Mechanism of C−H Activation by Diiron Methane Monooxygenases: Quantum Chemical Studies
Author:
Affiliation:
1. Contribution from the Department of Physics, Stockholm University, Box 6730, S-113 85 Stockholm, Sweden, and Chemistry Department, Yale University, 225 Prospect Street, New Haven, Connecticut, 06520-8107
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja963939m
Reference43 articles.
1. Reactions of Non-Heme Iron(II) Centers with Dioxygen in Biology and Chemistry
2. The nature of the copper ions in the membranes containing the particulate methane monooxygenase from Methylococcus capsulatus (Bath).
3. BIOCHEMISTRY OF THE SOLUBLE METHANE MONOOXYGENASE
4. Large Kinetic Isotope Effects in Methane Oxidation Catalyzed by Methane Monooxygenase: Evidence for C−H Bond Cleavage in a Reaction Cycle Intermediate
5. Dioxygen Activation by Enzymes Containing Binuclear Non-Heme Iron Clusters
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