystal structure of akt-1 complexed with substrate peptide and inhibitor','2','0.436686339285714','0.436686339285714'),
('WEE1_HUMAN','3cr0_A','A','wee1 kinase complex with inhibitor pd259_809','2.3','0.346830287267081','0.346830287267081'),
('ABL1_HUMAN','3cs9_A','A','human abl kinase in complex with nilotinib','2.21','0.391622288973282','0.391622288973282'),
('ABL1_HUMAN','3cs9_D','D','human abl kinase in complex with nilotinib','2.21','0.391622288973282','0.391622288973282'),
('MET_HUMAN','3cth_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor','2.3','0.290464736671843','0.290464736671843'),
('MET_HUMAN','3ctj_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor','2.5','0.263713571428571','0.263713571428571'),
('MK14_HUMAN','3ctq_A','A','structure of map kinase p38 in complex with a 1-o-tolyl-1,2, 3-triazole-4-carboxamide','1.95','0.400406971153846','0.400406971153846'),
('FGFR2_HUMAN','3cu1_A','A','crystal structure of 2:2:2 fgfr2d2:fgf1:sos complex','2.6','0.295568673305861','0.295568673305861'),
('FGFR2_HUMAN','3cu1_C','C','crystal structure of 2:2:2 fgfr2d2:fgf1:sos complex','2.6','0.295568673305861','0.295568673305861'),
('RAF1_HUMAN','3cu8_P','P','impaired binding of 14-3-3 to raf1 is linked to noonan and l syndrome','2.4','0.348787202380952','0.348787202380952'),
('RAF1_HUMAN','3cu8_Q','Q','impaired binding of 14-3-3 to raf1 is linked to noonan and l syndrome','2.4','0.348787202380952','0.348787202380952'),
('PIM1_HUMAN','3cxw_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and a beta carbo ligand i','2.1','0.442087946428571','0.442087946428571'),
('PIM1_HUMAN','3cy2_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and a beta carbo ligand ii','2.01','0.47906528007285','0.47906528007285'),
('PIM1_HUMAN','3cy3_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and the jnk inhi','2.15','0.44741092192691','0.44741092192691'),
('EPHA2_HUMAN','3czu_A','A','crystal structure of the human ephrin a2- ephrin a1 complex','2.65','0.304510633423181','0.304510633423181'),
('AKT2_HUMAN','3d0e_A','A','crystal structure of human akt2 in complex with gsk690693','2','0.437811116071429','0.437811116071429'),
('AKT2_HUMAN','3d0e_B','B','crystal structure of human akt2 in complex with gsk690693','2','0.437811116071429','0.437811116071429'),
('MK01_HUMAN','3d42_A','A','crystal structure of heptp in complex with a monophosphoryla peptide','2.46','0.348195210873984','0.348195210873984'),
('MK01_HUMAN','3d44_A','A','crystal structure of heptp in complex with a dually phosphor erk2 peptide mimetic','1.9','0.490795090068922','0.490795090068922'),
('BRAF_HUMAN','3d4q_A','A','pyrazole-based inhibitors of b-raf kinase','2.8','0.253154583333333','0.253154583333333'),
('BRAF_HUMAN','3d4q_B','B','pyrazole-based inhibitors of b-raf kinase','2.8','0.253154583333333','0.253154583333333'),
('LRRK2_HUMAN','3d6t_B','B','structure of the roc domain from the parkinson\'s disease-ass leucine-rich repeat kinase 2 reveals a dimeric gtpase','2.43','0.304453958149618','0.304453958149618'),
('CSK_HUMAN','3d7u_A','A','structural basis for the recognition of c-src by its inactivator csk','4.11','0.0640958774330901','0.0640958774330901'),
('CSK_HUMAN','3d7u_C','C','structural basis for the recognition of c-src by its inactivator csk','4.11','0.0640958774330901','0.0640958774330901'),
('MK14_HUMAN','3d7z_A','A','crystal structure of p38 kinase in complex with a biphenyl a inhibitor','2.1','0.446239732142857','0.446239732142857'),
('MK14_HUMAN','3d83_A','A','crystal structure of p38 kinase in complex with a biphenyl a inhibitor','1.9','0.490394346021303','0.490394346021303'),
('IGF1R_HUMAN','3d94_A','A','crystal structure of the insulin-like growth factor-1 receptor kinase in complex with pqip','2.3','0.360728055124224','0.360728055124224'),
('ROCK1_HUMAN','3d9v_A','A','crystal structure of rock i bound to h-1152p a di- methylated variant of fasudil','3.3','0.170660704816017','0.170660704816017'),
('ROCK1_HUMAN','3d9v_B','B','crystal structure of rock i bound to h-1152p a di- methylated variant of fasudil','3.3','0.170660704816017','0.170660704816017'),
('MK10_HUMAN','3da6_A','A','crystal structure of human jnk3 complexed with n-(3-methyl- 4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy) naphthalen-1-yl)-1h-benzo[d]imidazol-2-amine','2','0.353966145833333','0.353966145833333'),
('OXSR1_HUMAN','3dak_A','A','crystal structure of domain-swapped osr1 kinase domain','2.25','0.364635590277778','0.364635590277778'),
('OXSR1_HUMAN','3dak_B','B','crystal structure of domain-swapped osr1 kinase domain','2.25','0.364635590277778','0.364635590277778'),
('OXSR1_HUMAN','3dak_C','C','crystal structure of domain-swapped osr1 kinase domain','2.25','0.364635590277778','0.364635590277778'),
('OXSR1_HUMAN','3dak_D','D','crystal structure of domain-swapped osr1 kinase domain','2.25','0.364635590277778','0.364635590277778'),
('FGFR2_HUMAN','3dar_A','A','crystal structure of d2 domain from human fgfr2','2.2','0.378069070616883','0.378069070616883'),
('FGFR2_HUMAN','3dar_B','B','crystal structure of d2 domain from human fgfr2','2.2','0.378069070616883','0.378069070616883'),
('TTK_HUMAN','3dbq_A','A','crystal structure of ttk kinase domain','2.7','0.258169016203704','0.258169016203704'),
('PIM1_HUMAN','3dcv_A','A','crystal structure of human pim1 kinase complexed with 4-(4- hydroxy-3-methyl-phenyl)-6-phenylpyrimidin-2(1h)-one','2.7','0.305418391203704','0.305418391203704'),
('CDK2_HUMAN','3ddp_C','C','structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor cr8','2.7','0.26875443287037','0.26875443287037'),
('CDK2_HUMAN','3ddq_A','A','structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor roscovitine','1.8','0.504856760912698','0.504856760912698'),
('DAPK1_HUMAN','3dfc_B','B','crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain with amppnp','1.9','0.505899896616541','0.505899896616541'),
('DAPK1_HUMAN','3dgk_A','A','crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain','1.7','0.566649356617647','0.566649356617647'),
('MET_HUMAN','3dkc_A','A','sgx clone 5698a65kfg1h1','1.52','0.616947713032581','0.616947713032581'),
('MET_HUMAN','3dkf_A','A','sgx clone 5698a65kfg1h1','1.8','0.509047891865079','0.509047891865079'),
('MET_HUMAN','3dkg_A','A','sgx clone 5698a109kfg1h1','1.91','0.473930879066941','0.473930879066941'),
('EPHA7_HUMAN','3dko_A','A','complex between the kinase domain of human ephrin type-a receptor 7 (epha7) and inhibitor alw-ii-49-7','2','0.458590684523809','0.458590684523809'),
('PASK_HUMAN','3dls_A','A','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('B7Z7V7_HUMAN','3dls_B','B','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('B7Z7V7_HUMAN','3dls_C','C','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('B7Z7V7_HUMAN','3dls_D','D','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('B7Z7V7_HUMAN','3dls_E','E','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('B7Z7V7_HUMAN','3dls_F','F','crystal structure of human pas kinase bound to adp','2.3','0.303097459886128','0.303097459886128'),
('HASP_HUMAN','3dlz_A','A','crystal structure of human haspin in complex with amp','1.85','0.520149082207207','0.520149082207207'),
('CDK2_HUMAN','3dog_A','A','structure of thr 160 phosphorylated cdk2/cyclin a in complex with the inhibitor n-&-n1','2.7','0.289422215608466','0.289422215608466'),
('CDK2_HUMAN','3dog_C','C','structure of thr 160 phosphorylated cdk2/cyclin a in complex with the inhibitor n-&-n1','2.7','0.289422215608466','0.289422215608466'),
('CSF1R_HUMAN','3dpk_A','A','cfms tyrosine kinase in complex with a pyridopyrimidinone inhibitor','1.95','0.463464188415751','0.463464188415751'),
('MK14_HUMAN','3ds6_A','A','p38 complex with a phthalazine inhibitor','2.9','0.219029505849754','0.219029505849754'),
('MK14_HUMAN','3ds6_B','B','p38 complex with a phthalazine inhibitor','2.9','0.219029505849754','0.219029505849754'),
('MK14_HUMAN','3ds6_C','C','p38 complex with a phthalazine inhibitor','2.9','0.219029505849754','0.219029505849754'),
('MK14_HUMAN','3ds6_D','D','p38 complex with a phthalazine inhibitor','2.9','0.219029505849754','0.219029505849754'),
('MK14_HUMAN','3dt1_A','A','p38 complexed with a quinazoline inhibitor','2.8','0.252593199404762','0.252593199404762'),
('M3K9_HUMAN','3dtc_A','A','crystal structure of mixed-lineage kinase mlk1 complexed with compound 16','2.6','0.278585473901099','0.278585473901099'),
('VGFR2_HUMAN','3dtw_A','A','crystal structure of the vegfr2 kinase domain in complex with a benzisoxazole inhibitor','2.9','0.249934505849754','0.249934505849754'),
('VGFR2_HUMAN','3dtw_B','B','crystal structure of the vegfr2 kinase domain in complex with a benzisoxazole inhibitor','2.9','0.249934505849754','0.249934505849754'),
('GSK3B_HUMAN','3du8_B','B','crystal structure of gsk-3 beta in complex with nms-869553a','2.2','0.37821849025974','0.37821849025974'),
('MP2K1_HUMAN','3dv3_A','A','mek1 with pf-04622664 bound','2.3','0.374566001552795','0.374566001552795'),
('PAK1_HUMAN','3dvp_C','C','pak1 peptide bound lc8','2.5','0.306180416666667','0.306180416666667'),
('PAK1_HUMAN','3dvp_D','D','pak1 peptide bound lc8','2.5','0.306180416666667','0.306180416666667'),
('MP2K1_HUMAN','3dy7_A','A','x-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp','2.7','0.229124447751323','0.229124447751323'),
('EPHA3_HUMAN','3dzq_A','A','human epha3 kinase domain in complex with inhibitor awl-ii- 38.3','1.75','0.559041264880952','0.559041264880952'),
('CSK22_HUMAN','3e3b_X','X','crystal structure of catalytic subunit of human protein kinase ck2alpha prime with a potent indazole-derivative inhibitor','3.2','0.0612772172619047','0.0612772172619047'),
('AURKA_HUMAN','3e5a_A','A','crystal structure of aurora a in complex with vx-680 and tpx','2.3','0.349442400362319','0.349442400362319'),
('JAK2_HUMAN','3e62_A','A','fragment based discovery of jak-2 inhibitors','1.92','0.500384375','0.500384375'),
('JAK2_HUMAN','3e63_A','A','fragment based discovery of jak-2 inhibitors','1.9','0.473142485902256','0.473142485902256'),
('JAK2_HUMAN','3e64_A','A','fragment based discovery of jak-2 inhibitors','1.8','0.528711016865079','0.528711016865079'),
('BUB1_HUMAN','3e7e_A','A','structure and substrate recruitment of the human spindle che kinase bub','2.31','0.31802766504329','0.31802766504329'),
('MK09_HUMAN','3e7o_A','A','crystal structure of jnk2','2.14','0.373250151173787','0.373250151173787'),
('HASP_HUMAN','3e7v_A','A','crystal structure of human haspin with a pyrazolo-pyrimidine','2','0.476332306547619','0.476332306547619'),
('AKT2_HUMAN','3e87_A','A','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.3','0.358138977743271','0.358138977743271'),
('AKT2_HUMAN','3e87_B','B','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.3','0.358138977743271','0.358138977743271'),
('GSK3B_HUMAN','3e87_C','C','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.3','0.358138977743271','0.358138977743271'),
('GSK3B_HUMAN','3e87_D','D','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.3','0.358138977743271','0.358138977743271'),
('AKT2_HUMAN','3e88_A','A','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.5','0.312390044642857','0.312390044642857'),
('AKT2_HUMAN','3e88_B','B','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.5','0.312390044642857','0.312390044642857'),
('GSK3B_HUMAN','3e88_C','C','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.5','0.312390044642857','0.312390044642857'),
('GSK3B_HUMAN','3e88_D','D','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.5','0.312390044642857','0.312390044642857'),
('AKT2_HUMAN','3e8d_A','A','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.7','0.297674313822751','0.297674313822751'),
('AKT2_HUMAN','3e8d_B','B','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.7','0.297674313822751','0.297674313822751'),
('GSK3B_HUMAN','3e8d_C','C','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.7','0.297674313822751','0.297674313822751'),
('GSK3B_HUMAN','3e8d_D','D','crystal structures of the kinase domain of akt2 in complex w competitive inhibitors','2.7','0.297674313822751','0.297674313822751'),
('MP2K1_HUMAN','3e8n_A','A','x-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) complexed with a potent inhibitor rdea119 and mgatp','2.5','0.300714151785714','0.300714151785714'),
('MK14_HUMAN','3e92_A','A','crystal structure of p38 kinase in complex with a biaryl ami inhibitor','2','0.472731711309524','0.472731711309524'),
('MK14_HUMAN','3e93_A','A','crystal structure of p38 kinase in complex with a biaryl ami inhibitor','2','0.472444821428571','0.472444821428571'),
('CSK_HUMAN','3eac_A','A','crystal structure of sh2 domain of human csk (carboxyl- terminal src kinase), oxidized form.','1.37','0.650130474561175','0.650130474561175'),
('CSK_HUMAN','3eaz_A','A','crystal structure of sh2 domain of human csk (carboxyl- terminal src kinase), c122s mutant.','1.31','0.708838748864049','0.708838748864049'),
('MET_HUMAN','3efj_A','A','structure of c-met with pyrimidone inhibitor 7','2.6','0.25642910485348','0.25642910485348'),
('Q59EB3_HUMAN','3efj_B','B','structure of c-met with pyrimidone inhibitor 7','2.6','0.25642910485348','0.25642910485348'),
('MET_HUMAN','3efk_A','A','structure of c-met with pyrimidone inhibitor 50','2.2','0.319333147997836','0.319333147997836'),
('MET_HUMAN','3efk_B','B','structure of c-met with pyrimidone inhibitor 50','2.2','0.319333147997836','0.319333147997836'),
('VGFR2_HUMAN','3efl_A','A','crystal structure of the vegfr2 kinase domain in complex wit motesanib','2.2','0.354510528950216','0.354510528950216'),
('VGFR2_HUMAN','3efl_B','B','crystal structure of the vegfr2 kinase domain in complex wit motesanib','2.2','0.354510528950216','0.354510528950216'),
('B4DX16_HUMAN','3efw_A','A','structure of auroraa with pyridyl-pyrimidine urea inhibitor','2.29','0.322116773302662','0.322116773302662'),
('AURKA_HUMAN','3efw_B','B','structure of auroraa with pyridyl-pyrimidine urea inhibitor','2.29','0.322116773302662','0.322116773302662'),
('ABL1_HUMAN','3eg0_A','A','crystal structure of the n114t mutant of abl-sh3 domain','2.3','0.332618828933747','0.332618828933747'),
('ABL1_HUMAN','3eg1_A','A','crystal structure of the n114q mutant of abl-sh3 domain comp a designed high-affinity peptide ligand: implications for s interactions','1.85','0.468328769707207','0.468328769707207'),
('ABL1_HUMAN','3eg2_A','A','crystal structure of the n114q mutant of abl-sh3 domain','1.8','0.481952743055556','0.481952743055556'),
('ABL1_HUMAN','3eg3_A','A','crystal structure of the n114a mutant of abl-sh3 domain','1.4','0.649963898809524','0.649963898809524'),
('ABL1_HUMAN','3egu_A','A','crystal structure of the n114a mutant of abl-sh3 domain','2.25','0.339159191468254','0.339159191468254'),
('DAPK1_HUMAN','3eh9_A','A','crystal structure of death associated protein kinase complexed with adp','1.7','0.557373151260504','0.557373151260504'),
('DAPK1_HUMAN','3eha_A','A','crystal structure of death associated protein kinase complexed with amppnp','1.6','0.595597113095238','0.595597113095238'),
('CDK2_HUMAN','3eid_A','A','cdk2/cyclina complexed with a pyrazolopyridazine inhibitor','3.15','0.229298933531746','0.229298933531746'),
('CDK2_HUMAN','3ej1_A','A','cdk2/cyclina complexed with a pyrazolopyridazine inhibitor','3.22','0.211513232401656','0.211513232401656'),
('INSR_HUMAN','3ekk_A','A','insulin receptor kinase complexed with an inhibitor','2.1','0.423007470238095','0.423007470238095'),
('INSR_HUMAN','3ekn_A','A','insulin receptor kinase complexed with an inhibitor','2.2','0.387704130140693','0.387704130140693'),
('MK08_HUMAN','3elj_A','A','jnk1 complexed with a bis-anilino-pyrrolopyrimidine inhibito','1.8','0.521336329365079','0.521336329365079'),
('KSYK_HUMAN','3emg_A','A','discovery and sar of novel 4-thiazolyl-2- phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (syk)','2.6','0.295876009615385','0.295876009615385'),
('MP2K6_HUMAN','3enm_B','B','the structure of the map2k mek6 reveals an autoinhibitory di','2.35','0.328033358345998','0.328033358345998'),
('MP2K6_HUMAN','3enm_D','D','the structure of the map2k mek6 reveals an autoinhibitory di','2.35','0.328033358345998','0.328033358345998'),
('CDK2_HUMAN','3eoc_A','A','cdk2/cyclina complexed with a imidazo triazin-2-amine','3.2','0.219495967261905','0.219495967261905'),
('MP2K1_HUMAN','3eqb_A','A','x-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp','2.62','0.280898169074882','0.280898169074882'),
('MP2K1_HUMAN','3eqc_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a ternary complex with compound 1, atp-gs and mg2','1.8','0.478389097222222','0.478389097222222'),
('MP2K1_HUMAN','3eqd_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a binary complex with atp-gs and mg2p','2.1','0.353868645833333','0.353868645833333'),
('MP2K1_HUMAN','3eqf_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a binary complex with k252a and mg2p','2.7','0.122498792989418','0.122498792989418'),
('MP2K1_HUMAN','3eqg_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a ternary complex with pd, adp and mg2p','2.5','0.284613869047619','0.284613869047619'),
('MP2K1_HUMAN','3eqh_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a ternary complex with u0126, adp and mg2p','2','0.356276458333333','0.356276458333333'),
('MP2K1_HUMAN','3eqi_A','A','x-ray structure of the human mitogen-activated protein kinas (mek1) in a binary complex with adp and mg2p','1.9','0.37226663768797','0.37226663768797'),
('ACK1_HUMAN','3eqp_A','A','crystal structure of ack1 with compound t95','2.3','0.327807385481367','0.327807385481367'),
('ACK1_HUMAN','3eqp_B','B','crystal structure of ack1 with compound t95','2.3','0.327807385481367','0.327807385481367'),
('ACK1_HUMAN','3eqr_A','A','crystal structure of ack1 with compound t74','2','0.412786532738095','0.412786532738095'),
('ACK1_HUMAN','3eqr_B','B','crystal structure of ack1 with compound t74','2','0.412786532738095','0.412786532738095'),
('FAK2_HUMAN','3et7_A','A','crystal structure of pyk2 complexed with pf-2318841','2.7','0.175440920965608','0.175440920965608'),
('INSR_HUMAN','3eta_A','A','kinase domain of insulin receptor complexed with a pyrrolo p inhibitor','2.6','0.325190637591575','0.325190637591575'),
('INSR_HUMAN','3eta_B','B','kinase domain of insulin receptor complexed with a pyrrolo p inhibitor','2.6','0.325190637591575','0.325190637591575'),
('FGFR2_HUMAN','3euu_A','A','crystal structure of the fgfr2 d2 domain','2.34','0.360577079136142','0.360577079136142'),
('FGFR2_HUMAN','3euu_B','B','crystal structure of the fgfr2 d2 domain','2.34','0.360577079136142','0.360577079136142'),
('VGFR2_HUMAN','3ewh_A','A','crystal structure of the vegfr2 kinase domain in complex with a pyridyl-pyrimidine benzimidazole inhibitor','1.6','0.570598363095238','0.570598363095238'),
('JAK1_HUMAN','3eyg_A','A','crystal structures of jak1 and jak2 inhibitor complexes','1.9','0.479190610902256','0.479190610902256'),
('JAK1_HUMAN','3eyh_A','A','crystal structures of jak1 and jak2 inhibitor complexes','2','0.462326800595238','0.462326800595238'),
('CDK2_HUMAN','3ezr_A','A','cdk-2 with indazole inhibitor 17 bound at its active site','1.9','0.446911816259398','0.446911816259398'),
('CDK2_HUMAN','3ezv_A','A','cdk-2 with indazole inhibitor 9 bound at its active site','1.99','0.416007012218832','0.416007012218832'),
('PIM1_HUMAN','3f2a_A','A','crystal structure of human pim-1 in complex with dappa','1.9','0.386933468045113','0.386933468045113'),
('HASP_HUMAN','3f2n_A','A','crystal structure of human haspin with an imidazo-pyridazine','1.8','0.546811731150794','0.546811731150794'),
('DAPK1_HUMAN','3f5g_A','A','crystal structure of death associated protein kinase in complex with adp and mg2+','1.85','0.49841091256435','0.49841091256435'),
('IGF1R_HUMAN','3f5p_A','A','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_C','C','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_E','E','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_F','F','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_G','G','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_H','H','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_I','I','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_J','J','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_K','K','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_L','L','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_M','M','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_R','R','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_S','S','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('IGF1R_HUMAN','3f5p_T','T','complex structure of insulin-like growth factor receptor and cyanoquinoline inhibitor','2.9','0.249300026683087','0.249300026683087'),
('DAPK1_HUMAN','3f5u_A','A','crystal structure of the death associated protein kinase in complex with amppnp and mg2+','2','0.46250125','0.46250125'),
('CDK2_HUMAN','3f5x_C','C','cdk-2-cyclin complex with indazole inhibitor 9 bound at its site','2.4','0.273110744047619','0.273110744047619'),
('MET_HUMAN','3f66_A','A','human c-met kinase in complex with quinoxaline inhibitor','1.4','0.675240491071428','0.675240491071428'),
('B4DPY6_HUMAN','3f66_B','B','human c-met kinase in complex with quinoxaline inhibitor','1.4','0.675240491071428','0.675240491071428'),
('ILK_HUMAN','3f6q_A','A','crystal structure of integrin-linked kinase ankyrin repeat domain in complex with pinch1 lim1 domain','1.6','0.615147827380952','0.615147827380952'),
('B5BUC0_HUMAN','3f7z_A','A','x-ray co-crystal structure of glycogen synthase kinase 3beta complex with an inhibitor','2.4','0.332039598214286','0.332039598214286'),
('GSK3B_HUMAN','3f7z_B','B','x-ray co-crystal structure of glycogen synthase kinase 3beta complex with an inhibitor','2.4','0.332039598214286','0.332039598214286'),
('MET_HUMAN','3f82_A','A','crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with n- (4-(2-amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4- ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3- carboxamide','2.5','0.314520892857143','0.314520892857143'),
('GSK3B_HUMAN','3f88_A','A','glycogen synthase kinase 3beta inhibitor complex','2.6','0.288114342948718','0.288114342948718'),
('GSK3B_HUMAN','3f88_B','B','glycogen synthase kinase 3beta inhibitor complex','2.6','0.288114342948718','0.288114342948718'),
('CHK1_HUMAN','3f9n_A','A','crystal structure of chk1 kinase in complex with inhibitor 38','1.9','0.460366235902256','0.460366235902256'),
('TGFR1_HUMAN','3faa_C','C','crystal structure of tgfbri complexed with a 2- aminoimidazole inhibitor','3.35','0.154070037091329','0.154070037091329'),
('TGFR1_HUMAN','3faa_D','D','crystal structure of tgfbri complexed with a 2- aminoimidazole inhibitor','3.35','0.154070037091329','0.154070037091329'),
('TGFR1_HUMAN','3faa_E','E','crystal structure of tgfbri complexed with a 2- aminoimidazole inhibitor','3.35','0.154070037091329','0.154070037091329'),
('MK14_HUMAN','3fc1_X','X','crystal structure of p38 kinase bound to pyrimido-pyridazino inhibitor','2.4','0.355963556547619','0.355963556547619'),
('PLK1_HUMAN','3fc2_A','A','plk1 in complex with bi6727','2.45','0.346584604591837','0.346584604591837'),
('AURKA_HUMAN','3fdn_A','A','structure-based drug design of novel aurora kinase a inhibitors: structure basis for potency and specificity','1.9','0.419332843045113','0.419332843045113'),
('MARK3_HUMAN','3fe3_A','A','crystal structure of the kinase mark3/par-1: t211a-s215a dou','1.9','0.456642411497494','0.456642411497494'),
('MARK3_HUMAN','3fe3_B','B','crystal structure of the kinase mark3/par-1: t211a-s215a dou','1.9','0.456642411497494','0.456642411497494'),
('MAPK3_HUMAN','3fhr_A','A','high resolution crystal structure of mitogen-activated protein kinase-activated protein kinase 3 (mk3)-inhibitor complex','1.9','0.420069301378446','0.420069301378446'),
('MK10_HUMAN','3fi2_A','A','crystal structure of jnk3 with amino-pyrazole inhibitor, sr- 3451','2.28','0.367881372180451','0.367881372180451'),
('MK10_HUMAN','3fi3_A','A','crystal structure of jnk3 with indazole inhibitor, sr-3737','2.2','0.405732359307359','0.405732359307359'),
('MK14_HUMAN','3fi4_A','A','p38 kinase crystal structure in complex with ro4499','2.2','0.387914100378788','0.387914100378788'),
('MK14_HUMAN','3fkl_A','A','p38 kinase crystal structure in complex with ro9552','2','0.425943020833333','0.425943020833333'),
('MK14_HUMAN','3fkn_A','A','p38 kinase crystal structure in complex with ro7125','2','0.426964434523809','0.426964434523809'),
('MK14_HUMAN','3fko_A','A','p38 kinase crystal structure in complex with ro3668','2','0.4305546875','0.4305546875'),
('MK14_HUMAN','3fl4_A','A','p38 kinase crystal structure in complex with ro5634','1.8','0.487548293650794','0.487548293650794'),
('EPHA2_HUMAN','3fl7_A','A','crystal structure of the human ephrin a2 ectodomain','2.5','0.263834330357143','0.263834330357143'),
('MK14_HUMAN','3fln_C','C','p38 kinase crystal structure in complex with r1487','1.9','0.459357976973684','0.459357976973684'),
('MK14_HUMAN','3flq_A','A','p38 kinase crystal structure in complex with 6-(2,4- difluoro-phenoxy)-2-((s)-2-methanesulfonyl-1-methyl- ethylamino)-8-methyl-8h-pyrido[2,3-d]pyrimidin','1.9','0.433435506735589','0.433435506735589'),
('MK14_HUMAN','3fls_A','A','p38 kinase crystal structure in complex with 6-(2,4- difluoro-phenoxy)-2-((r)-2-methanesulfonyl-1-methyl- ethylamino)-8-methyl-8h-pyrido[2,3-d]pyrimidin-7-one','2.3','0.305095078933747','0.305095078933747'),
('MK14_HUMAN','3flw_A','A','p38 kinase crystal structure in complex with pamapimod','2.1','0.407346845238095','0.407346845238095'),
('MK14_HUMAN','3fly_A','A','p38 kinase crystal structure in complex with 6-(2,4- difluoro-phenoxy)-2-isopropylamino-8-methyl-8h-pyrido[2,3- d]pyrimidin-7-one','1.8','0.480913040674603','0.480913040674603'),
('MK14_HUMAN','3flz_A','A','p38 kinase crystal structure in complex with 8-methyl-6-phen (tetrahydro-pyran-4-ylamino)-8h-pyrido[2,3-d]pyrimidin-7-on','2.23','0.379286951606876','0.379286951606876'),
('HASP_HUMAN','3fmd_A','A','crystal structure of human haspin with an isoquinoline ligan','2','0.419693497023809','0.419693497023809'),
('MP2K6_HUMAN','3fme_A','A','crystal structure of human mitogen-activated protein kinase (mek6) activated mutant (s207d, t211d)','2.26','0.35326434932048','0.35326434932048'),
('MK14_HUMAN','3fmh_A','A','p38 kinase crystal structure in complex with 6-(2,4-difluoro 8-methyl-2-((r)-1-methyl-2-tetrazol-2-yl-ethylamino)-8h-pyr d]pyrimidin-7-one','1.9','0.45361788768797','0.45361788768797'),
('MK14_HUMAN','3fmj_A','A','p38 kinase crystal structure in complex with 4-(5-methyl-3-p isoxazol-4-yl)-pyrimidin-2-ylamine','2','0.431440372023809','0.431440372023809'),
('MK14_HUMAN','3fmk_A','A','p38 kinase crystal structure in complex with 6-(2,4-difluoro 8-methyl-2-((s)-1-methyl-2-tetrazol-2-yl-ethylamino)-8h-pyr d]pyrimidin-7-one','1.7','0.537283508403361','0.537283508403361'),
('MK14_HUMAN','3fml_A','A','p38 kinase crystal structure in complex with ro6224','2.1','0.409513005952381','0.409513005952381'),
('MK14_HUMAN','3fmm_A','A','p38 kinase crystal structure in complex with ro6226','2','0.429675997023809','0.429675997023809'),
('MK14_HUMAN','3fmn_A','A','p38 kinase crystal structure in complex with ro2530','1.9','0.467522917449875','0.467522917449875'),
('MAPK2_HUMAN','3fpm_A','A','crystal structure of a squarate inhibitor bound to mapkap kinase-2','3.3','0.132607386363636','0.132607386363636'),
('KSYK_HUMAN','3fqe_A','A','crystal structure of spleen tyrosine kinase complexed with y','2.5','0.318666473214286','0.318666473214286'),
('KSYK_HUMAN','3fqh_A','A','crystal structure of spleen tyrosine kinase complexed with a 2-substituted 7-azaindole','2.26','0.347911626106195','0.347911626106195'),
('KSYK_HUMAN','3fqh_B','B','crystal structure of spleen tyrosine kinase complexed with a 2-substituted 7-azaindole','2.26','0.347911626106195','0.347911626106195'),
('KSYK_HUMAN','3fqs_A','A','crystal structure of spleen tyrosine kinase complexed with r','2.1','0.401866011904762','0.401866011904762'),
('MK14_HUMAN','3fsf_A','A','p38 kinase crystal structure in complex with 3-(2,6- dichloro-phenyl)-7-[4-(2-diethylamino-ethoxy)-phenylamino]- 1-methyl-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one','2.1','0.392046398809524','0.392046398809524'),
('MK14_HUMAN','3fsk_A','A','p38 kinase crystal structure in complex with ro6257','2','0.437296785714286','0.437296785714286'),
('Q8IXP2_HUMAN','3fup_A','A','crystal structures of jak1 and jak2 inhibitor complexes','2.4','0.347174464285714','0.347174464285714'),
('JAK2_HUMAN','3fup_B','B','crystal structures of jak1 and jak2 inhibitor complexes','2.4','0.347174464285714','0.347174464285714'),
('MK10_HUMAN','3fv8_A','A','jnk3 bound to piperazine amide inhibitor, sr2774.','2.28','0.350124095394737','0.350124095394737'),
('PLK1_HUMAN','3fvh_A','A','polo-like kinase 1 polo box domain in complex with ac-lhspta peptide','1.58','0.601279085857444','0.601279085857444'),
('CSK21_HUMAN','3fwq_A','A','inactive conformation of human protein kinase ck2 catalytic','2.3','0.38394284679089','0.38394284679089'),
('CSK21_HUMAN','3fwq_B','B','inactive conformation of human protein kinase ck2 catalytic','2.3','0.38394284679089','0.38394284679089'),
('MAPK3_HUMAN','3fxw_A','A','high resolution crystal structure of mitogen-activated prote activated protein kinase 3/inhibitor 2 complex','2','0.390649434523809','0.390649434523809'),
('EPHA3_HUMAN','3fxx_A','A','human epha3 kinase and juxtamembrane region bound to substra kqwdnye[ptyr]iw','1.7','0.574387615546218','0.574387615546218'),
('PAK1_HUMAN','3fxz_A','A','crystal structure of pak1 kinase domain with ruthenium complex lambda-fl172','1.64','0.559580740418118','0.559580740418118'),
('PAK1_HUMAN','3fy0_A','A','crystal structure of pak1 kinase domain with ruthenium compl','2.35','0.361172108345998','0.361172108345998'),
('EPHA3_HUMAN','3fy2_A','A','human epha3 kinase and juxtamembrane region bound to substra kqwdnyefiw','1.8','0.529065138888889','0.529065138888889'),
('MAPK2_HUMAN','3fyj_X','X','crystal structure of an optimzied benzothiophene inhibitor bound to mapkap kinase-2 (mk-2)','3.8','-0.0713959594298246','-0.0713959594298246'),
('MAPK2_HUMAN','3fyk_X','X','crystal structure of a benzthiophene lead bound to mapkap kinase-2 (mk-2)','3.5','0.0568434821428571','0.0568434821428571'),
('CDK2_HUMAN','3fz1_A','A','crystal structure of a benzthiophene inhibitor bound to human cyclin-dependent kinase-2 (cdk-2)','1.9','0.439159375783208','0.439159375783208'),
('FAK2_HUMAN','3fzo_A','A','crystal structure of pyk2-apo, proline-rich tyrosine kinase','2.2','0.368254457521645','0.368254457521645'),
('FAK2_HUMAN','3fzp_A','A','crystal structure of pyk2 complexed with atpgs','2.1','0.381481845238095','0.381481845238095'),
('FAK2_HUMAN','3fzr_A','A','crystal structure of pyk2 complexed with pf-431396','2.7','0.21937261739418','0.21937261739418'),
('FAK2_HUMAN','3fzs_A','A','crystal structure of pyk2 complexed with birb796','1.75','0.527656979166667','0.527656979166667'),
('FAK2_HUMAN','3fzt_A','A','crystal structure of pyk2 complexed with pf-4618433','1.95','0.45971936698718','0.45971936698718'),
('KIT_HUMAN','3g0e_A','A','kit kinase domain in complex with sunitinib','1.6','0.571333526785714','0.571333526785714'),
('KIT_HUMAN','3g0f_A','A','kit kinase domain mutant d816h in complex with sunitinib','2.6','0.29560410485348','0.29560410485348'),
('KIT_HUMAN','3g0f_B','B','kit kinase domain mutant d816h in complex with sunitinib','2.6','0.29560410485348','0.29560410485348'),
('BMPR2_HUMAN','3g2f_A','A','crystal structure of the kinase domain of bone morphogenetic receptor type ii (bmpr2) at 2.35 a resolution','2.35','0.356846319655522','0.356846319655522'),
('CDK4_HUMAN','3g33_A','A','crystal structure of cdk4/cyclin d3','3','0.167686964285714','0.167686964285714'),
('CDK4_HUMAN','3g33_C','C','crystal structure of cdk4/cyclin d3','3','0.167686964285714','0.167686964285714'),
('EGFR_HUMAN','3g5v_C','C','antibodies specifically targeting a locally misfolded region associated egfr','2','0.391463764880952','0.391463764880952'),
('EGFR_HUMAN','3g5y_E','E','antibodies specifically targeting a locally misfolded region associated egfr','1.59','0.571973793800539','0.571973793800539'),
('MK10_HUMAN','3g90_X','X','jnk-3 bound to (z)-5-fluoro-1-((6-fluoro-4h-benzo[d][1,3]dio methyl)-3-(hydroxyimino)indolin-2-one','2.4','0.319996636904762','0.319996636904762'),
('MK10_HUMAN','3g9l_X','X','jnk3 bound to (z)-1-((6-fluoro-4h-benzo[d][1,3]dioxin-8-yl)m (hydroxyimino)-4-styrylindolin-2-one','2.2','0.35191661525974','0.35191661525974'),
('MK10_HUMAN','3g9n_A','A','jnk3 bound to (z)-1-((6-fluoro-4h-benzo[d][1,3]dioxin-8-yl)m (hydroxyimino)-4-phenylindolin-2-one','2.8','0.227798080357143','0.227798080357143'),
('GSK3B_HUMAN','3gb2_A','A','gsk3beta inhibitor complex','2.4','0.286938988095238','0.286938988095238'),
('MK14_HUMAN','3gc7_A','A','the structure of p38alpha in complex with a dihydroquinazoli','1.8','0.522776984126984','0.522776984126984'),
('MK11_HUMAN','3gc8_A','A','the structure of p38beta c162s in complex with a dihydroquin','2.4','0.32471349702381','0.32471349702381'),
('MK11_HUMAN','3gc8_B','B','the structure of p38beta c162s in complex with a dihydroquin','2.4','0.32471349702381','0.32471349702381'),
('MK11_HUMAN','3gc9_A','A','the structure of p38beta c119s, c162s in complex with a dihydroquinazolinone inhibitor','2.05','0.387491961382114','0.387491961382114'),
('MK11_HUMAN','3gc9_B','B','the structure of p38beta c119s, c162s in complex with a dihydroquinazolinone inhibitor','2.05','0.387491961382114','0.387491961382114'),
('MK14_HUMAN','3gcp_A','A','human p38 map kinase in complex with sb203580','2.25','0.363364712301587','0.363364712301587'),
('MK14_HUMAN','3gcq_A','A','human p38 map kinase in complex with rl45','2','0.403133363095238','0.403133363095238'),
('MK14_HUMAN','3gcs_A','A','human p38 map kinase in complex with sorafenib','2.1','0.398968303571429','0.398968303571429'),
('MK14_HUMAN','3gcu_A','A','human p38 map kinase in complex with rl48','2.1','0.412757321428571','0.412757321428571'),
('MK14_HUMAN','3gcv_A','A','human p38 map kinase in complex with rl62','2.3','0.357491998576605','0.357491998576605'),
('BTK_HUMAN','3gen_A','A','the 1.6 a crystal structure of human bruton\'s tyrosine kinase bound to a pyrrolopyrimidine-containing compound','1.6','0.576616443452381','0.576616443452381'),
('MK14_HUMAN','3gfe_A','A','crystal structure of p38a mitogen-activated protein kinase in complex with a pyrazolopyridinone inhibitor','2.1','0.384585654761905','0.384585654761905'),
('TTK_HUMAN','3gfw_A','A','crystal structure of human dual specificity protein kinase ( complex with a pyrolo-pyridin ligand','2.74','0.276697104840111','0.276697104840111'),
('MST4_HUMAN','3ggf_A','A','crystal structure of human serine/threonine-protein kinase m complex with an quinazolin','2.35','0.34426368572695','0.34426368572695'),
('MST4_HUMAN','3ggf_B','B','crystal structure of human serine/threonine-protein kinase m complex with an quinazolin','2.35','0.34426368572695','0.34426368572695'),
('MK14_HUMAN','3gi3_A','A','crystal structure of a n-phenyl-n\'-naphthylurea analog in complex with p38 map kinase','2.4','0.303131369047619','0.303131369047619'),
('FAK2_HUMAN','3gm1_A','A','crystal structure of the focal adhesion targeting (fat) domain of pyk2 in complex with paxillin ld4 motif-derived peptides','2.95','0.207086860371267','0.207086860371267'),
('FAK2_HUMAN','3gm1_B','B','crystal structure of the focal adhesion targeting (fat) domain of pyk2 in complex with paxillin ld4 motif-derived peptides','2.95','0.207086860371267','0.207086860371267'),
('FAK2_HUMAN','3gm2_A','A','crystal structure of the focal adhesion targeting (fat) domain of pyk2','2.71','0.219348853727377','0.219348853727377'),
('FAK2_HUMAN','3gm3_A','A','crystal structure of the focal adhesion targeting (fat) domain of pyk2','2.6','0.258530726877289','0.258530726877289'),
('STRAA_HUMAN','3gni_B','B','structure of strad and mo25','2.35','0.339779920845998','0.339779920845998'),
('MAPK2_HUMAN','3gok_A','A','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_B','B','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_C','C','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_D','D','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_E','E','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_F','F','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_G','G','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_H','H','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_I','I','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_J','J','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_K','K','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('MAPK2_HUMAN','3gok_L','L','binding site mapping of protein ligands','3.2','0.185049747023809','0.185049747023809'),
('EGFR_HUMAN','3gop_A','A','crystal structure of the egf receptor juxtamembrane and kina','2.8','0.267089241071429','0.267089241071429'),
('MK11_HUMAN','3gp0_A','A','crystal structure of human mitogen activated protein kinase beta) in complex with nilotinib','1.9','0.472789346021303','0.472789346021303'),
('KCC2D_HUMAN','3gp2_B','B','calmodulin bound to peptide from calmodulin kinase ii (camkii)','1.46','0.702187563396934','0.702187563396934'),
('FGFR1_HUMAN','3gqi_A','A','crystal structure of activated receptor tyrosine kinase in c with substrates','2.5','0.267974389880952','0.267974389880952'),
('FGFR1_HUMAN','3gql_A','A','crystal structure of activated receptor tyrosine kinase in c with substrates','2.8','0.230225833333333','0.230225833333333'),
('D3DSX2_HUMAN','3gql_B','B','crystal structure of activated receptor tyrosine kinase in c with substrates','2.8','0.230225833333333','0.230225833333333'),
('D3DSX2_HUMAN','3gql_C','C','crystal structure of activated receptor tyrosine kinase in c with substrates','2.8','0.230225833333333','0.230225833333333'),
('Q8NI16_HUMAN','3grw_A','A','fgfr3 in complex with a fab','2.1','0.407762946428571','0.407762946428571'),
('EGFR_HUMAN','3gt8_A','A','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.96','0.225998403314028','0.225998403314028'),
('EGFR_HUMAN','3gt8_B','B','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.96','0.225998403314028','0.225998403314028'),
('Q59FL8_HUMAN','3gt8_C','C','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.96','0.225998403314028','0.225998403314028'),
('EGFR_HUMAN','3gt8_D','D','crystal structure of the inactive egfr kinase domain in complex with amp-pnp','2.96','0.225998403314028','0.225998403314028'),
('DAPK1_HUMAN','3gu4_A','A','crystal structure of dapkq23v-amppnp','1.35','0.705211380621693','0.705211380621693'),
('DAPK1_HUMAN','3gu5_A','A','crystal structure of dapkq23v-amppnp-mg2+','1.65','0.559333835227273','0.559333835227273'),
('DAPK1_HUMAN','3gu6_A','A','crystal structure of dapkq23v-adp','1.49','0.63566852888303','0.63566852888303'),
('DAPK1_HUMAN','3gu7_A','A','crystal structure of dapkq23v-adp-mg2+','1.9','0.501756563283208','0.501756563283208'),
('DAPK1_HUMAN','3gu8_A','A','crystal structure of dapkl93g with n6-cyclopentyladenosine','1.6','0.567170059523809','0.567170059523809'),
('DAPK1_HUMAN','3gub_A','A','crystal structure of dapkl93g complexed with n6-(2- phenylethyl)adenosine','1.71','0.535236363304094','0.535236363304094'),
('ABL2_HUMAN','3gvu_A','A','the crystal structure of human abl2 in complex with gleevec','2.05','0.443774892929733','0.443774892929733'),
('TGFR1_HUMAN','3gxl_A','A','alk-5 kinase complex with gw857175','1.8','0.478016552579365','0.478016552579365'),
('EPHA4_HUMAN','3gxu_A','A','crystal structure of eph receptor and ephrin complex','2.5','0.28673412202381','0.28673412202381'),
('FYN_HUMAN','3h0f_A','A','crystal structure of the human fyn sh3 r96w mutant','2.61','0.289373324952107','0.289373324952107'),
('FYN_HUMAN','3h0h_A','A','human fyn sh3 domain r96i mutant, crystal form i','1.76','0.525900270562771','0.525900270562771'),
('FYN_HUMAN','3h0i_A','A','human fyn sh3 domain r96i mutant, crystal form ii','2.2','0.407620320616883','0.407620320616883'),
('FYN_HUMAN','3h0i_B','B','human fyn sh3 domain r96i mutant, crystal form ii','2.2','0.407620320616883','0.407620320616883'),
('AURKA_HUMAN','3h0y_A','A','aurora a in complex with a bisanilinopyrimidine','2.5','0.306255699404762','0.306255699404762'),
('AURKA_HUMAN','3h0z_A','A','aurora a in complex with a bisanilinopyrimidine','2.92','0.244783878424658','0.244783878424658'),
('B4DX16_HUMAN','3h0z_B','B','aurora a in complex with a bisanilinopyrimidine','2.92','0.244783878424658','0.244783878424658'),
('B4DX16_HUMAN','3h0z_C','C','aurora a in complex with a bisanilinopyrimidine','2.92','0.244783878424658','0.244783878424658'),
('AURKA_HUMAN','3h10_A','A','aurora a inhibitor complex','2.2','0.386482403950216','0.386482403950216'),
('AURKA_HUMAN','3h10_B','B','aurora a inhibitor complex','2.2','0.386482403950216','0.386482403950216'),
('B4DX16_HUMAN','3h10_D','D','aurora a inhibitor complex','2.2','0.386482403950216','0.386482403950216'),
('CSK21_HUMAN','3h30_A','A','crystal structure of the catalytic subunit of human protein kinase ck2 with 5,6-dichloro-1-beta-d- ribofuranosylbenzimidazole','1.56','0.623650373168498','0.623650373168498'),
('CSK21_HUMAN','3h30_B','B','crystal structure of the catalytic subunit of human protein kinase ck2 with 5,6-dichloro-1-beta-d- ribofuranosylbenzimidazole','1.56','0.623650373168498','0.623650373168498'),
('ERBB2_HUMAN','3h3b_A','A','crystal structure of the single-chain fv (scfv) fragment of erbb2 antibody cha21 in complex with residues 1-192 of erbb extracellular domain','2.45','0.327257595663265','0.327257595663265'),
('FAK2_HUMAN','3h3c_A','A','crystal structure of pyk2 in complex with sulfoximine- substituted trifluoromethylpyrimidine analog','2','0.398707961309524','0.398707961309524'),
('EPHA7_HUMAN','3h8m_B','B','sam domain of human ephrin type-a receptor 7 (epha7)','2.1','0.422141160714286','0.422141160714286'),
('TTK_HUMAN','3h9f_A','A','crystal structure of human dual specificity protein kinase ( complex with a pyrimido-diazepin ligand','2.6','0.298335265567766','0.298335265567766'),
('PDPK1_HUMAN','3h9o_A','A','phosphoinositide-dependent protein kinase 1 (pdk-1) in complex with compound 9','2.3','0.345944230719462','0.345944230719462'),
('ACVR1_HUMAN','3h9r_A','A','crystal structure of the kinase domain of type i activin rec (acvr1) in complex with fkbp12 and dorsomorphin','2.35','0.377515158941236','0.377515158941236'),
('AURKA_HUMAN','3ha6_A','A','crystal structure of aurora a in complex with tpx2 and compo','2.36','0.330013768916465','0.330013768916465'),
('MK14_HUMAN','3ha8_A','A','the complex structure of the map kinase p38/compound 14b','2.48','0.307998544546851','0.307998544546851'),
('HCK_HUMAN','3hck_A','A','nmr ensemble of the uncomplexed human hck sh2 domain, 20 structures',NULL,'0.0248003869047619','0.0248003869047619'),
('SGK1_HUMAN','3hdm_A','A','crystal structure of serum and glucocorticoid-regulated kina complex with compound 1','2.6','0.305087869734432','0.305087869734432'),
('SGK1_HUMAN','3hdn_A','A','crystal structure of serum and glucocorticoid-regulated kina complex with compound 2','3.1','0.21272033266129','0.21272033266129'),
('MK14_HUMAN','3hec_A','A','p38 in complex with imatinib','2.5','0.268247113095238','0.268247113095238'),
('MK14_HUMAN','3heg_A','A','p38 in complex with sorafenib','2.2','0.330964130140693','0.330964130140693'),
