Versatility of Prolyl Oligopeptidase B in Peptide Macrocyclization
Author:
Affiliation:
1. Department of Biochemistry and Molecular Biology, ‡Department of Energy-Plant Research Laboratory, and §Department of Plant Biology, Michigan State University, East Lansing, Michigan 48824, United States
Funder
Basic Energy Sciences
Michigan Economic Development Corporation
Michigan State University
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Biochemistry, Genetics and Molecular Biology (miscellaneous),Biomedical Engineering,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/acssynbio.7b00264
Reference35 articles.
1. The exploration of macrocycles for drug discovery — an underexploited structural class
2. Testing the Conformational Hypothesis of Passive Membrane Permeability Using Synthetic Cyclic Peptide Diastereomers
3. Conformational Selection of Inhibitors and Substrates by Proteolytic Enzymes: Implications for Drug Design and Polypeptide Processing
4. Design of Cyclic Peptides That Bind Protein Surfaces with Antibody-Like Affinity
5. Cyclic peptide therapeutics: past, present and future
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