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TitleCrystal structure of human cyclin-dependent kinase-2 complex with MK2 inhibitor TEI-I01800: insight into the selectivity.
Journal, issue, pagesJ. SYNCHROTRON RADIAT., Vol. 20, Page 905-909, Year 2013
Publish dateMay 20, 2013 (structure data deposition date)
AuthorsFujino, A. / Fukushima, K. / Kubota, T. / Kosugi, T. / Takimoto-Kamimura, M.
External linksJ. SYNCHROTRON RADIAT. / PubMed:24121337
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3wbl:
Crystal structure of CDK2 in complex with pyrazolopyrimidine inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-ACT:
ACETATE ION

ChemComp-PDY:
N~7~-(4-ethoxyphenyl)-6-methyl-N~5~-[(3S)-piperidin-3-yl]pyrazolo[1,5-a]pyrimidine-5,7-diamine

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / Binding Sites / Tumor / Cyclin-Dependent Kinase 2 / Drug Design / MAP Kinase Kinase 2 / MK2 / Protein Kinase Inhibitors / Pyrazoles / Pyrimidines / Structure-Activity Relationship / TRANSFERASE-TRANSFERASE INHIBITOR complex

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