Stereochemical dynamics of aliphatic hydroxylation by cytochrome P-450

This publication has 18 references indexed in Scilit:

• Functional differences between peroxidase compound I and the cytochrome P-450 reactive oxygen intermediate.
  Journal of Biological Chemistry, 1983
• The complete amino acid sequence of rabbit phenobarbital-induced liver microsomal cytochrome P-450.
  Journal of Biological Chemistry, 1983
• Steric course of hydroxylation at primary carbon atoms. Biosynthesis of 1-octanol from (1R)- and (1S)-[1-3H,2H,1H; 1-14C]octane by rat liver microsomes
  Journal of the American Chemical Society, 1982
• Stereochemistry and deuterium isotope effects in camphor hydroxylation by the cytochrome P450cam monooxygenase system
  Biochemistry, 1982
• Electron pathways in catalase and peroxidase enzymic catalysis. Metal and macrocycle oxidations of iron porphyrins and chlorins
  Journal of the American Chemical Society, 1981
• Quantum-chemical studies of model cytochrome P450 hydrocarbon oxidation mechanisms. 1. A MINDO/3 study of hydroxylation and epoxidation pathways for methane and ethylene
  Journal of the American Chemical Society, 1980
• Steroid binding properties of beef adrenal cortical cytochrome P-450 which catalyzes the conversion of cholesterol into pregnenolone.
  Journal of Biological Chemistry, 1979
• Aliphatic hydroxylation by highly purified liver microsomal cytochrome P-450. Evidence for a carbon radical intermediate
  Biochemical and Biophysical Research Communications, 1978
• Properties of electrophoretically homogeneous phenobarbital-inducible and beta-naphthoflavone-inducible forms of liver microsomal cytochrome P-450
  Journal of Biological Chemistry, 1976
• Haem accessibility in cytochrome P-450 from rabbit liver. A proton magnetic relaxation study by stereochemical probes
  Biochimica et Biophysica Acta (BBA) - Protein Structure, 1976