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Structure paper

TitleDistinctive binding modes and inhibitory mechanisms of two peptidic inhibitors of urokinase-type plasminogen activator with isomeric P1 residues.
Journal, issue, pagesInt. J. Biochem. Cell Biol., Vol. 62, Page 88-92, Year 2015
Publish dateNov 24, 2014 (structure data deposition date)
AuthorsJiang, L. / Zhao, B. / Xu, P. / Srensen, H.P. / Jensen, J.K. / Christensen, A. / Hosseini, M. / Nielsen, N.C. / Jensen, K.J. / Andreasen, P.A. / Huang, M.
External linksInt. J. Biochem. Cell Biol. / PubMed:25744057
MethodsX-ray diffraction
Resolution1.6 - 2.1 Å
Structure data

PDB-4x0w:
The crystal structure of mupain-1-17 in complex with murinised human uPA
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-4x1p:
The crystal structure of mupain-1-17 in complex with murinised human uPA at pH4.6
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

Chemicals

ChemComp-MRZ:
piperidine-1-carboximidamide

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

ChemComp-PGE:
TRIETHYLENE GLYCOL

Source
  • homo sapiens (human)
  • synthetic construct (others)
KeywordsHYDROLASE INHIBITOR/HYDROLASE / Serine protease / peptidic inhibitor / HYDROLASE-HYDROLASE INHIBITOR complex / HYDROLASE INHIBITOR-HYDROLASE complex / HYDROLASE/HYDROLASE INHIBITOR / uPA

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