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NADH结合位点与NADH过氧化物酶的催化作用

NADH binding site and catalysis of NADH peroxidase.

作者信息

Stehle T, Claiborne A, Schulz G E

机构信息

Institut für Organische Chemie und Biochemie der Universität, Freiburg im Breisgau, Federal Republic of Germany.

出版信息

Eur J Biochem. 1993 Jan 15;211(1-2):221-6. doi: 10.1111/j.1432-1033.1993.tb19889.x.

Abstract

The structure of the complex between cofactor NADH and the enzyme NADH peroxidase from Streptococcus faecalis 10C1 (Enterococcus faecalis) has been determined by crystal soaking, X-ray data collection, model building of NADH and refinement at 0.24-nm resolution based on the known enzyme structure [Stehle, T., Ahmed, S. A., Claiborne, A. & Schulz, G. E. (1991) J. Mol. Biol. 221, 1325-1344]. Apart from NADH, the catalytic center of the enzyme contains FAD and a cysteine that shuttles between thiolate and sulfenic acid states. Unfortunately, this cysteine was irreversibly oxidized to a cysteine sulfonic acid in the established enzyme structure. Based on the geometry of the catalytic center, we discuss the stabilization of the oxidation-sensitive sulfenic acid and propose a reaction mechanism.

摘要

已通过晶体浸泡、X射线数据收集、NADH的模型构建以及基于已知酶结构在0.24纳米分辨率下的精修,确定了辅因子NADH与粪肠球菌10C1(屎肠球菌)的NADH过氧化物酶之间复合物的结构[施特勒,T.,艾哈迈德,S. A.,克莱伯恩,A. & 舒尔茨,G. E.(1991年)《分子生物学杂志》221卷,1325 - 1344页]。除NADH外,该酶的催化中心含有FAD和一个在硫醇盐和亚磺酸状态之间穿梭的半胱氨酸。不幸的是,在已确立的酶结构中,这个半胱氨酸不可逆地氧化成了半胱氨酸磺酸。基于催化中心的几何结构,我们讨论了对氧化敏感的亚磺酸的稳定性,并提出了一种反应机制。

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