3rjc:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR L4-12  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3e64:A   (MET865) to   (ILE992)  FRAGMENT BASED DISCOVERY OF JAK-2 INHIBITORS  |   DRUG DISCOVERY, JAK2, FRAGMENT BASED, ATP-BINDING, DISEASE MUTATION, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, SH2 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE 
3rk5:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-72  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rk7:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-71  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rk9:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-74  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rm6:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-2-80  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rm7:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-91  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4gt3:A    (GLY35) to   (ILE163)  ATP-BOUND FORM OF THE ERK2 KINASE  |   KINASE, TRANSFERASE 
3e8n:A    (GLY80) to   (LEU206)  X-RAY STRUCTURE OF THE HUMAN MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1 (MEK1) COMPLEXED WITH A POTENT INHIBITOR RDEA119 AND MGATP  |   PROTEIN KINASE-LIGAND-MGATP COMPLEX, RDEA119, RDEA-119, MEK1, MEK1-RDEA119 COMPLEX, ACETYLATION, ATP-BINDING, DISEASE MUTATION, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, TYROSINE-PROTEIN KINASE 
3e92:A    (SER37) to   (ASP168)  CRYSTAL STRUCTURE OF P38 KINASE IN COMPLEX WITH A BIARYL AMIDE INHIBITOR  |   P38, SERINE/THREONINE PROTEIN KINASE, MAP KINASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3rmf:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-33  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rni:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-3-86  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3roy:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-154  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rpr:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-49  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rpv:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-88  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rpy:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-40  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2oic:A   (GLY198) to   (SER328)  CRYSTAL STRUCTURE OF IRAK4 KINASE DOMAIN COMPLEXED WITH STAUROSPORINE  |   KINASE, TRANSFERASE 
2oic:C   (GLY198) to   (SER328)  CRYSTAL STRUCTURE OF IRAK4 KINASE DOMAIN COMPLEXED WITH STAUROSPORINE  |   KINASE, TRANSFERASE 
2ojg:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF ERK2 IN COMPLEX WITH N,N-DIMETHYL-4-(4- PHENYL-1H-PYRAZOL-3-YL)-1H-PYRROLE-2-CARBOXAMIDE  |   KINASE INHIBITOR, TRANSFERASE 
2oji:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF ERK2 IN COMPLEX WITH N-BENZYL-4-(4-(3- CHLOROPHENYL)-1H-PYRAZOL-3-YL)-1H-PYRROLE-2-CARBOXAMIDE  |   KINASE INHIBITOR, TRANSFERASE 
2okr:D    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF THE P38A-MAPKAP KINASE 2 HETERODIMER  |   KINASE, NLS, NES, HETERODIMER, DOCKING GROOVE, TRANSFERASE 
2onl:A    (SER37) to   (ALA172)  CRYSTAL STRUCTURE OF THE P38A-MAPKAP KINASE 2 HETERODIMER  |   HETERODIMER, KINASE, NLS, NES, DOCKING GROOVE, TRANSFERASE 
4h39:A    (GLY76) to   (ASP207)  CRYSTAL STRUCTURE OF JNK3 IN COMPLEX WITH JIP1 PEPTIDE  |   MAPK, KINASE, TRANSFERASE 
4h3b:C    (GLY76) to   (ASP207)  CRYSTAL STRUCTURE OF JNK3 IN COMPLEX WITH SAB PEPTIDE  |   SH3BP-5, MAPK, KINASE, TRANSFERASE 
4h3p:D    (GLY37) to   (ILE165)  CRYSTAL STRUCTURE OF HUMAN ERK2 COMPLEXED WITH A MAPK DOCKING PEPTIDE  |   KINASE DOMAIN, SIGNALING, LINEAR MOTIF, SURFACE MUTATION, TRANSFERASE 
1aq1:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR STAUROSPORINE  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, STAUROSPORINE, CELL DIVISION, MITOSIS, INHIBITION 
2b52:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) COMPLEXED WITH DPH- 042562  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, CELL DIVISION, MITOSIS, INHIBITION, TRANSFERASE 
2b54:A    (LYS20) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 (CKD2)COMPLEXED WITH DIN- 232305  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, CELL DIVISION, MITOSIS, INHIBITION, TRANSFERASE 
3elj:A    (GLY38) to   (ASP169)  JNK1 COMPLEXED WITH A BIS-ANILINO-PYRROLOPYRIMIDINE INHIBITOR.  |   C-JUN N-TERMINAL KINASE, MITOGEN-ACTIVATED PROTEIN KINASE, ATP- BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, JNK1 
3s1h:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-39  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2bal:A    (GLY36) to   (ASP168)  P38ALPHA MAP KINASE BOUND TO PYRAZOLOAMINE  |   P38, MAP KINASE, SERINE/THREONINE KINASE, TRANSFERASE 
2p33:A    (GLY76) to   (ASP207)  SYNTHESIS AND SAR OF AMINOPYRIMIDINES AS NOVEL C-JUN N- TERMINAL KINASE (JNK) INHIBITORS  |   JNK3 KINASE, INHIBITOR, TRANSFERASE 
4x21:A    (ILE77) to   (ASP207)  THE MAP KINASE JNK3 AS TARGET FOR HALOGEN BONDING  |   MAPK, HALOGEN BOND COMPLEX, TRANSFERASE 
4x3f:A    (GLY25) to   (ASP159)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF THE M. TUBERCULOSIS SER/THR KINASE PKNA  |   KINASE, AUTOINHIBITION, PHOSPHORYLATION, TRANSFERASE 
4x3f:B    (GLY25) to   (ASP159)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF THE M. TUBERCULOSIS SER/THR KINASE PKNA  |   KINASE, AUTOINHIBITION, PHOSPHORYLATION, TRANSFERASE 
4x3f:C    (GLY25) to   (THR158)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF THE M. TUBERCULOSIS SER/THR KINASE PKNA  |   KINASE, AUTOINHIBITION, PHOSPHORYLATION, TRANSFERASE 
1bl7:A    (GLY36) to   (ILE166)  THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB220025  |   TRANSFERASE, INHIBITOR, MAP KINASE, SERINE/ THREONINE- PROTEIN KINASE, P38 
1bmk:A    (SER37) to   (ILE166)  THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB218655  |   TRANSFERASE, INHIBITORS, MAP KINASE, SERINE/ THREONINE- PROTEIN KINASE, P38 
3f66:B  (HIS1094) to  (VAL1220)  HUMAN C-MET KINASE IN COMPLEX WITH QUINOXALINE INHIBITOR  |   C-MET, PROTEIN KINASE, QUINOXALINE, ALTERNATIVE SPLICING; ATP-BINDING; CHROMOSOMAL REARRANGEMENT; DISEASE MUTATION; GLYCOPROTEIN; KINASE; MEMBRANE; NUCLEOTIDE-BINDING; PHOSPHOPROTEIN; POLYMORPHISM; PROTO-ONCOGENE; RECEPTOR; REPEAT; SIGNAL; TRANSFERASE; TRANSMEMBRANE; TYROSINE- PROTEIN KINASE. 
4x7j:A   (GLY605) to   (GLY954)  CO-CRYSTAL STRUCTURE OF PERK WITH 2-AMINO-N-[4-METHOXY-3- (TRIFLUOROMETHYL)PHENYL]-4-METHYL-3-[2-(METHYLAMINO)QUINAZOLIN-6- YL]BENZAMIDE INHIBITOR  |   CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR, COMPLEX 
4x7k:A   (GLY605) to   (GLY954)  CO-CRYSTAL STRUCTURE OF PERK BOUND TO 4-{2-AMINO-3-[5-FLUORO-2- (METHYLAMINO)QUINAZOLIN-6-YL]-4-METHYLBENZOYL}-1-METHYL-2,5-DIPHENYL- 1,2-DIHYDRO-3H-PYRAZOL-3-ONE INHIBITOR  |   CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR, COMPLEX 
4x7l:A   (GLY605) to   (GLY954)  CO-CRYSTAL STRUCTURE OF PERK BOUND TO 4-{2-AMINO-4-METHYL-3-[2- (METHYLAMINO)-1,3-BENZOTHIAZOL-6-YL]BENZOYL}-1-METHYL-2,5-DIPHENYL-1, 2-DIHYDRO-3H-PYRAZOL-3-ONE INHIBITOR  |   CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR, COMPLEX 
1o9u:A    (GLY68) to   (LEU198)  GLYCOGEN SYNTHASE KINASE 3 BETA COMPLEXED WITH AXIN PEPTIDE  |   TRANSFERASE-TRANSFERASE SUBSTRATE COMPLEX, KINASE, INSULIN PATHWAY, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, MULTIGENE FAMILY, PHOSPHORYLATION, DEVELOPMENTAL PROTEIN, ANTI-ONCOGENE, APOPTOSIS, TRANSFERASE- TRANSFERASE SUBSTRATE COMPLEX 
1ob3:A    (GLY16) to   (ASP143)  STRUCTURE OF P. FALCIPARUM PFPK5  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
1ob3:B    (GLY16) to   (ASP143)  STRUCTURE OF P. FALCIPARUM PFPK5  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
2pvl:A    (SER51) to   (LEU173)  STRUCTURE-BASED DESIGN OF PYRAZOLO[1,5-A][1,3,5]TRIAZINE DERIVATIVES AS POTENT INHIBITORS OF PROTEIN KINASE CK2  |   STRUCTURE-BASED DRUG DESIGN, ENZYME-INHIBITOR COMPLEX, CASEIN KINASE II, PROTEIN KINASE CK2, TRANSFERASE 
4i5h:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF A DOUBLE MUTANT RAT ERK2 COMPLEXED WITH A TYPE II QUINAZOLINE INHIBITOR  |   MAP KINASE, DFG-OUT, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3sls:A    (GLY80) to   (LEU206)  CRYSTAL STRUCTURE OF HUMAN MEK-1 KINASE IN COMPLEX WITH UCB1353770 AND AMPPNP  |   SERINE-THREONINE KINASE, SIGNALLING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3sls:B    (LYS84) to   (LEU206)  CRYSTAL STRUCTURE OF HUMAN MEK-1 KINASE IN COMPLEX WITH UCB1353770 AND AMPPNP  |   SERINE-THREONINE KINASE, SIGNALLING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1opj:B   (GLU274) to   (VAL398)  STRUCTURAL BASIS FOR THE AUTO-INHIBITION OF C-ABL TYROSINE KINASE  |   TRANSFERASE 
1cm8:A    (ALA40) to   (ILE169)  PHOSPHORYLATED MAP KINASE P38-GAMMA  |   P38-GAMMA, GAMMA, PHOSPHORYLATION, MAP KINASE, TRANSFERASE 
1cm8:B  (ALA1040) to  (ILE1169)  PHOSPHORYLATED MAP KINASE P38-GAMMA  |   P38-GAMMA, GAMMA, PHOSPHORYLATION, MAP KINASE, TRANSFERASE 
4xmo:A  (GLY1090) to  (VAL1220)  CRYSTAL STRUCTURE OF C-MET IN COMPLEX WITH (R)-5-(8-FLUORO-3-(1- FLUORO-1-(3-METHOXYQUINOLIN-6-YL)ETHYL)-[1,2,4]TRIAZOLO[4,3- A]PYRIDIN-6-YL)-3-METHYLISOXAZOLE  |   RECEPTOR TYROSINE KINASE, INTRACELLULAR CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3sw4:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF THE CDK2 IN COMPLEX WITH THIAZOLYLPYRIMIDINE INHIBITOR  |   ALPHA AND BETA PROTEIN (A+B), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3sw7:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF THE CDK2 IN COMPLEX WITH THIAZOLYLPYRIMIDINE INHIBITOR  |   ALPHA AND BETA PROTEIN (A+B), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2cch:A    (GLY16) to   (LEU143)  THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA- LINKED ATP ANALOGUE  |   COMPLEX(TRANSFERASE/CELL DIVISION), ATP-BINDING, CDK2, CELL CYCLE, CELL DIVISION, CYCLIN, MITOSIS, NUCLEAR PROTEIN, PEPTIDE SPECIFICITY, PHOSPHORYLATION, POLYMORPHISM, PROTEIN KINASE, RECRUITMENT, SERINE-THREONINE-PROTEIN KINASE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3g0f:A   (ALA616) to   (ILE808)  KIT KINASE DOMAIN MUTANT D816H IN COMPLEX WITH SUNITINIB  |   KIT KINASE DOMAIN, SUTENT BINDING, DRUG RESISTANCE, ATP- BINDING, DISEASE MUTATION, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, PROTO-ONCOGENE, RECEPTOR, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSFERASE 
2qc6:A    (GLU55) to   (LEU173)  PROTEIN KINASE CK2 IN COMPLEX WITH DBC  |   CK2, DBC, KINASE INHIBITORS, COUMARINS, TRANSFERASE 
1daw:A    (GLU55) to   (LEU173)  CRYSTAL STRUCTURE OF A BINARY COMPLEX OF PROTEIN KINASE CK2 (ALPHA-SUBUNIT) AND MG-AMPPNP  |   PROTEIN KINASE CK2, DUAL-COSUBSTRATE SPECIFICITY, BINARY COMPLEX, TRANSFERASE 
1day:A    (GLU55) to   (LEU173)  CRYSTAL STRUCTURE OF A BINARY COMPLEX OF PROTEIN KINASE CK2 (ALPHA-SUBUNIT) AND MG-GMPPNP  |   PROTEIN KINASE CK2, DUAL-COSUBSTRATE SPECIFICITY, BINARY COMPLEX WITH MG-GMPPNP, TRANSFERASE 
1pf8:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF HUMAN CYCLIN-DEPENDENT KINASE 2 COMPLEXED WITH A NUCLEOSIDE INHIBITOR  |   TRANSFERASE, SERINE/THREONINE PROTEIN KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION, SU9516, INHIBITOR 
1di9:A    (GLY36) to   (ILE166)  THE STRUCTURE OF P38 MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH 4-[3-METHYLSULFANYLANILINO]-6,7- DIMETHOXYQUINAZOLINE  |   SERINE/THREONINE PROTEIN KINASE, MAP KINASE, P38, TRANSFERASE 
3g90:X    (ILE77) to   (ASP207)  JNK-3 BOUND TO (Z)-5-FLUORO-1-((6-FLUORO-4H-BENZO[D][1,3]DIOXIN-8-YL) METHYL)-3-(HYDROXYIMINO)INDOLIN-2-ONE  |   KINASE, INHIBITOR, PHOSPHORYLATION, ATP-BINDING, EPILEPSY, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3g9n:A    (GLY32) to   (ASP163)  JNK3 BOUND TO (Z)-1-((6-FLUORO-4H-BENZO[D][1,3]DIOXIN-8-YL)METHYL)-3- (HYDROXYIMINO)-4-PHENYLINDOLIN-2-ONE  |   KINASE, INHIBITOR, PHOSPHORYLATION, ATP-BINDING, EPILEPSY, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gcq:A    (GLY36) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH RL45  |   DFG-OUT, TYPE II, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1pkd:A    (GLY16) to   (LEU143)  THE CRYSTAL STRUCTURE OF UCN-01 IN COMPLEX WITH PHOSPHO- CDK2/CYCLIN A  |   PROTEIN KINASE-DRUG COMPLEX, TRANSFERASE/CELL CYCLE COMPLEX 
4iti:A    (LYS30) to   (ASP156)  CRYSTAL STRUCTURE OF RIP1 KINASE IN COMPLEX WITH NECROSTATIN-3 ANALOG  |   ALPHA/BETA, RIP1 KINASE, NECROPTOSIS, NECROSTATINS, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3gfe:A    (SER37) to   (ASP168)  CRYSTAL STRUCTURE OF P38A MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH A PYRAZOLOPYRIDINONE INHIBITOR  |   SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE- BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM 
1pme:A    (GLY37) to   (ILE165)  STRUCTURE OF PENTA MUTANT HUMAN ERK2 MAP KINASE COMPLEXED WITH A SPECIFIC INHIBITOR OF HUMAN P38 MAP KINASE  |   MAP KINASE, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
4xyf:A  (GLY1090) to  (VAL1220)  CRYSTAL STRUCTURE OF C-MET IN COMPLEX WITH (S)-5-(8-FLUORO-3-(1-(3-(2- METHOXYETHOXY)QUINOLIN-6-YL)ETHYL)-[1,2,4]TRIAZOLO[4,3-A]PYRIDIN-6- YL)-3-METHYLISOXAZOLE  |   RECEPTOR TYROSINE KINASE, INHIBITOR, COMPLEX, INTRACELLULAR CATALYTIC DOMAIN 
3gi3:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF A N-PHENYL-N'-NAPHTHYLUREA ANALOG IN COMPLEX WITH P38 MAP KINASE  |   TWO LOBE KINASE STRUCTURE, N-LOBE BETA-SHEET, C-LOBE ALPHA- HELIX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gql:A   (ASN506) to   (ASP641)  CRYSTAL STRUCTURE OF ACTIVATED RECEPTOR TYROSINE KINASE IN COMPLEX WITH SUBSTRATES  |   PHOSPHORYLATED KINASE, ACTIVATION, ATP ANALOG, ATP-BINDING, CRANIOSYNOSTOSIS, DISEASE MUTATION, DISULFIDE BOND, DWARFISM, GLYCOPROTEIN, HEPARIN-BINDING, HYPOGONADOTROPIC HYPOGONADISM, IMMUNOGLOBULIN DOMAIN, KALLMANN SYNDROME, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1pxl:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-DIMETHYL-THIAZOL-5-YL)-PYRIMIDIN-2-YL]- (4-TRIFLUOROMETHYL-PHENYL)-AMINE  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, CELL DIVISION, MITOSIS, INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, 3D-STRUCTURE. 
