4gsb:A    (HIS59) to   (SER264)  MONOCLINIC CRYSTAL FORM OF THE APO-ERK2  |   KINASE, TRANSFERASE 
4wd5:B   (SER752) to   (ASP974)  CRYSTAL STRUCTURE OF EGFR 696-1022 T790M IN COMPLEX WITH QL-X138  |   EGFR, T790M, GATEKEEPER MUTATION, INHIBITOR, TRANSFERASE-INHIBITOR COMPLEX 
3e8e:I    (GLN84) to   (ALA298)  CRYSTAL STRUCTURES OF THE KINASE DOMAIN OF PKA IN COMPLEX WITH ATP- COMPETITIVE INHIBITORS  |   PKA, AKT2, KINASE, PKI, BOVINE, INHIBITOR, ATP-BINDING, CAMP, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
2oiq:B   (SER303) to   (TYR519)  CRYSTAL STRUCTURE OF CHICKEN C-SRC KINASE DOMAIN IN COMPLEX WITH THE CANCER DRUG IMATINIB.  |   SRC,KINASE,IMATINIB,INACTIVE, TRANSFERASE 
2onl:D    (CYS98) to   (GLN327)  CRYSTAL STRUCTURE OF THE P38A-MAPKAP KINASE 2 HETERODIMER  |   HETERODIMER, KINASE, NLS, NES, DOCKING GROOVE, TRANSFERASE 
3eh9:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DEATH ASSOCIATED PROTEIN KINASE COMPLEXED WITH ADP  |   KINASE CATALYTIC DOMAIN GLYCINE-RICH LOOP, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3eha:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DEATH ASSOCIATED PROTEIN KINASE COMPLEXED WITH AMPPNP  |   KINASE DOMAIN S/T KINASE, ANK REPEAT, APOPTOSIS, ATP- BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE 
3ej1:C    (PRO45) to   (HIS283)  CDK2/CYCLINA COMPLEXED WITH A PYRAZOLOPYRIDAZINE INHIBITOR  |   CDK, CYCLIN, KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX 
3el8:A   (PRO304) to   (TYR519)  CRYSTAL STRUCTURE OF C-SRC IN COMPLEX WITH PYRAZOLOPYRIMIDINE 5  |   C-SRC, KINASE, PYRAZOLOPYRIMIDINE 5, ATP-BINDING, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO-ONCOGENE, SH2 DOMAIN, SH3 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE 
3eoc:C    (PRO45) to   (HIS283)  CDK2/CYCLINA COMPLEXED WITH A IMIDAZO TRIAZIN-2-AMINE  |   CDK, CYCLIN, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX 
2bfx:A   (GLU135) to   (HIS340)  MECHANISM OF AURORA-B ACTIVATION BY INCENP AND INHIBITION BY HESPERADIN.  |   TRANSFERASE, KINASE, MITOSIS, INHIBITION, TRANSFERASE COMPLEX 
2bfy:A   (VAL134) to   (HIS340)  COMPLEX OF AURORA-B WITH INCENP AND HESPERADIN.  |   TRANSFERASE, KINASE, MITOSIS, INHIBITION, TRANSFERASE COMPLEX 
1bkx:A    (GLN84) to   (HIS294)  A BINARY COMPLEX OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE AND ADENOSINE FURTHER DEFINES CONFORMATIONAL FLEXIBILITY  |   CONFORMATIONAL CHANGES, ELECTROSTATIC COMPLEMENTARITY, PHOSPHORYLATION, PROTEIN KINASE, TRANSFERASE, COMPLEX (PHOSPHOTRANSFERASE/ADENOSINE), PHOSPHOTRANSFERASE 
2bpm:A    (PRO45) to   (GLN287)  STRUCTURE OF CDK2-CYCLIN A WITH PHA-630529  |   PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN 
3f5p:A  (SER1040) to  (SER1265)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:B  (SER1040) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:C  (SER1040) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:D  (SER1040) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:K  (SER1040) to  (SER1265)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:M  (SER1040) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:S  (SER1040) to  (SER1265)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f5p:T  (SER1040) to  (SER1265)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND 3- CYANOQUINOLINE INHIBITOR  |   IGF-1R, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP-BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3f6x:D   (SER303) to   (TYR519)  C-SRC KINASE DOMAIN IN COMPLEX WITH SMALL MOLECULE INHIBITOR  |   KINASE, ATP-BINDING, ALTERNATIVE SPLICING, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, SH2 DOMAIN, SH3 DOMAIN, TRANSFERASE, TYROSINE- PROTEIN KINASE 
3s95:A   (GLU375) to   (HIS614)  CRYSTAL STRUCTURE OF THE HUMAN LIMK1 KINASE DOMAIN IN COMPLEX WITH STAUROSPORINE  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, LIM DOMAIN KINASE, TRANSFERASE-ANTIBIOTIC COMPLEX 
3fc2:A    (LYS91) to   (THR306)  PLK1 IN COMPLEX WITH BI6727  |   PROTEIN KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
4xbr:A   (ARG360) to   (HIS569)  IN CELLULO CRYSTAL STRUCTURE OF PAK4 IN COMPLEX WITH INKA  |   PAK4, INKA, CRYSTALLIZATION, TRANSFERASE 
1oec:A   (THR524) to   (THR764)  FGFR2 KINASE DOMAIN  |   TRANSFERASE, FGFR2 KINASE DOMAIN, RECEPTOR TYROSINE KINASE, 
1oi9:A    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1oiu:C    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1oiy:A    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
4xj0:A    (GLN62) to   (HIS310)  CRYSTAL STRUCTURE OF ERK2 IN COMPLEX WITH AN INHIBITOR 14K  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4xj0:B    (GLN62) to   (HIS310)  CRYSTAL STRUCTURE OF ERK2 IN COMPLEX WITH AN INHIBITOR 14K  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4i3z:A    (PRO45) to   (GLN287)  STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 2 MAGNESIUM IONS  |   ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX 
4i3z:C    (PRO45) to   (GLN287)  STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 2 MAGNESIUM IONS  |   ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX 
1okw:A    (PRO45) to   (GLN287)  CYCLIN A BINDING GROOVE INHIBITOR AC-ARG-ARG-LEU-ASN-(M-CL-PHE)-NH2  |   CELL CYCLE, COMPLEX(KINASE-CYCLIN), CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1okw:C    (PRO45) to   (HIS283)  CYCLIN A BINDING GROOVE INHIBITOR AC-ARG-ARG-LEU-ASN-(M-CL-PHE)-NH2  |   CELL CYCLE, COMPLEX(KINASE-CYCLIN), CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1okv:C    (PRO45) to   (GLN287)  CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ILE-PHE-NH2  |   KINASE-CYCLIN COMPLEX, CYCLIN A, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, PEPTIDOMIMETICS, CELL CYCLE, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1ol1:A    (PRO45) to   (GLN287)  CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CELL CYCLE, KINASE-CYCLIN COMPLEX, CYCLIN A, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, PEPTIDOMIMETICS 
1ol1:C    (PRO45) to   (GLN287)  CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CELL CYCLE, KINASE-CYCLIN COMPLEX, CYCLIN A, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, PEPTIDOMIMETICS 
1ol2:A    (PRO45) to   (GLN287)  CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ASN-(P-F-PHE)-NH2  |   CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, KINASE 
2pvy:C   (THR524) to   (THR764)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC K659N MUTATION RESPONSIBLE FOR AN UNCLASSIFIED CRANIOSYNOSTOSIS SYNDROME.  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
4i5m:A    (LYS91) to   (GLN307)  SELECTIVE & BRAIN-PERMEABLE POLO-LIKE KINASE-2 (PLK-2) INHIBITORS THAT REDUCE -SYNUCLEIN PHOSPHORYLATION IN RAT BRAIN  |   POLO-LIKE KINASE-2 (PLK-2), SYNUCLEIN, PARKINSON'S DISEASE, KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2pwl:A   (LYS526) to   (THR764)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC N549H MUTATION RESPONSIBLE FOR CROUZON SYNDROME.  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2pwl:B   (THR524) to   (THR765)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC N549H MUTATION RESPONSIBLE FOR CROUZON SYNDROME.  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
4i6f:A   (HIS122) to   (HIS331)  SELECTIVE & BRAIN-PERMEABLE POLO-LIKE KINASE-2 (PLK-2) INHIBITORS THAT REDUCE -SYNUCLEIN PHOSPHORYLATION IN RAT BRAIN  |   POLO-LIKE KINASE-2 (PLK-2), SYNUCLEIN, PARKINSONS DISEASE, KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2c4g:A    (PRO45) to   (HIS283)  STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514  |   PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, NUCLEOTIDE-BINDING, POLYMORPHISM 
2c4g:C    (PRO45) to   (HIS283)  STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514  |   PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, NUCLEOTIDE-BINDING, POLYMORPHISM 
2py3:A   (THR524) to   (THR765)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC E565G MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2py3:B   (GLU525) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC E565G MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2c5o:C    (PRO45) to   (GLN287)  DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND  INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN  |   DIFFERENTIAL INHIBITION, TRANSFERASE, CDK2, ATP-BINDING, CELL CYCLE, CELL DIVISION, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN, KINASE, MITOSIS, CYCLIN 
2c5n:A    (PRO45) to   (GLN287)  DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND  INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN  |   DIFFERENTIAL INHIBITION, TRANSFERASE, CDK2, ATP-BINDING, CELL CYCLE, CELL DIVISION, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN, KINASE, MITOSIS, CYCLIN 
