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TitleBicyclic peptide inhibitor reveals large contact interface with a protease target
Journal, issue, pagesAcs Chem. Biol., Vol. 7, Page 817-821, Year 2012
Publish dateFeb 8, 2011 (structure data deposition date)
AuthorsAngelini, A. / Cendron, L. / Chen, S. / Touati, J. / Winter, G. / Zanotti, G. / Heinis, C.
External linksAcs Chem. Biol. / PubMed:22304751
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-3qn7:
Potent and selective bicyclic peptide inhibitor (UK18) of human urokinase-type plasminogen activator(uPA)
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-ZBR:
1,3,5-tris(bromomethyl)benzene

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Bicyclic peptide inhibitor / Chymotrypsin fold / Serine protease / Urokinase receptor (uPAR) / Extracellular / HYDROLASE-HYDROLASE INHIBITOR complex

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