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Structure paper

TitleStructural basis for high-affinity peptide inhibition of human Pin1.
Journal, issue, pagesAcs Chem. Biol., Vol. 2, Page 320-328, Year 2007
Publish dateOct 19, 2006 (structure data deposition date)
AuthorsZhang, Y. / Daum, S. / Wildemann, D. / Zhou, X.Z. / Verdecia, M.A. / Bowman, M.E. / Lucke, C. / Hunter, T. / Lu, K.P. / Fischer, G. / Noel, J.P.
External linksAcs Chem. Biol. / PubMed:17518432
MethodsX-ray diffraction
Resolution1.45 - 1.5 Å
Structure data

PDB-2itk:
human Pin1 bound to D-PEPTIDE
Method: X-RAY DIFFRACTION / Resolution: 1.45 Å

PDB-2q5a:
human Pin1 bound to L-PEPTIDE
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

Chemicals

ChemComp-PE4:
2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL / precipitant*YM

ChemComp-HOH:
WATER

ChemComp-16P:
3,6,9,12,15,18-HEXAOXAICOSANE

Source
  • homo sapiens (human)
KeywordsISOMERASE/ISOMERASE INHIBITOR / Pin1 / isomerase / WW domain / ISOMERASE-ISOMERASE INHIBITOR COMPLEX / ISOMERASE WW domain

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