Search PepX: kinase
Results 1 - 50 of 57
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1O9U | GLYCOGEN SYNTHASE KINASE 3 BETA COMPLEXED WITH AXIN PEPTIDE | B | A | Protein kinase-like (PK-like) |
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1OKV | CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ILE-PHE-NH2 | E | B | Cyclin-like |
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1WBP | SRPK1 BOUND TO 9MER DOCKING MOTIF PEPTIDE | B | C |
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2BFY | COMPLEX OF AURORA-B WITH INCENP AND HESPERIDIN. | D | A |
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2BZK | CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE | A | B |
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2C3I | CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I | A | B |
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2G1T | A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain | G | C |
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2GU8 | Discovery of 2-Pyrimidyl-5-Amidothiophenes as Novel and Potent Inhibitors for AKT: Synthesis and SAR Studies | C | A |
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2IZX | MOLECULAR BASIS OF AKAP SPECIFICITY FOR PKA REGULATORY SUBUNITS | C | AB |
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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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2ODB | The crystal structure of human cdc42 in complex with the CRIB domain of human p21-activated kinase 6 (PAK6) | B | A |
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2OKR | Crystal Structure of the P38a-MAPKAP kinase 2 Heterodimer | C | A | Protein kinase-like (PK-like) |
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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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2UZU | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS | I | E |
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2UZV | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS | 2 | A |
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2UZW | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS | I | E |
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2V3S | STRUCTURAL INSIGHTS INTO THE RECOGNITION OF SUBSTRATES AND ACTIVATORS BY THE OSR1 KINASE | D | A |
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2VNW | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE | I | A |
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2VNY | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)AMINE | I | A |
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2VO0 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE | I | A |
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2VO3 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE | I | A |
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2VO6 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE | I | A |
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2VO7 | STRUCTURE OF PKA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE | I | A | Protein kinase-like (PK-like) |
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3BU3 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide | B | A | Protein kinase-like (PK-like) |
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3BU5 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide and ATP | B | C |
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3C5I | Crystal structure of Plasmodium knowlesi choline kinase, PKH_134520 | E | C |
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3CBL | Crystal structure of human feline sarcoma viral oncogene homologue (v-FES) in complex with staurosporine and a consensus peptide | B | A |
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3CD3 | Crystal structure of phosphorylated human feline sarcoma viral oncogene homologue (v-FES) in complex with staurosporine and a consensus peptide | B | A |
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3CQU | Crystal Structure of Akt-1 complexed with substrate peptide and inhibitor | C | A |
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3CQW | Crystal Structure of Akt-1 complexed with substrate peptide and inhibitor | C | A |
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3CXW | Crystal structure of human proto-oncogene serine threonine kinase (PIM1) in complex with a consensus peptide and a beta carboline ligand I | B | A |
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