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TitleCharacterization of the CHK1 allosteric inhibitor binding site.
Journal, issue, pagesBiochemistry, Vol. 48, Page 9823-9830, Year 2009
Publish dateSep 17, 2009 (structure data deposition date)
AuthorsVanderpool, D. / Johnson, T.O. / Ping, C. / Bergqvist, S. / Alton, G. / Phonephaly, S. / Rui, E. / Luo, C. / Deng, Y.L. / Grant, S. ...Vanderpool, D. / Johnson, T.O. / Ping, C. / Bergqvist, S. / Alton, G. / Phonephaly, S. / Rui, E. / Luo, C. / Deng, Y.L. / Grant, S. / Quenzer, T. / Margosiak, S. / Register, J. / Brown, E. / Ermolieff, J.
External linksBiochemistry / PubMed:19743875
MethodsX-ray diffraction
Resolution1.76 - 1.9 Å
Structure data

PDB-3jvr:
Characterization of the Chk1 allosteric inhibitor binding site
Method: X-RAY DIFFRACTION / Resolution: 1.76 Å

PDB-3jvs:
Characterization of the Chk1 allosteric inhibitor binding site
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-AGX:
(1S)-1-(1H-benzimidazol-2-yl)ethyl (3,4-dichlorophenyl)carbamate

ChemComp-HOH:
WATER

ChemComp-AGY:
2-[(4-tert-butyl-3-nitrophenyl)carbonyl]-N-naphthalen-1-ylhydrazinecarboxamide

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Protein Kinase / ATP-binding / Cell cycle / Cytoplasm / DNA damage / DNA repair / Isopeptide bond / Kinase / Nucleotide-binding / Nucleus / Phosphoprotein / Polymorphism / Serine/threonine-protein kinase / Ubl conjugation

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