1pxm:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 3-[4-(2,4-DIMETHYL-THIAZOL-5-YL)-PYRIMIDIN-2- YLAMINO]-PHENOL  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, CELL DIVISION, MITOSIS, INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, 3D-STRUCTURE. 
1pxp:A    (GLY16) to   (LEU143)  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  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, CELL DIVISION, MITOSIS, INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, 3D-STRUCTURE. 
3gt8:D   (LYS713) to   (ILE829)  CRYSTAL STRUCTURE OF THE INACTIVE EGFR KINASE DOMAIN IN COMPLEX WITH AMP-PNP  |   INACTIVE KINASE, DIMER, ALTERNATIVE SPLICING, ANTI-ONCOGENE, ATP-BINDING, CELL CYCLE, CELL MEMBRANE, DISEASE MUTATION, DISULFIDE BOND, GLYCOPROTEIN, ISOPEPTIDE BOND, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE- PROTEIN KINASE, UBL CONJUGATION 
4y73:B   (GLY198) to   (ILE327)  CRYSTAL STRUCTURE OF IRAK4 KINASE DOMAIN WITH INHIBITOR  |   KINASE, INHIBITOR 
3tg1:A    (GLY36) to   (ILE166)  CRYSTAL STRUCTURE OF P38ALPHA IN COMPLEX WITH A MAPK DOCKING PARTNER  |   KINASE/RHODANESE-LIKE DOMAIN, DOCKING INTERACTION, TRANSFERASE- HYDROLASE COMPLEX 
1e9h:C    (TYR15) to   (LEU143)  THR 160 PHOSPHORYLATED CDK2 - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR INDIRUBIN-5-SULPHONATE BOUND  |   CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), KINASES, INHIBITOR, CYCLIN, COMPLEX, PHOSPHORYLATION 
3tiy:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH NSC 35676  |   PROTEIN KINASE, ALLOSTERIC LIGAND, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3tiz:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH NSC 111848  |   PROTEIN KINASE, ALLOSTERIC LIGAND, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3tt0:B   (ALA495) to   (ASP641)  CO-STRUCTURE OF FIBROBLAST GROWTH FACTOR RECEPTOR 1 KINASE DOMAIN WITH 3-(2,6-DICHLORO-3,5-DIMETHOXY-PHENYL)-1-{6-[4-(4-ETHYL-PIPERAZIN-1- YL)-PHENYLAMINO]-PYRIMIDIN-4-YL}-1-METHYL-UREA (BGJ398)  |   KINASE DOMAIN, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3tv6:B   (LYS473) to   (GLY593)  HUMAN B-RAF KINASE DOMAIN IN COMPLEX WITH A METHOXYPYRAZOLOPYRIDINYL BENZAMIDE INHIBITOR  |   B-RAF, KINASE, KINASE INHIBITOR, TRANSFERASE, C-RAF, RAS, MEK, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4joa:A  (GLU1132) to  (ILE1268)  CRYSTAL STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH 7-AZAINDOLE BASED INHIBITOR  |   ANAPLASTIC LYMPHOMA KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3u4w:A   (GLY279) to   (VAL402)  SRC IN COMPLEX WITH DNA-TEMPLATED MACROCYCLIC INHIBITOR MC4B  |   PROTEIN KINASE, SRC-LIKE INACTIVE CONFORMATION, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3hec:A    (SER37) to   (LEU167)  P38 IN COMPLEX WITH IMATINIB  |   TRANSFERASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE 
1r39:A    (GLY36) to   (ILE166)  THE STRUCTURE OF P38ALPHA  |   SERINE/THREONINE KINASE, MUTAGENESIS, STABILIZATION, TRANSFERASE 
4yp8:B   (GLY198) to   (SER328)  IRAK4-INHIBITOR CO-STRUCTURE  |   KINASE, PHOSPHATASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4yr8:F    (GLY38) to   (ASP169)  CRYSTAL STRUCTURE OF JNK IN COMPLEX WITH A REGULATOR PROTEIN  |   KINASE DOMAIN, CATALYTIC DOMAIN, TRANSFERASE-HYDROLASE COMPLEX 
4ysj:A    (GLY40) to   (ILE171)  CALCIUM-DEPENDENT PROTEIN KINASE FROM EIMERIA TENELLA IN COMPLEX WITH ADP  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE, CALCIUM-BINDING, ATP- BINDING 
4ysj:B    (GLY40) to   (ILE170)  CALCIUM-DEPENDENT PROTEIN KINASE FROM EIMERIA TENELLA IN COMPLEX WITH ADP  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE, CALCIUM-BINDING, ATP- BINDING 
3ugc:A   (GLY861) to   (ILE992)  STRUCTURAL BASIS OF JAK2 INHIBITION BY THE TYPE II INHIBTOR NVP-BBT594  |   SMALL MOLECULE INHIBITOR, ATP BINDING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ytc:A   (GLY861) to   (ILE992)  DISCOVERY OF VX-509 (DECERNOTINIB): A POTENT AND SELECTIVE JANUS KINASE (JAK) 3 INHIBITOR FOR THE TREATMENT OF AUTOIMMUNE DISEASE  |   JANUS KINASE, KINASE, INHIBITOR, AUTOIMMUNE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4yuq:A    (GLU41) to   (ILE170)  CDPK1 FROM EIMERIA TENELLA IN COMPLEX WITH INHIBITOR UW1354  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE, CALCIUM-BINDING, ATP- BINDING, BUMPED KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4yuq:B    (GLU41) to   (ILE170)  CDPK1 FROM EIMERIA TENELLA IN COMPLEX WITH INHIBITOR UW1354  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE, CALCIUM-BINDING, ATP- BINDING, BUMPED KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ka3:A    (GLY36) to   (LEU167)  STRUCTURE OF MAP KINASE IN COMPLEX WITH A DOCKING PEPTIDE  |   KINASE DOMAIN, PHOSPHORYLATION, KIM, TRANSFERASE-PROTEIN BINDING COMPLEX 
3uli:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) BOUND TO AZABENZIMIDAZOLE DERIVATIVE  |   AZABENZIMIDAZOLE DERIVATIVE, PHOSPHOTRANSFER, COMPLEX WITH CYCLIN A OR CYCLIN E, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4yzb:A    (ILE43) to   (ILE171)  CDPK1 FROM EIMERIA TENELLA IN COMPLEX WITH INHIBITOR UW1521  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE, CALCIUM-BINDING, ATP- BINDING, BUMPED KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3hng:A   (ALA844) to  (LEU1043)  CRYSTAL STRUCTURE OF VEGFR1 IN COMPLEX WITH N-(4-CHLOROPHENYL)-2- ((PYRIDIN-4-YLMETHYL)AMINO)BENZAMIDE  |   RECEPTOR TYROSINE KINASE, VEGFR1,FLT1,KINASE DOMAIN,INHIBITOR, ACTIVATION LOOP,VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR, STRUCTURAL GENOMICS,STRUCTURAL GENOMICS CONSORTIUM,SGC,SGC STOCKHOLM, ANGIOGENESIS, ATP-BINDING, CELL MEMBRANE, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, DISULFIDE BOND, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3unk:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR YL5-083  |   PROTEIN KINASE, ALLOSTERIC LIGAND, ANS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1g5s:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH THE INHIBITOR H717  |   PROTEIN-INHIBITOR COMPLEX, CELL CYCLE/TRANSFERASE COMPLEX 
4kin:B    (GLY36) to   (ASP168)  CRYSTAL STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE 14 (P38-H5) COMPLEX WITH 5-(2-CHLOROPHENYL)-N-(5-(CYCLOPROPYLCARBAMOYL)-2- METHYLPHENYL)-2-THIOPHENECARBOXAMIDE  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4kin:D    (SER37) to   (ASP168)  CRYSTAL STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE 14 (P38-H5) COMPLEX WITH 5-(2-CHLOROPHENYL)-N-(5-(CYCLOPROPYLCARBAMOYL)-2- METHYLPHENYL)-2-THIOPHENECARBOXAMIDE  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4kiq:A    (GLY36) to   (ASP168)  CRYSTAL STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE 14 (P38-H5) COMPLEX WITH ETHYL 6-((5-(CYCLOPROPYLCARBAMOYL)-2-METHYLPHENYL) CARBAMOYL)-1H-INDOLE-1-CARBOXYLATE  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3hv5:B    (GLY36) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH RL24  |   DFG-OUT, TYPE II, RL24, QUINOLINE-PYRAZOLOUREA, HYBRID, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1gii:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE CDK4 INHIBITOR  |   PROTEIN KINASE, CELL CYCLE, INHIBITION, TRANSFERASE 
4knb:C  (GLY1090) to  (ALA1221)  C-MET IN COMPLEX WITH OSI LIGAND  |   PROTEIN KINASE, TRANSFERASE 
2fvd:A    (GLY16) to   (LEU143)  CYCLIN DEPENDENT KINASE 2 (CDK2) WITH DIAMINOPYRIMIDINE INHIBITOR  |   CDK2 LIGAND, TRANSFERASE 
3hzt:A    (GLY88) to   (ILE218)  CRYSTAL STRUCTURE OF TOXOPLASMA GONDII CDPK3, TGME49_105860  |   CALCIUM DEPENDENT KINASE, CALMODULIN, TROPONIN PARASITE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3v6s:A    (ILE77) to   (ASP207)  DISCOVERY OF POTENT AND SELECTIVE COVALENT INHIBITORS OF JNK  |   KINASE FOLD, APOPTOSIS, MAP KINASE, CYS MODIFICATION, JNK, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3v6s:B    (GLY76) to   (ASP207)  DISCOVERY OF POTENT AND SELECTIVE COVALENT INHIBITORS OF JNK  |   KINASE FOLD, APOPTOSIS, MAP KINASE, CYS MODIFICATION, JNK, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2g2i:A   (GLY254) to   (VAL379)  A SRC-LIKE INACTIVE CONFORMATION IN THE ABL TYROSINE KINASE DOMAIN  |   PROTEIN KINASE, TRANSFERASE 
2g2i:B   (GLU258) to   (VAL379)  A SRC-LIKE INACTIVE CONFORMATION IN THE ABL TYROSINE KINASE DOMAIN  |   PROTEIN KINASE, TRANSFERASE 
2vti:A    (GLY16) to   (LEU143)  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.  |   TRANSFERASE, MITOSIS, CELL CYCLE, SERINE/THREONINE PROTEIN KINASE 
4zji:C   (GLY282) to   (LEU405)  PAK1 IN COMPLEX WITH 2-CHLORO-5-ETHYL-8-FLUORO-11-(4-METHYLPIPERAZIN- 1-YL)-DIBENZODIAZEPINE  |   INHIBITOR, KINASE, PAK1, ALLOSTERIC, TRANSFERASE 
4l00:A   (SER599) to   (ASP739)  CRYSTAL STRUCTURE OF THE APO JAK1 PSEUDOKINASE DOMAIN  |   KINASE DOMAIN FOLD, REGULATORY, TRANSFERASE 
1h1r:C    (GLY16) to   (GLY147)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6086  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1h1s:A    (GLY16) to   (LEU143)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6102  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1h25:C    (VAL17) to   (LEU143)  CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM RETINOBLASTOMA-ASSOCIATED PROTEIN  |   TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY 
4zlo:A   (GLY282) to   (LEU405)  SERINE/THREONINE-PROTEIN KINASE PAK1 COMPLEXED WITH A DIBENZODIAZEPINE: IDENTIFICATION OF AN ALLOSTERIC SITE ON PAK1  |   DIBENZODAZEPINE, PAK1, KINASE, ALLOSTERIC INHIBITOR, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
2w5b:A    (GLY20) to   (ASP159)  HUMAN NEK2 KINASE ATPGAMMAS-BOUND  |   TRANSFERASE, MEIOSIS, MITOSIS, CYTOPLASM, METAL-BINDING, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, MAGNESIUM, CELL CYCLE, ATP-BINDING, CENTROSOME SPLITTING, CELL DIVISION 
2w5h:A    (GLY20) to   (LEU157)  HUMAN NEK2 KINASE APO  |   SER/THR PROTEIN KINASE, KINASE, NUCLEUS, MEIOSIS, MITOSIS, CYTOPLASM, SERINE/THREONINE-PROTEIN KINASE, METAL-BINDING, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, MAGNESIUM, CELL CYCLE, ATP-BINDING, TRANSFERASE, CENTROSOME SPLITTING, ALTERNATIVE SPLICING, COILED COIL, POLYMORPHISM, CELL DIVISION 
4zth:A    (GLY36) to   (ASP168)  STRUCTURE OF HUMAN P38AMAPK-ARYLPYRIDAZINYLPYRIDINE FRAGMENT COMPLEX USED IN INHIBITOR DISCOVERY  |   TRANSFERASE 
4lgd:C    (PHE42) to   (LEU162)  STRUCTURAL BASIS FOR AUTOACTIVATION OF HUMAN MST2 KINASE AND ITS REGULATION BY RASSF5  |   HIPPO, MST AUTOACTIVATION, RASSF, SARAH DOMAIN, DIMERIZATION, SIGNALING PROTEIN 
