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TitleTruncation and Optimisation of Peptide Inhibitors of Cyclin-Dependent Kinase 2-Cyclin a Through Structure-Guided Design.
Journal, issue, pagesChemmedchem, Vol. 4, Page 1120-, Year 2009
Publish dateApr 1, 2009 (structure data deposition date)
AuthorsKontopidis, G. / Andrews, M.J. / Mcinnes, C. / Plater, A. / Innes, L. / Renachowski, S. / Cowan, A. / Fischer, P.M.
External linksChemmedchem / PubMed:19472269
MethodsX-ray diffraction
Resolution2.3 - 2.9 Å
Structure data

PDB-2wev:
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

PDB-2wfy:
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design
Method: X-RAY DIFFRACTION / Resolution: 2.53 Å

PDB-2whb:
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design
Method: X-RAY DIFFRACTION / Resolution: 2.9 Å

Chemicals

ChemComp-CK7:
[4-(2-AMINO-4-METHYL-THIAZOL-5-YL)-PYRIMIDIN-2-YL]-(3-NITRO-PHENYL)-AMINE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • synthetic construct (others)
KeywordsTRANSFERASE / CDK2 / KINASE / CYCLIN / ACTIVE / NUCLEUS / MITOSIS / SERINE/THREONINE-PROTEIN KINASE / CYTOPLASM / INHIBITION / CELL CYCLE / ATP-BINDING / CELL DIVISION / PHOSPHOPROTEIN / NUCLEOTIDE-BINDING / POLYMORPHISM / BETA-PEPTIDE / CYCLIN GROOVE

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