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

被引:88
|
作者
Altun, A
Guallar, V
Friesner, RA
Shaik, S
Thiel, W
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
[2] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63108 USA
[3] Univ Nacl Colombia, Dept Chem, New York, NY 10027 USA
[4] Univ Nacl Colombia, Ctr Biomol Simulat, New York, NY 10027 USA
[5] Hebrew Univ Jerusalem, Dept Organ Chem, IL-91904 Jerusalem, Israel
[6] Hebrew Univ Jerusalem, Lise Meitner Minerva Ctr Computat Quantum Chem, IL-91904 Jerusalem, Israel
关键词
D O I
10.1021/ja058196w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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. Copyright © 2006 American Chemical Society.
引用
收藏
页码:3924 / 3925
页数:2
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