3iph:A    (GLY36) to   (ASP168)  CRYSTAL STRUCTURE OF P38 IN COMPLEX WITH A BIPHENYLAMIDE INHIBITOR  |   P38, SERINE/THREONINE PROTEIN KINASE, MAP KINASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3is5:B   (GLY147) to   (ASP281)  CRYSTAL STRUCTURE OF CDPK KINASE DOMAIN FROM TOXOPLASMA GONDII, TGME49_018720  |   TOXOPLASMA GONDII, CDPK, STRUCTURAL GENOMICS, PARASITOLOGY, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3is5:C   (PHE146) to   (ILE280)  CRYSTAL STRUCTURE OF CDPK KINASE DOMAIN FROM TOXOPLASMA GONDII, TGME49_018720  |   TOXOPLASMA GONDII, CDPK, STRUCTURAL GENOMICS, PARASITOLOGY, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3is5:F   (LEU151) to   (ASP281)  CRYSTAL STRUCTURE OF CDPK KINASE DOMAIN FROM TOXOPLASMA GONDII, TGME49_018720  |   TOXOPLASMA GONDII, CDPK, STRUCTURAL GENOMICS, PARASITOLOGY, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3itz:A    (SER37) to   (ASP168)  CRYSTAL STRUCTURE OF P38A MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH A PYRAZOLOPYRIDAZINE INHIBITOR  |   SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE- BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM 
2wd1:A  (GLY1095) to  (ALA1221)  HUMAN C-MET KINASE IN COMPLEX WITH AZAINDOLE INHIBITOR  |   HUMAN KINASE, C-MET, AZAINDOLE, INHIBITOR, TRANSFERASE, KINASE, NUCLEOTIDE-BINDING, ATP-BINDING, TYROSINE-PROTEIN KINASE 
2wgj:A  (HIS1094) to  (ALA1221)  X-RAY STRUCTURE OF PF-02341066 BOUND TO THE KINASE DOMAIN OF C-MET  |   C-MET, KINASE, INHIBITOR, TRANSFERASE, ATP-BINDING, NUCLEOTIDE-BINDING, TYROSINE-PROTEIN KINASE 
4loo:A    (GLY36) to   (ILE166)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (MONOCLINIC CRYSTAL FORM)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4lop:A    (GLY36) to   (ASP168)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4lop:B    (GLY36) to   (ILE166)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4lop:C    (GLY36) to   (ILE166)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4lop:D    (GLY36) to   (ASP168)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
3vug:A    (GLY38) to   (ILE167)  CRYSTAL STRUCTURE OF A CYSTEINE-DEFICIENT MUTANT M2 IN MAP KINASE JNK1  |   MAP KINASE, TRANSCRIPTION, PHOSPHORYLATION, ATP BINDING, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3vvh:A    (GLY80) to   (LEU206)  X-RAY STRUCTURE OF THE HUMAN MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1 (MEK1) IN COMPLEX WITH AN INHIBITOR AND MGATP  |   KINASE DOMAIN, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2wma:A    (VAL17) to   (LEU143)  STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A  |   CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE 
2wma:C    (GLY16) to   (LEU143)  STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A  |   CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE 
3w2c:A   (LEU149) to   (ASP274)  STRUCTURE OF AURORA KINASE A COMPLEXED TO BENZOIMIDAZOLE-INDAZOLE INHIBITOR XV  |   KINASE, ATP COMPETITOR, TRANSFERASE 
3w2c:C   (LEU149) to   (ASP274)  STRUCTURE OF AURORA KINASE A COMPLEXED TO BENZOIMIDAZOLE-INDAZOLE INHIBITOR XV  |   KINASE, ATP COMPETITOR, TRANSFERASE 
3w2r:A   (LYS737) to   (ILE853)  EGFR KINASE DOMAIN T790M/L858R MUTANT WITH COMPOUND 4  |   ANTI-ONCOGENE, CELL CYCLE, DISEASE MUTATION, KINASE DOMAIN, RECEPTOR, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2hw7:A    (HIS95) to   (ASP226)  CRYSTAL STRUCTURE OF MNK2-D228G IN COMPLEX WITH STAUROSPORINE  |   PROTEIN KINASES, DRUG, INHIBITOR, PHOSPHORYLATION, TRANSFERASE 
1uki:A    (GLY38) to   (ASP169)  STRUCTURAL BASIS FOR THE SELECTIVE INHIBITION OF JNK1 BY THE SCAFFOLDING PROTEIN JIP1 AND SP600125  |   TRANSFERASE, PHOSPHORYLATION 
5a9u:A  (GLY1128) to  (ILE1268)  STRUCTURE OF C1156Y MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH PF-06463922 ((10R)-7-AMINO-12-FLUORO-2,10, 16-TRIMETHYL-15-OXO-10,15,16,17-TETRAHYDRO-2H-8,4-(METHENO) PYRAZOLO(4,3-H)(2,5,11)BENZOXADIAZACYCLOTETRADECINE-3- CARBONITRILE).  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, ANAPLASTIC LYMPHOMA KINASE, INHIBITOR, MUTANT 
5aa9:A  (PHE1127) to  (ILE1268)  STRUCTURE OF L1198F MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH PF-06463922 ((10R)-7-AMINO-12-FLUORO-2,10, 16-TRIMETHYL-15-OXO-10,15,16,17-TETRAHYDRO-2H-8,4-(METHENO) PYRAZOLO(4,3-H)(2,5,11)BENZOXADIAZACYCLOTETRADECINE-3- CARBONITRILE).  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR, MUTANT 
5aac:A  (GLY1128) to  (ILE1268)  STRUCTURE OF C1156Y MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH CRIZOTINIB  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, ANAPLASTIC LYMPHOMA KINASE, INHIBITOR, MUTANT 
2wzj:A    (LYS66) to   (ASP193)  CATALYTIC AND UBA DOMAIN OF KINASE MARK2/(PAR-1) K82R, T208E DOUBLE MUTANT  |   UBA DOMAIN, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, SIGNALING PROTEIN, S/T PROTEIN KINASE, DIFFERENTIATION, DEVELOPMENTAL PROTEIN 
2wzj:E    (ALA65) to   (ASP193)  CATALYTIC AND UBA DOMAIN OF KINASE MARK2/(PAR-1) K82R, T208E DOUBLE MUTANT  |   UBA DOMAIN, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, SIGNALING PROTEIN, S/T PROTEIN KINASE, DIFFERENTIATION, DEVELOPMENTAL PROTEIN 
5acb:C   (GLY739) to   (LEU875)  CRYSTAL STRUCTURE OF THE HUMAN CDK12-CYCLINK COMPLEX  |   TRANSFERASE 
5acb:D   (GLY739) to   (LEU875)  CRYSTAL STRUCTURE OF THE HUMAN CDK12-CYCLINK COMPLEX  |   TRANSFERASE 
3wf6:A   (GLN107) to   (LEU234)  CRYSTAL STRUCTURE OF S6K1 KINASE DOMAIN IN COMPLEX WITH A PYRAZOLOPYRIMIDINE DERIVATIVE 4-[4-(1H-INDOL-3-YL)-3,6- DIHYDROPYRIDIN-1(2H)-YL]-1H-PYRAZOLO[3,4-D]PYRIMIDINE  |   SERINE/THREONINE PROTEIN KINASE DOMAIN, TRANSFERASE, PHOSPHORYLATION, ATP-BINDING, ZINC-BINDING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1v0b:A    (GLY16) to   (ASP143)  CRYSTAL STRUCTURE OF THE T198A MUTANT OF PFPK5  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
1v0b:B    (GLY16) to   (ASP143)  CRYSTAL STRUCTURE OF THE T198A MUTANT OF PFPK5  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
1v0p:A    (GLY16) to   (ASP143)  STRUCTURE OF P. FALCIPARUM PFPK5-PURVALANOL B LIGAND COMPLEX  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
5ajq:A    (GLY48) to   (ASP175)  HUMAN LOK (STK10) IN COMPLEX WITH BOSUTINIB  |   TRANSFERASE 
2x7f:C    (GLY37) to   (VAL170)  CRYSTAL STRUCTURE OF THE KINASE DOMAIN OF HUMAN TRAF2- AND NCK-INTERACTING KINASE WITH WEE1CHK1 INHIBITOR  |   SERINE/THREONINE-PROTEIN KINASE, PHOSPHOPROTEIN, KINASE, TRANSFERASE 
2itx:A   (LYS737) to   (ILE853)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN IN COMPLEX WITH AMP- PNP  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, POLYMORPHISM, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, ALTERNATIVE SPLICING, ANP, EGFR, KINASE, AMP-PNP, MEMBRANE, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
1jam:A    (GLU55) to   (LEU173)  CRYSTAL STRUCTURE OF APO-FORM OF Z. MAYS CK2 PROTEIN KINASE ALPHA SUBUNIT  |   PROTEIN KINASE FOLD, TRANSFERASE 
4mne:E    (GLY80) to   (LEU206)  CRYSTAL STRUCTURE OF THE BRAF:MEK1 COMPLEX  |   RAF, MAPK, KINASE DOMAIN, ATP-BINDING, ERK, RAS, PAK, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
2xba:A  (GLU1132) to  (ILE1268)  STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH PHA-E429  |   ATP-BINDING, RECEPTOR, TRANSFERASE 
3wow:A    (SER51) to   (LEU173)  CRYSTAL STRUCTURE OF HUMAN CK2A WITH AMPPNP  |   TYPICAL KINASE FOLD, TRANSFERASE 
5ap6:A   (GLN541) to   (ASP664)  NATURALLY OCCURRING MUTATIONS IN THE MPS1 GENE PREDISPOSE CELLS TO KINASE INHIBITOR DRUG RESISTANCE.  |   TRANSFERASE, MPS1, MITOSIS 
2j7t:A    (GLY48) to   (LEU173)  CRYSTAL STRUCTURE OF HUMAN SERINE THREONINE KINASE-10 BOUND TO SU11274  |   KINASE, TRANSFERASE, ATP-BINDING, CELL CYCLE PROGRESSION, PHOSPHORYLATION, DISEASE MUTATION, NUCLEOTIDE- BINDING, LYMPHOCYTE ORIENTED KINASE (LOK), SERINE/THREONINE- PROTEIN KINASE, SERINE/THREONINE KINASE (STK10A) 
2xkd:A    (GLY20) to   (LEU157)  STRUCTURE OF NEK2 BOUND TO AMINOPYRAZINE COMPOUND 12  |   TRANSFERASE, CENTROSOME, MITOSIS 
4mxc:A  (GLY1095) to  (VAL1220)  CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH NOVEL INHIBITOR  |   CMET INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2j9m:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF CDK2 IN COMPLEX WITH MACROCYCLIC AMINOPYRIMIDINE  |   SERINE-THREONINE PROTEIN KINASE, SERINE/THREONINE-PROTEIN KINASE, NUCLEOTIDE-BINDING, ARYLAMINE N-ACETYLTRANSFERASE, CELL DIVISION, DRUG METABOLISM, PHOSPHORYLATION, ATP-BINDING, TRANSFERASE, MYCOBACTERIA, POLYMORPHISM, NAT, KINASE, MITOSIS, ISONIAZID, CELL CYCLE 
1jwh:A    (GLU55) to   (LEU173)  CRYSTAL STRUCTURE OF HUMAN PROTEIN KINASE CK2 HOLOENZYME  |   CASEIN KINASE 2, CK2 HOLOENZYME, PROTEIN KINASE CK2, TRANSFERASE 
2xno:A    (GLY20) to   (LEU157)  STRUCTURE OF NEK2 BOUND TO CCT243779  |   TRANSFERASE, CENTROSOME, MITOSIS, CELL CYCLE 
2xp2:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH CRIZOTINIB (PF-02341066)  |   CRIZOTINIB, TRANSFERASE 
2xs0:A    (GLY38) to   (ASP169)  LINEAR BINDING MOTIFS FOR JNK AND FOR CALCINEURIN ANTAGONISTICALLY CONTROL THE NUCLEAR SHUTTLING OF NFAT4  |   TRANSCRIPTION, TRANSFERASE, MAPK SIGNALING PATHWAYS, LINEAR BINDING MOTIFS 
5b7v:A   (ASN506) to   (ASP641)  HUMAN FGFR1 KINASE IN COMPLEX WITH CH5183284  |   PROTEIN KINASE, ATP-BINDING, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5bmm:A   (PHE278) to   (VAL402)  SRC IN COMPLEX WITH DNA-TEMPLATED MACROCYCLIC INHIBITOR MC25B  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1wbw:A    (SER37) to   (LEU167)  IDENTIFICATION OF NOVEL P38 ALPHA MAP KINASE INHIBITORS USING FRAGMENT-BASED LEAD GENERATION.  |   P38, MAP KINASE, INHIBITOR STRUCTURE, ALTERNATIVE SPLICING, ATP-BINDING, NUCLEAR PROTEIN, PHOSPHORYLATION, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
2jld:A    (GLY68) to   (LEU198)  EXTREMELY TIGHT BINDING OF RUTHENIUM COMPLEX TO GLYCOGEN SYNTHASE KINASE 3  |   WNT SIGNALING PATHWAY, SERINE/THREONINE-PROTEIN KINASE, RUTHENIUM GLYCOGEN SYNTHASE KINASE PICOMOLAR, NUCLEOTIDE-BINDING, ALTERNATIVE SPLICING, KINASE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN 
5bvd:A    (GLY35) to   (ILE163)  TETRAHYDROPYRROLO-DIAZEPENONES AS INHIBITORS OF ERK2 KINASE  |   INHIBITOR, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1wfc:A    (SER37) to   (LEU167)  STRUCTURE OF APO, UNPHOSPHORYLATED, P38 MITOGEN ACTIVATED PROTEIN KINASE P38 (P38 MAP KINASE) THE MAMMALIAN HOMOLOGUE OF THE YEAST HOG1 PROTEIN  |   P38 MAP KINASE, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
4nj3:A    (GLY16) to   (LEU143)  MODULATING THE INTERACTION BETWEEN CDK2 AND CYCLIN A WITH A QUINOLINE- BASED INHIBITOR  |   CELL CYCLE, INHIBITION, CYCLIN-DEPENDENT KINASE, CANCER, ATP-BINDING, CELL DIVISION,MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
2y4i:C    (VAL81) to   (LEU206)  KSR2-MEK1 HETERODIMER  |   TRANSFERASE, KSR1 
3zos:B   (GLY622) to   (ILE782)  STRUCTURE OF THE DDR1 KINASE DOMAIN IN COMPLEX WITH PONATINIB  |   TRANSFERASE, RTK, COLLAGEN, DISCOIDIN DOMAIN 
2lgc:A    (SER37) to   (ILE166)  JOINT NMR AND X-RAY REFINEMENT REVEALS THE STRUCTURE OF A NOVEL DIBENZO[A,D]CYCLOHEPTENONE INHIBITOR/P38 MAP KINASE COMPLEX IN SOLUTION  |   P38 MAPK KINASE-INHIBITOR COMPLEX, HYBRID NMR/X-RAY STRUCTURE, TRANSFERASE 
