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Structure paper

TitleSelection of High-Affinity Peptidic Serine Protease Inhibitors with Increased Binding Entropy from a Back-Flip Library of Peptide-Protease Fusions.
Journal, issue, pagesJ. Mol. Biol., Vol. 427, Page 3110-3122, Year 2015
Publish dateApr 25, 2015 (structure data deposition date)
AuthorsSrensen, H.P. / Xu, P. / Jiang, L. / Kromann-Hansen, T. / Jensen, K.J. / Huang, M. / Andreasen, P.A.
External linksJ. Mol. Biol. / PubMed:26281711
MethodsX-ray diffraction
Resolution1.9 - 2.06 Å
Structure data

PDB-4zhl:
The crystal structure of mupain-1-IG in complex with murinised human uPA at pH7.4
Method: X-RAY DIFFRACTION / Resolution: 2.06 Å

PDB-4zhm:
The crystal structure of mupain-1--16-IG in complex with murinised human uPA at pH7.4
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-HOH:
WATER

ChemComp-MRZ:
piperidine-1-carboximidamide

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

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