2pzp:A   (THR524) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC K526E MUTATION RESPONSIBLE FOR CROUZON SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2pzp:B   (GLU526) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC K526E MUTATION RESPONSIBLE FOR CROUZON SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2pzr:A   (THR524) to   (THR765)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC K641R MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2c5v:A    (PRO45) to   (GLN287)  DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN  |   ATP-BINDING, CELL CYCLE, CELL DIVISION, COMPLEX (KINASE/CYCLIN), CYCIN A, CYCLIN, DRUG DESIGN, LIGAND EXCHANGE, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, COMPLEX (TRANSFERASE/CYCLIN) 
2c5v:C    (PRO45) to   (GLN287)  DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN  |   ATP-BINDING, CELL CYCLE, CELL DIVISION, COMPLEX (KINASE/CYCLIN), CYCIN A, CYCLIN, DRUG DESIGN, LIGAND EXCHANGE, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, COMPLEX (TRANSFERASE/CYCLIN) 
2c5x:A    (PRO45) to   (GLN287)  DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN  |   TRANSFERASE/INHIBITOR, INHIBITION, ACTIVE, INACTIVE, CDK2, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ATP-BINDING, COMPLEX (TRANSFERASE/INHIBITOR) 
2pzy:A    (PRO99) to   (HIS322)  STRUCTURE OF MK2 COMPLEXED WITH COMPOUND 76  |   MK2, PROTEIN KINASE, TRANSFERASE 
2pzy:B    (PRO99) to   (LYS307)  STRUCTURE OF MK2 COMPLEXED WITH COMPOUND 76  |   MK2, PROTEIN KINASE, TRANSFERASE 
1cmk:E    (GLN84) to   (HIS294)  CRYSTAL STRUCTURES OF THE MYRISTYLATED CATALYTIC SUBUNIT OF CAMP- DEPENDENT PROTEIN KINASE REVEAL OPEN AND CLOSED CONFORMATIONS  |   PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2q0b:B   (THR524) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC E565A MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2c6t:A    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR  |   SERINE/THREONINE PROTEIN KINASE, CDK2, ATP-BINDING, CELL CYCLE, MITOSIS, PHOSPHORYLATION, TRIAZOLOPYRIMIDINE INHIBITOR, COMPLEX (TRANSFERASE/CYCLIN2) 
2c6t:C    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR  |   SERINE/THREONINE PROTEIN KINASE, CDK2, ATP-BINDING, CELL CYCLE, MITOSIS, PHOSPHORYLATION, TRIAZOLOPYRIMIDINE INHIBITOR, COMPLEX (TRANSFERASE/CYCLIN2) 
4idt:B   (ARG437) to   (GLY659)  CRYSTAL STRUCTURE OF NIK WITH 11-BROMO-5,6,7,8-TETRAHYDROPYRIMIDO[4', 5':3,4]CYCLOHEPTA[1,2-B]INDOL-2-AMINE (T28)  |   NIK, NUCLEAR FACTOR (NF)-KB, P100 PROCESSING, 2-AMINOPYRIMIDINE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4idv:A   (ALA438) to   (GLY659)  CRYSTAL STRUCTURE OF NIK WITH COMPOUND 4-{3-[2-AMINO-5-(2- METHOXYETHOXY)PYRIMIDIN-4-YL]-1H-INDOL-5-YL}-2-METHYLBUT-3-YN-2-OL (13V)  |   NIK, NUCLEAR FACTOR (NF)-KB, P100 PROCESSING, 2-AMINOPYRIMIDINE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4idv:B   (ALA438) to   (GLY659)  CRYSTAL STRUCTURE OF NIK WITH COMPOUND 4-{3-[2-AMINO-5-(2- METHOXYETHOXY)PYRIMIDIN-4-YL]-1H-INDOL-5-YL}-2-METHYLBUT-3-YN-2-OL (13V)  |   NIK, NUCLEAR FACTOR (NF)-KB, P100 PROCESSING, 2-AMINOPYRIMIDINE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4idv:D   (ALA438) to   (GLY659)  CRYSTAL STRUCTURE OF NIK WITH COMPOUND 4-{3-[2-AMINO-5-(2- METHOXYETHOXY)PYRIMIDIN-4-YL]-1H-INDOL-5-YL}-2-METHYLBUT-3-YN-2-OL (13V)  |   NIK, NUCLEAR FACTOR (NF)-KB, P100 PROCESSING, 2-AMINOPYRIMIDINE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3fxw:A    (SER78) to   (HIS301)  HIGH RESOLUTION CRYSTAL STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE- ACTIVATED PROTEIN KINASE 3/INHIBITOR 2 COMPLEX  |   KINASE DOMAIN FOLD, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
2cci:C    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF PHOSPHO-CDK2 CYCLIN A IN COMPLEX WITH A PEPTIDE CONTAINING BOTH THE SUBSTRATE AND RECRUITMENT SITES OF CDC6  |   COMPLEX (TRANSFERASE/CELL DIVISION), PROTEIN KINASES, CELL CYCLE, RECRUITMENT, SUBSTRATE RECOGNITION, ATP-BINDING, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, CYCLIN, DNA REPLICATION, NUCLEAR PROTEIN, COMPLEX 
1p5e:A    (PRO45) to   (GLN287)  THE STRUCURE OF PHOSPHO-CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR 4,5,6,7-TETRABROMOBENZOTRIAZOLE (TBS)  |   KINASE INHIBITOR, CDK2, TBS, CELL CYCLE 
1p5e:C    (PRO45) to   (GLN287)  THE STRUCURE OF PHOSPHO-CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR 4,5,6,7-TETRABROMOBENZOTRIAZOLE (TBS)  |   KINASE INHIBITOR, CDK2, TBS, CELL CYCLE 
2clq:A   (GLN720) to   (LYS939)  STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 5  |   TRANSFERASE, METAL-BINDING, APOPTOSIS 
2clq:B   (GLN720) to   (LYS939)  STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 5  |   TRANSFERASE, METAL-BINDING, APOPTOSIS 
2qok:A   (THR660) to   (ASN884)  HUMAN EPHA3 KINASE AND JUXTAMEMBRANE REGION, Y596F:Y602F:S768A TRIPLE MUTANT  |   RECEPTOR TYROSINE KINASE, JUXTAMEMBRANE SEGMENT, STRUCTURAL GENOMICS, MUTANT, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP- BINDING, NUCLEOTIDE-BINDING, PHOSPHORYLATION, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
1pkd:C    (PRO45) to   (GLN287)  THE CRYSTAL STRUCTURE OF UCN-01 IN COMPLEX WITH PHOSPHO- CDK2/CYCLIN A  |   PROTEIN KINASE-DRUG COMPLEX, TRANSFERASE/CELL CYCLE COMPLEX 
4j53:A    (LYS91) to   (ASP302)  CRYSTAL STRUCTURE OF PLK1 IN COMPLEX WITH TAK-960  |   PROTEIN SERINE/THREONINE KINASE, MITOSIS, ONCOGENESIS, REGULATION OF CELL CYCLE, KINASE DOMAIN, ATP BINDING, NUCLEAR, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4y72:A    (PRO45) to   (ASN288)  HUMAN CDK1/CYCLINB1/CKS2 WITH INHIBITOR  |   CDK1, CYCLINB1, CKS2, INHIBITOR, TRANSFERASE 
4j99:A   (THR524) to   (THR764)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE GAIN-OF-FUNCTION K659T MUTATION.  |   BILOBATE PROTEIN KINASE FOLD, RECEPTOR TYROSINE KINASE, ATP BINDING, TRANSFERASE 
4j99:D   (THR524) to   (THR764)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE GAIN-OF-FUNCTION K659T MUTATION.  |   BILOBATE PROTEIN KINASE FOLD, RECEPTOR TYROSINE KINASE, ATP BINDING, TRANSFERASE 
4y85:A   (LYS175) to   (HIS385)  CRYSTAL STRUCTURE OF COT KINASE DOMAIN IN COMPLEX WITH 5-(5-(1H-INDOL- 3-YL)-1H-PYRROLO[2,3-B]PYRIDIN-3-YL)-1,3,4-OXADIAZOL-2-AMINE  |   COT, TPL-2, MAP3K8, KINASE, INHIBITOR, COMPLEX, TRANSFERASE 
4y85:B   (LYS175) to   (HIS385)  CRYSTAL STRUCTURE OF COT KINASE DOMAIN IN COMPLEX WITH 5-(5-(1H-INDOL- 3-YL)-1H-PYRROLO[2,3-B]PYRIDIN-3-YL)-1,3,4-OXADIAZOL-2-AMINE  |   COT, TPL-2, MAP3K8, KINASE, INHIBITOR, COMPLEX, TRANSFERASE 
4y85:C   (LYS175) to   (HIS385)  CRYSTAL STRUCTURE OF COT KINASE DOMAIN IN COMPLEX WITH 5-(5-(1H-INDOL- 3-YL)-1H-PYRROLO[2,3-B]PYRIDIN-3-YL)-1,3,4-OXADIAZOL-2-AMINE  |   COT, TPL-2, MAP3K8, KINASE, INHIBITOR, COMPLEX, TRANSFERASE 
1q41:B    (ASN95) to   (LEU320)  GSK-3 BETA COMPLEXED WITH INDIRUBIN-3'-MONOXIME  |   KINASE, INSULIN PATHWAY, INDIRUBIN-3'-MONOXIME, TRANSFERASE 
4jbq:A   (VAL174) to   (HIS380)  NOVEL AURORA KINASE INHIBITORS REVEAL MECHANISMS OF HURP IN NUCLEATION OF CENTROSOMAL AND KINETOCHORE MICROTUBULES  |   AURORA KINASE INHIBITORS, HURP, MITOTIC SPINDLE, TRANSFERASE 
3gu4:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPKQ23V-AMPPNP  |   GLYCINE-RICH LOOP MUTANT, KINASE-AMPPNP COMPLEX, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN- BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gu5:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPKQ23V-AMPPNP-MG2+  |   GLYCINE-RICH LOOP MUTANT, KINASE-AMPPNP-MG2+ COMPLEX, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gu6:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPKQ23V-ADP  |   GLYCINE-RICH LOOP MUTANT, KINASE-ADP COMPLEX, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN- BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gu7:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPKQ23V-ADP-MG2+  |   GLYCINE-RICH LOOP MUTANT, KINASE-ADP-MG2+ COMPLEX, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3gub:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPKL93G COMPLEXED WITH N6-(2- PHENYLETHYL)ADENOSINE  |   GATEKEEPER MUTANT, KINASE-ADP COMPLEX, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3tnw:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH CAN508  |   CYCLIN DEPENDENT KINASE, KINASE CYCLIN, PHOSPHOTRANSFERASE, CYCLIN A, PHOSPHORYLATION AT CDK2 THREONINE 160, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4yc3:A    (PRO45) to   (ASN288)  CDK1/CYCLINB1/CKS2 APO  |   CDK1, CYCLIN B1, CKS2, CELL CYCLE 