1koa:A  (GLY5954) to  (LEU6081)  TWITCHIN KINASE FRAGMENT (C.ELEGANS), AUTOREGULATED PROTEIN KINASE AND IMMUNOGLOBULIN DOMAINS  |   KINASE, TWITCHIN, INTRASTERIC REGULATION 
4nst:A   (GLY739) to   (LEU875)  CRYSTAL STRUCTURE OF HUMAN CDK12/CYCLIN K IN COMPLEX WITH ADP-ALUMINUM FLUORIDE  |   TRANSCRIPTION, RNA POLYMERASE II, PHOSPHORYLATION, TRANSFERASE- TRANSCRIPTION COMPLEX 
2yfx:A  (GLY1128) to  (ILE1268)  STRUCTURE OF L1196M MUTANT ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH CRIZOTINIB  |   NUCLEOTIDE-BINDING, TRANSFERASE, RECEPTOR 
1ksw:A   (GLY279) to   (VAL402)  STRUCTURE OF HUMAN C-SRC TYROSINE KINASE (THR338GLY MUTANT) IN COMPLEX WITH N6-BENZYL ADP  |   SH3, SH2, KINASE, BUMP HOLE, BUMP-HOLE, CHEMICAL GENETICS, ORTHOGONAL SUBSTRATE, ATP, TRANSFERASE 
2yhv:A  (PHE1127) to  (ILE1268)  STRUCTURE OF L1196M MUTANT ANAPLASTIC LYMPHOMA KINASE  |   TRANSFERASE, RECEPTOR 
3zya:A    (SER37) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH 2-AMINO-PHENYLAMINO- DIBENZOSUBERONE  |   TRANSFERASE, ALLOSTERIC REGULATION, PROTEIN KINASE INHIBITOR, STRUCTURE-ACTIVITY RELATIONSHIP, P38 MITOGEN-ACTIVATED PROTEIN KINASES 
4o0r:B   (GLY282) to   (LEU405)  BACK POCKET FLEXIBILITY PROVIDES GROUP-II PAK SELECTIVITY FOR TYPE 1 KINASE INHIBITORS  |   PAK1, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2no3:A    (GLY38) to   (ILE167)  NOVEL 4-ANILINOPYRIMIDINES AS POTENT JNK1 INHIBITORS  |   JNK1, C-JUN N-TERMINAL KINASE, JNK1 INHIBITORS, ANILINOPYRIMIDINES JNK1 INHIBITORS, SIGNALING PROTEIN/INHIBITOR COMPLEX 
4o0t:B   (GLY282) to   (LEU405)  BACK POCKET FLEXIBILITY PROVIDES GROUP-II PAK SELECTIVITY FOR TYPE 1 KINASE INHIBITORS  |   PAK1, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4o2p:A   (GLY279) to   (VAL402)  KINASE DOMAIN OF CSRC IN COMPLEX WITH A SUBSTITUTED PYRAZOLOPYRIMIDINE  |   PYRAZOLO-PYRIMIDINE LIGAND, TYPE I, DFG-IN, TYROSINE PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5cei:A    (GLY33) to   (ALA172)  CRYSTAL STRUCTURE OF CDK8:CYCLIN C COMPLEX WITH COMPOUND 22  |   KINASE, INHIBITOR, CDK8, CYCLIN DEPENDENT KINASE, CYCLIN, TRANSCRIPTION-TRANSFERASE-INHIBITOR COMPLEX 
4obo:A    (GLN38) to   (ASP171)  MAP4K4 IN COMPLEX WITH INHIBITOR (COMPOUND 22), 6-(3-CHLOROPHENYL) QUINAZOLIN-4-AMINE  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5ci6:B    (GLY75) to   (ILE205)  CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA MPK6  |   KINASE, APOENZYME, TRANSFERASE 
1lew:A    (GLY36) to   (LEU167)  CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS NUCLEAR SUBSTRATE MEF2A  |   PROTEIN-PEPTIDE COMPLEX, TRANSFERASE, MAP KINASE, SERINE/THREONINE- PROTEIN KINASE, P38, MEF2A 
1lez:A    (GLY36) to   (ALA172)  CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS ACTIVATOR MKK3B  |   PROTEIN-PEPTIDE COMPLEX, TRANSFERASE, MAP KINASE, SERINE/THREONINE- PROTEIN KINASE, P38, MKK3B 
5ckw:B    (TYR86) to   (LEU211)  CRYSTAL STRUCTURE OF LEGK4_AMPPNP KINASE  |   LEGIONELLA, BACTERIAL EFFECTORS, SERINE/THREONINE KINASE, TYPE IV SECRETION SYSTEM, TRANSFERASE 
5ckw:A    (TYR86) to   (LEU211)  CRYSTAL STRUCTURE OF LEGK4_AMPPNP KINASE  |   LEGIONELLA, BACTERIAL EFFECTORS, SERINE/THREONINE KINASE, TYPE IV SECRETION SYSTEM, TRANSFERASE 
4ogr:A    (GLY31) to   (LEU165)  CRYSTAL STRUCTURE OF P-TEFB COMPLEX WITH AFF4 AND TAT  |   P-TEFB, CYCLIN-DEPENDENT KINASE 9, CYCLIN FOLD, INTRINSICALLY UNSTRUCTURED AFF4, TRANSCRIPTIONAL REGULATION AT HIV PROMOTER, BINDS TAR, N-TERMINAL ACETYLATION OF TAT, TRANSFERASE-VIRAL PROTEIN COMPLEX 
4ogr:I    (GLU32) to   (LEU165)  CRYSTAL STRUCTURE OF P-TEFB COMPLEX WITH AFF4 AND TAT  |   P-TEFB, CYCLIN-DEPENDENT KINASE 9, CYCLIN FOLD, INTRINSICALLY UNSTRUCTURED AFF4, TRANSCRIPTIONAL REGULATION AT HIV PROMOTER, BINDS TAR, N-TERMINAL ACETYLATION OF TAT, TRANSFERASE-VIRAL PROTEIN COMPLEX 
5cnn:B   (LYS713) to   (ILE829)  CRYSTAL STRUCTURE OF THE EGFR KINASE DOMAIN MUTANT I682Q  |   KINASE EGFR, TRANSFERASE 
1lp4:A    (SER51) to   (LEU173)  CRYSTAL STRUCTURE OF A BINARY COMPLEX OF THE CATALYTIC SUBUNIT OF PROTEIN KINASE CK2 WITH MG-AMPPNP  |   PROTEIN KINASE, CK2, CASEIN KINASE 2, DUAL-COSUBSTRATE SPECIFICITY, TRANSFERASE 
1luf:A   (ALA591) to   (ILE740)  CRYSTAL STRUCTURE OF THE MUSK TYROSINE KINASE: INSIGHTS INTO RECEPTOR AUTOREGULATION  |   PHOSPHORYLATION, SIGNAL TRANSDUCTION, MASS SPECTROMETRY, TRANSFERASE 
2zaz:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF P38 IN COMPLEX WITH 4-ANILINO QUINOLINE INHIBITOR  |   SERINE/THREONINE PROTEIN KINASE, MAP KINASE, P38, ATP-BINDING, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHORYLATION, TRANSFERASE 
2zb1:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF P38 IN COMPLEX WITH BIPHENYL AMIDE INHIBITOR  |   SERINE/THREONINE PROTEIN KINASE, MAP KINASE, P38, ATP-BINDING, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHORYLATION, TRANSFERASE 
2zdt:A    (GLY76) to   (ASP207)  CRYSTAL STRUCTURE OF HUMAN JNK3 COMPLEXED WITH AN ISOQUINOLONE INHIBITOR  |   PROTEIN KINASE, ATP-BINDING, EPILEPSY, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
4or5:F    (GLU32) to   (LEU165)  CRYSTAL STRUCTURE OF HIV-1 TAT COMPLEXED WITH HUMAN P-TEFB AND AFF4  |   CDK9, TAT, AFF4, ZINC FINGER, TRANSCRIPTION, RNA BINDING, PHOSPHORYLATION, TRANSFERASE-TRANSCRIPTION COMPLEX 
1m7q:A    (GLY36) to   (ILE166)  CRYSTAL STRUCTURE OF P38 MAP KINASE IN COMPLEX WITH A DIHYDROQUINAZOLINONE INHIBITOR  |   SERINE/THREONINE KINASE, ATP-BINDING DOMAIN, INHIBITOR, TRANSFERASE 
2zoq:B    (MET55) to   (ILE182)  STRUCTURAL DISSECTION OF HUMAN MITOGEN-ACTIVATED KINASE ERK1  |   SERINE/THREONINE KINASE, ERK1, ACETYLATION, ATP-BINDING, CELL CYCLE, HOST-VIRUS INTERACTION, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
4acg:A    (GLY68) to   (LEU198)  GSK3B IN COMPLEX WITH INHIBITOR  |   TRANSFERASE 
3kq7:A    (GLY36) to   (ILE166)  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  |   P38ALPHA KINASE, ALTERNATIVE SPLICING, ATP BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
4p90:B   (GLY282) to   (LEU405)  CRYSTAL STRUCTURE OF THE KINASE DOMAIN OF HUMAN PAK1 IN COMPLEX WITH COMPOUND 15  |   INHIBITOR, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3kul:A   (GLY652) to   (VAL776)  KINASE DOMAIN OF HUMAN EPHRIN TYPE-A RECEPTOR 8 (EPHA8)  |   ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, RECEPTOR, TRANSFERASE, PHOSPHORYLATION, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, MEMBRANE, PHOSPHOPROTEIN 
5dbx:A    (ALA87) to   (ILE220)  CRYSTAL STRUCTURE OF MURINE SPAK(T243D) IN COMPLEX WITH AMPPNP  |   KINASE, TRANSFERASE 
5dg5:B  (HIS1094) to  (ALA1221)  CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HEPATOCYTE GROWTH FACTOR RECEPTOR C-MET IN COMPLEX WITH ALTIRATINIB ANALOG DP- 4157  |   TYROSINE KINASE DOMAIN, HEPATOCYTE GROWTH FACTOR RECEPTOR C-MET, C- MET, ALTIRATINIB ANALOG, DP-4157, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3l8s:A    (GLY36) to   (ASP168)  HUMAN P38 MAP KINASE IN COMPLEX WITH CP-547632  |   DFG-OUT, GLYCINE-RICH LOOP, CP-547632, ALTERNATIVE SPLICING, ATP- BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3lct:A  (GLU1132) to  (ILE1268)  CRYSTAL STRUCTURE OF THE ANAPLASTIC LYMPHOMA KINASE CATALYTIC DOMAIN  |   KINASE CATALYTIC DOMAIN, ATP-BINDING, GLYCOPROTEIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO-ONCOGENE, RECEPTOR, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSFERASE 
3lfb:A    (SER37) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH RL98  |   THIAZOLE-UREA, DFG-OUT, SAR, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3lff:A    (GLY36) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH RL166  |   THIAZOLE-UREA, DFG-OUT, SAR, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3lfn:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF CDK2 WITH SAR57, AN AMINOINDAZOLE TYPE INHIBITOR  |   PROTEIN KINASE FOLD, ACETYLATION, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3alo:A   (GLY114) to   (LEU245)  CRYSTAL STRUCTURE OF HUMAN NON-PHOSPHORYLATED MKK4 KINASE DOMAIN TERNARY COMPLEX WITH AMP-PNP AND P38 PEPTIDE  |   KINASE, ALLOSTERIC BINDING, ACTIVATION HELIX, TRANSFERASE 
4anl:A  (PHE1127) to  (ILE1268)  STRUCTURE OF G1269A MUTANT ANAPLASTIC LYMPHOMA KINASE  |   TRANSFERASE, CRIZOTINIB 
4ans:A  (PHE1127) to  (ILE1268)  STRUCTURE OF L1196M,G1269A DOUBLE MUTANT ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH CRIZOTINIB  |   TRANSFERASE 
5drb:A   (PHE232) to   (ILE366)  CRYSTAL STRUCTURE OF WNK1 IN COMPLEX WITH WNK463  |   KINASE, INHIBITOR, COMPLEX, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3lhj:A    (SER37) to   (ASP168)  CRYSTAL STRUCTURE OF P38A MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH A PYRAZOLOPYRIDINONE INHIBITOR.  |   SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE- BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM 
4ap7:A  (LYS1103) to  (ALA1221)  CRYSTAL STRUCTURE OF C-MET KINASE DOMAIN IN COMPLEX WITH 4-( (6-(4- FLUOROPHENYL)-(1,2,4)TRIAZOLO(4,3-B)(1,2,4)TRIAZIN-3-YL)METHYL) PHENOL  |   TRANSFERASE 
4ase:A   (ALA851) to  (ILE1044)  CRYSTAL STRUCTURE OF VEGFR2 (JUXTAMEMBRANE AND KINASE DOMAINS) IN COMPLEX WITH TIVOZANIB (AV-951)  |   TRANSFERASE, ANGIOGENESIS, SIGNALING PROTEIN, PHOSPHORYLATION, RECEPTOR, INHIBITOR 
1zoe:A    (SER51) to   (LEU173)  CRYSTAL STRUCTURE OF PROTEIN KINASE CK2 IN COMPLEX WITH TBB- DERIVATIVES INHIBITORS  |   PROTEIN KINASE, INHIBITOR, COMPLEX, TRANSFERASE 
3lq5:A    (GLY31) to   (LEU165)  STRUCTURE OF CDK9/CYCLINT IN COMPLEX WITH S-CR8  |   TRANSCRIPTIONAL CDK-CYCLIN COMPLEX, PHOSPHORYLATED, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSCRIPTION REGULATION, TRANSFERASE, CELL CYCLE, CELL DIVISION, HOST-VIRUS INTERACTION,, TRANSCRIPTION-INHIBITOR COMPLEX 
5efq:A   (GLY717) to   (LEU853)  CRYSTAL STRUCTURE OF HUMAN CDK13/CYCLIN K IN COMPLEX WITH ADP-ALUMINUM FLUORIDE  |   KINASE, CYCLIN, ADP, TRANSFERASE 
5efq:C   (GLY717) to   (LEU853)  CRYSTAL STRUCTURE OF HUMAN CDK13/CYCLIN K IN COMPLEX WITH ADP-ALUMINUM FLUORIDE  |   KINASE, CYCLIN, ADP, TRANSFERASE 
2ac3:A    (HIS95) to   (ASP226)  STRUCTURE OF HUMAN MNK2 KINASE DOMAIN  |   DFD MOTIF, TRANSFERASE 
2ac5:A    (HIS95) to   (ASP226)  STRUCTURE OF HUMAN MNK2 KINASE DOMAIN MUTANT D228G  |   DFG MOTIF, TRANSFERASE 
4bbm:A    (GLY16) to   (ASP144)  CRYSTAL STRUCTURE OF THE HUMAN CDKL2 KINASE DOMAIN WITH BOUND TCS 2312  |   TRANSFERASE, PHOSPHO-MIMETIC 
3b8q:B   (GLN847) to  (ILE1044)  CRYSTAL STRUCTURE OF THE VEGFR2 KINASE DOMAIN IN COMPLEX WITH A NAPHTHAMIDE INHIBITOR  |   RECEPTOR TYROSINE KINASE, ANGIOGENESIS, ATP-BINDING, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, GLYCOPROTEIN, HOST- VIRUS INTERACTION, IMMUNOGLOBULIN DOMAIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
4bcg:A    (GLY31) to   (LEU165)  STRUCTURE OF CDK9 IN COMPLEX WITH CYCLIN T AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR  |   TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, TRANSCRIPTION-PROTEIN BINDING, STRUCTURE-BASED DRUG DESIGN 
