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CDK-2 with indazole inhibitor 9 bound at its active site[TRANSFERASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
CDK-2 with indazole inhibitor 17 bound at its active site[TRANSFERASE/Transferase inhibitor]
Human cyclin dependent kinase 2 complexed with the CDK4 inhibitor[TRANSFERASE]
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE CDK4 INHIBITOR[TRANSFERASE]
Structure of CDK2 in complex with a Pyrazolo[4,3-d]pyrimidine Bioisostere of Roscovitine[TRANSFERASE/TRANSFERASE INHIBITOR]
CDK2 ternary complex with SU9516 and ANS[TRANSFERASE/TRANSFERASE INHIBITOR]
CDK2 in complex with inhibitor SU9516[TRANSFERASE/TRANSFERASE INHIBITOR]
CDK2 ternary complex with JWS648 and ANS[TRANSFERASE/TRANSFERASE INHIBITOR]
CDK2 in complex with inhibitor JWS648[TRANSFERASE/TRANSFERASE INHIBITOR]
Apo CDK2 crystallized from Jeffamine[TRANSFERASE]
CDK2 in complex with 3 molecules of 8-anilino-1-naphthalene sulfonate[TRANSFERASE]
CDK2 in complex with two molecules of 8-anilino-1-naphthalene sulfonate[TRANSFERASE]
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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]
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