2rku:A    (PRO92) to   (ASP302)  STRUCTURE OF PLK1 IN COMPLEX WITH BI2536  |   STRUCTURE OF PLK1, SELECTIVITY RESIDUES, KINASE, POLO-LIKE KINASE, STRUCTURE BASED DRUG DESIGN, ATP-BINDING, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1qmz:A    (PRO45) to   (GLN287)  PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX  |   CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, SUBSTRATE COMPLEX 
1qmz:C    (PRO45) to   (GLN287)  PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX  |   CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, SUBSTRATE COMPLEX 
2uue:A    (PRO45) to   (HIS283)  REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS  |   POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING 
2uue:C    (PRO45) to   (GLN287)  REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS  |   POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING 
3ha6:A   (VAL174) to   (ASN386)  CRYSTAL STRUCTURE OF AURORA A IN COMPLEX WITH TPX2 AND COMPOUND 10  |   AURORA A, SERINE/THREONINE-PROTEIN KINASE, COFACTOR, TPX2, INHIBITOR, PHOSPHORYLATION, ATP-BINDING, CELL CYCLE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, TRANSFERASE, NUCLEUS, KINASE 
1f5q:A    (SER46) to   (GLN287)  CRYSTAL STRUCTURE OF MURINE GAMMA HERPESVIRUS CYCLIN COMPLEXED TO HUMAN CYCLIN DEPENDENT KINASE 2  |   HERPESVIRAL CYCLIN, CYCLIN DEPENDENT KINASE. PROTEIN/PROTEIN COMPLEX, TRANSFERASE 
1f5q:C    (SER46) to   (GLN287)  CRYSTAL STRUCTURE OF MURINE GAMMA HERPESVIRUS CYCLIN COMPLEXED TO HUMAN CYCLIN DEPENDENT KINASE 2  |   HERPESVIRAL CYCLIN, CYCLIN DEPENDENT KINASE. PROTEIN/PROTEIN COMPLEX, TRANSFERASE 
2uw6:A    (ILE85) to   (HIS294)  STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH  (S)-2-(4- CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE  |   TRANSFERASE/INHIBITOR, CAMP, KINASE, MYRISTATE, TRANSFERASE, LIPOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, NUCLEOTIDE-BINDING, PROTEIN KINASE INHIBITOR, ATP-BINDING, NUCLEAR PROTEIN, PHOSPHORYLATION, TRANSFERASE/INHIBITOR COMPLEX 
2uzd:A    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF HUMAN CDK2 COMPLEXED WITH A THIAZOLIDINONE INHIBITOR  |   TRANSFERASE, ATP-BINDING, PHOSPHORYLATION, CDK2, KINASE, CYCLIN, MITOSIS, CELL CYCLE, CELL DIVISION, NUCLEOTIDE- BINDING, SERINE/THREONINE-PROTEIN KINASE, THIAZOLIDINONE LIGAND 
2uze:A    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF HUMAN CDK2 COMPLEXED WITH A THIAZOLIDINONE INHIBITOR  |   TRANSFERASE, ATP-BINDING, PHOSPHORYLATION, CDK2, KINASE, CYCLIN, MITOSIS, CELL CYCLE, CELL DIVISION, NUCLEOTIDE- BINDING, SERINE/THREONINE-PROTEIN KINASE, THIAZOLIDINONE LIGAND 
2uze:C    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF HUMAN CDK2 COMPLEXED WITH A THIAZOLIDINONE INHIBITOR  |   TRANSFERASE, ATP-BINDING, PHOSPHORYLATION, CDK2, KINASE, CYCLIN, MITOSIS, CELL CYCLE, CELL DIVISION, NUCLEOTIDE- BINDING, SERINE/THREONINE-PROTEIN KINASE, THIAZOLIDINONE LIGAND 
2uzl:A    (PRO45) to   (HIS283)  CRYSTAL STRUCTURE OF HUMAN CDK2 COMPLEXED WITH A THIAZOLIDINONE INHIBITOR  |   TRANSFERASE, ATP-BINDING, PHOSPHORYLATION, CDK2, KINASE, CYCLIN, MITOSIS, CELL CYCLE, CELL DIVISION, NUCLEOTIDE- BINDING, SERINE/THREONINE-PROTEIN KINASE, THIAZOLIDINONE LIGAND 
2uzt:A    (ILE85) to   (HIS294)  PKA STRUCTURES OF AKT, INDAZOLE-PYRIDINE INHIBITORS  |   CAMP, KINASE, MYRISTATE, TRANSFERASE, LIPOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, PROTEIN KINASE A, NUCLEOTIDE-BINDING, PROTEIN KINASE INHIBITOR, ATP- BINDING, AKT INHIBITORS, NUCLEAR PROTEIN 
2v22:C    (PRO45) to   (GLN287)  REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS  |   POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING 
1fin:A    (PRO45) to   (GLN287)  CYCLIN A-CYCLIN-DEPENDENT KINASE 2 COMPLEX  |   COMPLEX (TRANSFERASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION 
1fot:A   (VAL129) to   (HIS338)  STRUCTURE OF THE UNLIGANDED CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT FROM SACCHAROMYCES CEREVISIAE  |   CAMP-DEPENDENT PROTEIN KINASE, OPEN CONFORMATION, PROTEIN KINASE, TRANSFERASE 
1rek:A    (GLN84) to   (HIS294)  CRYSTAL STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH BALANOL ANALOG 8  |   PROTEIN KINASE, NATURAL PRODUCT INHIBITOR, LIGAND BINDING, SPECIFITY DETERMINANTS, CONFORMATIONAL MALLEABILITY, TRANSFERASE 
3uiu:A   (LYS304) to   (TRP539)  CRYSTAL STRUCTURE OF APO-PKR KINASE DOMAIN  |   KINASE DOMAIN, TRANSFERASE 
3uiu:B   (LYS304) to   (TRP539)  CRYSTAL STRUCTURE OF APO-PKR KINASE DOMAIN  |   KINASE DOMAIN, TRANSFERASE 
4yu2:A   (LYS194) to   (LYS393)  CRYSTAL STRUCTURE OF DYRK1A WITH HARMINE-DERIVATIZED ANNH-75 INHIBITOR  |   TRANSFERASE, DYRK1A, DOWN SYNDROME, INHIBITOR, HARMINE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
4yu2:B   (LYS194) to   (LYS393)  CRYSTAL STRUCTURE OF DYRK1A WITH HARMINE-DERIVATIZED ANNH-75 INHIBITOR  |   TRANSFERASE, DYRK1A, DOWN SYNDROME, INHIBITOR, HARMINE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
1fvv:A    (PRO45) to   (GLN287)  THE STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH AN OXINDOLE INHIBITOR  |   CYCLIN-DEPENDENT KINASE, CYCLIN A, TRANSFERASE, CELL CYCLE 
2vgo:A   (VAL134) to   (HIS340)  CRYSTAL STRUCTURE OF AURORA B KINASE IN COMPLEX WITH REVERSINE INHIBITOR  |   NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, TRANSFERASE, COILED COIL, CELL DIVISION, KINASE, CANCER, INCENP, NUCLEUS, MITOSIS, AURORA B, METAL-BINDING, AMINOTHIAZOLE, PHOSPHORYLATION, MAGNESIUM, CELL CYCLE, CENTROMERE, MICROTUBULE 
2vrx:A   (VAL134) to   (HIS340)  STRUCTURE OF AURORA B KINASE IN COMPLEX WITH ZM447439  |   SERINE/THREONINE-PROTEIN KINASE, KINASE, NUCLEUS, MITOSIS, MAGNESIUM, CELL CYCLE/TRANSFERASE, CENTROMERE, MICROTUBULE, ATP-BINDING, TRANSFERASE, ANTI-CANCER DRUG TARGET, PHOSPHOPROTEIN, PROTEIN KINASE, NUCLEOTIDE-BINDING, COILED COIL, CELL DIVISION, METAL-BINDING 
2g9x:C    (PRO45) to   (GLN287)  STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR NU6271  |   TRANSFERASE, SERINE/THREONINE PROTEIN KINASE, ATP-BINDING, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX 
4zjj:B   (GLU310) to   (LEU502)  PAK1 IN COMPLEX WITH (S)-N-(TERT-BUTYL)-3-((2-CHLORO-5-ETHYL-8-FLUORO- DIBENZODIAZEPIN-11-YL)AMINO)PYRROLIDINE-1-CARBOXAMIDE  |   PAK1, INHIBITOR, KINASE, ALLOSTERIC, TRANSFERASE 
1h1p:A    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU2058  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1h1q:C    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6094  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1h24:C    (PRO45) to   (GLN287)  CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F  |   TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
1h26:C    (PRO45) to   (GLN287)  CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P53  |   CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY 
1h27:C    (PRO45) to   (GLN287)  CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27  |   CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3idb:A    (ILE85) to   (HIS294)  CRYSTAL STRUCTURE OF (108-268)RIIB:C HOLOENZYME OF CAMP- DEPENDENT PROTEIN KINASE  |   PKA, CAMP, SPR, AFFINITY, KINASE, LINKER, CRYSTAL STRUCTURE, RII HOLOENZYME, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ACETYLATION, CAMP-BINDING 
1h4l:A    (PRO45) to   (SER287)  STRUCTURE AND REGULATION OF THE CDK5-P25(NCK5A) COMPLEX  |   KINASE/KINASE ACTIVATOR, COMPLEX(CYCLINS/CDK), CYCLINS, CYCLIN-DEPENDENT KINASES, CDK5, P35, P25, TRANSFERASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, PHOSPHORYLATION 
2gsf:A   (THR660) to   (ASN884)  THE HUMAN EPHA3 RECEPTOR TYROSINE KINASE AND JUXTAMEMBRANE REGION  |   ATP-BINDING, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, RECEPTOR, SIGNAL, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
4ztq:A   (VAL174) to   (HIS380)  HUMAN AURORA A CATALYTIC DOMAIN BOUND TO FK932  |   AURORA, KINASE, INHIBITOR, TRANSFERASE 
3ion:A   (LYS123) to   (HIS339)  PDK1 IN COMPLEX WITH COMPOUND 8H  |   PDK-1, INHIBITOR, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
2wev:C    (PRO45) to   (GLN287)  TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN  |   CDK2, KINASE, CYCLIN, ACTIVE, NUCLEUS, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, CYTOPLASM, INHIBITION, CELL CYCLE, ATP-BINDING, CELL DIVISION, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, TRANSFERASE, POLYMORPHISM, BETA-PEPTIDE, CYCLIN GROOVE 
2wfy:C    (PRO45) to   (GLN287)  TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN  |   CDK2, KINASE, CYCLIN, ACTIVE, NUCLEUS, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, CYTOPLASM, INHIBITION, CELL CYCLE, ATP-BINDING, CELL DIVISION, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, TRANSFERASE, POLYMORPHISM, BETA-PEPTIDE, CYCLIN GROOVE 
