Search PepX: serine/threonine-protein kinase
Results 1 - 50 of 69
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1H24 | CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F | E | B | Cyclin-like |
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1H27 | CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 | E | B | Cyclin-like |
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1LEW | CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS NUCLEAR SUBSTRATE MEF2A | B | A | Protein kinase-like (PK-like) |
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1LEZ | CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS ACTIVATOR MKK3B | B | A | Protein kinase-like (PK-like) |
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1O6K | STRUCTURE OF ACTIVATED FORM OF PKB KINASE DOMAIN S474D WITH GSK3 PEPTIDE AND AMP-PNP | C | A | Protein kinase-like (PK-like) |
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1O6L | CRYSTAL STRUCTURE OF AN ACTIVATED AKT/PROTEIN KINASE B (PKB-PIF CHIMERA) TERNARY COMPLEX WITH AMP-PNP AND GSK3 PEPTIDE | C | A | Protein kinase-like (PK-like) |
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1Q8T | The Catalytic Subunit of cAMP-dependent Protein Kinase (PKA) in Complex with Rho-kinase Inhibitor Y-27632 | B | A | Protein kinase-like (PK-like) |
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1Q8U | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor H-1152P | B | A | Protein kinase-like (PK-like) |
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1Q8W | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor Fasudil (HA-1077) | B | A | Protein kinase-like (PK-like) |
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1STC | CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH STAUROSPORINE | I | E | Protein kinase-like (PK-like) |
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1SVE | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 1 | B | A | Protein kinase-like (PK-like) |
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1SVG | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 4 | B | A | Protein kinase-like (PK-like) |
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1SVH | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 8 | B | A | Protein kinase-like (PK-like) |
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1WBP | SRPK1 BOUND TO 9MER DOCKING MOTIF PEPTIDE | B | C |
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1XH4 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH5 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH6 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH7 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH8 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH9 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A |
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1XHA | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1YDR | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H7 PROTEIN KINASE INHIBITOR 1-(5-ISOQUINOLINESULFONYL)-2-METHYLPIPERAZINE | I | E | Protein kinase-like (PK-like) |
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1YDS | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H8 PROTEIN KINASE INHIBITOR [N-(2-METHYLAMINO)ETHYL]-5-ISOQUINOLINESULFONAMIDE | I | E | Protein kinase-like (PK-like) |
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1YDT | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H89 PROTEIN KINASE INHIBITOR N-[2-(4-BROMOCINNAMYLAMINO)ETHYL]-5-ISOQUINOLINE | I | E | Protein kinase-like (PK-like) |
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2BZK | CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE | A | B |
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2C1A | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL)AMIDE | I | A | Protein kinase-like (PK-like) |
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2C1B | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH (4R,2S)-5\'-(4-(4-CHLOROBENZYLOXY)PYRROLIDIN-2-YLMETHANESULFONYL)ISOQUINOLINE | I | A | Protein kinase-like (PK-like) |
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2C3I | CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I | A | B |
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2CCH | THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA-LINKED ATP ANALOGUE | E | B | Cyclin-like |
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2JAM | CRYSTAL STRUCTURE OF HUMAN CALMODULIN-DEPENDENT PROTEIN KINASE I G | D | A |
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2JDO | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE | C | A | Protein kinase-like (PK-like) |
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2JDR | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH THE INHIBITOR A-443654 | C | A | Protein kinase-like (PK-like) |
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2JDS | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A-443654 | I | A | Protein kinase-like (PK-like) |
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2JDT | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE | I | A |
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2JDV | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH A-443654 | I | A |
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2JLD | EXTREMELY TIGHT BINDING OF RUTHENIUM COMPLEX TO GLYCOGEN SYNTHASE KINASE 3 | E | A |
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2Q0N | Structure of human p21 activating kinase 4 (PAK4) in complex with a consensus peptide | B | A |
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2QME | Crystal structure of human RAC3 in complex with CRIB domain of human p21-activated kinase 1 (PAK1) | I | A |
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2UVX | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 7-AZAINDOLE | I | A |
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2UVY | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH METHYL-(4-(9H-PURIN-6-YL)-BENZYL)-AMINE | I | A |
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2UVZ | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-PHENYL-C-(4-(9H-PURIN-6-YL)-PHENYL)-METHYLAMINE | I | A |
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2UW0 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 6-(4-(4-(4-CHLORO-PHENYL)-PIPERIDIN-4-YL)-PHENYL)-9H-PURINE | I | A |
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2UW3 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE | I | A |
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2UW4 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-(5-METHYL-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
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2UW5 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (R)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
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2UW6 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (S)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
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2UW7 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE | I | A |
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2UW8 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-CHLORO-PHENYL)-2-PHENYL-ETHYLAMINE | I | A |
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2UW9 | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE | C | A | Protein kinase-like (PK-like) |
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2UZT | PKA STRUCTURES OF AKT, INDAZOLE-PYRIDINE INHIBITORS | B | A |
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