4qny:A    (GLY33) to   (ILE165)  CRYSTAL STRUCTURE OF MAPK FROM LEISHMANIA DONOVANI, LDBPK_331470  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, LEISHMANIA, KINASE, TRANSFERASE 
4bcq:A    (VAL17) to   (LYS142)  STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR  |   TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN A, CYCLIN- DEPENDENT KINASE 2, STRUCTURE-BASED DRUG DESIGN 
3mh0:A    (SER37) to   (ASP168)  MUTAGENESIS OF P38 MAP KINASE ESHTABLISHES KEY ROLES OF PHE169 IN FUNCTION AND STRUCTURAL DYNAMICS AND REVEALS A NOVEL DFG-OUT STATE  |   SIGNALING PROTEIN,TRANSFERASE, TRANSFERASE 
3mh3:A    (GLY36) to   (ASP168)  MUTAGENESIS OF P38 MAP KINASE ESTABLISHES KEY ROLES OF PHE169 IN FUNCTION AND STRUCTURAL DYNAMICS AND REVEALS A NOVEL DFG-OUT STATE  |   SIGNALING PROTEIN, TRANSFERASE 
4qqj:A   (GLN496) to   (ASP630)  CRYSTAL STRUCTURE OF FGF RECEPTOR (FGFR) 4 KINASE DOMAIN HARBORING THE V550L GATE-KEEPER MUTATION  |   KINASE DOMAIN FOLD, CELL SIGNALING, PHOSPHOTRANSFERASE, PLASMAMEMBRANE, TRANSFERASE 
5eob:A  (LYS1103) to  (VAL1220)  CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH NOVEL INHIBITOR  |   CMET INHIBITOR, TRANSFERASE 
4bi2:A   (SER537) to   (ASP664)  SCAFFOLD FOCUSED VIRTUAL SCREENING: PROSPECTIVE APPLICATION TO THE DISCOVERY OF TTK INHIBITOR  |   TRANSFERASE, MITOSIS 
5eta:B    (SER37) to   (ILE166)  STRUCTURE OF MAPK14 WITH BOUND THE KIM DOMAIN OF THE TOXOPLASMA PROTEIN GRA24  |   MAPK14, GRA24, KIM DOMAIN, PEPTIDE-PROTEIN COMPLEX, TRANSFERASE 
5eta:A    (SER37) to   (ILE166)  STRUCTURE OF MAPK14 WITH BOUND THE KIM DOMAIN OF THE TOXOPLASMA PROTEIN GRA24  |   MAPK14, GRA24, KIM DOMAIN, PEPTIDE-PROTEIN COMPLEX, TRANSFERASE 
3mss:B   (GLU255) to   (VAL379)  ABL KINASE IN COMPLEX WITH IMATINIB AND FRAGMENT (FRAG2) IN THE MYRISTATE SITE  |   KINASE, FRAGMENT-BASED SCREENING, FBS, TRANSFERASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3mss:C   (GLU255) to   (VAL379)  ABL KINASE IN COMPLEX WITH IMATINIB AND FRAGMENT (FRAG2) IN THE MYRISTATE SITE  |   KINASE, FRAGMENT-BASED SCREENING, FBS, TRANSFERASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3blh:A    (GLY31) to   (LEU165)  CRYSTAL STRUCTURE OF HUMAN CDK9/CYCLINT1  |   TRANSCRIPTIONAL CDK/CYCLIN COMPLEX, PHOSPHORYLATED, ALTERNATIVE SPLICING, ATP-BINDING, KINASE, NUCLEOTIDE- BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSCRIPTION REGULATION, TRANSFERASE, ACETYLATION, CELL CYCLE, CELL DIVISION, COILED COIL, HOST-VIRUS INTERACTION 
3blr:A    (GLY31) to   (LEU165)  CRYSTAL STRUCTURE OF HUMAN CDK9/CYCLINT1 IN COMPLEX WITH FLAVOPIRIDOL  |   TRANSCRIPTIONAL CDK/CYCLIN COMPLEX, PHOSPHORYLATED, FLAVOPIRIDOL, ALTERNATIVE SPLICING, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSCRIPTION REGULATION, TRANSFERASE, ACETYLATION, CELL CYCLE, CELL DIVISION, COILED COIL, HOST-VIRUS INTERACTION 
5eyd:A  (GLY1090) to  (VAL1220)  CRYSTAL STRUCTURE OF C-MET IN COMPLEX WITH AMG 337  |   PHOSPHOTRANSFERASE, INHIBITOR, CANCER, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3mvl:A    (ALA41) to   (ASP168)  P38 ALPHA MAP KINASE COMPLEXED WITH PYRROLOTRIAZINE INHIBITOR 7K  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE 
3mvl:B    (SER37) to   (ASP168)  P38 ALPHA MAP KINASE COMPLEXED WITH PYRROLOTRIAZINE INHIBITOR 7K  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE 
3mvm:A    (SER37) to   (ASP168)  P38 ALPHA MAP KINASE COMPLEXED WITH PYRROLOTRIAZINE INHIBITOR 7V  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3mvm:B    (SER37) to   (ASP168)  P38 ALPHA MAP KINASE COMPLEXED WITH PYRROLOTRIAZINE INHIBITOR 7V  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3bv2:A    (TYR35) to   (ILE166)  MORPHOLINO PYRROLOTRIAZINE P38 ALPHA MAP KINASE INHIBITOR COMPOUND 30  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN 
5f95:A    (GLY68) to   (LEU198)  CRYSTAL STRUCTURE OF GSK3B IN COMPLEX WITH COMPOUND 18: 2- [(CYCLOPROPYLCARBONYL)AMINO]-N-(4-PHENYLPYRIDIN-3-YL)PYRIDINE-4- CARBOXAMIDE  |   GSK3B, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4btf:A   (SER204) to   (ALA335)  STRUCTURE OF MLKL  |   TRANSFERASE, PSEDUOKINASE, NECROPTOSIS 
3bx5:A    (SER37) to   (ILE166)  P38 ALPHA MAP KINASE COMPLEXED WITH BMS-640994  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE, SIGNALING PROTEIN 
4r1y:A  (GLY1090) to  (VAL1220)  IDENTIFICATION AND OPTIMIZATION OF PYRIDAZINONES AS POTENT AND SELECTIVE C-MET KINASE INHIBITOR  |   TRANSFERASE INHIBITOR, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5fdp:A   (GLY622) to   (ILE782)  STRUCTURE OF DDR1 RECEPTOR TYROSINE KINASE IN COMPLEX WITH D2099 INHIBITOR AT 2.25 ANGSTROMS RESOLUTION.  |   TRANSFERASE, DDR1 KINASE, INHIBITORS, STRUCTURAL GENOMICS, PSI- BIOLOGY, STRUCTURAL GENOMICS CONSORTIUM, SGC 
4bwx:B   (PRO284) to   (LEU423)  STRUCTURE OF NEUROSPORA CRASSA PAN3 PSEUDOKINASE MUTANT  |   GENE REGULATION, DEADENYLASE, PAN2, MIRNA, MRNA DECAY 
4r3c:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF P38 ALPHA MAP KINASE IN COMPLEX WITH A NOVEL ISOFORM SELECTIVE DRUG CANDIDATE  |   SERINE/THREONINE-PROTEIN KINASE, PROTEIN KINASE DOMAIN, TRANSFERASE, ATP BINDING, PHOSPHORYLATION, CYTOSOL, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4r5y:B   (GLY469) to   (GLY593)  THE COMPLEX STRUCTURE OF BRAF V600E KINASE DOMAIN WITH A NOVEL BRAF INHIBITOR  |   KINASE, SIGNAL TRANSDUCTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4bzd:A    (GLY16) to   (LEU143)  STRUCTURE OF CDK2 IN COMPLEX WITH A BENZIMIDAZOPYRIMIDINE  |   TRANSFERASE, KINASE INHIBITOR 
3cgo:A    (ILE77) to   (ASP207)  IRAK-4 INHIBITORS (PART II)- A STRUCTURE BASED ASSESSMENT OF IMIDAZO[1,2 A]PYRIDINE BINDING  |   JNK3 KINASE, INHIBITOR, ALTERNATIVE SPLICING, ATP-BINDING, CHROMOSOMAL REARRANGEMENT, CYTOPLASM, EPILEPSY, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3new:A    (GLY36) to   (ILE166)  P38-ALPHA COMPLEXED WITH COMPOUND 10  |   KINASE, SER/THR KINASE, INTRACELLULAR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3nnv:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF P38 ALPHA IN COMPLEX WITH DP437  |   KINASE, TRANSFERASE 
3nnw:A    (GLY36) to   (ILE166)  CRYSTAL STRUCTURE OF P38 ALPHA IN COMPLEX WITH DP802  |   KINASE, TRANSFERASE 
3npc:A    (GLY38) to   (ILE167)  CRYSTAL STRUCTURE OF JNK2 COMPLEXED WITH BIRB796  |   DFG-OUT, PROTEIN KINASE, TRANSFERASE, ATP BINDING, TYPE II KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3npc:B    (GLY38) to   (ILE167)  CRYSTAL STRUCTURE OF JNK2 COMPLEXED WITH BIRB796  |   DFG-OUT, PROTEIN KINASE, TRANSFERASE, ATP BINDING, TYPE II KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ccu:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH 2-(5-(6-AMINO-5-((R)-1-(5-FLUORO-2-(2H-1,2,3-TRIAZOL-2-YL) PHENYL)ETHOXY)PYRIDIN-3-YL)-4-METHYLTHIAZOL-2-YL)PROPAN-2-OL  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
5fto:A  (GLY1128) to  (ILE1268)  CRYSTAL STRUCTURE OF THE ALK KINASE DOMAIN IN COMPLEX WITH ENTRECTINIB  |   TRANSFERASE, KINASE INHIBITORS, CANCER, DRUG DISCOVERY, ALK, TRK, ROS1, ANAPLASTIC LARGE CELL LYMPHOMA (ALCL), NON SMALL CELL LARGE CANCER (NSCLC), NEUROBLASTOMA, COLORECTAL CANCER (CRC) 
5ftq:A  (GLU1132) to  (ILE1268)  CRYSTAL STRUCTURE OF THE ALK KINASE DOMAIN IN COMPLEX WITH CMPD 17  |   TRANSFERASE, KINASE INHIBITORS, CANCER, DRUG DISCOVERY, ALK, TRK, ROS1, ANAPLASTIC LARGE CELL LYMPHOMA (ALCL), NON SMALL CELL LARGE CANCER (NSCLC), NEUROBLASTOMA, COLORECTAL CANCER (CRC) 
3nup:A    (GLY25) to   (LEU161)  CDK6 (MONOMERIC) IN COMPLEX WITH INHIBITOR  |   KINASE, PROTEIN KINASE, ATP BINDING, PHOSPHORYLATION, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4cfw:A    (GLY16) to   (LEU143)  STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS.  |   CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE 
4cfx:C    (VAL17) to   (LEU143)  STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS.  |   CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE 
3cs9:A   (GLU255) to   (VAL379)  HUMAN ABL KINASE IN COMPLEX WITH NILOTINIB  |   NILOTINIB, AMN107, KINASE, ABL, ALTERNATIVE SPLICING, ATP- BINDING, CELL ADHESION, CHROMOSOMAL REARRANGEMENT, CYTOPLASM, CYTOSKELETON, LIPOPROTEIN, MAGNESIUM, MANGANESE, METAL-BINDING, MYRISTATE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTO-ONCOGENE, SH2 DOMAIN, SH3 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE, ABL KINASE WT IN COMPLEX WITH NVP-AMN107 
3nww:A    (GLY36) to   (ASP168)  P38 ALPHA KINASE COMPLEXED WITH A 2-AMINOTHIAZOL-5-YL-PYRIMIDINE BASED INHIBITOR  |   P38 MAP KINASE, SERINE/THREONINE-PROTINE KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3ctq:A    (SER37) to   (ILE166)  STRUCTURE OF MAP KINASE P38 IN COMPLEX WITH A 1-O-TOLYL-1,2, 3-TRIAZOLE-4-CARBOXAMIDE  |   TWO LOBE KINASE FOLD, N-TERMINAL BETA-SHEET, C-TERMINAL ALPHA-HELIX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3o0g:B    (GLY16) to   (LEU142)  CRYSTAL STRUCTURE OF CDK5:P25 IN COMPLEX WITH AN ATP ANALOGUE  |   KINASE, KINASE ACTIVATOR COMPLEX, KINASE INHIBITOR COMPLEX, TRANSFERASE-TRANSFERASE ACTIVATOR COMPLEX 
4cmo:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR 2-((1R)-1-((3-AMINO-6-(2- METHOXYPYRIDIN- -YL)PYRAZIN-2-YL)OXY)ETHYL)-4-FLUORO-N-METHYLBENZAMIDE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE INHIBITOR 
4cmt:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR 3-((1R)-1-(5-FLUORO-2-(2H-1,2,3-TRIAZOL-2-YL) PHENYL)ETHOXY)-5-(3-(METHYLSULFONYL)PHENYL)PYRIDIN-2-AMINE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
4cmu:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR (10R)-7-AMINO-12-FLUORO-1,3,10, 16-TETRAMETHYL-16,17-DIHYDRO-1H-8,4-(METHENO)PYRAZOLO(4,3- H)(2,5,11)BENZOXADIAZACYCLOTETRADECIN-15(10H)-ONE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
4cnh:A  (GLU1129) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR 3-((1R)-1-(5-FLUORO-2- METHOXYPHENYL)ETHOXY)-5-(1-METHYL-1H-1,2,3-TRIAZOL-5-YL) PYRIDIN-2-AMINE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
4cnh:B  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR 3-((1R)-1-(5-FLUORO-2- METHOXYPHENYL)ETHOXY)-5-(1-METHYL-1H-1,2,3-TRIAZOL-5-YL) PYRIDIN-2-AMINE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
3o8p:A    (SER37) to   (GLY168)  CONFORMATIONAL PLASTICITY OF P38 MAP KINASE DFG MOTIF MUTANTS IN RESPONSE TO INHIBITOR BINDING  |   TRANSFERASE 
3o8t:A    (GLY36) to   (ILE166)  CONFORMATIONAL PLASTICITY OF P38 MAP KINASE DFG-MOTIF MUTANTS IN RESPONSE TO INHIBITOR BINDING  |   TRANSFERASE 
3d4q:A   (LYS473) to   (ILE592)  PYRAZOLE-BASED INHIBITORS OF B-RAF KINASE  |   KINASE, ATP-BINDING, CARDIOMYOPATHY, DISEASE MUTATION, METAL-BINDING, NUCLEOTIDE-BINDING, PHORBOL-ESTER BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ZINC-FINGER 