2whb:C    (PRO45) to   (GLN287)  TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN  |   CDK2, KINASE, CYCLIN, ACTIVE, NUCLEUS, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, CYTOPLASM, INHIBITION, CELL CYCLE, ATP-BINDING, CELL DIVISION, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, TRANSFERASE, POLYMORPHISM, BETA-PEPTIDE, CYCLIN GROOVE 
2wmb:C    (PRO45) to   (GLN287)  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 
3vw6:A   (PRO721) to   (LYS939)  CRYSTAL STRUCTURE OF HUMAN APOPTOSIS SIGNAL-REGULATING KINASE 1 (ASK1) WITH IMIDAZOPYRIDINE INHIBITOR  |   TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1ig1:A    (ARG58) to   (HIS272)  1.8A X-RAY STRUCTURE OF TERNARY COMPLEX OF A CATALYTIC DOMAIN OF DEATH-ASSOCIATED PROTEIN KINASE WITH ATP ANALOGUE AND MN.  |   TRANSFERASE 
2i40:A    (PRO45) to   (GLN287)  CDK2/CYCLIN A COMPLEXED WITH A THIOPHENE CARBOXAMIDE INHIBITOR  |   CDK2, CYCLIN, KINASE, TRANSFERASE-CELL CYCLE COMPLEX 
2i40:C    (PRO45) to   (GLN287)  CDK2/CYCLIN A COMPLEXED WITH A THIOPHENE CARBOXAMIDE INHIBITOR  |   CDK2, CYCLIN, KINASE, TRANSFERASE-CELL CYCLE COMPLEX 
2wxv:A    (PRO45) to   (HIS283)  STRUCTURE OF CDK2-CYCLIN A WITH A PYRAZOLO(4,3-H) QUINAZOLINE-3-CARBOXAMIDE INHIBITOR  |   NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, TRANSFERASE, KINASE, CYCLIN 
2wxv:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2-CYCLIN A WITH A PYRAZOLO(4,3-H) QUINAZOLINE-3-CARBOXAMIDE INHIBITOR  |   NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, TRANSFERASE, KINASE, CYCLIN 
1urc:A    (PRO45) to   (HIS283)  CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY  |   TRANSFERASE-INHIBITOR COMPLEX, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, PEPTIDOMIMETICS 
1v0o:A    (SER45) to   (HIS281)  STRUCTURE OF P. FALCIPARUM PFPK5-INDIRUBIN-5-SULPHONATE LIGAND COMPLEX  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, PHOSPHORYLATION, CDK 
2itn:A   (PRO753) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN G719S MUTATION 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, G719S, KINASE, AMP-PNP, MEMBRANE, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2ito:A   (SER752) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN G719S MUTATION IN COMPLEX WITH IRESSA  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, IRESSA, EGFR, G719S, ZD1839, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2itt:A   (PRO753) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN L858R MUTATION IN COMPLEX WITH AEE788  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, POLYMORPHISM, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, ALTERNATIVE SPLICING, AEE788, EGFR, L858R, KINASE, MEMBRANE, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2itu:A   (SER752) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN L858R MUTATION IN COMPLEX WITH AFN941  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, POLYMORPHISM, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, ALTERNATIVE SPLICING, AFN941, EGFR, L858R, STAUROSPORINE, MEMBRANE TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2itv:A   (PRO753) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN L858R MUTATION 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, L858R, KINASE, AMP-PNP, MEMBRANE, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2ity:A   (SER752) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN IN COMPLEX WITH IRESSA  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, IRESSA, EGFR, ZD1839, MEMBRANE TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2itz:A   (PRO753) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN L858R MUTATION IN COMPLEX WITH IRESSA  |   RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, POLYMORPHISM, GLYCOPROTEIN, ANTI-ONCOGENE, NUCLEOTIDE- BINDING, ALTERNATIVE SPLICING, IRESSA, EGFR, L858R, GEFITINIB, ZD1839, MEMBRANE, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR 
2ivs:B   (PRO766) to  (ARG1012)  CRYSTAL STRUCTURE OF NON-PHOSPHORYLATED RET TYROSINE KINASE DOMAIN  |   NUCLEOTIDE-BINDING, HIRSCHSPRUNG DISEASE, PHOSPHORYLATION, DISEASE MUTATION, PHOSPHOTRANSFERASE, TYROSINE-PROTEIN KINASE, CHROMOSOMAL TRANSLOCATION, POLYMORPHISM, GDNF RECEPTOR, TRANSMEMBRANE, PROTO-ONCOGENE, TYROSINE KINASE, RET, KINASE, MEMBRANE, ATP-BINDING, TRANSFERASE 
2iw6:C    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A COMPLEXED WITH A BISANILINOPYRIMIDINE INHIBITOR  |   PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING 
2iw8:A    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A F82H-L83V- H84D MUTANT WITH AN O6-CYCLOHEXYLMETHYLGUANINE INHIBITOR  |   PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE 
2j0l:A   (LEU469) to   (GLN686)  CRYSTAL STRUCTURE OF A THE ACTIVE CONFORMATION OF THE KINASE DOMAIN OF FOCAL ADHESION KINASE WITH A PHOSPHORYLATED ACTIVATION LOOP.  |   FOCAL ADHESION, CELL MIGRATION, PHOSPHORYLATION, FERM, KINASE, TRANSFERASE, ATP-BINDING, INTEGRIN SIGNALING, NUCLEOTIDE-BINDING, TYROSINE-PROTEIN KINASE 
1jkl:A    (SER57) to   (HIS272)  1.6A X-RAY STRUCTURE OF BINARY COMPLEX OF A CATALYTIC DOMAIN OF DEATH-ASSOCIATED PROTEIN KINASE WITH ATP ANALOGUE  |   TRANSFERASE 
5aut:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH ANS.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERIN/THREONINE PROTEIN KINASE, COMPLEX 
5auv:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH APIGENIN.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5auw:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH QUERCETIN.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5aux:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH KAEMPFEROL.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5auy:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH MORIN.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5auz:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN COMPLEX WITH GENISTEIN.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5av1:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 IN THE PRESENCE OF BROMIDE IONS.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5av3:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1-KAEMPFEROL COMPLEX IN THE PRESENCE OF IODIDE IONS.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
5av4:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1-GENISTEIN COMPLEX IN THE PRESENCE OF BROMIDE IONS.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
2j5f:A   (PRO753) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN IN COMPLEX WITH AN IRREVERSIBLE INHIBITOR 34-JAB  |   CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, IRREVERSIBLE INHIBITOR, TYROSINE-PROTEIN KINASE, EGFR, KINASE, 34-JAB, MEMBRANE, RECEPTOR, WILD-TYPE, EPIDERMAL GROWTH FACTOR, ANTI-ONCOGENE, TRANSMEMBRANE, NUCLEOTIDE- BINDING, ALTERNATIVE SPLICING, UBL CONJUGATION, PHOSPHORYLATION, DISEASE MUTATION, GLYCOPROTEIN 
2j6m:A   (SER752) to   (ARG973)  CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN IN COMPLEX WITH AEE788  |   CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, NUCLEOTIDE-BINDING, ALTERNATIVE SPLICING, TYROSINE-PROTEIN KINASE, EPIDERMAL GROWTH FACTOR, UBL CONJUGATION, PHOSPHORYLATION, DISEASE MUTATION, GLYCOPROTEIN, ANTI- ONCOGENE, TRANSMEMBRANE, EGFR, KINASE, AEE788, MEMBRANE, RECEPTOR, WILD-TYPE 
1jst:A    (PRO45) to   (GLN287)  PHOSPHORYLATED CYCLIN-DEPENDENT KINASE-2 BOUND TO CYCLIN A  |   COMPLEX (PROTEIN KINASE-CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, COMPLEX (PROTEIN KINASE-CYCLIN) COMPLEX 
1jst:C    (PRO45) to   (GLN287)  PHOSPHORYLATED CYCLIN-DEPENDENT KINASE-2 BOUND TO CYCLIN A  |   COMPLEX (PROTEIN KINASE-CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, COMPLEX (PROTEIN KINASE-CYCLIN) COMPLEX 
1vyw:A    (PRO45) to   (HIS283)  STRUCTURE OF CDK2/CYCLIN A WITH PNU-292137  |   TRANSFERASE/COMPLEX, PROTEIN KINASE/COMPLEX, PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN 
1vyw:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2/CYCLIN A WITH PNU-292137  |   TRANSFERASE/COMPLEX, PROTEIN KINASE/COMPLEX, PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN 
2jbp:C    (PRO99) to   (LYS307)  PROTEIN KINASE MK2 IN COMPLEX WITH AN INHIBITOR (CRYSTAL FORM-2, CO-CRYSTALLIZATION)  |   SER-THR KINASE, MAPKAP KINASE 2, PHOSPHORYLATION, SMALL MOLECULE INHIBITOR, MK2, KINASE, ATP SITE, TRANSFERASE, ATP- BINDING, SERINE/THREONINE-PROTEIN KINASE, CO- CRYSTALLIZATION, NUCLEOTIDE-BINDING 
2jbp:D    (PRO99) to   (HIS322)  PROTEIN KINASE MK2 IN COMPLEX WITH AN INHIBITOR (CRYSTAL FORM-2, CO-CRYSTALLIZATION)  |   SER-THR KINASE, MAPKAP KINASE 2, PHOSPHORYLATION, SMALL MOLECULE INHIBITOR, MK2, KINASE, ATP SITE, TRANSFERASE, ATP- BINDING, SERINE/THREONINE-PROTEIN KINASE, CO- CRYSTALLIZATION, NUCLEOTIDE-BINDING 
3zbf:A  (ASP1988) to  (SER2229)  STRUCTURE OF HUMAN ROS1 KINASE DOMAIN IN COMPLEX WITH CRIZOTINIB  |   TRANSFERASE, TYROSINE KINASE 