('EPHA2_HUMAN','3hei_A','A','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_C','C','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_E','E','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_G','G','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_I','I','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_K','K','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_M','M','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('EPHA2_HUMAN','3hei_O','O','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2','0.445076086309524','0.445076086309524'),
('PLK1_HUMAN','3hih_A','A','structure of human plk1-pbd with glycerol and sulfate in the phophopeptide binding site','1.7','0.563495785189076','0.563495785189076'),
('B4E083_HUMAN','3hih_B','B','structure of human plk1-pbd with glycerol and sulfate in the phophopeptide binding site','1.7','0.563495785189076','0.563495785189076'),
('PLK1_HUMAN','3hik_A','A','structure of human plk1-pbd in complex with plhspt','1.77','0.484075337721953','0.484075337721953'),
('EPHA1_HUMAN','3hil_A','A','sam domain of human ephrin type-a receptor 1 (epha1)','2','0.407742172619048','0.407742172619048'),
('A8K2T6_HUMAN','3hil_B','B','sam domain of human ephrin type-a receptor 1 (epha1)','2','0.407742172619048','0.407742172619048'),
('MK14_HUMAN','3hl7_A','A','crystal structure of human p38alpha complexed with sd-0006','1.88','0.456721158497974','0.456721158497974'),
('MK14_HUMAN','3hll_A','A','crystal structure of human p38alpha complexed with ph-797804','1.95','0.422967015796703','0.422967015796703'),
('ABL2_HUMAN','3hmi_A','A','the crystal structure of human abl2 in complex with 5-amino- (aminosulfonyl)phenyl]amino}-n-(2,6-difluorophenyl)-1h-1,2, triazole-1-carbothioamide','1.65','0.566790516774892','0.566790516774892'),
('TGFR1_HUMAN','3hmm_A','A','structure of alk5 + gw855857','1.7','0.512656722689076','0.512656722689076'),
('TTK_HUMAN','3hmn_A','A','crystal structure of human mps1 catalytic domain in complex','2.7','0.291653525132275','0.291653525132275'),
('TTK_HUMAN','3hmo_A','A','crystal structure of human mps1 catalytic domain in complex inhibitor staurosporine','2.4','0.345884300595238','0.345884300595238'),
('TTK_HUMAN','3hmp_A','A','crystal structure of human mps1 catalytic domain in complex quinazolin ligand compound 4','2.3','0.352800480719462','0.352800480719462'),
('VGFR1_HUMAN','3hng_A','A','crystal structure of vegfr1 in complex with n-(4-chloropheny ((pyridin-4-ylmethyl)amino)benzamide','2.7','0.290804938822751','0.290804938822751'),
('MK14_HUMAN','3hp2_A','A','crystal structure of human p38alpha complexed with a pyridin compound','2.15','0.387712350498339','0.387712350498339'),
('MK14_HUMAN','3hp5_A','A','crystal structure of human p38alpha complexed with a pyrimidopyridazinone compound','2.3','0.344630808100414','0.344630808100414'),
('EPHA2_HUMAN','3hpn_A','A','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('EPHA2_HUMAN','3hpn_B','B','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('EPHA2_HUMAN','3hpn_C','C','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('EPHA2_HUMAN','3hpn_D','D','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('EPHA2_HUMAN','3hpn_E','E','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('EPHA2_HUMAN','3hpn_F','F','ligand recognition by a-class eph receptors: crystal structu epha2 ligand-binding domain and the epha2/ephrin-a1 complex','2.52','0.261077926587302','0.261077926587302'),
('MK14_HUMAN','3hrb_A','A','p38 kinase crystal structure in complex with small molecule inhibitor','2.2','0.378716005140693','0.378716005140693'),
('PDPK1_HUMAN','3hrc_A','A','crystal structure of a mutant of human pdk1 kinase domain in with atp','1.91','0.484250328471703','0.484250328471703'),
('PDPK1_HUMAN','3hrf_A','A','crystal structure of human pdk1 kinase domain in complex wit allosteric activator bound to the pif-pocket','1.9','0.511923006735589','0.511923006735589'),
('MK14_HUMAN','3hub_A','A','human p38 map kinase in complex with scios-469','2.25','0.344923968253968','0.344923968253968'),
('MK14_HUMAN','3huc_A','A','human p38 map kinase in complex with rl40','1.8','0.504363338293651','0.504363338293651'),
('MK14_HUMAN','3hv3_A','A','human p38 map kinase in complex with rl49','2','0.390721041666667','0.390721041666667'),
('MK14_HUMAN','3hv4_A','A','human p38 map kinase in complex with rl51','2.6','0.298724551282051','0.298724551282051'),
('MK14_HUMAN','3hv4_B','B','human p38 map kinase in complex with rl51','2.6','0.298724551282051','0.298724551282051'),
('MK14_HUMAN','3hv5_A','A','human p38 map kinase in complex with rl24','2.25','0.371927316468254','0.371927316468254'),
('MK14_HUMAN','3hv5_B','B','human p38 map kinase in complex with rl24','2.25','0.371927316468254','0.371927316468254'),
('MK14_HUMAN','3hv6_A','A','human p38 map kinase in complex with rl39','1.95','0.428484664606227','0.428484664606227'),
('MK14_HUMAN','3hv7_A','A','human p38 map kinase in complex with rl38','2.4','0.325939464285714','0.325939464285714'),
('MK14_HUMAN','3hvc_A','A','crystal structure of human p38alpha map kinase','2.1','0.392507693452381','0.392507693452381'),
('GSK3B_HUMAN','3i4b_A','A','crystal structure of gsk3b in complex with a pyrimidylpyrrole inhibitor','2.3','0.377143412267081','0.377143412267081'),
('MET_HUMAN','3i5n_A','A','crystal structure of c-met with triazolopyridazine inhibitor 13','2','0.417815089285714','0.417815089285714'),
('MK01_HUMAN','3i5z_A','A','crystal structure of erk2 bound to (s)-n-(2-hydroxy-1-phenyl (5-methyl-2-(phenylamino)pyrimidin-4-yl)-1h-pyrrole-2-carbo','2.2','0.357187686688312','0.357187686688312'),
('MK01_HUMAN','3i60_A','A','crystal structure of erk2 bound to (s)-4-(2-(2-chlorophenyla methylpyrimidin-4-yl)-n-(2-hydroxy-1-phenylethyl)-1h-pyrrol carboxamide','2.5','0.310889806547619','0.310889806547619'),
('CHK2_HUMAN','3i6u_A','A','structure and activation mechanism of the chk2 dna-damage ch kinase','3','0.185965848214286','0.185965848214286'),
('CHK2_HUMAN','3i6u_B','B','structure and activation mechanism of the chk2 dna-damage ch kinase','3','0.185965848214286','0.185965848214286'),
('CHK2_HUMAN','3i6w_A','A','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_B','B','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_C','C','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_D','D','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_E','E','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_F','F','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_G','G','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('CHK2_HUMAN','3i6w_H','H','structure and activation mechanism of the chk2 dna-damage ch kinase','3.25','0.173685849358974','0.173685849358974'),
('IGF1R_HUMAN','3i81_A','A','crystal structure of insulin-like growth factor 1 receptor (igf-1r-wt) complex with bms-754807 [1-(4-((5-cyclopropyl- 1h-pyrazol-3-yl)amino)pyrrolo[2,1-f][1,2,4]triazin-2-yl)-n- (6-fluoro-3-pyridinyl)-2-methyl-l-prolinamide]','2.08','0.399576641483516','0.399576641483516'),
('BRAF_HUMAN','3idp_B','B','b-raf v600e kinase domain in complex with an aminoisoquinoli inhibitor','2.7','0.285107944775132','0.285107944775132'),
('A9CP04_HUMAN','3iec_A','A','helicobacter pylori caga inhibits par1/mark family kinases b mimicking host substrates','2.2','0.395991332521645','0.395991332521645'),
('MARK2_HUMAN','3iec_B','B','helicobacter pylori caga inhibits par1/mark family kinases b mimicking host substrates','2.2','0.395991332521645','0.395991332521645'),
('A9CP04_HUMAN','3iec_C','C','helicobacter pylori caga inhibits par1/mark family kinases b mimicking host substrates','2.2','0.395991332521645','0.395991332521645'),
('A9CP04_HUMAN','3iec_D','D','helicobacter pylori caga inhibits par1/mark family kinases b mimicking host substrates','2.2','0.395991332521645','0.395991332521645'),
('CDK2_HUMAN','3ig7_A','A','novel cdk-5 inhibitors - crystal structure of inhibitor efp with cdk-2','1.8','0.465376552579365','0.465376552579365'),
('CDK2_HUMAN','3igg_A','A','novel cdk-5 inhibitors - crystal structure of inhibitor efq with cdk-2','1.8','0.472048129960318','0.472048129960318'),
('BRAF_HUMAN','3ii5_A','A','the complex of wild-type b-raf with pyrazolo pyrimidine inhibitor','2.79','0.262564040258577','0.262564040258577'),
('EGFR_HUMAN','3ika_A','A','crystal structure of egfr 696-1022 t790m mutant covalently binding to wz4002','2.9','0.22437310704023','0.22437310704023'),
('Q59FL8_HUMAN','3ika_B','B','crystal structure of egfr 696-1022 t790m mutant covalently binding to wz4002','2.9','0.22437310704023','0.22437310704023'),
('JAK2_HUMAN','3io7_A','A','2-aminopyrazolo[1,5-a]pyrimidines as potent and selective inhibitors of jak2','2.6','0.294294744734432','0.294294744734432'),
('JAK2_HUMAN','3iok_A','A','2-aminopyrazolo[1,5-a]pyrimidines as potent and selective inhibitors of jak2','2.1','0.388706071428571','0.388706071428571'),
('PDPK1_HUMAN','3ion_A','A','pdk1 in complex with compound 8h','2.4','0.311586041666667','0.311586041666667'),
('PDPK1_HUMAN','3iop_A','A','pdk-1 in complex with the inhibitor compound-8i','2.2','0.356646942640693','0.356646942640693'),
('MK14_HUMAN','3iph_A','A','crystal structure of p38 in complex with a biphenylamide inh','2.1','0.435797470238095','0.435797470238095'),
('HASP_HUMAN','3iq7_A','A','crystal structure of human haspin in complex with 5-iodotube','2','0.473708764880952','0.473708764880952'),
('RAF1_HUMAN','3iqj_P','P','crystal structure of human 14-3-3 sigma in complex with raf1 (10mer)','1.15','0.9207136251294','0.9207136251294'),
('RAF1_HUMAN','3iqu_P','P','crystal structure of human 14-3-3 sigma in complex with raf1 (6mer)','1.05','1.0022825','1.0022825'),
('RAF1_HUMAN','3iqv_P','P','crystal structure of human 14-3-3 sigma in complex with raf1 (6mer) and stabilisator fusicoccin','1.2','0.88652568452381','0.88652568452381'),
('MK14_HUMAN','3itz_A','A','crystal structure of p38a mitogen-activated protein kinase in complex with a pyrazolopyridazine inhibitor','2.25','0.350690515873016','0.350690515873016'),
('KPCA_HUMAN','3iw4_A','A','crystal structure of pkc alpha in complex with nvp-aeb071','2.8','0.267313764880952','0.267313764880952'),
('KPCA_HUMAN','3iw4_C','C','crystal structure of pkc alpha in complex with nvp-aeb071','2.8','0.267313764880952','0.267313764880952'),
('MK14_HUMAN','3iw5_A','A','human p38 map kinase in complex with an indole derivative','2.5','0.305984375','0.305984375'),
('MK14_HUMAN','3iw6_A','A','human p38 map kinase in complex with a benzylpiperazin- pyrrol','2.1','0.385874255952381','0.385874255952381'),
('MK14_HUMAN','3iw7_A','A','human p38 map kinase in complex with an imidazo-pyridine','2.4','0.336475535714286','0.336475535714286'),
('MK14_HUMAN','3iw8_A','A','structure of inactive human p38 map kinase in complex with a thiazole-urea','2','0.404831517857143','0.404831517857143'),
('ILK_HUMAN','3ixe_A','A','structural basis of competition between pinch1 and pinch2 for binding to the ankyrin repeat domain of integrin-linked kinase',NULL,'-0.3','-0.3'),
('PIM1_HUMAN','3jpv_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and a pyrrolo[2, a]carbazole ligand','2.35','0.379550069655522','0.379550069655522'),
('FGFR1_HUMAN','3js2_A','A','crystal structure of minimal kinase domain of fibroblast growth factor receptor 1 in complex with 5-(2-thienyl) nicotinic acid','2.2','0.382459130140693','0.382459130140693'),
('CSK21_HUMAN','3juh_A','A','crystal structure of a mutant of human protein kinase ck2alp altered cosubstrate specificity','1.66','0.566776320101836','0.566776320101836'),
('CSK21_HUMAN','3juh_B','B','crystal structure of a mutant of human protein kinase ck2alp altered cosubstrate specificity','1.66','0.566776320101836','0.566776320101836'),
('CHK1_HUMAN','3jvr_A','A','characterization of the chk1 allosteric inhibitor binding site','1.76','0.512832993777056','0.512832993777056'),
('CHK1_HUMAN','3jvs_A','A','characterization of the chk1 allosteric inhibitor binding site','1.9','0.48370695018797','0.48370695018797'),
('PIM1_HUMAN','3jxw_A','A','discovery of 3h-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective and orally bioavailable pim kinases inhibitors','2.8','0.249463898809524','0.249463898809524'),
('PIM1_HUMAN','3jy0_A','A','discovery of 3h-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective and orally bioavailable pim kinases inhibitors','2.4','0.308487217261905','0.308487217261905'),
('JAK2_HUMAN','3jy9_A','A','janus kinase 2 inhibitors','2.1','0.396798794642857','0.396798794642857'),
('PIM1_HUMAN','3jya_A','A','discovery of 3h-benzo[4,5]thieno[3,2-d]pyrimidin-4-ones as potent, highly selective and orally bioavailable pim kinases inhibitors','2.1','0.387225803571428','0.387225803571428'),
('DYRK2_HUMAN','3k2l_A','A','crystal structure of dual-specificity tyrosine phosphorylati regulated kinase 2 (dyrk2)','2.36','0.333733069511703','0.333733069511703'),
('ABL1_HUMAN','3k2m_A','A','crystal structure of monobody ha4/abl1 sh2 domain complex','1.75','0.533997395833333','0.533997395833333'),
('MK14_HUMAN','3k3i_A','A','p38alpha bound to novel dgf-out compound pf-00215955','1.7','0.537853538165266','0.537853538165266'),
('MK14_HUMAN','3k3j_A','A','p38alpha bound to novel dfg-out compound pf-00416121','2','0.431821770833333','0.431821770833333'),
('BTK_HUMAN','3k54_A','A','structures of human bruton\'s tyrosine kinase in active and i conformations suggests a mechanism of activation for tec fa kinases.','1.94','0.440251610978154','0.440251610978154'),
('AURKA_HUMAN','3k5u_A','A','identification, sar studies and x-ray cocrystal analysis of furano-pyrimidine aurora kinase a inhibitor','2.35','0.29855968275076','0.29855968275076'),
('MAPK2_HUMAN','3ka0_A','A','mk2 complex with inhibitor 6-(5-(2-aminopyrimidin-4-ylamino) hydroxyphenyl)-n-methylbenzo[b]thiophene-2-carboxamide','2.9','0.231642749897373','0.231642749897373'),
('PLK1_HUMAN','3kb7_A','A','crystal structure of polo-like kinase 1 in complex with a pyrazoloquinazoline inhibitor','2.5','0.302817752976191','0.302817752976191'),
('MAPK2_HUMAN','3kc3_A','A','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_B','B','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_C','C','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_E','E','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_F','F','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_G','G','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_H','H','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_I','I','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_J','J','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_K','K','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('MAPK2_HUMAN','3kc3_L','L','mk2 complexed to inhibitor n4-(7-(benzofuran-2-yl)-1h-indazo pyrimidine-2,4-diamine','2.9','0.201845666564039','0.201845666564039'),
('TGFR1_HUMAN','3kcf_C','C','crystal structure of tgfbri complexed with a pyrazolone inhibitor','2.8','0.225885357142857','0.225885357142857'),
('TGFR1_HUMAN','3kcf_D','D','crystal structure of tgfbri complexed with a pyrazolone inhibitor','2.8','0.225885357142857','0.225885357142857'),
('TGFR1_HUMAN','3kcf_E','E','crystal structure of tgfbri complexed with a pyrazolone inhibitor','2.8','0.225885357142857','0.225885357142857'),
('JAK2_HUMAN','3kck_A','A','a novel chemotype of kinase inhibitors','2.2','0.325369219426407','0.325369219426407'),
('ERBB3_HUMAN','3kex_A','A','crystal structure of the catalytically inactive kinase domain of the human epidermal growth factor receptor 3 (her3)','2.8','0.217277633928571','0.217277633928571'),
('ERBB3_HUMAN','3kex_B','B','crystal structure of the catalytically inactive kinase domain of the human epidermal growth factor receptor 3 (her3)','2.8','0.217277633928571','0.217277633928571'),
('MK14_HUMAN','3kf7_A','A','crystal structure of human p38alpha complexed with a triazolopyrimidine compound','2','0.385970788690476','0.385970788690476'),
('MYLK2_HUMAN','3kf9_B','B','crystal structure of the sdcen/skmlck complex','2.6','0.299763941163004','0.299763941163004'),
('MYLK2_HUMAN','3kf9_D','D','crystal structure of the sdcen/skmlck complex','2.6','0.299763941163004','0.299763941163004'),
('A3QNQ0_HUMAN','3kfd_E','E','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('TGFR2_HUMAN','3kfd_F','F','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('TGFR2_HUMAN','3kfd_G','G','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('TGFR2_HUMAN','3kfd_H','H','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('TGFR1_HUMAN','3kfd_J','J','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('TGFR1_HUMAN','3kfd_L','L','ternary complex of tgf-b1 reveals isoform-specific ligand re and receptor recruitment in the superfamily','3','0.195011949404762','0.195011949404762'),
('MAPK2_HUMAN','3kga_A','A','crystal structure of mapkap kinase 2 (mk2) complexed with a potent 3-aminopyrazole atp site inhibitor','2.55','0.326849675245098','0.326849675245098'),
('MAST3_HUMAN','3khf_A','A','the crystal structure of the pdz domain of human microtubule associated serine/threonine kinase 3 (mast3)','1.2','0.826314523809524','0.826314523809524'),
('MAST3_HUMAN','3khf_B','B','the crystal structure of the pdz domain of human microtubule associated serine/threonine kinase 3 (mast3)','1.2','0.826314523809524','0.826314523809524'),
('EPHA1_HUMAN','3kka_A','A','co-crystal structure of the sam domains of epha1 and epha2','2.4','0.330082113095238','0.330082113095238'),
('A8K2T6_HUMAN','3kka_B','B','co-crystal structure of the sam domains of epha1 and epha2','2.4','0.330082113095238','0.330082113095238'),
('Q96HF4_HUMAN','3kka_C','C','co-crystal structure of the sam domains of epha1 and epha2','2.4','0.330082113095238','0.330082113095238'),
('EPHA2_HUMAN','3kka_D','D','co-crystal structure of the sam domains of epha1 and epha2','2.4','0.330082113095238','0.330082113095238'),
('Q96HF4_HUMAN','3kka_E','E','co-crystal structure of the sam domains of epha1 and epha2','2.4','0.330082113095238','0.330082113095238'),
('LCK_HUMAN','3kmm_A','A','structure of human lck kinase with a small molecule inhibito','2.8','0.329256116071429','0.329256116071429'),
('ILK_HUMAN','3kmu_A','A','crystal structure of the ilk/alpha-parvin core complex (apo)','1.8','0.494871567460318','0.494871567460318'),
('ILK_HUMAN','3kmw_A','A','crystal structure of the ilk/alpha-parvin core complex (mgatp)','2','0.442435520833333','0.442435520833333'),
('KS6A5_HUMAN','3kn5_A','A','crystal structure of the c-terminal kinase domain of msk1 in with amp-pnp','2.4','0.319075357142857','0.319075357142857'),
('KS6A5_HUMAN','3kn5_B','B','crystal structure of the c-terminal kinase domain of msk1 in with amp-pnp','2.4','0.319075357142857','0.319075357142857'),
('KS6A5_HUMAN','3kn6_A','A','crystal structure of the c-terminal kinase domain of msk1','2','0.403009285714286','0.403009285714286'),
('KS6A5_HUMAN','3kn6_B','B','crystal structure of the c-terminal kinase domain of msk1','2','0.403009285714286','0.403009285714286'),
('TITIN_HUMAN','3knb_A','A','crystal structure of the titin c-terminus in complex with ob like 1','1.4','0.69854693452381','0.69854693452381'),
('MK14_HUMAN','3kq7_A','A','structure of human p38alpha with n-[4-methyl-3-(6-{[2-(1- methylpyrrolidin-2-yl)ethyl]amino}pyridine-3-amido)phenyl]- 2-(morpholin-4-yl)pyridine-4-carboxamide','1.8','0.506415808531746','0.506415808531746'),
('FGFR1_HUMAN','3krj_A','A','cfms tyrosine kinase in complex with 4-cyano-1h-imidazole-2- acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide','2.1','0.263190476190476','0.263190476190476'),
('FGFR1_HUMAN','3krl_A','A','cfms tyrosine kinase in complex with 5-cyano-furan-2-carboxy [4-(4-methyl-piperazin-1-yl)-2-piperidin-1-yl-phenyl]-amide','2.4','0.204666666666667','0.204666666666667'),
('JAK2_HUMAN','3krr_A','A','crystal structure of jak2 complexed with a potent quinoxalin inhibitor','1.8','0.536043159722222','0.536043159722222'),
('ARBK1_HUMAN','3krw_A','A','human grk2 in complex with gbetgamma subunits and balanol (soak)','2.9','0.258997615968801','0.258997615968801'),
('ARBK1_HUMAN','3krx_A','A','human grk2 in complex with gbetgamma subunits and balanol (c','3.1','0.223404915994624','0.223404915994624'),
('RAF1_HUMAN','3kuc_B','B','complex of rap1a(e30d/k31e)gdp with rafrbd(a85k/n71r)','1.92','0.484149761904762','0.484149761904762'),
('RAF1_HUMAN','3kud_B','B','complex of ras-gdp with rafrbd(a85k)','2.15','0.299181725498339','0.299181725498339'),
('EPHA8_HUMAN','3kul_A','A','kinase domain of human ephrin type-a receptor 8 (epha8)','2.15','0.404986160022148','0.404986160022148'),
('EPHA8_HUMAN','3kul_B','B','kinase domain of human ephrin type-a receptor 8 (epha8)','2.15','0.404986160022148','0.404986160022148'),
('VGFR2_HUMAN','3kvq_A','A','crystal structure of vegfr2 extracellular domain d7','2.7','0.236324819775132','0.236324819775132'),
('DYRK2_HUMAN','3kvw_A','A','crystal structure of dual-specificity tyrosine phosphorylati regulated kinase 2 (dyrk2) in complex with an indirubin lig','2.28','0.365716327537594','0.365716327537594'),
('MK10_HUMAN','3kvx_A','A','jnk3 bound to aminopyrimidine inhibitor, sr-3562','2.4','0.312075714285714','0.312075714285714'),
('FGFR1_HUMAN','3kxx_A','A','structure of the mutant fibroblast growth factor receptor 1','3.2','0.224323244047619','0.224323244047619'),
('D3DSX2_HUMAN','3kxx_B','B','structure of the mutant fibroblast growth factor receptor 1','3.2','0.224323244047619','0.224323244047619'),
('LCK_HUMAN','3kxz_A','A','the complex crystal structure of lck with a probe molecule w','2.37','0.369498264579566','0.369498264579566'),
('FGFR1_HUMAN','3ky2_A','A','crystal structure of fibroblast growth factor receptor 1 kinase domain','2.7','0.313246947751323','0.313246947751323'),
('GSK3B_HUMAN','3l1s_A','A','3-aryl-4-(arylhydrazono)-1h-pyrazol-5-ones: highly ligand ef and potent inhibitors of gsk3','2.9','0.282283523706897','0.282283523706897'),
('TIE2_HUMAN','3l8p_A','A','crystal structure of cytoplasmic kinase domain of tie2 compl inhibitor cep11207','2.4','0.300945863095238','0.300945863095238'),
('MK14_HUMAN','3l8s_A','A','human p38 map kinase in complex with cp-547632','2.35','0.293536364298379','0.293536364298379'),
('MET_HUMAN','3l8v_A','A','crystal structure of the tyrosine kinase domain of the hepat growth factor receptor c-met in complex with a biarylamine inhibitor','2.4','0.348581741071429','0.348581741071429'),
('MK14_HUMAN','3l8x_A','A','p38 alpha kinase complexed with a pyrazolo-pyrimidine based inhibitor','2.4','0.277918705357143','0.277918705357143'),
('KAPCA_HUMAN','3l9l_A','A','crystal structure of pka with compound 36','2','0.407626755952381','0.407626755952381'),
('KAPCA_HUMAN','3l9l_B','B','crystal structure of pka with compound 36','2','0.407626755952381','0.407626755952381'),
('KAPCA_HUMAN','3l9m_A','A','crystal structure of pkab3 (pka triple mutant v123a, l173m, with compound 18','1.9','0.428683527568922','0.428683527568922'),
('KAPCA_HUMAN','3l9m_B','B','crystal structure of pkab3 (pka triple mutant v123a, l173m, with compound 18','1.9','0.428683527568922','0.428683527568922'),
('KAPCA_HUMAN','3l9n_A','A','crystal structure of pkab3 (pka triple mutant v123a, l173m, with compound 27','2','0.409292916666667','0.409292916666667'),
('ALK_HUMAN','3l9p_A','A','crystal structure of the anaplastic lymphoma kinase catalyti','1.8','0.489523635912698','0.489523635912698'),
('AURKA_HUMAN','3lau_A','A','crystal structure of aurora2 kinase in complex with a gsk3beta inhibitor','2.1','0.398452455357143','0.398452455357143'),
('CSF1R_HUMAN','3lcd_A','A','inhibitor bound to a dfg-in structure of the kinase domain o','2.5','0.328552797619048','0.328552797619048'),
('LCK_HUMAN','3lck_A','A','the kinase domain of human lymphocyte kinase (lck), activated form (auto-phosphorylated on tyr394)','1.7','0.561077883403361','0.561077883403361'),
('CSF1R_HUMAN','3lco_A','A','inhibitor bound to a dfg-out structure of the kinase domain','3.4','0.189970608368347','0.189970608368347'),
('ALK_HUMAN','3lcs_A','A','crystal structure of the anaplastic lymphoma kinase catalyti','1.95','0.438231331272894','0.438231331272894'),
('ALK_HUMAN','3lct_A','A','crystal structure of the anaplastic lymphoma kinase catalyti','2.1','0.379722395833333','0.379722395833333'),
('TITIN_HUMAN','3lcy_A','A','titin ig tandem domains a164-a165','2.5','0.334874047619048','0.334874047619048'),
('TITIN_HUMAN','3lcy_B','B','titin ig tandem domains a164-a165','2.5','0.334874047619048','0.334874047619048'),
('TITIN_HUMAN','3lcy_C','C','titin ig tandem domains a164-a165','2.5','0.334874047619048','0.334874047619048'),
('TITIN_HUMAN','3lcy_D','D','titin ig tandem domains a164-a165','2.5','0.334874047619048','0.334874047619048'),
('CDK2_HUMAN','3le6_A','A','the structure of cyclin dependent kinase 2 (ckd2) with a pyrazolobenzodiazepine inhibitor','2','0.433466547619048','0.433466547619048'),
('MK14_HUMAN','3lfa_A','A','human p38 map kinase in complex with dasatinib','2.1','0.400461011904762','0.400461011904762'),
('MK14_HUMAN','3lfb_A','A','human p38 map kinase in complex with rl98','2.6','0.266284179258242','0.266284179258242'),
('MK14_HUMAN','3lfc_A','A','human p38 map kinase in complex with rl99','2.8','0.230098095238095','0.230098095238095'),
('MK14_HUMAN','3lfd_A','A','human p38 map kinase in complex with rl113','3.4','0.157143941701681','0.157143941701681'),
('MK14_HUMAN','3lfe_A','A','human p38 map kinase in complex with rl116','2.3','0.343090480719462','0.343090480719462'),
('MK14_HUMAN','3lff_A','A','human p38 map kinase in complex with rl166','1.5','0.614350907738095','0.614350907738095'),
('CDK2_HUMAN','3lfn_A','A','crystal structure of cdk2 with sar57, an aminoindazole type inhibitor','2.28','0.363315390037594','0.363315390037594'),
('CDK2_HUMAN','3lfq_A','A','crystal structure of cdk2 with sar60, an aminoindazole type inhibitor','2.03','0.425676343390805','0.425676343390805'),
('CDK2_HUMAN','3lfs_A','A','crystal structure of cdk2 with sar37, an aminoindazole type inhibitor','2.4','0.328083928571429','0.328083928571429'),
('MK14_HUMAN','3lhj_A','A','crystal structure of p38a mitogen-activated protein kinase in complex with a pyrazolopyridinone inhibitor.','3.31','0.193587154815854','0.193587154815854'),
('GAK_HUMAN','3ll6_A','A','crystal structure of the human cyclin g associated kinase (g','2.1','0.416690625','0.416690625'),
('GAK_HUMAN','3ll6_B','B','crystal structure of the human cyclin g associated kinase (g','2.1','0.416690625','0.416690625'),
('ST17B_HUMAN','3lm0_A','A','crystal structure of human serine/threonine kinase 17b (stk1','2.35','0.368107554774569','0.368107554774569'),
('ST17B_HUMAN','3lm5_A','A','crystal structure of human serine/threonine kinase 17b (stk1 complex with quercetin','2.29','0.382323335802662','0.382323335802662'),
('ERBB3_HUMAN','3lmg_A','A','crystal structure of the erbb3 kinase domain in complex with','2.8','0.242838839285714','0.242838839285714'),
('ERBB3_HUMAN','3lmg_B','B','crystal structure of the erbb3 kinase domain in complex with','2.8','0.242838839285714','0.242838839285714'),
('INSR_HUMAN','3loh_E','E','structure of the insulin receptor ectodomain, including ct p','3.8','0.0543786536654135','0.0543786536654135'),
('Q8IXP2_HUMAN','3lpb_A','A','crystal structure of jak2 complexed with a potent 2,8-diaryl quinoxaline inhibitor','2','0.465492797619048','0.465492797619048'),
('JAK2_HUMAN','3lpb_B','B','crystal structure of jak2 complexed with a potent 2,8-diaryl quinoxaline inhibitor','2','0.465492797619048','0.465492797619048'),
('TITIN_HUMAN','3lpw_A','A','crystal structure of the fniii-tandem a77-a78 from the a-ban','1.65','0.574105710227273','0.574105710227273'),
('TITIN_HUMAN','3lpw_B','B','crystal structure of the fniii-tandem a77-a78 from the a-ban','1.65','0.574105710227273','0.574105710227273'),
('CDK9_HUMAN','3lq5_A','A','structure of cdk9/cyclint in complex with s-cr8','3','0.282745744047619','0.282745744047619'),
('MET_HUMAN','3lq8_A','A','structure of the kinase domain of c-met bound to xl880 (gsk1','2.02','0.44417978768859','0.44417978768859'),
('IGF1R_HUMAN','3lvp_B','B','crystal structure of bisphosphorylated igf1-r kinase domain complex with a bis-azaindole inhibitor','3','0.215075550595238','0.215075550595238'),
('C9J5X1_HUMAN','3lvp_C','C','crystal structure of bisphosphorylated igf1-r kinase domain complex with a bis-azaindole inhibitor','3','0.215075550595238','0.215075550595238'),
('C9J5X1_HUMAN','3lvp_D','D','crystal structure of bisphosphorylated igf1-r kinase domain complex with a bis-azaindole inhibitor','3','0.215075550595238','0.215075550595238'),
('IGF1R_HUMAN','3lw0_A','A','igf-1rk in complex with ligand msc1609119a-1','1.79','0.551290423234238','0.551290423234238'),
('IGF1R_HUMAN','3lw0_B','B','igf-1rk in complex with ligand msc1609119a-1','1.79','0.551290423234238','0.551290423234238'),
('IGF1R_HUMAN','3lw0_C','C','igf-1rk in complex with ligand msc1609119a-1','1.79','0.551290423234238','0.551290423234238'),
('IGF1R_HUMAN','3lw0_D','D','igf-1rk in complex with ligand msc1609119a-1','1.79','0.551290423234238','0.551290423234238'),
('JAK3_HUMAN','3lxk_A','A','structural and thermodynamic characterization of the tyk2 an kinase domains in complex with cp-690550 and cmp-6','2','0.438818333333333','0.438818333333333'),
('JAK3_HUMAN','3lxl_A','A','structural and thermodynamic characterization of the tyk2 an kinase domains in complex with cp-690550 and cmp-6','1.74','0.526348566297208','0.526348566297208'),
('TYK2_HUMAN','3lxn_A','A','structural and thermodynamic characterization of the tyk2 an kinase domains in complex with cp-690550 and cmp-6','2.5','0.288988526785714','0.288988526785714'),
('TYK2_HUMAN','3lxp_A','A','structural and thermodynamic characterization of the tyk2 an kinase domains in complex with cp-690550 and cmp-6','1.65','0.557878269751082','0.557878269751082'),
('EGFR_HUMAN','3lzb_A','A','egfr kinase domain complexed with an imidazo[2,1-b]thiazole','2.7','0.258584135251323','0.258584135251323'),
('EGFR_HUMAN','3lzb_B','B','egfr kinase domain complexed with an imidazo[2,1-b]thiazole','2.7','0.258584135251323','0.258584135251323'),
('EGFR_HUMAN','3lzb_C','C','egfr kinase domain complexed with an imidazo[2,1-b]thiazole','2.7','0.258584135251323','0.258584135251323'),
('EGFR_HUMAN','3lzb_D','D','egfr kinase domain complexed with an imidazo[2,1-b]thiazole','2.7','0.258584135251323','0.258584135251323'),
('AURKA_HUMAN','3m11_A','A','crystal structure of aurora a kinase complexed with inhibito','2.75','0.250978015422078','0.250978015422078'),
('GSK3B_HUMAN','3m1s_B','B','structure of ruthenium half-sandwich complex bound to glycog synthase kinase 3','3.13','0.248552121462802','0.248552121462802'),
('MAPK2_HUMAN','3m2w_A','A','crystal structure of mapkak kinase 2 (mk2) complexed with a spiroazetidine-tetracyclic atp site inhibitor','2.41','0.349484961717052','0.349484961717052'),
('MAPK2_HUMAN','3m42_A','A','crystal structure of mapkap kinase 2 (mk2) complexed with a tetracyclic atp site inhibitor','2.68','0.325346515858209','0.325346515858209'),
('PIM1_HUMAN','3ma3_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and a naphtho-di ligand','2.3','0.386983263457557','0.386983263457557'),
('CSK21_HUMAN','3mb6_A','A','human ck2 catalytic domain in complex with a difurane deriva inhibitor (cpa)','1.75','0.525843913690476','0.525843913690476'),
('CSK21_HUMAN','3mb7_A','A','human ck2 catalytic domain in complex with a difurane deriva inhibitor (amr)','1.65','0.540170635822511','0.540170635822511'),
('MP2K1_HUMAN','3mbl_A','A','crystal structure of the human mitogen-activated protein kin 1 (mek 1) in complex with ligand and mgadp','2.6','0.330374789377289','0.330374789377289'),
('EPHA2_HUMAN','3mbw_A','A','crystal structure of the human ephrin a2 lbd and crd domains complex with ephrin a1','2.81','0.221001677787663','0.221001677787663'),
('BMR1B_HUMAN','3mdy_C','C','crystal structure of the cytoplasmic domain of the bone morp protein receptor type-1b (bmpr1b) in complex with fkbp12 an 193189','2.05','0.408463553644019','0.408463553644019'),
('CSKP_HUMAN','3mfr_A','A','cask-4m cam kinase domain, native','2','0.427872440476191','0.427872440476191'),
('CSKP_HUMAN','3mfs_A','A','cask-4m cam kinase domain, amppnp','2.1','0.382203005952381','0.382203005952381'),
('CSKP_HUMAN','3mft_A','A','cask-4m cam kinase domain, mn2+','2.2','0.363102731331169','0.363102731331169'),
('CSKP_HUMAN','3mfu_A','A','cask-4m cam kinase domain, amppnp-mn2+','2.3','0.377256016433747','0.377256016433747'),
('MK14_HUMAN','3mgy_A','A','mutagenesis of p38 map kinase eshtablishes key roles of phe1 function and structural dynamics and reveals a novel dfg-ou','2.1','0.349285104166667','0.349285104166667'),
('MK14_HUMAN','3mh0_A','A','mutagenesis of p38 map kinase eshtablishes key roles of phe1 function and structural dynamics and reveals a novel dfg-ou','2','0.383622678571429','0.383622678571429'),
('MK14_HUMAN','3mh1_A','A','mutagenesis of p38 map kinase establishes key roles of phe16 function and structural dynamics and reveals a novel dfg-ou','2.2','0.331160767045455','0.331160767045455'),
('MK14_HUMAN','3mh2_A','A','mutagenesis of p38 map kinase establishes key roles of phe16 function and structural dynamics and reveals a novel dfg-ou','2.3','0.297884245600414','0.297884245600414'),
('MK14_HUMAN','3mh3_A','A','mutagenesis of p38 map kinase establishes key roles of phe16 function and structural dynamics and reveals a novel dfg-ou','2.2','0.331964963474026','0.331964963474026'),
('PLK1_HUMAN','3mhn_A','A','human plk1-pbd in complex with poloxime ((e)-4-(hydroxyimino isopropyl-5-methylcyclohexa-2,5-dienone)','1.93','0.483486128716383','0.483486128716383'),
('PLK1_HUMAN','3mhq_A','A','human plk1-pbd with a glycerol bound at the phophopeptide bi','1.95','0.469337715201465','0.469337715201465'),
('CDK9_HUMAN','3mi9_A','A','crystal structure of hiv-1 tat complexed with human p-tefb','2.1','0.392531845238095','0.392531845238095'),
('CDK9_HUMAN','3mia_A','A','crystal structure of hiv-1 tat complexed with atp-bound huma','3','0.221704002976191','0.221704002976191'),
('ITK_HUMAN','3miy_B','B','x-ray crystal structure of itk complexed with sunitinib','1.67','0.5407181392572','0.5407181392572'),
('ITK_HUMAN','3mj1_A','A','x-ray crystal structure of itk complexed with inhibitor ro51','1.72','0.489299708956257','0.489299708956257'),
('ITK_HUMAN','3mj2_A','A','x-ray crystal structure of itk complexed with inhibitor bms-','1.9','0.450021087092732','0.450021087092732'),
('PGFRB_HUMAN','3mjg_X','X','the structure of a platelet derived growth factor receptor c','2.3','0.2867719688147','0.2867719688147'),
('PGFRB_HUMAN','3mjg_Y','Y','the structure of a platelet derived growth factor receptor c','2.3','0.2867719688147','0.2867719688147'),
('IRAK4_HUMAN','3mop_G','G','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK4_HUMAN','3mop_H','H','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK4_HUMAN','3mop_I','I','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK4_HUMAN','3mop_J','J','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK2_HUMAN','3mop_K','K','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK2_HUMAN','3mop_L','L','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK2_HUMAN','3mop_M','M','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('IRAK2_HUMAN','3mop_N','N','the ternary death domain complex of myd88, irak4, and irak2','3.4','0.090986218487395','0.090986218487395'),
('MK14_HUMAN','3mpa_A','A','conformational plasticity of p38 map kinase dfg motif mutant response to inhibitor binding','2.1','0.356646592261905','0.356646592261905'),
('LCK_HUMAN','3mpm_A','A','lck complexed with a pyrazolopyrimidine','1.95','0.48788711996337','0.48788711996337'),
('MK14_HUMAN','3mpt_A','A','crystal structure of p38 kinase in complex with a pyrrole-2- carboxamide inhibitor','1.89','0.409322314814815','0.409322314814815'),
('PLK1_HUMAN','3mq8_A','A','human plk1-pbd in complex with thymoquinone at the phophopep binding site','2.75','0.274597226731602','0.274597226731602'),
('PLK1_HUMAN','3mq8_B','B','human plk1-pbd in complex with thymoquinone at the phophopep binding site','2.75','0.274597226731602','0.274597226731602'),
('ACVR1_HUMAN','3mtf_B','B','crystal structure of the acvr1 kinase in complex with a 2- aminopyridine inhibitor','2.15','0.418147052879291','0.418147052879291'),
('CDK16_HUMAN','3mtl_A','A','crystal structure of the pctaire1 kinase in complex with ind e804','2.4','0.33204724702381','0.33204724702381'),
('AKT1_HUMAN','3mv5_A','A','crystal structure of akt-1-inhibitor complexes','2.47','0.313033254952285','0.313033254952285'),
('AKT1_HUMAN','3mvh_A','A','crystal structure of akt-1-inhibitor complexes','2.01','0.456503047929993','0.456503047929993'),
('KAPCA_HUMAN','3mvj_A','A','human cyclic amp-dependent protein kinase pka inhibitor comp','2.49','0.297989134036145','0.297989134036145'),
('KAPCA_HUMAN','3mvj_B','B','human cyclic amp-dependent protein kinase pka inhibitor comp','2.49','0.297989134036145','0.297989134036145'),
('KAPCA_HUMAN','3mvj_E','E','human cyclic amp-dependent protein kinase pka inhibitor comp','2.49','0.297989134036145','0.297989134036145'),
('MK14_HUMAN','3mvl_A','A','p38 alpha map kinase complexed with pyrrolotriazine inhibito','2.8','0.187415714285714','0.187415714285714'),
('MK14_HUMAN','3mvl_B','B','p38 alpha map kinase complexed with pyrrolotriazine inhibito','2.8','0.187415714285714','0.187415714285714'),
('MK14_HUMAN','3mvm_A','A','p38 alpha map kinase complexed with pyrrolotriazine inhibito','2','0.425124285714286','0.425124285714286'),
('MK14_HUMAN','3mvm_B','B','p38 alpha map kinase complexed with pyrrolotriazine inhibito','2','0.425124285714286','0.425124285714286'),
('MK14_HUMAN','3mw1_A','A','p38 kinase crystal structure in complex with small molecule','2.8','0.21170630952381','0.21170630952381'),
('EPHA2_HUMAN','3mx0_A','A','crystal structure of epha2 ectodomain in complex with ephrin','3.51','0.0892209991859992','0.0892209991859992'),
('EPHA2_HUMAN','3mx0_C','C','crystal structure of epha2 ectodomain in complex with ephrin','3.51','0.0892209991859992','0.0892209991859992'),
('ACVL1_HUMAN','3my0_A','A','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_B','B','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_C','C','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_D','D','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_E','E','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_F','F','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_G','G','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_H','H','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_I','I','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_L','L','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_M','M','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_N','N','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_O','O','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_Q','Q','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_R','R','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_S','S','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('ACVL1_HUMAN','3my0_T','T','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('B4DUF0_HUMAN','3my0_U','U','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('B4DUF0_HUMAN','3my0_V','V','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('B4DUF0_HUMAN','3my0_W','W','crystal structure of the acvrl1 (alk1) kinase domain bound t 193189','2.65','0.280733148304133','0.280733148304133'),
('CDK9_HUMAN','3my1_A','A','structure of cdk9/cyclint1 in complex with drb','2.8','0.302954419642857','0.302954419642857'),
('CDK2_HUMAN','3my5_A','A','cdk2/cyclina in complex with drb','2.1','0.440805997023809','0.440805997023809'),
('CDK2_HUMAN','3my5_C','C','cdk2/cyclina in complex with drb','2.1','0.440805997023809','0.440805997023809'),
('AURKA_HUMAN','3myg_A','A','aurora a kinase complexed with sch 1473759','2.4','0.313264211309524','0.313264211309524'),
('ERBB2_HUMAN','3mzw_A','A','her2 extracelluar region with affinity matured 3-helix affib zher2:342','2.9','0.244224371921182','0.244224371921182'),
('ERBB2_HUMAN','3n85_A','A','crystallographic trimer of her2 extracellular regions in com tryptophan-rich antibody fragment','3.2','0.215015014880952','0.215015014880952'),
('PDPK1_HUMAN','3nax_A','A','pdk1 in complex with inhibitor mp7','1.75','0.556852485119048','0.556852485119048'),
('PDPK1_HUMAN','3nay_A','A','pdk1 in complex with inhibitor mp6','2.6','0.289636709020146','0.289636709020146'),
('PDPK1_HUMAN','3nay_B','B','pdk1 in complex with inhibitor mp6','2.6','0.289636709020146','0.289636709020146'),
('ROCK1_HUMAN','3ncz_A','A','x-ray co-structure of rho-associated protein kinase (rock1) potent 2h-isoquinolin-1-one inhibitor','3','0.150758526785714','0.150758526785714'),
('D9ZGF8_HUMAN','3ncz_B','B','x-ray co-structure of rho-associated protein kinase (rock1) potent 2h-isoquinolin-1-one inhibitor','3','0.150758526785714','0.150758526785714'),
('ROCK1_HUMAN','3ncz_C','C','x-ray co-structure of rho-associated protein kinase (rock1) potent 2h-isoquinolin-1-one inhibitor','3','0.150758526785714','0.150758526785714'),
('ROCK1_HUMAN','3ncz_D','D','x-ray co-structure of rho-associated protein kinase (rock1) potent 2h-isoquinolin-1-one inhibitor','3','0.150758526785714','0.150758526785714'),
('D9ZGF8_HUMAN','3ndm_A','A','crystal structure of rho-associated protein kinase (rock1) w potent isoquinolone derivative','3.3','0.125540794101732','0.125540794101732'),
('ROCK1_HUMAN','3ndm_B','B','crystal structure of rho-associated protein kinase (rock1) w potent isoquinolone derivative','3.3','0.125540794101732','0.125540794101732'),
('D9ZGF8_HUMAN','3ndm_C','C','crystal structure of rho-associated protein kinase (rock1) w potent isoquinolone derivative','3.3','0.125540794101732','0.125540794101732'),
('ROCK1_HUMAN','3ndm_D','D','crystal structure of rho-associated protein kinase (rock1) w potent isoquinolone derivative','3.3','0.125540794101732','0.125540794101732'),
('MK14_HUMAN','3new_A','A','p38-alpha complexed with compound 10','2.51','0.286139454859135','0.286139454859135'),
('CSK21_HUMAN','3nga_A','A','human ck2 catalytic domain in complex with cx-4945','2.71','0.303676725751186','0.303676725751186'),
('CSK21_HUMAN','3nga_B','B','human ck2 catalytic domain in complex with cx-4945','2.71','0.303676725751186','0.303676725751186'),
('BMR1A_HUMAN','3nh7_A','A','crystal structure of the neutralizing fab fragment abd1556 b the bmp type i receptor ia','2.7','0.229465727513227','0.229465727513227'),
('BMR1A_HUMAN','3nh7_B','B','crystal structure of the neutralizing fab fragment abd1556 b the bmp type i receptor ia','2.7','0.229465727513227','0.229465727513227'),
('BMR1A_HUMAN','3nh7_C','C','crystal structure of the neutralizing fab fragment abd1556 b the bmp type i receptor ia','2.7','0.229465727513227','0.229465727513227'),
('BMR1A_HUMAN','3nh7_D','D','crystal structure of the neutralizing fab fragment abd1556 b the bmp type i receptor ia','2.7','0.229465727513227','0.229465727513227'),
('HCK_HUMAN','3nhn_A','A','crystal structure of the src-family kinase hck sh3-sh2-linke regulatory region','2.61','0.331598786261631','0.331598786261631'),
('EGFR_HUMAN','3njp_A','A','the extracellular and transmembrane domain interfaces in epi growth factor receptor signaling','3.3','0.127955556006494','0.127955556006494'),
('EGFR_HUMAN','3njp_B','B','the extracellular and transmembrane domain interfaces in epi growth factor receptor signaling','3.3','0.127955556006494','0.127955556006494'),
('RAF1_HUMAN','3nkx_P','P','impaired binding of 14-3-3 to raf1 is linked to noonan and l syndrome','2.4','0.326975119047619','0.326975119047619'),
('RAF1_HUMAN','3nkx_Q','Q','impaired binding of 14-3-3 to raf1 is linked to noonan and l syndrome','2.4','0.326975119047619','0.326975119047619'),
