Angewandte Chemie International Edition · 2007 · 74 citations · 19 references
Life SciencesBiochemistryToxicologyEnzymologyMetabolismRedox BiochemistryCytochrome P450 EnzymesCytochrome P450-mediated MetabolismOxidative MetabolismRedox EnzymesSulfur ChemistrySulfur MetabolismCytochrome P450 CatalysisCytochrome P450 IsoenzymesCytochrome P450 Metabolic PathwaysCytochrome P450 OxidationCytochrome P450 PathwaysCytochrome P450 Reaction MechanismsCytochrome P450-mediated OxidationSulfur Oxidation
Clarifying a conundrum: The question of whether Compound I or Compound 0 (Cpd I or Cpd 0) is the reactive oxidant in the sulfoxidation of thiafatty acids by P450 is addressed by theory, which demonstrates that Cpd I leads to an extremely fast process, while Cpd 0 is at least six orders of magnitude slower. Most likely, thiafatty acids promote Cpd I formation even in the T→A mutant of P450BM3.
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Epoxidation of Olefins by Hydroperoxo−Ferric Cytochrome P450
Shengxi Jin, Thomas M. Makris, Thomas A. Bryson et al. · Journal of the American Chemical Society · 2003 · 145 citations