Insights into the mechanisms of adenosylcobalamin (coenzyme B12)-dependent enzymes from rapid chemical quench experiments
Author:
Affiliation:
1. Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, U.S.A., and Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, U.S.A.
Abstract
Publisher
Portland Press Ltd.
Subject
Biochemistry
Link
https://portlandpress.com/biochemsoctrans/article-pdf/37/2/336/543600/bst0370336.pdf
Reference39 articles.
1. Coenzyme B12 (cobalamin)-dependent enzymes;Marsh;Essays Biochem.,1999
2. Coenzyme B12-dependent glutamate mutase;Marsh;Bioorganic Chem.,2000
3. Radical peregrinations catalyzed by coenzyme B12-dependent enzymes;Banerjee;Biochemistry,2001
4. Adenosylcobalamin-dependent isomerases: new insights into structure and mechanism;Marsh;Curr. Opin. Chem. Biol.,2001
5. Radical carbon skeleton rearrangements: catalysis by coenzyme B12-dependent mutases;Banerjee;Chem. Rev.,2003
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2. Structure‐Based Demystification of Radical Catalysis by a Coenzyme B 12 Dependent Enzyme—Crystallographic Study of Glutamate Mutase with Cofactor Homologues;Angewandte Chemie International Edition;2022-07-21
3. Structure‐Based Demystification of Radical Catalysis by a Coenzyme B 12 Dependent Enzyme—Crystallographic Study of Glutamate Mutase with Cofactor Homologues;Angewandte Chemie;2022-07-21
4. Optimal electrostatic interactions between substrate and protein are essential for radical chemistry in ornithine 4,5-aminomutase;Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics;2017-08
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