| PDB ID | Description | |
|---|---|---|
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1XH7 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants |
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2GNI | PKA fivefold mutant model of Rho-kinase with inhibitor Fasudil (HA1077) |
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2JDT | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE |
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2UVX | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 7-AZAINDOLE |
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2UZW | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS |
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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 |
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3CY3 | Crystal structure of human proto-oncogene serine threonine kinase (PIM1) in complex with a consensus peptide and the JNK inhibitor V |
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1Q62 | PKA double mutant model of PKB |
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2ERZ | Crystal Structure of c-AMP Dependent Kinase (PKA) bound to hydroxyfasudil |
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2VNW | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE |