The effect of heme environment on the hydrogen abstraction reaction of camphor in P450cam catalysis: a QM/MM study

J Am Chem Soc. 2006 Mar 29;128(12):3924-5. doi: 10.1021/ja058196w.

Abstract

The discrepancies between the published QM/MM studies (Schöneboom, J. C.; Cohen, S.; Lin, H.; Shaik, S.; Thiel, W. J. Am. Chem. Soc. 2004, 126, 4017; Guallar, V.; Friesner, R. A. J. Am. Chem. Soc. 2004, 126, 8501) on H-abstraction of camphor in P450cam have largely been resolved. The crystallographic water molecule 903 situated near the oxo atom of Compound I acts as a catalyst for H-abstraction, lowering the barrier by about 4 kcal/mol. Spin density at the A-propionate side chain of heme can occur in the case of incomplete screening but has no major effect on the computed barrier.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Camphor / chemistry*
  • Camphor / metabolism
  • Camphor 5-Monooxygenase / chemistry*
  • Camphor 5-Monooxygenase / metabolism
  • Catalysis
  • Heme / chemistry*
  • Heme / metabolism
  • Hydrogen / chemistry
  • Hydrogen / metabolism
  • Hydroxylation
  • Quantum Theory

Substances

  • Heme
  • Camphor
  • Hydrogen
  • Camphor 5-Monooxygenase