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Structural diversity of the active conformation of the N-terminal kinase domain of p90 ribosomal S6 kinase 2[TRANSFERASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Crystal Structure of the N-terminal Kinase Domain of Human RSK1 bound to Purvalnol A[TRANSFERASE]
Crystal Structure of the N-terminal Kinase Domain of Human RSK1 bound to Staurosporine[TRANSFERASE]
Crystal structure of the N-terminal kinase domain of human RSK-1 bound to AMP-PCP[TRANSFERASE]
STRUCTURE OF THE MAMMALIAN CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE AND AN INHIBITOR PEPTIDE DISPLAYS AN OPEN CONFORMATION[TRANSFERASE/TRANSFERASE INHIBITOR]
CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT (E.C.2.7.1.37) (PROTEIN KINASE A) COMPLEXED WITH PROTEIN KINASE INHIBITOR PEPTIDE FRAGMENT 5-24 (PKI(5-24) ISOELECTRIC VARIANT CA) AND MN2+ ADENYLYL IMI...
human cAMP-dependent protein kinase in complex with an inhibitor[TRANSFERASE/TRANSFERASE INHIBITOR]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Complex of PKA with the bisubstrate protein kinase inhibitor ARC-670[TRANSFERASE/TRANSFERASE INHIBITOR]
Human cAMP-dependent protein kinase in complex with an inhibitor[TRANSFERASE]
Human Camp-Dependent Protein Kinase In Complex With An Inhibitor[Transferase, EC: 2.7.11.11]
Human Camp-Dependent Protein Kinase In Complex With An Inhibitor[TransferaseTRANSFERASE INHIBITOR, EC: 2.7.11.11]
Human Camp-Dependent Protein Kinase In Complex With A Small Fragment[Transferase, EC: 2.7.11.11]
Crystal structure of pka with compound 36[TRANSFERASE/TRANSFERASE INHIBITOR]
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Complex of PKA with the bisubstrate protein kinase inhibitor ARC-1039[TRANSFERASE/TRANSFERASE INHIBITOR]
CRYSTAL STRUCTURES OF THE MYRISTYLATED CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE REVEAL OPEN AND CLOSED CONFORMATIONS[TRANSFERASE/TRANSFERASE INHIBITOR]
Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants[TRANSFERASE/TRANSFERASE INHIBITOR]
Protein kinase A variant complex with completely ordered N-terminal helix[SIGNALING PROTEIN,TRANSFERASE/INHIBITOR]
Discovery of dihydrothieno- and dihydrofuropyrimidines as potent pan Akt inhibitors[TRANSFERASE/TRANSFERASE inhibitor]
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