('CHK1_HUMAN','3nlb_A','A','novel kinase profile highlights the temporal basis of contex dependent checkpoint pathways to cell death','1.9','0.466817709116541','0.466817709116541'),
('KGP1_HUMAN','3nmd_A','A','crystal structure of the leucine zipper domain of cgmp depen protein kinase i beta','2.27','0.405678009361233','0.405678009361233'),
('KGP1_HUMAN','3nmd_B','B','crystal structure of the leucine zipper domain of cgmp depen protein kinase i beta','2.27','0.405678009361233','0.405678009361233'),
('KGP1_HUMAN','3nmd_C','C','crystal structure of the leucine zipper domain of cgmp depen protein kinase i beta','2.27','0.405678009361233','0.405678009361233'),
('KGP1_HUMAN','3nmd_D','D','crystal structure of the leucine zipper domain of cgmp depen protein kinase i beta','2.27','0.405678009361233','0.405678009361233'),
('KGP1_HUMAN','3nmd_E','E','crystal structure of the leucine zipper domain of cgmp depen protein kinase i beta','2.27','0.405678009361233','0.405678009361233'),
('MK14_HUMAN','3nnu_A','A','crystal structure of p38 alpha in complex with dp1376','2.4','0.354905357142857','0.354905357142857'),
('MK14_HUMAN','3nnv_A','A','crystal structure of p38 alpha in complex with dp437','2.1','0.410204940476191','0.410204940476191'),
('MK14_HUMAN','3nnw_A','A','crystal structure of p38 alpha in complex with dp802','1.89','0.505229249338625','0.505229249338625'),
('MK14_HUMAN','3nnx_A','A','crystal structure of phosphorylated p38 alpha in complex wit','2.28','0.329073128132832','0.329073128132832'),
('MK09_HUMAN','3npc_A','A','crystal structure of jnk2 complexed with birb796','2.35','0.333284042869808','0.333284042869808'),
('D7R526_HUMAN','3npc_B','B','crystal structure of jnk2 complexed with birb796','2.35','0.333284042869808','0.333284042869808'),
('CLK2_HUMAN','3nr9_A','A','structure of human cdc2-like kinase 2 (clk2)','2.89','0.265299913031389','0.265299913031389'),
('CLK2_HUMAN','3nr9_B','B','structure of human cdc2-like kinase 2 (clk2)','2.89','0.265299913031389','0.265299913031389'),
('CLK2_HUMAN','3nr9_C','C','structure of human cdc2-like kinase 2 (clk2)','2.89','0.265299913031389','0.265299913031389'),
('AURKA_HUMAN','3nrm_A','A','imidazo[1,2-a]pyrazine-based aurora kinase inhibitors','3.05','0.213419611387588','0.213419611387588'),
('EPHA7_HUMAN','3nru_A','A','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_B','B','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_C','C','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_D','D','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_E','E','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_F','F','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_G','G','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_H','H','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_I','I','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_J','J','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_K','K','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('EPHA7_HUMAN','3nru_L','L','ligand binding domain of epha7','2.3','0.318998620600414','0.318998620600414'),
('CDK2_HUMAN','3ns9_A','A','crystal structure of cdk2 in complex with inhibitor bs-194','1.78','0.477709434356608','0.477709434356608'),
('CSK21_HUMAN','3nsz_A','A','human ck2 catalytic domain in complex with amppn','1.3','0.746071156135531','0.746071156135531'),
('PDPK1_HUMAN','3nun_A','A','phosphoinositide-dependent kinase-1 (pdk1) with lead compoun','2.2','0.422647389069264','0.422647389069264'),
('CDK6_HUMAN','3nup_A','A','cdk6 (monomeric) in complex with inhibitor','2.6','0.281800191163004','0.281800191163004'),
('PDPK1_HUMAN','3nus_A','A','phosphoinositide-dependent kinase-1 (pdk1) with fragment8','2.75','0.333571333874459','0.333571333874459'),
('PDPK1_HUMAN','3nuu_A','A','phosphoinositide-dependent kinase-1 (pdk1) with fragment11','1.98','0.464486636002886','0.464486636002886'),
('CDK6_HUMAN','3nux_A','A','cdk6 (monomeric) in complex with inhibitor','2.7','0.260440102513227','0.260440102513227'),
('PDPK1_HUMAN','3nuy_A','A','phosphoinositide-dependent kinase-1 (pdk1) with fragment17','2.1','0.439861577380952','0.439861577380952'),
('IGF1R_HUMAN','3nw5_A','A','crystal structure of insulin-like growth factor 1 receptor ( complex with a carbon-linked proline isostere inhibitor (11','2.14','0.406424749388073','0.406424749388073'),
('IGF1R_HUMAN','3nw6_A','A','crystal structure of insulin-like growth factor 1 receptor ( complex with a carbon-linked proline isostere inhibitor (11','2.2','0.388675796807359','0.388675796807359'),
('IGF1R_HUMAN','3nw7_A','A','crystal structure of insulin-like growth factor 1 receptor ( complex with a carbon-linked proline isostere inhibitor (34','2.11','0.42651296476529','0.42651296476529'),
('MK14_HUMAN','3nww_A','A','p38 alpha kinase complexed with a 2-aminothiazol-5-yl-pyrimi inhibitor','2.09','0.385116935235817','0.385116935235817'),
('KAPCA_HUMAN','3nx8_A','A','human camp dependent protein kinase in complex with phenol','2','0.398363273809524','0.398363273809524'),
('BRAF_HUMAN','3ny5_B','B','crystal structure of the rbd domain of serine/threonine-prot b-raf from homo sapiens. northeast structural genomics cons target hr4694f','1.99','0.416622681861689','0.416622681861689'),
('GRK6_HUMAN','3nyn_A','A','crystal structure of g protein-coupled receptor kinase 6 in with sangivamycin','2.72','0.252265764180672','0.252265764180672'),
('GRK6_HUMAN','3nyn_B','B','crystal structure of g protein-coupled receptor kinase 6 in with sangivamycin','2.72','0.252265764180672','0.252265764180672'),
('GRK6_HUMAN','3nyo_A','A','crystal structure of g protein-coupled receptor kinase 6 in with amp','2.92','0.22458639330561','0.22458639330561'),
('GRK6_HUMAN','3nyo_B','B','crystal structure of g protein-coupled receptor kinase 6 in with amp','2.92','0.22458639330561','0.22458639330561'),
('TYK2_HUMAN','3nyx_A','A','non-phosphorylated tyk2 jh1 domain with quinoline-thiadiazol thiophene inhibitor','2.5','0.291770669642857','0.291770669642857'),
('TYK2_HUMAN','3nz0_A','A','non-phosphorylated tyk2 kinase with cmp6','2','0.430425238095238','0.430425238095238'),
('CDK5_HUMAN','3o0g_A','A','crystal structure of cdk5:p25 in complex with an atp analogu','1.95','0.405594292582418','0.405594292582418'),
('CDK5_HUMAN','3o0g_B','B','crystal structure of cdk5:p25 in complex with an atp analogu','1.95','0.405594292582418','0.405594292582418'),
('ROCK1_HUMAN','3o0z_D','D','crystal structure of a coiled-coil domain from human rock i','2.33','0.297504236856223','0.297504236856223'),
('MK08_HUMAN','3o17_A','A','crystal structure of jnk1-alpha1 isoform','3','0.13166900297619','0.13166900297619'),
('MK08_HUMAN','3o17_B','B','crystal structure of jnk1-alpha1 isoform','3','0.13166900297619','0.13166900297619'),
('IGF1R_HUMAN','3o23_A','A','human unphosphorylated igf1-r kinase domain in complex with hydantoin inhibitor','2.1','0.3822625','0.3822625'),
('MK08_HUMAN','3o2m_A','A','crystal structure of jnk1-alpha1 isoform complex with a biar tetrazol (a-82118)','2.7','0.250056709656085','0.250056709656085'),
('MK08_HUMAN','3o2m_B','B','crystal structure of jnk1-alpha1 isoform complex with a biar tetrazol (a-82118)','2.7','0.250056709656085','0.250056709656085'),
('B2R6Z3_HUMAN','3o50_A','A','crystal structure of benzamide 9 bound to auroraa','2','0.315779136904762','0.315779136904762'),
('AURKA_HUMAN','3o50_B','B','crystal structure of benzamide 9 bound to auroraa','2','0.315779136904762','0.315779136904762'),
('AURKA_HUMAN','3o51_A','A','crystal structure of anthranilamide 10 bound to auroraa','3.2','0.136898169642857','0.136898169642857'),
('RAF1_HUMAN','3o8i_B','B','structure of 14-3-3 isoform sigma in complex with a c-raf1 p a stabilizing small molecule fragment','2','0.476867931547619','0.476867931547619'),
('MK14_HUMAN','3o8p_A','A','conformational plasticity of p38 map kinase dfg motif mutant response to inhibitor binding','2.1','0.376144880952381','0.376144880952381'),
('MK14_HUMAN','3o8t_A','A','conformational plasticity of p38 map kinase dfg-motif mutant response to inhibitor binding','2','0.390625669642857','0.390625669642857'),
('MK14_HUMAN','3o8u_A','A','conformational plasticity of p38 map kinase dfg motif mutant response to inhibitor binding','2.1','0.370101607142857','0.370101607142857'),
('AKT1_HUMAN','3o96_A','A','crystal structure of human akt1 with an allosteric inhibitor','2.7','0.230387736441799','0.230387736441799'),
('EGFR_HUMAN','3ob2_A','A','crystal structure of c-cbl tkb domain in complex with double phosphorylated egfr peptide','2.1','0.412956383928571','0.412956383928571'),
('MK14_HUMAN','3obg_A','A','conformational plasticity of p38 map kinase dfg mutants in r inhibitor binding','2.8','0.215722901785714','0.215722901785714'),
('MK14_HUMAN','3obj_A','A','conformational plasticity of p38 map kinase dfg mutants in r inhibitor binding','2.4','0.306811235119048','0.306811235119048'),
('MK14_HUMAN','3oc1_A','A','conformational plasticity of p38 map kinase dfg motif mutant response to inhibitor binding','2.59','0.244338392052767','0.244338392052767'),
('B7Z5R1_HUMAN','3ocb_A','A','akt1 kinase domain with pyrrolopyrimidine inhibitor','2.7','0.266601769179894','0.266601769179894'),
('AKT1_HUMAN','3ocb_B','B','akt1 kinase domain with pyrrolopyrimidine inhibitor','2.7','0.266601769179894','0.266601769179894'),
('MK14_HUMAN','3ocg_A','A','p38 alpha kinase complexed with a 5-amino-pyrazole based inh','2.21','0.337389446711377','0.337389446711377'),
('KGP1_HUMAN','3ocp_A','A','crystal structure of camp bound cgmp-dependent protein kinas','2.49','0.327642273917097','0.327642273917097'),
('KGP1_HUMAN','3ocp_B','B','crystal structure of camp bound cgmp-dependent protein kinas','2.49','0.327642273917097','0.327642273917097'),
('BTK_HUMAN','3ocs_A','A','crystal structure of bruton\'s tyrosine kinase in complex wit inhibitor cgi1746','1.8','0.515681954365079','0.515681954365079'),
('BTK_HUMAN','3oct_A','A','crystal structure of bruton\'s tyrosine kinase mutant v555r i with dasatinib','1.95','0.456181733058608','0.456181733058608'),
('KGP1_HUMAN','3od0_A','A','crystal structure of cgmp bound cgmp-dependent protein kinas','2.9','0.256969699302135','0.256969699302135'),
('KGP1_HUMAN','3od0_B','B','crystal structure of cgmp bound cgmp-dependent protein kinas','2.9','0.256969699302135','0.256969699302135'),
('MK14_HUMAN','3od6_X','X','crystal structure of p38alpha y323t active mutant','2.68','0.255493405739161','0.255493405739161'),
('MK14_HUMAN','3ody_X','X','crystal structure of p38alpha y323q active mutant','2.2','0.336872850378788','0.336872850378788'),
('MK14_HUMAN','3odz_X','X','crystal structure of p38alpha y323r active mutant','2.3','0.326319662267081','0.326319662267081'),
('MK14_HUMAN','3oef_X','X','crystal structure of y323f inactive mutant of p38alpha map k','1.6','0.568321160714286','0.568321160714286'),
('CSK22_HUMAN','3ofm_A','A','structure of a human ck2alpha prime, the paralog isoform of catalytic subunit of protein kinase ck2 from homo sapiens','2','0.47229224702381','0.47229224702381'),
('BRAF_HUMAN','3og7_B','B','b-raf kinase v600e oncogenic mutant in complex with plx4032','2.45','0.311530854591837','0.311530854591837'),
('KGP1_HUMAN','3ogj_A','A','crystal structure of partial apo (92-227) of cgmp-dependent kinase','2.75','0.301127196969697','0.301127196969697'),
('KGP1_HUMAN','3ogj_B','B','crystal structure of partial apo (92-227) of cgmp-dependent kinase','2.75','0.301127196969697','0.301127196969697'),
('KGP1_HUMAN','3ogj_C','C','crystal structure of partial apo (92-227) of cgmp-dependent kinase','2.75','0.301127196969697','0.301127196969697'),
('KGP1_HUMAN','3ogj_D','D','crystal structure of partial apo (92-227) of cgmp-dependent kinase','2.75','0.301127196969697','0.301127196969697'),
('FGFR2_HUMAN','3oj2_C','C','crystal structure of fgf1 complexed with the ectodomain of f harboring the a172f pfeiffer syndrome mutation','2.2','0.315618267045455','0.315618267045455'),
('FGFR2_HUMAN','3oj2_D','D','crystal structure of fgf1 complexed with the ectodomain of f harboring the a172f pfeiffer syndrome mutation','2.2','0.315618267045455','0.315618267045455'),
('FGFR2_HUMAN','3ojm_B','B','crystal structure of fgf1 complexed with the ectodomain of f harboring p253r apert mutation','2.1','0.392936979166667','0.392936979166667'),
('FGFR1_HUMAN','3ojv_C','C','crystal structure of fgf1 complexed with the ectodomain of f exhibiting an ordered ligand specificity-determining betac\' loop','2.6','0.228049402472527','0.228049402472527'),
('FGFR1_HUMAN','3ojv_D','D','crystal structure of fgf1 complexed with the ectodomain of f exhibiting an ordered ligand specificity-determining betac\' loop','2.6','0.228049402472527','0.228049402472527'),
('RAF1_HUMAN','3omv_A','A','crystal structure of c-raf (raf-1)','4','0.0659673363095238','0.0659673363095238'),
('RAF1_HUMAN','3omv_B','B','crystal structure of c-raf (raf-1)','4','0.0659673363095238','0.0659673363095238'),
('KAPCA_HUMAN','3oog_A','A','human camp-dependent protein kinase in complex with a small','2','0.393295982142857','0.393295982142857'),
('ACVR1_HUMAN','3oom_A','A','crystal structure of the acvr1 kinase domain in complex with imidazo[1,2-b]pyridazine inhibitor k00507','2','0.474083229166667','0.474083229166667'),
('EGFR_HUMAN','3op0_C','C','crystal structure of cbl-c (cbl-3) tkb domain in complex wit py1069 peptide','2.52','0.297458387896825','0.297458387896825'),
('EGFR_HUMAN','3op0_D','D','crystal structure of cbl-c (cbl-3) tkb domain in complex wit py1069 peptide','2.52','0.297458387896825','0.297458387896825'),
('VRK1_HUMAN','3op5_A','A','human vaccinia-related kinase 1','2.4','0.383278139880952','0.383278139880952'),
('VRK1_HUMAN','3op5_B','B','human vaccinia-related kinase 1','2.4','0.383278139880952','0.383278139880952'),
('VRK1_HUMAN','3op5_C','C','human vaccinia-related kinase 1','2.4','0.383278139880952','0.383278139880952'),
('VRK1_HUMAN','3op5_D','D','human vaccinia-related kinase 1','2.4','0.383278139880952','0.383278139880952'),
('MP2K1_HUMAN','3orn_A','A','mitogen-activated protein kinase kinase 1 (mek1) in complex ch4987655 and mgamp-pnp','2.8','0.236921502976191','0.236921502976191'),
('PDPK1_HUMAN','3orx_A','A','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('Q9UPJ8_HUMAN','3orx_B','B','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('PDPK1_HUMAN','3orx_C','C','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('Q9UPJ8_HUMAN','3orx_D','D','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('PDPK1_HUMAN','3orx_E','E','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('C9JWR9_HUMAN','3orx_F','F','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('C9JWR9_HUMAN','3orx_G','G','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('C9JWR9_HUMAN','3orx_H','H','pdk1 mutant bound to allosteric disulfide fragment inhibitor','2.2','0.369951272997836','0.369951272997836'),
('PDPK1_HUMAN','3orz_A','A','pdk1 mutant bound to allosteric disulfide fragment activator','2','0.409789508928571','0.409789508928571'),
('PDPK1_HUMAN','3orz_B','B','pdk1 mutant bound to allosteric disulfide fragment activator','2','0.409789508928571','0.409789508928571'),
('PDPK1_HUMAN','3orz_C','C','pdk1 mutant bound to allosteric disulfide fragment activator','2','0.409789508928571','0.409789508928571'),
('PDPK1_HUMAN','3orz_D','D','pdk1 mutant bound to allosteric disulfide fragment activator','2','0.409789508928571','0.409789508928571'),
('MP2K1_HUMAN','3os3_A','A','mitogen-activated protein kinase kinase 1 (mek1) in complex ch4858061 and mgatp','2.8','0.152137589285714','0.152137589285714'),
('MARK1_HUMAN','3ose_A','A','structure of the kinase associated domain 1 (ka1) from mark1','1.7','0.56460081495098','0.56460081495098'),
('CHK1_HUMAN','3ot3_A','A','x-ray crystal structure of compound 22k bound to human chk1 domain','1.44','0.635371319444445','0.635371319444445'),
('CHK1_HUMAN','3ot8_A','A','x-ray crystal structure of compound 17r bound to human chk1 domain','1.65','0.551374088203463','0.551374088203463'),
('PDPK1_HUMAN','3otu_A','A','pdk1 mutant bound to allosteric disulfide fragment activator','2.1','0.402341607142857','0.402341607142857'),
('KAPCA_HUMAN','3ovv_A','A','human camp-dependent protein kinase in complex with an inhib','1.58','0.596953163238397','0.596953163238397'),
('AKT1_HUMAN','3ow4_A','A','discovery of dihydrothieno- and dihydrofuropyrimidines as po akt inhibitors','2.6','0.298135726877289','0.298135726877289'),
('AKT1_HUMAN','3ow4_B','B','discovery of dihydrothieno- and dihydrofuropyrimidines as po akt inhibitors','2.6','0.298135726877289','0.298135726877289'),
('CSK21_HUMAN','3owj_A','A','human ck2 catalytic domain in complex with a pyridocarbazole derivative inhibitor','1.85','0.46298778756435','0.46298778756435'),
('CSK21_HUMAN','3owk_A','A','human ck2 catalytic domain in complex with a benzopyridoindo derivative inhibitor','1.8','0.475037356150794','0.475037356150794'),
('CSK21_HUMAN','3owl_A','A','human ck2 catalytic domain in complex with a benzopyridoindo derivative inhibitor','2.1','0.384271205357143','0.384271205357143'),
('KAPCA_HUMAN','3owp_A','A','human camp-dependent protein kinase in complex with an inhib','1.88','0.511129938259878','0.511129938259878'),
('MK10_HUMAN','3oxi_A','A','design and synthesis of disubstituted thiophene and thiazole inhibitors of jnk for the treatment of neurodegenerative di','2.2','0.335738014069264','0.335738014069264'),
('KAPCA_HUMAN','3oxt_A','A','human camp-dependent protein kinase in complex with an inhib','2.2','0.420319695616883','0.420319695616883'),
('MK10_HUMAN','3oy1_A','A','highly selective c-jun n-terminal kinase (jnk) 2 and 3 inhib in vitro cns-like pharmacokinetic properties','1.7','0.472794178046218','0.472794178046218'),
('BTK_HUMAN','3p08_B','B','crystal structure of the human btk kinase domain','2.3','0.327941581909938','0.327941581909938'),
('KAPCA_HUMAN','3p0m_A','A','human camp-dependent protein kinase in complex with an inhib','2.03','0.474320257081281','0.474320257081281'),
('EGFR_HUMAN','3p0y_A','A','anti-egfr/her3 fab dl11 in complex with domain iii of egfr extracellular region','1.8','0.51908408234127','0.51908408234127'),
('ERBB3_HUMAN','3p11_A','A','anti-egfr/her3 fab dl11 in complex with domains i-iii of the extracellular region','3.7','0.111767398246461','0.111767398246461'),
('PMYT1_HUMAN','3p1a_A','A','structure of human membrane-associated tyrosine- and threoni specific cdc2-inhibitory kinase myt1 (pkmyt1)','1.7','0.606833121498599','0.606833121498599'),
('EPHB3_HUMAN','3p1i_A','A','ligand binding domain of human ephrin type-b receptor 3','2.1','0.409413839285714','0.409413839285714'),
('EPHB3_HUMAN','3p1i_B','B','ligand binding domain of human ephrin type-b receptor 3','2.1','0.409413839285714','0.409413839285714'),
('EPHB3_HUMAN','3p1i_C','C','ligand binding domain of human ephrin type-b receptor 3','2.1','0.409413839285714','0.409413839285714'),
('ERN1_HUMAN','3p23_A','A','crystal structure of the human kinase and rnase domains in c with adp','2.7','0.234465712632275','0.234465712632275'),
('ERN1_HUMAN','3p23_B','B','crystal structure of the human kinase and rnase domains in c with adp','2.7','0.234465712632275','0.234465712632275'),
('ERN1_HUMAN','3p23_C','C','crystal structure of the human kinase and rnase domains in c with adp','2.7','0.234465712632275','0.234465712632275'),
('ERN1_HUMAN','3p23_D','D','crystal structure of the human kinase and rnase domains in c with adp','2.7','0.234465712632275','0.234465712632275'),
('PLK1_HUMAN','3p2w_A','A','unliganded form of polo-like kinase i polo-box domain','1.66','0.560951959982788','0.560951959982788'),
('PLK1_HUMAN','3p2z_A','A','polo-like kinase i polo-box domain in complex with plhspta phosphopeptide from pbip1','1.79','0.521567685139','0.521567685139'),
('PLK1_HUMAN','3p34_A','A','polo-like kinase i polo-box domain in complex with mqsptpl phosphopeptide','1.4','0.648594613095238','0.648594613095238'),
('PLK1_HUMAN','3p35_A','A','polo-like kinase i polo-box domain in complex with mqspspl phosphopeptide','2.09','0.395528214997722','0.395528214997722'),
('PLK1_HUMAN','3p35_B','B','polo-like kinase i polo-box domain in complex with mqspspl phosphopeptide','2.09','0.395528214997722','0.395528214997722'),
('PLK1_HUMAN','3p35_C','C','polo-like kinase i polo-box domain in complex with mqspspl phosphopeptide','2.09','0.395528214997722','0.395528214997722'),
('PLK1_HUMAN','3p36_A','A','polo-like kinase i polo-box domain in complex with dpplhspta phosphopeptide from pbip1','1.59','0.574624448562444','0.574624448562444'),
('PLK1_HUMAN','3p37_A','A','polo-like kinase i polo-box domain in complex with fdpplhspt phosphopeptide from pbip1','2.38','0.306263826155462','0.306263826155462'),
('PLK1_HUMAN','3p37_B','B','polo-like kinase i polo-box domain in complex with fdpplhspt phosphopeptide from pbip1','2.38','0.306263826155462','0.306263826155462'),
('PLK1_HUMAN','3p37_C','C','polo-like kinase i polo-box domain in complex with fdpplhspt phosphopeptide from pbip1','2.38','0.306263826155462','0.306263826155462'),
('AURKA_HUMAN','3p9j_A','A','aurora a kinase domain with phthalazinone pyrazole inhibitor','2.8','0.298865342261905','0.298865342261905'),
('CHK1_HUMAN','3pa3_A','A','x-ray crystal structure of compound 70 bound to human chk1 k domain','1.4','0.647912321428571','0.647912321428571'),
('CHK1_HUMAN','3pa4_A','A','x-ray crystal structure of compound 2a bound to human chk1 k domain','1.59','0.528025921776729','0.528025921776729'),
('CHK1_HUMAN','3pa5_A','A','x-ray crystal structure of compound 1 bound to human chk1 ki domain','1.7','0.527778582808123','0.527778582808123'),
('PAK2_HUMAN','3pcs_E','E','structure of espg-pak2 autoinhibitory ialpha3 helix complex','2.86','0.270826748459874','0.270826748459874'),
('CSK21_HUMAN','3pe1_A','A','crystal structure of human protein kinase ck2 alpha subunit with the inhibitor cx-4945','1.6','0.608067738095238','0.608067738095238'),
('CSK21_HUMAN','3pe2_A','A','crystal structure of human protein kinase ck2 in complex wit inhibitor cx-5011','1.9','0.48507626566416','0.48507626566416'),
('CSK21_HUMAN','3pe4_B','B','structure of human o-glcnac transferase and its complex with substrate','1.95','0.434935914606227','0.434935914606227'),
('CSK21_HUMAN','3pe4_D','D','structure of human o-glcnac transferase and its complex with substrate','1.95','0.434935914606227','0.434935914606227'),
('EGFR_HUMAN','3pfv_C','C','crystal structure of cbl-b tkb domain in complex with egfr p peptide','2.27','0.357851833765995','0.357851833765995'),
('EGFR_HUMAN','3pfv_D','D','crystal structure of cbl-b tkb domain in complex with egfr p peptide','2.27','0.357851833765995','0.357851833765995'),
('MK14_HUMAN','3pg3_A','A','human p38 map kinase in complex with rl182','2','0.409701755952381','0.409701755952381'),
('BTK_HUMAN','3pix_A','A','crystal structure of btk kinase domain complexed with 2-isop (4-methyl-piperazin-1-yl)-4-(5-methyl-2h-pyrazol-3-ylamino) phthalazin-1-one','1.85','0.464360927445302','0.464360927445302'),
('BTK_HUMAN','3piy_A','A','crystal structure of btk kinase domain complexed with r406','2.55','0.286903871673669','0.286903871673669'),
('BTK_HUMAN','3piz_A','A','crystal structure of btk kinase domain complexed with (5-ami tolyl-1h-pyrazol-4-yl)-[3-(1-methanesulfonyl-piperidin-4-yl methanone','2.21','0.354162274092329','0.354162274092329'),
('BTK_HUMAN','3pj1_A','A','crystal structure of btk kinase domain complexed with 3-(2,6 phenyl)-7-[4-(2-diethylamino-ethoxy)-phenylamino]-1-methyl- dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one','2','0.41020943452381','0.41020943452381'),
('BTK_HUMAN','3pj2_A','A','crystal structure of btk kinase domain complexed with 2-[4-( diethylamino-ethoxy)-phenylamino]-6-(4-fluoro-phenoxy)-8-me pyrido[2,3-d]pyrimidin-7-one','1.75','0.493070892857143','0.493070892857143'),
('BTK_HUMAN','3pj3_A','A','crystal structure of btk kinase domain complexed with 2-meth (3-phenyl-acryloyl)amino]-n-(2-phenyl-3h-imidazo[4,5-b]pyri benzamide','1.85','0.457985986969112','0.457985986969112'),
('CDK2_HUMAN','3pj8_A','A','structure of cdk2 in complex with a pyrazolo[4,3-d]pyrimidin bioisostere of roscovitine.','1.96','0.431895733418367','0.431895733418367'),
('JAK3_HUMAN','3pjc_A','A','crystal structure of jak3 complexed with a potent atp site i showing high selectivity within the janus kinase family','2.2','0.41876567775974','0.41876567775974'),
('RON_HUMAN','3pls_A','A','ron in complex with ligand amp-pnp','2.24','0.328862663690476','0.328862663690476'),
('KAPCA_HUMAN','3poo_A','A','human camp-dependent protein kinase in complex with an inhib','1.6','0.592106279761905','0.592106279761905'),
('EGFR_HUMAN','3poz_A','A','egfr kinase domain complexed with tak-285','1.5','0.5980428125','0.5980428125'),
('B4DTR1_HUMAN','3pp0_A','A','crystal structure of the kinase domain of human her2 (erbb2)','2.25','0.380877584325397','0.380877584325397'),
('ERBB2_HUMAN','3pp0_B','B','crystal structure of the kinase domain of human her2 (erbb2)','2.25','0.380877584325397','0.380877584325397'),
('MP2K1_HUMAN','3pp1_A','A','crystal structure of the human mitogen-activated protein kin 1 (mek 1) in complex with ligand and mgatp','2.7','0.302883420965608','0.302883420965608'),
('D7PBN4_HUMAN','3ppj_A','A','human b-raf kinase in complex with a furopyridine inhibitor','3.7','0.129533067889318','0.129533067889318'),
('BRAF_HUMAN','3ppj_B','B','human b-raf kinase in complex with a furopyridine inhibitor','3.7','0.129533067889318','0.129533067889318'),
('D7PBN4_HUMAN','3ppk_A','A','human b-raf kinase in complex with a non-oxime furopyridine','3','0.208464717261905','0.208464717261905'),
('BRAF_HUMAN','3ppk_B','B','human b-raf kinase in complex with a non-oxime furopyridine','3','0.208464717261905','0.208464717261905'),
('BRAF_HUMAN','3prf_A','A','crystal structure of human b-raf kinase domain in complex wi oxime furopyridine inhibitor','2.9','0.180924565373563','0.180924565373563'),
('BRAF_HUMAN','3prf_B','B','crystal structure of human b-raf kinase domain in complex wi oxime furopyridine inhibitor','2.9','0.180924565373563','0.180924565373563'),
('BRAF_HUMAN','3pri_A','A','crystal structure of human b-raf kinase in complex with a no furopyridine inhibitor','3.5','0.124981130952381','0.124981130952381'),
('BRAF_HUMAN','3pri_B','B','crystal structure of human b-raf kinase in complex with a no furopyridine inhibitor','3.5','0.124981130952381','0.124981130952381'),
('MAST1_HUMAN','3ps4_A','A','pdz domain from human microtubule-associated serine/threonin kinase 1','1.85','0.471404320302445','0.471404320302445'),
('MAST1_HUMAN','3ps4_B','B','pdz domain from human microtubule-associated serine/threonin kinase 1','1.85','0.471404320302445','0.471404320302445'),
('MAST1_HUMAN','3ps4_C','C','pdz domain from human microtubule-associated serine/threonin kinase 1','1.85','0.471404320302445','0.471404320302445'),
('MAST1_HUMAN','3ps4_D','D','pdz domain from human microtubule-associated serine/threonin kinase 1','1.85','0.471404320302445','0.471404320302445'),
('D7PBN4_HUMAN','3psb_A','A','furo[2,3-c]pyridine-based indanone oximes as potent and sele raf inhibitors','3.4','0.179292111344538','0.179292111344538'),
('BRAF_HUMAN','3psb_B','B','furo[2,3-c]pyridine-based indanone oximes as potent and sele raf inhibitors','3.4','0.179292111344538','0.179292111344538'),
('BRAF_HUMAN','3psd_A','A','non-oxime pyrazole based inhibitors of b-raf kinase','3.6','0.121288625992063','0.121288625992063'),
('BRAF_HUMAN','3psd_B','B','non-oxime pyrazole based inhibitors of b-raf kinase','3.6','0.121288625992063','0.121288625992063'),
('MK10_HUMAN','3ptg_A','A','design and synthesis of a novel, orally efficacious tri-subs thiophene based jnk inhibitor','2.43','0.269269568268665','0.269269568268665'),
('TITIN_HUMAN','3puc_A','A','atomic resolution structure of titin domain m7','0.96','0.925666666666667','0.925666666666667'),
('GSK3B_HUMAN','3pup_B','B','structure of glycogen synthase kinase 3 beta (gsk3b) in comp ruthenium octasporine ligand (os1)','2.99','0.244755348035117','0.244755348035117'),
('PDPK1_HUMAN','3pwy_A','A','crystal structure of an extender (spd28345)-modified human p complex 2','3.5','0.185836443452381','0.185836443452381'),
('CDK2_HUMAN','3pxf_A','A','cdk2 in complex with two molecules of 8-anilino-1-naphthalen sulfonate','1.8','0.503016046626984','0.503016046626984'),
('Q8IYN9_HUMAN','3pxk_A','A','focal adhesion kinase catalytic domain in complex with pyrro d]thiazole','1.79','0.525356345853285','0.525356345853285'),
('FAK1_HUMAN','3pxk_B','B','focal adhesion kinase catalytic domain in complex with pyrro d]thiazole','1.79','0.525356345853285','0.525356345853285'),
('CDK2_HUMAN','3pxq_A','A','cdk2 in complex with 3 molecules of 8-anilino-1-naphthalene','1.9','0.472006860902256','0.472006860902256'),
('CDK2_HUMAN','3pxr_A','A','apo cdk2 crystallized from jeffamine','2','0.443119270833333','0.443119270833333'),
('CDK2_HUMAN','3pxy_A','A','cdk2 in complex with inhibitor jws648','1.8','0.486226359126984','0.486226359126984'),
('CDK2_HUMAN','3pxz_A','A','cdk2 ternary complex with jws648 and ans','1.7','0.51940056197479','0.51940056197479'),
('CDK2_HUMAN','3py0_A','A','cdk2 in complex with inhibitor su9516','1.75','0.505003958333333','0.505003958333333'),
('CDK2_HUMAN','3py1_A','A','cdk2 ternary complex with su9516 and ans','2.05','0.433902973286876','0.433902973286876'),
('ABL1_HUMAN','3pyy_A','A','discovery and characterization of a cell-permeable, small-mo abl kinase activator that binds to the myristoyl binding si','1.85','0.49790741554054','0.49790741554054'),
('MK08_HUMAN','3pze_A','A','jnk1 in complex with inhibitor','2','0.419024181547619','0.419024181547619'),
('CSK21_HUMAN','3q04_A','A','crystal structure of the apo-form of human ck2 alpha at ph 8','1.8','0.390555555555556','0.390555555555556'),
('PLK1_HUMAN','3q1i_A','A','polo-like kinase i polo-box domain in complex with fmpppmsps phosphopeptide from tcerg1','1.4','0.663900029761905','0.663900029761905'),
('Q8IXP2_HUMAN','3q32_A','A','structure of janus kinase 2 with a pyrrolotriazine inhibitor','2.5','0.334189895833333','0.334189895833333'),
('JAK2_HUMAN','3q32_B','B','structure of janus kinase 2 with a pyrrolotriazine inhibitor','2.5','0.334189895833333','0.334189895833333'),
('GSK3B_HUMAN','3q3b_A','A','6-amino-4-(pyrimidin-4-yl)pyridones: novel glycogen synthase inhibitors','2.7','0.263228584656085','0.263228584656085'),
('GSK3B_HUMAN','3q3b_B','B','6-amino-4-(pyrimidin-4-yl)pyridones: novel glycogen synthase inhibitors','2.7','0.263228584656085','0.263228584656085'),
('BRAF_HUMAN','3q4c_A','A','crystal structure of wild type braf kinase domain in complex organometallic inhibitor cns292','3.2','0.184332306547619','0.184332306547619'),
('BRAF_HUMAN','3q4c_B','B','crystal structure of wild type braf kinase domain in complex organometallic inhibitor cns292','3.2','0.184332306547619','0.184332306547619'),
('AVR2A_HUMAN','3q4t_A','A','crystal structure of activin receptor type-iia (acvr2a) kina in complex with dorsomorphin','1.96','0.48117387329932','0.48117387329932'),
('ACVR1_HUMAN','3q4u_D','D','crystal structure of the acvr1 kinase domain in complex with 193189','1.82','0.526883778617216','0.526883778617216'),
('PAK1_HUMAN','3q4z_A','A','structure of unphosphorylated pak1 kinase domain','1.89','0.468224576719577','0.468224576719577'),
('PAK1_HUMAN','3q4z_B','B','structure of unphosphorylated pak1 kinase domain','1.89','0.468224576719577','0.468224576719577'),
('PAK1_HUMAN','3q52_A','A','structure of phosphorylated pak1 kinase domain','1.8','0.514998888888889','0.514998888888889'),
('PAK1_HUMAN','3q53_A','A','structure of phosphorylated pak1 kinase domain in complex wi','2.09','0.443331994759626','0.443331994759626'),
('TITIN_HUMAN','3q5o_A','A','crystal structure of human titin domain m10','2.05','0.444787169715447','0.444787169715447'),
('TITIN_HUMAN','3q5o_B','B','crystal structure of human titin domain m10','2.05','0.444787169715447','0.444787169715447'),
('MET_HUMAN','3q6u_A','A','structure of the apo met receptor kinase in the dually-phosp activated state','1.6','0.590877901785714','0.590877901785714'),
('MET_HUMAN','3q6w_A','A','structure of dually-phosphorylated met receptor kinase in co an mk-2461 analog with specificity for the activated recept','1.75','0.512197425595238','0.512197425595238'),
('BRAF_HUMAN','3q96_A','A','b-raf kinase domain in complex with a tetrahydronaphthalene','3.1','0.206750927899386','0.206750927899386'),
('BRAF_HUMAN','3q96_B','B','b-raf kinase domain in complex with a tetrahydronaphthalene','3.1','0.206750927899386','0.206750927899386'),
('CSK21_HUMAN','3q9w_A','A','crystal structure of human ck2 alpha in complex with emodin','1.7','0.563049118522409','0.563049118522409'),
('CSK21_HUMAN','3q9x_A','A','crystal structure of human ck2 alpha in complex with emodin','2.2','0.384527984307359','0.384527984307359'),
('CSK21_HUMAN','3q9x_B','B','crystal structure of human ck2 alpha in complex with emodin','2.2','0.384527984307359','0.384527984307359'),
('CSK21_HUMAN','3q9y_A','A','crystal structure of human ck2 alpha in complex with quinali ph 8.5','1.8','0.514224156746032','0.514224156746032'),
('CSK21_HUMAN','3q9z_A','A','crystal structure of human ck2 alpha in complex with quinali ph 6.5','2.2','0.364661496212121','0.364661496212121'),
('CSK21_HUMAN','3q9z_B','B','crystal structure of human ck2 alpha in complex with quinali ph 6.5','2.2','0.364661496212121','0.364661496212121'),
('CSK21_HUMAN','3qa0_A','A','crystal structure of the apo-form of human ck2 alpha at ph 6','2.5','0.315315833333333','0.315315833333333'),
('CSK21_HUMAN','3qa0_B','B','crystal structure of the apo-form of human ck2 alpha at ph 6','2.5','0.315315833333333','0.315315833333333'),
('BMR1A_HUMAN','3qb4_B','B','crystal structure of a tgf-beta ligand-receptor complex','2.28','0.332121684680451','0.332121684680451'),
('BMR1A_HUMAN','3qb4_D','D','crystal structure of a tgf-beta ligand-receptor complex','2.28','0.332121684680451','0.332121684680451'),
('AURKA_HUMAN','3qbn_A','A','structure of human aurora a in complex with a diaminopyrimid','3.5','0.0973085863095238','0.0973085863095238'),
('PDPK1_HUMAN','3qc4_A','A','pdk1 in complex with dfg-out inhibitor xxx','1.8','0.510744439484127','0.510744439484127'),
('PDPK1_HUMAN','3qc4_B','B','pdk1 in complex with dfg-out inhibitor xxx','1.8','0.510744439484127','0.510744439484127'),
('PDPK1_HUMAN','3qcq_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit amino-1h-indazol-6-yl)-n4-ethyl-2,4-pyrimidinediamine','2.5','0.357993556547619','0.357993556547619'),
('PDPK1_HUMAN','3qcs_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit amino-6-(4-morpholinyl)-4-pyrimidinyl]-1h-indazol-3-amine','2.49','0.341006023917097','0.341006023917097'),
('PDPK1_HUMAN','3qcx_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit amino-6-[(3r)-3-methyl-4-morpholinyl]-4-pyrimidinyl}-1h-ind amine','2.3','0.379244825957557','0.379244825957557'),
('PDPK1_HUMAN','3qcy_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit amino-6-(3-amino-1h-indazol-6-yl)-4-pyrimidinyl]-n-phenyl-2 morpholinecarboxamide','2.2','0.421932895021645','0.421932895021645'),
('PDPK1_HUMAN','3qd0_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit 1-[2-amino-6-(3-amino-1h-indazol-6-yl)-4-pyrimidinyl]-6-met phenyl-3-piperidinecarboxamide','1.99','0.463168291980737','0.463168291980737'),
('PDPK1_HUMAN','3qd3_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit dimethylethyl {(3r,6s)-1-[2-amino-6-(3-amino-1h-indazol-6-y pyrimidinyl]-6-methyl-3-piperidinyl}carbamate','2','0.4627940625','0.4627940625'),
('PDPK1_HUMAN','3qd4_A','A','phosphoinositide-dependent kinase-1 (pdk1) kinase domain wit dimethylethyl{(3r,5r)-1-[2-amino-6-(3-amino-1h-indazol-6-yl pyrimidinyl]-5-methyl-3-piperidinyl}carbamate','2.3','0.3829275938147','0.3829275938147'),
('PIM1_HUMAN','3qf9_A','A','crystal structure of human proto-oncogene serine threonine k (pim1) in complex with a consensus peptide and a furan- thiazolidinedione ligand','2.2','0.391218966450217','0.391218966450217'),
('Q86XZ8_HUMAN','3qfv_A','A','mrck beta in complex with tpca-1','2.65','0.274624413185085','0.274624413185085'),
('MRCKB_HUMAN','3qfv_B','B','mrck beta in complex with tpca-1','2.65','0.274624413185085','0.274624413185085'),
('ITK_HUMAN','3qgw_A','A','crystal structure of itk kinase bound to an inhibitor','2.1','0.352112351190476','0.352112351190476'),
('ITK_HUMAN','3qgw_B','B','crystal structure of itk kinase bound to an inhibitor','2.1','0.352112351190476','0.352112351190476'),
('ITK_HUMAN','3qgy_A','A','crystal structure of itk inhibitor complex','2.1','0.391204479166667','0.391204479166667'),
('ITK_HUMAN','3qgy_B','B','crystal structure of itk inhibitor complex','2.1','0.391204479166667','0.391204479166667'),
('CDK2_HUMAN','3qhr_A','A','structure of a pcdk2/cyclina transition-state mimic','2.17','0.407339478206605','0.407339478206605'),
('CDK2_HUMAN','3qhr_C','C','structure of a pcdk2/cyclina transition-state mimic','2.17','0.407339478206605','0.407339478206605'),
('CDK2_HUMAN','3qhw_A','A','structure of a pcdk2/cyclina transition-state mimic','1.91','0.48311162311456','0.48311162311456'),
('CDK2_HUMAN','3qhw_C','C','structure of a pcdk2/cyclina transition-state mimic','1.91','0.48311162311456','0.48311162311456'),
('AKT1_HUMAN','3qkk_A','A','spirochromane akt inhibitors','2.3','0.373646135481367','0.373646135481367'),
('AKT1_HUMAN','3qkl_A','A','spirochromane akt inhibitors','1.9','0.457857917449875','0.457857917449875'),
('AKT1_HUMAN','3qkm_A','A','spirocyclic sulfonamides as akt inhibitors','2.2','0.410580707521645','0.410580707521645'),
('CDK2_HUMAN','3ql8_A','A','cdk2 in complex with inhibitor jws-6-260','1.9','0.448863274592732','0.448863274592732'),
('TITIN_HUMAN','3qp3_A','A','crystal structure of titin domain m4, tetragonal form','2','0.465365699404762','0.465365699404762'),
('TITIN_HUMAN','3qp3_B','B','crystal structure of titin domain m4, tetragonal form','2','0.465365699404762','0.465365699404762'),
('TITIN_HUMAN','3qp3_C','C','crystal structure of titin domain m4, tetragonal form','2','0.465365699404762','0.465365699404762'),
('CDK2_HUMAN','3qqf_A','A','cdk2 in complex with inhibitor l1','1.75','0.517934642857143','0.517934642857143'),
('CDK2_HUMAN','3qqg_A','A','cdk2 in complex with inhibitor l2-5','1.9','0.464563006735589','0.464563006735589'),
('CDK2_HUMAN','3qqh_A','A','cdk2 in complex with inhibitor l2-2','1.87','0.47801679876496','0.47801679876496'),
('CDK2_HUMAN','3qqj_A','A','cdk2 in complex with inhibitor l2','1.7','0.527825234593837','0.527825234593837'),
('CDK2_HUMAN','3qqk_A','A','cdk2 in complex with inhibitor l4','1.86','0.480483634792627','0.480483634792627'),
('CDK2_HUMAN','3qql_A','A','cdk2 in complex with inhibitor l3','1.85','0.501787326254826','0.501787326254826'),
('IGF1R_HUMAN','3qqu_A','A','cocrystal structure of unphosphorylated igf with pyrimidine','2.9','0.167481693349754','0.167481693349754'),
('IGF1R_HUMAN','3qqu_B','B','cocrystal structure of unphosphorylated igf with pyrimidine','2.9','0.167481693349754','0.167481693349754'),
('IGF1R_HUMAN','3qqu_C','C','cocrystal structure of unphosphorylated igf with pyrimidine','2.9','0.167481693349754','0.167481693349754'),
('IGF1R_HUMAN','3qqu_D','D','cocrystal structure of unphosphorylated igf with pyrimidine','2.9','0.167481693349754','0.167481693349754'),
('ABL1_HUMAN','3qri_A','A','the crystal structure of human abl1 kinase domain in complex 2036','2.1','0.410882425595238','0.410882425595238'),
('ABL1_HUMAN','3qri_B','B','the crystal structure of human abl1 kinase domain in complex 2036','2.1','0.410882425595238','0.410882425595238'),
('ABL1_HUMAN','3qrj_A','A','the crystal structure of human abl1 kinase domain t315i muta complex with dcc-2036','1.82','0.443787811355311','0.443787811355311'),
('ABL1_HUMAN','3qrj_B','B','the crystal structure of human abl1 kinase domain t315i muta complex with dcc-2036','1.82','0.443787811355311','0.443787811355311'),
('ABL1_HUMAN','3qrk_A','A','the crystal structure of human abl1 kinase domain in complex 987','2.3','0.365178546195652','0.365178546195652'),
('CDK2_HUMAN','3qrt_A','A','cdk2 in complex with inhibitor nsk-mc2-55','1.75','0.518226488095238','0.518226488095238'),
('CDK2_HUMAN','3qru_A','A','cdk2 in complex with inhibitor nsk-mc1-12','1.95','0.457960274725275','0.457960274725275'),
('FLT3_HUMAN','3qs7_F','F','crystal structure of a human flt3 ligand-receptor ternary co','4.3','0.0715603419158361','0.0715603419158361'),
('FLT3_HUMAN','3qs9_E','E','crystal structure of a human flt3 ligand-receptor ternary co','7.8','-0.108533621794872','-0.108533621794872'),
('FLT3_HUMAN','3qs9_G','G','crystal structure of a human flt3 ligand-receptor ternary co','7.8','-0.108533621794872','-0.108533621794872'),
('FLT3_HUMAN','3qs9_H','H','crystal structure of a human flt3 ligand-receptor ternary co','7.8','-0.108533621794872','-0.108533621794872'),
('MET_HUMAN','3qti_A','A','c-met kinase in complex with nvp-bvu972','2','0.465067857142857','0.465067857142857'),
('MET_HUMAN','3qti_B','B','c-met kinase in complex with nvp-bvu972','2','0.465067857142857','0.465067857142857'),
('CDK2_HUMAN','3qtq_A','A','cdk2 in complex with inhibitor rc-1-137','1.8','0.495512504960317','0.495512504960317'),
('CDK2_HUMAN','3qtr_A','A','cdk2 in complex with inhibitor rc-1-148','1.85','0.485863129826255','0.485863129826255'),
('CDK2_HUMAN','3qts_A','A','cdk2 in complex with inhibitor rc-2-12','1.9','0.440845878759398','0.440845878759398'),
('CDK2_HUMAN','3qtu_A','A','cdk2 in complex with inhibitor rc-2-132','1.82','0.496859760760073','0.496859760760073'),
('CDK2_HUMAN','3qtw_A','A','cdk2 in complex with inhibitor rc-2-13','1.85','0.465692356016731','0.465692356016731'),
('CDK2_HUMAN','3qtx_A','A','cdk2 in complex with inhibitor rc-2-35','1.95','0.454221986034799','0.454221986034799'),
('CDK2_HUMAN','3qtz_A','A','cdk2 in complex with inhibitor rc-2-36','2','0.439933288690476','0.439933288690476'),
('CDK2_HUMAN','3qu0_A','A','cdk2 in complex with inhibitor rc-2-38','1.95','0.45656430746337','0.45656430746337'),
('MK14_HUMAN','3qud_A','A','human p38 map kinase in complex with 2-amino-phenylamino-ben','2','0.394354925595238','0.394354925595238'),
('MK14_HUMAN','3que_A','A','human p38 map kinase in complex with skepinone-l','2.7','0.250726486441799','0.250726486441799'),
('CDK2_HUMAN','3qwj_A','A','cdk2 in complex with inhibitor kvr-1-142','1.75','0.512298809523809','0.512298809523809'),
('CDK2_HUMAN','3qwk_A','A','cdk2 in complex with inhibitor kvr-1-150','1.85','0.479120034588159','0.479120034588159'),
('EGFR_HUMAN','3qwq_A','A','crystal structure of the extracellular domain of the epiderm factor receptor in complex with an adnectin','2.75','0.270719860660173','0.270719860660173'),
('CDK2_HUMAN','3qx2_A','A','cdk2 in complex with inhibitor kvr-1-190','1.75','0.515892678571429','0.515892678571429'),
('CDK2_HUMAN','3qx4_A','A','cdk2 in complex with inhibitor kvr-1-78','1.92','0.462054166666667','0.462054166666667'),
('CDK2_HUMAN','3qxo_A','A','cdk2 in complex with inhibitor kvr-1-84','1.75','0.499183377976191','0.499183377976191'),
('CDK2_HUMAN','3qxp_A','A','cdk2 in complex with inhibitor rc-3-89','1.75','0.503388020833333','0.503388020833333'),
('CDK2_HUMAN','3qzf_A','A','cdk2 in complex with inhibitor jws-6-52','2','0.425691101190476','0.425691101190476'),
('CDK2_HUMAN','3qzg_A','A','cdk2 in complex with inhibitor jws-6-76','1.75','0.496754821428571','0.496754821428571'),
('CDK2_HUMAN','3qzh_A','A','cdk2 in complex with inhibitor kvr-1-124','1.95','0.458546941391941','0.458546941391941'),
('CDK2_HUMAN','3qzi_A','A','cdk2 in complex with inhibitor kvr-1-126','1.75','0.508525208333333','0.508525208333333'),
('PIM1_HUMAN','3r00_A','A','the discovery of novel benzofuran-2-carboxylic acids as pote inhibitors','2.1','0.447079583333333','0.447079583333333'),
('PIM1_HUMAN','3r01_A','A','the discovery of novel benzofuran-2-carboxylic acids as pote inhibitors','2.6','0.285075235805861','0.285075235805861'),
('PIM1_HUMAN','3r02_A','A','the discovery of novel benzofuran-2-carboxylic acids as pote inhibitors','1.95','0.492739381868132','0.492739381868132'),
('PIM1_HUMAN','3r04_A','A','the discovery of novel benzofuran-2-carboxylic acids as pote inhibitors','1.7','0.556565859593838','0.556565859593838'),
('CSK21_HUMAN','3r0t_A','A','crystal structure of human protein kinase ck2 alpha subunit with the inhibitor cx-5279','1.75','0.557687098214286','0.557687098214286'),
('MAPK3_HUMAN','3r1n_A','A','mk3 kinase bound to compound 5b','2.09','0.385167917378674','0.385167917378674'),
('CDK2_HUMAN','3r1q_A','A','cdk2 in complex with inhibitor kvr-1-102','1.85','0.48034591256435','0.48034591256435'),
('CDK2_HUMAN','3r1s_A','A','cdk2 in complex with inhibitor kvr-1-127','1.8','0.505567624007937','0.505567624007937'),
('CDK2_HUMAN','3r1y_A','A','cdk2 in complex with inhibitor kvr-1-134','1.8','0.477668531746032','0.477668531746032'),
('AURKA_HUMAN','3r21_A','A','design, synthesis, and biological evaluation of pyrazolopyri sulfonamides as potent multiple-mitotic kinase (mmk) inhibi i)','2.9','0.17474966954023','0.17474966954023'),
('AURKA_HUMAN','3r22_A','A','design, synthesis, and biological evaluation of pyrazolopyri sulfonamides as potent multiple-mitotic kinase (mmk) inhibi i)','2.9','0.142297184421182','0.142297184421182'),
('CDK2_HUMAN','3r28_A','A','cdk2 in complex with inhibitor kvr-1-140','1.75','0.514823125','0.514823125'),
('MAPK2_HUMAN','3r2b_A','A','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_B','B','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_C','C','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_D','D','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_E','E','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_F','F','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_G','G','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_H','H','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_I','I','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_J','J','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_K','K','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2b_L','L','mk2 kinase bound to compound 5b','2.9','0.204762720135468','0.204762720135468'),
('MAPK2_HUMAN','3r2y_A','A','mk2 kinase bound to compound 1','3','0.130370014880952','0.130370014880952'),
('MAPK2_HUMAN','3r30_A','A','mk2 kinase bound to compound 2','3.2','0.123246383928571','0.123246383928571'),
('CDK2_HUMAN','3r6x_A','A','cdk2 in complex with inhibitor kvr-1-158','1.75','0.521285714285714','0.521285714285714'),
('CDK2_HUMAN','3r71_A','A','cdk2 in complex with inhibitor kvr-1-162','1.75','0.492374970238095','0.492374970238095'),
('CDK2_HUMAN','3r73_A','A','cdk2 in complex with inhibitor kvr-1-164','1.7','0.534668657212885','0.534668657212885'),
('CDK2_HUMAN','3r7e_A','A','cdk2 in complex with inhibitor kvr-1-67','1.9','0.472041622807017','0.472041622807017'),
('CDK2_HUMAN','3r7i_A','A','cdk2 in complex with inhibitor kvr-1-74','1.85','0.492819111969112','0.492819111969112'),
('MET_HUMAN','3r7o_A','A','structure of dually phosphorylated c-met in complex with mk-','2.3','0.341169349767081','0.341169349767081'),
('CDK2_HUMAN','3r7u_A','A','cdk2 in complex with inhibitor kvr-1-75','1.75','0.521084880952381','0.521084880952381'),
('CDK2_HUMAN','3r7v_A','A','cdk2 in complex with inhibitor kvr-1-9','1.95','0.454024009844322','0.454024009844322'),
('CDK2_HUMAN','3r7y_A','A','cdk2 in complex with inhibitor kvr-2-88','1.9','0.464273884711779','0.464273884711779'),
('CDK2_HUMAN','3r83_A','A','cdk2 in complex with inhibitor kvr-2-92','1.75','0.536556711309524','0.536556711309524'),
('CDK2_HUMAN','3r8l_A','A','cdk2 in complex with inhibitor l3-4','1.9','0.451698721021303','0.451698721021303'),
('CDK2_HUMAN','3r8m_A','A','cdk2 in complex with inhibitor l3-3','1.8','0.495104900793651','0.495104900793651'),
('CDK2_HUMAN','3r8p_A','A','cdk2 in complex with inhibitor nsk-mc1-6','1.8','0.517163174603175','0.517163174603175'),
('CDK2_HUMAN','3r8u_A','A','cdk2 in complex with inhibitor rc-1-132','2','0.424884598214286','0.424884598214286'),
('CDK2_HUMAN','3r8v_A','A','cdk2 in complex with inhibitor rc-1-135','1.9','0.461440968045113','0.461440968045113'),
('CDK2_HUMAN','3r8z_A','A','cdk2 in complex with inhibitor rc-1-136','1.85','0.478203367921493','0.478203367921493'),
('CDK2_HUMAN','3r9d_A','A','cdk2 in complex with inhibitor rc-2-135','1.95','0.447915393772894','0.447915393772894'),
('CDK2_HUMAN','3r9h_A','A','cdk2 in complex with inhibitor rc-2-142','2.1','0.401760535714286','0.401760535714286'),
('CDK2_HUMAN','3r9n_A','A','cdk2 in complex with inhibitor rc-2-21','1.75','0.530709523809524','0.530709523809524'),
('CDK2_HUMAN','3r9o_A','A','cdk2 in complex with inhibitor rc-2-143','1.9','0.461253527568922','0.461253527568922'),
('CDK2_HUMAN','3rah_A','A','cdk2 in complex with inhibitor rc-2-22','1.75','0.523555104166667','0.523555104166667'),
('CDK2_HUMAN','3rai_A','A','cdk2 in complex with inhibitor kvr-1-160','1.7','0.529890398284314','0.529890398284314'),
('CDK2_HUMAN','3rak_A','A','cdk2 in complex with inhibitor rc-2-32','1.75','0.524816889880952','0.524816889880952'),
('CDK2_HUMAN','3ral_A','A','cdk2 in complex with inhibitor rc-2-34','1.75','0.5209365625','0.5209365625'),
('CLK3_HUMAN','3raw_A','A','crystal structure of human cdc-like kinase 3 isoform in comp leucettine l41','2.09','0.442757887616769','0.442757887616769'),
('CLK3_HUMAN','3raw_B','B','crystal structure of human cdc-like kinase 3 isoform in comp leucettine l41','2.09','0.442757887616769','0.442757887616769'),
('HCK_HUMAN','3rbb_B','B','hiv-1 nef protein in complex with engineered hck sh3 domain','2.35','0.34636556072695','0.34636556072695'),
('HCK_HUMAN','3rbb_D','D','hiv-1 nef protein in complex with engineered hck sh3 domain','2.35','0.34636556072695','0.34636556072695'),
('ERBB2_HUMAN','3rcd_A','A','her2 kinase domain complexed with tak-285','3.21','0.0845264797507788','0.0845264797507788'),
('ERBB2_HUMAN','3rcd_B','B','her2 kinase domain complexed with tak-285','3.21','0.0845264797507788','0.0845264797507788'),
('ERBB2_HUMAN','3rcd_C','C','her2 kinase domain complexed with tak-285','3.21','0.0845264797507788','0.0845264797507788'),
('ERBB2_HUMAN','3rcd_D','D','her2 kinase domain complexed with tak-285','3.21','0.0845264797507788','0.0845264797507788'),
('PDPK1_HUMAN','3rcj_A','A','rapid preparation of triazolyl substituted nh-heterocyclic k inhibitors via one-pot sonogashira coupling tms-deprotectio sequence','1.7','0.522876544117647','0.522876544117647'),
('HCK_HUMAN','3rea_B','B','hiv-1 nef protein in complex with engineered hck-sh3 domain','2','0.47580568452381','0.47580568452381'),
('HCK_HUMAN','3rea_D','D','hiv-1 nef protein in complex with engineered hck-sh3 domain','2','0.47580568452381','0.47580568452381'),
('HCK_HUMAN','3reb_B','B','hiv-1 nef protein in complex with engineered hck-sh3 domain','3.45','0.164605697463768','0.164605697463768'),
('HCK_HUMAN','3reb_D','D','hiv-1 nef protein in complex with engineered hck-sh3 domain','3.45','0.164605697463768','0.164605697463768'),
('ILK_HUMAN','3rep_A','A','crystal structure of the ilk/alpha-parvin core complex (mnat','1.8','0.498867251984127','0.498867251984127'),
('CDK8_HUMAN','3rgf_A','A','crystal structure of human cdk8/cycc','2.2','0.423597433712121','0.423597433712121'),
('MET_HUMAN','3rhk_A','A','crystal structure of the catalytic domain of c-met kinase in with arq 197','1.94','0.458490137763868','0.458490137763868'),
('MET_HUMAN','3rhk_B','B','crystal structure of the catalytic domain of c-met kinase in with arq 197','1.94','0.458490137763868','0.458490137763868'),
('FGFR1_HUMAN','3rhx_A','A','crystal structure of the catalytic domain of fgfr1 kinase in with arq 069','2.01','0.44212121757285','0.44212121757285'),
('FGFR1_HUMAN','3rhx_B','B','crystal structure of the catalytic domain of fgfr1 kinase in with arq 069','2.01','0.44212121757285','0.44212121757285'),
('FGFR2_HUMAN','3ri1_A','A','crystal structure of the catalytic domain of fgfr2 kinase in with arq 069','2.1','0.408271443452381','0.408271443452381'),
('FGFR2_HUMAN','3ri1_B','B','crystal structure of the catalytic domain of fgfr2 kinase in with arq 069','2.1','0.408271443452381','0.408271443452381'),
('MK14_HUMAN','3rin_A','A','p38 kinase crystal structure in complex with small molecule','2.2','0.30820761228355','0.30820761228355'),
('CDK2_HUMAN','3rjc_A','A','cdk2 in complex with inhibitor l4-12','1.85','0.475295495897683','0.475295495897683'),
('CDK2_HUMAN','3rk5_A','A','cdk2 in complex with inhibitor rc-2-72','2','0.43453775297619','0.43453775297619'),
('CDK2_HUMAN','3rk7_A','A','cdk2 in complex with inhibitor rc-2-71','1.8','0.492104365079365','0.492104365079365'),
('CDK2_HUMAN','3rk9_A','A','cdk2 in complex with inhibitor rc-2-74','1.85','0.474486567326255','0.474486567326255'),
('CDK2_HUMAN','3rkb_A','A','cdk2 in complex with inhibitor rc-2-73','2','0.435224479166667','0.435224479166667'),
('CDK2_HUMAN','3rm6_A','A','cdk2 in complex with inhibitor kvr-2-80','1.6','0.551753080357143','0.551753080357143'),
('CDK2_HUMAN','3rm7_A','A','cdk2 in complex with inhibitor kvr-1-91','1.85','0.467091924469112','0.467091924469112'),
('CDK2_HUMAN','3rmf_A','A','cdk2 in complex with inhibitor rc-2-33','1.75','0.513671964285714','0.513671964285714'),
('CDK2_HUMAN','3rni_A','A','cdk2 in complex with inhibitor rc-3-86','1.95','0.445244709249084','0.445244709249084'),
('KS6A1_HUMAN','3rny_A','A','crystal structure of human rsk1 c-terminal kinase domain','2.7','0.295619849537037','0.295619849537037'),
('KS6A1_HUMAN','3rny_B','B','crystal structure of human rsk1 c-terminal kinase domain','2.7','0.295619849537037','0.295619849537037'),
('MK14_HUMAN','3roc_A','A','crystal structure of human p38 alpha complexed with a pyrimi compound','1.7','0.476788359593838','0.476788359593838'),
('CDK2_HUMAN','3roy_A','A','cdk2 in complex with inhibitor kvr-1-154','1.75','0.513549672619047','0.513549672619047'),
('CDK2_HUMAN','3rpo_A','A','cdk2 in complex with inhibitor kvr-1-156','1.75','0.519111755952381','0.519111755952381'),
('CDK2_HUMAN','3rpr_A','A','cdk2 in complex with inhibitor rc-2-49','1.75','0.531529270833333','0.531529270833333'),
('CSK21_HUMAN','3rps_A','A','structure of human ck2alpha in complex with the atp-competit inhibitor 3-(4,5,6,7-tetrabromo-1h-benzotriazol-1-yl)propan','2.3','0.386037013457557','0.386037013457557'),
('CSK21_HUMAN','3rps_B','B','structure of human ck2alpha in complex with the atp-competit inhibitor 3-(4,5,6,7-tetrabromo-1h-benzotriazol-1-yl)propan','2.3','0.386037013457557','0.386037013457557'),
('CDK2_HUMAN','3rpv_A','A','cdk2 in complex with inhibitor rc-2-88','1.8','0.495881314484127','0.495881314484127'),
('CDK2_HUMAN','3rpy_A','A','cdk2 in complex with inhibitor rc-2-40','1.9','0.468896295426065','0.468896295426065'),
('PLK1_HUMAN','3rq7_A','A','polo-like kinase 1 polo box domain in complex with a c6h5(ch derivatized peptide inhibitor','1.55','0.6554539093702','0.6554539093702'),
('JAK2_HUMAN','3rvg_A','A','crystals structure of jak2 with a 1-amino-5h-pyrido[4,3-b]in carboxamide inhibitor','2.5','0.291563556547619','0.291563556547619'),
('PDPK1_HUMAN','3rwp_A','A','discovery of a novel, potent and selective inhibitor of 3- phosphoinositide dependent kinase (pdk1)','1.92','0.498687589285714','0.498687589285714'),
('PDPK1_HUMAN','3rwq_A','A','discovery of a novel, potent and selective inhibitor of 3- phosphoinositide dependent kinase (pdk1)','2.55','0.337098142507003','0.337098142507003'),
('CDK2_HUMAN','3rzb_A','A','cdk2 in complex with inhibitor rc-2-23','1.9','0.465837902568922','0.465837902568922'),
('CDK2_HUMAN','3s00_A','A','cdk2 in complex with inhibitor l4-14','1.8','0.465340555555556','0.465340555555556'),
('CDK2_HUMAN','3s0o_A','A','cdk2 in complex with inhibitor rc-1-138','2','0.413133616071429','0.413133616071429'),
('CDK2_HUMAN','3s1h_A','A','cdk2 in complex with inhibitor rc-2-39','1.75','0.511011696428571','0.511011696428571'),
('CDK2_HUMAN','3s2p_A','A','crystal structure of cdk2 with a 2-aminopyrimidine compound','2.3','0.307181224767081','0.307181224767081'),
('VGFR2_HUMAN','3s35_X','X','structural basis for the function of two anti-vegf receptor','2.2','0.37171911525974','0.37171911525974'),
('VGFR2_HUMAN','3s36_X','X','structural basis for the function of two anti-vegf receptor','3.2','0.1700621875','0.1700621875'),
('VGFR2_HUMAN','3s37_X','X','structural basis for the function of two anti-vegf receptor','2.7','0.227478480489418','0.227478480489418'),
('MK14_HUMAN','3s3i_A','A','p38 kinase crystal structure in complex with small molecule','1.8','0.440182534722222','0.440182534722222'),
('MK14_HUMAN','3s4q_A','A','p38 alpha kinase complexed with a pyrazolo-triazine based in','2.27','0.255429274242186','0.255429274242186'),
('LIMK1_HUMAN','3s95_A','A','crystal structure of the human limk1 kinase domain in comple staurosporine','1.65','0.599432019751082','0.599432019751082'),
('LIMK1_HUMAN','3s95_B','B','crystal structure of the human limk1 kinase domain in comple staurosporine','1.65','0.599432019751082','0.599432019751082'),
('FAK1_HUMAN','3s9o_A','A','the focal adhesion targeting (fat) domain of the focal adhes showing n-terminal interactions in cis','2.6','0.246727259615385','0.246727259615385'),
('FAK1_HUMAN','3s9o_B','B','the focal adhesion targeting (fat) domain of the focal adhes showing n-terminal interactions in cis','2.6','0.246727259615385','0.246727259615385'),
('FAK1_HUMAN','3s9o_C','C','the focal adhesion targeting (fat) domain of the focal adhes showing n-terminal interactions in cis','2.6','0.246727259615385','0.246727259615385'),
('MK01_HUMAN','3sa0_A','A','complex of erk2 with norathyriol','1.59','0.610065475348158','0.610065475348158'),
('GSK3B_HUMAN','3say_A','A','crystal structure of human glycogen synthase kinase 3 beta ( complex with inhibitor 142','2.23','0.369984987321162','0.369984987321162'),
('GSK3B_HUMAN','3say_B','B','crystal structure of human glycogen synthase kinase 3 beta ( complex with inhibitor 142','2.23','0.369984987321162','0.369984987321162'),
('PDPK1_HUMAN','3sc1_A','A','novel isoquinolone pdk1 inhibitors discovered through fragme lead discovery','2.7','0.295541233465608','0.295541233465608'),
('GSK3B_HUMAN','3sd0_A','A','identification of a glycogen synthase kinase-3b inhibitor th attenuates hyperactivity in clock mutant mice','2.7','0.303826754298942','0.303826754298942'),
('GSK3B_HUMAN','3sd0_B','B','identification of a glycogen synthase kinase-3b inhibitor th attenuates hyperactivity in clock mutant mice','2.7','0.303826754298942','0.303826754298942'),
('MAPK3_HUMAN','3she_A','A','novel atp-competitive mk2 inhibitors with potent biochemical based activity throughout the series','2.25','0.321953611111111','0.321953611111111'),
('BUB1B_HUMAN','3si5_A','A','kinetochore-bubr1 kinase complex','2.2','0.422849918831169','0.422849918831169'),
('BUB1B_HUMAN','3si5_B','B','kinetochore-bubr1 kinase complex','2.2','0.422849918831169','0.422849918831169'),
('BRAF_HUMAN','3skc_A','A','human b-raf kinase in complex with an amide linked pyrazolop inhibitor','3.2','0.0775','0.0775'),
('BRAF_HUMAN','3skc_B','B','human b-raf kinase in complex with an amide linked pyrazolop inhibitor','3.2','0.0775','0.0775'),
('EPHA2_HUMAN','3skj_E','E','structural and functional characterization of an agonistic a epha2 monoclonal antibody','2.5','0.29849693452381','0.29849693452381'),
('EPHA2_HUMAN','3skj_F','F','structural and functional characterization of an agonistic a epha2 monoclonal antibody','2.5','0.29849693452381','0.29849693452381'),
('MP2K1_HUMAN','3sls_A','A','crystal structure of human mek-1 kinase in complex with ucb1 amppnp','2.3','0.349320331909938','0.349320331909938'),
('MP2K1_HUMAN','3sls_B','B','crystal structure of human mek-1 kinase in complex with ucb1 amppnp','2.3','0.349320331909938','0.349320331909938'),
('KCC2A_HUMAN','3soa_A','A','full-length human camkii','3.55','0.0926367331069752','0.0926367331069752'),
('AVR2A_HUMAN','3soc_A','A','crystal structure of activin receptor type-iia (acvr2a) kina in complex with a quinazolin','1.95','0.492525036630037','0.492525036630037'),
('AVR2A_HUMAN','3soc_B','B','crystal structure of activin receptor type-iia (acvr2a) kina in complex with a quinazolin','1.95','0.492525036630037','0.492525036630037'),
('CDK2_HUMAN','3sqq_A','A','cdk2 in complex with inhibitor rc-3-96','1.85','0.483831954231017','0.483831954231017'),
('KSYK_HUMAN','3srv_A','A','crystal structure of spleen tyrosine kinase (syk) in complex diaminopyrimidine carboxamide inhibitor','1.95','0.473760542582418','0.473760542582418'),
('KSYK_HUMAN','3srv_B','B','crystal structure of spleen tyrosine kinase (syk) in complex diaminopyrimidine carboxamide inhibitor','1.95','0.473760542582418','0.473760542582418'),
('CDK2_HUMAN','3sw4_A','A','crystal structure of the cdk2 in complex with thiazolylpyrim inhibitor','1.7','0.553834713760504','0.553834713760504'),
('CDK2_HUMAN','3sw7_A','A','crystal structure of the cdk2 in complex with thiazolylpyrim inhibitor','1.8','0.521568234126984','0.521568234126984'),
('BMX_HUMAN','3sxr_A','A','crystal structure of bmx non-receptor tyrosine kinase comple dasatinib','2.4','0.349155505952381','0.349155505952381'),
('BMX_HUMAN','3sxr_B','B','crystal structure of bmx non-receptor tyrosine kinase comple dasatinib','2.4','0.349155505952381','0.349155505952381'),
('BMX_HUMAN','3sxs_A','A','crystal structure of bmx non-receptor tyrosine kinase comple pp2','1.89','0.479604740410053','0.479604740410053'),
('ABL1_HUMAN','3t04_A','A','crystal structure of monobody 7c12/abl1 sh2 domain complex','2.1','0.426305148809524','0.426305148809524'),
('PIM1_HUMAN','3t9i_A','A','pim1 complexed with a novel 3,6-disubstituted indole at 2.6 resolution','2.6','0.368228539377289','0.368228539377289'),
('ITK_HUMAN','3t9t_A','A','crystal structure of btk mutant (f435t,k596r) complexed with imidazo[1,5-a]quinoxaline','1.65','0.581650635822511','0.581650635822511'),
('CSKP_HUMAN','3tac_A','A','crystal structure of the liprin-alpha/cask complex','2.2','0.387796124188312','0.387796124188312'),
('CSK21_HUMAN','3tax_B','B','a neutral diphosphate mimic crosslinks the active site of hu glcnac transferase','1.88','0.46058507218845','0.46058507218845'),
('CSK21_HUMAN','3tax_D','D','a neutral diphosphate mimic crosslinks the active site of hu glcnac transferase','1.88','0.46058507218845','0.46058507218845'),
('MERTK_HUMAN','3tcp_A','A','crystal structure of the catalytic domain of the proto-oncog tyrosine-protein kinase mer in complex with inhibitor unc56','2.69','0.266417226776863','0.266417226776863'),
('MERTK_HUMAN','3tcp_B','B','crystal structure of the catalytic domain of the proto-oncog tyrosine-protein kinase mer in complex with inhibitor unc56','2.69','0.266417226776863','0.266417226776863'),
('MK01_HUMAN','3tei_A','A','crystal structure of human erk2 complexed with a mapk dockin','2.4','0.340589583333333','0.340589583333333'),
('KS6A1_HUMAN','3tei_B','B','crystal structure of human erk2 complexed with a mapk dockin','2.4','0.340589583333333','0.340589583333333'),
('PLK1_HUMAN','3thb_A','A','structure of plk1 kinase domain in complex with a benzolacta inhibitor','2.5','0.266675758928571','0.266675758928571'),
('CDK2_HUMAN','3ti1_A','A','cdk2 in complex with sunitinib','1.99','0.418630241385499','0.418630241385499'),
('CDK2_HUMAN','3tiy_A','A','cdk2 in complex with nsc 35676','1.84','0.503618022774327','0.503618022774327'),
('CDK2_HUMAN','3tiz_A','A','cdk2 in complex with nsc 111848','2.02','0.427513493045733','0.427513493045733'),
('JAK2_HUMAN','3tjc_A','A','co-crystal structure of jak2 with thienopyridine 8','2.4','0.28228224702381','0.28228224702381'),
('JAK2_HUMAN','3tjc_B','B','co-crystal structure of jak2 with thienopyridine 8','2.4','0.28228224702381','0.28228224702381'),
('JAK2_HUMAN','3tjd_A','A','co-crystal structure of jak2 with thienopyridine 19','2.9','0.179038627873563','0.179038627873563'),
('JAK2_HUMAN','3tjd_B','B','co-crystal structure of jak2 with thienopyridine 19','2.9','0.179038627873563','0.179038627873563'),
('CHK1_HUMAN','3tkh_A','A','crystal structure of chk1 in complex with inhibitor s01','1.79','0.501943072043762','0.501943072043762'),
('CHK1_HUMAN','3tki_A','A','crystal structure of chk1 in complex with inhibitor s25','1.6','0.580864761904762','0.580864761904762'),
('MRCKB_HUMAN','3tku_A','A','mrck beta in complex with fasudil','2.15','0.363953496331672','0.363953496331672'),
('MRCKB_HUMAN','3tku_B','B','mrck beta in complex with fasudil','2.15','0.363953496331672','0.363953496331672'),
('CDK9_HUMAN','3tn8_A','A','cdk9/cyclin t in complex with can508','2.95','0.27957306572841','0.27957306572841'),
('CDK9_HUMAN','3tnh_A','A','cdk9/cyclin t in complex with can508','3.2','0.259096919642857','0.259096919642857'),
('CDK9_HUMAN','3tni_A','A','structure of cdk9/cyclin t f241l','3.23','0.268374591672195','0.268374591672195'),
('CDK2_HUMAN','3tnw_A','A','structure of cdk2/cyclin a in complex with can508','2','0.460955','0.460955'),
('CDK2_HUMAN','3tnw_C','C','structure of cdk2/cyclin a in complex with can508','2','0.460955','0.460955'),
('FGFR1_HUMAN','3tt0_A','A','co-structure of fibroblast growth factor receptor 1 kinase d 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-pipe yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (bgj398)','2.8','0.279337901785714','0.279337901785714'),
('FGFR1_HUMAN','3tt0_B','B','co-structure of fibroblast growth factor receptor 1 kinase d 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-pipe yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (bgj398)','2.8','0.279337901785714','0.279337901785714'),
('MK10_HUMAN','3tti_A','A','crystal structure of jnk3 complexed with cc-930, an orally a anti-fibrotic jnk inhibitor','2.2','0.322092180735931','0.322092180735931'),
('MK10_HUMAN','3ttj_A','A','crystal structure of jnk3 complexed with cc-359, a jnk inhib the prevention of ischemia-reperfusion injury','2.1','0.383703645833333','0.383703645833333'),
('KSYK_HUMAN','3tub_A','A','crystal structure of syk kinase domain with 1-(5-(6,7- dimethoxyquinolin-4-yloxy)pyridin-2-yl)-3-((1r,2s)-2- phenylcyclopropyl)urea','2.23','0.397310448630686','0.397310448630686'),
('KSYK_HUMAN','3tuc_A','A','crystal structure of syk kinase domain with 1-benzyl-n-(5-(6 dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-1,2-dihydropy carboxamide','2.1','0.389226473214286','0.389226473214286'),
('KSYK_HUMAN','3tud_A','A','crystal structure of syk kinase domain with n-(4-methyl-3-(8 oxo-2-(phenylamino)-7,8-dihydropyrido[2,3-d]pyrimidin-6-yl) (trifluoromethyl)benzamide','2.33','0.356875471975271','0.356875471975271'),
('BRAF_HUMAN','3tv4_A','A','human b-raf kinase domain in complex with an bromopyridine b inhibitor','3.4','0.136612929796919','0.136612929796919'),
('BRAF_HUMAN','3tv4_B','B','human b-raf kinase domain in complex with an bromopyridine b inhibitor','3.4','0.136612929796919','0.136612929796919'),
('BRAF_HUMAN','3tv6_A','A','human b-raf kinase domain in complex with a methoxypyrazolop benzamide inhibitor','3.3','0.147188874458875','0.147188874458875'),
('BRAF_HUMAN','3tv6_B','B','human b-raf kinase domain in complex with a methoxypyrazolop benzamide inhibitor','3.3','0.147188874458875','0.147188874458875'),
('ROCK1_HUMAN','3tv7_A','A','human rho-associated protein kinase 1 (rock 1) in complex wi','2.75','0.266845009469697','0.266845009469697'),
('ROCK1_HUMAN','3tv7_B','B','human rho-associated protein kinase 1 (rock 1) in complex wi','2.75','0.266845009469697','0.266845009469697'),
('ROCK1_HUMAN','3tv7_C','C','human rho-associated protein kinase 1 (rock 1) in complex wi','2.75','0.266845009469697','0.266845009469697'),
('ROCK1_HUMAN','3tv7_D','D','human rho-associated protein kinase 1 (rock 1) in complex wi','2.75','0.266845009469697','0.266845009469697'),
('ROCK1_HUMAN','3twj_A','A','rho-associated protein kinase 1 (rock 1) in complex with rki','2.9','0.191830383825944','0.191830383825944'),
('ROCK1_HUMAN','3twj_B','B','rho-associated protein kinase 1 (rock 1) in complex with rki','2.9','0.191830383825944','0.191830383825944'),
('ROCK1_HUMAN','3twj_C','C','rho-associated protein kinase 1 (rock 1) in complex with rki','2.9','0.191830383825944','0.191830383825944'),
('ROCK1_HUMAN','3twj_D','D','rho-associated protein kinase 1 (rock 1) in complex with rki','2.9','0.191830383825944','0.191830383825944'),
('KPCL_HUMAN','3txo_A','A','pkc eta kinase in complex with a naphthyridine','2.05','0.410037080429733','0.410037080429733'),
('TGFR1_HUMAN','3tzm_A','A','tgf-beta receptor type 1 in complex with sb431542','1.7','0.551135889355742','0.551135889355742'),
('ERBB4_HUMAN','3u2p_A','A','crystal structure of n-terminal three extracellular domains erbb4/her4','2.57','0.309807796460997','0.309807796460997'),
('FAK2_HUMAN','3u3c_A','A','structural basis for the interaction of pyk2 pat domain with ld motifs','3.7','0.131969436936937','0.131969436936937'),
('FAK2_HUMAN','3u3f_A','A','structural basis for the interaction of pyk2 pat domain with ld motifs','3.1','0.219832788018433','0.219832788018433'),
('FAK2_HUMAN','3u3f_B','B','structural basis for the interaction of pyk2 pat domain with ld motifs','3.1','0.219832788018433','0.219832788018433'),
('FAK2_HUMAN','3u3f_C','C','structural basis for the interaction of pyk2 pat domain with ld motifs','3.1','0.219832788018433','0.219832788018433'),
('FAK2_HUMAN','3u3f_D','D','structural basis for the interaction of pyk2 pat domain with ld motifs','3.1','0.219832788018433','0.219832788018433'),
('CSK21_HUMAN','3u4u_A','A','casein kinase 2 in complex with az-inhibitor','2.2','0.370873624188312','0.370873624188312'),
('MET_HUMAN','3u6h_A','A','crystal structure of c-met in complex with pyrazolone inhibi','2','0.4255771875','0.4255771875'),
('MET_HUMAN','3u6i_A','A','crystal structure of c-met in complex with pyrazolone inhibi','2.1','0.415391845238095','0.415391845238095'),
('VGFR2_HUMAN','3u6j_A','A','crystal structure of the vegfr2 kinase domain in complex wit pyrazolone inhibitor','2.15','0.418075415974529','0.418075415974529'),
('ERBB4_HUMAN','3u7u_A','A','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('ERBB4_HUMAN','3u7u_B','B','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('ERBB4_HUMAN','3u7u_C','C','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('ERBB4_HUMAN','3u7u_D','D','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('ERBB4_HUMAN','3u7u_E','E','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('ERBB4_HUMAN','3u7u_F','F','crystal structure of extracellular region of human epidermal factor receptor 4 in complex with neuregulin-1 beta','3.03','0.253624283062235','0.253624283062235'),
('MK14_HUMAN','3u8w_A','A','crystal structure of p38a mitogen-activated protein kinase i with a triazolopyridazinone inhibitor','2.15','0.359371844545958','0.359371844545958'),
('CSK21_HUMAN','3u9c_A','A','structure of a c-terminal deletion mutant of human protein k catalytic subunit with the atp-competitive inhibitor resoru','3.2','0.261337693452381','0.261337693452381'),
('CSK21_HUMAN','3u9c_B','B','structure of a c-terminal deletion mutant of human protein k catalytic subunit with the atp-competitive inhibitor resoru','3.2','0.261337693452381','0.261337693452381'),
('CHK1_HUMAN','3u9n_A','A','x-ray crystal structure of compound 1 bound to human chk1 ki domain','1.85','0.464724439350064','0.464724439350064'),
('ERBB4_HUMAN','3u9u_E','E','crystal structure of extracellular domain of human erbb4/her complex with the fab fragment of mab1479','3.42','0.147090220342523','0.147090220342523'),
('ERBB4_HUMAN','3u9u_F','F','crystal structure of extracellular domain of human erbb4/her complex with the fab fragment of mab1479','3.42','0.147090220342523','0.147090220342523'),
('FYN_HUMAN','3ua6_A','A','crystal structure of the human fyn sh3 domain','1.85','0.494467579231017','0.494467579231017'),
('FYN_HUMAN','3ua6_B','B','crystal structure of the human fyn sh3 domain','1.85','0.494467579231017','0.494467579231017'),
('FYN_HUMAN','3ua7_A','A','crystal structure of the human fyn sh3 domain in complex wit peptide from the hepatitis c virus ns5a-protein','1.5','0.62887','0.62887'),
('FYN_HUMAN','3ua7_B','B','crystal structure of the human fyn sh3 domain in complex wit peptide from the hepatitis c virus ns5a-protein','1.5','0.62887','0.62887'),
('FYN_HUMAN','3ua7_C','C','crystal structure of the human fyn sh3 domain in complex wit peptide from the hepatitis c virus ns5a-protein','1.5','0.62887','0.62887'),
('FYN_HUMAN','3ua7_D','D','crystal structure of the human fyn sh3 domain in complex wit peptide from the hepatitis c virus ns5a-protein','1.5','0.62887','0.62887'),
('ABL1_HUMAN','3ue4_A','A','structural and spectroscopic analysis of the kinase inhibito bosutinib binding to the abl tyrosine kinase domain','2.42','0.346052024424439','0.346052024424439'),
('ABL1_HUMAN','3ue4_B','B','structural and spectroscopic analysis of the kinase inhibito bosutinib binding to the abl tyrosine kinase domain','2.42','0.346052024424439','0.346052024424439'),
('EGFR_HUMAN','3ug1_A','A','crystal structure of the mutated egfr kinase domain (g719s/t the apo form','2.75','0.262308878517316','0.262308878517316'),
('EGFR_HUMAN','3ug2_A','A','crystal structure of the mutated egfr kinase domain (g719s/t complex with gefitinib','2.5','0.328579851190476','0.328579851190476'),
('JAK2_HUMAN','3ugc_A','A','structural basis of jak2 inhibition by the type ii inhibtor','1.34','0.721585903740227','0.721585903740227'),
('E2AK2_HUMAN','3uiu_A','A','crystal structure of apo-pkr kinase domain','2.9','0.143986336206897','0.143986336206897'),
('E2AK2_HUMAN','3uiu_B','B','crystal structure of apo-pkr kinase domain','2.9','0.143986336206897','0.143986336206897'),
('PIM1_HUMAN','3uix_A','A','crystal structure of pim1 kinase in complex with small molec inhibitor','2.2','0.433664293831169','0.433664293831169'),
('ABL2_HUMAN','3ulr_C','C','lysozyme contamination facilitates crystallization of a hete trimericcortactin:arg:lysozyme complex','1.65','0.56260444534632','0.56260444534632'),
('PIM1_HUMAN','3umw_A','A','crystal structure of pim1 kinase in complex with inhibitor ( indazol-3-yl)methylene]-6-methoxy-7-(piperazin-1-ylmethyl)b 3(2h)-one','2.08','0.453987281364469','0.453987281364469'),
('PIM1_HUMAN','3umx_A','A','crystal structure of pim1 kinase in complex with inhibitor ( indol-3-yl)methylene]-7-(azepan-1-ylmethyl)-6-hydroxybenzof 3(2h)-one','2.55','0.336822115721289','0.336822115721289'),
('CDK2_HUMAN','3unj_A','A','cdk2 in complex with inhibitor yl1-038-31','1.9','0.467214375783208','0.467214375783208'),
('CDK2_HUMAN','3unk_A','A','cdk2 in complex with inhibitor yl5-083','2.1','0.419242247023809','0.419242247023809'),
('AURKA_HUMAN','3unz_A','A','aurora a in complex with rpm1679','2.8','0.237246711309524','0.237246711309524'),
('AURKA_HUMAN','3unz_B','B','aurora a in complex with rpm1679','2.8','0.237246711309524','0.237246711309524'),
('AURKA_HUMAN','3uo4_A','A','aurora a in complex with rpm1680','2.45','0.308429783163265','0.308429783163265'),
('AURKA_HUMAN','3uo5_A','A','aurora a in complex with yl1-038-31','2.7','0.269211233465608','0.269211233465608'),
('AURKA_HUMAN','3uo6_A','A','aurora a in complex with yl5-083','2.8','0.236364508928571','0.236364508928571'),
('AURKA_HUMAN','3uo6_B','B','aurora a in complex with yl5-083','2.8','0.236364508928571','0.236364508928571'),
('AURKA_HUMAN','3uod_A','A','aurora a in complex with rpm1693','2.5','0.315233735119048','0.315233735119048'),
('AURKA_HUMAN','3uoh_A','A','aurora a in complex with rpm1722','2.8','0.236912366071429','0.236912366071429'),
('AURKA_HUMAN','3uoh_B','B','aurora a in complex with rpm1722','2.8','0.236912366071429','0.236912366071429'),
('AURKA_HUMAN','3uoj_A','A','aurora a in complex with rpm1715','2.9','0.227757556444992','0.227757556444992'),
('AURKA_HUMAN','3uoj_B','B','aurora a in complex with rpm1715','2.9','0.227757556444992','0.227757556444992'),
('AURKA_HUMAN','3uok_A','A','aurora a in complex with yl5-81-1','2.95','0.213766979418886','0.213766979418886'),
('AURKA_HUMAN','3uok_B','B','aurora a in complex with yl5-81-1','2.95','0.213766979418886','0.213766979418886'),
('AURKA_HUMAN','3uol_A','A','aurora a in complex with so2-162','2.4','0.274959732142857','0.274959732142857'),
('AURKA_HUMAN','3uol_B','B','aurora a in complex with so2-162','2.4','0.274959732142857','0.274959732142857'),
('AURKA_HUMAN','3up2_A','A','aurora a in complex with rpm1686','2.3','0.3492750938147','0.3492750938147'),
('AURKA_HUMAN','3up7_A','A','aurora a in complex with yl1-038-09','3.05','0.210689536982826','0.210689536982826'),
('MATK_HUMAN','3us4_A','A','crystal structure of a sh2 domain of a megakaryocyte-associa tyrosine kinase (matk) from homo sapiens at 1.50 a resoluti','1.5','0.620806145833333','0.620806145833333'),
('MK14_HUMAN','3uvp_A','A','human p38 map kinase in complex with km048','2.4','0.314699315476191','0.314699315476191'),
('MK14_HUMAN','3uvq_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','3uvr_A','A',NULL,NULL,NULL,NULL),
('ABL1_HUMAN','3uyo_A','A','crystal structure of monobody sh13/abl1 sh2 domain complex','1.83','0.501111718384075','0.501111718384075'),
('KC1D_HUMAN','3uys_A','A','crystal structure of apo human ck1d','2.3','0.318406016433747','0.318406016433747'),
('KC1D_HUMAN','3uys_B','B','crystal structure of apo human ck1d','2.3','0.318406016433747','0.318406016433747'),
('KC1D_HUMAN','3uys_C','C','crystal structure of apo human ck1d','2.3','0.318406016433747','0.318406016433747'),
('KC1D_HUMAN','3uys_D','D','crystal structure of apo human ck1d','2.3','0.318406016433747','0.318406016433747'),
('KC1D_HUMAN','3uyt_A','A','crystal structure of ck1d with pf670462 from p1 crystal form','2','0.379149419642857','0.379149419642857'),
('KC1D_HUMAN','3uyt_B','B','crystal structure of ck1d with pf670462 from p1 crystal form','2','0.379149419642857','0.379149419642857'),
('KC1D_HUMAN','3uyt_C','C','crystal structure of ck1d with pf670462 from p1 crystal form','2','0.379149419642857','0.379149419642857'),
('KC1D_HUMAN','3uyt_D','D','crystal structure of ck1d with pf670462 from p1 crystal form','2','0.379149419642857','0.379149419642857'),
('KC1D_HUMAN','3uzp_A','A','crystal structure of ck1d with pf670462 from p21 crystal for','1.94','0.420687563359107','0.420687563359107'),
('KC1D_HUMAN','3uzp_B','B','crystal structure of ck1d with pf670462 from p21 crystal for','1.94','0.420687563359107','0.420687563359107'),
('MP2K1_HUMAN','3v01_A','A','discovery of novel allosteric mek inhibitors possessing clas non-classical bidentate ser212 interactions.','2.71','0.320934969798805','0.320934969798805'),
('MP2K1_HUMAN','3v04_A','A','discovery of novel allosteric mek inhibitors possessing clas non-classical bidentate ser212 interactions.','2.7','0.302368941798942','0.302368941798942'),
('VGFR2_HUMAN','3v2a_R','R','vegfr-2/vegf-a complex structure','3.2','0.163497648809524','0.163497648809524'),
('MK08_HUMAN','3v3v_A','A',NULL,NULL,NULL,NULL),
('ITK_HUMAN','3v5j_A','A','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 090','2.59','0.264712767052767','0.264712767052767'),
('ITK_HUMAN','3v5j_B','B','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 090','2.59','0.264712767052767','0.264712767052767'),
('ITK_HUMAN','3v5l_A','A','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 542','1.86','0.452966090149769','0.452966090149769'),
('ITK_HUMAN','3v5l_B','B','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 542','1.86','0.452966090149769','0.452966090149769'),
('ITK_HUMAN','3v5l_C','C','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 542','1.86','0.452966090149769','0.452966090149769'),
('ITK_HUMAN','3v5l_D','D','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 542','1.86','0.452966090149769','0.452966090149769'),
('NTRK3_HUMAN','3v5q_A','A','discovery of a selective trk inhibitor with efficacy in rode tumor models','2.2','0.360798713474026','0.360798713474026'),
('NTRK3_HUMAN','3v5q_B','B','discovery of a selective trk inhibitor with efficacy in rode tumor models','2.2','0.360798713474026','0.360798713474026'),
('ARBK1_HUMAN','3v5w_A','A','human g protein-coupled receptor kinase 2 in complex with so gbetagamma subunits and paroxetine','2.07','0.413408037439614','0.413408037439614'),
('VGFR2_HUMAN','3v6b_R','R','vegfr-2/vegf-e complex structure','3.21','0.178168667250779','0.178168667250779'),
('MK10_HUMAN','3v6r_A','A','discovery of potent and selective covalent inhibitors of jnk','2.6','0.295662899496337','0.295662899496337'),
('MK10_HUMAN','3v6r_B','B','discovery of potent and selective covalent inhibitors of jnk','2.6','0.295662899496337','0.295662899496337'),
('MK10_HUMAN','3v6s_A','A','discovery of potent and selective covalent inhibitors of jnk','2.97','0.23854710753367','0.23854710753367'),
('MK10_HUMAN','3v6s_B','B','discovery of potent and selective covalent inhibitors of jnk','2.97','0.23854710753367','0.23854710753367'),
('ROCK1_HUMAN','3v8s_A','A','human rho-associated protein kinase 1 (rock 1) in complex wi indazole derivative (compound 18)','2.29','0.374756564969328','0.374756564969328'),
('ROCK1_HUMAN','3v8s_B','B','human rho-associated protein kinase 1 (rock 1) in complex wi indazole derivative (compound 18)','2.29','0.374756564969328','0.374756564969328'),
('ROCK1_HUMAN','3v8s_C','C','human rho-associated protein kinase 1 (rock 1) in complex wi indazole derivative (compound 18)','2.29','0.374756564969328','0.374756564969328'),
('ROCK1_HUMAN','3v8s_D','D','human rho-associated protein kinase 1 (rock 1) in complex wi indazole derivative (compound 18)','2.29','0.374756564969328','0.374756564969328'),
('ITK_HUMAN','3v8t_A','A','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 477','2','0.424240357142857','0.424240357142857'),
('ITK_HUMAN','3v8t_B','B','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 477','2','0.424240357142857','0.424240357142857'),
('ITK_HUMAN','3v8w_A','A','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 469','2.27','0.313926982575519','0.313926982575519'),
('ITK_HUMAN','3v8w_B','B','crystal structure of interleukin-2 inducible t-cell kinase i catalytic domain with thienopyrazolylindole inhibitor 469','2.27','0.313926982575519','0.313926982575519'),
('CHK2_HUMAN','3va4_C','C','crystal structure of the mammalian mdc1 fha domain complexed pthr68 peptide','1.54','0.612234191017316','0.612234191017316'),
('AURKA_HUMAN','3vap_A','A','synthesis and sar studies of imidazo-[1,2-a]-pyrazine aurora inhibitors with improved off target kinase selectivity','2.66','0.291960593671679','0.291960593671679'),
('PIM1_HUMAN','3vbq_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','1.85','0.511352981016731','0.511352981016731'),
('PIM1_HUMAN','3vbt_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.23','0.365771490297352','0.365771490297352'),
('PIM1_HUMAN','3vbv_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.08','0.399861939102564','0.399861939102564'),
('PIM1_HUMAN','3vbw_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.48','0.296440330261137','0.296440330261137'),
('PIM1_HUMAN','3vbx_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.03','0.417660301724138','0.417660301724138'),
('PIM1_HUMAN','3vby_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.27','0.3563512385279','0.3563512385279'),
('PIM1_HUMAN','3vc4_A','A','exploitation of hydrogen bonding constraints and flat hydrop energy landscapes in pim-1 kinase needle screening and inhi design','2.23','0.311517398035447','0.311517398035447'),
('KSYK_HUMAN','3vf8_A','A','crystal structure of spleen tyrosine kinase syk catalytic do pyrazolylbenzimidazole inhibitor 416','2.08','0.393179439102564','0.393179439102564'),
('KSYK_HUMAN','3vf9_A','A','crystal structure of spleen tyrosine kinase syk catalytic do thienopyrazolylindole inhibitor 027','2.3','0.305801626552795','0.305801626552795'),
('VGFR2_HUMAN','3vhe_A','A','crystal structure of human vegfr2 kinase domain with a novel pyrrolopyrimidine inhibitor.','1.55','0.609226945084485','0.609226945084485'),
('VGFR2_HUMAN','3vhk_A','A','crystal structure of the vegfr2 kinase domain in complex wit pocket binder','2.49','0.320635026893287','0.320635026893287'),
('VGFR2_HUMAN','3vid_A','A','crystal structure of human vegfr2 kinase domain with compoun','2.3','0.332693575957557','0.332693575957557'),
('EGFR_HUMAN','3vjn_A','A','crystal structure of the mutated egfr kinase domain (g719s/t complex with amppnp.','2.34','0.357414519612332','0.357414519612332'),
('EGFR_HUMAN','3vjo_A','A','crystal structure of the wild-type egfr kinase domain in com amppnp.','2.64','0.304626628787879','0.304626628787879'),
('MP2K6_HUMAN','3vn9_A','A','rifined crystal structure of non-phosphorylated map2k6 in a auto-inhibition state','2.6','0.201151947115385','0.201151947115385'),
('VGFR2_HUMAN','3vnt_A','A','crystal structure of the kinase domain of human vegfr2 with 3]thiazolo[5,4-b]pyridine derivative','1.64','0.60868987732288','0.60868987732288'),
('KAPCA_HUMAN','3vqh_A','A','bromine sad partially resolves multiple binding modes for pk inhibitor h-89','1.95','0.471444084249084','0.471444084249084'),
('TTK_HUMAN','3vqu_A','A','crystal structure of human mps1 catalytic domain in complex [(4-amino-5-cyano-6-ethoxypyridin-2- yl)amino]benzamide','2.4','0.284444985119048','0.284444985119048'),
('A1L4K2_HUMAN','3vud_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vug_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vuh_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vui_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vuk_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vul_A','A',NULL,NULL,NULL,NULL),
('A1L4K2_HUMAN','3vum_A','A',NULL,NULL,NULL,NULL),
('MP2K4_HUMAN','3vut_A','A','crystal structures of non-phosphorylated map2k4','3.5','-0.0324996428571429','-0.0324996428571429'),
('MP2K4_HUMAN','3vut_B','B','crystal structures of non-phosphorylated map2k4','3.5','-0.0324996428571429','-0.0324996428571429'),
('M3K5_HUMAN','3vw6_A','A','crystal structure of human apoptosis signal-regulating kinas with imidazopyridine inhibitor','2.4','0.332771026785714','0.332771026785714'),
('M3K5_HUMAN','3vw6_B','B','crystal structure of human apoptosis signal-regulating kinas with imidazopyridine inhibitor','2.4','0.332771026785714','0.332771026785714'),
('INSR_HUMAN','3w11_E','E',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w11_F','F',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w12_E','E',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w12_F','F',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w13_E','E',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w13_F','F',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w14_E','E',NULL,NULL,NULL,NULL),
('INSR_HUMAN','3w14_F','F',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','3w2o_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','3w2p_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','3w2q_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','3w2r_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','3w2s_A','A',NULL,NULL,NULL,NULL),
('MK01_HUMAN','3w55_A','A',NULL,NULL,NULL,NULL),
('GSK3B_HUMAN','3zdi_A','A',NULL,NULL,NULL,NULL),
('MELK_HUMAN','3zgw_A','A',NULL,NULL,NULL,NULL),
('KPCI_HUMAN','3zh8_A','A',NULL,NULL,NULL,NULL),
('KPCI_HUMAN','3zh8_B','B',NULL,NULL,NULL,NULL),
('KPCI_HUMAN','3zh8_C','C',NULL,NULL,NULL,NULL),
('STK24_HUMAN','3zhp_C','C',NULL,NULL,NULL,NULL),