3zfx:A   (SER658) to   (ASN884)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:B   (SER658) to   (ILE882)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:D   (SER658) to   (ILE882)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:E   (SER658) to   (ILE882)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:F   (SER658) to   (ASN884)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:G   (SER667) to   (ASN884)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:H   (SER658) to   (ASN884)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
3zfx:I   (SER658) to   (ASN884)  CRYSTAL STRUCTURE OF EPHB1  |   TRANSFERASE 
1w98:A    (PRO45) to   (HIS283)  THE STRUCTURAL BASIS OF CDK2 ACTIVATION BY CYCLIN E  |   CELL CYCLE, TRANSFERASE 
5bvf:A    (HIS59) to   (SER264)  TETRAHYDROPYRROLO-DIAZEPENONES AS INHIBITORS OF ERK2 KINASE  |   INHIBITOR, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2ya9:B    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF THE AUTOINHIBITED FORM OF MOUSE DAPK2  |   TRANSFERASE, APOPTOSIS 
1wzy:A    (GLN62) to   (SER266)  CRYSTAL STRUCTURE OF HUMAN ERK2 COMPLEXED WITH A PYRAZOLOPYRIDAZINE DERIVATIVE  |   ERK2, INHIBITOR, KINASE, TRANSFERASE 
4nst:C   (PRO768) to  (SER1017)  CRYSTAL STRUCTURE OF HUMAN CDK12/CYCLIN K IN COMPLEX WITH ADP-ALUMINUM FLUORIDE  |   TRANSCRIPTION, RNA POLYMERASE II, PHOSPHORYLATION, TRANSFERASE- TRANSCRIPTION COMPLEX 
3zxt:B    (SER57) to   (HIS272)  DIMERIC STRUCTURE OF DAPK-1 CATALYTIC DOMAIN IN COMPLEX WITH AMPPCP-MG  |   APOPTOSIS, TRANSFERASE, ATP BINDING 
4o0r:A   (LYS308) to   (HIS518)  BACK POCKET FLEXIBILITY PROVIDES GROUP-II PAK SELECTIVITY FOR TYPE 1 KINASE INHIBITORS  |   PAK1, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5cas:A   (PRO753) to   (ARG973)  EGFR KINASE DOMAIN MUTANT "TMLR" WITH COMPOUND 41A  |   PROTEIN KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5cau:A   (LYS754) to   (ARG973)  EGFR KINASE DOMAIN MUTANT "TMLR" WITH COMPOUND 41B  |   PROTEIN KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4o2p:B   (SER303) to   (TYR519)  KINASE DOMAIN OF CSRC IN COMPLEX WITH A SUBSTITUTED PYRAZOLOPYRIMIDINE  |   PYRAZOLO-PYRIMIDINE LIGAND, TYPE I, DFG-IN, TYROSINE PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1xh8:A    (GLN84) to   (HIS294)  CRYSTAL STRUCTURES OF PROTEIN KINASE B SELECTIVE INHIBITORS IN COMPLEX WITH PROTEIN KINASE A AND MUTANTS  |   PKA, KINASE-INHIBITOR-COMPLEX, SERINE/THREONINE-PROTEIN KINASE, BALANOL DERIVATIVE, TRANSFERASE/TRANSFERASE INHIBITOR COMPLEX 
1xh9:A    (ILE85) to   (ALA298)  CRYSTAL STRUCTURES OF PROTEIN KINASE B SELECTIVE INHIBITORS IN COMPLEX WITH PROTEIN KINASE A AND MUTANTS  |   PKA, KINASE-INHIBITOR-COMPLEX, SERINE/THREONINE-PROTEIN KINASE, BALANOL DERIVATIVE, TRANSFERASE/TRANSFERASE INHIBITOR COMPLEX 
1xha:A    (GLU84) to   (ALA298)  CRYSTAL STRUCTURES OF PROTEIN KINASE B SELECTIVE INHIBITORS IN COMPLEX WITH PROTEIN KINASE A AND MUTANTS  |   PKA, KINASE-INHIBITOR-COMPLEX, SERINE/THREONINE-PROTEIN KINASE, BALANOL DERIVATIVE, TRANSFERASE/TRANSFERASE INHIBITOR COMPLEX 
4oau:C   (SER398) to   (HIS568)  COMPLETE HUMAN RNASE L IN COMPLEX WITH BIOLOGICAL ACTIVATORS.  |   RNASE L, RNASEL, 2-5A, 2',5'-OLIGOADENYLATE, INTERFERON, KEN, PSEUDOKINASE, KINASE, INFLAMMATION, IRE1, RIDD, REGULATED RNA DECAY, SPLICING CLEAVAGE, HPC1, HEREDITARY PROSTATE CANCER 1, RNASE L KINASE-HOMOLOGY AND KEN DOMAIN-CONTAINING, INNATE IMMUNITY, INTERFERON RESPONSE, ANTIVIRAL RESPONSE, 2-5A (2',5'-LINKED OLIGOADENYLATE)AND RNA, HYDROLASE-RNA COMPLEX 
5ci7:A    (LEU53) to   (ASP279)  STRUCTURE OF ULK1 BOUND TO A SELECTIVE INHIBITOR  |   INHIBITOR, KINASE, AUTOPHAGY, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2z8c:A  (SER1037) to  (LEU1262)  PHOSPHORYLATED INSULIN RECEPTOR TYROSINE KINASE IN COMPLEX WITH (4-{[5-CARBAMOYL-4-(3-METHYLANILINO)PYRIMIDIN-2- YL]AMINO}PHENYL)ACETIC ACID  |   TRANSFERASE, ALTERNATIVE SPLICING, ATP-BINDING, CARBOHYDRATE METABOLISM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DIABETES MELLITUS, DISEASE MUTATION, GLYCOPROTEIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, RECEPTOR, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TRANSDUCER 
4a4o:A    (PRO92) to   (ASP302)  CRYSTAL STRUCTURE OF POLO-LIKE KINASE 1 IN COMPLEX WITH A 2- (2-AMINO-PYRIMIDIN-4-YL)-1,5,6,7-TETRAHYDRO-PYRROLOPYRIDIN- 4-ONE INHIBITOR  |   TRANSFERASE 
3kb7:A    (PRO92) to   (THR306)  CRYSTAL STRUCTURE OF POLO-LIKE KINASE 1 IN COMPLEX WITH A PYRAZOLOQUINAZOLINE INHIBITOR  |   PROTEIN KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
2zm3:B  (MET1054) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND ISOQUINOLINEDIONE INHIBITOR  |   IGFR, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP- BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
2zm3:D  (MET1054) to  (ILE1266)  COMPLEX STRUCTURE OF INSULIN-LIKE GROWTH FACTOR RECEPTOR AND ISOQUINOLINEDIONE INHIBITOR  |   IGFR, PROTEIN-INHIBITOR COMPLEX, TYROSINE KINASE, ATP- BINDING, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3kkv:A    (ILE85) to   (ALA298)  STRUCTURE OF PKA WITH A PROTEIN KINASE B-SELECTIVE INHIBITOR.  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ae6:A    (ILE85) to   (HIS294)  STRUCTURE AND FUNCTION OF THE HUMAN SPERM-SPECIFIC ISOFORM OF PROTEIN KINASE A (PKA) CATALYTIC SUBUNIT CALPHA 2  |   TRANSFERASE 
4pf4:A    (SER57) to   (GLN271)  1.1A X-RAY STRUCTURE OF THE APO CATALYTIC DOMAIN OF DEATH-ASSOCIATED PROTEIN KINASE 1, AA 1-277  |   TRANSFERASE 
5dh3:A    (LEU64) to   (HIS275)  CRYSTAL STRUCTURE OF MST2 IN COMPLEX WITH XMU-MP-1  |   MST2, MST1, HIPPO PATHWAY, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5dn3:A   (GLU175) to   (ASN386)  AURORA A IN COMPLEX WITH ATP AND AA35.  |   AURORA A KINASE, MITOTIC KINASE, PPI, TRANSFERASE 
3l9l:A    (GLN84) to   (ALA298)  CRYSTAL STRUCTURE OF PKA WITH COMPOUND 36  |   PKB, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3l9l:B    (GLN84) to   (ALA298)  CRYSTAL STRUCTURE OF PKA WITH COMPOUND 36  |   PKB, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3l9m:A    (GLN84) to   (ALA298)  CRYSTAL STRUCTURE OF PKAB3 (PKA TRIPLE MUTANT V123A, L173M, Q181K) WITH COMPOUND 18  |   PKB, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3l9m:B    (GLN84) to   (HIS294)  CRYSTAL STRUCTURE OF PKAB3 (PKA TRIPLE MUTANT V123A, L173M, Q181K) WITH COMPOUND 18  |   PKB, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5dpv:A   (VAL174) to   (HIS380)  AURORA A KINASE IN COMPLEX WITH AA35 AND JNJ-7706621 IN SPACE GROUP P6122  |   AURORA A KINASE, MITOTIC KINASE, PPI, TRANSFERASE 
5dyk:A   (GLN582) to   (HIS795)  CRYSTAL STRUCTURE OF PF3D7_1436600  |   TRANSFERASE, KINASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
5dzc:A   (GLN575) to   (GLY792)  CRYSTAL STRUCTURE OF PVX_084705 IN COMPLEX WITH AMP-PNP  |   STRUCTURAL GENOMICS CONSORTIUM (SGC), KINASE, TRANSFERASE 
2a19:B   (ASN302) to   (LYS540)  PKR KINASE DOMAIN- EIF2ALPHA- AMP-PNP COMPLEX.  |   TRANSFERASE, KINASE, PROTEIN BIOSYNTHESIS, PROTEIN SYNTHESIS- TRANSFERASE COMPLEX 
4b6l:A   (PRO101) to   (HIS311)  DISCOVERY OF ORAL POLO-LIKE KINASE (PLK) INHIBITORS WITH ENHANCED SELECTIVITY PROFILE USING RESIDUE TARGETED DRUG DESIGN  |   TRANSFERASE, KINASE INHIBITORS, WATER-MEDIATED H-BOND 
3b2t:A   (THR524) to   (THR765)  STRUCTURE OF PHOSPHOTRANSFERASE  |   PHOSPHOTRANSFERASE, CELL SIGNALING, ALTERNATIVE SPLICING, ATP-BINDING, DISEASE MUTATION, ECTODERMAL DYSPLASIA, GLYCOPROTEIN, HEPARIN-BINDING, IMMUNOGLOBULIN DOMAIN, KINASE, LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, RECEPTOR, SECRETED, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
3b2t:B   (THR524) to   (THR764)  STRUCTURE OF PHOSPHOTRANSFERASE  |   PHOSPHOTRANSFERASE, CELL SIGNALING, ALTERNATIVE SPLICING, ATP-BINDING, DISEASE MUTATION, ECTODERMAL DYSPLASIA, GLYCOPROTEIN, HEPARIN-BINDING, IMMUNOGLOBULIN DOMAIN, KINASE, LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, RECEPTOR, SECRETED, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
4b8m:A   (VAL134) to   (HIS340)  AURORA B KINASE IN COMPLEX WITH VX-680  |   CELL CYCLE, CANCER 
2acx:A   (GLU228) to   (HIS445)  CRYSTAL STRUCTURE OF G PROTEIN COUPLED RECEPTOR KINASE 6 BOUND TO AMPPNP  |   KINASE, G PROTEIN, GRK, G PROTEIN COUPLED RECEPTOR KINASE, GRK6, TRANSFERASE 
2acx:B   (GLU228) to   (HIS445)  CRYSTAL STRUCTURE OF G PROTEIN COUPLED RECEPTOR KINASE 6 BOUND TO AMPPNP  |   KINASE, G PROTEIN, GRK, G PROTEIN COUPLED RECEPTOR KINASE, GRK6, TRANSFERASE 
4bcn:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR  |   TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN 
4bcp:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR  |   TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN 