4ctb:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH THE INHIBITOR (5R)-8-AMINO-3-FLUORO-5,19-DIMETHYL-20-OXO-5,18,19,20- TETRAHYDRO-7,11-(AZENO)PYRIDO(2',1':2,3)IMIDAZO(4,5-H)(2,5,11) BENZOXADIAZACYCLOTETRADECINE-14-CARBONITRILE  |   TRANSFERASE, INHIBITOR 
4cv8:A   (SER537) to   (ASP664)  MPS1 KINASE WITH 3-AMINOPYRIDIN-2-ONE INHIBITORS  |   TRANSFERASE, INHIBITOR 
3oc1:A    (GLY36) to   (LEU167)  CONFORMATIONAL PLASTICITY OF P38 MAP KINASE DFG MOTIF MUTANTS IN RESPONSE TO INHIBITOR BINDING  |   TRANSFERASE 
3dak:B    (ALA29) to   (ILE162)  CRYSTAL STRUCTURE OF DOMAIN-SWAPPED OSR1 KINASE DOMAIN  |   SERINE/THREONINE PROTEIN KINASE, STE20, DOMAIN-SWAPPING, ATP-BINDING, KINASE, MAGNESIUM, METAL-BINDING, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE 
3ocg:A    (GLY36) to   (ASP168)  P38 ALPHA KINASE COMPLEXED WITH A 5-AMINO-PYRAZOLE BASED INHIBITOR  |   P38 MAP KINASE, SERINE/THREONINE-PROTINE KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4cxa:A   (GLN740) to   (LEU875)  CRYSTAL STRUCTURE OF THE HUMAN CDK12-CYCLIN K COMPLEX BOUND TO AMPPNP  |   TRANSFERASE, KINASE 
3oht:A    (SER38) to   (ASP169)  CRYSTAL STRUCTURE OF SALMO SALAR P38ALPHA  |   KINASE SERINE/THREONINE-PROTEIN KINASE TRANSFERASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3oht:B    (SER38) to   (ASP169)  CRYSTAL STRUCTURE OF SALMO SALAR P38ALPHA  |   KINASE SERINE/THREONINE-PROTEIN KINASE TRANSFERASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4tyg:A   (GLN496) to   (ASP630)  STRUCTURAL ANALYSIS OF THE HUMAN FIBROBLAST GROWTH FACTOR RECEPTOR 4 KINASE  |   FIBROBLAST GROWTH FACTOR RECEPTOR, KINASE, TRANSFERASE, DOVITINIB, PONATINB, PROTEROS BIOSTRUCTURES GMBH 
4tyh:A    (GLY76) to   (LEU205)  TERNARY COMPLEX OF P38 AND MK2 WITH A P38 INHIBITOR  |   P38, MK2, P38 INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3ds6:A    (SER37) to   (ASP168)  P38 COMPLEX WITH A PHTHALAZINE INHIBITOR  |   KINASE INHIBITOR COMPLEX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3ds6:B    (SER37) to   (ASP168)  P38 COMPLEX WITH A PHTHALAZINE INHIBITOR  |   KINASE INHIBITOR COMPLEX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3ds6:C    (SER37) to   (ASP168)  P38 COMPLEX WITH A PHTHALAZINE INHIBITOR  |   KINASE INHIBITOR COMPLEX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3dt1:A    (SER37) to   (ASP168)  P38 COMPLEXED WITH A QUINAZOLINE INHIBITOR  |   KINASE INHIBITOR COMPLEX, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3os3:A    (LYS84) to   (LEU206)  MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1 (MEK1) IN COMPLEX WITH CH4858061 AND MGATP  |   KINASE, KINASE INHIBITOR, ALLOSTERIC, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5hbe:A    (GLY33) to   (ALA172)  CDK8-CYCC IN COMPLEX WITH 8-[3-CHLORO-5-(1-METHYL-2,2-DIOXO-2, 3- DIHYDRO-1H-2L6-BENZO[C]ISOTHIAZOL-5-YL)-PYRIDIN- 4-YL]-1-OXA-3,8- DIAZA-SPIRO[4.5]DECAN-2-ONE  |   CDK8 KINASE / CYCLIN C, TRANSFERASE 
3dv3:A    (LYS84) to   (LYS205)  MEK1 WITH PF-04622664 BOUND  |   KINASE, KINASE INHIBITORS, MEK, ATP-BINDING, DISEASE MUTATION, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, TYROSINE-PROTEIN KINASE 
3otv:A    (GLN45) to   (LEU166)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF RV3910 FROM MYCOBACTERIUM TUBERCULOSIS  |   PEPTIDOGLYCAN, SER/THR KINASE, PSEUDOKINASE, REGULATION, MEMBRANE, TRANSFERASE 
4u3y:A    (GLY37) to   (LEU169)  APO MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE KINASE 4 (MAP4K4)  |   KINASE, TRANSFERASE 
4u3z:A    (TYR40) to   (LEU169)  APO MAP4K4 T181E PHOSPHOMIMETIC MUTANT  |   KINASE, TRANSFERASE 
4u41:A    (GLN38) to   (ASP171)  MAP4K4 BOUND TO INHIBITOR COMPOUND 1  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4deh:A  (GLY1090) to  (VAL1220)  CRYSTAL STRUCTURE OF C-MET IN COMPLEX WITH TRIAZOLOPYRIDINONE INHIBITOR 3  |   PROTO-ONCOGENE, RECEPTOR TYROSINE KINASE, RTK, ATP-BINDING, HEPATOCYTE GROWTH FACTOR/SCATTER FACTOR, HGF/SF, PHOSPHOPROTEIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4dei:A  (GLY1090) to  (VAL1220)  CRYSTAL STRUCTURE OF C-MET IN COMPLEX WITH TRIAZOLOPYRIDINONE INHIBITOR 24  |   PROTO-ONCOGENE, INHIBITOR, RECEPTOR TYROSINE KINASE, RTK, ATP- BINDING, HEPATOCYTE GROWTH FACTOR/SCATTER FACTOR, HGF/SF, PHOSPHOPROTEIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3dxn:A    (GLY35) to   (ILE165)  CRYSTAL STRUCTURE OF THE CALCIUM-DEPENDENT KINASE FROM TOXOPLASMA GONDII, 541.M00134, KINASE DOMAIN.  |   CDPK, CALCIUM DEPENDENT KINASE, CALMODULIN, PARASITE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, TRANSFERASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
3p4k:A    (GLY36) to   (ILE166)  THE THIRD CONFORMATION OF P38A MAP KINASE OBSERVED IN PHOSPHORYLATED P38A AND IN SOLUTION  |   KINASE, PHOSPHORYLATION, TRANSFERASE 
3p5k:A    (SER37) to   (ILE166)  P38 INHIBITOR-BOUND  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5hnb:A    (GLY33) to   (ALA172)  CDK8-CYCC IN COMPLEX WITH [6-HYDROXY-3-(3-METHYL-BENZYL)-1H-INDAZOL-5- YL]-((S)-3-HYDROXY-PYRROLIDIN-1-YL)-METHANONE  |   CDK8 KINASE / CYCLIN C, TRANSFERASE 
3p7b:A    (GLY36) to   (ILE166)  P38 INHIBITOR-BOUND  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3p7c:A    (SER37) to   (ILE166)  P38 INHIBITOR-BOUND  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3p86:A   (THR564) to   (VAL692)  CRYSTAL STRUCTURE OF CTR1 KINASE DOMAIN MUTANT D676N IN COMPLEX WITH STAUROSPORINE  |   KINASE, ETR1, ERS1, ETR2, PHOSPHORYLATION, TRANSFERASE 
3p86:B   (ALA568) to   (ASP694)  CRYSTAL STRUCTURE OF CTR1 KINASE DOMAIN MUTANT D676N IN COMPLEX WITH STAUROSPORINE  |   KINASE, ETR1, ERS1, ETR2, PHOSPHORYLATION, TRANSFERASE 
4u97:B   (GLY198) to   (SER328)  CRYSTAL STRUCTURE OF ASYMMETRIC IRAK4 DIMER  |   KINASE, AUTOPHOSPHORYLATION, DIMER, TRANSFERASE 
3e3b:X    (GLU56) to   (LEU174)  CRYSTAL STRUCTURE OF CATALYTIC SUBUNIT OF HUMAN PROTEIN KINASE CK2ALPHA PRIME WITH A POTENT INDAZOLE-DERIVATIVE INHIBITOR  |   CRYSTAL STRUCTURE, CASEIN KINASE 2, CK2ALPHA PRIME, CK2ALPHA INHIBITOR, SELECTIVE KINASE INHIBITOR, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, POLYMORPHISM, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, WNT SIGNALING PATHWAY 
4u9a:B   (GLY198) to   (ASP329)  SULPHUR ANOMALOUS CRYSTAL STRUCTURE OF ASYMMETRIC IRAK4 DIMER  |   KINASE, SULPHUR ANOMALOUS, AUTOPHOSPHORYLATION, TRANSFERASE 
3pp1:A    (LYS84) to   (LEU206)  CRYSTAL STRUCTURE OF THE HUMAN MITOGEN-ACTIVATED PROTEIN KINASE KINASE 1 (MEK 1) IN COMPLEX WITH LIGAND AND MGATP  |   KINASE DOMAIN, KINASE, ATP BINDING, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5iey:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF A CDK INHIBITOR BOUND TO CDK2  |   ANTINEOPLASTIC AGENTS, CYCLIN-DEPENDENT KINASES, DOSE-RESPONSE RELATIONSHIP, DRUG, DRUG DISCOVERY, HELA CELLS, MOLECULAR STRUCTURE, NEOPLASMS, PROTEIN KINASE INHIBITORS, PYRIMIDINES, STRUCTURE- ACTIVITY RELATIONSHIP, STRUCTURE-KINETICS RELATIONSHIP, SULFOXIDES, BIOPHYSICAL ASSAYS, TUMOR, HUMANS, TRANSFERASE 
4e73:A    (GLY38) to   (ILE167)  CRYSTAL STRUCTURE OF JNK1BETA-JIP IN COMPLEX WITH AN AZAQUINOLONE INHBITOR  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4usd:A    (LYS49) to   (ASP175)  HUMAN STK10 (LOK) WITH SB-633825  |   TRANSFERASE 
4usd:B    (LYS49) to   (ASP175)  HUMAN STK10 (LOK) WITH SB-633825  |   TRANSFERASE 
4use:A    (GLY48) to   (ASP175)  HUMAN STK10 (LOK) WITH SB-633825  |   TRANSFERASE 
4use:B    (GLY48) to   (ASP175)  HUMAN STK10 (LOK) WITH SB-633825  |   TRANSFERASE 
3ptg:A    (GLY76) to   (ASP207)  DESIGN AND SYNTHESIS OF A NOVEL, ORALLY EFFICACIOUS TRI-SUBSTITUTED THIOPHENE BASED JNK INHIBITOR  |   JNK INHIBITOR, THIOPHENE, NEURODEGENERATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eh2:A    (GLY36) to   (ASP168)  HUMAN P38 MAP KINASE IN COMPLEX WITH NP-F1 AND RL87  |   MAP KINASE INSERT, KINASE-LIGAND COMPLEX, NP-FRAGMENT, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4eh6:A    (GLY36) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH NP-F5 AND RL87  |   MAP KINASE INSERT, KINASE-LIGAND COMPLEX, NP-FRAGMENT, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4eh7:A    (GLY36) to   (ASP168)  HUMAN P38 MAP KINASE IN COMPLEX WITH NP-F6 AND RL87  |   MAP KINASE INSERT, KINASE-LIGAND COMPLEX, NP-FRAGMENT, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4ehg:A   (THR470) to   (ILE592)  B-RAF KINASE DOMAIN IN COMPLEX WITH AN AMINOPYRIDIMINE-BASED INHIBITOR  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3pxq:A    (VAL17) to   (LEU143)  CDK2 IN COMPLEX WITH 3 MOLECULES OF 8-ANILINO-1-NAPHTHALENE SULFONATE  |   PROTEIN KINASE, CDK2, ALLOSTERIC LIGAND, ANS, TRANSFERASE 
3pxy:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR JWS648  |   PROTEIN KINASE, CDK2, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3pxz:A    (GLY16) to   (LEU143)  CDK2 TERNARY COMPLEX WITH JWS648 AND ANS  |   PROTEIN KINASE, CDK2, ALLOSTERIC LIGAND, ANS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3py0:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR SU9516  |   PROTEIN KINASE, CDK2, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3py1:A    (GLY16) to   (LEU143)  CDK2 TERNARY COMPLEX WITH SU9516 AND ANS  |   PROTEIN KINASE, CDK2, ALLOSTERIC LIGAND, ANS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3pyy:A   (GLU274) to   (VAL398)  DISCOVERY AND CHARACTERIZATION OF A CELL-PERMEABLE, SMALL-MOLECULE C- ABL KINASE ACTIVATOR THAT BINDS TO THE MYRISTOYL BINDING SITE  |   TYROSINE KINASE, TRANSFERASE 
3pze:A    (GLY38) to   (ASP169)  JNK1 IN COMPLEX WITH INHIBITOR  |   KINASE JNK1, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eol:A    (GLY16) to   (LEU143)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eqm:D    (SER22) to   (ASP151)  STRUCTURAL ANALYSIS OF STAPHYLOCOCCUS AUREUS SERINE/THREONINE KINASE PKNB  |   KINASE, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
4eqm:E    (SER22) to   (ASP151)  STRUCTURAL ANALYSIS OF STAPHYLOCOCCUS AUREUS SERINE/THREONINE KINASE PKNB  |   KINASE, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
4eqm:F    (SER22) to   (ASP151)  STRUCTURAL ANALYSIS OF STAPHYLOCOCCUS AUREUS SERINE/THREONINE KINASE PKNB  |   KINASE, SERINE/THREONINE PROTEIN KINASE, TRANSFERASE 
4equ:A    (GLY48) to   (LEU173)  HUMAN STK-10 (LOK) KINASE DOMAIN IN DFG-OUT CONFORMATION WITH INHIBITOR DSA-7  |   SERINE/THREONINE KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4equ:B    (GLY48) to   (LEU173)  HUMAN STK-10 (LOK) KINASE DOMAIN IN DFG-OUT CONFORMATION WITH INHIBITOR DSA-7  |   SERINE/THREONINE KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3q5i:A    (TYR68) to   (GLY213)  CRYSTAL STRUCTURE OF PBANKA_031420  |   CDPK, PLASMODIUM, MALARIA, CALCIUM DEPENDENT PROTEIN KINASE, PHOSPHOTRANSFERASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
5iui:A  (GLU1129) to  (ILE1268)  CRYSTAL STRUCTURE OF ANAPLASTIC LYPHOMA KINASE (ALK) IN COMPLEX WITH 4  |   CATALYTIC DOMAIN, TRANSFERASE 
