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Crystal Structure of CDK4 in complex with a D-type cyclin[TRANSFERASE]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
Crystal Structure of CDK4 in complex with a D-type cyclin[CELL CYCLE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
X-ray structure of human CDK6-Vcyclinwith the inhibitor aminopurvalanol[CELL CYCLE/TRANSFERASE]
X-ray structure of human CDK6-Vcyclin in complex with the inhibitor PD0332991[CELL CYCLE/TRANSFERASE]
Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin[CELL CYCLE/TRANSFERASE]
Crystal structure of a complex of human CDK6 and a viral cyclin[CELL CYCLE/TRANSFERASE]
Differential Binding Of Inhibitors To Active And Inactive Cdk2 Provides Insights For Drug Design[CELL CYCLE]
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design[TRANSFERASE]
Structure of CDK2-CYCLIN A with a Pyrazolo(4,3-h) quinazoline-3- carboxamide inhibitor[TRANSFERASE]
Optimisation of 6,6-Dimethyl Pyrrolo 3,4-c pyrazoles: Identification of PHA-793887, a Potent CDK Inhibitor Suitable for Intravenous Dosing[CELL CYCLE]
STRUCTURE OF CDK2-CYCLIN A COMPLEXED WITH 8-ANILINO-1-METHYL-4,5-DIHYDRO- 1H-PYRAZOLO[4,3-H] QUINAZOLINE-3-CARBOXYLIC ACID[TRANSFERASE]
View in iCn3D PubMedProteinsConserved DomainsPubChem Compound
STRUCTURE OF CDK2-CYCLIN A WITH PHA-848125[TRANSFERASE]
Cyclin A binding groove inhibitor Ace-Arg-Lys-Leu-Phe-Gly[TRANSFERASE/INHIBITOR]
Cyclin A binding groove inhibitor H-Arg-Arg-Leu-Asn-(p-F-Phe)-NH2[TRANSFERASE/TRANSFERASE INHIBITOR]
Cyclin A binding groove inhibitor Ac-Arg-Arg-Leu-Asn-(m-Cl-Phe)-NH2[TRANSFERASE/TRANSFERASE INHIBITOR]
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