4qp2:B    (GLN62) to   (HIS310)  CRYSTAL STRUCTURE OF ERKS IN COMPLEX WITH 5-CHLOROBENZO[D]OXAZOL-2- AMINE  |   KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4bf2:A   (GLU724) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
4bf2:B   (GLU724) to   (ASP935)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
4bhn:A   (HIS723) to   (ASP935)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE, STRUCTURE BASED DESIGN 
4bhn:B   (GLN720) to   (ASP935)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE, STRUCTURE BASED DESIGN 
4bic:A   (GLN720) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
4bic:B   (GLN720) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
4bie:A   (GLU724) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE, STRUCTURE BASED DESGIN 
3bht:A    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 3  |   SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN 
3bht:C    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 3  |   SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN 
5f0a:A   (GLN575) to   (GLY792)  CRYSTAL STRUCTURE OF PVX_084705 WITH BOUND 1-TERT-BUTYL-3-(3- CHLOROPHENOXY)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE INHIBITOR  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3mvj:E    (ILE85) to   (ALA298)  HUMAN CYCLIC AMP-DEPENDENT PROTEIN KINASE PKA INHIBITOR COMPLEX  |   KINASE INHIBITOR, TRANSFERASE 
4qyy:A    (GLN60) to   (LEU265)  DISCOVERY OF NOVEL, DUAL MECHANISM ERK INHIBITORS BY AFFINITY SELECTION SCREENING OF AN INACTIVE KINASE STATE  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3my5:A    (PRO45) to   (GLN287)  CDK2/CYCLINA IN COMPLEX WITH DRB  |   CDK, CYCLIN, INHIBITOR, DRB, TRANSFERASE-PROTEIN BINDING-INHIBITOR COMPLEX 
3my5:C    (PRO45) to   (GLN287)  CDK2/CYCLINA IN COMPLEX WITH DRB  |   CDK, CYCLIN, INHIBITOR, DRB, TRANSFERASE-PROTEIN BINDING-INHIBITOR COMPLEX 
5fee:A   (PRO753) to   (ARG973)  EGFR KINASE DOMAIN T790M MUTANT IN COMPLEX WITH A COVALENT AMINOBENZIMIDAZOLE INHIBITOR.  |   KINASE, INHIBITOR, COVALENTLY BOUND, T790M, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5feq:A   (SER752) to   (ARG973)  EGFR KINASE DOMAIN IN COMPLEX WITH A COVALENT AMINOBENZIMIDAZOLE  |   KINASE, INHIBITOR, COVALENTLY BOUND, T790M, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4r5s:A   (SER752) to   (ALA972)  CRYSTAL STRUCTURE OF EGFR 696-1022 L858R IN COMPLEX WITH FIIN-3  |   EGFR, L858R, KINASE, FIIN-3, TRANSFERASE 
3c4w:A   (GLY228) to   (ILE455)  CRYSTAL STRUCTURE OF G PROTEIN COUPLED RECEPTOR KINASE 1 BOUND TO ATP AND MAGNESIUM CHLORIDE AT 2.7A  |   SER/THR KINASE, RGS HOMOLOGY DOMAIN, G PROTEIN COUPLED RECEPTOR KINASE, GRK, GRK1, RHODOPSIN KINASE, P-LOOP, PHOSPHOTHREONINE, AUTOPHOSPHORYLATION, AMPHIPATHIC, ATP-BINDING, LIPOPROTEIN, MEMBRANE, METHYLATION, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PRENYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3c4w:B   (TYR229) to   (ILE455)  CRYSTAL STRUCTURE OF G PROTEIN COUPLED RECEPTOR KINASE 1 BOUND TO ATP AND MAGNESIUM CHLORIDE AT 2.7A  |   SER/THR KINASE, RGS HOMOLOGY DOMAIN, G PROTEIN COUPLED RECEPTOR KINASE, GRK, GRK1, RHODOPSIN KINASE, P-LOOP, PHOSPHOTHREONINE, AUTOPHOSPHORYLATION, AMPHIPATHIC, ATP-BINDING, LIPOPROTEIN, MEMBRANE, METHYLATION, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PRENYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3c51:B   (GLY228) to   (ILE455)  CRYSTAL STRUCTURE OF G PROTEIN COUPLED RECEPTOR KINASE 1 BOUND TO ADP AND MAGNESIUM CHLORIDE AT 3.55A  |   SER/THR KINASE, RGS HOMOLOGY DOMAIN, G PROTEIN COUPLED RECEPTOR KINASE, GRK, GRK1, RHODOPSIN KINASE, P-LOOP, AUTOPHOSPHORYLATION, ADP, ATP-BINDING, LIPOPROTEIN, MEMBRANE, METHYLATION, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, PRENYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
4c2v:A   (HIS136) to   (HIS340)  AURORA B KINASE IN COMPLEX WITH THE SPECIFIC INHIBITOR BARASERTIB  |   TRANSFERASE-CELL CYCLE COMPLEX, AZD1152 
4c2w:A   (GLU135) to   (HIS340)  CRYSTAL STRUCTURE OF AURORA B IN COMPLEX WITH AMP-PNP  |   TRANSFERASE 
4c33:A    (ILE85) to   (HIS294)  PKA-S6K1 CHIMERA APO  |   TRANSFERASE-INHIBITOR COMPLEX 
3cjg:A   (HIS874) to  (ALA1166)  CRYSTAL STRUCTURE OF VEGFR2 IN COMPLEX WITH A 3,4,5-TRIMETHOXY ANILINE CONTAINING PYRIMIDINE  |   VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 2. VEGFR-2, KINASE INSERT DOMAIN RECEPTOR, PROTEIN-TYROSINE KINASE RECEPTOR FLK-1, ANGIOGENESIS, ATP-BINDING, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNOGLOBULIN DOMAIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE 
4rj7:A   (PRO753) to   (PRO975)  EGFR KINASE (T790M/L858R) WITH INHIBITOR COMPOUND 1  |   PROTEIN KINASE, PHOSPHOTRANSFER CATALYST, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3nuy:A   (LYS123) to   (HIS339)  PHOSPHOINOSITIDE-DEPENDENT KINASE-1 (PDK1) WITH FRAGMENT17  |   KINASE DOMAIN, TRANSFERASE 
4cfh:A    (VAL57) to   (HIS265)  STRUCTURE OF AN ACTIVE FORM OF MAMMALIAN AMPK  |   TRANSFERASE, TRANSFERASE PHOSPHORYLATION, ACTIVE FORM, NUCLEOTIDE- BINDING, STAUROSPORINE-BINDING, SERINE/THREONINE-PROTEIN KINASE 
4cfv:A    (PRO45) to   (GLN287)  STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS.  |   TRANSFERASE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE 
4rz7:A   (ASN578) to   (GLY792)  CRYSTAL STRUCTURE OF PVX_084705 WITH BOUND PCI32765  |   STRUCTURAL GENOMICS CONSORTIUM, SGC, KINASE, PCI32765, TRANSFERASE 
3o7l:B    (GLN84) to   (HIS294)  CRYSTAL STRUCTURE OF PHOSPHOLAMBAN (1-19):PKA C-SUBUNIT:AMP-PNP:MG2+ COMPLEX  |   PROTEIN KINASE A, PHOSPHOLAMBAN, ALLOSTERY, SUBSTRATE RECOGNITION, CONFORMATIONAL SELECTION, INTRINSICALLY DISORDERED PROTEINS, MEMBRANE PROTEINS, TRANSFERASE 
3dbe:A    (LYS77) to   (THR292)  CRYSTAL STRUCTURE OF AN ACTIVATED (THR->ASP) POLO-LIKE KINASE 1 (PLK1) CATALYTIC DOMAIN IN COMPLEX WITH COMPOUND 557  |   POLO-LIKE KINASE 1, PLK1, CATALYTIC DOMAIN, SMALL-MOLECULE INHIBITOR, KINASE, TRANSFERASE 
4tpt:A   (VAL377) to   (GLY609)  CRYSTAL STRUCTURE OF THE HUMAN LIMK2 KINASE DOMAIN IN COMPLEX WITH A NON-ATP COMPETITIVE INHIBITOR  |   LIMK2 KINASE, DFG INHIBITOR 
3dfc:B    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF A GLYCINE-RICH LOOP MUTANT OF THE DEATH ASSOCIATED PROTEIN KINASE CATALYTIC DOMAIN WITH AMPPNP  |   KINASE DOMAIN, GLYCINE-RICH LOOP MUTATION, AMPPNP, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3dgk:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF A GLYCINE-RICH LOOP MUTANT OF THE DEATH ASSOCIATED PROTEIN KINASE CATALYTIC DOMAIN  |   KINASE DOMAIN, GLYCINE-RICH LOOP MUTATION, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3dne:A    (ILE85) to   (ALA298)  CAMP-DEPENDENT PROTEIN KINASE PKA CATALYTIC SUBUNIT WITH PKI-5-24  |   ATP-BINDING, KINASE, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CAMP, PROTEIN KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3dog:C    (PRO45) to   (GLN287)  STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR N-&-N1  |   SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CYCLIN, CYTOPLASM, NUCLEUS 
3dqx:B   (SER303) to   (TYR519)  CHICKEN C-SRC KINASE DOMAIN IN COMPLEX WITH ATPGS  |   SRC, KINASE, ACTIVE, ATP-BINDING, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, PROTO-ONCOGENE, SH2 DOMAIN, SH3 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE 
3orz:B   (VAL124) to   (HIS339)  PDK1 MUTANT BOUND TO ALLOSTERIC DISULFIDE FRAGMENT ACTIVATOR 2A2  |   C HELIX, SER/THR-KINASE, AGC KINASE, ALLOSTERY, TRANSFERASE, ALLOSTERIC ACTIVATOR, BISINDOLYLMALEIMIDE, DISULFIDE, KINASE, PDK1, TRANSFERASE-TRANSFERASE ACTIVATOR COMPLEX 
5hcy:A   (PRO753) to   (ARG973)  EGFR KINASE DOMAIN MUTANT "TMLR" WITH 3-CARBOXAMIDE AZAINDOLE COMPOUND 13  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5hd4:A    (GLN60) to   (LEU265)  DISSECTING THERAPEUTIC RESISTANCE TO ERK INHIBITION RAT WILD TYPE SCH772984 IN COMPLEX WITH (3R)-1-(2-OXO-2-{4-[4-(PYRIMIDIN-2-YL) PHENYL]PIPERAZIN-1-YL}ETHYL)-N-[3-(PYRIDIN-4-YL)-2H-INDAZOL-5- YL]PYRROLIDINE-3-CARBOXAMIDE  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5hd7:A    (GLN60) to   (LEU265)  DISSECTING THERAPEUTIC RESISTANCE TO ERK INHIBITION RAT MUTANT SCH772984 IN COMPLEX WITH (3R)-1-(2-OXO-2-{4-[4-(PYRIMIDIN-2-YL) PHENYL]PIPERAZIN-1-YL}ETHYL)-N-[3-(PYRIDIN-4-YL)-2H-INDAZOL-5- YL]PYRROLIDINE-3-CARBOXAMIDE  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4dfz:E    (ILE85) to   (HIS294)  CRYSTAL STRUCTURE OF MYRISTOYLATED K7C CATALYTIC SUBUNIT OF CAMP- DEPENDENT PROTEIN KINASE IN COMPLEX WITH SP20  |   PROTEIN KINASE, MYRISTOYLATED, PHOSPHOTRANSFERASE OF SER/THR, MG, PKI, PKA REGULATORY SUBUNITS, PHOSPHORYLATED ON S139, T197, S338, MYRISTOYLATED ON G1, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5hic:A   (SER752) to   (ARG973)  EGFR KINASE DOMAIN MUTANT "TMLR" WITH A IMIDAZOPYRIDINYL- AMINOPYRIMIDINE INHIBITOR  |   PROTEIN KINASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4u5j:A   (SER303) to   (TYR519)  C-SRC IN COMPLEX WITH RUXOLITINIB  |   C-SRC, RUXOLITINIB, KINASE, INHIBITOR 