('STK24_HUMAN','3zhp_D','D',NULL,NULL,NULL,NULL),
('GSK3B_HUMAN','3zrk_A','A','identification of 2-(4-pyridyl)thienopyridinones as gsk-3bet inhibitors','2.37','0.347518651484328','0.347518651484328'),
('GSK3B_HUMAN','3zrk_B','B','identification of 2-(4-pyridyl)thienopyridinones as gsk-3bet inhibitors','2.37','0.347518651484328','0.347518651484328'),
('GSK3B_HUMAN','3zrl_A','A','identification of 2-(4-pyridyl)thienopyridinones as gsk-3bet inhibitors','2.48','0.339834586213518','0.339834586213518'),
('GSK3B_HUMAN','3zrl_B','B','identification of 2-(4-pyridyl)thienopyridinones as gsk-3bet inhibitors','2.48','0.339834586213518','0.339834586213518'),
('GSK3B_HUMAN','3zrm_A','A','identification of 2-(4-pyridyl)thienopyridinones as gsk- 3beta inhibitors','2.49','0.336348360226621','0.336348360226621'),
('GSK3B_HUMAN','3zrm_B','B','identification of 2-(4-pyridyl)thienopyridinones as gsk- 3beta inhibitors','2.49','0.336348360226621','0.336348360226621'),
('MK14_HUMAN','3zs5_A','A','structural basis for kinase selectivity of three clinical p38alpha inhibitors','1.6','0.592042589285714','0.592042589285714'),
('MK14_HUMAN','3zsg_A','A','x-ray structure of p38alpha bound to tak-715','1.89','0.48927322255291','0.48927322255291'),
('MK14_HUMAN','3zsh_A','A','x-ray structure of p38alpha bound to scio-469','2.05','0.4098556220964','0.4098556220964'),
('MK14_HUMAN','3zsi_A','A','x-ray structure of p38alpha bound to vx-745','2.4','0.31256724702381','0.31256724702381'),
('DAPK1_HUMAN','3zxt_A','A','dimeric structure of dapk-1 catalytic domain in complex with amppcp-mg','2.65','0.272541794137466','0.272541794137466'),
('DAPK1_HUMAN','3zxt_B','B','dimeric structure of dapk-1 catalytic domain in complex with amppcp-mg','2.65','0.272541794137466','0.272541794137466'),
('DAPK1_HUMAN','3zxt_C','C','dimeric structure of dapk-1 catalytic domain in complex with amppcp-mg','2.65','0.272541794137466','0.272541794137466'),
('DAPK1_HUMAN','3zxt_D','D','dimeric structure of dapk-1 catalytic domain in complex with amppcp-mg','2.65','0.272541794137466','0.272541794137466'),
('MET_HUMAN','3zxz_A','A','x-ray structure of pf-04217903 bound to the kinase domain of','1.8','0.523312385912698','0.523312385912698'),
('MK14_HUMAN','3zya_A','A','human p38 map kinase in complex with 2-amino-phenylamino- dibenzosuberone','1.9','0.50180788768797','0.50180788768797'),
('MET_HUMAN','3zze_A','A','crystal structure of c-met kinase domain in complex with n\'- ((3z)-4-chloro-7-methyl-2-oxo-1,2-dihydro-3h-indol-3- ylidene)-2-(4-hydroxyphenyl)propanohydrazide','1.87','0.494102676741151','0.494102676741151'),
('ROR2_HUMAN','3zzw_A','A','crystal structure of the kinase domain of ror2','2.9','0.273237987992611','0.273237987992611'),
('ROR2_HUMAN','3zzw_B','B','crystal structure of the kinase domain of ror2','2.9','0.273237987992611','0.273237987992611'),
('PDPK1_HUMAN','4a06_A','A','human pdk1 kinase domain in complex with allosteric activato bound to the pif-pocket','2','0.488165848214286','0.488165848214286'),
('PDPK1_HUMAN','4a07_A','A','human pdk1 kinase domain in complex with allosteric activato bound to the pif-pocket','1.85','0.37964054054054','0.37964054054054'),
('BUB1_HUMAN','4a1g_A','A','the crystal structure of the human bub1 tpr domain in comple the ki motif of knl1','2.6','0.305558539377289','0.305558539377289'),
('BUB1_HUMAN','4a1g_B','B','the crystal structure of the human bub1 tpr domain in comple the ki motif of knl1','2.6','0.305558539377289','0.305558539377289'),
('BUB1_HUMAN','4a1g_C','C','the crystal structure of the human bub1 tpr domain in comple the ki motif of knl1','2.6','0.305558539377289','0.305558539377289'),
('BUB1_HUMAN','4a1g_D','D','the crystal structure of the human bub1 tpr domain in comple the ki motif of knl1','2.6','0.305558539377289','0.305558539377289'),
('ZAP70_HUMAN','4a4b_B','B','structure of modified phosphotyr371-c-cbl-ubch5b-zap-70 comp','2.79','0.285683296210958','0.285683296210958'),
('ZAP70_HUMAN','4a4c_B','B','structure of phosphotyr371-c-cbl-ubch5b-zap-70 complex','2.7','0.279537602513227','0.279537602513227'),
('PLK1_HUMAN','4a4l_A','A','crystal structure of polo-like kinase 1 in complex with a 5-(2-amino-pyrimidin-4-yl)-1h-pyrrole inhibitor','2.35','0.323481304774569','0.323481304774569'),
('PLK1_HUMAN','4a4o_A','A','crystal structure of polo-like kinase 1 in complex with a 2- (2-amino-pyrimidin-4-yl)-1,5,6,7-tetrahydro-pyrrolopyridin- 4-one inhibitor','2.7','0.253919269179894','0.253919269179894'),
('NEK2_HUMAN','4a4x_A','A','nek2-ede bound to cct248662','2.4','0.328840178571429','0.328840178571429'),
('PIM1_HUMAN','4a7c_A','A','crystal structure of pim1 kinase with etp46546','2.3','0.410554439052795','0.410554439052795'),
('CHK2_HUMAN','4a9r_A','A','crystal structure of human chk2 in complex with benzimidazol carboxamide inhibitor','2.85','0.290499246553885','0.290499246553885'),
('CHK2_HUMAN','4a9s_A','A','crystal structure of human chk2 in complex with benzimidazole carboxamide inhibitor','2.66','0.317211025219298','0.317211025219298'),
('CHK2_HUMAN','4a9t_A','A','crystal structure of human chk2 in complex with benzimidazole carboxamide inhibitor','2.7','0.329207409060847','0.329207409060847'),
('CHK2_HUMAN','4a9u_A','A','crystal structure of human chk2 in complex with benzimidazole carboxamide inhibitor','2.48','0.369876624903994','0.369876624903994'),
('MK14_HUMAN','4a9y_A','A','p38alpha map kinase bound to cmpd 8','2.2','0.355242508116883','0.355242508116883'),
('MK14_HUMAN','4aa0_A','A','p38alpha map kinase bound to cmpd 2','1.8','0.470797743055555','0.470797743055555'),
('MK14_HUMAN','4aa4_A','A','p38alpha map kinase bound to cmpd 22','2.3','0.340605614648033','0.340605614648033'),
('MK14_HUMAN','4aa5_A','A','p38alpha map kinase bound to cmpd 33','2.38','0.342655864845938','0.342655864845938'),
('CDKL2_HUMAN','4aaa_A','A','crystal structure of the human cdkl2 kinase domain','1.53','0.47181477124183','0.47181477124183'),
('MK14_HUMAN','4aac_A','A','p38alpha map kinase bound to cmpd 29','2.5','0.282121324404762','0.282121324404762'),
('GSK3B_HUMAN','4acc_A','A','gsk3b in complex with inhibitor','2.21','0.387363211592329','0.387363211592329'),
('GSK3B_HUMAN','4acc_B','B','gsk3b in complex with inhibitor','2.21','0.387363211592329','0.387363211592329'),
('GSK3B_HUMAN','4acd_A','A','gsk3b in complex with inhibitor','2.6','0.325828122710623','0.325828122710623'),
('GSK3B_HUMAN','4acd_B','B','gsk3b in complex with inhibitor','2.6','0.325828122710623','0.325828122710623'),
('GSK3B_HUMAN','4acg_A','A','gsk3b in complex with inhibitor','2.6','0.331165697115385','0.331165697115385'),
('GSK3B_HUMAN','4acg_B','B','gsk3b in complex with inhibitor','2.6','0.331165697115385','0.331165697115385'),
('GSK3B_HUMAN','4ach_A','A','gsk3b in complex with inhibitor','2.6','0.276804506639194','0.276804506639194'),
('GSK3B_HUMAN','4ach_B','B','gsk3b in complex with inhibitor','2.6','0.276804506639194','0.276804506639194'),
('CDK2_HUMAN','4acm_A','A','cdk2 in complex with 3-amino-6-(4-{[2-(dimethylamino)ethyl] sulfamoyl}-phenyl)-n-pyridin-3-ylpyrazine-2-carboxamide','1.63','0.55793132239629','0.55793132239629'),
('KAPCA_HUMAN','4ae6_A','A','structure and function of the human sperm-specific isoform o protein kinase a (pka) catalytic subunit calpha 2','2.1','0.378353154761905','0.378353154761905'),
('KAPCA_HUMAN','4ae6_B','B','structure and function of the human sperm-specific isoform o protein kinase a (pka) catalytic subunit calpha 2','2.1','0.378353154761905','0.378353154761905'),
('KAPCA_HUMAN','4ae9_A','A','structure and function of the human sperm-specific isoform of protein kinase a (pka) catalytic subunit c alpha 2','2.3','0.355024200957557','0.355024200957557'),
('KAPCA_HUMAN','4ae9_B','B','structure and function of the human sperm-specific isoform of protein kinase a (pka) catalytic subunit c alpha 2','2.3','0.355024200957557','0.355024200957557'),
('AURKB_HUMAN','4af3_A','A','human aurora b kinase in complex with incenp and vx-680','2.75','0.291478893398268','0.291478893398268'),
('NEK2_HUMAN','4afe_A','A','nek2 bound to hybrid compound 21','2.6','0.287552066163004','0.287552066163004'),
('GSK3B_HUMAN','4afj_A','A','5-aryl-4-carboxamide-1,3-oxazoles: potent and selective gsk- inhibitors','1.98','0.452332112193362','0.452332112193362'),
('GSK3B_HUMAN','4afj_B','B','5-aryl-4-carboxamide-1,3-oxazoles: potent and selective gsk- inhibitors','1.98','0.452332112193362','0.452332112193362'),
('DDR1_HUMAN','4ag4_A','A','crystal structure of a ddr1-fab complex','2.8','0.252779583333333','0.252779583333333'),
('VGFR2_HUMAN','4ag8_A','A','crystal structure of the vegfr2 kinase domain in complex with axitinib (ag-013736) (n-methyl-2-(3-((e)-2-pyridin-2- yl-vinyl)-1h-indazol-6-ylsulfanyl)-benzamide)','1.95','0.444410542582418','0.444410542582418'),
('VGFR2_HUMAN','4agc_A','A','crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with axitinib (ag-013736) (n-methyl-2-( 3-((e)-2-pyridin-2-yl-vinyl)-1h-indazol-6-ylsulfanyl)- benzamide)','2','0.442692113095238','0.442692113095238'),
('VGFR2_HUMAN','4agd_A','A','crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sunitinib (su11248) (n-2- diethylaminoethyl)-5-((z)-(5-fluoro-2-oxo-1h-indol-3- ylidene)methyl)-2,4-dimethyl-1h-pyrrole-3-carboxamide)','2.81','0.257757302787663','0.257757302787663'),
('CDKL1_HUMAN','4agu_A','A','crystal structure of the human cdkl1 kinase domain','2.4','0.352541904761905','0.352541904761905'),
('CDKL1_HUMAN','4agu_B','B','crystal structure of the human cdkl1 kinase domain','2.4','0.352541904761905','0.352541904761905'),
('CDKL1_HUMAN','4agu_C','C','crystal structure of the human cdkl1 kinase domain','2.4','0.352541904761905','0.352541904761905'),
('PIM1_HUMAN','4alu_A','A',NULL,NULL,NULL,NULL),
('PIM1_HUMAN','4alv_A','A',NULL,NULL,NULL,NULL),
('PIM1_HUMAN','4alw_A','A',NULL,NULL,NULL,NULL),
('MP2K1_HUMAN','4an2_A','A',NULL,NULL,NULL,NULL),
('MP2K1_HUMAN','4an3_A','A',NULL,NULL,NULL,NULL),
('MP2K1_HUMAN','4an9_A','A',NULL,NULL,NULL,NULL),
('MP2K1_HUMAN','4anb_A','A',NULL,NULL,NULL,NULL),
('MET_HUMAN','4aoi_A','A','crystal structure of c-met kinase domain in complex with 4-( pyrrolo(2,3-b)pyridin-3-yl)methyl)-(1,2,4)triazolo( 4,3-b)( triazin-6-yl)benzonitrile','1.9','0.505688646616541','0.505688646616541'),
('NTRK1_HUMAN','4aoj_A','A','human trka in complex with the inhibitor az-23','2.75','0.247675426136364','0.247675426136364'),
('NTRK1_HUMAN','4aoj_B','B','human trka in complex with the inhibitor az-23','2.75','0.247675426136364','0.247675426136364'),
('NTRK1_HUMAN','4aoj_C','C','human trka in complex with the inhibitor az-23','2.75','0.247675426136364','0.247675426136364'),
('STK10_HUMAN','4aot_A','A','crystal structure of human serine threonine kinase-10 (lok) bound to gw830263a','2.33','0.341486558284795','0.341486558284795'),
('STK10_HUMAN','4aot_B','B','crystal structure of human serine threonine kinase-10 (lok) bound to gw830263a','2.33','0.341486558284795','0.341486558284795'),
('MET_HUMAN','4ap7_A','A','crystal structure of c-met kinase domain in complex with 4-( fluorophenyl)-(1,2,4)triazolo(4,3-b)(1,2,4)triazin-3-yl)met phenol','1.8','0.516787728174603','0.516787728174603'),
('NEK1_HUMAN','4apc_A','A','crystal structure of human nima-related kinase 1 (nek1)','2.1','0.412503348214286','0.412503348214286'),
('NEK1_HUMAN','4apc_B','B','crystal structure of human nima-related kinase 1 (nek1)','2.1','0.412503348214286','0.412503348214286'),
('PAK4_HUMAN','4app_A','A','crystal structure of the human p21-activated kinase 4 in complex with (s)-n-(5-(3-benzyl-1-methylpiperazine-4- carbonyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo(3,4-c) pyrazol-3-yl)-3-phenoxybenzamide','2.2','0.414362656926407','0.414362656926407'),
('JAK2_HUMAN','4aqc_A','A','triazolopyridine-based inhibitor of janus kinase 2','1.9','0.476503304354637','0.476503304354637'),
('JAK2_HUMAN','4aqc_B','B','triazolopyridine-based inhibitor of janus kinase 2','1.9','0.476503304354637','0.476503304354637'),
('PIM1_HUMAN','4as0_A','A','cyclometalated phthalimides as protein kinase inhibitors','2.3','0.409740644409938','0.409740644409938'),
('VGFR2_HUMAN','4asd_A','A','crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with sorafenib (bay 43-9006)','2.03','0.441011328509852','0.441011328509852'),
('VGFR2_HUMAN','4ase_A','A','crystal structure of vegfr2 (juxtamembrane and kinase domains) in complex with tivozanib (av-951)','1.83','0.486261465407884','0.486261465407884'),
('AVR2A_HUMAN','4asx_A','A','crystal structure of activin receptor type-iia (acvr2a) kinase domain in complex with dihydro-bauerine c','2.05','0.444602645905923','0.444602645905923'),
('AVR2A_HUMAN','4asx_B','B','crystal structure of activin receptor type-iia (acvr2a) kinase domain in complex with dihydro-bauerine c','2.05','0.444602645905923','0.444602645905923'),
('NTRK2_HUMAN','4asz_A','A','crystal structure of apo trkb kinase domain','1.7','0.560504341736695','0.560504341736695'),
('NTRK2_HUMAN','4at3_A','A','crystal structure of trkb kinase domain in complex with cpd5','1.77','0.511978730579096','0.511978730579096'),
('NTRK2_HUMAN','4at4_A','A','crystal structure of trkb kinase domain in complex with ex42','2.36','0.387039810583132','0.387039810583132'),
('NTRK2_HUMAN','4at5_A','A','crystal structure of trkb kinase domain in complex with gw25','1.71','0.570894220446951','0.570894220446951'),
('CDK6_HUMAN','4aua_A','A',NULL,NULL,NULL,NULL),
('PDPK1_HUMAN','4aw0_A','A','human pdk1 kinase domain in complex with allosteric compound bound to the pif-pocket','1.43','0.679797708229271','0.679797708229271'),
('PDPK1_HUMAN','4aw1_A','A','human pdk1 kinase domain in complex with allosteric compound ps210 bound to the pif-pocket','1.68','0.581411086309524','0.581411086309524'),
('EPHB4_HUMAN','4aw5_A','A','complex of the ephb4 kinase domain with an oxindole inhibito','2.33','0.357444266618128','0.357444266618128'),
('DYR1A_HUMAN','4aze_A','A','human dyrk1a in complex with leucettine l41','3.15','0.218529841269841','0.218529841269841'),
('DYR1A_HUMAN','4aze_B','B','human dyrk1a in complex with leucettine l41','3.15','0.218529841269841','0.218529841269841'),
('DYR1A_HUMAN','4aze_C','C','human dyrk1a in complex with leucettine l41','3.15','0.218529841269841','0.218529841269841'),
('DYRK2_HUMAN','4azf_A','A','human dyrk2 in complex with leucettine l41','2.55','0.316961267507003','0.316961267507003'),
('GSK3B_HUMAN','4b7t_A','A',NULL,NULL,NULL,NULL),
('MK07_HUMAN','4b99_A','A','crystal structure of mapk7 (erk5) with inhibitor','2.8','0.271387946428572','0.271387946428572'),
('NEK1_HUMAN','4b9d_A','A','crystal structure of human nima-related kinase 1 (nek1) with inhibitor.','1.9','0.483002962092732','0.483002962092732'),
('NEK1_HUMAN','4b9d_B','B','crystal structure of human nima-related kinase 1 (nek1) with inhibitor.','1.9','0.483002962092732','0.483002962092732'),
('EPHB4_HUMAN','4bb4_A','A',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbe_A','A',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbe_B','B',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbe_C','C',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbe_D','D',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbf_A','A',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbf_B','B',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbf_C','C',NULL,NULL,NULL,NULL),
('JAK2_HUMAN','4bbf_D','D',NULL,NULL,NULL,NULL),
('CDKL2_HUMAN','4bbm_A','A','crystal structure of the human cdkl2 kinase domain with bound tcs 2312','2','0.403257455357143','0.403257455357143'),
('CDKL2_HUMAN','4bbm_B','B','crystal structure of the human cdkl2 kinase domain with bound tcs 2312','2','0.403257455357143','0.403257455357143'),
('STK10_HUMAN','4bc6_A','A','crystal structure of human serine threonine kinase-10 bound novel bosutinib isoform 1, previously thought to be bosutin','2.2','0.366206764069264','0.366206764069264'),
('CDK9_HUMAN','4bcf_A','A',NULL,NULL,NULL,NULL),
('CDK9_HUMAN','4bch_A','A',NULL,NULL,NULL,NULL),
('CDK9_HUMAN','4bci_A','A',NULL,NULL,NULL,NULL),
('CDK9_HUMAN','4bcj_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4bco_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4bco_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4bcq_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4bcq_C','C',NULL,NULL,NULL,NULL),
('FYN_HUMAN','4d8d_A','A',NULL,NULL,NULL,NULL),
('FYN_HUMAN','4d8d_C','C',NULL,NULL,NULL,NULL),
('LCK_HUMAN','4d8k_A','A','crystal structure of a sh3-sh2 domains of a lymphocyte-speci protein tyrosine kinase (lck) from homo sapiens at 2.36 a r','2.36','0.356909721297417','0.356909721297417'),
('KS6A3_HUMAN','4d9t_A','A','rsk2 c-terminal kinase domain with inhibitor (e)-methyl 3-(4 (3-hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl cyanoacrylate','2.4','0.316474494047619','0.316474494047619'),
('KS6A3_HUMAN','4d9u_A','A','rsk2 c-terminal kinase domain, (e)-tert-butyl 3-(4-amino-7-( hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl)-2 cyanoacrylate','2.4','0.328353154761905','0.328353154761905'),
('PAK1_HUMAN','4daw_A','A','crystal structure of pak1 kinase domain with the ruthenium p complex','2','0.427047544642857','0.427047544642857'),
('BRAF_HUMAN','4dbn_A','A','crystal structure of the kinase domain of human b-raf with a 3]thiazolo[5,4-b]pyridine derivative','3.15','0.237401150793651','0.237401150793651'),
('BRAF_HUMAN','4dbn_B','B','crystal structure of the kinase domain of human b-raf with a 3]thiazolo[5,4-b]pyridine derivative','3.15','0.237401150793651','0.237401150793651'),
('ALK_HUMAN','4dce_A','A','crystal structure of human anaplastic lymphoma kinase in com a piperidine-carboxamide inhibitor','2.03','0.42895406660509','0.42895406660509'),
('ALK_HUMAN','4dce_B','B','crystal structure of human anaplastic lymphoma kinase in com a piperidine-carboxamide inhibitor','2.03','0.42895406660509','0.42895406660509'),
('AURKA_HUMAN','4dea_A','A','aurora a in complex with yl1-038-18','2.45','0.333217580782313','0.333217580782313'),
('AURKA_HUMAN','4deb_A','A','aurora a in complex with rk2-17-01','3.05','0.225672706625683','0.225672706625683'),
('AURKA_HUMAN','4ded_A','A','aurora a in complex with yl1-038-21','3.05','0.209226694720921','0.209226694720921'),
('AURKA_HUMAN','4dee_A','A','aurora a in complex with adp','2.3','0.367912950957557','0.367912950957557'),
('MET_HUMAN','4deg_A','A','crystal structure of c-met in complex with triazolopyridazin inhibitor 2','2','0.440078303571429','0.440078303571429'),
('MET_HUMAN','4deh_A','A','crystal structure of c-met in complex with triazolopyridinon inhibitor 3','2','0.439056651785714','0.439056651785714'),
('MET_HUMAN','4dei_A','A','crystal structure of c-met in complex with triazolopyridinon inhibitor 24','2.05','0.411200994120209','0.411200994120209'),
('KSYK_HUMAN','4dfl_A','A','crystal structure of spleen tyrosine kinase complexed with a sulfonamidopyrazine piperidine inhibitor','1.98','0.458016338383838','0.458016338383838'),
('KSYK_HUMAN','4dfn_A','A','crystal structure of spleen tyrosine kinase complexed with a adamantylpyrazine inhibitor','2.48','0.332319630856375','0.332319630856375'),
('PLK1_HUMAN','4dfw_A','A','oxime-based post solid-phase peptide diversification: identi of high affinity polo-like kinase 1 (plk1) polo-box domain peptides','1.55','0.65665041234639','0.65665041234639'),
('CSK21_HUMAN','4dgl_C','C','crystal structure of the ck2 tetrameric holoenzyme','3','0.256956354166667','0.256956354166667'),
('CSK21_HUMAN','4dgl_D','D','crystal structure of the ck2 tetrameric holoenzyme','3','0.256956354166667','0.256956354166667'),
('AURKA_HUMAN','4dhf_A','A','structure of aurora a mutant bound to biogenidec cpd 15','2.8','0.240045238095238','0.240045238095238'),
('AURKA_HUMAN','4dhf_B','B','structure of aurora a mutant bound to biogenidec cpd 15','2.8','0.240045238095238','0.240045238095238'),
('GSK3B_HUMAN','4dit_A','A','crystal structure of gsk3beta in complex with a imidazopyrid inhibitor','2.6','0.259731366758242','0.259731366758242'),
('CSF1R_HUMAN','4dkd_C','C','crystal structure of human interleukin-34 bound to human csf','3','0.189342380952381','0.189342380952381'),
('MK14_HUMAN','4dli_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4dlj_A','A',NULL,NULL,NULL,NULL),
('M3K14_HUMAN','4dn5_A','A','crystal structure of nf-kb-inducing kinase (nik)','2.5','0.337669568452381','0.337669568452381'),
('M3K14_HUMAN','4dn5_B','B','crystal structure of nf-kb-inducing kinase (nik)','2.5','0.337669568452381','0.337669568452381'),
('KPCA_HUMAN','4dnl_A','A','crystal structure of a c2 domain of a protein kinase c alpha from homo sapiens at 1.90 a resolution','1.9','0.481686340068922','0.481686340068922'),
('PIM1_HUMAN','4dtk_A','A','novel and selective pan-pim kinase inhibitor','1.86','0.520123456221198','0.520123456221198'),
('FES_HUMAN','4dyl_A','A','f-bar domain of human fes tyrosine kinase','2.18','0.406187768949323','0.406187768949323'),
('ACVR1_HUMAN','4dym_A','A','crystal structure of the acvr1 kinase domain in complex with imidazo[1,2-b]pyridazine inhibitor k00135','2.42','0.308716458948249','0.308716458948249'),
('BRAF_HUMAN','4e26_A','A','braf in complex with an organic inhibitor 7898734','2.55','0.291454824054622','0.291454824054622'),
('BRAF_HUMAN','4e26_B','B','braf in complex with an organic inhibitor 7898734','2.55','0.291454824054622','0.291454824054622'),
('JAK1_HUMAN','4e4l_A','A','jak1 kinase (jh1 domain) in complex with compound 30','2','0.458344434523809','0.458344434523809'),
('JAK1_HUMAN','4e4l_B','B','jak1 kinase (jh1 domain) in complex with compound 30','2','0.458344434523809','0.458344434523809'),
('JAK1_HUMAN','4e4l_D','D','jak1 kinase (jh1 domain) in complex with compound 30','2','0.458344434523809','0.458344434523809'),
('JAK1_HUMAN','4e4l_E','E','jak1 kinase (jh1 domain) in complex with compound 30','2','0.458344434523809','0.458344434523809'),
('JAK2_HUMAN','4e4m_A','A','jak2 kinase (jh1 domain) in complex with compound 30','2.25','0.395386825396825','0.395386825396825'),
('JAK2_HUMAN','4e4m_B','B','jak2 kinase (jh1 domain) in complex with compound 30','2.25','0.395386825396825','0.395386825396825'),
('JAK2_HUMAN','4e4m_D','D','jak2 kinase (jh1 domain) in complex with compound 30','2.25','0.395386825396825','0.395386825396825'),
('JAK2_HUMAN','4e4m_E','E','jak2 kinase (jh1 domain) in complex with compound 30','2.25','0.395386825396825','0.395386825396825'),
('JAK1_HUMAN','4e4n_A','A','jak1 kinase (jh1 domain) in complex with compound 49','1.9','0.495610432330827','0.495610432330827'),
('JAK1_HUMAN','4e4n_B','B','jak1 kinase (jh1 domain) in complex with compound 49','1.9','0.495610432330827','0.495610432330827'),
('BRAF_HUMAN','4e4x_A','A','crystal structure of b-raf kinase domain in complex with a dihydropyrido[2,3-d]pyrimidinone-based inhibitor','3.6','0.0987004861111111','0.0987004861111111'),
('BRAF_HUMAN','4e4x_B','B','crystal structure of b-raf kinase domain in complex with a dihydropyrido[2,3-d]pyrimidinone-based inhibitor','3.6','0.0987004861111111','0.0987004861111111'),
('MK14_HUMAN','4e5a_X','X','the w197a mutant of p38a map kinase','1.87','0.450651218407818','0.450651218407818'),
('MK14_HUMAN','4e5b_A','A','structure of p38a map kinase without bog','2','0.405501622023809','0.405501622023809'),
('JAK1_HUMAN','4e5w_A','A','jak1 kinase (jh1 domain) in complex with compound 26','1.86','0.50260546514977','0.50260546514977'),
('JAK1_HUMAN','4e5w_B','B','jak1 kinase (jh1 domain) in complex with compound 26','1.86','0.50260546514977','0.50260546514977'),
('PLK1_HUMAN','4e67_A','A','the structure of the polo-box domain (pbd) of polo-like kina (plk1) in complex with hydrocinnamoyl-derivatized plhspta p','2.1','0.403777485119048','0.403777485119048'),
('MK14_HUMAN','4e6a_A','A','p38a-pia23 complex','2.09','0.379522411426293','0.379522411426293'),
('MK14_HUMAN','4e6c_A','A','p38a-perifosine complex','2.39','0.305612913864814','0.305612913864814'),
('JAK2_HUMAN','4e6d_A','A','jak2 kinase (jh1 domain) triple mutant in complex with compo','2.22','0.41613894747426','0.41613894747426'),
('JAK2_HUMAN','4e6d_B','B','jak2 kinase (jh1 domain) triple mutant in complex with compo','2.22','0.41613894747426','0.41613894747426'),
('JAK2_HUMAN','4e6q_A','A','jak2 kinase (jh1 domain) triple mutant in complex with compo','1.95','0.447591390796703','0.447591390796703'),
('JAK2_HUMAN','4e6q_B','B','jak2 kinase (jh1 domain) triple mutant in complex with compo','1.95','0.447591390796703','0.447591390796703'),
('MK14_HUMAN','4e8a_A','A','the crystal structure of p38a map kinase in complex with pia','2.7','0.258632736441799','0.258632736441799'),
('FES_HUMAN','4e93_A','A','crystal structure of human feline sarcoma viral oncogene hom fes)in complex with tae684','1.84','0.484995463250518','0.484995463250518'),
('PLK1_HUMAN','4e9c_A','A','the structure of the polo-box domain (pbd) of polo-like kina (plk1) in complex with ldpplhspta phosphopeptide','1.7','0.541768910189076','0.541768910189076'),
('PLK1_HUMAN','4e9d_A','A','the structure of the polo-box domain (pbd) of polo-like kina (plk1) in complex with 3-(1-benzothiophen-2-yl)propanoyl-de dpplhspta peptide','2.75','0.210050738636364','0.210050738636364'),
('FAK1_HUMAN','4ebv_A','A','structure of focal adhesion kinase catalytic domain in compl novel allosteric inhibitor','1.67','0.561008169019105','0.561008169019105'),
('FAK1_HUMAN','4ebw_A','A','structure of focal adhesion kinase catalytic domain in compl novel allosteric inhibitor','2.65','0.335299978661276','0.335299978661276'),
('CDK9_HUMAN','4ec8_A','A','structure of full length cdk9 in complex with cyclint and dr','3.6','0.202905783730159','0.202905783730159'),
('CDK9_HUMAN','4ec9_A','A','crystal structure of full-length cdk9 in complex with cyclin','3.21','0.250112952965065','0.250112952965065'),
('TBK1_HUMAN','4efo_A','A','crystal structure of the ubiquitin-like domain of human tbk1','1.77','0.55328256986481','0.55328256986481'),
('TBK1_HUMAN','4efo_B','B','crystal structure of the ubiquitin-like domain of human tbk1','1.77','0.55328256986481','0.55328256986481'),
('MK14_HUMAN','4eh2_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh3_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh4_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh5_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh6_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh7_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh8_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4eh9_A','A',NULL,NULL,NULL,NULL),
('MK14_HUMAN','4ehv_A','A',NULL,NULL,NULL,NULL),
('JAK1_HUMAN','4ehz_A','A','the jak1 kinase domain in complex with inhibitor','2.17','0.431856888920891','0.431856888920891'),
('JAK1_HUMAN','4ehz_B','B','the jak1 kinase domain in complex with inhibitor','2.17','0.431856888920891','0.431856888920891'),
('JAK1_HUMAN','4ehz_C','C','the jak1 kinase domain in complex with inhibitor','2.17','0.431856888920891','0.431856888920891'),
('JAK1_HUMAN','4ehz_D','D','the jak1 kinase domain in complex with inhibitor','2.17','0.431856888920891','0.431856888920891'),
('JAK1_HUMAN','4ei4_A','A','jak1 kinase (jh1 domain) in complex with compound 20','2.22','0.395939215331403','0.395939215331403'),
('JAK1_HUMAN','4ei4_B','B','jak1 kinase (jh1 domain) in complex with compound 20','2.22','0.395939215331403','0.395939215331403'),
('AKT1_HUMAN','4ejn_A','A','crystal structure of autoinhibited form of akt1 in complex w (5-(3-acetamidophenyl)-2-(2-aminopyridin-3-yl)-3h-imidazo[4 b]pyridin-3-yl)benzyl)-3-fluorobenzamide','2.19','0.340396793256686','0.340396793256686'),
('AKT1_HUMAN','4ekk_A','A','akt1 with amp-pnp','2.8','0.258170327380952','0.258170327380952'),
('AKT1_HUMAN','4ekk_B','B','akt1 with amp-pnp','2.8','0.258170327380952','0.258170327380952'),
('GSK3B_HUMAN','4ekk_C','C','akt1 with amp-pnp','2.8','0.258170327380952','0.258170327380952'),
('GSK3B_HUMAN','4ekk_D','D','akt1 with amp-pnp','2.8','0.258170327380952','0.258170327380952'),
('AKT1_HUMAN','4ekl_A','A','akt1 with gdc0068','2','0.470699508928571','0.470699508928571'),
('FAK2_HUMAN','4eku_A','A','crystal structure of ferm domain of proline-rich tyrosine ki','3.25','0.184799271978022','0.184799271978022'),
('PIM1_HUMAN','4enx_A','A','crystal structure of pim-1 kinase in complex with inhibitor (2-chlorophenylimino)-5-(4-hydroxy-3-nitrobenzylidene)thiaz one','2.8','0.314795297619048','0.314795297619048'),
('PIM1_HUMAN','4eny_A','A','crystal structure of pim-1 kinase in complex with (2e,5z)-2- chlorophenylimino)-5-(4-hydroxy-3-methoxybenzylidene)thiazo one','2.8','0.317971770833333','0.317971770833333'),
('CDK2_HUMAN','4eoi_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoi_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoj_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoj_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eok_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eok_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eol_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eol_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eom_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eom_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eon_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eon_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoo_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoo_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eop_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eop_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoq_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eoq_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eor_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eor_C','C',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eos_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4eos_C','C',NULL,NULL,NULL,NULL),
('STK10_HUMAN','4equ_A','A','human stk-10 (lok) kinase domain in dfg-out conformation wit inhibitor dsa-7','2','0.420813214285714','0.420813214285714'),
('STK10_HUMAN','4equ_B','B','human stk-10 (lok) kinase domain in dfg-out conformation wit inhibitor dsa-7','2','0.420813214285714','0.420813214285714'),
('CDK2_HUMAN','4erw_A','A','cdk2 in complex with staurosporine','2','0.428422261904762','0.428422261904762'),
('TBK1_HUMAN','4eut_A','A','structure of bx-795 complexed with unphosphorylated human tb uld domain','2.6','0.293501664377289','0.293501664377289'),
('TBK1_HUMAN','4eut_B','B','structure of bx-795 complexed with unphosphorylated human tb uld domain','2.6','0.293501664377289','0.293501664377289'),
('TBK1_HUMAN','4euu_A','A','structure of bx-795 complexed with human tbk1 kinase domain phosphorylated on ser172','1.8','0.537381493055556','0.537381493055556'),
('TBK1_HUMAN','4euu_B','B','structure of bx-795 complexed with human tbk1 kinase domain phosphorylated on ser172','1.8','0.537381493055556','0.537381493055556'),
('ACK1_HUMAN','4ewh_A','A','co-crystal structure of ack1 with inhibitor','2.5','0.237272098214286','0.237272098214286'),
('ACK1_HUMAN','4ewh_B','B','co-crystal structure of ack1 with inhibitor','2.5','0.237272098214286','0.237272098214286'),
('MK14_HUMAN','4ewq_A','A','human p38 alpha mapk in complex with a pyridazine based inhi','2.1','0.44481625','0.44481625'),
('MK13_HUMAN','4exu_A','A',NULL,NULL,NULL,NULL),
('MK13_HUMAN','4eyj_A','A',NULL,NULL,NULL,NULL),
('MK13_HUMAN','4eym_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4ez3_A','A','cdk2 in complex with nsc 134199','2','0.407903333333333','0.407903333333333'),
('CDK6_HUMAN','4ez5_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4ez7_A','A','cdk2 in complex with staurosporine and 2 molecules of 8-anil naphthalene sulfonic acid','2.49','0.298948821536145','0.298948821536145'),
('JAK2_HUMAN','4f08_A','A','discovery and optimization of c-2 methyl imidazo-pyrrolopyri potent and orally bioavailable jak1 inhibitors with selecti jak2','2.82','0.260285985625633','0.260285985625633'),
('JAK2_HUMAN','4f08_B','B','discovery and optimization of c-2 methyl imidazo-pyrrolopyri potent and orally bioavailable jak1 inhibitors with selecti jak2','2.82','0.260285985625633','0.260285985625633'),
('JAK2_HUMAN','4f09_A','A','discovery and optimization of c-2 methyl imidazo-pyrrolopyri potent and orally bioavailable jak1 inhibitors with selecti jak2','2.4','0.342832544642857','0.342832544642857'),
('NTRK1_HUMAN','4f0i_A','A','crystal structure of apo trka','2.3','0.378306537267081','0.378306537267081'),
('NTRK1_HUMAN','4f0i_B','B','crystal structure of apo trka','2.3','0.378306537267081','0.378306537267081'),
('KSYK_HUMAN','4f4p_A','A',NULL,NULL,NULL,NULL),
('SRC_HUMAN','4f59_A','A','triple mutant src sh2 domain','1.71','0.521712479375522','0.521712479375522'),
('SRC_HUMAN','4f5a_A','A','triple mutant src sh2 domain bound to phosphate ion','1.8','0.488931984126984','0.488931984126984'),
('SRC_HUMAN','4f5b_A','A','triple mutant src sh2 domain bound to phosphotyrosine','1.57','0.585145219802093','0.585145219802093'),
('FGFR1_HUMAN','4f63_A','A','crystal structure of human fibroblast growth factor receptor domain in complex with compound 1','2.55','0.288542026435574','0.288542026435574'),
('FGFR1_HUMAN','4f63_B','B','crystal structure of human fibroblast growth factor receptor domain in complex with compound 1','2.55','0.288542026435574','0.288542026435574'),
('FGFR1_HUMAN','4f64_A','A','crystal structure of human fibroblast growth factor receptor domain in complex with compound 6','2.05','0.422833241144019','0.422833241144019'),
('FGFR1_HUMAN','4f64_B','B','crystal structure of human fibroblast growth factor receptor domain in complex with compound 6','2.05','0.422833241144019','0.422833241144019'),
('FGFR1_HUMAN','4f65_A','A','crystal structure of human fibroblast growth factor receptor domain in complex with compound 8','2.26','0.389927652891909','0.389927652891909'),
('FGFR1_HUMAN','4f65_B','B','crystal structure of human fibroblast growth factor receptor domain in complex with compound 8','2.26','0.389927652891909','0.389927652891909'),
('CDC7_HUMAN','4f99_A','A','human cdc7 kinase in complex with dbf4 and nucleotide','2.33','0.359891186260985','0.359891186260985'),
('CDC7_HUMAN','4f9a_A','A','human cdc7 kinase in complex with dbf4 and nucleotide','2.17','0.375859656778034','0.375859656778034'),
('CDC7_HUMAN','4f9a_C','C','human cdc7 kinase in complex with dbf4 and nucleotide','2.17','0.375859656778034','0.375859656778034'),
('CDC7_HUMAN','4f9b_A','A','human cdc7 kinase in complex with dbf4 and pha767491','2.5','0.330194776785714','0.330194776785714'),
('CDC7_HUMAN','4f9b_C','C','human cdc7 kinase in complex with dbf4 and pha767491','2.5','0.330194776785714','0.330194776785714'),
('CDC7_HUMAN','4f9c_A','A','human cdc7 kinase in complex with dbf4 and xl413','2.08','0.403769230769231','0.403769230769231'),
('ACVL1_HUMAN','4fao_c','c','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_C','C','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_d','d','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_D','D','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_e','e','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_E','E','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_f','f','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_F','F','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_i','i','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_I','I','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_j','j','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_J','J','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_k','k','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_K','K','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_l','l','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_L','L','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_O','O','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_P','P','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_Q','Q','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_R','R','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_U','U','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('ACVL1_HUMAN','4fao_V','V','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_W','W','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('AVR2B_HUMAN','4fao_X','X','specificity and structure of a high affinity activin-like 1 signaling complex','3.36','0.179722276785714','0.179722276785714'),
('CSK21_HUMAN','4fbx_A','A','complex structure of human protein kinase ck2 catalytic subu crystallized in the presence of a bisubstrate inhibitor','2.33','0.375107213046699','0.375107213046699'),
('KCC1A_HUMAN','4fg7_A','A',NULL,NULL,NULL,NULL),
('KCC1A_HUMAN','4fg8_A','A',NULL,NULL,NULL,NULL),
('KCC1A_HUMAN','4fg8_B','B',NULL,NULL,NULL,NULL),
('KCC1A_HUMAN','4fg9_A','A',NULL,NULL,NULL,NULL),
('KCC1A_HUMAN','4fg9_B','B',NULL,NULL,NULL,NULL),
('KCC1A_HUMAN','4fgb_A','A',NULL,NULL,NULL,NULL),
('PAK4_HUMAN','4fie_A','A','full-length human pak4','3.11','0.185227842883938','0.185227842883938'),
('PAK4_HUMAN','4fie_B','B','full-length human pak4','3.11','0.185227842883938','0.185227842883938'),
('PAK4_HUMAN','4fif_A','A','catalytic domain of human pak4 with rpkplvdp peptide','2.6','0.323190697115385','0.323190697115385'),
('PAK4_HUMAN','4fif_B','B','catalytic domain of human pak4 with rpkplvdp peptide','2.6','0.323190697115385','0.323190697115385'),
('PAK4_HUMAN','4fif_C','C','catalytic domain of human pak4 with rpkplvdp peptide','2.6','0.323190697115385','0.323190697115385'),
('PAK4_HUMAN','4fif_D','D','catalytic domain of human pak4 with rpkplvdp peptide','2.6','0.323190697115385','0.323190697115385'),
('PAK4_HUMAN','4fig_A','A','catalytic domain of human pak4','3.01','0.257351746954596','0.257351746954596'),
('PAK4_HUMAN','4fig_B','B','catalytic domain of human pak4','3.01','0.257351746954596','0.257351746954596'),
('PAK4_HUMAN','4fih_A','A','catalytic domain of human pak4 with qkftglprqw peptide','1.97','0.471346356055112','0.471346356055112'),
('PAK4_HUMAN','4fii_A','A','catalytic domain of human pak4 with rpkplvdp peptide','2','0.439402678571429','0.439402678571429'),
('PAK4_HUMAN','4fii_B','B','catalytic domain of human pak4 with rpkplvdp peptide','2','0.439402678571429','0.439402678571429'),
('PAK4_HUMAN','4fij_A','A','catalytic domain of human pak4','2.3','0.347873174171843','0.347873174171843'),
('RAF1_HUMAN','4fj3_P','P','14-3-3 isoform zeta in complex with a diphoyphorylated c-raf','1.95','0.523437105082418','0.523437105082418'),
('BRAF_HUMAN','4fk3_A','A','b-raf kinase v600e oncogenic mutant in complex with plx3203','2.65','0.212194576875562','0.212194576875562'),
('BRAF_HUMAN','4fk3_B','B','b-raf kinase v600e oncogenic mutant in complex with plx3203','2.65','0.212194576875562','0.212194576875562'),
('JAK1_HUMAN','4fk6_A','A','jak1 kinase (jh1 domain) in complex with compound 72','2.2','0.37160323728355','0.37160323728355'),
('JAK1_HUMAN','4fk6_B','B','jak1 kinase (jh1 domain) in complex with compound 72','2.2','0.37160323728355','0.37160323728355'),
('KSYK_HUMAN','4fl1_A','A',NULL,NULL,NULL,NULL),
('KSYK_HUMAN','4fl2_A','A',NULL,NULL,NULL,NULL),
('KSYK_HUMAN','4fl3_A','A',NULL,NULL,NULL,NULL),
('MK01_HUMAN','4fmq_A','A','crystal structure of human erk2 complexed with a mapk dockin','2.1','0.437503363095238','0.437503363095238'),
('ALK_HUMAN','4fnw_A','A','crystal structure of the apo f1174l anaplastic lymphoma kina catalytic domain','1.75','0.541397663690476','0.541397663690476'),
('ALK_HUMAN','4fnx_A','A','crystal structure of the apo r1275q anaplastic lymphoma kina catalytic domain','1.7','0.546611082808123','0.546611082808123'),
('ALK_HUMAN','4fny_A','A','crystal structure of the r1275q anaplastic lymphoma kinase c domain in complex with a benzoxazole inhibitor','2.45','0.342263369472789','0.342263369472789'),
('ALK_HUMAN','4fnz_A','A','crystal structure of human anaplastic lymphoma kinase in com piperidine-carboxamide inhibitor 2','2.6','0.310617408424908','0.310617408424908'),
('ALK_HUMAN','4fob_A','A','crystal structure of human anaplastic lymphoma kinase in com acyliminobenzimidazole inhibitor 1','1.9','0.470195343045113','0.470195343045113'),
('ALK_HUMAN','4foc_A','A','crystal structure of human anaplastic lymphoma kinase in com acyliminobenzimidazole inhibitor 2','1.7','0.546126737570028','0.546126737570028'),
('ALK_HUMAN','4fod_A','A','crystal structure of human anaplastic lymphoma kinase in com acyliminobenzimidazole inhibitor 36','2','0.469209598214286','0.469209598214286'),
('ST32A_HUMAN','4fr4_A','A','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('ST32A_HUMAN','4fr4_B','B','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('ST32A_HUMAN','4fr4_C','C','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('ST32A_HUMAN','4fr4_D','D','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('ST32A_HUMAN','4fr4_E','E','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('ST32A_HUMAN','4fr4_F','F','crystal structure of human serine/threonine-protein kinase 3','2.29','0.355564481635995','0.355564481635995'),
('CHK1_HUMAN','4fsm_A','A','crystal structure of the chk1','2.3','0.400677802148033','0.400677802148033'),
('CHK1_HUMAN','4fsn_A','A','crystal structure of the chk1','2.1','0.44285962797619','0.44285962797619'),
('CHK1_HUMAN','4fsq_A','A','crystal structure of the chk1','2.4','0.365264389880952','0.365264389880952'),
('CHK1_HUMAN','4fsr_A','A','crystal structure of the chk1','2.5','0.365280818452381','0.365280818452381'),
('CHK1_HUMAN','4fst_A','A','crystal structure of the chk1','1.9','0.508686786497494','0.508686786497494'),
('CHK1_HUMAN','4fsu_A','A','crystal structure of the chk1','2.1','0.450410238095238','0.450410238095238'),
('CHK1_HUMAN','4fsw_A','A','crystal structure of the chk1','2.3','0.3783682188147','0.3783682188147'),
('CHK1_HUMAN','4fsy_A','A','crystal structure of the chk1','2.3','0.395816864648033','0.395816864648033'),
('CHK1_HUMAN','4fsz_A','A','crystal structure of the chk1','2.3','0.404034334886128','0.404034334886128'),
('CHK1_HUMAN','4ft0_A','A','crystal structure of the chk1','2.3','0.402749855719462','0.402749855719462'),
('CHK1_HUMAN','4ft3_A','A','crystal structure of the chk1','2.5','0.373516175595238','0.373516175595238'),
('CHK1_HUMAN','4ft5_A','A','crystal structure of the chk1','2.4','0.363702544642857','0.363702544642857'),
('CHK1_HUMAN','4ft7_A','A','crystal structure of the chk1','2.2','0.427347017045455','0.427347017045455'),
('CHK1_HUMAN','4ft9_A','A','crystal structure of the chk1','2.2','0.42151042478355','0.42151042478355'),
('CHK1_HUMAN','4fta_A','A','crystal structure of the chk1','2.4','0.388938392857143','0.388938392857143'),
('CHK1_HUMAN','4ftc_A','A','crystal structure of the chk1','2','0.478356428571429','0.478356428571429'),
('CHK1_HUMAN','4fti_A','A','crystal structure of the chk1','2.2','0.424095900974026','0.424095900974026'),
('CHK1_HUMAN','4ftj_A','A','crystal structure of the chk1','2.2','0.417930930735931','0.417930930735931'),
('CHK1_HUMAN','4ftk_A','A','crystal structure of the chk1','2.3','0.410647891433747','0.410647891433747'),
('CHK1_HUMAN','4ftl_A','A','crystal structure of the chk1','2.5','0.345408020833333','0.345408020833333'),
('CHK1_HUMAN','4ftm_A','A','crystal structure of the chk1','1.9','0.502119167449875','0.502119167449875'),
('CHK1_HUMAN','4ftn_A','A','crystal structure of the chk1','2.02','0.469192198402876','0.469192198402876'),
('CHK1_HUMAN','4fto_A','A','crystal structure of the chk1','2.1','0.444401205357143','0.444401205357143'),
('CHK1_HUMAN','4ftq_A','A','crystal structure of the chk1','2','0.444746383928571','0.444746383928571'),
('CHK1_HUMAN','4ftr_A','A','crystal structure of the chk1','2.25','0.416005530753968','0.416005530753968'),
