Folding Then Binding vs Folding Through Binding in Macrocyclic Peptide Inhibitors of Human Pancreatic α-Amylase
Author:
Affiliation:
1. Department of Chemical Biology and Drug Discovery, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, 3584 CG Utrecht, The Netherlands
Funder
Government of Canada
European Commission
U.S. Department of Energy
U.S. Department of Health and Human Services
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Publisher
American Chemical Society (ACS)
Subject
Molecular Medicine,General Medicine,Biochemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acschembio.9b00290
Reference54 articles.
1. Structure-Based Design of Inhibitors of Protein-Protein Interactions: Mimicking Peptide Binding Epitopes
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4. RNA Display Methods for the Discovery of Bioactive Macrocycles
5. Model foldamers: applications and structures of stable macrocyclic peptides identified using in vitro selection
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