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TitleImidazole Piperazines: Sar and Development of a Potent Class of Cyclin-Dependent Kinase Inhibitors with a Novel Binding Mode.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 4442-, Year 2008
Publish dateJun 4, 2008 (structure data deposition date)
AuthorsFinlay, M.R. / Acton, D.G. / Andrews, D.M. / Barker, A.J. / Dennis, M. / Fisher, E. / Graham, M.A. / Green, C.P. / Heaton, D.W. / Karoutchi, G. ...Finlay, M.R. / Acton, D.G. / Andrews, D.M. / Barker, A.J. / Dennis, M. / Fisher, E. / Graham, M.A. / Green, C.P. / Heaton, D.W. / Karoutchi, G. / Loddick, S.A. / Morgentin, R. / Roberts, A. / Tucker, J.A. / Weir, H.M.
External linksBioorg. Med. Chem. Lett. / PubMed:18617397
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-2vv9:
CDK2 in complex with an imidazole piperazine
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-IM9:
2-{4-[4-({4-[2-methyl-1-(1-methylethyl)-1H-imidazol-5-yl]pyrimidin-2-yl}amino)phenyl]piperazin-1-yl}-2-oxoethanol

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / KINASE / MITOSIS / CELL CYCLE / SERINE/THREONINE-PROTEIN KINASE / ATP-BINDING / CELL DIVISION / PHOSPHOPROTEIN / PHOSPHORYLATION / NUCLEOTIDE-BINDING

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