('CHK1_HUMAN','4ftt_A','A','crystal structure of the chk1','2.3','0.40654690929089','0.40654690929089'),
('CHK1_HUMAN','4ftu_A','A','crystal structure of the chk1','2.1','0.431443497023809','0.431443497023809'),
('MK01_HUMAN','4fux_A','A','crystal structure of the erk2 complexed with e75','2.2','0.395856466450216','0.395856466450216'),
('MK01_HUMAN','4fuy_A','A','crystal structure of the erk2 complexed with ek2','2','0.459013125','0.459013125'),
('MK01_HUMAN','4fv0_A','A','crystal structure of the erk2 complexed with ek3','2.1','0.447171919642857','0.447171919642857'),
('MK01_HUMAN','4fv1_A','A','crystal structure of the erk2 complexed with ek4','1.99','0.47034105983788','0.47034105983788'),
('MK01_HUMAN','4fv2_A','A','crystal structure of the erk2 complexed with ek5','2','0.46682125','0.46682125'),
('MK01_HUMAN','4fv3_A','A','crystal structure of the erk2 complexed with ek6','2.2','0.407448772997835','0.407448772997835'),
('MK01_HUMAN','4fv4_A','A','crystal structure of the erk2 complexed with ek7','2.5','0.325644866071429','0.325644866071429'),
('MK01_HUMAN','4fv5_A','A','crystal structure of the erk2 complexed with ek9','2.4','0.35592125','0.35592125'),
('MK01_HUMAN','4fv6_A','A','crystal structure of the erk2 complexed with e57','2.5','0.321939657738095','0.321939657738095'),
('MK01_HUMAN','4fv7_A','A','crystal structure of the erk2 complexed with e94','1.9','0.490995982926065','0.490995982926065'),
('MK01_HUMAN','4fv8_A','A','crystal structure of the erk2 complexed with e63','2','0.442669479166667','0.442669479166667'),
('MK01_HUMAN','4fv9_A','A','crystal structure of the erk2 complexed with e71','2.11','0.422805092741481','0.422805092741481'),
('JAK2_HUMAN','4fvp_A','A','crystal structure of the jak2 pseudokinase domain (apo form)','2.01','0.466960250310945','0.466960250310945'),
('JAK2_HUMAN','4fvq_A','A','crystal structure of the jak2 pseudokinase domain (mg-atp-bo','1.75','0.544688720238095','0.544688720238095'),
('JAK2_HUMAN','4fvr_A','A','crystal structure of the jak2 pseudokinase domain mutant v61 atp-bound form)','2','0.448380342261905','0.448380342261905'),
('RON_HUMAN','4fww_A','A','crystal structure of the sema-psi extracellular domains of h receptor tyrosine kinase','1.85','0.465163174469112','0.465163174469112'),
('KSYK_HUMAN','4fyn_A','A',NULL,NULL,NULL,NULL),
('KSYK_HUMAN','4fyo_A','A',NULL,NULL,NULL,NULL),
('KSYK_HUMAN','4fz6_A','A',NULL,NULL,NULL,NULL),
('EPHA3_HUMAN','4g2f_A','A','human epha3 kinase domain in complex with compound 7','1.7','0.562531231617647','0.562531231617647'),
('E2AK3_HUMAN','4g31_A','A','crystal structure of gsk6414 bound to perk (r587-r1092, dele t867) at 2.28 a resolution','2.28','0.366171416823308','0.366171416823308'),
('E2AK3_HUMAN','4g34_A','A','crystal structure of gsk6924 bound to perk (r587-r1092, dele t867) at 2.70 a resolution','2.7','0.293364998346561','0.293364998346561'),
('M3K14_HUMAN','4g3d_A','A','crystal structure of human nf-kappab inducing kinase (nik)','2.9','0.259640160611659','0.259640160611659'),
('M3K14_HUMAN','4g3d_B','B','crystal structure of human nf-kappab inducing kinase (nik)','2.9','0.259640160611659','0.259640160611659'),
('M3K14_HUMAN','4g3d_D','D','crystal structure of human nf-kappab inducing kinase (nik)','2.9','0.259640160611659','0.259640160611659'),
('M3K14_HUMAN','4g3d_E','E','crystal structure of human nf-kappab inducing kinase (nik)','2.9','0.259640160611659','0.259640160611659'),
('EGFR_HUMAN','4g5j_A','A','crystal structure of egfr kinase in complex with bibw2992','2.8','0.292508586309524','0.292508586309524'),
('EGFR_HUMAN','4g5p_A','A','crystal structure of egfr kinase t790m in complex with bibw2','3.17','0.181471207892069','0.181471207892069'),
('EGFR_HUMAN','4g5p_B','B','crystal structure of egfr kinase t790m in complex with bibw2','3.17','0.181471207892069','0.181471207892069'),
('MK01_HUMAN','4g6n_A','A','crystal structure of the erk2','2','0.458426026785714','0.458426026785714'),
('MK01_HUMAN','4g6o_A','A','crystal structure of the erk2','2.2','0.419993713474026','0.419993713474026'),
('RN5A_HUMAN','4g8k_A','A','intact sensor domain of human rnase l in the inactive signal','2.4','0.33478943452381','0.33478943452381'),
('RN5A_HUMAN','4g8k_B','B','intact sensor domain of human rnase l in the inactive signal','2.4','0.33478943452381','0.33478943452381'),
('RN5A_HUMAN','4g8l_A','A','active state of intact sensor domain of human rnase l with 2','2.8','0.252554404761905','0.252554404761905'),
('RN5A_HUMAN','4g8l_B','B','active state of intact sensor domain of human rnase l with 2','2.8','0.252554404761905','0.252554404761905'),
('RN5A_HUMAN','4g8l_C','C','active state of intact sensor domain of human rnase l with 2','2.8','0.252554404761905','0.252554404761905'),
('RN5A_HUMAN','4g8l_D','D','active state of intact sensor domain of human rnase l with 2','2.8','0.252554404761905','0.252554404761905'),
('BRAF_HUMAN','4g9c_A','A','human b-raf kinase domain bound to a type ii pyrazolopyridin inhibitor','3.5','0.136676800595238','0.136676800595238'),
('BRAF_HUMAN','4g9c_B','B','human b-raf kinase domain bound to a type ii pyrazolopyridin inhibitor','3.5','0.136676800595238','0.136676800595238'),
('BRAF_HUMAN','4g9r_A','A','b-raf v600e kinase domain bound to a type ii dihydroquinazol inhibitor','3.2','0.199408050595238','0.199408050595238'),
('BRAF_HUMAN','4g9r_B','B','b-raf v600e kinase domain bound to a type ii dihydroquinazol inhibitor','3.2','0.199408050595238','0.199408050595238'),
('CDK2_HUMAN','4gcj_A','A','cdk2 in complex with inhibitor rc-3-89','1.42','0.661247956279343','0.661247956279343'),
('MET_HUMAN','4gg5_A','A','crystal structure of cmet in complex with novel inhibitor','2.42','0.321560759543487','0.321560759543487'),
('MET_HUMAN','4gg7_A','A','crystal structure of cmet in complex with novel inhibitor','2.27','0.355286312932662','0.355286312932662'),
('BUB1B_HUMAN','4ggd_C','C','structural analysis of human cdc20 supports multisite degron recognition by apc/c.','2.44','0.372747330454723','0.372747330454723'),
('BUB1B_HUMAN','4ggd_D','D','structural analysis of human cdc20 supports multisite degron recognition by apc/c.','2.44','0.372747330454723','0.372747330454723'),
('CHK1_HUMAN','4gh2_A','A','crystal structure of the chk1','2.03','0.47333750410509','0.47333750410509'),
('Q6P4R6_HUMAN','4gk2_A','A',NULL,NULL,NULL,NULL),
('Q6P4R6_HUMAN','4gk3_A','A',NULL,NULL,NULL,NULL),
('Q6P4R6_HUMAN','4gk4_A','A',NULL,NULL,NULL,NULL),
('M3K7_HUMAN','4gs6_A','A',NULL,NULL,NULL,NULL),
('ROR2_HUMAN','4gt4_A','A','structure of unliganded, inactive ror2 kinase domain','2.41','0.388383905169433','0.388383905169433'),
('ROR2_HUMAN','4gt4_B','B','structure of unliganded, inactive ror2 kinase domain','2.41','0.388383905169433','0.388383905169433'),
('NTRK1_HUMAN','4gt5_A','A','crystal structure of the inactive trka kinase domain','2.4','0.359765729166667','0.359765729166667'),
('AKT1_HUMAN','4gv1_A','A',NULL,NULL,NULL,NULL),
('PIM1_HUMAN','4gw8_A','A','human proto-oncogene serine threonine kinase (pim1) in compl consensus peptide and leucettine l41','2','0.47057130952381','0.47057130952381'),
('CSK21_HUMAN','4gyw_B','B','crystal structure of human o-glcnac transferase in complex w and a glycopeptide','1.7','0.572739029236695','0.572739029236695'),
('CSK21_HUMAN','4gyw_D','D','crystal structure of human o-glcnac transferase in complex w and a glycopeptide','1.7','0.572739029236695','0.572739029236695'),
('CSK21_HUMAN','4gyy_B','B','crystal structure of human o-glcnac transferase with udp-5sg a peptide substrate','1.85','0.477684067326255','0.477684067326255'),
('CSK21_HUMAN','4gyy_D','D','crystal structure of human o-glcnac transferase with udp-5sg a peptide substrate','1.85','0.477684067326255','0.477684067326255'),
('CSK21_HUMAN','4gz3_B','B','crystal structure of human o-glcnac transferase with udp and thioglycopeptide','1.9','0.454612485902256','0.454612485902256'),
('CSK21_HUMAN','4gz3_D','D','crystal structure of human o-glcnac transferase with udp and thioglycopeptide','1.9','0.454612485902256','0.454612485902256'),
('FAK2_HUMAN','4h1j_A','A',NULL,NULL,NULL,NULL),
('FAK2_HUMAN','4h1m_A','A',NULL,NULL,NULL,NULL),
('MK10_HUMAN','4h36_A','A',NULL,NULL,NULL,NULL),
('MK10_HUMAN','4h39_A','A',NULL,NULL,NULL,NULL),
('MK10_HUMAN','4h3b_A','A',NULL,NULL,NULL,NULL),
('MK10_HUMAN','4h3b_C','C',NULL,NULL,NULL,NULL),
('MK01_HUMAN','4h3p_A','A',NULL,NULL,NULL,NULL),
('KS6A1_HUMAN','4h3p_B','B',NULL,NULL,NULL,NULL),
('MK01_HUMAN','4h3p_D','D',NULL,NULL,NULL,NULL),
('KS6A1_HUMAN','4h3p_E','E',NULL,NULL,NULL,NULL),
('MK01_HUMAN','4h3q_A','A',NULL,NULL,NULL,NULL),
('MP2K2_HUMAN','4h3q_B','B',NULL,NULL,NULL,NULL),
('BRAF_HUMAN','4h58_A','A',NULL,NULL,NULL,NULL),
('BRAF_HUMAN','4h58_B','B',NULL,NULL,NULL,NULL),
('BRAF_HUMAN','4h58_C','C',NULL,NULL,NULL,NULL),
('PLK1_HUMAN','4h5x_A','A','human plk1-pbd with a glycerol bound at the phophopeptide bi','1.95','0.455885334249084','0.455885334249084'),
('PLK1_HUMAN','4h5x_B','B','human plk1-pbd with a glycerol bound at the phophopeptide bi','1.95','0.455885334249084','0.455885334249084'),
('PLK1_HUMAN','4h71_A','A','human plk1-pbd in complex with poloxime ((e)-4-(hydroxyimino isopropyl-5-methylcyclohexa-2,5-dienone)','1.93','0.471827587049716','0.471827587049716'),
('PLK1_HUMAN','4h71_B','B','human plk1-pbd in complex with poloxime ((e)-4-(hydroxyimino isopropyl-5-methylcyclohexa-2,5-dienone)','1.93','0.471827587049716','0.471827587049716'),
('TTK_HUMAN','4h7x_A','A',NULL,NULL,NULL,NULL),
('TTK_HUMAN','4h7x_B','B',NULL,NULL,NULL,NULL),
('TTK_HUMAN','4h7y_A','A',NULL,NULL,NULL,NULL),
('TTK_HUMAN','4h7y_B','B',NULL,NULL,NULL,NULL),
('TTK_HUMAN','4h7y_C','C',NULL,NULL,NULL,NULL),
('TTK_HUMAN','4h7y_D','D',NULL,NULL,NULL,NULL),
('HCK_HUMAN','4hck_A','A','human hck sh3 domain, nmr, 25 structures',NULL,'0.0327482589285714','0.0327482589285714'),
('PLK1_HUMAN','4hco_A','A','human plk1-pbd in complex with thymoquinone at the phophopep binding site','2.75','0.270340827922078','0.270340827922078'),
('PLK1_HUMAN','4hco_B','B','human plk1-pbd in complex with thymoquinone at the phophopep binding site','2.75','0.270340827922078','0.270340827922078'),
('ITK_HUMAN','4hct_A','A','crystal structure of itk in complex with compound 52','1.48','0.656133220318533','0.656133220318533'),
('ITK_HUMAN','4hcu_A','A','crystal structure of itk in complext with compound 40','1.43','0.683292589181652','0.683292589181652'),
('ITK_HUMAN','4hcv_A','A','crystal structure of itk in complex with compound 53','1.48','0.657234723294723','0.657234723294723'),
('JAK2_HUMAN','4hge_A','A','jak2 kinase (jh1 domain) in complex with compound 8','2.3','0.401264989648033','0.401264989648033'),
('JAK2_HUMAN','4hge_B','B','jak2 kinase (jh1 domain) in complex with compound 8','2.3','0.401264989648033','0.401264989648033'),
('KC1G3_HUMAN','4hgl_A','A',NULL,NULL,NULL,NULL),
('KC1G3_HUMAN','4hgs_A','A',NULL,NULL,NULL,NULL),
('KC1D_HUMAN','4hgt_A','A',NULL,NULL,NULL,NULL),
('KC1D_HUMAN','4hgt_B','B',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4hjo_A','A','crystal structure of the inactive egfr tyrosine kinase domai erlotinib','2.75','0.277640976731602','0.277640976731602'),
('KC1D_HUMAN','4hnf_A','A','crystal structure of ck1d in complex with pf4800567','2.07','0.365073468987233','0.365073468987233'),
('KC1D_HUMAN','4hnf_B','B','crystal structure of ck1d in complex with pf4800567','2.07','0.365073468987233','0.365073468987233'),
('KC1E_HUMAN','4hni_A','A','crystal structure of ck1e in complex with pf4800567','2.74','0.251759947102016','0.251759947102016'),
('KC1E_HUMAN','4hni_B','B','crystal structure of ck1e in complex with pf4800567','2.74','0.251759947102016','0.251759947102016'),
('KC1E_HUMAN','4hok_A','A','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_C','C','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_E','E','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_G','G','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_I','I','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_K','K','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_M','M','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_O','O','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_Q','Q','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_S','S','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_U','U','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('KC1E_HUMAN','4hok_W','W','crystal structure of apo ck1e','2.77','0.213486991039195','0.213486991039195'),
('JAK3_HUMAN','4hvd_A','A',NULL,NULL,NULL,NULL),
('JAK3_HUMAN','4hvg_A','A',NULL,NULL,NULL,NULL),
('JAK3_HUMAN','4hvh_A','A',NULL,NULL,NULL,NULL),
('JAK3_HUMAN','4hvi_A','A',NULL,NULL,NULL,NULL),
('SRC_HUMAN','4hxj_A','A',NULL,NULL,NULL,NULL),
('SRC_HUMAN','4hxj_B','B',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzr_A','A',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzr_B','B',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzs_A','A',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzs_B','B',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzs_C','C',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4hzs_D','D',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i1z_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i20_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i21_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i21_B','B',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i22_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i23_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i24_A','A',NULL,NULL,NULL,NULL),
('EGFR_HUMAN','4i24_B','B',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4i3z_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4i3z_C','C',NULL,NULL,NULL,NULL),
('FAK1_HUMAN','4i4f_A','A',NULL,NULL,NULL,NULL),
('MK07_HUMAN','4ic7_A','A',NULL,NULL,NULL,NULL),
('MP2K5_HUMAN','4ic7_B','B',NULL,NULL,NULL,NULL),
('MK07_HUMAN','4ic7_D','D',NULL,NULL,NULL,NULL),
('MP2K5_HUMAN','4ic7_E','E',NULL,NULL,NULL,NULL),
('MK07_HUMAN','4ic8_A','A',NULL,NULL,NULL,NULL),
('MK07_HUMAN','4ic8_B','B',NULL,NULL,NULL,NULL),
('ACK1_HUMAN','4id7_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4ii5_A','A',NULL,NULL,NULL,NULL),
('CDK2_HUMAN','4ii5_C','C',NULL,NULL,NULL,NULL),
('HCK_HUMAN','5hck_A','A','human hck sh3 domain, nmr, minimized average structure',NULL,'0.0364212053571429','0.0364212053571429');INSERT INTO `kindriver_v82`.`Pfam_Domain` (`pfam_domain_id`,`pfam_id`,`uniprot_id`,`start`,`end`) VALUES 
('E3WH17_HUMAN/310-577','PF07714','E3WH17_HUMAN','310','577'),
('MATK_HUMAN/235-478','PF07714','MATK_HUMAN','235','478'),
('B4DES9_HUMAN/363-633','PF07714','B4DES9_HUMAN','363','633'),
('Q59GM4_HUMAN/430-684','PF07714','Q59GM4_HUMAN','430','684'),
('H0Y8F1_HUMAN/94-356','PF07714','H0Y8F1_HUMAN','94','356'),
('H7C560_HUMAN/65-322','PF07714','H7C560_HUMAN','65','322'),
('H7C074_HUMAN/63-285','PF07714','H7C074_HUMAN','63','285'),
('H3BVG6_HUMAN/208-475','PF07714','H3BVG6_HUMAN','208','475'),
('ABL1_HUMAN/242-493','PF07714','ABL1_HUMAN','242','493'),
('B7Z2I3_HUMAN/659-915','PF07714','B7Z2I3_HUMAN','659','915'),
('EPHA1_HUMAN/624-880','PF07714','EPHA1_HUMAN','624','880'),
('GUC2F_HUMAN/583-809','PF07714','GUC2F_HUMAN','583','809'),
('BTK_HUMAN/402-651','PF07714','BTK_HUMAN','402','651'),
('NTRK1_HUMAN/510-781','PF07714','NTRK1_HUMAN','510','781'),
('Q3MS92_HUMAN/1-200','PF07714','Q3MS92_HUMAN','1','200'),
('B3KUV3_HUMAN/2-234','PF07714','B3KUV3_HUMAN','2','234'),
('F8TLW0_HUMAN/724-1005','PF07714','F8TLW0_HUMAN','724','1005'),
('C9J1X3_HUMAN/158-417','PF07714','C9J1X3_HUMAN','158','417'),
('Q2VJ45_HUMAN/386-667','PF07714','Q2VJ45_HUMAN','386','667'),
('Q16176_HUMAN/194-436','PF07714','Q16176_HUMAN','194','436'),
('H0YM90_HUMAN/530-705','PF07714','H0YM90_HUMAN','530','705'),
('Q59FX1_HUMAN/10-261','PF07714','Q59FX1_HUMAN','10','261'),
('B6D4Y3_HUMAN/1116-1383','PF07714','B6D4Y3_HUMAN','1116','1383'),
('B2RDR6_HUMAN/235-478','PF07714','B2RDR6_HUMAN','235','478'),
('PGFRB_HUMAN/600-958','PF07714','PGFRB_HUMAN','600','958'),
('Q53TA0_HUMAN/346-603','PF07714','Q53TA0_HUMAN','346','603'),
('EPHB6_HUMAN/670-915','PF07714','EPHB6_HUMAN','670','915'),
('Q59EB0_HUMAN/929-1255','PF07714','Q59EB0_HUMAN','929','1255'),
('FGR_HUMAN/263-512','PF07714','FGR_HUMAN','263','512'),
('JAK3_HUMAN/521-777','PF07714','JAK3_HUMAN','521','777'),
('Q05D26_HUMAN/241-487','PF07714','Q05D26_HUMAN','241','487'),
('Q6ZNH1_HUMAN/140-395','PF07714','Q6ZNH1_HUMAN','140','395'),
('B3KQJ1_HUMAN/48-303','PF07714','B3KQJ1_HUMAN','48','303'),
('B6D4Y8_HUMAN/1116-1383','PF07714','B6D4Y8_HUMAN','1116','1383'),
('D1MAM4_HUMAN/1116-1383','PF07714','D1MAM4_HUMAN','1116','1383'),
('JAK1_HUMAN/583-845','PF07714','JAK1_HUMAN','583','845'),
('Q5U0C9_HUMAN/36-284','PF07714','Q5U0C9_HUMAN','36','284'),
('H0YBP1_HUMAN/433-687','PF07714','H0YBP1_HUMAN','433','687'),
('B2RDI6_HUMAN/117-376','PF07714','B2RDI6_HUMAN','117','376'),
('TESK2_HUMAN/59-309','PF07714','TESK2_HUMAN','59','309'),
('Q15516_HUMAN/242-500','PF07714','Q15516_HUMAN','242','500'),
('F8VP57_HUMAN/676-933','PF07714','F8VP57_HUMAN','676','933'),
('H7BYU0_HUMAN/327-591','PF07714','H7BYU0_HUMAN','327','591'),
('Q59FL8_HUMAN/583-839','PF07714','Q59FL8_HUMAN','583','839'),
('H0YE48_HUMAN/1-189','PF07714','H0YE48_HUMAN','1','189'),
('H2E273_HUMAN/357-492','PF07714','H2E273_HUMAN','357','492'),
('H0Y9P2_HUMAN/99-280','PF07714','H0Y9P2_HUMAN','99','280'),
('Q506Q0_HUMAN/545-805','PF07714','Q506Q0_HUMAN','545','805'),
('INSRR_HUMAN/979-1246','PF07714','INSRR_HUMAN','979','1246'),
('A9YLN5_HUMAN/322-592','PF07714','A9YLN5_HUMAN','322','592'),
('Q9H7V3_HUMAN/1-234','PF07714','Q9H7V3_HUMAN','1','234'),
('Q2TTR7_HUMAN/712-968','PF07714','Q2TTR7_HUMAN','712','968'),
('F2YGG7_HUMAN/667-923','PF07714','F2YGG7_HUMAN','667','923'),
('ROR1_HUMAN/473-746','PF07714','ROR1_HUMAN','473','746'),
('Q8IYN9_HUMAN/422-676','PF07714','Q8IYN9_HUMAN','422','676'),
('VGFR3_HUMAN/845-1169','PF07714','VGFR3_HUMAN','845','1169'),
('H0YNK6_HUMAN/473-741','PF07714','H0YNK6_HUMAN','473','741'),
('A8K2P1_HUMAN/621-878','PF07714','A8K2P1_HUMAN','621','878'),
('Q59GM6_HUMAN/374-628','PF07714','Q59GM6_HUMAN','374','628'),
('A6P4V4_HUMAN/806-1073','PF07714','A6P4V4_HUMAN','806','1073'),
('FGFR3_HUMAN/472-748','PF07714','FGFR3_HUMAN','472','748'),
('D1MAM3_HUMAN/1116-1383','PF07714','D1MAM3_HUMAN','1116','1383'),
('KSR1_HUMAN/611-875','PF07714','KSR1_HUMAN','611','875'),
('F8VUG4_HUMAN/126-364','PF07714','F8VUG4_HUMAN','126','364'),
('F0UY65_HUMAN/1116-1383','PF07714','F0UY65_HUMAN','1116','1383'),
('B7Z418_HUMAN/134-385','PF07714','B7Z418_HUMAN','134','385'),
('H0YBZ1_HUMAN/120-374','PF07714','H0YBZ1_HUMAN','120','374'),
('E9PG71_HUMAN/621-878','PF07714','E9PG71_HUMAN','621','878'),
('Q15850_HUMAN/87-368','PF07714','Q15850_HUMAN','87','368'),
('E9PC47_HUMAN/369-634','PF07714','E9PC47_HUMAN','369','634'),
('D3DNT9_HUMAN/591-850','PF07714','D3DNT9_HUMAN','591','850'),
('G9BXQ3_HUMAN/116-377','PF07714','G9BXQ3_HUMAN','116','377'),
('E7EU09_HUMAN/389-665','PF07714','E7EU09_HUMAN','389','665'),
('E7BSV0_HUMAN/712-968','PF07714','E7BSV0_HUMAN','712','968'),
('D3DRD5_HUMAN/498-774','PF07714','D3DRD5_HUMAN','498','774'),
('Q8IXP2_HUMAN/846-1120','PF07714','Q8IXP2_HUMAN','846','1120'),
('FGFR1_HUMAN/478-754','PF07714','FGFR1_HUMAN','478','754'),
('H7C265_HUMAN/73-335','PF07714','H7C265_HUMAN','73','335'),
('FER_HUMAN/563-814','PF07714','FER_HUMAN','563','814'),
('Q541P7_HUMAN/615-874','PF07714','Q541P7_HUMAN','615','874'),
('FGFR2_HUMAN/481-757','PF07714','FGFR2_HUMAN','481','757'),
('F8VW56_HUMAN/1-206','PF07714','F8VW56_HUMAN','1','206'),
('TIE2_HUMAN/824-1092','PF07714','TIE2_HUMAN','824','1092'),
('Q5VTU6_HUMAN/610-946','PF07714','Q5VTU6_HUMAN','610','946'),
('STYK1_HUMAN/114-380','PF07714','STYK1_HUMAN','114','380'),
('E7EML7_HUMAN/140-395','PF07714','E7EML7_HUMAN','140','395'),
('A2VCQ3_HUMAN/476-749','PF07714','A2VCQ3_HUMAN','476','749'),
('GUC2C_HUMAN/499-745','PF07714','GUC2C_HUMAN','499','745'),
('E9PFD7_HUMAN/659-915','PF07714','E9PFD7_HUMAN','659','915'),
('Q1RMG3_HUMAN/411-678','PF07714','Q1RMG3_HUMAN','411','678'),
('ROS1_HUMAN/1945-2215','PF07714','ROS1_HUMAN','1945','2215'),
('D3DRD4_HUMAN/384-660','PF07714','D3DRD4_HUMAN','384','660'),
('B3KTB2_HUMAN/180-439','PF07714','B3KTB2_HUMAN','180','439'),
('Q53EL3_HUMAN/195-439','PF07714','Q53EL3_HUMAN','195','439'),
('H7C155_HUMAN/228-485','PF07714','H7C155_HUMAN','228','485'),
('B5BU52_HUMAN/195-440','PF07714','B5BU52_HUMAN','195','440'),
('Q4LDX3_HUMAN/571-833','PF07714','Q4LDX3_HUMAN','571','833'),
('H9N1E7_HUMAN/1-249','PF07714','H9N1E7_HUMAN','1','249'),
('B6EXY4_HUMAN/128-395','PF07714','B6EXY4_HUMAN','128','395'),
('Q9NPI3_HUMAN/1-166','PF07714','Q9NPI3_HUMAN','1','166'),
('E9PBI4_HUMAN/171-425','PF07714','E9PBI4_HUMAN','171','425'),
('B4DGQ7_HUMAN/709-911','PF07714','B4DGQ7_HUMAN','709','911'),
('B7Z6W7_HUMAN/197-446','PF07714','B7Z6W7_HUMAN','197','446'),
('A9UEZ6_HUMAN/745-996','PF07714','A9UEZ6_HUMAN','745','996'),
('ERBB4_HUMAN/718-974','PF07714','ERBB4_HUMAN','718','974'),
('E9PM19_HUMAN/404-681','PF07714','E9PM19_HUMAN','404','681'),
('F5H8L5_HUMAN/141-407','PF07714','F5H8L5_HUMAN','141','407'),
('UFO_HUMAN/536-803','PF07714','UFO_HUMAN','536','803'),
('G8FPZ9_HUMAN/14-191','PF07714','G8FPZ9_HUMAN','14','191'),
('B4DSE0_HUMAN/563-822','PF07714','B4DSE0_HUMAN','563','822'),
('ANPRA_HUMAN/543-801','PF07714','ANPRA_HUMAN','543','801'),
('B6EXY3_HUMAN/593-860','PF07714','B6EXY3_HUMAN','593','860'),
('FLT3_HUMAN/610-943','PF07714','FLT3_HUMAN','610','943'),
('A8K3B6_HUMAN/195-440','PF07714','A8K3B6_HUMAN','195','440'),
('E9PHX8_HUMAN/411-678','PF07714','E9PHX8_HUMAN','411','678'),
('DDR2_HUMAN/563-849','PF07714','DDR2_HUMAN','563','849'),
('HCK_HUMAN/262-511','PF07714','HCK_HUMAN','262','511'),
('E7ENM8_HUMAN/498-673','PF07714','E7ENM8_HUMAN','498','673'),
('B4E123_HUMAN/336-613','PF07714','B4E123_HUMAN','336','613'),
('ERBB3_HUMAN/709-965','PF07714','ERBB3_HUMAN','709','965'),
('B0YIV3_HUMAN/25-285','PF07714','B0YIV3_HUMAN','25','285'),
('E9PR11_HUMAN/13-230','PF07714','E9PR11_HUMAN','13','230'),
('KIT_HUMAN/589-924','PF07714','KIT_HUMAN','589','924'),
('Q9P0L3_HUMAN/1-164','PF07714','Q9P0L3_HUMAN','1','164'),
('LCK_HUMAN/245-494','PF07714','LCK_HUMAN','245','494'),
('Q5R3A8_HUMAN/219-468','PF07714','Q5R3A8_HUMAN','219','468'),
('B3KP36_HUMAN/141-406','PF07714','B3KP36_HUMAN','141','406'),
('C9J5X1_HUMAN/998-1265','PF07714','C9J5X1_HUMAN','998','1265'),
('A9UF02_HUMAN/756-1007','PF07714','A9UF02_HUMAN','756','1007'),
('B2RE75_HUMAN/587-854','PF07714','B2RE75_HUMAN','587','854'),
('D3DSX2_HUMAN/42-318','PF07714','D3DSX2_HUMAN','42','318'),
('Q6ZNR9_HUMAN/277-432','PF07714','Q6ZNR9_HUMAN','277','432'),
('D7RF68_HUMAN/288-545','PF07714','D7RF68_HUMAN','288','545'),
('SRMS_HUMAN/230-480','PF07714','SRMS_HUMAN','230','480'),
('FGFR4_HUMAN/467-743','PF07714','FGFR4_HUMAN','467','743'),
('D4Q8H0_HUMAN/16-260','PF07714','D4Q8H0_HUMAN','16','260'),
('B2R6Q4_HUMAN/195-440','PF07714','B2R6Q4_HUMAN','195','440'),
('FRK_HUMAN/234-487','PF07714','FRK_HUMAN','234','487'),
('Q4JFK8_HUMAN/1-203','PF07714','Q4JFK8_HUMAN','1','203'),
('Q6MZT2_HUMAN/563-849','PF07714','Q6MZT2_HUMAN','563','849'),
('NTRK3_HUMAN/538-824','PF07714','NTRK3_HUMAN','538','824'),
('E9PEI4_HUMAN/50-304','PF07714','E9PEI4_HUMAN','50','304'),
('E9PPF2_HUMAN/589-826','PF07714','E9PPF2_HUMAN','589','826'),
('Q8NI16_HUMAN/437-713','PF07714','Q8NI16_HUMAN','437','713'),
('H7C3Z8_HUMAN/103-270','PF07714','H7C3Z8_HUMAN','103','270'),
('A8K3Z4_HUMAN/507-778','PF07714','A8K3Z4_HUMAN','507','778'),
('B4DQ47_HUMAN/1-159','PF07714','B4DQ47_HUMAN','1','159'),
('B4DZS7_HUMAN/289-521','PF07714','B4DZS7_HUMAN','289','521'),
('Q8TDJ5_HUMAN/299-566','PF07714','Q8TDJ5_HUMAN','299','566'),
('H0YB16_HUMAN/94-348','PF07714','H0YB16_HUMAN','94','348'),
('TYK2_HUMAN/897-1169','PF07714','TYK2_HUMAN','897','1169'),
('Q12787_HUMAN/333-599','PF07714','Q12787_HUMAN','333','599'),
('Q8NFJ4_HUMAN/1-227','PF07714','Q8NFJ4_HUMAN','1','227'),
('Q548C2_HUMAN/538-807','PF07714','Q548C2_HUMAN','538','807'),
('B4DVT5_HUMAN/1-207','PF07714','B4DVT5_HUMAN','1','207'),
('E7EVR7_HUMAN/367-643','PF07714','E7EVR7_HUMAN','367','643'),
('Q6ZRA8_HUMAN/171-425','PF07714','Q6ZRA8_HUMAN','171','425'),
('A8E633_HUMAN/146-422','PF07714','A8E633_HUMAN','146','422'),
('D6RA14_HUMAN/1-175','PF07714','D6RA14_HUMAN','1','175'),
('H0YCC9_HUMAN/145-391','PF07714','H0YCC9_HUMAN','145','391'),
('B4E0X2_HUMAN/268-525','PF07714','B4E0X2_HUMAN','268','525'),
('B4DP99_HUMAN/144-389','PF07714','B4DP99_HUMAN','144','389'),
('B4DU06_HUMAN/288-547','PF07714','B4DU06_HUMAN','288','547'),
('EPHB4_HUMAN/615-874','PF07714','EPHB4_HUMAN','615','874'),
('Q4LE53_HUMAN/639-898','PF07714','Q4LE53_HUMAN','639','898'),
('A8K710_HUMAN/16-260','PF07714','A8K710_HUMAN','16','260'),
('BMX_HUMAN/417-666','PF07714','BMX_HUMAN','417','666'),
('Q75MF2_HUMAN/1-145','PF07714','Q75MF2_HUMAN','1','145'),
('Q9NPI2_HUMAN/1-166','PF07714','Q9NPI2_HUMAN','1','166'),
('FES_HUMAN/561-814','PF07714','FES_HUMAN','561','814'),
('B6D4Y7_HUMAN/1116-1383','PF07714','B6D4Y7_HUMAN','1116','1383'),
('Q53T57_HUMAN/1-145','PF07714','Q53T57_HUMAN','1','145'),
('EPHA5_HUMAN/675-932','PF07714','EPHA5_HUMAN','675','932'),
('B7Z1I0_HUMAN/59-312','PF07714','B7Z1I0_HUMAN','59','312'),
('B4DQQ3_HUMAN/1-229','PF07714','B4DQQ3_HUMAN','1','229'),
('C1PHA1_HUMAN/601-868','PF07714','C1PHA1_HUMAN','601','868'),
('A9UF07_HUMAN/902-1153','PF07714','A9UF07_HUMAN','902','1153'),
('JAK2_HUMAN/849-1123','PF07714','JAK2_HUMAN','849','1123'),
('C0LYZ4_HUMAN/1-215','PF07714','C0LYZ4_HUMAN','1','215'),
('MUSK_HUMAN/575-856','PF07714','MUSK_HUMAN','575','856'),
('F1T0G6_HUMAN/235-478','PF07714','F1T0G6_HUMAN','235','478'),
('Q59GQ9_HUMAN/40-367','PF07714','Q59GQ9_HUMAN','40','367'),
('ACK1_HUMAN/126-385','PF07714','ACK1_HUMAN','126','385'),
('D1MAM0_HUMAN/1116-1383','PF07714','D1MAM0_HUMAN','1116','1383'),
('B2R8Z4_HUMAN/417-666','PF07714','B2R8Z4_HUMAN','417','666'),
('Q5H8Y1_HUMAN/1939-2209','PF07714','Q5H8Y1_HUMAN','1939','2209'),
('Q53R53_HUMAN/155-422','PF07714','Q53R53_HUMAN','155','422'),
('NTRK2_HUMAN/538-807','PF07714','NTRK2_HUMAN','538','807'),
('G9JXB8_HUMAN/976-1235','PF07714','G9JXB8_HUMAN','976','1235'),
('ZAP70_HUMAN/338-593','PF07714','ZAP70_HUMAN','338','593'),
('EPHB1_HUMAN/619-878','PF07714','EPHB1_HUMAN','619','878'),
('E7EUC1_HUMAN/85-355','PF07714','E7EUC1_HUMAN','85','355'),
('B4DPY6_HUMAN/1-207','PF07714','B4DPY6_HUMAN','1','207'),
('C1PHA2_HUMAN/979-1246','PF07714','C1PHA2_HUMAN','979','1246'),
('D1MAM5_HUMAN/1116-1383','PF07714','D1MAM5_HUMAN','1116','1383'),
('VGFR1_HUMAN/827-1154','PF07714','VGFR1_HUMAN','827','1154'),
('D2CGD1_HUMAN/392-668','PF07714','D2CGD1_HUMAN','392','668'),
('PTK7_HUMAN/796-1061','PF07714','PTK7_HUMAN','796','1061'),
('B3XZM0_HUMAN/292-559','PF07714','B3XZM0_HUMAN','292','559'),
('A8K5U6_HUMAN/621-878','PF07714','A8K5U6_HUMAN','621','878'),
('JAK2_HUMAN/545-805','PF07714','JAK2_HUMAN','545','805'),
('Q9HBS4_HUMAN/122-390','PF07714','Q9HBS4_HUMAN','122','390'),
('E9PB13_HUMAN/637-899','PF07714','E9PB13_HUMAN','637','899'),
('D3DRD6_HUMAN/44-320','PF07714','D3DRD6_HUMAN','44','320'),
('FAK2_HUMAN/425-679','PF07714','FAK2_HUMAN','425','679'),
('INSR_HUMAN/1023-1290','PF07714','INSR_HUMAN','1023','1290'),
('IGF1R_HUMAN/999-1266','PF07714','IGF1R_HUMAN','999','1266'),
('A8KAM8_HUMAN/600-958','PF07714','A8KAM8_HUMAN','600','958'),
('F8TLS5_HUMAN/724-1005','PF07714','F8TLS5_HUMAN','724','1005'),
('Q9UMQ4_HUMAN/700-982','PF07714','Q9UMQ4_HUMAN','700','982'),
('Q59FM9_HUMAN/579-847','PF07714','Q59FM9_HUMAN','579','847'),
('SRC_HUMAN/270-519','PF07714','SRC_HUMAN','270','519'),
('F8W9W0_HUMAN/512-769','PF07714','F8W9W0_HUMAN','512','769'),
('Q59FQ5_HUMAN/12-221','PF07714','Q59FQ5_HUMAN','12','221'),
('B6D4Y2_HUMAN/1116-1383','PF07714','B6D4Y2_HUMAN','1116','1383'),
('B4DH13_HUMAN/117-371','PF07714','B4DH13_HUMAN','117','371'),
('B4E123_HUMAN/644-916','PF07714','B4E123_HUMAN','644','916'),
('Q59F19_HUMAN/62-312','PF07714','Q59F19_HUMAN','62','312'),
('Q4LDX3_HUMAN/863-1136','PF07714','Q4LDX3_HUMAN','863','1136'),
('H0Y9F4_HUMAN/1-228','PF07714','H0Y9F4_HUMAN','1','228'),
('A8K2T6_HUMAN/624-880','PF07714','A8K2T6_HUMAN','624','880'),
('D7PBN3_HUMAN/762-1019','PF07714','D7PBN3_HUMAN','762','1019'),
('A8K910_HUMAN/545-805','PF07714','A8K910_HUMAN','545','805'),
('TEX14_HUMAN/263-509','PF07714','TEX14_HUMAN','263','509'),
('B6D4Y5_HUMAN/1116-1383','PF07714','B6D4Y5_HUMAN','1116','1383'),
('A8K709_HUMAN/417-666','PF07714','A8K709_HUMAN','417','666'),
('B4DQP7_HUMAN/180-439','PF07714','B4DQP7_HUMAN','180','439'),
('Q8IXP2_HUMAN/542-802','PF07714','Q8IXP2_HUMAN','542','802'),
('Q506Q0_HUMAN/849-1123','PF07714','Q506Q0_HUMAN','849','1123'),
('Q0IJ44_HUMAN/146-422','PF07714','Q0IJ44_HUMAN','146','422'),
('B4DY49_HUMAN/92-345','PF07714','B4DY49_HUMAN','92','345'),
('Q2VXS9_HUMAN/498-673','PF07714','Q2VXS9_HUMAN','498','673'),
('MET_HUMAN/1078-1337','PF07714','MET_HUMAN','1078','1337'),
('Q59EB3_HUMAN/400-659','PF07714','Q59EB3_HUMAN','400','659'),
('Q15300_HUMAN/248-529','PF07714','Q15300_HUMAN','248','529'),
('B1AKC9_HUMAN/616-875','PF07714','B1AKC9_HUMAN','616','875'),
('Q8N6J3_HUMAN/146-414','PF07714','Q8N6J3_HUMAN','146','414'),
('B6D4Y1_HUMAN/1116-1383','PF07714','B6D4Y1_HUMAN','1116','1383'),
('PGFRA_HUMAN/593-950','PF07714','PGFRA_HUMAN','593','950'),
('LYN_HUMAN/247-497','PF07714','LYN_HUMAN','247','497'),
('ROR2_HUMAN/473-746','PF07714','ROR2_HUMAN','473','746'),
('B3KSH7_HUMAN/85-355','PF07714','B3KSH7_HUMAN','85','355'),
('E9PJX5_HUMAN/170-419','PF07714','E9PJX5_HUMAN','170','419'),
('A8K4G2_HUMAN/371-626','PF07714','A8K4G2_HUMAN','371','626'),
('F5H5U8_HUMAN/396-656','PF07714','F5H5U8_HUMAN','396','656'),
('Q6P4R6_HUMAN/621-878','PF07714','Q6P4R6_HUMAN','621','878'),
('F8W9L4_HUMAN/473-658','PF07714','F8W9L4_HUMAN','473','658'),
('A8K2T7_HUMAN/712-968','PF07714','A8K2T7_HUMAN','712','968'),
('H0Y3C5_HUMAN/261-510','PF07714','H0Y3C5_HUMAN','261','510'),
('Q8TCG9_HUMAN/17-153','PF07714','Q8TCG9_HUMAN','17','153'),
('E9PD35_HUMAN/845-1169','PF07714','E9PD35_HUMAN','845','1169'),
('B4DV85_HUMAN/176-433','PF07714','B4DV85_HUMAN','176','433'),
('B7Z7U4_HUMAN/440-617','PF07714','B7Z7U4_HUMAN','440','617'),
('SG196_HUMAN/81-225','PF07714','SG196_HUMAN','81','225'),
('F0UY66_HUMAN/1116-1383','PF07714','F0UY66_HUMAN','1116','1383'),
('Q3MS96_HUMAN/73-311','PF07714','Q3MS96_HUMAN','73','311'),
('B4DLF5_HUMAN/648-907','PF07714','B4DLF5_HUMAN','648','907'),
('A8K379_HUMAN/247-497','PF07714','A8K379_HUMAN','247','497'),
('Q5JPC5_HUMAN/208-423','PF07714','Q5JPC5_HUMAN','208','423'),
('Q504U8_HUMAN/667-923','PF07714','Q504U8_HUMAN','667','923'),
('B3KWB3_HUMAN/1-206','PF07714','B3KWB3_HUMAN','1','206'),
('B4DMZ0_HUMAN/116-361','PF07714','B4DMZ0_HUMAN','116','361'),
('A9CB80_HUMAN/712-968','PF07714','A9CB80_HUMAN','712','968'),
('H7BZZ3_HUMAN/44-290','PF07714','H7BZZ3_HUMAN','44','290'),
('H7C3L9_HUMAN/1-178','PF07714','H7C3L9_HUMAN','1','178'),
('Q5U0D0_HUMAN/36-284','PF07714','Q5U0D0_HUMAN','36','284'),
('H7C224_HUMAN/2-267','PF07714','H7C224_HUMAN','2','267'),
('EGFR_HUMAN/712-968','PF07714','EGFR_HUMAN','712','968'),
('B4DTW8_HUMAN/794-1062','PF07714','B4DTW8_HUMAN','794','1062'),
('B4DYR0_HUMAN/177-447','PF07714','B4DYR0_HUMAN','177','447'),
('B2RAW9_HUMAN/310-580','PF07714','B2RAW9_HUMAN','310','580'),
('EPHA6_HUMAN/736-929','PF07714','EPHA6_HUMAN','736','929'),
('B4DR56_HUMAN/253-523','PF07714','B4DR56_HUMAN','253','523'),
('EPHA3_HUMAN/621-878','PF07714','EPHA3_HUMAN','621','878'),
('Q59GN8_HUMAN/342-596','PF07714','Q59GN8_HUMAN','342','596'),
('MERTK_HUMAN/587-854','PF07714','MERTK_HUMAN','587','854'),
('C1PHA0_HUMAN/578-845','PF07714','C1PHA0_HUMAN','578','845'),
('A8K4G3_HUMAN/242-491','PF07714','A8K4G3_HUMAN','242','491'),
('Q7Z635_HUMAN/615-874','PF07714','Q7Z635_HUMAN','615','874'),
('RYK_HUMAN/327-593','PF07714','RYK_HUMAN','327','593'),
('B5BU33_HUMAN/331-601','PF07714','B5BU33_HUMAN','331','601'),
('Q9P0M0_HUMAN/1-149','PF07714','Q9P0M0_HUMAN','1','149'),
('H0Y8A4_HUMAN/310-576','PF07714','H0Y8A4_HUMAN','310','576'),
('Q9NSQ6_HUMAN/108-355','PF07714','Q9NSQ6_HUMAN','108','355'),
('B7Z4Y7_HUMAN/50-280','PF07714','B7Z4Y7_HUMAN','50','280'),
('B4E058_HUMAN/1-220','PF07714','B4E058_HUMAN','1','220'),
('TNK1_HUMAN/116-377','PF07714','TNK1_HUMAN','116','377'),
('TXK_HUMAN/271-520','PF07714','TXK_HUMAN','271','520'),
('RET_HUMAN/724-1005','PF07714','RET_HUMAN','724','1005'),
('EPHA2_HUMAN/613-871','PF07714','EPHA2_HUMAN','613','871'),
('A6P4T4_HUMAN/555-822','PF07714','A6P4T4_HUMAN','555','822'),
('B4DYV1_HUMAN/396-656','PF07714','B4DYV1_HUMAN','396','656'),
('B4DTR1_HUMAN/444-700','PF07714','B4DTR1_HUMAN','444','700'),
('A2ABM8_HUMAN/342-493','PF07714','A2ABM8_HUMAN','342','493'),
('EPHA4_HUMAN/621-878','PF07714','EPHA4_HUMAN','621','878'),
('B4DYV1_HUMAN/700-974','PF07714','B4DYV1_HUMAN','700','974'),
('TYRO3_HUMAN/518-786','PF07714','TYRO3_HUMAN','518','786'),
('GUC2D_HUMAN/552-805','PF07714','GUC2D_HUMAN','552','805'),
('F8WEA9_HUMAN/613-877','PF07714','F8WEA9_HUMAN','613','877'),
('B4E1N6_HUMAN/134-391','PF07714','B4E1N6_HUMAN','134','391'),
('PTK6_HUMAN/191-441','PF07714','PTK6_HUMAN','191','441'),
('B4DQ79_HUMAN/158-408','PF07714','B4DQ79_HUMAN','158','408'),
('TIE1_HUMAN/839-1107','PF07714','TIE1_HUMAN','839','1107'),
('F1JU33_HUMAN/5-256','PF07714','F1JU33_HUMAN','5','256'),
('Q59HG2_HUMAN/857-1125','PF07714','Q59HG2_HUMAN','857','1125'),
('E9PM19_HUMAN/712-984','PF07714','E9PM19_HUMAN','712','984'),
('RON_HUMAN/1082-1341','PF07714','RON_HUMAN','1082','1341'),
('B4DFN2_HUMAN/1-226','PF07714','B4DFN2_HUMAN','1','226'),
('E7ESA6_HUMAN/466-720','PF07714','E7ESA6_HUMAN','466','720'),
('JAK3_HUMAN/822-1095','PF07714','JAK3_HUMAN','822','1095'),
('ABL2_HUMAN/288-539','PF07714','ABL2_HUMAN','288','539'),
('B4DUD9_HUMAN/543-796','PF07714','B4DUD9_HUMAN','543','796'),
('H7C175_HUMAN/78-348','PF07714','H7C175_HUMAN','78','348'),
('D7PBN4_HUMAN/20-277','PF07714','D7PBN4_HUMAN','20','277'),
('B2RA70_HUMAN/277-526','PF07714','B2RA70_HUMAN','277','526'),
('Q658W2_HUMAN/444-698','PF07714','Q658W2_HUMAN','444','698'),
('H3BPR7_HUMAN/1-244','PF07714','H3BPR7_HUMAN','1','244'),
('EPHB3_HUMAN/633-892','PF07714','EPHB3_HUMAN','633','892'),
('Q6NUK7_HUMAN/317-567','PF07714','Q6NUK7_HUMAN','317','567'),
('TEC_HUMAN/370-619','PF07714','TEC_HUMAN','370','619'),
('Q59F17_HUMAN/614-873','PF07714','Q59F17_HUMAN','614','873'),
('B7Z6Q8_HUMAN/570-827','PF07714','B7Z6Q8_HUMAN','570','827'),
('Q573B4_HUMAN/261-501','PF07714','Q573B4_HUMAN','261','501'),
('YES_HUMAN/277-526','PF07714','YES_HUMAN','277','526'),
('A9YLN6_HUMAN/219-489','PF07714','A9YLN6_HUMAN','219','489'),
('F5H5U8_HUMAN/700-974','PF07714','F5H5U8_HUMAN','700','974'),
('VGFR2_HUMAN/834-1160','PF07714','VGFR2_HUMAN','834','1160'),
('Q59FT4_HUMAN/689-946','PF07714','Q59FT4_HUMAN','689','946'),
('EPHAA_HUMAN/645-900','PF07714','EPHAA_HUMAN','645','900'),
('ALK_HUMAN/1116-1383','PF07714','ALK_HUMAN','1116','1383'),
('A9YLN7_HUMAN/292-559','PF07714','A9YLN7_HUMAN','292','559'),
('G5EKE5_HUMAN/307-574','PF07714','G5EKE5_HUMAN','307','574'),
('A8K297_HUMAN/339-604','PF07714','A8K297_HUMAN','339','604'),
('A9YLN4_HUMAN/301-571','PF07714','A9YLN4_HUMAN','301','571'),
('Q9P0L5_HUMAN/1-166','PF07714','Q9P0L5_HUMAN','1','166'),
('KSYK_HUMAN/371-626','PF07714','KSYK_HUMAN','371','626'),
('Q96L35_HUMAN/615-874','PF07714','Q96L35_HUMAN','615','874'),
('F5H3M4_HUMAN/197-446','PF07714','F5H3M4_HUMAN','197','446'),
('ANPRB_HUMAN/518-786','PF07714','ANPRB_HUMAN','518','786'),
('A8K910_HUMAN/849-1123','PF07714','A8K910_HUMAN','849','1123'),
('B2R601_HUMAN/621-878','PF07714','B2R601_HUMAN','621','878'),
('Q53HA9_HUMAN/589-822','PF07714','Q53HA9_HUMAN','589','822'),
('B3XZL9_HUMAN/281-548','PF07714','B3XZL9_HUMAN','281','548'),
('Q8NI15_HUMAN/435-711','PF07714','Q8NI15_HUMAN','435','711'),
('BLK_HUMAN/241-490','PF07714','BLK_HUMAN','241','490'),
('H7C459_HUMAN/2-152','PF07714','H7C459_HUMAN','2','152'),
('Q59F04_HUMAN/271-629','PF07714','Q59F04_HUMAN','271','629'),
('D3DRD3_HUMAN/384-660','PF07714','D3DRD3_HUMAN','384','660'),
('A1L4F5_HUMAN/473-746','PF07714','A1L4F5_HUMAN','473','746'),
('C9JXA2_HUMAN/621-878','PF07714','C9JXA2_HUMAN','621','878'),
('DDR1_HUMAN/610-905','PF07714','DDR1_HUMAN','610','905'),
('B4DIA4_HUMAN/1-264','PF07714','B4DIA4_HUMAN','1','264'),
('B4DGF4_HUMAN/1-184','PF07714','B4DGF4_HUMAN','1','184'),
('B4DVP5_HUMAN/399-675','PF07714','B4DVP5_HUMAN','399','675'),
('B6D4Y6_HUMAN/1116-1383','PF07714','B6D4Y6_HUMAN','1116','1383'),
('B7ZKW7_HUMAN/654-911','PF07714','B7ZKW7_HUMAN','654','911'),
('B6EXY5_HUMAN/167-434','PF07714','B6EXY5_HUMAN','167','434'),
('B3KPS6_HUMAN/219-468','PF07714','B3KPS6_HUMAN','219','468'),
('ITK_HUMAN/363-612','PF07714','ITK_HUMAN','363','612'),
('H7BXU9_HUMAN/390-666','PF07714','H7BXU9_HUMAN','390','666'),
('Q59FK4_HUMAN/279-530','PF07714','Q59FK4_HUMAN','279','530'),
('MLKL_HUMAN/209-466','PF07714','MLKL_HUMAN','209','466'),
('Q8N9D7_HUMAN/90-344','PF07714','Q8N9D7_HUMAN','90','344'),
('E9PG63_HUMAN/484-752','PF07714','E9PG63_HUMAN','484','752'),
('LTK_HUMAN/510-777','PF07714','LTK_HUMAN','510','777'),
('C9JQR6_HUMAN/64-257','PF07714','C9JQR6_HUMAN','64','257'),
('ERBB2_HUMAN/720-976','PF07714','ERBB2_HUMAN','720','976'),
('B2R8C2_HUMAN/234-487','PF07714','B2R8C2_HUMAN','234','487'),
('FAK1_HUMAN/422-676','PF07714','FAK1_HUMAN','422','676'),
('Q8WTZ8_HUMAN/118-384','PF07714','Q8WTZ8_HUMAN','118','384'),
('B4DTB5_HUMAN/3-207','PF07714','B4DTB5_HUMAN','3','207'),
('Q5IBP5_HUMAN/1183-1440','PF07714','Q5IBP5_HUMAN','1183','1440'),
('B7ZKJ3_HUMAN/676-933','PF07714','B7ZKJ3_HUMAN','676','933'),
('F5H0K8_HUMAN/591-855','PF07714','F5H0K8_HUMAN','591','855'),
('FYN_HUMAN/271-520','PF07714','FYN_HUMAN','271','520'),
('C7TPG7_HUMAN/532-789','PF07714','C7TPG7_HUMAN','532','789'),
('Q9P0L7_HUMAN/1-166','PF07714','Q9P0L7_HUMAN','1','166'),
('CSF1R_HUMAN/582-910','PF07714','CSF1R_HUMAN','582','910'),
('A6NJF2_HUMAN/1-138','PF07714','A6NJF2_HUMAN','1','138'),
('EPHA8_HUMAN/635-892','PF07714','EPHA8_HUMAN','635','892'),
('H2E272_HUMAN/7-195','PF07714','H2E272_HUMAN','7','195'),
('B1APY4_HUMAN/333-606','PF07714','B1APY4_HUMAN','333','606'),
('B4DGX8_HUMAN/470-751','PF07714','B4DGX8_HUMAN','470','751'),
('Q96II5_HUMAN/313-570','PF07714','Q96II5_HUMAN','313','570'),
('Q96HF4_HUMAN/1-148','PF07714','Q96HF4_HUMAN','1','148'),
('CSK_HUMAN/195-440','PF07714','CSK_HUMAN','195','440'),
('EPHB2_HUMAN/621-880','PF07714','EPHB2_HUMAN','621','880'),
('B4E110_HUMAN/16-214','PF07714','B4E110_HUMAN','16','214'),
('JAK1_HUMAN/875-1149','PF07714','JAK1_HUMAN','875','1149'),
('D1MAM2_HUMAN/1116-1383','PF07714','D1MAM2_HUMAN','1116','1383'),
('B4DL04_HUMAN/291-549','PF07714','B4DL04_HUMAN','291','549'),
('B4DKW0_HUMAN/484-752','PF07714','B4DKW0_HUMAN','484','752'),
('TYK2_HUMAN/589-866','PF07714','TYK2_HUMAN','589','866'),
('EPHA7_HUMAN/633-890','PF07714','EPHA7_HUMAN','633','890'),
('F5GWP9_HUMAN/1-226','PF07714','F5GWP9_HUMAN','1','226'),
('Q58F15_HUMAN/621-878','PF07714','Q58F15_HUMAN','621','878'),
('A8MY87_HUMAN/476-740','PF07714','A8MY87_HUMAN','476','740'),
('Q59F30_HUMAN/699-975','PF07714','Q59F30_HUMAN','699','975'),
('Q9P0L6_HUMAN/1-166','PF07714','Q9P0L6_HUMAN','1','166'),
('KSR2_HUMAN/666-928','PF07714','KSR2_HUMAN','666','928'),
('B4DFQ0_HUMAN/1-253','PF07714','B4DFQ0_HUMAN','1','253'),
('D1MAM1_HUMAN/1116-1383','PF07714','D1MAM1_HUMAN','1116','1383'),
('Q59FX2_HUMAN/82-249','PF00069','Q59FX2_HUMAN','82','249'),
('TAOK2_HUMAN/28-281','PF00069','TAOK2_HUMAN','28','281'),
('MK14_HUMAN/24-308','PF00069','MK14_HUMAN','24','308'),
('Q9H4D1_HUMAN/22-283','PF00069','Q9H4D1_HUMAN','22','283'),
('Q6E0B2_HUMAN/15-210','PF00069','Q6E0B2_HUMAN','15','210'),
('B7ZMH9_HUMAN/198-456','PF00069','B7ZMH9_HUMAN','198','456'),
('H0YF68_HUMAN/4-175','PF00069','H0YF68_HUMAN','4','175'),
('TTBK2_HUMAN/21-266','PF00069','TTBK2_HUMAN','21','266'),
('LATS2_HUMAN/668-833','PF00069','LATS2_HUMAN','668','833'),
('CTRO_HUMAN/97-360','PF00069','CTRO_HUMAN','97','360'),
('CDK15_HUMAN/103-387','PF00069','CDK15_HUMAN','103','387'),
('Q6IAW3_HUMAN/4-286','PF00069','Q6IAW3_HUMAN','4','286'),
('B4DXU2_HUMAN/111-353','PF00069','B4DXU2_HUMAN','111','353'),
('B7Z3V5_HUMAN/25-289','PF00069','B7Z3V5_HUMAN','25','289'),
('OBSCN_HUMAN/7672-7924','PF00069','OBSCN_HUMAN','7672','7924'),
('B4DLF9_HUMAN/33-291','PF00069','B4DLF9_HUMAN','33','291'),
('NTKL_HUMAN/32-246','PF00069','NTKL_HUMAN','32','246'),
('B4E104_HUMAN/1-183','PF00069','B4E104_HUMAN','1','183'),
('E2AK3_HUMAN/863-1077','PF00069','E2AK3_HUMAN','863','1077'),
('Q6FI27_HUMAN/56-340','PF00069','Q6FI27_HUMAN','56','340'),
('AURKA_HUMAN/133-383','PF00069','AURKA_HUMAN','133','383'),
('F8W872_HUMAN/7-276','PF00069','F8W872_HUMAN','7','276'),
('Q32ND9_HUMAN/15-297','PF00069','Q32ND9_HUMAN','15','297'),
('E5RI85_HUMAN/4-144','PF00069','E5RI85_HUMAN','4','144'),
('IKKE_HUMAN/9-301','PF00069','IKKE_HUMAN','9','301'),
('E9PLM7_HUMAN/1-210','PF00069','E9PLM7_HUMAN','1','210'),
('CSK21_HUMAN/39-324','PF00069','CSK21_HUMAN','39','324'),
('H0Y894_HUMAN/374-630','PF00069','H0Y894_HUMAN','374','630'),
('Q15136_HUMAN/27-204','PF00069','Q15136_HUMAN','27','204'),
('MAST2_HUMAN/512-785','PF00069','MAST2_HUMAN','512','785'),
('C9JCC0_HUMAN/1-162','PF00069','C9JCC0_HUMAN','1','162'),
('B7Z2B0_HUMAN/14-272','PF00069','B7Z2B0_HUMAN','14','272'),
('A8MPP7_HUMAN/37-186','PF00069','A8MPP7_HUMAN','37','186'),
('B4DVS7_HUMAN/5-196','PF00069','B4DVS7_HUMAN','5','196'),
('LRRK2_HUMAN/1882-2132','PF00069','LRRK2_HUMAN','1882','2132'),
('SBK2_HUMAN/62-329','PF00069','SBK2_HUMAN','62','329'),
('E9PJN1_HUMAN/33-301','PF00069','E9PJN1_HUMAN','33','301'),
('Q5U045_HUMAN/9-280','PF00069','Q5U045_HUMAN','9','280'),
('BRSK2_HUMAN/19-270','PF00069','BRSK2_HUMAN','19','270'),
('B7Z2X1_HUMAN/29-289','PF00069','B7Z2X1_HUMAN','29','289'),
('Q5TBH0_HUMAN/29-200','PF00069','Q5TBH0_HUMAN','29','200'),
('E2AK4_HUMAN/315-539','PF00069','E2AK4_HUMAN','315','539'),
('B2RAJ6_HUMAN/26-312','PF00069','B2RAJ6_HUMAN','26','312'),
('B7ZAN7_HUMAN/29-295','PF00069','B7ZAN7_HUMAN','29','295'),
('TSSK6_HUMAN/12-267','PF00069','TSSK6_HUMAN','12','267'),
('Q6NSL2_HUMAN/299-569','PF00069','Q6NSL2_HUMAN','299','569'),
('ARBK2_HUMAN/191-453','PF00069','ARBK2_HUMAN','191','453'),
('KS6A5_HUMAN/427-687','PF00069','KS6A5_HUMAN','427','687'),
('IRAK1_HUMAN/212-518','PF00069','IRAK1_HUMAN','212','518'),
('F8WBA3_HUMAN/593-847','PF00069','F8WBA3_HUMAN','593','847'),
('Q5QPD4_HUMAN/133-271','PF00069','Q5QPD4_HUMAN','133','271'),
('F8VZZ0_HUMAN/2-174','PF00069','F8VZZ0_HUMAN','2','174'),
('Q5H9N4_HUMAN/4-293','PF00069','Q5H9N4_HUMAN','4','293'),
('M3K9_HUMAN/144-404','PF00069','M3K9_HUMAN','144','404'),
('Q6FG83_HUMAN/33-293','PF00069','Q6FG83_HUMAN','33','293'),
('B4DGP5_HUMAN/139-420','PF00069','B4DGP5_HUMAN','139','420'),
('MP2K7_HUMAN/120-380','PF00069','MP2K7_HUMAN','120','380'),
('A8MPY5_HUMAN/79-228','PF00069','A8MPY5_HUMAN','79','228'),
('STK36_HUMAN/4-254','PF00069','STK36_HUMAN','4','254'),
('C9J9E2_HUMAN/24-286','PF00069','C9J9E2_HUMAN','24','286'),
('B1APG2_HUMAN/39-209','PF00069','B1APG2_HUMAN','39','209'),
('DYRK3_HUMAN/209-522','PF00069','DYRK3_HUMAN','209','522'),
('B4DUB1_HUMAN/27-211','PF00069','B4DUB1_HUMAN','27','211'),
('Q5Y191_HUMAN/40-290','PF00069','Q5Y191_HUMAN','40','290'),
('Q8N774_HUMAN/1-180','PF00069','Q8N774_HUMAN','1','180'),
('HIPK2_HUMAN/199-527','PF00069','HIPK2_HUMAN','199','527'),
('B7Z9H7_HUMAN/23-281','PF00069','B7Z9H7_HUMAN','23','281'),
('E7EN07_HUMAN/30-316','PF00069','E7EN07_HUMAN','30','316'),
('OXSR1_HUMAN/17-291','PF00069','OXSR1_HUMAN','17','291'),
('Q2TU65_HUMAN/18-290','PF00069','Q2TU65_HUMAN','18','290'),
('M3K5_HUMAN/682-938','PF00069','M3K5_HUMAN','682','938'),
('E9PC69_HUMAN/53-304','PF00069','E9PC69_HUMAN','53','304'),