4u5j:B   (GLU305) to   (TYR519)  C-SRC IN COMPLEX WITH RUXOLITINIB  |   C-SRC, RUXOLITINIB, KINASE, INHIBITOR 
3p1a:A   (LYS149) to   (LEU356)  STRUCTURE OF HUMAN MEMBRANE-ASSOCIATED TYROSINE- AND THREONINE- SPECIFIC CDC2-INHIBITORY KINASE MYT1 (PKMYT1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, TYROSINE- AND THREONINE-SPECIFIC KINASE, MEMBRANE-ASSOCIATED PROTEIN KINASE, TRANSFERASE 
4dn5:B   (ALA438) to   (GLY659)  CRYSTAL STRUCTURE OF NF-KB-INDUCING KINASE (NIK)  |   NON-RD KINASE, PROTEIN SERINE/THREONINE KINASE, TRANSFERASE, ATP BINDING 
5hq0:A    (PRO45) to   (ASN288)  TERNARY COMPLEX OF HUMAN PROTEINS CDK1, CYCLIN B AND CKS2, BOUND TO AN INHIBITOR  |   CDK1, CYCLIN B, CKS2, CELL-CYCLE, PROTEIN KINASE, INHIBITOR, TRANSFERASE 
3e5a:A   (GLU175) to   (HIS380)  CRYSTAL STRUCTURE OF AURORA A IN COMPLEX WITH VX-680 AND TPX2  |   AURORA A, SERINE/THREONINE-PROTEIN KINASE, COFACTOR, TPX2, VX-680, INHIBITOR, PHOSPHORYLATION, ATP-BINDING, CELL CYCLE, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, TRANSFERASE, NUCLEUS 
4ueu:A    (SER45) to   (THR261)  TYROSINE KINASE AS - A COMMON ANCESTOR OF SRC AND ABL  |   TRANSFERASE, ANCESTOR PROTEIN, AMPPCP, DFG-IN 
5i9u:A   (THR653) to   (ALA877)  CRYSTAL STRUCTURE OF EPHRIN A2 (EPHA2) RECEPTOR PROTEIN KINASE  |   TRANSFERASE, TYROSINE-PROTEIN KINASE, RECEPTOR, ATP-BINDING 
5i9v:A   (THR653) to   (ALA877)  CRYSTAL STRUCTURE OF EPHRIN A2 (EPHA2) RECEPTOR PROTEIN KINASE WITH AGS  |   TRANSFERASE, TYROSINE-PROTEIN KINASE, RECEPTOR, ATP-BINDING 
5if1:A    (PRO45) to   (HIS283)  CRYSTAL STRUCTURE APO CDK2/CYCLIN A  |   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 
5if1:C    (PRO45) to   (HIS283)  CRYSTAL STRUCTURE APO CDK2/CYCLIN A  |   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 
4utd:A   (VAL174) to   (ASN386)  STRUCTURE OF DEPHOSPHORYLATED AURORA A (122-403) BOUND TO AMPPCP IN AN ACTIVE CONFORMATION  |   TRANSFERASE, ACTIVATION, CELL CYCLE, CANCER 
3pvw:A   (GLY232) to   (SER450)  BOVINE GRK2 IN COMPLEX WITH GBETAGAMMA SUBUNITS AND A SELECTIVE KINASE INHIBITOR (CMPD103A)  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, INHIBITOR, MEMBRANE, TRANSFERASE-SIGNALING PROTEIN-INHIBITOR COMPLEX 
4eoi:A    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 K89D, Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eoi:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 K89D, Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eoj:A    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
4eok:A    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR NU6102  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eol:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eom:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
4eon:A    (PRO45) to   (HIS283)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eon:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eoo:A    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
4eoo:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
4eop:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306  |   PROTEIN KINASE, CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4eoq:A    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
4eoq:C    (PRO45) to   (GLN287)  THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH ATP  |   PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE 
3qhr:A    (PRO45) to   (GLN287)  STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC  |   KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, TRANSFERASE-PROTEIN BINDING COMPLEX 
3qhr:C    (PRO45) to   (GLN287)  STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC  |   KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, TRANSFERASE-PROTEIN BINDING COMPLEX 
3qhw:A    (PRO45) to   (GLN287)  STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC  |   KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, PHOSPHORYLATED ON THR-160, TRANSFERASE-PROTEIN BINDING COMPLEX 
3qhw:C    (PRO45) to   (GLN287)  STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC  |   KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, PHOSPHORYLATED ON THR-160, TRANSFERASE-PROTEIN BINDING COMPLEX 
4uxl:A  (THR1987) to  (SER2229)  STRUCTURE OF HUMAN ROS1 KINASE DOMAIN IN COMPLEX WITH PF-06463922  |   TRANSFERASE, INHIBITOR, ROS 
4uy9:A   (ASP180) to   (SER409)  STRUCTURE OF MLK1 KINASE DOMAIN WITH LEUCINE ZIPPER 1  |   MLK FAMILY, MLK1 AND MLK3 SUBTYPE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, SH3 DOMAIN, TRANSFERASE 
3r22:A   (GLU175) to   (HIS380)  DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF PYRAZOLOPYRIDINE- SULFONAMIDES AS POTENT MULTIPLE-MITOTIC KINASE (MMK) INHIBITORS (PART I)  |   KINASE DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3r30:A    (PRO99) to   (HIS322)  MK2 KINASE BOUND TO COMPOUND 2  |   KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fr4:A    (GLU64) to   (LYS292)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fr4:B    (GLU64) to   (PHE278)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fr4:C    (GLU64) to   (PHE278)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fr4:D    (GLU64) to   (PHE278)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fr4:E    (GLU64) to   (PHE278)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fr4:F    (GLU64) to   (PHE278)  CRYSTAL STRUCTURE OF HUMAN SERINE/THREONINE-PROTEIN KINASE 32A (YANK1)  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4fux:A    (GLN60) to   (SER264)  CRYSTAL STRUCTURE OF THE ERK2 COMPLEXED WITH E75  |   TRANSFERASE 
4g3c:A   (VAL440) to   (VAL660)  CRYSTAL STRUCTURE OF APO MURINE NF-KAPPAB INDUCING KINASE (NIK)  |   NON-RD KINASE, PROTEIN SERINE/THREONINE KINASE, NF-KAPPAB, MAP3K14, TRANSFERASE 
4g3d:D   (ARG437) to   (GLN657)  CRYSTAL STRUCTURE OF HUMAN NF-KAPPAB INDUCING KINASE (NIK)  |   NON-RD KINASE, PROTEIN SERINE/THREONINE KINASE, NF-KAPPAB, MAP3K14, TRANSFERASE 
4g6n:A    (GLN60) to   (SER264)  CRYSTAL STRUCTURE OF THE ERK2  |   TRANSFERASE 
5ke0:A    (HIS59) to   (LEU265)  DISCOVERY OF 1-1H-PYRAZOLO 4,3-C PYRIDINE-6-YL UREA INHIBITORS OF EXTRACELLULAR SIGNAL REGULATED KINASE ERK FOR THE TREATMENT OF CANCERS  |   TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, MAP KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5l2w:A    (PRO45) to   (HIS283)  THE X-RAY CO-CRYSTAL STRUCTURE OF HUMAN CDK2/CYCLINE AND DINACICLIB.  |   CYCLIN-DEPENDENT KINASE, KINASE INHIBITOR, KINASE SELECTIVITY, TRANSFERASE-CELL CYCLE-INHIBITOR COMPLEX 
5li1:A   (ASP293) to   (HIS519)  STRUCTURE OF A PAR3-INHIBITORY PEPTIDE BOUND TO PKCIOTA CORE KINASE DOMAIN  |   APKC, POLARITY, COMPLEX, TRANSFERASE 
5lxm:A   (VAL174) to   (HIS380)  CRYSTAL STRUCTURE OF AURORA-A BOUND TO A HYDROCARBON-STAPLED PROTEOMIMETIC OF TPX2  |   PROTEIN KINASE, PROTEOMIMETIC, STAPLED HELIX PEPTIDE, MITOSIS, TRANSFERASE 
1nxk:C    (PRO99) to   (HIS322)  CRYSTAL STRUCTURE OF STAUROSPORINE BOUND TO MAP KAP KINASE 2  |   PROTEIN KINASE, MK2, PHOSPHORYLATION, STAUROSPORINE, TRANSFERASE 
3f5g:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DEATH ASSOCIATED PROTEIN KINASE IN COMPLEX WITH ADP AND MG2+  |   KINASE-ADP COMPLEX,, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1ogu:C    (PRO45) to   (GLN287)  STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 2-ARYLAMINO-4-CYCLOHEXYLMETHYL-5-NITROSO-6-AMINOPYRIMIDINE INHIBITOR  |   KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION 
2pz5:A   (THR524) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC N549T MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
2pz5:B   (LYS526) to   (ASN766)  CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC N549T MUTATION RESPONSIBLE FOR PFEIFFER SYNDROME  |   KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, TRANSFERASE 
4iac:A    (ILE85) to   (HIS294)  X-RAY STRUCTURE OF CAMP DEPENDENT PROTEIN KINASE A IN COMPLEX WITH HIGH MG2+ CONCENTRATION, AMP-PCP AND PSEUDO-SUBSTRATE PEPTIDE SP20  |   KINASE, PHOSPHORYLATION, AUTO-PHOSPHORYLATED, TRANSFERASE-PEPTIDE COMPLEX 
4ie9:A    (ILE85) to   (ALA298)  BOVINE PKA C-ALPHA IN COMPLEX WITH 3-PYRIDYLMETHYL-5-METHYL-1H- PYRAZOLE-3-CARBOXYLATE  |   PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4ii5:A    (PRO45) to   (GLN287)  STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 1 MAGNESIUM ION  |   ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX 
