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Structure paper

TitleDiscovery of b-homophenylalanine based pyrrolidin-2-ylmethyl amides and sulfonamides as highly potent and selective inhibitors of dipeptidyl peptidase IV
Journal, issue, pagesTo be Published
Publish dateApr 9, 2009 (structure data deposition date)
AuthorsNordhoff, S. / Cerezo-Galvez, S. / Deppe, H. / Hill, O. / Lopez-Canet, M. / Rummey, C. / Thiemann, M. / Matassa, V.G. / Edwards, P.J. / Feurer, A.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution2.66 Å
Structure data

PDB-3h0c:
Crystal Structure of Human Dipeptidyl Peptidase IV (CD26) in Complex with a Reversed Amide Inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.66 Å

Chemicals

ChemComp-NAG:
2-acetamido-2-deoxy-beta-D-glucopyranose

ChemComp-PS4:
N-({(2S)-1-[(3R)-3-amino-4-(3-chlorophenyl)butanoyl]pyrrolidin-2-yl}methyl)-3-(methylsulfonyl)benzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / COMPLEX (HYDROLASE-INHIBITOR) / DPP-IV / DIABETES MELLITUS / DRUG DESIGN / SERINE PROTEASE / AMINOPEPTIDASE / GLYCOPROTEIN / PROTEASE / SIGNAL-ANCHOR / TRANSMEMBRANE / Cell membrane / Disulfide bond / Membrane / Secreted

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