('D2JYI1_HUMAN/269-563','PF00069','D2JYI1_HUMAN','269','563'),
('MYLK4_HUMAN/106-361','PF00069','MYLK4_HUMAN','106','361'),
('F8WBF5_HUMAN/161-355','PF00069','F8WBF5_HUMAN','161','355'),
('E7ER02_HUMAN/712-926','PF00069','E7ER02_HUMAN','712','926'),
('KKCC2_HUMAN/165-446','PF00069','KKCC2_HUMAN','165','446'),
('KS6A1_HUMAN/62-321','PF00069','KS6A1_HUMAN','62','321'),
('B5MC51_HUMAN/253-471','PF00069','B5MC51_HUMAN','253','471'),
('A5YM56_HUMAN/375-634','PF00069','A5YM56_HUMAN','375','634'),
('B5BUB8_HUMAN/26-321','PF00069','B5BUB8_HUMAN','26','321'),
('C9JV82_HUMAN/23-163','PF00069','C9JV82_HUMAN','23','163'),
('E7EWQ5_HUMAN/391-664','PF00069','E7EWQ5_HUMAN','391','664'),
('KPCL_HUMAN/355-614','PF00069','KPCL_HUMAN','355','614'),
('E9PIX7_HUMAN/4-259','PF00069','E9PIX7_HUMAN','4','259'),
('C9J338_HUMAN/25-263','PF00069','C9J338_HUMAN','25','263'),
('A9CP04_HUMAN/20-271','PF00069','A9CP04_HUMAN','20','271'),
('H7BYT1_HUMAN/2-223','PF00069','H7BYT1_HUMAN','2','223'),
('M3K4_HUMAN/1343-1601','PF00069','M3K4_HUMAN','1343','1601'),
('B2R841_HUMAN/53-305','PF00069','B2R841_HUMAN','53','305'),
('Q6AI46_HUMAN/366-524','PF00069','Q6AI46_HUMAN','366','524'),
('A8K8B2_HUMAN/80-232','PF00069','A8K8B2_HUMAN','80','232'),
('MK03_HUMAN/42-330','PF00069','MK03_HUMAN','42','330'),
('KS6B2_HUMAN/67-328','PF00069','KS6B2_HUMAN','67','328'),
('B4DQN3_HUMAN/1-153','PF00069','B4DQN3_HUMAN','1','153'),
('Q86V37_HUMAN/212-465','PF00069','Q86V37_HUMAN','212','465'),
('B3KY86_HUMAN/18-264','PF00069','B3KY86_HUMAN','18','264'),
('A4D1G0_HUMAN/13-300','PF00069','A4D1G0_HUMAN','13','300'),
('Q0VG04_HUMAN/20-312','PF00069','Q0VG04_HUMAN','20','312'),
('B7Z2K7_HUMAN/402-594','PF00069','B7Z2K7_HUMAN','402','594'),
('WNK3_HUMAN/147-405','PF00069','WNK3_HUMAN','147','405'),
('B7ZKY2_HUMAN/12-276','PF00069','B7ZKY2_HUMAN','12','276'),
('B4DV95_HUMAN/136-396','PF00069','B4DV95_HUMAN','136','396'),
('BRSK1_HUMAN/34-285','PF00069','BRSK1_HUMAN','34','285'),
('CDK7_HUMAN/12-295','PF00069','CDK7_HUMAN','12','295'),
('Q05DF6_HUMAN/6-261','PF00069','Q05DF6_HUMAN','6','261'),
('NEK6_HUMAN/45-306','PF00069','NEK6_HUMAN','45','306'),
('RK_HUMAN/190-455','PF00069','RK_HUMAN','190','455'),
('B4DMX3_HUMAN/439-682','PF00069','B4DMX3_HUMAN','439','682'),
('TLK1_HUMAN/456-734','PF00069','TLK1_HUMAN','456','734'),
('ARBK1_HUMAN/191-453','PF00069','ARBK1_HUMAN','191','453'),
('GAK_HUMAN/40-313','PF00069','GAK_HUMAN','40','313'),
('B7Z6U2_HUMAN/20-279','PF00069','B7Z6U2_HUMAN','20','279'),
('B4DG79_HUMAN/90-347','PF00069','B4DG79_HUMAN','90','347'),
('B3KUU7_HUMAN/83-399','PF00069','B3KUU7_HUMAN','83','399'),
('Q5JPA7_HUMAN/1-276','PF00069','Q5JPA7_HUMAN','1','276'),
('MK12_HUMAN/27-311','PF00069','MK12_HUMAN','27','311'),
('E9PGT3_HUMAN/62-310','PF00069','E9PGT3_HUMAN','62','310'),
('ULK4_HUMAN/4-280','PF00069','ULK4_HUMAN','4','280'),
('MARK1_HUMAN/60-311','PF00069','MARK1_HUMAN','60','311'),
('A3KFJ0_HUMAN/133-347','PF00069','A3KFJ0_HUMAN','133','347'),
('Q1RLL8_HUMAN/366-524','PF00069','Q1RLL8_HUMAN','366','524'),
('B4DV01_HUMAN/1-182','PF00069','B4DV01_HUMAN','1','182'),
('C9J319_HUMAN/75-211','PF00069','C9J319_HUMAN','75','211'),
('B4DDM0_HUMAN/47-308','PF00069','B4DDM0_HUMAN','47','308'),
('A0PJF8_HUMAN/33-301','PF00069','A0PJF8_HUMAN','33','301'),
('A8K8V9_HUMAN/793-966','PF00069','A8K8V9_HUMAN','793','966'),
('Q6PIN8_HUMAN/28-281','PF00069','Q6PIN8_HUMAN','28','281'),
('F8W9I9_HUMAN/159-479','PF00069','F8W9I9_HUMAN','159','479'),
('B4DWB2_HUMAN/81-343','PF00069','B4DWB2_HUMAN','81','343'),
('KCC1D_HUMAN/23-279','PF00069','KCC1D_HUMAN','23','279'),
('F5H049_HUMAN/25-313','PF00069','F5H049_HUMAN','25','313'),
('KALRN_HUMAN/2683-2937','PF00069','KALRN_HUMAN','2683','2937'),
('KC1D_HUMAN/9-280','PF00069','KC1D_HUMAN','9','280'),
('F5H2M7_HUMAN/221-479','PF00069','F5H2M7_HUMAN','221','479'),
('A8K8J5_HUMAN/23-335','PF00069','A8K8J5_HUMAN','23','335'),
('ST32B_HUMAN/23-283','PF00069','ST32B_HUMAN','23','283'),
('B4DIG8_HUMAN/101-243','PF00069','B4DIG8_HUMAN','101','243'),
('E9PKQ3_HUMAN/9-204','PF00069','E9PKQ3_HUMAN','9','204'),
('B2RD76_HUMAN/166-419','PF00069','B2RD76_HUMAN','166','419'),
('TESK1_HUMAN/57-311','PF00069','TESK1_HUMAN','57','311'),
('Q5QPR3_HUMAN/422-707','PF00069','Q5QPR3_HUMAN','422','707'),
('B0QY34_HUMAN/9-280','PF00069','B0QY34_HUMAN','9','280'),
('STK39_HUMAN/63-337','PF00069','STK39_HUMAN','63','337'),
('KPCD3_HUMAN/577-832','PF00069','KPCD3_HUMAN','577','832'),
('A4D160_HUMAN/770-943','PF00069','A4D160_HUMAN','770','943'),
('Q8IWY7_HUMAN/28-246','PF00069','Q8IWY7_HUMAN','28','246'),
('D3DUX0_HUMAN/25-307','PF00069','D3DUX0_HUMAN','25','307'),
('B4DQK5_HUMAN/23-238','PF00069','B4DQK5_HUMAN','23','238'),
('Q6FG81_HUMAN/24-274','PF00069','Q6FG81_HUMAN','24','274'),
('B4DW31_HUMAN/60-307','PF00069','B4DW31_HUMAN','60','307'),
('PACE1_HUMAN/25-277','PF00069','PACE1_HUMAN','25','277'),
('B4DDN2_HUMAN/1-139','PF00069','B4DDN2_HUMAN','1','139'),
('Q9NT28_HUMAN/1-270','PF00069','Q9NT28_HUMAN','1','270'),
('B4E0A7_HUMAN/6-237','PF00069','B4E0A7_HUMAN','6','237'),
('H0Y630_HUMAN/1-192','PF00069','H0Y630_HUMAN','1','192'),
('STK24_HUMAN/36-286','PF00069','STK24_HUMAN','36','286'),
('E9PS17_HUMAN/32-246','PF00069','E9PS17_HUMAN','32','246'),
('Q59FL1_HUMAN/192-480','PF00069','Q59FL1_HUMAN','192','480'),
('E7EPE6_HUMAN/439-682','PF00069','E7EPE6_HUMAN','439','682'),
('B4E3B5_HUMAN/78-328','PF00069','B4E3B5_HUMAN','78','328'),
('KCC2G_HUMAN/14-272','PF00069','KCC2G_HUMAN','14','272'),
('Q5JPB0_HUMAN/4-252','PF00069','Q5JPB0_HUMAN','4','252'),
('Q96T11_HUMAN/22-283','PF00069','Q96T11_HUMAN','22','283'),
('B9EGA7_HUMAN/77-343','PF00069','B9EGA7_HUMAN','77','343'),
('F5H5C4_HUMAN/351-604','PF00069','F5H5C4_HUMAN','351','604'),
('PASK_HUMAN/999-1251','PF00069','PASK_HUMAN','999','1251'),
('Q4G0X2_HUMAN/21-246','PF00069','Q4G0X2_HUMAN','21','246'),
('ST17B_HUMAN/33-293','PF00069','ST17B_HUMAN','33','293'),
('PI3R4_HUMAN/26-312','PF00069','PI3R4_HUMAN','26','312'),
('CD11A_HUMAN/426-711','PF00069','CD11A_HUMAN','426','711'),
('KC1AL_HUMAN/17-292','PF00069','KC1AL_HUMAN','17','292'),
('E7EPP6_HUMAN/111-281','PF00069','E7EPP6_HUMAN','111','281'),
('SIK3_HUMAN/8-259','PF00069','SIK3_HUMAN','8','259'),
('B5BU16_HUMAN/53-314','PF00069','B5BU16_HUMAN','53','314'),
('H3BPI9_HUMAN/1-163','PF00069','H3BPI9_HUMAN','1','163'),
('F5H0U9_HUMAN/21-287','PF00069','F5H0U9_HUMAN','21','287'),
('B7Z7V7_HUMAN/783-1035','PF00069','B7Z7V7_HUMAN','783','1035'),
('B2RA25_HUMAN/16-268','PF00069','B2RA25_HUMAN','16','268'),
('CDK19_HUMAN/23-335','PF00069','CDK19_HUMAN','23','335'),
('STK25_HUMAN/20-270','PF00069','STK25_HUMAN','20','270'),
('KC1A_HUMAN/17-293','PF00069','KC1A_HUMAN','17','293'),
('B5BUC0_HUMAN/56-340','PF00069','B5BUC0_HUMAN','56','340'),
('Q6ZN64_HUMAN/25-278','PF00069','Q6ZN64_HUMAN','25','278'),
('KS6A4_HUMAN/33-301','PF00069','KS6A4_HUMAN','33','301'),
('B2RCU6_HUMAN/268-519','PF00069','B2RCU6_HUMAN','268','519'),
('Q9BRG8_HUMAN/2-318','PF00069','Q9BRG8_HUMAN','2','318'),
('KKCC1_HUMAN/128-409','PF00069','KKCC1_HUMAN','128','409'),
('PKN1_HUMAN/615-874','PF00069','PKN1_HUMAN','615','874'),
('F5GWT4_HUMAN/221-479','PF00069','F5GWT4_HUMAN','221','479'),
('A5YM46_HUMAN/468-729','PF00069','A5YM46_HUMAN','468','729'),
('C9J840_HUMAN/25-171','PF00069','C9J840_HUMAN','25','171'),
('F5GYC4_HUMAN/392-649','PF00069','F5GYC4_HUMAN','392','649'),
('WEE1_HUMAN/299-569','PF00069','WEE1_HUMAN','299','569'),
('A9NIU4_HUMAN/460-713','PF00069','A9NIU4_HUMAN','460','713'),
('MST4_HUMAN/24-274','PF00069','MST4_HUMAN','24','274'),
('TOPK_HUMAN/33-318','PF00069','TOPK_HUMAN','33','318'),
('E9PF82_HUMAN/14-272','PF00069','E9PF82_HUMAN','14','272'),
('B4DTG1_HUMAN/91-329','PF00069','B4DTG1_HUMAN','91','329'),
('CDK14_HUMAN/135-419','PF00069','CDK14_HUMAN','135','419'),
('B4DH08_HUMAN/4-287','PF00069','B4DH08_HUMAN','4','287'),
('Q2TB16_HUMAN/22-283','PF00069','Q2TB16_HUMAN','22','283'),
('B4E2S6_HUMAN/126-368','PF00069','B4E2S6_HUMAN','126','368'),
('C9JMC3_HUMAN/106-361','PF00069','C9JMC3_HUMAN','106','361'),
('PHKG2_HUMAN/24-291','PF00069','PHKG2_HUMAN','24','291'),
('B7Z5H7_HUMAN/36-196','PF00069','B7Z5H7_HUMAN','36','196'),
('B4DJG4_HUMAN/43-213','PF00069','B4DJG4_HUMAN','43','213'),
('MAPK3_HUMAN/44-304','PF00069','MAPK3_HUMAN','44','304'),
('SRPK2_HUMAN/81-230','PF00069','SRPK2_HUMAN','81','230'),
('MAST3_HUMAN/367-640','PF00069','MAST3_HUMAN','367','640'),
('B5BU53_HUMAN/19-315','PF00069','B5BU53_HUMAN','19','315'),
('B7ZB17_HUMAN/40-299','PF00069','B7ZB17_HUMAN','40','299'),
('D6REC6_HUMAN/1-149','PF00069','D6REC6_HUMAN','1','149'),
('Q32NE9_HUMAN/103-357','PF00069','Q32NE9_HUMAN','103','357'),
('MK15_HUMAN/13-304','PF00069','MK15_HUMAN','13','304'),
('Q59FC5_HUMAN/231-547','PF00069','Q59FC5_HUMAN','231','547'),
('F8VZ51_HUMAN/2-208','PF00069','F8VZ51_HUMAN','2','208'),
('KS6B1_HUMAN/91-352','PF00069','KS6B1_HUMAN','91','352'),
('H7C5L6_HUMAN/119-293','PF00069','H7C5L6_HUMAN','119','293'),
('Q05CR6_HUMAN/29-312','PF00069','Q05CR6_HUMAN','29','312'),
('D3DPA4_HUMAN/208-495','PF00069','D3DPA4_HUMAN','208','495'),
('PXK_HUMAN/186-479','PF00069','PXK_HUMAN','186','479'),
('B1AVT0_HUMAN/161-477','PF00069','B1AVT0_HUMAN','161','477'),
('F8W998_HUMAN/12-276','PF00069','F8W998_HUMAN','12','276'),
('B7Z9Y5_HUMAN/1-249','PF00069','B7Z9Y5_HUMAN','1','249'),
('B7Z708_HUMAN/1-216','PF00069','B7Z708_HUMAN','1','216'),
('B4DY26_HUMAN/136-423','PF00069','B4DY26_HUMAN','136','423'),
('Q4VAU9_HUMAN/1-269','PF00069','Q4VAU9_HUMAN','1','269'),
('Q5R3E4_HUMAN/25-298','PF00069','Q5R3E4_HUMAN','25','298'),
('B4DDG2_HUMAN/1-153','PF00069','B4DDG2_HUMAN','1','153'),
('MOK_HUMAN/4-285','PF00069','MOK_HUMAN','4','285'),
('H7C041_HUMAN/451-697','PF00069','H7C041_HUMAN','451','697'),
('Q17RV3_HUMAN/1882-2132','PF00069','Q17RV3_HUMAN','1882','2132'),
('A8K5P5_HUMAN/16-269','PF00069','A8K5P5_HUMAN','16','269'),
('SBK1_HUMAN/53-315','PF00069','SBK1_HUMAN','53','315'),
('B4E083_HUMAN/1-208','PF00069','B4E083_HUMAN','1','208'),
('PDK1L_HUMAN/8-328','PF00069','PDK1L_HUMAN','8','328'),
('SGK1_HUMAN/98-355','PF00069','SGK1_HUMAN','98','355'),
('G3V105_HUMAN/15-296','PF00069','G3V105_HUMAN','15','296'),
('KC1G3_HUMAN/43-308','PF00069','KC1G3_HUMAN','43','308'),
('B2R9M8_HUMAN/23-283','PF00069','B2R9M8_HUMAN','23','283'),
('A4D1R9_HUMAN/1-144','PF00069','A4D1R9_HUMAN','1','144'),
('KCC1A_HUMAN/20-276','PF00069','KCC1A_HUMAN','20','276'),
('E7EWI5_HUMAN/486-740','PF00069','E7EWI5_HUMAN','486','740'),
('CDKL1_HUMAN/4-287','PF00069','CDKL1_HUMAN','4','287'),
('B3KU51_HUMAN/186-459','PF00069','B3KU51_HUMAN','186','459'),
('F8WA18_HUMAN/1-172','PF00069','F8WA18_HUMAN','1','172'),
('D3DUP1_HUMAN/221-479','PF00069','D3DUP1_HUMAN','221','479'),
('F5H5M9_HUMAN/25-289','PF00069','F5H5M9_HUMAN','25','289'),
('B7Z8N6_HUMAN/1-251','PF00069','B7Z8N6_HUMAN','1','251'),
('B4DZC9_HUMAN/25-269','PF00069','B4DZC9_HUMAN','25','269'),
('A6NK28_HUMAN/8-229','PF00069','A6NK28_HUMAN','8','229'),
('B4DMM9_HUMAN/105-342','PF00069','B4DMM9_HUMAN','105','342'),
('TNIK_HUMAN/25-289','PF00069','TNIK_HUMAN','25','289'),
('M4K2_HUMAN/16-273','PF00069','M4K2_HUMAN','16','273'),
('C9JWR9_HUMAN/82-239','PF00069','C9JWR9_HUMAN','82','239'),
('NUAK2_HUMAN/53-303','PF00069','NUAK2_HUMAN','53','303'),
('F5GZ00_HUMAN/34-233','PF00069','F5GZ00_HUMAN','34','233'),
('H0Y411_HUMAN/2289-2539','PF00069','H0Y411_HUMAN','2289','2539'),
('B4DER5_HUMAN/55-336','PF00069','B4DER5_HUMAN','55','336'),
('H0YME5_HUMAN/565-779','PF00069','H0YME5_HUMAN','565','779'),
('F8W9F9_HUMAN/195-453','PF00069','F8W9F9_HUMAN','195','453'),
('TAOK3_HUMAN/24-277','PF00069','TAOK3_HUMAN','24','277'),
('UHMK1_HUMAN/23-304','PF00069','UHMK1_HUMAN','23','304'),
('Q8NBY1_HUMAN/24-274','PF00069','Q8NBY1_HUMAN','24','274'),
('H0Y7T5_HUMAN/191-449','PF00069','H0Y7T5_HUMAN','191','449'),
('Q8N7M6_HUMAN/75-327','PF00069','Q8N7M6_HUMAN','75','327'),
('B7Z2Y5_HUMAN/348-608','PF00069','B7Z2Y5_HUMAN','348','608'),
('KPCG_HUMAN/351-604','PF00069','KPCG_HUMAN','351','604'),
('B4DG22_HUMAN/40-299','PF00069','B4DG22_HUMAN','40','299'),
('SPEG_HUMAN/2966-3218','PF00069','SPEG_HUMAN','2966','3218'),
('F8W1R9_HUMAN/209-381','PF00069','F8W1R9_HUMAN','209','381'),
('Q8N2N5_HUMAN/1-176','PF00069','Q8N2N5_HUMAN','1','176'),
('ULK1_HUMAN/16-278','PF00069','ULK1_HUMAN','16','278'),
('B4E0K5_HUMAN/1-231','PF00069','B4E0K5_HUMAN','1','231'),
('NLK_HUMAN/138-427','PF00069','NLK_HUMAN','138','427'),
('C9JCU6_HUMAN/16-179','PF00069','C9JCU6_HUMAN','16','179'),
('Q59GD0_HUMAN/65-248','PF00069','Q59GD0_HUMAN','65','248'),
('A4QPA9_HUMAN/68-361','PF00069','A4QPA9_HUMAN','68','361'),
('Q96CA8_HUMAN/107-392','PF00069','Q96CA8_HUMAN','107','392'),
('STK4_HUMAN/30-281','PF00069','STK4_HUMAN','30','281'),
('C9J6L2_HUMAN/2-160','PF00069','C9J6L2_HUMAN','2','160'),
('M4K1_HUMAN/17-274','PF00069','M4K1_HUMAN','17','274'),
('E9PRU3_HUMAN/1-175','PF00069','E9PRU3_HUMAN','1','175'),
('AAK1_HUMAN/46-312','PF00069','AAK1_HUMAN','46','312'),
('B3KP61_HUMAN/53-310','PF00069','B3KP61_HUMAN','53','310'),
('BUB1_HUMAN/787-1033','PF00069','BUB1_HUMAN','787','1033'),
('B4DZE2_HUMAN/71-339','PF00069','B4DZE2_HUMAN','71','339'),
('KPCD2_HUMAN/553-807','PF00069','KPCD2_HUMAN','553','807'),
('Q5TBH2_HUMAN/45-220','PF00069','Q5TBH2_HUMAN','45','220'),
('B4E2L0_HUMAN/91-345','PF00069','B4E2L0_HUMAN','91','345'),
('D3DTD6_HUMAN/1-161','PF00069','D3DTD6_HUMAN','1','161'),
('H0Y9X2_HUMAN/2-139','PF00069','H0Y9X2_HUMAN','2','139'),
('NRBP_HUMAN/80-327','PF00069','NRBP_HUMAN','80','327'),
('H7C4V0_HUMAN/3-235','PF00069','H7C4V0_HUMAN','3','235'),
('C9J185_HUMAN/742-956','PF00069','C9J185_HUMAN','742','956'),
('TRIO_HUMAN/2796-3050','PF00069','TRIO_HUMAN','2796','3050'),
('MK11_HUMAN/24-308','PF00069','MK11_HUMAN','24','308'),
('B2RB89_HUMAN/44-298','PF00069','B2RB89_HUMAN','44','298'),
('MK09_HUMAN/26-321','PF00069','MK09_HUMAN','26','321'),
('B4DF67_HUMAN/527-783','PF00069','B4DF67_HUMAN','527','783'),
('AVR2B_HUMAN/190-478','PF00069','AVR2B_HUMAN','190','478'),
('B4E3D9_HUMAN/415-700','PF00069','B4E3D9_HUMAN','415','700'),
('DCLK3_HUMAN/356-613','PF00069','DCLK3_HUMAN','356','613'),
('LATS1_HUMAN/705-879','PF00069','LATS1_HUMAN','705','879'),
('G3V202_HUMAN/4-257','PF00069','G3V202_HUMAN','4','257'),
('A8K730_HUMAN/24-308','PF00069','A8K730_HUMAN','24','308'),
('A0JLR0_HUMAN/150-423','PF00069','A0JLR0_HUMAN','150','423'),
('GRK7_HUMAN/191-449','PF00069','GRK7_HUMAN','191','449'),
('B7ZKK7_HUMAN/267-535','PF00069','B7ZKK7_HUMAN','267','535'),
('ULK3_HUMAN/14-270','PF00069','ULK3_HUMAN','14','270'),
('A8K8I6_HUMAN/39-186','PF00069','A8K8I6_HUMAN','39','186'),
('MK08_HUMAN/26-321','PF00069','MK08_HUMAN','26','321'),
('F8VYH9_HUMAN/6-170','PF00069','F8VYH9_HUMAN','6','170'),
('F2Z3C8_HUMAN/35-282','PF00069','F2Z3C8_HUMAN','35','282'),
('Q5JXL9_HUMAN/4-142','PF00069','Q5JXL9_HUMAN','4','142'),
('Q96E92_HUMAN/18-196','PF00069','Q96E92_HUMAN','18','196'),
('RIPK3_HUMAN/21-283','PF00069','RIPK3_HUMAN','21','283'),
('B4DUC2_HUMAN/408-687','PF00069','B4DUC2_HUMAN','408','687'),
('E9PRI4_HUMAN/402-659','PF00069','E9PRI4_HUMAN','402','659'),
('Q6P5Y5_HUMAN/118-403','PF00069','Q6P5Y5_HUMAN','118','403'),
('F8WCQ3_HUMAN/13-186','PF00069','F8WCQ3_HUMAN','13','186'),
('HASP_HUMAN/484-699','PF00069','HASP_HUMAN','484','699'),
('B4E0Y9_HUMAN/24-296','PF00069','B4E0Y9_HUMAN','24','296'),
('A8JZZ5_HUMAN/220-486','PF00069','A8JZZ5_HUMAN','220','486'),
('C9JB09_HUMAN/15-224','PF00069','C9JB09_HUMAN','15','224'),
('SPEG_HUMAN/1601-1854','PF00069','SPEG_HUMAN','1601','1854'),
('F6UYM1_HUMAN/91-329','PF00069','F6UYM1_HUMAN','91','329'),
('B4DXZ7_HUMAN/32-259','PF00069','B4DXZ7_HUMAN','32','259'),
('Q9BWF9_HUMAN/1-234','PF00069','Q9BWF9_HUMAN','1','234'),
('B3KX76_HUMAN/1-142','PF00069','B3KX76_HUMAN','1','142'),
('Q5H8Y5_HUMAN/35-198','PF00069','Q5H8Y5_HUMAN','35','198'),
('MYLK2_HUMAN/285-540','PF00069','MYLK2_HUMAN','285','540'),
('H7C3H0_HUMAN/1-145','PF00069','H7C3H0_HUMAN','1','145'),
('Q2I0Y7_HUMAN/39-324','PF00069','Q2I0Y7_HUMAN','39','324'),
('PIM2_HUMAN/32-286','PF00069','PIM2_HUMAN','32','286'),
('A0JLT6_HUMAN/38-292','PF00069','A0JLT6_HUMAN','38','292'),
('CDK3_HUMAN/4-286','PF00069','CDK3_HUMAN','4','286'),
('IRAK3_HUMAN/165-443','PF00069','IRAK3_HUMAN','165','443'),
('TSSK1_HUMAN/12-272','PF00069','TSSK1_HUMAN','12','272'),
('Q6FG25_HUMAN/140-388','PF00069','Q6FG25_HUMAN','140','388'),
('D6RAD4_HUMAN/98-258','PF00069','D6RAD4_HUMAN','98','258'),
('Q59GL9_HUMAN/13-247','PF00069','Q59GL9_HUMAN','13','247'),
('B3KR49_HUMAN/1-216','PF00069','B3KR49_HUMAN','1','216'),
('B4DFV1_HUMAN/276-530','PF00069','B4DFV1_HUMAN','276','530'),
('D3DPG0_HUMAN/32770-33024','PF00069','D3DPG0_HUMAN','32770','33024'),
('B4DZU0_HUMAN/1-228','PF00069','B4DZU0_HUMAN','1','228'),
('H0YDJ3_HUMAN/267-583','PF00069','H0YDJ3_HUMAN','267','583'),
('A8K3Y2_HUMAN/53-314','PF00069','A8K3Y2_HUMAN','53','314'),
('H0Y9H3_HUMAN/1-272','PF00069','H0Y9H3_HUMAN','1','272'),
('B7Z474_HUMAN/813-1065','PF00069','B7Z474_HUMAN','813','1065'),
('Q53TE4_HUMAN/66-344','PF00069','Q53TE4_HUMAN','66','344'),
('M4K3_HUMAN/16-273','PF00069','M4K3_HUMAN','16','273'),
('Q59FI5_HUMAN/250-452','PF00069','Q59FI5_HUMAN','250','452'),
('C9IYV2_HUMAN/23-189','PF00069','C9IYV2_HUMAN','23','189'),
('Q86VY5_HUMAN/21-246','PF00069','Q86VY5_HUMAN','21','246'),
('HIPK1_HUMAN/190-518','PF00069','HIPK1_HUMAN','190','518'),
('KAPCG_HUMAN/44-298','PF00069','KAPCG_HUMAN','44','298'),
('SGK71_HUMAN/28-297','PF00069','SGK71_HUMAN','28','297'),
('Q5JP05_HUMAN/1-231','PF00069','Q5JP05_HUMAN','1','231'),
('Q5U0E6_HUMAN/24-274','PF00069','Q5U0E6_HUMAN','24','274'),
('AURKB_HUMAN/77-327','PF00069','AURKB_HUMAN','77','327'),
('Q9BRL4_HUMAN/117-398','PF00069','Q9BRL4_HUMAN','117','398'),
('DAPK3_HUMAN/13-275','PF00069','DAPK3_HUMAN','13','275'),
('Q59H88_HUMAN/16-278','PF00069','Q59H88_HUMAN','16','278'),
('Q56A86_HUMAN/148-405','PF00069','Q56A86_HUMAN','148','405'),
('A0ZT98_HUMAN/12-272','PF00069','A0ZT98_HUMAN','12','272'),
('D6R938_HUMAN/14-272','PF00069','D6R938_HUMAN','14','272'),
('F5GYW7_HUMAN/813-1065','PF00069','F5GYW7_HUMAN','813','1065'),
('B7ZB17_HUMAN/394-651','PF00069','B7ZB17_HUMAN','394','651'),
('STRAA_HUMAN/69-379','PF00069','STRAA_HUMAN','69','379'),
('A6NIA0_HUMAN/1-185','PF00069','A6NIA0_HUMAN','1','185'),
('B4DFH4_HUMAN/29-180','PF00069','B4DFH4_HUMAN','29','180'),
('ST32C_HUMAN/93-352','PF00069','ST32C_HUMAN','93','352'),
('CDK5_HUMAN/4-286','PF00069','CDK5_HUMAN','4','286'),
('SRPK2_HUMAN/516-686','PF00069','SRPK2_HUMAN','516','686'),
('GRK5_HUMAN/186-448','PF00069','GRK5_HUMAN','186','448'),
('B3KVF3_HUMAN/10-325','PF00069','B3KVF3_HUMAN','10','325'),
('A8K6N9_HUMAN/14-272','PF00069','A8K6N9_HUMAN','14','272'),
('B5TY33_HUMAN/24-167','PF00069','B5TY33_HUMAN','24','167'),
('B4DM54_HUMAN/68-320','PF00069','B4DM54_HUMAN','68','320'),
('A1L4K2_HUMAN/26-321','PF00069','A1L4K2_HUMAN','26','321'),
('B4DJZ5_HUMAN/21-159','PF00069','B4DJZ5_HUMAN','21','159'),
('NEK1_HUMAN/4-258','PF00069','NEK1_HUMAN','4','258'),
('H0YM36_HUMAN/1-165','PF00069','H0YM36_HUMAN','1','165'),
('Q1PBM3_HUMAN/358-618','PF00069','Q1PBM3_HUMAN','358','618'),
('Q9H5M4_HUMAN/1-174','PF00069','Q9H5M4_HUMAN','1','174'),
('Q75MR0_HUMAN/93-339','PF00069','Q75MR0_HUMAN','93','339'),
('B5BUG9_HUMAN/234-521','PF00069','B5BUG9_HUMAN','234','521'),
('TGFR1_HUMAN/205-492','PF00069','TGFR1_HUMAN','205','492'),
('Q53EZ1_HUMAN/9-279','PF00069','Q53EZ1_HUMAN','9','279'),
('B7ZL90_HUMAN/426-683','PF00069','B7ZL90_HUMAN','426','683'),
('B3KRI8_HUMAN/304-620','PF00069','B3KRI8_HUMAN','304','620'),
('SGK2_HUMAN/95-352','PF00069','SGK2_HUMAN','95','352'),
('B4DXY6_HUMAN/20-190','PF00069','B4DXY6_HUMAN','20','190'),
('B1AXG1_HUMAN/39-227','PF00069','B1AXG1_HUMAN','39','227'),
('Q59EB4_HUMAN/674-839','PF00069','Q59EB4_HUMAN','674','839'),
('B4DE88_HUMAN/126-376','PF00069','B4DE88_HUMAN','126','376'),
('B4DHU6_HUMAN/44-325','PF00069','B4DHU6_HUMAN','44','325'),
('B4DMA5_HUMAN/1-176','PF00069','B4DMA5_HUMAN','1','176'),
('SIK2_HUMAN/20-271','PF00069','SIK2_HUMAN','20','271'),
('B4DEQ4_HUMAN/1-237','PF00069','B4DEQ4_HUMAN','1','237'),
('B4DJN5_HUMAN/194-453','PF00069','B4DJN5_HUMAN','194','453'),
('G5E9R2_HUMAN/408-583','PF00069','G5E9R2_HUMAN','408','583'),
('A8K9I1_HUMAN/23-283','PF00069','A8K9I1_HUMAN','23','283'),
('DCLK2_HUMAN/394-651','PF00069','DCLK2_HUMAN','394','651'),
('B4DM56_HUMAN/29-293','PF00069','B4DM56_HUMAN','29','293'),
('Q59F75_HUMAN/38-204','PF00069','Q59F75_HUMAN','38','204'),
('A6YR18_HUMAN/49-309','PF00069','A6YR18_HUMAN','49','309'),
('M3K6_HUMAN/650-906','PF00069','M3K6_HUMAN','650','906'),
('F5H6Z0_HUMAN/139-420','PF00069','F5H6Z0_HUMAN','139','420'),
('GWL_HUMAN/35-203','PF00069','GWL_HUMAN','35','203'),
('Q0IJ40_HUMAN/30-177','PF00069','Q0IJ40_HUMAN','30','177'),
('Q69FE3_HUMAN/187-455','PF00069','Q69FE3_HUMAN','187','455'),
('D6RHX8_HUMAN/186-448','PF00069','D6RHX8_HUMAN','186','448'),
('B5BUJ6_HUMAN/50-333','PF00069','B5BUJ6_HUMAN','50','333'),
('A4D2J9_HUMAN/14-272','PF00069','A4D2J9_HUMAN','14','272'),
('SRPK1_HUMAN/80-232','PF00069','SRPK1_HUMAN','80','232'),
('KPSH1_HUMAN/98-355','PF00069','KPSH1_HUMAN','98','355'),
('B7ZA62_HUMAN/2-239','PF00069','B7ZA62_HUMAN','2','239'),
('B7Z5K4_HUMAN/83-340','PF00069','B7Z5K4_HUMAN','83','340'),
('A8K8M5_HUMAN/187-449','PF00069','A8K8M5_HUMAN','187','449'),
('B3KUN5_HUMAN/76-342','PF00069','B3KUN5_HUMAN','76','342'),
('KS6A1_HUMAN/418-675','PF00069','KS6A1_HUMAN','418','675'),
('Q96AD6_HUMAN/186-448','PF00069','Q96AD6_HUMAN','186','448'),
('B3KTJ2_HUMAN/398-535','PF00069','B3KTJ2_HUMAN','398','535'),
('E9PPA5_HUMAN/1-186','PF00069','E9PPA5_HUMAN','1','186'),
('Q5U4A5_HUMAN/25-206','PF00069','Q5U4A5_HUMAN','25','206'),
('E2AK4_HUMAN/765-1001','PF00069','E2AK4_HUMAN','765','1001'),
('B4DKZ2_HUMAN/392-649','PF00069','B4DKZ2_HUMAN','392','649'),
('Q9UFE3_HUMAN/1-213','PF00069','Q9UFE3_HUMAN','1','213'),
('NEK5_HUMAN/4-259','PF00069','NEK5_HUMAN','4','259'),
('STK40_HUMAN/37-328','PF00069','STK40_HUMAN','37','328'),
('B7Z302_HUMAN/1-234','PF00069','B7Z302_HUMAN','1','234'),
('B7Z5U3_HUMAN/48-234','PF00069','B7Z5U3_HUMAN','48','234'),
('BMPR2_HUMAN/203-501','PF00069','BMPR2_HUMAN','203','501'),
('B2R757_HUMAN/20-288','PF00069','B2R757_HUMAN','20','288'),
('MINK1_HUMAN/25-289','PF00069','MINK1_HUMAN','25','289'),
('Q53EW6_HUMAN/162-419','PF00069','Q53EW6_HUMAN','162','419'),
('PIM3_HUMAN/40-293','PF00069','PIM3_HUMAN','40','293'),
('B4DYG2_HUMAN/767-1013','PF00069','B4DYG2_HUMAN','767','1013'),
('Q0VD65_HUMAN/21-287','PF00069','Q0VD65_HUMAN','21','287'),
('F5H7T0_HUMAN/655-844','PF00069','F5H7T0_HUMAN','655','844'),
('C9J232_HUMAN/1-176','PF00069','C9J232_HUMAN','1','176'),
('KCC1B_HUMAN/15-270','PF00069','KCC1B_HUMAN','15','270'),
('MRCKA_HUMAN/77-343','PF00069','MRCKA_HUMAN','77','343'),
('Q9BRS0_HUMAN/67-328','PF00069','Q9BRS0_HUMAN','67','328'),
('H0YEZ7_HUMAN/50-211','PF00069','H0YEZ7_HUMAN','50','211'),
('B7Z5H7_HUMAN/327-541','PF00069','B7Z5H7_HUMAN','327','541'),
('B3KRS6_HUMAN/2-193','PF00069','B3KRS6_HUMAN','2','193'),
('MK13_HUMAN/25-308','PF00069','MK13_HUMAN','25','308'),
('A6NGQ3_HUMAN/5306-5558','PF00069','A6NGQ3_HUMAN','5306','5558'),
('C0JYZ2_HUMAN/31251-31505','PF00069','C0JYZ2_HUMAN','31251','31505'),
('A6NF29_HUMAN/26-208','PF00069','A6NF29_HUMAN','26','208'),
('STK33_HUMAN/116-381','PF00069','STK33_HUMAN','116','381'),
('A6NGQ3_HUMAN/4102-4355','PF00069','A6NGQ3_HUMAN','4102','4355'),
('B2RC06_HUMAN/77-327','PF00069','B2RC06_HUMAN','77','327'),
('KC1G1_HUMAN/44-315','PF00069','KC1G1_HUMAN','44','315'),
('E7ETV6_HUMAN/146-295','PF00069','E7ETV6_HUMAN','146','295'),
('Q1HBJ4_HUMAN/25-313','PF00069','Q1HBJ4_HUMAN','25','313'),
('A8K8B2_HUMAN/476-653','PF00069','A8K8B2_HUMAN','476','653'),
('H0YJ50_HUMAN/1-184','PF00069','H0YJ50_HUMAN','1','184'),
('Q15523_HUMAN/152-411','PF00069','Q15523_HUMAN','152','411'),
('B1APF7_HUMAN/48-186','PF00069','B1APF7_HUMAN','48','186'),
('A4VCI5_HUMAN/185-470','PF00069','A4VCI5_HUMAN','185','470'),
('B4DNF9_HUMAN/1-175','PF00069','B4DNF9_HUMAN','1','175'),
('VRK2_HUMAN/29-312','PF00069','VRK2_HUMAN','29','312'),
('D6R9G1_HUMAN/1-202','PF00069','D6R9G1_HUMAN','1','202'),
('E9PQW4_HUMAN/42-328','PF00069','E9PQW4_HUMAN','42','328'),
('B2R779_HUMAN/91-352','PF00069','B2R779_HUMAN','91','352'),
('B0LPE5_HUMAN/150-408','PF00069','B0LPE5_HUMAN','150','408'),
('MARK2_HUMAN/53-304','PF00069','MARK2_HUMAN','53','304'),
('E7EU96_HUMAN/39-324','PF00069','E7EU96_HUMAN','39','324'),
('B2R928_HUMAN/20-277','PF00069','B2R928_HUMAN','20','277'),
('B7Z2K7_HUMAN/46-305','PF00069','B7Z2K7_HUMAN','46','305'),
('KCC4_HUMAN/46-300','PF00069','KCC4_HUMAN','46','300'),
('MELK_HUMAN/11-263','PF00069','MELK_HUMAN','11','263'),
('B3KUS6_HUMAN/4-280','PF00069','B3KUS6_HUMAN','4','280'),
('Q53SF4_HUMAN/2-139','PF00069','Q53SF4_HUMAN','2','139'),
('B7ZM71_HUMAN/27-293','PF00069','B7ZM71_HUMAN','27','293'),
('A8K4I7_HUMAN/15-296','PF00069','A8K4I7_HUMAN','15','296'),
('KS6A6_HUMAN/426-683','PF00069','KS6A6_HUMAN','426','683'),
('MP2K2_HUMAN/72-369','PF00069','MP2K2_HUMAN','72','369'),
('A8K2S4_HUMAN/20-271','PF00069','A8K2S4_HUMAN','20','271'),
('NEK9_HUMAN/52-308','PF00069','NEK9_HUMAN','52','308'),
('Q9NRL6_HUMAN/132-447','PF00069','Q9NRL6_HUMAN','132','447'),
('B5BUH5_HUMAN/39-324','PF00069','B5BUH5_HUMAN','39','324'),
('MK06_HUMAN/20-316','PF00069','MK06_HUMAN','20','316'),
('O75271_HUMAN/159-340','PF00069','O75271_HUMAN','159','340'),
('B4DUG0_HUMAN/1-221','PF00069','B4DUG0_HUMAN','1','221'),
('E7ETV6_HUMAN/454-632','PF00069','E7ETV6_HUMAN','454','632'),
('A0MZF5_HUMAN/16-268','PF00069','A0MZF5_HUMAN','16','268'),
('MYO3A_HUMAN/21-287','PF00069','MYO3A_HUMAN','21','287'),
('Q53HJ9_HUMAN/82-341','PF00069','Q53HJ9_HUMAN','82','341'),
('F8VSH4_HUMAN/1-150','PF00069','F8VSH4_HUMAN','1','150'),
('F8VWX7_HUMAN/6-203','PF00069','F8VWX7_HUMAN','6','203'),
('H3BNQ5_HUMAN/9-158','PF00069','H3BNQ5_HUMAN','9','158'),
('KCC2A_HUMAN/13-271','PF00069','KCC2A_HUMAN','13','271'),
('ACV1C_HUMAN/195-482','PF00069','ACV1C_HUMAN','195','482'),
('B7Z7D1_HUMAN/74-265','PF00069','B7Z7D1_HUMAN','74','265'),
('H0YCG5_HUMAN/2-242','PF00069','H0YCG5_HUMAN','2','242'),
('MP2K1_HUMAN/68-361','PF00069','MP2K1_HUMAN','68','361'),
('F5GYC4_HUMAN/39-298','PF00069','F5GYC4_HUMAN','39','298'),
('NUAK1_HUMAN/55-306','PF00069','NUAK1_HUMAN','55','306'),
('B7Z7K5_HUMAN/65-331','PF00069','B7Z7K5_HUMAN','65','331'),
('C7DUW4_HUMAN/64-325','PF00069','C7DUW4_HUMAN','64','325'),
('B2R6Z3_HUMAN/133-383','PF00069','B2R6Z3_HUMAN','133','383'),
('Q6PJ06_HUMAN/17-261','PF00069','Q6PJ06_HUMAN','17','261'),
('B3KQ65_HUMAN/8-229','PF00069','B3KQ65_HUMAN','8','229'),
('SCYL2_HUMAN/32-327','PF00069','SCYL2_HUMAN','32','327'),
('STK16_HUMAN/20-290','PF00069','STK16_HUMAN','20','290'),
('CDC7_HUMAN/58-224','PF00069','CDC7_HUMAN','58','224'),
('CDK1_HUMAN/4-287','PF00069','CDK1_HUMAN','4','287'),
('E7ESS2_HUMAN/35-269','PF00069','E7ESS2_HUMAN','35','269'),
('DCLK1_HUMAN/390-647','PF00069','DCLK1_HUMAN','390','647'),
('B4DM55_HUMAN/1-250','PF00069','B4DM55_HUMAN','1','250'),
('PDPK2_HUMAN/55-314','PF00069','PDPK2_HUMAN','55','314'),
('HIPK3_HUMAN/197-525','PF00069','HIPK3_HUMAN','197','525'),
('B2R5T1_HUMAN/351-604','PF00069','B2R5T1_HUMAN','351','604'),
('D6W660_HUMAN/1-255','PF00069','D6W660_HUMAN','1','255'),
('B4DIP4_HUMAN/213-459','PF00069','B4DIP4_HUMAN','213','459'),
('A8K0J3_HUMAN/24-277','PF00069','A8K0J3_HUMAN','24','277'),
('F6UYG0_HUMAN/221-388','PF00069','F6UYG0_HUMAN','221','388'),
('Q53QE7_HUMAN/33-293','PF00069','Q53QE7_HUMAN','33','293'),
('B1APF9_HUMAN/32-244','PF00069','B1APF9_HUMAN','32','244'),
('Q562E6_HUMAN/15-297','PF00069','Q562E6_HUMAN','15','297'),
('CDKL5_HUMAN/13-297','PF00069','CDKL5_HUMAN','13','297'),
('E9PGR2_HUMAN/37-234','PF00069','E9PGR2_HUMAN','37','234'),
('C9JDH9_HUMAN/1-148','PF00069','C9JDH9_HUMAN','1','148'),
('B4DP95_HUMAN/17-208','PF00069','B4DP95_HUMAN','17','208'),
('A0JP11_HUMAN/26-312','PF00069','A0JP11_HUMAN','26','312'),
('Q86YC8_HUMAN/11-232','PF00069','Q86YC8_HUMAN','11','232'),
('Q499L9_HUMAN/24-274','PF00069','Q499L9_HUMAN','24','274'),
('B5BU77_HUMAN/355-614','PF00069','B5BU77_HUMAN','355','614'),
('SIK1_HUMAN/27-278','PF00069','SIK1_HUMAN','27','278'),
('Q5QPR4_HUMAN/389-674','PF00069','Q5QPR4_HUMAN','389','674'),
('B3KU24_HUMAN/44-191','PF00069','B3KU24_HUMAN','44','191'),
('A0PJ48_HUMAN/28-281','PF00069','A0PJ48_HUMAN','28','281'),
('B5MDL5_HUMAN/1-221','PF00069','B5MDL5_HUMAN','1','221'),
('SG494_HUMAN/107-272','PF00069','SG494_HUMAN','107','272'),
('B3KUZ9_HUMAN/1-187','PF00069','B3KUZ9_HUMAN','1','187'),
('Q8NCK8_HUMAN/396-650','PF00069','Q8NCK8_HUMAN','396','650'),
('B7ZA25_HUMAN/33-291','PF00069','B7ZA25_HUMAN','33','291'),
('E5RGW5_HUMAN/15-297','PF00069','E5RGW5_HUMAN','15','297'),
('M3K2_HUMAN/356-616','PF00069','M3K2_HUMAN','356','616'),
('AAPK2_HUMAN/16-268','PF00069','AAPK2_HUMAN','16','268'),
('AMHR2_HUMAN/203-505','PF00069','AMHR2_HUMAN','203','505'),
('MK10_HUMAN/64-359','PF00069','MK10_HUMAN','64','359'),
('G3V1W8_HUMAN/216-504','PF00069','G3V1W8_HUMAN','216','504'),
('ERN2_HUMAN/520-781','PF00069','ERN2_HUMAN','520','781'),
('E7ENQ1_HUMAN/25-289','PF00069','E7ENQ1_HUMAN','25','289'),
('B4DSE5_HUMAN/376-649','PF00069','B4DSE5_HUMAN','376','649'),
('MP2K5_HUMAN/166-419','PF00069','MP2K5_HUMAN','166','419'),
('Q59GQ4_HUMAN/1-157','PF00069','Q59GQ4_HUMAN','1','157'),
('B7Z325_HUMAN/133-311','PF00069','B7Z325_HUMAN','133','311'),
('B4DW95_HUMAN/4-258','PF00069','B4DW95_HUMAN','4','258'),
('D3DQU7_HUMAN/116-381','PF00069','D3DQU7_HUMAN','116','381'),
('MRCKG_HUMAN/71-337','PF00069','MRCKG_HUMAN','71','337'),
('B7Z3W6_HUMAN/351-604','PF00069','B7Z3W6_HUMAN','351','604'),
('Q6FHV7_HUMAN/95-352','PF00069','Q6FHV7_HUMAN','95','352'),
('E5KR08_HUMAN/81-349','PF00069','E5KR08_HUMAN','81','349'),
('Q5SQQ7_HUMAN/23-279','PF00069','Q5SQQ7_HUMAN','23','279'),
('B4E0Y5_HUMAN/97-347','PF00069','B4E0Y5_HUMAN','97','347'),
('B3KS97_HUMAN/1-179','PF00069','B3KS97_HUMAN','1','179'),
('F8WAQ9_HUMAN/573-846','PF00069','F8WAQ9_HUMAN','573','846'),
('B5BUJ8_HUMAN/44-304','PF00069','B5BUJ8_HUMAN','44','304'),
('Q86V29_HUMAN/299-569','PF00069','Q86V29_HUMAN','299','569'),
('STRAB_HUMAN/58-369','PF00069','STRAB_HUMAN','58','369'),
('KC1E_HUMAN/9-280','PF00069','KC1E_HUMAN','9','280'),
('B7ZLC4_HUMAN/46-312','PF00069','B7ZLC4_HUMAN','46','312'),
('B4E0D4_HUMAN/30-316','PF00069','B4E0D4_HUMAN','30','316'),
('PLK1_HUMAN/53-305','PF00069','PLK1_HUMAN','53','305'),
('Q59FN2_HUMAN/7-255','PF00069','Q59FN2_HUMAN','7','255'),
('D3DPF9_HUMAN/24754-25008','PF00069','D3DPF9_HUMAN','24754','25008'),
('G3V5T9_HUMAN/4-220','PF00069','G3V5T9_HUMAN','4','220'),
('BMR1A_HUMAN/234-521','PF00069','BMR1A_HUMAN','234','521'),
('D7R526_HUMAN/26-321','PF00069','D7R526_HUMAN','26','321'),
('B5BU64_HUMAN/50-333','PF00069','B5BU64_HUMAN','50','333'),
('NRBP2_HUMAN/56-306','PF00069','NRBP2_HUMAN','56','306'),
('E9PD56_HUMAN/153-446','PF00069','E9PD56_HUMAN','153','446'),
('B4DTS2_HUMAN/553-817','PF00069','B4DTS2_HUMAN','553','817'),
('B1APG0_HUMAN/47-206','PF00069','B1APG0_HUMAN','47','206'),
('TRIB2_HUMAN/72-308','PF00069','TRIB2_HUMAN','72','308'),
('Q1KKQ2_HUMAN/587-841','PF00069','Q1KKQ2_HUMAN','587','841'),
('F8VSC5_HUMAN/32-327','PF00069','F8VSC5_HUMAN','32','327'),
('E7EX48_HUMAN/28-172','PF00069','E7EX48_HUMAN','28','172'),
('A6H8V9_HUMAN/597-874','PF00069','A6H8V9_HUMAN','597','874'),
('ACV1B_HUMAN/207-494','PF00069','ACV1B_HUMAN','207','494'),
('Q5TI62_HUMAN/1-158','PF00069','Q5TI62_HUMAN','1','158'),
('Q5TBG7_HUMAN/45-219','PF00069','Q5TBG7_HUMAN','45','219'),
('E7ERL6_HUMAN/442-715','PF00069','E7ERL6_HUMAN','442','715'),
('E9PJF0_HUMAN/42-295','PF00069','E9PJF0_HUMAN','42','295'),
('PHKG1_HUMAN/20-288','PF00069','PHKG1_HUMAN','20','288'),
('F8W6G1_HUMAN/80-335','PF00069','F8W6G1_HUMAN','80','335'),
('E7ETY4_HUMAN/20-271','PF00069','E7ETY4_HUMAN','20','271'),
('B4DMF2_HUMAN/14-249','PF00069','B4DMF2_HUMAN','14','249'),
('Q5U5J2_HUMAN/39-324','PF00069','Q5U5J2_HUMAN','39','324'),
('A8K8F7_HUMAN/104-400','PF00069','A8K8F7_HUMAN','104','400'),
('B4DPS1_HUMAN/12-172','PF00069','B4DPS1_HUMAN','12','172'),
('ERN1_HUMAN/571-832','PF00069','ERN1_HUMAN','571','832'),
('BMP2K_HUMAN/51-316','PF00069','BMP2K_HUMAN','51','316'),
('Q6P084_HUMAN/2-160','PF00069','Q6P084_HUMAN','2','160'),
('Q8WU40_HUMAN/1-207','PF00069','Q8WU40_HUMAN','1','207'),
('E5KR07_HUMAN/71-339','PF00069','E5KR07_HUMAN','71','339'),
('B1APF8_HUMAN/40-214','PF00069','B1APF8_HUMAN','40','214'),
('MRCKB_HUMAN/76-342','PF00069','MRCKB_HUMAN','76','342'),
('Q6P0Y1_HUMAN/24-274','PF00069','Q6P0Y1_HUMAN','24','274'),
('E7ETR1_HUMAN/101-243','PF00069','E7ETR1_HUMAN','101','243'),
('F5H5N0_HUMAN/77-343','PF00069','F5H5N0_HUMAN','77','343'),
('Q59FU6_HUMAN/118-386','PF00069','Q59FU6_HUMAN','118','386'),
('G3XAA2_HUMAN/25-289','PF00069','G3XAA2_HUMAN','25','289'),
('B8ZZI5_HUMAN/20-187','PF00069','B8ZZI5_HUMAN','20','187'),
('E9PBK7_HUMAN/13-153','PF00069','E9PBK7_HUMAN','13','153'),
('MARK3_HUMAN/56-307','PF00069','MARK3_HUMAN','56','307'),
('E9PBG7_HUMAN/14-272','PF00069','E9PBG7_HUMAN','14','272'),
('PAK6_HUMAN/408-658','PF00069','PAK6_HUMAN','408','658'),
('H7C1X3_HUMAN/2-215','PF00069','H7C1X3_HUMAN','2','215'),
('KPCZ_HUMAN/252-518','PF00069','KPCZ_HUMAN','252','518'),
('CDKL2_HUMAN/4-287','PF00069','CDKL2_HUMAN','4','287'),
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('SRPK1_HUMAN/476-653','PF00069','SRPK1_HUMAN','476','653'),
('DAPK1_HUMAN/13-275','PF00069','DAPK1_HUMAN','13','275'),
('A4D150_HUMAN/92-407','PF00069','A4D150_HUMAN','92','407'),
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('Q5SWX3_HUMAN/14-272','PF00069','Q5SWX3_HUMAN','14','272'),
('NEK7_HUMAN/34-292','PF00069','NEK7_HUMAN','34','292'),
('HUNK_HUMAN/63-320','PF00069','HUNK_HUMAN','63','320'),
('B3KY45_HUMAN/712-926','PF00069','B3KY45_HUMAN','712','926'),
('A8KAN3_HUMAN/270-520','PF00069','A8KAN3_HUMAN','270','520'),
('RPKL1_HUMAN/378-539','PF00069','RPKL1_HUMAN','378','539'),
('NEK10_HUMAN/519-783','PF00069','NEK10_HUMAN','519','783'),
('KPCB_HUMAN/342-600','PF00069','KPCB_HUMAN','342','600'),
('B4DS23_HUMAN/364-637','PF00069','B4DS23_HUMAN','364','637'),
('Q53H78_HUMAN/14-272','PF00069','Q53H78_HUMAN','14','272'),
('H7C3L8_HUMAN/1-155','PF00069','H7C3L8_HUMAN','1','155'),
('B4DS61_HUMAN/460-637','PF00069','B4DS61_HUMAN','460','637'),
('ROCK1_HUMAN/76-338','PF00069','ROCK1_HUMAN','76','338'),
('CDC7_HUMAN/355-569','PF00069','CDC7_HUMAN','355','569'),
('Q9UPJ8_HUMAN/74-333','PF00069','Q9UPJ8_HUMAN','74','333'),
('PMYT1_HUMAN/110-359','PF00069','PMYT1_HUMAN','110','359'),
('OBSCN_HUMAN/6468-6721','PF00069','OBSCN_HUMAN','6468','6721'),
('B4DT73_HUMAN/111-281','PF00069','B4DT73_HUMAN','111','281'),
('F5H2J1_HUMAN/36-302','PF00069','F5H2J1_HUMAN','36','302'),
('Q53EZ9_HUMAN/64-325','PF00069','Q53EZ9_HUMAN','64','325'),
('B4E2M4_HUMAN/4-280','PF00069','B4E2M4_HUMAN','4','280'),
('F5H538_HUMAN/1339-1597','PF00069','F5H538_HUMAN','1339','1597'),
('Q32MQ5_HUMAN/119-375','PF00069','Q32MQ5_HUMAN','119','375'),
('B4DDH2_HUMAN/75-340','PF00069','B4DDH2_HUMAN','75','340'),
('Q6N076_HUMAN/4-263','PF00069','Q6N076_HUMAN','4','263'),
('A8K5A6_HUMAN/787-1033','PF00069','A8K5A6_HUMAN','787','1033'),
('B4DFS6_HUMAN/1-180','PF00069','B4DFS6_HUMAN','1','180'),
('M4K5_HUMAN/20-277','PF00069','M4K5_HUMAN','20','277'),
('E9PJN1_HUMAN/406-667','PF00069','E9PJN1_HUMAN','406','667'),
('H7C2I6_HUMAN/1-139','PF00069','H7C2I6_HUMAN','1','139'),
('CDK17_HUMAN/192-473','PF00069','CDK17_HUMAN','192','473'),
('B5BUJ7_HUMAN/26-321','PF00069','B5BUJ7_HUMAN','26','321'),
('Q59G02_HUMAN/106-387','PF00069','Q59G02_HUMAN','106','387'),
('KPSH2_HUMAN/63-320','PF00069','KPSH2_HUMAN','63','320'),
('A8K8B9_HUMAN/36-290','PF00069','A8K8B9_HUMAN','36','290'),
('H0YCS6_HUMAN/1-169','PF00069','H0YCS6_HUMAN','1','169'),
('B3KNJ2_HUMAN/318-573','PF00069','B3KNJ2_HUMAN','318','573'),
('G5E9L9_HUMAN/393-650','PF00069','G5E9L9_HUMAN','393','650'),
('E9PG46_HUMAN/46-312','PF00069','E9PG46_HUMAN','46','312'),
('CDK13_HUMAN/705-998','PF00069','CDK13_HUMAN','705','998'),
('CDK6_HUMAN/13-300','PF00069','CDK6_HUMAN','13','300'),
('Q7Z370_HUMAN/1-272','PF00069','Q7Z370_HUMAN','1','272'),
('B4DNQ3_HUMAN/536-772','PF00069','B4DNQ3_HUMAN','536','772'),
('E5KR06_HUMAN/71-339','PF00069','E5KR06_HUMAN','71','339'),
('A8K342_HUMAN/58-369','PF00069','A8K342_HUMAN','58','369'),
('Q5TBH1_HUMAN/45-222','PF00069','Q5TBH1_HUMAN','45','222'),
('Q5T7S2_HUMAN/205-492','PF00069','Q5T7S2_HUMAN','205','492'),
('Q59FA7_HUMAN/79-312','PF00069','Q59FA7_HUMAN','79','312'),
('Q9Y6B5_HUMAN/265-516','PF00069','Q9Y6B5_HUMAN','265','516'),
('Q9NWE9_HUMAN/1-154','PF00069','Q9NWE9_HUMAN','1','154'),
('E7ET86_HUMAN/4-286','PF00069','E7ET86_HUMAN','4','286'),
('B4E185_HUMAN/1-176','PF00069','B4E185_HUMAN','1','176'),
('GRK6_HUMAN/186-448','PF00069','GRK6_HUMAN','186','448'),
('Q5T8F1_HUMAN/13-275','PF00069','Q5T8F1_HUMAN','13','275'),
('Q499Y8_HUMAN/1-214','PF00069','Q499Y8_HUMAN','1','214'),
('CDK4_HUMAN/6-295','PF00069','CDK4_HUMAN','6','295'),
('PLK4_HUMAN/12-265','PF00069','PLK4_HUMAN','12','265'),
('A8K8Z3_HUMAN/456-734','PF00069','A8K8Z3_HUMAN','456','734'),
('B0LPI0_HUMAN/174-432','PF00069','B0LPI0_HUMAN','174','432'),
('KS6A3_HUMAN/422-679','PF00069','KS6A3_HUMAN','422','679'),
('B4E359_HUMAN/63-331','PF00069','B4E359_HUMAN','63','331'),
('KS6A2_HUMAN/59-318','PF00069','KS6A2_HUMAN','59','318'),
('Q8TB93_HUMAN/450-700','PF00069','Q8TB93_HUMAN','450','700'),
('H3BLV9_HUMAN/492-669','PF00069','H3BLV9_HUMAN','492','669'),
('TAOK1_HUMAN/28-281','PF00069','TAOK1_HUMAN','28','281'),
('Q53SV1_HUMAN/208-355','PF00069','Q53SV1_HUMAN','208','355'),
('SGK3_HUMAN/162-419','PF00069','SGK3_HUMAN','162','419'),
('B7ZA00_HUMAN/7-261','PF00069','B7ZA00_HUMAN','7','261'),
('E9PRV7_HUMAN/191-369','PF00069','E9PRV7_HUMAN','191','369'),
('A8K161_HUMAN/13-271','PF00069','A8K161_HUMAN','13','271'),
('E9PK59_HUMAN/32-246','PF00069','E9PK59_HUMAN','32','246'),
('B4DZM6_HUMAN/110-359','PF00069','B4DZM6_HUMAN','110','359'),
('NRK_HUMAN/25-313','PF00069','NRK_HUMAN','25','313'),
('STK35_HUMAN/202-527','PF00069','STK35_HUMAN','202','527'),
('IRAK4_HUMAN/187-455','PF00069','IRAK4_HUMAN','187','455'),
('H9KV37_HUMAN/12-276','PF00069','H9KV37_HUMAN','12','276'),
('B4DM24_HUMAN/1-211','PF00069','B4DM24_HUMAN','1','211'),
('E7EX83_HUMAN/25-171','PF00069','E7EX83_HUMAN','25','171'),
('Q05DL3_HUMAN/17-232','PF00069','Q05DL3_HUMAN','17','232'),
('CDK20_HUMAN/4-288','PF00069','CDK20_HUMAN','4','288'),
('H7BXX9_HUMAN/199-527','PF00069','H7BXX9_HUMAN','199','527'),
('STK10_HUMAN/36-294','PF00069','STK10_HUMAN','36','294'),
('NEK2_HUMAN/8-271','PF00069','NEK2_HUMAN','8','271'),
('AKT3_HUMAN/148-405','PF00069','AKT3_HUMAN','148','405'),
('A0PJ51_HUMAN/30-281','PF00069','A0PJ51_HUMAN','30','281'),
('F5H4F6_HUMAN/20-161','PF00069','F5H4F6_HUMAN','20','161'),
('B4DPK7_HUMAN/16-273','PF00069','B4DPK7_HUMAN','16','273'),
('E9PGT3_HUMAN/407-664','PF00069','E9PGT3_HUMAN','407','664'),
('E2AK1_HUMAN/337-583','PF00069','E2AK1_HUMAN','337','583'),
('F8W9H1_HUMAN/128-447','PF00069','F8W9H1_HUMAN','128','447'),
('B4DVN6_HUMAN/1-203','PF00069','B4DVN6_HUMAN','1','203'),
('B4DJP1_HUMAN/15-187','PF00069','B4DJP1_HUMAN','15','187'),
('B4E3J8_HUMAN/9-290','PF00069','B4E3J8_HUMAN','9','290'),
('H7C3X8_HUMAN/1-220','PF00069','H7C3X8_HUMAN','1','220'),
('B2R9A0_HUMAN/6-295','PF00069','B2R9A0_HUMAN','6','295'),
('B4DMR0_HUMAN/24-274','PF00069','B4DMR0_HUMAN','24','274'),
('ST32A_HUMAN/23-281','PF00069','ST32A_HUMAN','23','281'),
('RIPK2_HUMAN/18-290','PF00069','RIPK2_HUMAN','18','290'),
('Q59GN5_HUMAN/3-173','PF00069','Q59GN5_HUMAN','3','173'),
('B5BUK7_HUMAN/245-513','PF00069','B5BUK7_HUMAN','245','513'),
('B4DJS8_HUMAN/49-342','PF00069','B4DJS8_HUMAN','49','342'),
('Q4VBY6_HUMAN/118-403','PF00069','Q4VBY6_HUMAN','118','403'),
('MAPK5_HUMAN/22-304','PF00069','MAPK5_HUMAN','22','304'),
('E9PHI8_HUMAN/29-295','PF00069','E9PHI8_HUMAN','29','295'),
('Q9NWX4_HUMAN/1-151','PF00069','Q9NWX4_HUMAN','1','151'),
('MARK4_HUMAN/59-310','PF00069','MARK4_HUMAN','59','310'),
('A8MT37_HUMAN/37-321','PF00069','A8MT37_HUMAN','37','321'),
('B5BTY5_HUMAN/25-308','PF00069','B5BTY5_HUMAN','25','308'),
('KPCE_HUMAN/408-668','PF00069','KPCE_HUMAN','408','668'),
('E5KR05_HUMAN/71-339','PF00069','E5KR05_HUMAN','71','339'),
('ST38L_HUMAN/90-383','PF00069','ST38L_HUMAN','90','383'),
('Q8IXN4_HUMAN/4-284','PF00069','Q8IXN4_HUMAN','4','284'),
('KPCD1_HUMAN/585-839','PF00069','KPCD1_HUMAN','585','839'),
('B7Z2Y5_HUMAN/1-239','PF00069','B7Z2Y5_HUMAN','1','239'),
('Q6FG98_HUMAN/33-293','PF00069','Q6FG98_HUMAN','33','293'),
('B2R859_HUMAN/174-487','PF00069','B2R859_HUMAN','174','487'),
('MKNK1_HUMAN/50-374','PF00069','MKNK1_HUMAN','50','374'),
('Q8IZN1_HUMAN/73-223','PF00069','Q8IZN1_HUMAN','73','223'),
('E7EQE4_HUMAN/34-173','PF00069','E7EQE4_HUMAN','34','173'),
('Q6FHG1_HUMAN/64-325','PF00069','Q6FHG1_HUMAN','64','325'),
('Q5SQL3_HUMAN/190-518','PF00069','Q5SQL3_HUMAN','190','518'),
('KGP1_HUMAN/360-619','PF00069','KGP1_HUMAN','360','619'),
('Q8IWQ7_HUMAN/77-343','PF00069','Q8IWQ7_HUMAN','77','343'),
('MOS_HUMAN/60-338','PF00069','MOS_HUMAN','60','338'),
('KS6A4_HUMAN/413-674','PF00069','KS6A4_HUMAN','413','674'),
('A0ZT99_HUMAN/12-272','PF00069','A0ZT99_HUMAN','12','272'),
('B2R7K0_HUMAN/186-448','PF00069','B2R7K0_HUMAN','186','448'),
('H7C279_HUMAN/1-152','PF00069','H7C279_HUMAN','1','152'),
('Q59FJ7_HUMAN/2-172','PF00069','Q59FJ7_HUMAN','2','172'),
('Q9P1M2_HUMAN/279-537','PF00069','Q9P1M2_HUMAN','279','537'),
('A8MWW6_HUMAN/1-214','PF00069','A8MWW6_HUMAN','1','214'),
('Q5H9Q5_HUMAN/162-419','PF00069','Q5H9Q5_HUMAN','162','419'),
('B9A038_HUMAN/2174-2426','PF00069','B9A038_HUMAN','2174','2426'),
('B1APG1_HUMAN/31-197','PF00069','B1APG1_HUMAN','31','197'),
('B3KQG4_HUMAN/4-284','PF00069','B3KQG4_HUMAN','4','284'),
('B7ZL90_HUMAN/73-330','PF00069','B7ZL90_HUMAN','73','330'),
('B4E125_HUMAN/172-426','PF00069','B4E125_HUMAN','172','426'),
('B7ZAU7_HUMAN/1-220','PF00069','B7ZAU7_HUMAN','1','220'),
('Q9BVE2_HUMAN/91-323','PF00069','Q9BVE2_HUMAN','91','323'),
('H0YD75_HUMAN/86-375','PF00069','H0YD75_HUMAN','86','375'),
('E2AK2_HUMAN/267-537','PF00069','E2AK2_HUMAN','267','537'),
('B9EG64_HUMAN/159-475','PF00069','B9EG64_HUMAN','159','475'),
('Q96BA2_HUMAN/20-270','PF00069','Q96BA2_HUMAN','20','270'),
('GSK3B_HUMAN/56-340','PF00069','GSK3B_HUMAN','56','340'),
('B3KYB0_HUMAN/408-583','PF00069','B3KYB0_HUMAN','408','583'),
('H0Y494_HUMAN/66-317','PF00069','H0Y494_HUMAN','66','317'),
('Q7Z319_HUMAN/23-238','PF00069','Q7Z319_HUMAN','23','238'),
('PAK3_HUMAN/283-534','PF00069','PAK3_HUMAN','283','534'),
('E7ETG2_HUMAN/468-729','PF00069','E7ETG2_HUMAN','468','729'),
('H0YAZ9_HUMAN/1-210','PF00069','H0YAZ9_HUMAN','1','210'),
('F6WCX7_HUMAN/162-422','PF00069','F6WCX7_HUMAN','162','422'),
('PAK4_HUMAN/322-572','PF00069','PAK4_HUMAN','322','572'),
('SG223_HUMAN/1080-1321','PF00069','SG223_HUMAN','1080','1321'),
('B4DIJ9_HUMAN/1-169','PF00069','B4DIJ9_HUMAN','1','169'),
('BMR1B_HUMAN/204-491','PF00069','BMR1B_HUMAN','204','491'),
('H0YME5_HUMAN/121-345','PF00069','H0YME5_HUMAN','121','345'),
('H7C5P0_HUMAN/1-199','PF00069','H7C5P0_HUMAN','1','199'),
('KGP2_HUMAN/453-711','PF00069','KGP2_HUMAN','453','711'),
('F5H1S7_HUMAN/2-184','PF00069','F5H1S7_HUMAN','2','184'),
('Q9BS11_HUMAN/4-196','PF00069','Q9BS11_HUMAN','4','196'),
('C9JSU7_HUMAN/10-193','PF00069','C9JSU7_HUMAN','10','193'),
('B4DKZ2_HUMAN/39-298','PF00069','B4DKZ2_HUMAN','39','298'),
('Q499G7_HUMAN/25-313','PF00069','Q499G7_HUMAN','25','313'),
('RIPK1_HUMAN/17-285','PF00069','RIPK1_HUMAN','17','285'),
('HIPK4_HUMAN/11-347','PF00069','HIPK4_HUMAN','11','347'),
('TSSK2_HUMAN/12-272','PF00069','TSSK2_HUMAN','12','272'),
('KS6A5_HUMAN/49-318','PF00069','KS6A5_HUMAN','49','318'),
('Q59FJ5_HUMAN/365-506','PF00069','Q59FJ5_HUMAN','365','506'),
('E9PR89_HUMAN/133-311','PF00069','E9PR89_HUMAN','133','311'),
