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TitleStructure-Based Design, Synthesis and Biological Evaluation of Potent and Selective Macrocyclic Chk1 Inhibitors
Journal, issue, pagesTo be Published
Publish dateJan 26, 2007 (structure data deposition date)
AuthorsTong, Y. / Claiborne, A. / Stewart, K.D. / Park, C. / Kovar, P. / Chen, Z. / Credo, R.B. / Gwaltney, S.L. / Zhang, H. / Rosenberg, S.H. ...Tong, Y. / Claiborne, A. / Stewart, K.D. / Park, C. / Kovar, P. / Chen, Z. / Credo, R.B. / Gwaltney, S.L. / Zhang, H. / Rosenberg, S.H. / Sham, H.L. / Sowin, T.J. / Lin, N.H.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution2.6 Å
Structure data

PDB-2e9p:
Structure of h-CHK1 complexed with A771129
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

ChemComp-77A:
1-(5-CHLORO-2-METHOXYPHENYL)-3-{6-[2-(DIMETHYLAMINO)-1-METHYLETHOXY]PYRAZIN-2-YL}UREA

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Protein-inhibitor Complex

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