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PMID: 15237977 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A predictive pattern of computed barriers for C-h hydroxylation by compound I of cytochrome p450.

Journal of the American Chemical Society ·Vol. 126 ·No. 27 ·2004-07-14 ·Pages 8362-3

de Visser SP, Kumar D, Cohen S, Shacham R, Shaik S

Abstract

The communication presents DFT calculations of 10 different C-H hydroxylation barriers by the active species of the enzyme cytochrome P450. The work demonstrates the existence of an excellent barrier-bond energy correlation. The so-obtained equation of the straight line is demonstrated to be useful for predicting barriers of related C-H activation processes, as well as for assessing barrier heights within the protein environment. This facility is demonstrated be estimating the barrier of camphor hydroxylation by P450cam.

MeSH Terms
Alkanes/chemistry,metabolism Benzene Derivatives/chemistry,metabolism Camphor 5-Monooxygenase/chemistry,metabolism Cytochrome P-450 Enzyme System/chemistry,metabolism Ferric Compounds/chemistry,metabolism Hydrogen/chemistry,metabolism Hydroxylation Iron Compounds/chemistry,metabolism Phenols/chemistry,metabolism Thermodynamics
Chemicals
Alkanes Benzene Derivatives Ferric Compounds Iron Compounds Phenols ferric oxide phenoxy radical Hydrogen Cytochrome P-450 Enzyme System Camphor 5-Monooxygenase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
de Visser Sam P
Department of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry, The Hebrew University of Jerusalem, 91904 Jerusalem, Israel.
Kumar Devesh
Cohen Shimrit
Shacham Ronen
Shaik Sason
Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2004-07-14
Pages
8362-3
Language
English
Region
United States
NLM ID
7503056
Subset
IM
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