('G5E9C7_HUMAN/1-272','PF00069','G5E9C7_HUMAN','1','272'),
('SRPK3_HUMAN/79-228','PF00069','SRPK3_HUMAN','79','228'),
('D7R527_HUMAN/26-321','PF00069','D7R527_HUMAN','26','321'),
('A6PVV2_HUMAN/195-453','PF00069','A6PVV2_HUMAN','195','453'),
('H0Y645_HUMAN/3-218','PF00069','H0Y645_HUMAN','3','218'),
('IRAK2_HUMAN/210-485','PF00069','IRAK2_HUMAN','210','485'),
('B7ZL31_HUMAN/159-307','PF00069','B7ZL31_HUMAN','159','307'),
('A3QNQ0_HUMAN/244-538','PF00069','A3QNQ0_HUMAN','244','538'),
('A8MPY5_HUMAN/354-532','PF00069','A8MPY5_HUMAN','354','532'),
('Q59GL6_HUMAN/762-1018','PF00069','Q59GL6_HUMAN','762','1018'),
('RIPK4_HUMAN/22-282','PF00069','RIPK4_HUMAN','22','282'),
('A8K0W0_HUMAN/23-277','PF00069','A8K0W0_HUMAN','23','277'),
('B2RCZ4_HUMAN/245-513','PF00069','B2RCZ4_HUMAN','245','513'),
('B0QYQ2_HUMAN/78-267','PF00069','B0QYQ2_HUMAN','78','267'),
('B4DIB3_HUMAN/60-311','PF00069','B4DIB3_HUMAN','60','311'),
('B4DL75_HUMAN/1-275','PF00069','B4DL75_HUMAN','1','275'),
('Q68D39_HUMAN/184-387','PF00069','Q68D39_HUMAN','184','387'),
('DYR1B_HUMAN/111-431','PF00069','DYR1B_HUMAN','111','431'),
('WNK2_HUMAN/195-453','PF00069','WNK2_HUMAN','195','453'),
('A4D151_HUMAN/78-393','PF00069','A4D151_HUMAN','78','393'),
('B2R6D7_HUMAN/39-324','PF00069','B2R6D7_HUMAN','39','324'),
('IKKB_HUMAN/15-296','PF00069','IKKB_HUMAN','15','296'),
('G8JLE8_HUMAN/81-343','PF00069','G8JLE8_HUMAN','81','343'),
('TGFR2_HUMAN/244-538','PF00069','TGFR2_HUMAN','244','538'),
('B4DK03_HUMAN/174-455','PF00069','B4DK03_HUMAN','174','455'),
('B4DHN0_HUMAN/13-301','PF00069','B4DHN0_HUMAN','13','301'),
('B3KPS5_HUMAN/156-418','PF00069','B3KPS5_HUMAN','156','418'),
('MYLK_HUMAN/1464-1719','PF00069','MYLK_HUMAN','1464','1719'),
('G3XAA9_HUMAN/33-301','PF00069','G3XAA9_HUMAN','33','301'),
('CSKP_HUMAN/12-276','PF00069','CSKP_HUMAN','12','276'),
('B8ZZN3_HUMAN/67-335','PF00069','B8ZZN3_HUMAN','67','335'),
('PDPK1_HUMAN/82-341','PF00069','PDPK1_HUMAN','82','341'),
('NIM1_HUMAN/74-325','PF00069','NIM1_HUMAN','74','325'),
('Q5JQZ9_HUMAN/1-244','PF00069','Q5JQZ9_HUMAN','1','244'),
('B3KNX7_HUMAN/270-520','PF00069','B3KNX7_HUMAN','270','520'),
('B4DER9_HUMAN/1-233','PF00069','B4DER9_HUMAN','1','233'),
('A6NHV6_HUMAN/101-350','PF00069','A6NHV6_HUMAN','101','350'),
('B3KTV2_HUMAN/1-251','PF00069','B3KTV2_HUMAN','1','251'),
('H3BRE4_HUMAN/1-187','PF00069','H3BRE4_HUMAN','1','187'),
('E5RGN0_HUMAN/165-389','PF00069','E5RGN0_HUMAN','165','389'),
('TITIN_HUMAN/32178-32432','PF00069','TITIN_HUMAN','32178','32432'),
('E9PRI4_HUMAN/46-305','PF00069','E9PRI4_HUMAN','46','305'),
('CDK10_HUMAN/39-323','PF00069','CDK10_HUMAN','39','323'),
('D9ZGF8_HUMAN/76-338','PF00069','D9ZGF8_HUMAN','76','338'),
('VRK3_HUMAN/229-452','PF00069','VRK3_HUMAN','229','452'),
('B3KYB1_HUMAN/7-276','PF00069','B3KYB1_HUMAN','7','276'),
('H0Y4E8_HUMAN/60-311','PF00069','H0Y4E8_HUMAN','60','311'),
('B3KY50_HUMAN/35-290','PF00069','B3KY50_HUMAN','35','290'),
('PAK7_HUMAN/450-700','PF00069','PAK7_HUMAN','450','700'),
('DMPK_HUMAN/71-339','PF00069','DMPK_HUMAN','71','339'),
('WEE2_HUMAN/212-486','PF00069','WEE2_HUMAN','212','486'),
('MAK_HUMAN/4-284','PF00069','MAK_HUMAN','4','284'),
('Q8IW76_HUMAN/267-502','PF00069','Q8IW76_HUMAN','267','502'),
('KAPCB_HUMAN/44-298','PF00069','KAPCB_HUMAN','44','298'),
('Q8NHX0_HUMAN/42-286','PF00069','Q8NHX0_HUMAN','42','286'),
('AAPK1_HUMAN/27-279','PF00069','AAPK1_HUMAN','27','279'),
('Q6NSZ4_HUMAN/20-291','PF00069','Q6NSZ4_HUMAN','20','291'),
('Q59HA5_HUMAN/5-209','PF00069','Q59HA5_HUMAN','5','209'),
('B2R9L6_HUMAN/19-315','PF00069','B2R9L6_HUMAN','19','315'),
('D3DW67_HUMAN/57-253','PF00069','D3DW67_HUMAN','57','253'),
('F2Z2J1_HUMAN/84-343','PF00069','F2Z2J1_HUMAN','84','343'),
('H7C360_HUMAN/1-251','PF00069','H7C360_HUMAN','1','251'),
('B4DUF0_HUMAN/1-227','PF00069','B4DUF0_HUMAN','1','227'),
('SLK_HUMAN/34-292','PF00069','SLK_HUMAN','34','292'),
('KS6A2_HUMAN/415-672','PF00069','KS6A2_HUMAN','415','672'),
('Q6ZNI2_HUMAN/39-297','PF00069','Q6ZNI2_HUMAN','39','297'),
('B4DX68_HUMAN/33-329','PF00069','B4DX68_HUMAN','33','329'),
('B4DX02_HUMAN/1-251','PF00069','B4DX02_HUMAN','1','251'),
('B7Z388_HUMAN/35-269','PF00069','B7Z388_HUMAN','35','269'),
('F2Z300_HUMAN/32-291','PF00069','F2Z300_HUMAN','32','291'),
('B4DSP6_HUMAN/378-539','PF00069','B4DSP6_HUMAN','378','539'),
('B2R8Z2_HUMAN/44-304','PF00069','B2R8Z2_HUMAN','44','304'),
('DUSTY_HUMAN/653-906','PF00069','DUSTY_HUMAN','653','906'),
('B4DPV1_HUMAN/1-238','PF00069','B4DPV1_HUMAN','1','238'),
('B4DID9_HUMAN/153-446','PF00069','B4DID9_HUMAN','153','446'),
('LRRK1_HUMAN/1243-1520','PF00069','LRRK1_HUMAN','1243','1520'),
('A0PJ70_HUMAN/484-699','PF00069','A0PJ70_HUMAN','484','699'),
('A8MU99_HUMAN/4-254','PF00069','A8MU99_HUMAN','4','254'),
('CD11B_HUMAN/438-723','PF00069','CD11B_HUMAN','438','723'),
('SNRK_HUMAN/16-269','PF00069','SNRK_HUMAN','16','269'),
('AURKC_HUMAN/43-293','PF00069','AURKC_HUMAN','43','293'),
('C9J8E1_HUMAN/44-304','PF00069','C9J8E1_HUMAN','44','304'),
('B3KR53_HUMAN/1-168','PF00069','B3KR53_HUMAN','1','168'),
('B3KTK0_HUMAN/23-277','PF00069','B3KTK0_HUMAN','23','277'),
('KS6A6_HUMAN/73-330','PF00069','KS6A6_HUMAN','73','330'),
('MAST4_HUMAN/573-846','PF00069','MAST4_HUMAN','573','846'),
('B4DHI4_HUMAN/13-275','PF00069','B4DHI4_HUMAN','13','275'),
('B4DG22_HUMAN/393-650','PF00069','B4DG22_HUMAN','393','650'),
('C9J8V9_HUMAN/1-143','PF00069','C9J8V9_HUMAN','1','143'),
('MP2K4_HUMAN/102-367','PF00069','MP2K4_HUMAN','102','367'),
('A1A5A9_HUMAN/1-158','PF00069','A1A5A9_HUMAN','1','158'),
('CLK4_HUMAN/159-475','PF00069','CLK4_HUMAN','159','475'),
('BUB1B_HUMAN/808-956','PF00069','BUB1B_HUMAN','808','956'),
('B4DFP8_HUMAN/4-167','PF00069','B4DFP8_HUMAN','4','167'),
('DAPK2_HUMAN/23-285','PF00069','DAPK2_HUMAN','23','285'),
('M3K14_HUMAN/401-650','PF00069','M3K14_HUMAN','401','650'),
('CDKL3_HUMAN/4-286','PF00069','CDKL3_HUMAN','4','286'),
('KAPCA_HUMAN/44-298','PF00069','KAPCA_HUMAN','44','298'),
('B4DWX2_HUMAN/1-312','PF00069','B4DWX2_HUMAN','1','312'),
('ST17A_HUMAN/61-321','PF00069','ST17A_HUMAN','61','321'),
('B4DI23_HUMAN/55-347','PF00069','B4DI23_HUMAN','55','347'),
('A8K245_HUMAN/37-325','PF00069','A8K245_HUMAN','37','325'),
('H3BSA1_HUMAN/48-206','PF00069','H3BSA1_HUMAN','48','206'),
('A4CYL7_HUMAN/91-375','PF00069','A4CYL7_HUMAN','91','375'),
('B3KVH4_HUMAN/150-408','PF00069','B3KVH4_HUMAN','150','408'),
('H7C1M9_HUMAN/27-293','PF00069','H7C1M9_HUMAN','27','293'),
('WNK1_HUMAN/221-479','PF00069','WNK1_HUMAN','221','479'),
('C9JIG9_HUMAN/17-291','PF00069','C9JIG9_HUMAN','17','291'),
('Q53GK9_HUMAN/22-225','PF00069','Q53GK9_HUMAN','22','225'),
('A8K7I0_HUMAN/163-479','PF00069','A8K7I0_HUMAN','163','479'),
('G5E948_HUMAN/25-289','PF00069','G5E948_HUMAN','25','289'),
('SRPK3_HUMAN/387-565','PF00069','SRPK3_HUMAN','387','565'),
('B7Z8T0_HUMAN/263-551','PF00069','B7Z8T0_HUMAN','263','551'),
('DYRK4_HUMAN/104-400','PF00069','DYRK4_HUMAN','104','400'),
('MYO3B_HUMAN/27-293','PF00069','MYO3B_HUMAN','27','293'),
('B2R748_HUMAN/210-485','PF00069','B2R748_HUMAN','210','485'),
('KCC1G_HUMAN/23-277','PF00069','KCC1G_HUMAN','23','277'),
('M3K3_HUMAN/362-622','PF00069','M3K3_HUMAN','362','622'),
('PINK1_HUMAN/263-509','PF00069','PINK1_HUMAN','263','509'),
('KCC2D_HUMAN/14-272','PF00069','KCC2D_HUMAN','14','272'),
('M4K4_HUMAN/25-289','PF00069','M4K4_HUMAN','25','289'),
('F5H277_HUMAN/61-213','PF00069','F5H277_HUMAN','61','213'),
('Q59FZ4_HUMAN/54-305','PF00069','Q59FZ4_HUMAN','54','305'),
('B2RA52_HUMAN/165-443','PF00069','B2RA52_HUMAN','165','443'),
('Q86VU2_HUMAN/33-301','PF00069','Q86VU2_HUMAN','33','301'),
('Q8IWE0_HUMAN/13-271','PF00069','Q8IWE0_HUMAN','13','271'),
('H3BT74_HUMAN/1-161','PF00069','H3BT74_HUMAN','1','161'),
('Q4W5L5_HUMAN/141-398','PF00069','Q4W5L5_HUMAN','141','398'),
('A8K9L2_HUMAN/29-312','PF00069','A8K9L2_HUMAN','29','312'),
('SG110_HUMAN/43-303','PF00069','SG110_HUMAN','43','303'),
('Q59FN4_HUMAN/557-731','PF00069','Q59FN4_HUMAN','557','731'),
('A4D159_HUMAN/793-966','PF00069','A4D159_HUMAN','793','966'),
('Q5SQU3_HUMAN/348-607','PF00069','Q5SQU3_HUMAN','348','607'),
('B7Z8Q0_HUMAN/238-454','PF00069','B7Z8Q0_HUMAN','238','454'),
('E9PBE1_HUMAN/65-331','PF00069','E9PBE1_HUMAN','65','331'),
('PAK1_HUMAN/270-521','PF00069','PAK1_HUMAN','270','521'),
('B4E0G1_HUMAN/2-223','PF00069','B4E0G1_HUMAN','2','223'),
('B4DH44_HUMAN/79-344','PF00069','B4DH44_HUMAN','79','344'),
('CHK2_HUMAN/220-486','PF00069','CHK2_HUMAN','220','486'),
('F5H6L9_HUMAN/219-515','PF00069','F5H6L9_HUMAN','219','515'),
('ULK2_HUMAN/9-271','PF00069','ULK2_HUMAN','9','271'),
('A8K869_HUMAN/191-453','PF00069','A8K869_HUMAN','191','453'),
('B1APG3_HUMAN/50-264','PF00069','B1APG3_HUMAN','50','264'),
('Q6FI23_HUMAN/64-325','PF00069','Q6FI23_HUMAN','64','325'),
('B7Z1Z6_HUMAN/1-143','PF00069','B7Z1Z6_HUMAN','1','143'),
('PLK2_HUMAN/82-334','PF00069','PLK2_HUMAN','82','334'),
('KS6C1_HUMAN/867-1056','PF00069','KS6C1_HUMAN','867','1056'),
('D3DU05_HUMAN/440-719','PF00069','D3DU05_HUMAN','440','719'),
('Q0IJ49_HUMAN/110-359','PF00069','Q0IJ49_HUMAN','110','359'),
('A8K724_HUMAN/322-572','PF00069','A8K724_HUMAN','322','572'),
('B4DJH7_HUMAN/5-176','PF00069','B4DJH7_HUMAN','5','176'),
('MP2K3_HUMAN/64-325','PF00069','MP2K3_HUMAN','64','325'),
('Q8IXA3_HUMAN/44-315','PF00069','Q8IXA3_HUMAN','44','315'),
('B2RDF9_HUMAN/24-286','PF00069','B2RDF9_HUMAN','24','286'),
('B1ANA3_HUMAN/21-197','PF00069','B1ANA3_HUMAN','21','197'),
('B3KQM3_HUMAN/18-290','PF00069','B3KQM3_HUMAN','18','290'),
('D3DUP2_HUMAN/221-479','PF00069','D3DUP2_HUMAN','221','479'),
('B7Z3K0_HUMAN/172-422','PF00069','B7Z3K0_HUMAN','172','422'),
('A8K602_HUMAN/16-273','PF00069','A8K602_HUMAN','16','273'),
('E9PER6_HUMAN/55-314','PF00069','E9PER6_HUMAN','55','314'),
('B7Z5R1_HUMAN/88-346','PF00069','B7Z5R1_HUMAN','88','346'),
('H3BTW6_HUMAN/24-266','PF00069','H3BTW6_HUMAN','24','266'),
('B9A038_HUMAN/809-1062','PF00069','B9A038_HUMAN','809','1062'),
('PKN2_HUMAN/657-916','PF00069','PKN2_HUMAN','657','916'),
('PAK2_HUMAN/249-500','PF00069','PAK2_HUMAN','249','500'),
('ACVL1_HUMAN/202-490','PF00069','ACVL1_HUMAN','202','490'),
('Q6IC53_HUMAN/27-301','PF00069','Q6IC53_HUMAN','27','301'),
('B7Z7R6_HUMAN/964-1216','PF00069','B7Z7R6_HUMAN','964','1216'),
('KPCT_HUMAN/380-634','PF00069','KPCT_HUMAN','380','634'),
('F5H5A3_HUMAN/1-210','PF00069','F5H5A3_HUMAN','1','210'),
('B7Z7X0_HUMAN/1-220','PF00069','B7Z7X0_HUMAN','1','220'),
('B7Z2T7_HUMAN/390-616','PF00069','B7Z2T7_HUMAN','390','616'),
('B2R6F9_HUMAN/89-382','PF00069','B2R6F9_HUMAN','89','382'),
('H7C521_HUMAN/5-202','PF00069','H7C521_HUMAN','5','202'),
('A8MPP7_HUMAN/312-490','PF00069','A8MPP7_HUMAN','312','490'),
('RN5A_HUMAN/366-524','PF00069','RN5A_HUMAN','366','524'),
('F8WAK5_HUMAN/1-194','PF00069','F8WAK5_HUMAN','1','194'),
('ACVR1_HUMAN/208-495','PF00069','ACVR1_HUMAN','208','495'),
('C9JUK9_HUMAN/55-241','PF00069','C9JUK9_HUMAN','55','241'),
('H3BP07_HUMAN/24-255','PF00069','H3BP07_HUMAN','24','255'),
('PRKX_HUMAN/49-303','PF00069','PRKX_HUMAN','49','303'),
('B4DRK0_HUMAN/655-844','PF00069','B4DRK0_HUMAN','655','844'),
('PLK3_HUMAN/62-314','PF00069','PLK3_HUMAN','62','314'),
('CLK3_HUMAN/304-620','PF00069','CLK3_HUMAN','304','620'),
('B0QY35_HUMAN/9-280','PF00069','B0QY35_HUMAN','9','280'),
('Q96HN9_HUMAN/330-590','PF00069','Q96HN9_HUMAN','330','590'),
('Q71TU5_HUMAN/17-292','PF00069','Q71TU5_HUMAN','17','292'),
('B3KVE9_HUMAN/1-210','PF00069','B3KVE9_HUMAN','1','210'),
('ICK_HUMAN/4-284','PF00069','ICK_HUMAN','4','284'),
('H7BYG4_HUMAN/169-462','PF00069','H7BYG4_HUMAN','169','462'),
('B4DT57_HUMAN/43-293','PF00069','B4DT57_HUMAN','43','293'),
('C9JJ18_HUMAN/15-226','PF00069','C9JJ18_HUMAN','15','226'),
('B5MCX4_HUMAN/72-217','PF00069','B5MCX4_HUMAN','72','217'),
('E5RIU6_HUMAN/4-189','PF00069','E5RIU6_HUMAN','4','189'),
('Q53GX0_HUMAN/11-263','PF00069','Q53GX0_HUMAN','11','263'),
('Q7LDD5_HUMAN/13-271','PF00069','Q7LDD5_HUMAN','13','271'),
('H0YEW1_HUMAN/5-197','PF00069','H0YEW1_HUMAN','5','197'),
('B3KRV2_HUMAN/9-280','PF00069','B3KRV2_HUMAN','9','280'),
('TTBK1_HUMAN/34-300','PF00069','TTBK1_HUMAN','34','300'),
('NEK11_HUMAN/29-287','PF00069','NEK11_HUMAN','29','287'),
('H0Y820_HUMAN/3-219','PF00069','H0Y820_HUMAN','3','219'),
('Q5TBG1_HUMAN/45-207','PF00069','Q5TBG1_HUMAN','45','207'),
('Q8N433_HUMAN/191-387','PF00069','Q8N433_HUMAN','191','387'),
('B5BU41_HUMAN/20-276','PF00069','B5BU41_HUMAN','20','276'),
('A5YM65_HUMAN/520-781','PF00069','A5YM65_HUMAN','520','781'),
('B4DR46_HUMAN/23-281','PF00069','B4DR46_HUMAN','23','281'),
('MYLK3_HUMAN/515-770','PF00069','MYLK3_HUMAN','515','770'),
('B2R6V2_HUMAN/58-224','PF00069','B2R6V2_HUMAN','58','224'),
('A8K9K0_HUMAN/484-699','PF00069','A8K9K0_HUMAN','484','699'),
('B0AZM9_HUMAN/450-700','PF00069','B0AZM9_HUMAN','450','700'),
('A8K4K4_HUMAN/44-304','PF00069','A8K4K4_HUMAN','44','304'),
('H3BTZ2_HUMAN/2-156','PF00069','H3BTZ2_HUMAN','2','156'),
('B4DJD8_HUMAN/48-313','PF00069','B4DJD8_HUMAN','48','313'),
('Q8N2H2_HUMAN/396-650','PF00069','Q8N2H2_HUMAN','396','650'),
('PIM1_HUMAN/129-381','PF00069','PIM1_HUMAN','129','381'),
('TRIB3_HUMAN/78-315','PF00069','TRIB3_HUMAN','78','315'),
('MAST1_HUMAN/374-647','PF00069','MAST1_HUMAN','374','647'),
('D6RJF7_HUMAN/29-196','PF00069','D6RJF7_HUMAN','29','196'),
('A9NIU4_HUMAN/1664-1916','PF00069','A9NIU4_HUMAN','1664','1916'),
('D3DSB5_HUMAN/20-277','PF00069','D3DSB5_HUMAN','20','277'),
('M3K15_HUMAN/654-908','PF00069','M3K15_HUMAN','654','908'),
('H7BXZ5_HUMAN/2653-2907','PF00069','H7BXZ5_HUMAN','2653','2907'),
('B4DMN4_HUMAN/374-647','PF00069','B4DMN4_HUMAN','374','647'),
('VRK1_HUMAN/37-325','PF00069','VRK1_HUMAN','37','325'),
('H3BPX2_HUMAN/8384-8634','PF00069','H3BPX2_HUMAN','8384','8634'),
('TRIB1_HUMAN/104-338','PF00069','TRIB1_HUMAN','104','338'),
('B7Z1Z1_HUMAN/1-245','PF00069','B7Z1Z1_HUMAN','1','245'),
('Q7Z3H5_HUMAN/1-274','PF00069','Q7Z3H5_HUMAN','1','274'),
('B4E0I7_HUMAN/37-308','PF00069','B4E0I7_HUMAN','37','308'),
('D6REM4_HUMAN/1-205','PF00069','D6REM4_HUMAN','1','205'),
('B7ZBF6_HUMAN/157-298','PF00069','B7ZBF6_HUMAN','157','298'),
('NEK8_HUMAN/4-258','PF00069','NEK8_HUMAN','4','258'),
('Q68D16_HUMAN/24-308','PF00069','Q68D16_HUMAN','24','308'),
('G5E959_HUMAN/148-449','PF00069','G5E959_HUMAN','148','449'),
('F8VTV8_HUMAN/6-181','PF00069','F8VTV8_HUMAN','6','181'),
('NEK3_HUMAN/4-257','PF00069','NEK3_HUMAN','4','257'),
('B3KY91_HUMAN/349-525','PF00069','B3KY91_HUMAN','349','525'),
('B4DGW1_HUMAN/11-221','PF00069','B4DGW1_HUMAN','11','221'),
('Q59GF4_HUMAN/519-697','PF00069','Q59GF4_HUMAN','519','697'),
('B4DZQ5_HUMAN/673-989','PF00069','B4DZQ5_HUMAN','673','989'),
('Q86XZ8_HUMAN/76-342','PF00069','Q86XZ8_HUMAN','76','342'),
('B7ZVY7_HUMAN/425-710','PF00069','B7ZVY7_HUMAN','425','710'),
('D3YTB5_HUMAN/238-541','PF00069','D3YTB5_HUMAN','238','541'),
('B2R6V2_HUMAN/355-569','PF00069','B2R6V2_HUMAN','355','569'),
('MK01_HUMAN/25-313','PF00069','MK01_HUMAN','25','313'),
('E9PBE8_HUMAN/14-168','PF00069','E9PBE8_HUMAN','14','168'),
('MAPK2_HUMAN/64-325','PF00069','MAPK2_HUMAN','64','325'),
('Q58A51_HUMAN/53-232','PF00069','Q58A51_HUMAN','53','232'),
('B5TY32_HUMAN/24-254','PF00069','B5TY32_HUMAN','24','254'),
('H3BRW9_HUMAN/12-185','PF00069','H3BRW9_HUMAN','12','185'),
('CLK2_HUMAN/163-479','PF00069','CLK2_HUMAN','163','479'),
('B3KV38_HUMAN/190-518','PF00069','B3KV38_HUMAN','190','518'),
('E9PM17_HUMAN/172-422','PF00069','E9PM17_HUMAN','172','422'),
('WNK4_HUMAN/174-432','PF00069','WNK4_HUMAN','174','432'),
('KPCI_HUMAN/254-522','PF00069','KPCI_HUMAN','254','522'),
('Q59ED6_HUMAN/37-289','PF00069','Q59ED6_HUMAN','37','289'),
('F5H865_HUMAN/25-289','PF00069','F5H865_HUMAN','25','289'),
('E7EUK8_HUMAN/23-290','PF00069','E7EUK8_HUMAN','23','290'),
('Q9HBS3_HUMAN/49-309','PF00069','Q9HBS3_HUMAN','49','309'),
('F8WAP0_HUMAN/1-251','PF00069','F8WAP0_HUMAN','1','251'),
('B9EIS4_HUMAN/190-455','PF00069','B9EIS4_HUMAN','190','455'),
('Q6LC83_HUMAN/2-221','PF00069','Q6LC83_HUMAN','2','221'),
('B3KQI0_HUMAN/111-431','PF00069','B3KQI0_HUMAN','111','431'),
('PEAK1_HUMAN/1443-1663','PF00069','PEAK1_HUMAN','1443','1663'),
('Q2NME9_HUMAN/4-286','PF00069','Q2NME9_HUMAN','4','286'),
('TSSK3_HUMAN/10-265','PF00069','TSSK3_HUMAN','10','265'),
('D6REE7_HUMAN/92-354','PF00069','D6REE7_HUMAN','92','354'),
('Q6FHR4_HUMAN/25-308','PF00069','Q6FHR4_HUMAN','25','308'),
('AKT2_HUMAN/152-409','PF00069','AKT2_HUMAN','152','409'),
('M3K8_HUMAN/140-388','PF00069','M3K8_HUMAN','140','388'),
('ROCK2_HUMAN/92-354','PF00069','ROCK2_HUMAN','92','354'),
('Q8IWB3_HUMAN/1-164','PF00069','Q8IWB3_HUMAN','1','164'),
('H7BZ84_HUMAN/28-288','PF00069','H7BZ84_HUMAN','28','288'),
('H0Y411_HUMAN/1085-1338','PF00069','H0Y411_HUMAN','1085','1338'),
('AKT1_HUMAN/150-408','PF00069','AKT1_HUMAN','150','408'),
('STK11_HUMAN/49-309','PF00069','STK11_HUMAN','49','309'),
('MKNK2_HUMAN/84-368','PF00069','MKNK2_HUMAN','84','368'),
('KS6A3_HUMAN/68-327','PF00069','KS6A3_HUMAN','68','327'),
('B4DPV1_HUMAN/350-611','PF00069','B4DPV1_HUMAN','350','611'),
('Q68DI6_HUMAN/712-926','PF00069','Q68DI6_HUMAN','712','926'),
('DYRK2_HUMAN/222-535','PF00069','DYRK2_HUMAN','222','535'),
('CDKL4_HUMAN/4-286','PF00069','CDKL4_HUMAN','4','286'),
('Q53TX8_HUMAN/1-229','PF00069','Q53TX8_HUMAN','1','229'),
('AVR2A_HUMAN/192-479','PF00069','AVR2A_HUMAN','192','479'),
('STK3_HUMAN/27-278','PF00069','STK3_HUMAN','27','278'),
('B3KNJ3_HUMAN/13-275','PF00069','B3KNJ3_HUMAN','13','275'),
('D7R525_HUMAN/26-212','PF00069','D7R525_HUMAN','26','212'),
('B3KS39_HUMAN/1-194','PF00069','B3KS39_HUMAN','1','194'),
('B4DK59_HUMAN/23-290','PF00069','B4DK59_HUMAN','23','290'),
('H7BXS4_HUMAN/14-272','PF00069','H7BXS4_HUMAN','14','272'),
('TSSK4_HUMAN/25-293','PF00069','TSSK4_HUMAN','25','293'),
('CDK9_HUMAN/19-315','PF00069','CDK9_HUMAN','19','315'),
('B4E1D9_HUMAN/1-195','PF00069','B4E1D9_HUMAN','1','195'),
('M3K1_HUMAN/1243-1508','PF00069','M3K1_HUMAN','1243','1508'),
('Q9BUD9_HUMAN/46-312','PF00069','Q9BUD9_HUMAN','46','312'),
('B7Z3V9_HUMAN/166-419','PF00069','B7Z3V9_HUMAN','166','419'),
('A8K574_HUMAN/189-502','PF00069','A8K574_HUMAN','189','502'),
('B0QY36_HUMAN/9-225','PF00069','B0QY36_HUMAN','9','225'),
('CLK1_HUMAN/161-477','PF00069','CLK1_HUMAN','161','477'),
('H3BLV9_HUMAN/96-248','PF00069','H3BLV9_HUMAN','96','248'),
('B7Z454_HUMAN/13-275','PF00069','B7Z454_HUMAN','13','275'),
('Q5R363_HUMAN/369-545','PF00069','Q5R363_HUMAN','369','545'),
('CAMKV_HUMAN/24-286','PF00069','CAMKV_HUMAN','24','286'),
('B3KVM3_HUMAN/284-541','PF00069','B3KVM3_HUMAN','284','541'),
('CDK18_HUMAN/142-423','PF00069','CDK18_HUMAN','142','423'),
('B2R9M7_HUMAN/408-668','PF00069','B2R9M7_HUMAN','408','668'),
('F2Z2J1_HUMAN/440-697','PF00069','F2Z2J1_HUMAN','440','697'),
('A0PJF8_HUMAN/413-556','PF00069','A0PJF8_HUMAN','413','556'),
('B4DX16_HUMAN/65-315','PF00069','B4DX16_HUMAN','65','315'),
('C9JDA4_HUMAN/4-254','PF00069','C9JDA4_HUMAN','4','254'),
('E7ETM0_HUMAN/1-232','PF00069','E7ETM0_HUMAN','1','232'),
('CDK2_HUMAN/4-286','PF00069','CDK2_HUMAN','4','286'),
('F5H2U2_HUMAN/673-989','PF00069','F5H2U2_HUMAN','673','989'),
('B4DV02_HUMAN/148-429','PF00069','B4DV02_HUMAN','148','429'),
('MK04_HUMAN/20-312','PF00069','MK04_HUMAN','20','312'),
('B4DS61_HUMAN/64-216','PF00069','B4DS61_HUMAN','64','216'),
('NEK4_HUMAN/6-261','PF00069','NEK4_HUMAN','6','261'),
('KPCA_HUMAN/339-597','PF00069','KPCA_HUMAN','339','597'),
('B4DFT0_HUMAN/41-281','PF00069','B4DFT0_HUMAN','41','281'),
('DYR1A_HUMAN/159-479','PF00069','DYR1A_HUMAN','159','479'),
('B4DS37_HUMAN/39-234','PF00069','B4DS37_HUMAN','39','234'),
('A8KAE3_HUMAN/204-491','PF00069','A8KAE3_HUMAN','204','491'),
('MK07_HUMAN/55-347','PF00069','MK07_HUMAN','55','347'),
('Q59GF4_HUMAN/211-360','PF00069','Q59GF4_HUMAN','211','360'),
('B7Z7J1_HUMAN/106-365','PF00069','B7Z7J1_HUMAN','106','365'),
('STK38_HUMAN/89-382','PF00069','STK38_HUMAN','89','382'),
('STK31_HUMAN/793-966','PF00069','STK31_HUMAN','793','966'),
('CDK8_HUMAN/23-335','PF00069','CDK8_HUMAN','23','335'),
('IKKA_HUMAN/15-297','PF00069','IKKA_HUMAN','15','297'),
('B2R8A5_HUMAN/140-388','PF00069','B2R8A5_HUMAN','140','388'),
('CDK16_HUMAN/165-446','PF00069','CDK16_HUMAN','165','446'),
('H3BPX2_HUMAN/7180-7433','PF00069','H3BPX2_HUMAN','7180','7433'),
('Q4G1A8_HUMAN/14-272','PF00069','Q4G1A8_HUMAN','14','272'),
('GRK4_HUMAN/187-449','PF00069','GRK4_HUMAN','187','449'),
('A8K7G8_HUMAN/156-472','PF00069','A8K7G8_HUMAN','156','472'),
('Q59GT1_HUMAN/22-304','PF00069','Q59GT1_HUMAN','22','304'),
('B2RAP9_HUMAN/187-455','PF00069','B2RAP9_HUMAN','187','455'),
('F8W9W2_HUMAN/247-414','PF00069','F8W9W2_HUMAN','247','414'),
('B7Z537_HUMAN/39-323','PF00069','B7Z537_HUMAN','39','323'),
('B7Z3B5_HUMAN/326-583','PF00069','B7Z3B5_HUMAN','326','583'),
('A8K8R5_HUMAN/203-501','PF00069','A8K8R5_HUMAN','203','501'),
('D6W5G0_HUMAN/46-312','PF00069','D6W5G0_HUMAN','46','312'),
('PKN3_HUMAN/559-818','PF00069','PKN3_HUMAN','559','818'),
('PRKY_HUMAN/50-272','PF00069','PRKY_HUMAN','50','272'),
('G3V2D1_HUMAN/49-214','PF00069','G3V2D1_HUMAN','49','214'),
('B7Z1G1_HUMAN/2-212','PF00069','B7Z1G1_HUMAN','2','212'),
('Q86UI9_HUMAN/1-161','PF00069','Q86UI9_HUMAN','1','161'),
('B2R747_HUMAN/46-300','PF00069','B2R747_HUMAN','46','300'),
('Q5JS74_HUMAN/12-276','PF00069','Q5JS74_HUMAN','12','276'),
('E9PQ51_HUMAN/2-160','PF00069','E9PQ51_HUMAN','2','160'),
('Q96K88_HUMAN/1-139','PF00069','Q96K88_HUMAN','1','139'),
('B4DKT8_HUMAN/376-649','PF00069','B4DKT8_HUMAN','376','649'),
('C9JGD6_HUMAN/181-439','PF00069','C9JGD6_HUMAN','181','439'),
('E7EN19_HUMAN/25-289','PF00069','E7EN19_HUMAN','25','289'),
('B4DR80_HUMAN/86-255','PF00069','B4DR80_HUMAN','86','255'),
('CHK1_HUMAN/9-265','PF00069','CHK1_HUMAN','9','265'),
('KPCD_HUMAN/349-603','PF00069','KPCD_HUMAN','349','603'),
('Q2TSD3_HUMAN/339-597','PF00069','Q2TSD3_HUMAN','339','597'),
('B8ZZR0_HUMAN/1-300','PF00069','B8ZZR0_HUMAN','1','300'),
('CDK12_HUMAN/727-1020','PF00069','CDK12_HUMAN','727','1020'),
('B7ZA12_HUMAN/203-519','PF00069','B7ZA12_HUMAN','203','519'),
('B4DZ33_HUMAN/261-589','PF00069','B4DZ33_HUMAN','261','589'),
('TBK1_HUMAN/9-329','PF00069','TBK1_HUMAN','9','329'),
('B0YIY3_HUMAN/20-276','PF00069','B0YIY3_HUMAN','20','276'),
('D3DVK8_HUMAN/1-143','PF00069','D3DVK8_HUMAN','1','143'),
('KCC2B_HUMAN/14-272','PF00069','KCC2B_HUMAN','14','272'),
('PRP4B_HUMAN/687-1003','PF00069','PRP4B_HUMAN','687','1003'),
('A8K341_HUMAN/50-333','PF00069','A8K341_HUMAN','50','333'),
('B7Z3B5_HUMAN/1-229','PF00069','B7Z3B5_HUMAN','1','229'),
('G3V4L3_HUMAN/1-150','PF00069','G3V4L3_HUMAN','1','150'),
('A8K0N1_HUMAN/35-292','PF00069','A8K0N1_HUMAN','35','292'),
('B3KTH7_HUMAN/2-168','PF00069','B3KTH7_HUMAN','2','168'),
('A8K5M4_HUMAN/249-500','PF00069','A8K5M4_HUMAN','249','500'),
('Q96GA5_HUMAN/64-345','PF00069','Q96GA5_HUMAN','64','345'),
('CSK22_HUMAN/40-325','PF00069','CSK22_HUMAN','40','325'),
('Q5MD60_HUMAN/25-171','PF00069','Q5MD60_HUMAN','25','171'),
('MP2K6_HUMAN/53-314','PF00069','MP2K6_HUMAN','53','314'),
('TLK2_HUMAN/462-741','PF00069','TLK2_HUMAN','462','741'),
('A8K6P8_HUMAN/4-167','PF00069','A8K6P8_HUMAN','4','167'),
('B2R8K8_HUMAN/34-292','PF00069','B2R8K8_HUMAN','34','292'),
('A1A4C4_HUMAN/20-312','PF00069','A1A4C4_HUMAN','20','312'),
('TBCK_HUMAN/33-273','PF00069','TBCK_HUMAN','33','273'),
('GSK3A_HUMAN/119-403','PF00069','GSK3A_HUMAN','119','403'),
('B4DMM6_HUMAN/1-172','PF00069','B4DMM6_HUMAN','1','172'),
('TTK_HUMAN/525-791','PF00069','TTK_HUMAN','525','791'),
('E9PJI4_HUMAN/9-170','PF00069','E9PJI4_HUMAN','9','170'),
('LIMK2_HUMAN/331-601','PF00069','LIMK2_HUMAN','331','601'),
('LIMK1_HUMAN/339-604','PF00069','LIMK1_HUMAN','339','604'),
('M3K10_HUMAN/98-357','PF00069','M3K10_HUMAN','98','357'),
('M3K11_HUMAN/117-376','PF00069','M3K11_HUMAN','117','376'),
('M3KL4_HUMAN/124-398','PF00069','M3KL4_HUMAN','124','398'),
('M3K12_HUMAN/126-364','PF00069','M3K12_HUMAN','126','364'),
('M3K13_HUMAN/168-407','PF00069','M3K13_HUMAN','168','407'),
('MLTK_HUMAN/16-260','PF00069','MLTK_HUMAN','16','260'),
('ANKK1_HUMAN/25-285','PF00069','ANKK1_HUMAN','25','285'),
('M3K7_HUMAN/36-284','PF00069','M3K7_HUMAN','36','284'),
('TNI3K_HUMAN/463-719','PF00069','TNI3K_HUMAN','463','719'),
('ARAF_HUMAN/310-567','PF00069','ARAF_HUMAN','310','567'),
('BRAF_HUMAN/457-714','PF00069','BRAF_HUMAN','457','714'),
('RAF1_HUMAN/349-606','PF00069','RAF1_HUMAN','349','606'),
('LMTK3_HUMAN/133-408','PF00069','LMTK3_HUMAN','133','408'),
('LMTK2_HUMAN/137-407','PF00069','LMTK2_HUMAN','137','407'),
('LMTK1_HUMAN/125-395','PF00069','LMTK1_HUMAN','125','395'),
('ILK_HUMAN/193-446','PF00069','ILK_HUMAN','193','446');INSERT INTO `kindriver_v82`.`Protein_has_Segment` (`Protein_has_Segment_id`,`segment_id`,`pfam_domain_id`,`start`,`end`,`length`) VALUES 
('1','1','Q59F17_HUMAN/614-873','614','638','24'),
('2','1','Q548C2_HUMAN/538-807','538','564','26'),
('3','1','JAK3_HUMAN/822-1095','822','847','25'),
('4','1','TYRO3_HUMAN/518-786','518','542','24'),
('5','1','Q12787_HUMAN/333-599','333','357','24'),
('6','1','B4DES9_HUMAN/363-633','364','384','20'),
('7','1','TESK2_HUMAN/59-309','61','79','18'),
('8','1','B4DTW8_HUMAN/794-1062','794','817','23'),
('9','1','D1MAM5_HUMAN/1116-1383','1116','1142','26'),
('10','1','TYK2_HUMAN/589-866','590','634','44'),
('11','1','Q573B4_HUMAN/261-501','270','272','2'),
('12','1','ZAP70_HUMAN/338-593','341','361','20'),
('13','1','NTRK3_HUMAN/538-824','538','564','26'),
('14','1','A6P4T4_HUMAN/555-822','555','581','26'),
('15','1','EPHA3_HUMAN/621-878','621','645','24'),
('16','1','B5BU33_HUMAN/331-601','332','352','20'),
('17','1','MLKL_HUMAN/209-466','218','222','4'),
('18','1','B4DR56_HUMAN/253-523','254','274','20'),
('19','1','E7EML7_HUMAN/140-395','140','164','24'),
('20','1','GUC2C_HUMAN/499-745','506','508','2'),
('21','1','B4DSE0_HUMAN/563-822','563','587','24'),
('22','1','C1PHA2_HUMAN/979-1246','979','1005','26'),
('23','1','EGFR_HUMAN/712-968','712','737','25'),
('24','1','Q1RMG3_HUMAN/411-678','411','435','24'),
('25','1','H7C074_HUMAN/63-285','66','84','18'),
('26','1','Q59FM9_HUMAN/579-847','579','603','24'),
('27','1','Q8TDJ5_HUMAN/299-566','299','325','26'),
('28','1','D1MAM4_HUMAN/1116-1383','1116','1142','26'),
('29','1','F2YGG7_HUMAN/667-923','667','692','25'),
('30','1','A9YLN7_HUMAN/292-559','292','318','26'),
('31','1','E9PFD7_HUMAN/659-915','659','684','25'),
('32','1','B3KSH7_HUMAN/85-355','86','106','20'),
('33','1','ERBB2_HUMAN/720-976','720','745','25'),
('34','1','B3KQJ1_HUMAN/48-303','50','71','21'),
('35','1','C1PHA0_HUMAN/578-845','578','604','26'),
('36','1','PTK7_HUMAN/796-1061','798','822','24'),
('37','1','H0YNK6_HUMAN/473-741','473','497','24'),
('38','1','A9YLN5_HUMAN/322-592','323','349','26'),
('39','1','ROR1_HUMAN/473-746','473','498','25'),
('40','1','Q9HBS4_HUMAN/122-390','122','145','23'),
('41','1','E9PPF2_HUMAN/589-826','590','634','44'),
('42','1','Q53HA9_HUMAN/589-822','590','634','44'),
('43','1','EPHB2_HUMAN/621-880','621','645','24'),
('44','1','A9CB80_HUMAN/712-968','712','737','25'),
('45','1','Q2TTR7_HUMAN/712-968','712','737','25'),
('46','1','ROR2_HUMAN/473-746','473','499','26'),
('47','1','Q7Z635_HUMAN/615-874','615','639','24'),
('48','1','H3BPR7_HUMAN/1-244','1','24','23'),
('49','1','Q59FX1_HUMAN/10-261','13','26','13'),
('50','1','F5H8L5_HUMAN/141-407','141','167','26'),
('51','1','D3DNT9_HUMAN/591-850','591','615','24'),
('52','1','Q8IXP2_HUMAN/542-802','542','570','28'),
('53','1','H7BZZ3_HUMAN/44-290','66','75','9'),
('54','1','Q8N6J3_HUMAN/146-414','146','170','24'),
('55','1','H0Y8A4_HUMAN/310-576','310','336','26'),
('56','1','MERTK_HUMAN/587-854','587','611','24'),
('57','1','B4E123_HUMAN/336-613','337','381','44'),
('58','1','B4DTR1_HUMAN/444-700','444','469','25'),
('59','1','EPHAA_HUMAN/645-900','645','669','24'),
('60','1','B6D4Y2_HUMAN/1116-1383','1116','1142','26'),
('61','1','D4Q8H0_HUMAN/16-260','16','37','21'),
('62','1','B7Z7U4_HUMAN/440-617','440','466','26'),
('63','1','D1MAM1_HUMAN/1116-1383','1116','1142','26'),
('64','1','A8K2T6_HUMAN/624-880','625','648','23'),
('65','1','C9JXA2_HUMAN/621-878','621','645','24'),
('66','1','B6EXY4_HUMAN/128-395','128','154','26'),
('67','1','MUSK_HUMAN/575-856','575','601','26'),
('68','1','H3BVG6_HUMAN/208-475','208','234','26'),
('69','1','EPHB3_HUMAN/633-892','633','657','24'),
('70','1','Q4LE53_HUMAN/639-898','639','663','24'),
('71','1','B4DIA4_HUMAN/1-264','1','20','19'),
('72','1','B6D4Y8_HUMAN/1116-1383','1116','1142','26'),
('73','1','A8K3Z4_HUMAN/507-778','508','533','25'),
('74','1','A8K5U6_HUMAN/621-878','621','645','24'),
('75','1','E9PG63_HUMAN/484-752','484','507','23'),
('76','1','ERBB3_HUMAN/709-965','709','734','25'),
('77','1','Q506Q0_HUMAN/545-805','545','573','28'),
('78','1','B3KP36_HUMAN/141-406','143','167','24'),
('79','1','A2VCQ3_HUMAN/476-749','476','501','25'),
('80','1','Q53R53_HUMAN/155-422','155','179','24'),
('81','1','JAK1_HUMAN/875-1149','875','900','25'),
('82','1','Q4LDX3_HUMAN/571-833','571','602','31'),
('83','1','STYK1_HUMAN/114-380','115','139','24'),
('84','1','Q4LDX3_HUMAN/863-1136','863','887','24'),
('85','1','D1MAM0_HUMAN/1116-1383','1116','1142','26'),
('86','1','Q59F19_HUMAN/62-312','65','82','17'),
('87','1','B0YIV3_HUMAN/25-285','27','43','16'),
('88','1','A8K4G2_HUMAN/371-626','373','394','21'),
('89','1','TIE1_HUMAN/839-1107','839','862','23'),
('90','1','E9PBI4_HUMAN/171-425','171','195','24'),
('91','1','JAK2_HUMAN/545-805','545','573','28'),
('92','1','RYK_HUMAN/327-593','327','353','26'),
('93','1','A1L4F5_HUMAN/473-746','473','499','26'),
('94','1','F5H5U8_HUMAN/396-656','396','424','28'),
('95','1','TNK1_HUMAN/116-377','118','140','22'),
('96','1','B6EXY3_HUMAN/593-860','593','619','26'),
('97','1','EPHA1_HUMAN/624-880','625','648','23'),
('98','1','H0YCC9_HUMAN/145-391','145','169','24'),
('99','1','E7EUC1_HUMAN/85-355','86','106','20'),
('100','1','H7C175_HUMAN/78-348','80','101','21'),
('101','1','LTK_HUMAN/510-777','510','536','26'),
('102','1','B1AKC9_HUMAN/616-875','616','640','24'),
('103','1','A8K910_HUMAN/545-805','545','573','28'),
('104','1','EPHA2_HUMAN/613-871','613','638','25'),
('105','1','FAK2_HUMAN/425-679','425','449','24'),
('106','1','C0LYZ4_HUMAN/1-215','1','7','6'),
('107','1','B4DGQ7_HUMAN/709-911','709','734','25'),
('108','1','Q5JPC5_HUMAN/208-423','217','221','4'),
('109','1','EPHB4_HUMAN/615-874','615','639','24'),
('110','1','B6EXY5_HUMAN/167-434','167','193','26'),
('111','1','H2E273_HUMAN/357-492','359','381','22'),
('112','1','UFO_HUMAN/536-803','536','559','23'),
('113','1','A8K2T7_HUMAN/712-968','712','737','25'),
('114','1','G5EKE5_HUMAN/307-574','307','333','26'),
('115','1','Q6ZNH1_HUMAN/140-395','140','164','24'),
('116','1','B6D4Y5_HUMAN/1116-1383','1116','1142','26'),
('117','1','E9PM19_HUMAN/404-681','405','449','44'),
('118','1','B2RE75_HUMAN/587-854','587','611','24'),
('119','1','A8K710_HUMAN/16-260','16','37','21'),
('120','1','D1MAM3_HUMAN/1116-1383','1116','1142','26'),
('121','1','Q15516_HUMAN/242-500','242','268','26'),
('122','1','B4DU06_HUMAN/288-547','304','305','1'),
('123','1','Q541P7_HUMAN/615-874','615','639','24'),
('124','1','NTRK1_HUMAN/510-781','511','536','25'),
('125','1','Q59FL8_HUMAN/583-839','583','608','25'),
('126','1','E9PC47_HUMAN/369-634','370','390','20'),
('127','1','INSRR_HUMAN/979-1246','979','1005','26'),
('128','1','H0YM90_HUMAN/530-705','530','556','26'),
('129','1','Q6ZRA8_HUMAN/171-425','171','195','24'),
('130','1','B4DYR0_HUMAN/177-447','178','198','20'),
('131','1','RON_HUMAN/1082-1341','1084','1106','22'),
('132','1','Q5H8Y1_HUMAN/1939-2209','1940','1966','26'),
('133','1','KSYK_HUMAN/371-626','373','394','21'),
('134','1','A9YLN4_HUMAN/301-571','302','328','26'),
('135','1','A9YLN6_HUMAN/219-489','220','246','26'),
('136','1','ALK_HUMAN/1116-1383','1116','1142','26'),
('137','1','B6D4Y3_HUMAN/1116-1383','1116','1142','26'),
('138','1','A6P4V4_HUMAN/806-1073','806','832','26'),
('139','1','ROS1_HUMAN/1945-2215','1946','1972','26'),
('140','1','B4DKW0_HUMAN/484-752','484','507','23'),
('141','1','B1APY4_HUMAN/333-606','333','359','26'),
('142','1','NTRK2_HUMAN/538-807','538','564','26'),
('143','1','G9BXQ3_HUMAN/116-377','118','140','22'),
('144','1','Q59GM4_HUMAN/430-684','430','454','24'),
('145','1','B3XZL9_HUMAN/281-548','281','307','26'),
('146','1','Q8WTZ8_HUMAN/118-384','118','144','26'),
('147','1','B4DYV1_HUMAN/396-656','396','424','28'),
('148','1','EPHB1_HUMAN/619-878','619','643','24'),
('149','1','B3XZM0_HUMAN/292-559','292','318','26'),
('150','1','Q9NSQ6_HUMAN/108-355','114','116','2'),
('151','1','B3KTB2_HUMAN/180-439','180','204','24'),
('152','1','E7BSV0_HUMAN/712-968','712','737','25'),
('153','1','Q504U8_HUMAN/667-923','667','692','25'),
('154','1','B6D4Y1_HUMAN/1116-1383','1116','1142','26'),
('155','1','D1MAM2_HUMAN/1116-1383','1116','1142','26'),
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('4023','12','LCK_HUMAN/245-494','465','490','25'),
('4024','12','C9J1X3_HUMAN/158-417','388','413','25'),
('4025','12','TYK2_HUMAN/897-1169','1140','1165','25'),
('4026','12','A2VCQ3_HUMAN/476-749','720','745','25'),
('4027','12','Q53R53_HUMAN/155-422','393','418','25'),
('4028','12','VGFR3_HUMAN/845-1169','1140','1165','25'),
('4029','12','JAK1_HUMAN/875-1149','1120','1145','25'),
('4030','12','Q5R3A8_HUMAN/219-468','439','464','25'),
('4031','12','D3DRD6_HUMAN/44-320','291','316','25'),
('4032','12','E9PEI4_HUMAN/50-304','275','300','25'),
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('4035','12','Q4LDX3_HUMAN/863-1136','1107','1132','25'),
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('4037','12','Q59F19_HUMAN/62-312','283','308','25'),
('4038','12','FGFR1_HUMAN/478-754','725','750','25'),
('4039','12','B0YIV3_HUMAN/25-285','253','281','28'),
('4040','12','BTK_HUMAN/402-651','622','647','25'),
('4041','12','A8K4G2_HUMAN/371-626','597','622','25'),
('4042','12','TIE1_HUMAN/839-1107','1078','1103','25'),
('4043','12','E9PBI4_HUMAN/171-425','396','421','25'),
('4044','12','RYK_HUMAN/327-593','564','589','25'),
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('4051','12','EPHA1_HUMAN/624-880','851','876','25'),
('4052','12','Q59F04_HUMAN/271-629','600','625','25'),
('4053','12','E7EUC1_HUMAN/85-355','326','351','25'),
('4054','12','F5H5U8_HUMAN/700-974','945','970','25'),
('4055','12','H7C175_HUMAN/78-348','320','344','24'),
('4056','12','LTK_HUMAN/510-777','748','773','25'),
('4057','12','B1AKC9_HUMAN/616-875','846','871','25'),
('4058','12','FRK_HUMAN/234-487','458','483','25'),
('4059','12','F5H3M4_HUMAN/197-446','417','442','25'),
('4060','12','Q15850_HUMAN/87-368','339','364','25'),
('4061','12','Q59GM6_HUMAN/374-628','599','624','25'),
('4062','12','EPHA2_HUMAN/613-871','842','867','25'),
('4063','12','D6RA14_HUMAN/1-175','146','171','25'),
('4064','12','FAK2_HUMAN/425-679','650','675','25'),
('4065','12','B2R8Z4_HUMAN/417-666','637','662','25'),
('4066','12','B2R601_HUMAN/621-878','849','874','25'),
('4067','12','A9UF07_HUMAN/902-1153','1124','1149','25'),
('4068','12','EPHB4_HUMAN/615-874','845','870','25'),
('4069','12','B6EXY5_HUMAN/167-434','405','430','25'),
('4070','12','A8K3B6_HUMAN/195-440','411','436','25'),
('4071','12','A8K297_HUMAN/339-604','575','600','25'),
('4072','12','UFO_HUMAN/536-803','774','799','25'),
('4073','12','A8K2T7_HUMAN/712-968','939','964','25'),
('4074','12','B4DGX8_HUMAN/470-751','722','747','25'),
('4075','12','G5EKE5_HUMAN/307-574','545','570','25'),
('4076','12','Q6ZNH1_HUMAN/140-395','366','391','25'),
('4077','12','B6D4Y5_HUMAN/1116-1383','1354','1379','25'),
('4078','12','FER_HUMAN/563-814','785','810','25'),
('4079','12','F5H0K8_HUMAN/591-855','826','851','25'),
('4080','12','B2RE75_HUMAN/587-854','825','850','25'),
('4081','12','A8K710_HUMAN/16-260','231','256','25'),
('4082','12','D1MAM3_HUMAN/1116-1383','1354','1379','25'),
('4083','12','Q9UMQ4_HUMAN/700-982','953','978','25'),
('4084','12','Q5IBP5_HUMAN/1183-1440','1411','1436','25'),
('4085','12','C9J5X1_HUMAN/998-1265','1236','1261','25'),
('4086','12','ABL1_HUMAN/242-493','464','489','25'),
('4087','12','B4DFN2_HUMAN/1-226','197','222','25'),
('4088','12','VGFR2_HUMAN/834-1160','1131','1156','25'),
('4089','12','F8VW56_HUMAN/1-206','177','202','25'),
('4090','12','E9PJX5_HUMAN/170-419','389','415','26'),
('4091','12','B4DU06_HUMAN/288-547','518','543','25'),
('4092','12','B7Z4Y7_HUMAN/50-280','251','276','25'),
('4093','12','F1JU33_HUMAN/5-256','228','253','25'),
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('4095','12','B2R6Q4_HUMAN/195-440','411','436','25'),
('4096','12','FYN_HUMAN/271-520','491','516','25'),
('4097','12','B4DVP5_HUMAN/399-675','646','671','25'),
('4098','12','B4DVT5_HUMAN/1-207','178','203','25'),
('4099','12','PTK6_HUMAN/191-441','412','437','25'),
('4100','12','B4DLF5_HUMAN/648-907','878','903','25'),
('4101','12','NTRK1_HUMAN/510-781','752','777','25'),
('4102','12','B4E123_HUMAN/644-916','887','912','25'),
('4103','12','ACK1_HUMAN/126-385','356','381','25'),
('4104','12','YES_HUMAN/277-526','497','522','25'),
('4105','12','H7BYU0_HUMAN/327-591','562','587','25'),
('4106','12','EPHA7_HUMAN/633-890','861','886','25'),
('4107','12','Q59FL8_HUMAN/583-839','810','835','25'),
('4108','12','E9PC47_HUMAN/369-634','605','630','25'),
('4109','12','INSRR_HUMAN/979-1246','1217','1242','25'),
('4110','12','KSR2_HUMAN/666-928','899','924','25'),
('4111','12','A9UEZ6_HUMAN/745-996','967','992','25'),
('4112','12','Q8NI16_HUMAN/437-713','684','709','25'),
('4113','12','Q2VXS9_HUMAN/498-673','644','669','25'),
('4114','12','Q6ZRA8_HUMAN/171-425','396','421','25'),
('4115','12','B4DYR0_HUMAN/177-447','418','443','25'),
('4116','12','Q96HF4_HUMAN/1-148','119','144','25'),
('4117','12','RON_HUMAN/1082-1341','1312','1337','25'),
('4118','12','Q5H8Y1_HUMAN/1939-2209','2180','2205','25'),
('4119','12','B4E0X2_HUMAN/268-525','496','521','25'),
('4120','12','KSYK_HUMAN/371-626','597','622','25'),
('4121','12','A9YLN4_HUMAN/301-571','542','567','25'),
('4122','12','A9YLN6_HUMAN/219-489','460','485','25'),
('4123','12','Q8NI15_HUMAN/435-711','682','707','25'),
('4124','12','ALK_HUMAN/1116-1383','1354','1379','25'),
('4125','12','B6D4Y3_HUMAN/1116-1383','1354','1379','25'),
('4126','12','FGFR2_HUMAN/481-757','728','753','25'),
('4127','12','D7RF68_HUMAN/288-545','516','541','25'),
('4128','12','A6P4V4_HUMAN/806-1073','1044','1069','25'),
('4129','12','ROS1_HUMAN/1945-2215','2186','2211','25'),
('4130','12','B4DKW0_HUMAN/484-752','723','748','25'),
('4131','12','A8KAM8_HUMAN/600-958','929','954','25'),
('4132','12','B1APY4_HUMAN/333-606','577','602','25'),
('4133','12','NTRK2_HUMAN/538-807','778','803','25'),
('4134','12','Q8IXP2_HUMAN/846-1120','1091','1116','25'),
('4135','12','G9BXQ3_HUMAN/116-377','348','373','25'),
('4136','12','Q59GM4_HUMAN/430-684','655','680','25'),
('4137','12','H7C3L9_HUMAN/1-178','149','174','25'),
('4138','12','B3XZL9_HUMAN/281-548','519','544','25'),
('4139','12','Q8WTZ8_HUMAN/118-384','355','380','25'),
('4140','12','HCK_HUMAN/262-511','482','507','25'),
('4141','12','TEC_HUMAN/370-619','590','615','25'),
('4142','12','EPHB1_HUMAN/619-878','849','874','25'),
('4143','12','Q59F30_HUMAN/699-975','946','971','25'),
('4144','12','B3XZM0_HUMAN/292-559','530','555','25'),
('4145','12','B4DTB5_HUMAN/3-207','178','203','25'),
('4146','12','Q9NPI3_HUMAN/1-166','137','162','25'),
('4147','12','Q9H7V3_HUMAN/1-234','205','230','25'),
('4148','12','D3DRD5_HUMAN/498-774','745','770','25'),
('4149','12','Q4JFK8_HUMAN/1-203','174','199','25'),
('4150','12','B4DP99_HUMAN/144-389','360','385','25'),
('4151','12','E9PD35_HUMAN/845-1169','1140','1165','25'),
('4152','12','Q9NSQ6_HUMAN/108-355','326','351','25'),
('4153','12','E9PB13_HUMAN/637-899','870','895','25'),
('4154','12','Q9NPI2_HUMAN/1-166','137','162','25'),
('4155','12','B7Z418_HUMAN/134-385','356','381','25'),
('4156','12','B3KWB3_HUMAN/1-206','177','202','25'),
('4157','12','D3DSX2_HUMAN/42-318','289','314','25'),
('4158','12','B3KTB2_HUMAN/180-439','410','435','25'),
('4159','12','E7BSV0_HUMAN/712-968','939','964','25'),
('4160','12','FES_HUMAN/561-814','785','810','25'),
('4161','12','Q504U8_HUMAN/667-923','894','919','25'),
('4162','12','B6D4Y1_HUMAN/1116-1383','1354','1379','25'),
('4163','12','D1MAM2_HUMAN/1116-1383','1354','1379','25'),
('4164','12','B4E058_HUMAN/1-220','191','216','25'),
('4165','12','Q96L35_HUMAN/615-874','845','870','25'),
('4166','12','B6D4Y6_HUMAN/1116-1383','1354','1379','25'),
('4167','12','B4DGF4_HUMAN/1-184','155','180','25'),
('4168','12','B7Z1I0_HUMAN/59-312','283','308','25'),
('4169','12','F8TLW0_HUMAN/724-1005','976','1001','25'),
('4170','12','D7PBN4_HUMAN/20-277','248','273','25'),
('4171','12','B2RAW9_HUMAN/310-580','551','576','25'),
('4172','12','B5BU52_HUMAN/195-440','411','436','25'),
('4173','12','JAK2_HUMAN/849-1123','1094','1119','25'),
('4174','12','DDR1_HUMAN/610-905','876','901','25'),
('4175','12','Q15300_HUMAN/248-529','500','525','25'),
('4176','12','EPHB6_HUMAN/670-915','886','911','25'),
('4177','12','VGFR1_HUMAN/827-1154','1125','1150','25'),
('4178','12','F8VUG4_HUMAN/126-364','335','360','25'),
('4179','12','H7C560_HUMAN/65-322','293','318','25'),
('4180','12','EPHA4_HUMAN/621-878','849','874','25'),
('4181','12','D2CGD1_HUMAN/392-668','639','664','25'),
('4182','12','INSR_HUMAN/1023-1290','1261','1286','25'),
('4183','12','ANPRB_HUMAN/518-786','757','782','25'),
('4184','12','F0UY66_HUMAN/1116-1383','1354','1379','25'),
('4185','12','B4DH13_HUMAN/117-371','342','367','25'),
('4186','12','F0UY65_HUMAN/1116-1383','1354','1379','25'),
('4187','12','E3WH17_HUMAN/310-577','548','573','25'),
('4188','12','Q0IJ44_HUMAN/146-422','393','418','25'),
('4189','12','Q58F15_HUMAN/621-878','849','874','25'),
('4190','12','B7ZKJ3_HUMAN/676-933','904','929','25'),
('4191','12','B4DQP7_HUMAN/180-439','410','435','25'),
('4192','12','FGFR4_HUMAN/467-743','714','739','25'),
('4193','12','A9UF02_HUMAN/756-1007','978','1003','25'),
('4194','12','Q6P4R6_HUMAN/621-878','849','874','25'),
('4195','12','ERBB4_HUMAN/718-974','945','970','25'),
('4196','12','B2RDR6_HUMAN/235-478','449','474','25'),
('4197','12','Q96II5_HUMAN/313-570','541','566','25'),
('4198','12','ANPRA_HUMAN/543-801','772','797','25'),
('4199','12','D3DRD4_HUMAN/384-660','631','656','25'),
('4200','12','Q5U0C9_HUMAN/36-284','255','280','25'),
('4201','12','A8MY87_HUMAN/476-740','711','736','25'),
('4202','12','A6NJF2_HUMAN/1-138','109','134','25'),
('4203','12','B4DFQ0_HUMAN/1-253','224','249','25'),
('4204','12','C1PHA1_HUMAN/601-868','839','864','25'),
('4205','12','B7Z6W7_HUMAN/197-446','417','442','25'),
('4206','12','B6D4Y7_HUMAN/1116-1383','1354','1379','25'),
('4207','12','G9JXB8_HUMAN/976-1235','1206','1231','25'),
('4208','12','B4E1N6_HUMAN/134-391','362','387','25'),
('4209','12','Q16176_HUMAN/194-436','407','432','25'),
('4210','12','Q9P0L5_HUMAN/1-166','137','162','25'),
('4211','12','Q59GN8_HUMAN/342-596','567','592','25'),
('4212','12','H0YBP1_HUMAN/433-687','658','683','25'),
('4213','12','Q59EB3_HUMAN/400-659','630','655','25'),
('4214','12','B4DL04_HUMAN/291-549','520','545','25'),
('4215','12','KSR1_HUMAN/611-875','846','871','25'),
('4216','12','B2RDI6_HUMAN/117-376','347','372','25'),
('4217','12','E9PHX8_HUMAN/411-678','649','674','25'),
('4218','12','ITK_HUMAN/363-612','583','608','25'),
('4219','12','H0Y8F1_HUMAN/94-356','327','352','25'),
('4220','12','Q6MZT2_HUMAN/563-849','820','845','25'),
('4221','12','RET_HUMAN/724-1005','976','1001','25'),
('4222','12','B7Z2I3_HUMAN/659-915','886','911','25');INSERT INTO `kindriver_v82`.`Protein_residue` (`uniprot_id`,`alignment_col`,`protein_res_number`,`aa_type`,`pfam_domain_id`,`protein_residue_id`) VALUES 
('E3WH17_HUMAN','41','310','I','E3WH17_HUMAN/310-577','E3WH17_HUMAN.310'),
('E3WH17_HUMAN','43','311','T','E3WH17_HUMAN/310-577','E3WH17_HUMAN.311'),
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