Molecular Basis for Olefin Rearrangement in the Gephyronic Acid Polyketide Synthase
Author:
Affiliation:
1. Department of Biological Chemistry and Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109, United States
2. Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, United States
Funder
Horace H. Rackham School of Graduate Studies, University of Michigan
National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
American Chemical Society (ACS)
Subject
Molecular Medicine,General Medicine,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acschembio.8b00645
Reference38 articles.
1. Tylosin polyketide synthase module 3: stereospecificity, stereoselectivity and steady-state kinetic analysis of β-processing domains via diffusible, synthetic substrates
2. Functional Characterization of a Dehydratase Domain from the Pikromycin Polyketide Synthase
3. Stereospecific Formation of E- and Z-Disubstituted Double Bonds by Dehydratase Domains from Modules 1 and 2 of the Fostriecin Polyketide Synthase
4. Structure and Stereospecificity of the Dehydratase Domain from the Terminal Module of the Rifamycin Polyketide Synthase
5. Vinylogous Dehydration by a Polyketide Dehydratase Domain in Curacin Biosynthesis
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