4erw:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH STAUROSPORINE  |   PROTEIN KINASE, TRANSFERASE-ANTIBIOTIC COMPLEX 
4ewq:A    (GLY36) to   (ILE166)  HUMAN P38 ALPHA MAPK IN COMPLEX WITH A PYRIDAZINE BASED INHIBITOR  |   SERINE/THREONINE-PROTEIN KINASE, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, PROTEIN KINASE DOMAIN, TRANSFERASE, ATP BINDING, PHOSPHORYLATION, CYTOSOL, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ez3:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH NSC 134199  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qgw:A   (LEU379) to   (VAL498)  CRYSTAL STRUCTURE OF ITK KINASE BOUND TO AN INHIBITOR  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3ql8:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR JWS-6-260  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4f9w:A    (GLY36) to   (ILE166)  HUMAN P38ALPHA MAPK IN COMPLEX WITH A NOVEL AND SELECTIVE SMALL MOLECULE INHIBITOR  |   PROTEIN KINASE CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4f9y:A    (GLY36) to   (ILE166)  HUMAN P38 ALPHA MAPK IN COMPLEX WITH A NOVEL AND SELECTIVE SMALL MOLECULE INHIBITOR  |   PROTEIN KINASE CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fa2:A    (GLY36) to   (ASP168)  HUMAN P38 ALPHA MITOGEN-ACTIVATED KINASE IN COMPLEX WITH SB239063  |   PROTEIN KINASE CATALYTIC DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qqg:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR L2-5  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qrk:A   (GLU258) to   (VAL379)  THE CRYSTAL STRUCTURE OF HUMAN ABL1 KINASE DOMAIN IN COMPLEX WITH DP- 987  |   ABL1, KINASE, KINASE DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qru:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR NSK-MC1-12  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qts:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-12  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qtu:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-132  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qtw:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-13  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qtx:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-35  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qtz:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-36  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qud:A    (SER37) to   (ASP168)  HUMAN P38 MAP KINASE IN COMPLEX WITH 2-AMINO-PHENYLAMINO-BENZOPHENONE  |   KINASE DOMAIN, PHOSPHATE TRANSFERASE, BENZOPHENONE DERIVATIVE, TRANSFERASE 
3qxp:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-3-89  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qzg:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR JWS-6-76  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qzh:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-124  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qzi:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-126  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r1s:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-127  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r28:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-140  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fko:A    (GLY16) to   (LEU143)  CRYSTAL STRUCTURE OF THE CDK2 IN COMPLEX WITH THIAZOLYLPYRIMIDINE INHIBITOR  |   ALPHA AND BETA PROTEIN (A+B), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r63:A    (GLY35) to   (ILE163)  STRUCTURE OF ERK2 (SPE) MUTANT (S246E)  |   NUCLEAR TRANSPORT, PHOSPHORYLATION, KINASE FOLD, KINASE, ATP BINDING, TRANSFERASE 
3r73:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-164  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r7e:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-67  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r8l:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR L3-4  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r8u:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-1-132  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r9d:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-135  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r9h:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-142  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rah:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-22  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rai:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-160  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3rak:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-32  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3ral:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-2-34  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fob:A  (GLY1128) to  (ILE1268)  CRYSTAL STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH ACYLIMINOBENZIMIDAZOLE INHIBITOR 1  |   RECEPTOR TYROSINE KINASE, INHIBITOR, CRIZOTINIB, NEUROBLASTOMA, CD246, PHOSPHOTRANSFERASE, NPM-ALK, EML4-ALK, IN SITU PROTEOLYSIS, TRANSFERASE-INHIBITOR COMPLEX 
4foc:A  (GLY1128) to  (ILE1268)  CRYSTAL STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH ACYLIMINOBENZIMIDAZOLE INHIBITOR 2  |   RECEPTOR TYROSINE KINASE, INHIBITOR, CRIZOTINIB, NEUROBLASTOMA, CD246, PHOSPHOTRANSFERASE, NPM-ALK, EML4-ALK, IN SITU PROTEOLYSIS, TRANSFERASE-INHIBITOR COMPLEX 
4fuy:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF THE ERK2 COMPLEXED WITH EK2  |   TRANSFERASE 
4fv3:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF THE ERK2 COMPLEXED WITH EK6  |   TRANSFERASE 
4fv7:A    (GLY35) to   (ILE163)  CRYSTAL STRUCTURE OF THE ERK2 COMPLEXED WITH E94  |   TRANSFERASE 
5jsm:A   (THR470) to   (ASP594)  BRAFV600E KINASE DOMAIN IN COMPLEX WITH CHEMICALLY LINKED VEMURAFENIB INHIBITOR VEM-3-VEM  |   KINASE, DIMER, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5jsm:B   (GLY469) to   (ASP594)  BRAFV600E KINASE DOMAIN IN COMPLEX WITH CHEMICALLY LINKED VEMURAFENIB INHIBITOR VEM-3-VEM  |   KINASE, DIMER, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5jsm:C   (LYS473) to   (ASP594)  BRAFV600E KINASE DOMAIN IN COMPLEX WITH CHEMICALLY LINKED VEMURAFENIB INHIBITOR VEM-3-VEM  |   KINASE, DIMER, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4g1w:A    (GLY38) to   (ASP169)  CRYSTAL STRUCTURE OF JNK1 IN COMPLEX WITH JIP1 PEPTIDE AND 7-FLUORO-3- [4-(2-HYDROXY-ETHANESULFONYL)-BENZYL]-4-OXO-1-PHENYL-1,4-DIHYDRO- QUINOLINE-2-CARBOXYLIC ACID METHYL ESTER  |   KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5kbr:B   (THR283) to   (LEU405)  PAK1 IN COMPLEX WITH 7-AZAINDOLE INHIBITOR  |   SERINE/THREONINE-PROTEIN KINASE PAK1, KINASE, TRANSFERASE 
4gg7:A  (GLY1095) to  (VAL1220)  CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH NOVEL INHIBITOR  |   C-MET INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5ko1:A   (SER215) to   (ALA348)  PSEUDOKINASE DOMAIN OF MLKL BOUND TO COMPOUND 4.  |   PSEUDOKINASE DOMAIN MLKL TYPE1 INHIBITOR, MEMBRANE PROTEINS-INHIBITOR COMPLEX 
5kz0:A  (PHE1127) to  (ILE1268)  STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH 2-[(1R)- 1-{[2-AMINO-5-(1,3-DIMETHYL-1H-PYRAZOL-4-YL)PYRIDIN-3-YL]OXY}ETHYL]- 4-FLUORO-N,N-DIMETHYLBENZAMIDE  |   KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5l1z:A    (GLU32) to   (LEU165)  TAR COMPLEX WITH HIV-1 TAT-AFF4-P-TEFB  |   HIV-1 TAR, PROTEIN-RNA COMPLEX, TRANSCRIPTION, PROTEIN KINASE, TRANSCRIPTION-RNA COMPLEX 
5lar:A    (SER37) to   (ILE166)  CRYSTAL STRUCTURE OF P38 ALPHA MAPK14 IN COMPLEX WITH VPC00628  |   TRANSFERASE, PROTEIN KINASE, MAPK, INHIBITOR COMPLEX, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
5ljj:A   (SER537) to   (ASP664)  CRYSTAL STRUCTURE OF HUMAN MPS1 (TTK) IN COMPLEX WITH REVERSINE  |   MPS1, REVERSINE, TTK, KINASE, MITOSIS CHECKPOINT, TRANSFERASE 
5t6i:A    (GLU64) to   (ASP195)  CRYSTAL STRUCTURE OF TGCDPK1 FROM TOXOPLASMA GONDII COMPLEXED WITH 5GB  |   STRUCTURAL GENOMICS CONSORTIUM, SGC, CDPKS, SERINE/THREONINE PROTEIN KINASE, NUCLEOTIDE-BINDING, TRANSFERASE 
3e93:A    (GLY36) to   (ILE166)  CRYSTAL STRUCTURE OF P38 KINASE IN COMPLEX WITH A BIARYL AMIDE INHIBITOR  |   P38, SERINE/THREONINE PROTEIN KINASE, MAP KINASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1a9u:A    (GLY36) to   (ILE166)  THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB203580  |   TRANSFERASE, MAP KINASE, SERINE/THREONINE-PROTEIN KINASE, P38 
2oib:C   (GLY198) to   (ILE327)  CRYSTAL STRUCTURE OF IRAK4 KINASE DOMAIN APO FORM  |   KINASE, HELIC C, TRANSFERASE 
3s00:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR L4-14  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3s0o:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-1-138  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1nxk:D    (GLY76) to   (LEU205)  CRYSTAL STRUCTURE OF STAUROSPORINE BOUND TO MAP KAP KINASE 2  |   PROTEIN KINASE, MK2, PHOSPHORYLATION, STAUROSPORINE, TRANSFERASE 
2bhe:A    (GLY16) to   (LEU143)  HUMAN CYCLIN DEPENDENT PROTEIN KINASE 2 IN COMPLEX WITH THE INHIBITOR 5-BROMO-INDIRUBINE  |   3D-STRUCTURE, ARYLAMINE N-ACETYLTRANSFERASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, DRUG METABOLISM, ISONIAZID, MITOSIS, MYCOBACTERIA, NAT, PHOSPHORYLATION, POLYMORPHISM, SERINE-THREONINE -PROTEIN KINASE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3sqq:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-3-96  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1p38:A    (SER37) to   (LEU167)  THE STRUCTURE OF THE MAP KINASE P38 AT 2.1 ANGSTOMS RESOLUTION  |   TRANSFERASE, MAP KINASE, SERINE/THREONINE-PROTEIN KINASE, P38 
4xs2:B   (GLY198) to   (SER328)  IRAK4-INHIBITOR CO-STRUCTURE  |   KINASE, PHOSPHATASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4imy:A    (GLU32) to   (LEU165)  THE AFF4 SCAFFOLD BINDS HUMAN P-TEFB ADJACENT TO HIV TAT  |   TRANSCRIPTIONAL CDK9-CYCT1 COMPLEX, PHOSPHORYLATED, INTRINSICALLY DISORDERED AFF4, REGULATION OF TRANSCRIPTION ELONGATION, SER/THR KINASE, PHOSPHORYLATION OF POLII-CTD, DSIF, AND NELF, HIV-1 TAT, HOST-VIRUS INTERACTION, PHOSPHOPROTEIN, NUCLEUS, TRANSFERASE 
4imy:E    (GLU32) to   (LEU165)  THE AFF4 SCAFFOLD BINDS HUMAN P-TEFB ADJACENT TO HIV TAT  |   TRANSCRIPTIONAL CDK9-CYCT1 COMPLEX, PHOSPHORYLATED, INTRINSICALLY DISORDERED AFF4, REGULATION OF TRANSCRIPTION ELONGATION, SER/THR KINASE, PHOSPHORYLATION OF POLII-CTD, DSIF, AND NELF, HIV-1 TAT, HOST-VIRUS INTERACTION, PHOSPHOPROTEIN, NUCLEUS, TRANSFERASE 
3gcv:A    (GLY36) to   (ILE166)  HUMAN P38 MAP KINASE IN COMPLEX WITH RL62  |   DFG-OUT, TYPE II, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1ds5:B    (SER51) to   (LEU173)  DIMERIC CRYSTAL STRUCTURE OF THE ALPHA SUBUNIT IN COMPLEX WITH TWO BETA PEPTIDES MIMICKING THE ARCHITECTURE OF THE TETRAMERIC PROTEIN KINASE CK2 HOLOENZYME.  |   PROTEIN-COMPLEX, TETRAMER, TRANSFERASE 
1ds5:C    (SER51) to   (LEU173)  DIMERIC CRYSTAL STRUCTURE OF THE ALPHA SUBUNIT IN COMPLEX WITH TWO BETA PEPTIDES MIMICKING THE ARCHITECTURE OF THE TETRAMERIC PROTEIN KINASE CK2 HOLOENZYME.  |   PROTEIN-COMPLEX, TETRAMER, TRANSFERASE 
1ds5:D    (SER51) to   (LEU173)  DIMERIC CRYSTAL STRUCTURE OF THE ALPHA SUBUNIT IN COMPLEX WITH TWO BETA PEPTIDES MIMICKING THE ARCHITECTURE OF THE TETRAMERIC PROTEIN KINASE CK2 HOLOENZYME.  |   PROTEIN-COMPLEX, TETRAMER, TRANSFERASE 
4izy:A    (ILE39) to   (ASP169)  CRYSTAL STRUCTURE OF JNK1 IN COMPLEX WITH JIP1 PEPTIDE AND 4-{4-[4-(4- METHANESULFONYL-PIPERIDIN-1-YL)-INDOL-1-YL]-PYRIMIDIN-2-YLAMINO}- CYCLOHEXAN  |   KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3tn8:A    (GLU32) to   (LEU165)  CDK9/CYCLIN T IN COMPLEX WITH CAN508  |   CYCLIN DEPENDENT KINASE, KINASE, CYCLIN, PHOSPHOTRANSFER, CDK-CYCLIN COMPLEX, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2rg6:A    (SER37) to   (ASP168)  PHENYLALANINE PYRROLOTRIAZINE P38 ALPHA MAP KINASE INHIBITOR COMPOUND 11J  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, TRANSFERASE, P38 MAP KINASE 
4z55:A  (GLU1132) to  (ILE1268)  ANAPLASTIC LYMPHOMA KINASE CATALYTIC DOMAIN COMPLEXED WITH PYRAZOLOPYRIMIDINE DERIVATIVE OF LDK378  |   CATALYTIC DOMAIN, TRANSFERASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3v6r:A    (GLY76) to   (ASP207)  DISCOVERY OF POTENT AND SELECTIVE COVALENT INHIBITORS OF JNK  |   KINASE FOLD, APOPTOSIS, MAP KINASE, CYS MODIFICATION, PHOSPHORYLATION, JNK, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3v6r:B    (GLY76) to   (ASP207)  DISCOVERY OF POTENT AND SELECTIVE COVALENT INHIBITORS OF JNK  |   KINASE FOLD, APOPTOSIS, MAP KINASE, CYS MODIFICATION, PHOSPHORYLATION, JNK, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4lg4:B    (GLY39) to   (LEU162)  STRUCTURAL BASIS FOR AUTOACTIVATION OF HUMAN MST2 KINASE AND ITS REGULATION BY RASSF5  |   HIPPO, MST AUTOACTIVATION, DIMERIZATION, SIGNALING PROTEIN 
4lg4:C    (GLY39) to   (LEU162)  STRUCTURAL BASIS FOR AUTOACTIVATION OF HUMAN MST2 KINASE AND ITS REGULATION BY RASSF5  |   HIPPO, MST AUTOACTIVATION, DIMERIZATION, SIGNALING PROTEIN 
2h8h:A   (MET283) to   (VAL402)  SRC KINASE IN COMPLEX WITH A QUINAZOLINE INHIBITOR  |   SRC KINASE, TRANSFERASE 
4loq:A    (GLY36) to   (LEU167)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM WITH BOUND SULPHATE)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4loq:B    (GLY36) to   (LEU167)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM WITH BOUND SULPHATE)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4loq:C    (GLY36) to   (LEU167)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM WITH BOUND SULPHATE)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
4loq:D    (GLY36) to   (LEU167)  STRUCTURAL BASIS OF AUTOACTIVATION OF P38 ALPHA INDUCED BY TAB1 (TETRAGONAL CRYSTAL FORM WITH BOUND SULPHATE)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, KINASE-REGULATORY PROTEIN COMPLEX, MAPK, AUTOACTIVATION, AUTOPHOSPHORYLATION, TRANSFERASE 
2wqo:A    (GLY20) to   (LEU157)  STRUCTURE OF NEK2 BOUND TO THE AMINOPYRIDINE CCT241950  |   KINASE, NUCLEUS, MEIOSIS, MITOSIS, CYTOPLASM, ALTERNATIVE SPLICING, SERINE/THREONINE-PROTEIN KINASE, METAL-BINDING, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, MAGNESIUM, CELL CYCLE, ATP-BINDING, TRANSFERASE, COILED COIL, POLYMORPHISM, CELL DIVISION 
5aa8:A  (GLY1128) to  (ILE1268)  STRUCTURE OF C1156Y,L1198F MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH PF-06463922 ((10R)-7-AMINO-12- FLUORO-2,10,16-TRIMETHYL-15-OXO-10,15,16,17-TETRAHYDRO-2H- 8,4-(METHENO)PYRAZOLO(4,3-H)(2,5,11) BENZOXADIAZACYCLOTETRADECINE-3-CARBONITRILE).  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR, MUTANT 
5aaa:A  (GLY1128) to  (ILE1268)  STRUCTURE OF L1198F MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH CRIZOTINIB  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, ANAPLASTIC LYMPHOMA KINASE, INHIBITOR, MUTANT 
2xnm:A    (GLY20) to   (LEU157)  STRUCTURE OF NEK2 BOUND TO CCT  |   TRANSFERASE, CENTROSOME, MITOSIS, CELL CYCLE 
3zdu:A    (THR17) to   (LEU141)  CRYSTAL STRUCTURE OF THE HUMAN CDKL3 KINASE DOMAIN  |   TRANSFERASE, PHOSPHO-MIMETIC 
1w83:A    (GLY36) to   (ILE166)  P38 KINASE CRYSTAL STRUCTURE IN COMPLEX WITH SMALL MOLECULE INHIBITOR  |   KINASE/INHIBITOR, KINASE/INHIBITOR COMPLEX, P38, KINASE, INHIBITOR COMPLEX 
2y8o:A    (GLY36) to   (LEU167)  CRYSTAL STRUCTURE OF HUMAN P38ALPHA COMPLEXED WITH A MAPK DOCKING PEPTIDE  |   TRANSFERASE, SIGNALLING, MAP KINASE PATHWAY, PROTEIN-PROTEIN INTERACTION 
3k5v:B   (GLU274) to   (VAL398)  STRUCTURE OF ABL KINASE IN COMPLEX WITH IMATINIB AND GNF-2  |   KINASE, ATP-BINDING, NUCLEOTIDE-BINDING, ONCOGENE, SH2 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE 
5dey:B   (GLY282) to   (ASP407)  CRYSTAL STRUCTURE OF PAK1 IN COMPLEX WITH AN INHIBITOR COMPOUND G-5555  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3l9p:A  (GLU1132) to  (ILE1268)  CRYSTAL STRUCTURE OF THE ANAPLASTIC LYMPHOMA KINASE CATALYTIC DOMAIN  |   KINASE DOMAIN, ATP-BINDING, GLYCOPROTEIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO-ONCOGENE, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3lco:A   (ALA599) to   (ILE794)  INHIBITOR BOUND TO A DFG-OUT STRUCTURE OF THE KINASE DOMAIN OF CSF-1R  |   ATP-BINDING, DISULFIDE BOND, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3lcs:A  (GLU1132) to  (ILE1268)  CRYSTAL STRUCTURE OF THE ANAPLASTIC LYMPHOMA KINASE CATALYTIC DOMAIN  |   KINASE DOMAIN, ATP-BINDING, GLYCOPROTEIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO-ONCOGENE, RECEPTOR, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSFERASE 
4aqc:B   (GLY861) to   (ILE992)  TRIAZOLOPYRIDINE-BASED INHIBITOR OF JANUS KINASE 2  |   TRANSFERASE, ATP-BINDING 
3mgy:A    (SER37) to   (ASP168)  MUTAGENESIS OF P38 MAP KINASE ESHTABLISHES KEY ROLES OF PHE169 IN FUNCTION AND STRUCTURAL DYNAMICS AND REVEALS A NOVEL DFG-OUT STATE  |   TRANSFERASE, SIGNALING PROTEIN 
3mpa:A    (SER37) to   (ILE166)  CONFORMATIONAL PLASTICITY OF P38 MAP KINASE DFG MOTIF MUTANTS IN RESPONSE TO INHIBITOR BINDING  |   TRANSFERASE 
5etf:A    (SER37) to   (ILE166)  STRUCTURE OF DEAD KINASE MAPK14 WITH BOUND THE KIM DOMAIN OF MKK6  |   MAPK14, MKK6, KIM DOMAIN, PEPTIDE-PROTEIN COMPLEX, TRANSFERASE 
4r1v:A  (LYS1103) to  (VAL1220)  IDENTIFICATION AND OPTIMIZATION OF PYRIDAZINONES AS POTENT AND SELECTIVE C-MET KINASE INHIBITORS  |   PROTEIN KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ccb:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH 3-((R)-1-(5-FLUORO-2-(2H-1,2,3-TRIAZOL-2-YL) PHENYL)ETHOXY)-5-(5-METHYL-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, ANAPLASTIC LYMPHOMA KINASE, INHIBITOR 
4cd0:A  (GLU1132) to  (ILE1268)  STRUCTURE OF L1196M MUTANT HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH 2-(5-(6-AMINO-5-((R)-1-(5-FLUORO-2-(2H-1,2,3-TRIAZOL-2-YL) PHENYL)ETHOXY)PYRIDIN-3-YL)-4-METHYLTHIAZOL-2-YL)PROPANE-1,2-DIOL  |   TRANSFERASE, RECEPTOR TYROSINE KINASE, INHIBITOR 
4cli:A  (GLY1128) to  (ILE1268)  STRUCTURE OF THE HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH PF-06463922 ((10R)-7-AMINO-12-FLUORO-2,10,16-TRIMETHYL-15 -OXO-10,15,16,17-TETRAHYDRO-2H-8,4-(METHENO)PYRAZOLO(4,3-H) (2,5,11)BENZOXADIAZACYCLOTETRADECINE-3-CARBONITRILE).  |   TRANSFERASE, INHIBITOR 
5g6v:A   (ALA177) to   (LEU302)  CRYSTAL STRUCTURE OF THE PCTAIRE1 KINASE IN COMPLEX WITH INHIBITOR  |   TRANSFERASE 
5g6v:B   (ALA177) to   (LEU302)  CRYSTAL STRUCTURE OF THE PCTAIRE1 KINASE IN COMPLEX WITH INHIBITOR  |   TRANSFERASE 
3oef:X    (GLY36) to   (ILE166)  CRYSTAL STRUCTURE OF Y323F INACTIVE MUTANT OF P38ALPHA MAP KINASE  |   MAP KINASE, INACTIVE MUTANT, TCR MEDIATED ACTIVATION, KINASE FOLD, KINASE, SUBSTRATES, PHOSPHOTASES, UPSTREAM ACTIVATORS, Y323F, TRANSFERASE 
3dkc:A  (GLY1095) to  (ALA1221)  STRUCTURE OF MET RECEPTOR TYROSINE KINASE IN COMPLEX WITH ATP  |   DRUG DISCOVERY, C-MET KINASE, FRAGMENT BASED, MEMBRANE, RECEPTOR, TRANSMEMBRANE, ONCOPROTEIN 
4usf:A    (LYS47) to   (ASP173)  HUMAN SLK WITH SB-440719  |   TRANSFERASE 
3psb:B   (THR470) to   (ILE592)  FURO[2,3-C]PYRIDINE-BASED INDANONE OXIMES AS POTENT AND SELECTIVE B- RAF INHIBITORS  |   KINASE, ATP-BINDING, CARDIOMYOPATHY, DISEASE MUTATION, METAL-BINDING, NUCLEOTIDE-BINDING, PHORBOL-ESTER BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, ZINC-FINGER, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3pxr:A    (GLY16) to   (LEU143)  APO CDK2 CRYSTALLIZED FROM JEFFAMINE  |   PROTEIN KINASE, CDK2, JEFFAMINE, TRANSFERASE 
4f7s:A    (GLY33) to   (ALA172)  CRYSTAL STRUCTURE OF HUMAN CDK8/CYCC IN THE DMG-IN CONFORMATION  |   PROTEIN KINASE COMPLEX, PROTEROS, TRANSFERASE-TRANSCRIPTION-INHIBITOR COMPLEX 
3qwk:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-150  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3qxo:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-84  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r1q:A    (VAL17) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-102  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r2b:H    (LYS77) to   (LEU205)  MK2 KINASE BOUND TO COMPOUND 5B  |   KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fl2:A   (GLY388) to   (ILE510)  STRUCTURAL AND BIOPHYSICAL CHARACTERIZATION OF THE SYK ACTIVATION SWITCH  |   TRANSFERASE, PROTEIN KINASE 
4fl3:A   (GLY388) to   (ILE510)  STRUCTURAL AND BIOPHYSICAL CHARACTERIZATION OF THE SYK ACTIVATION SWITCH  |   TRANSFERASE, PROTEIN KINASE 
3r6x:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR KVR-1-158  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r8v:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-1-135  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fod:A  (GLY1128) to  (ILE1268)  CRYSTAL STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH ACYLIMINOBENZIMIDAZOLE INHIBITOR 36  |   RECEPTOR TYROSINE KINASE, INHIBITOR, CRIZOTINIB, NEUROBLASTOMA, CD246, PHOSPHOTRANSFERASE, NPM-ALK, EML4-ALK, TRANSFERASE-INHIBITOR COMPLEX 
4fvr:A   (GLN572) to   (LEU697)  CRYSTAL STRUCTURE OF THE JAK2 PSEUDOKINASE DOMAIN MUTANT V617F (MG- ATP-BOUND FORM)  |   JANUS PROTEIN KINASE, PSEUDOKINASE, ATP BINDING, PHOSPHORYLATION, TRANSFERASE 
5jzn:B   (PHE401) to   (LEU531)  CRYSTAL STRUCTURE OF DCLK1-KD IN COMPLEX WITH NVP-TAE684  |   KINASE, DOUBLECORTIN, TRANSFERASE 
4g6l:A    (GLY33) to   (ALA172)  CRYSTAL STRUCTURE OF HUMAN CDK8/CYCC IN THE DMG-IN CONFORMATION  |   PROTEIN KINASE COMPLEX, PROTEROS, TRANSFERASE-TRANSCRIPTION COMPLEX 
4gcj:A    (GLY16) to   (LEU143)  CDK2 IN COMPLEX WITH INHIBITOR RC-3-89  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5knj:A   (SER215) to   (PHE350)  PSEUDOKINASE DOMAIN OF MLKL BOUND TO COMPOUND 1.  |   PSEUDOKINASE DOMAIN MLKL COMPOUND 1 GFE OUT TYPE 2 INHIBITOR, MEMBRANE PROTEINS-INHIBITOR COMPLEX