4ii5:C    (PRO45) to   (GLN287)  STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 1 MAGNESIUM ION  |   ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX 
4yo4:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 CATALYTIC DOMAIN IN COMPLEX WITH THE HINGE BINDING FRAGMENT PHTHALAZINE  |   TRANSFERASE 
4ypd:A    (ARG58) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1 CATALYTIC DOMAIN IN COMPLEX WITH THE HINGE BINDING FRAGMENT 4-METHYLPYRIDAZINE  |   TRANSFERASE 
2f2c:B    (PRO55) to   (HIS297)  X-RAY STRUCTURE OF HUMAN CDK6-VCYCLINWITH THE INHIBITOR AMINOPURVALANOL  |   SMALL MOLECULE INHIBITOR BOUND BETWEEN N-TERMINAL AND C-TERMINAL DOMAIN OF KINASE, CELL CYCLE-TRANSFERASE COMPLEX 
2vgp:A   (VAL134) to   (HIS340)  CRYSTAL STRUCTURE OF AURORA B KINASE IN COMPLEX WITH A AMINOTHIAZOLE INHIBITOR  |   NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, TRANSFERASE, COILED COIL, CELL DIVISION, KINASE, CANCER, INCENP, NUCLEUS, MITOSIS, AURORA B, METAL-BINDING, AMINOTHIAZOLE, PHOSPHORYLATION, MAGNESIUM, CELL CYCLE, CENTROMERE, MICROTUBULE 
1gjo:A   (THR524) to   (THR764)  THE FGFR2 TYROSINE KINASE DOMAIN  |   TRANSFERASE, TYROSINE KINASE, FGFR2 RECEPTOR 
2vo6:A    (ILE85) to   (ALA298)  STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH  4-(4- CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN- 4-YLAMINE  |   TRANSFERASE, LIPOPROTEIN, ATP-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, NUCLEOTIDE-BINDING, PROTEIN KINASE INHIBITOR, CAMP, KINASE, NUCLEUS, MYRISTATE, CYTOPLASM 
1smh:A    (ILE85) to   (HIS294)  PROTEIN KINASE A VARIANT COMPLEX WITH COMPLETELY ORDERED N- TERMINAL HELIX  |   PKA; PROTEIN KINASE A; CAMP-DEPENDENT PROTEIN KINASE; PHOSPHORYLATION; SER10; MYRISTOYLATION; POSTTRANSLATIONAL MODIFICATION; SIGNALING; MEMBRANE, ALPHA HELIX, SIGNALING PROTEIN,TRANSFERASE/INHIBITOR COMPLEX 
1svh:A    (GLN84) to   (ALA298)  CRYSTAL STRUCTURE OF PROTEIN KINASE A IN COMPLEX WITH AZEPANE DERIVATIVE 8  |   KINASE-INHIBITOR-COMPLEX, SERINE/THREONINE-PROTEIN KINASE, BALANOL DERIVATIVE, TRANSFERASE 
1gy3:A    (PRO45) to   (GLN287)  PCDK2/CYCLIN A IN COMPLEX WITH MGADP, NITRATE AND PEPTIDE SUBSTRATE  |   TRANSFERASE-TRANSFERASE SUBSTRATE COMPLEX, CELL CYCLE REGULATORY PROTEIN KINASE, THR160-PHOSPHO-CYCLIN DEPENDENT PROTEIN KINASE 2 IN ASSOCIATION WITH CYCLIN A, TRANSFERASE- TRANSFERASE SUBSTRATE COMPLEX 
2hel:A   (ASP661) to   (ASN884)  CRYSTAL STRUCTURE OF A MUTANT EPHA4 KINASE DOMAIN (Y742A)  |   TYR KINASE, ACTIVATION, SIGNALING PROTEIN, TRANSFERASE 
2wpa:A    (PRO45) to   (HIS283)  OPTIMISATION OF 6,6-DIMETHYL PYRROLO 3,4-C PYRAZOLES: IDENTIFICATION OF PHA-793887, A POTENT CDK INHIBITOR SUITABLE FOR INTRAVENOUS DOSING  |   SERINE/THREONINE-PROTEIN 2 KINASE, CYCLIN, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN, 
2wpa:C    (PRO45) to   (GLN287)  OPTIMISATION OF 6,6-DIMETHYL PYRROLO 3,4-C PYRAZOLES: IDENTIFICATION OF PHA-793887, A POTENT CDK INHIBITOR SUITABLE FOR INTRAVENOUS DOSING  |   SERINE/THREONINE-PROTEIN 2 KINASE, CYCLIN, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN, 
2x1n:A    (PRO45) to   (HIS283)  TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN  |   INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, CELL DIVISION 
2x1n:C    (PRO45) to   (GLN287)  TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN  |   INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, CELL DIVISION 
1j3h:A    (GLN84) to   (HIS294)  CRYSTAL STRUCTURE OF APOENZYME CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT  |   CRYSTAL STRUCTURE, APOENZYME, CAMP-DEPENDENT PROTEIN KINASE, CATALYTIC SUBUNIT, OPEN CONFORMATION, PREFORMED ACTIVE SITE, TRANSFERASE 
1j3h:B    (GLU86) to   (HIS294)  CRYSTAL STRUCTURE OF APOENZYME CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT  |   CRYSTAL STRUCTURE, APOENZYME, CAMP-DEPENDENT PROTEIN KINASE, CATALYTIC SUBUNIT, OPEN CONFORMATION, PREFORMED ACTIVE SITE, TRANSFERASE 
1jks:A    (SER57) to   (HIS272)  1.5A X-RAY STRUCTURE OF APO FORM OF A CATALYTIC DOMAIN OF DEATH-ASSOCIATED PROTEIN KINASE  |   TRANSFERASE 
5av2:A    (SER57) to   (HIS272)  CRYSTAL STRUCTURE OF DAPK1-KAEMPFEROL COMPLEX IN THE PRESENCE OF BROMIDE IONS.  |   DEATH-ASSOCIATED PROTEIN KINASE 1, SERINE/THREONINE PROTEIN KINASE, NATURAL FLAVONOID 
1kwp:A    (PRO99) to   (LYS307)  CRYSTAL STRUCTURE OF MAPKAP2  |   MAPKAP2, PROTEIN KINASE, SIGNAL TRANSDUCTION, TRANSFERASE 
1kwp:B   (LYS100) to   (HIS322)  CRYSTAL STRUCTURE OF MAPKAP2  |   MAPKAP2, PROTEIN KINASE, SIGNAL TRANSDUCTION, TRANSFERASE 
3kc3:C    (CYS98) to   (HIS322)  MK2 COMPLEXED TO INHIBITOR N4-(7-(BENZOFURAN-2-YL)-1H-INDAZOL-5-YL) PYRIMIDINE-2,4-DIAMINE  |   MAPKAP-K2, MK2, TNFALPHA, DIAMINOPYRIMIDINE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3a2c:E    (CYS98) to   (LEU305)  CRYSTAL STRUCTURE OF A PYRAZOLOPYRIMIDINE INHIBITOR COMPLEX BOUND TO MAPKAP KINASE-2 (MK2)  |   GLY-RICH LOOP FORMED, AIPHA-HELIX, ALTERNATIVE SPLICING, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3a2c:H    (CYS98) to   (LEU305)  CRYSTAL STRUCTURE OF A PYRAZOLOPYRIMIDINE INHIBITOR COMPLEX BOUND TO MAPKAP KINASE-2 (MK2)  |   GLY-RICH LOOP FORMED, AIPHA-HELIX, ALTERNATIVE SPLICING, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
3a2c:K    (CYS98) to   (HIS322)  CRYSTAL STRUCTURE OF A PYRAZOLOPYRIMIDINE INHIBITOR COMPLEX BOUND TO MAPKAP KINASE-2 (MK2)  |   GLY-RICH LOOP FORMED, AIPHA-HELIX, ALTERNATIVE SPLICING, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
1ydr:E    (ILE85) to   (ALA298)  STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H7 PROTEIN KINASE INHIBITOR 1-(5- ISOQUINOLINESULFONYL)-2-METHYLPIPERAZINE  |   COMPLEX (PHOSPHOTRANSFERASE/INHIBITOR), TRANSFERASE, CAMP, PHOSPHORYLATION, ISOQUINOLINE SULFONAMIDE, SERINE/THREONINE- PROTEIN KINASE, ATP-BINDING 
4ann:A    (PHE45) to   (GLN204)  CRYSTAL STRUCTURE STAPHYLOCOCCUS AUREUS ESSB CYTOPLASMIC FRAGMENT  |   MEMBRANE PROTEIN, MEMBRANE SECRETION, ESS TYPE VII SECRETION SYSTEM, VIRULENCE 
5dyl:A   (GLN575) to   (HIS788)  CRYSTAL STRUCTURE OF PVX_084705  |   TRANSFERASE, KINASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
3lvp:A  (MET1041) to  (SER1265)  CRYSTAL STRUCTURE OF BISPHOSPHORYLATED IGF1-R KINASE DOMAIN (2P) IN COMPLEX WITH A BIS-AZAINDOLE INHIBITOR  |   PROTEIN KINASE, TYROSINE KINASE, TYROSINE PHOSPHORYLATION, PROTEIN- SUBSTRATE COMPLEX, TRANSFERASE 
4bco:C    (PRO45) to   (GLN287)  STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR  |   TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN 
4bib:A   (LEU722) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
4bib:B   (GLN720) to   (LYS939)  CRYSTAL STRUCTURES OF ASK1-INHIBITOR COMPLEXES  |   TRANSFERASE 
3bhu:A    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 5  |   SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN 
3bhv:A    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR VARIOLIN B  |   SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE- PROTEIN KINASE, CYCLIN 
5fet:A   (GLN575) to   (GLY792)  CRYSTAL STRUCTURE OF PVX_084705 IN PRESENCE OF COMPOUND 2  |   AGC KINASE, PKG, STRUCTURAL GENOMICS, MALARIA, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE 
4cff:A    (VAL57) to   (HIS265)  STRUCTURE OF FULL LENGTH HUMAN AMPK IN COMPLEX WITH A SMALL MOLECULE ACTIVATOR, A THIENOPYRIDONE DERIVATIVE (A-769662)  |   TRANSFERASE, NUCLEOTIDE-BINDING, STAUROSPORINE-BINDING, SERINE/THREONINE-PROTEIN KINASE, ACTIVATOR, CARBOHYDRATE BINDING MODULE (CBM) 
4cfu:A    (PRO45) to   (GLN287)  STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS.  |   TRANSFERASE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE 
3ddp:C    (PRO45) to   (HIS283)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR CR8  |   SER/THR PROTEIN KINASE; PHOSPHORYLATION; CELL CYCLE, ATP- BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX 
3ddq:A    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR ROSCOVITINE  |   SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX 
3ddq:C    (PRO45) to   (GLN287)  STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR ROSCOVITINE  |   SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX 
4d55:A   (SER461) to   (LEU685)  FOCAL ADHESION KINASE CATALYTIC DOMAIN  |   TRANSFERASE, KINASE INHIBITOR, ATP-BINDING, INTEGRIN SIGNALING 
4fx3:A    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF THE CDK2/CYCLIN A COMPLEX WITH OXINDOLE INHIBITOR  |   COMPLEX (TRANSFERASE-CYCLIN), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fx3:C    (PRO45) to   (GLN287)  CRYSTAL STRUCTURE OF THE CDK2/CYCLIN A COMPLEX WITH OXINDOLE INHIBITOR  |   COMPLEX (TRANSFERASE-CYCLIN), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5lih:B   (GLN300) to   (LYS533)  STRUCTURE OF A PEPTIDE-SUBSTRATE BOUND TO PKCIOTA CORE KINASE DOMAIN  |   APKC, POLARITY, COMPLEX, TRANSFERASE