| PDB ID | Description | |
|---|---|---|
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1ATP | 2.2 angstrom refined crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with MNATP and a peptide inhibitor |
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1XH4 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants |
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2GNF | Protein kinase A fivefold mutant model of Rho-kinase with Y-27632 |
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2UW0 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 6-(4-(4-(4-CHLORO-PHENYL)-PIPERIDIN-4-YL)-PHENYL)-9H-PURINE |
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2UZU | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS |
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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 |
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1Q8W | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor Fasudil (HA-1077) |
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1XHA | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants |
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2UW8 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-CHLORO-PHENYL)-2-PHENYL-ETHYLAMINE |
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1RDQ | Hydrolysis of ATP in the crystal of Y204A mutant of cAMP-dependent protein kinase |