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TitleFolding Then Binding vs Folding Through Binding in Macrocyclic Peptide Inhibitors of Human Pancreatic alpha-Amylase.
Journal, issue, pagesAcs Chem. Biol., Vol. 14, Page 1751-1759, Year 2019
Publish dateDec 1, 2016 (structure data deposition date)
AuthorsGoldbach, L. / Vermeulen, B.J.A. / Caner, S. / Liu, M. / Tysoe, C. / van Gijzel, L. / Yoshisada, R. / Trellet, M. / van Ingen, H. / Brayer, G.D. ...Goldbach, L. / Vermeulen, B.J.A. / Caner, S. / Liu, M. / Tysoe, C. / van Gijzel, L. / Yoshisada, R. / Trellet, M. / van Ingen, H. / Brayer, G.D. / Bonvin, A.M.J.J. / Jongkees, S.A.K.
External linksAcs Chem. Biol. / PubMed:31241898
MethodsX-ray diffraction
Resolution0.95 - 2.55 Å
Structure data

PDB-5u3a:
Ultra High Resolution Crystal Structure of Human Pancreatic Alpha Amylase
Method: X-RAY DIFFRACTION / Resolution: 0.95 Å

PDB-5va9:
Human pancreatic alpha amylase in complex with peptide inhibitor piHA-L5(d10Y)
Method: X-RAY DIFFRACTION / Resolution: 2.55 Å

Chemicals

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

ChemComp-CL:
Unknown entry

ChemComp-CA:
Unknown entry

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • synthetic construct (others)
KeywordsHYDROLASE / Amylase / Diabetes / Obesity / Glucosyl hydrolase / hydrolase/hydrolase inhibitor / peptide inhibitor complex / hydrolase-hydrolase inhibitor complex

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