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-Structure paper
Title | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design. |
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Journal, issue, pages | Chem. Biol., Vol. 13, Page 201-, Year 2006 |
Publish date | Oct 30, 2005 (structure data deposition date) |
Authors | Kontopidis, G. / Mcinnes, C. / Pandalaneni, S.R. / Mcnae, I. / Gibson, D. / Mezna, M. / Thomas, M. / Wood, G. / Wang, S. / Walkinshaw, M.D. / Fischer, P.M. |
External links | Chem. Biol. / PubMed:16492568 |
Methods | X-ray diffraction |
Resolution | 2.1 - 2.9 Å |
Structure data | PDB-2c5n: PDB-2c5o: PDB-2c5v: PDB-2c5x: PDB-2c5y: |
Chemicals | ChemComp-CK8: ChemComp-HOH: ChemComp-CK2: ChemComp-CK4: ChemComp-MTW: |
Source |
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Keywords | TRANSFERASE / DIFFERENTIAL INHIBITION / CDK2 / ATP-BINDING / CELL CYCLE / CELL DIVISION / POLYMORPHISM / PHOSPHORYLATION / NUCLEOTIDE-BINDING / SERINE/THREONINE-PROTEIN / KINASE / MITOSIS / CYCLIN / COMPLEX (KINASE-CYCLIN) / CYCIN A / DRUG DESIGN / LIGAND EXCHANGE / SERINE/THREONINE-PROTEIN KINASE / COMPLEX (TRANSFERASE-CYCLIN) / TRANSFERASE/INHIBITOR / INHIBITION / ACTIVE / INACTIVE / COMPLEX (TRANSFERASE-INHIBITOR) / TRANSFERASE-INHIBITOR complex |