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关于NADH的酶促激活作用。

On the enzymatic activation of NADH.

作者信息

Meijers R, Morris R J, Adolph H W, Merli A, Lamzin V S, Cedergren-Zeppezauer E S

机构信息

European Molecular Biology Laboratory, c/o DESY, Notkestrasse 85, 22603 Hamburg, Germany.

出版信息

J Biol Chem. 2001 Mar 23;276(12):9316-21. doi: 10.1074/jbc.M010870200. Epub 2000 Dec 28.

Abstract

Atomic (1 A) resolution x-ray structures of horse liver alcohol dehydrogenase in complex with NADH revealed the formation of an adduct in the active site between a metal-bound water and NADH. Furthermore, a pronounced distortion of the pyridine ring of NADH was observed. A series of quantum chemical calculations on the water-nicotinamide adduct showed that the puckering of the pyridine ring in the crystal structures can only be reproduced when the water is considered a hydroxide ion. These observations provide fundamental insight into the enzymatic activation of NADH for hydride transfer.

摘要

与烟酰胺腺嘌呤二核苷酸(NADH)结合的马肝醇脱氢酶的原子分辨率(1埃)X射线结构显示,在活性位点中,金属结合水与NADH之间形成了加合物。此外,还观察到NADH吡啶环有明显扭曲。对水-烟酰胺加合物进行的一系列量子化学计算表明,只有将水视为氢氧根离子时,才能重现晶体结构中吡啶环的褶皱。这些观察结果为NADH进行氢化物转移的酶促活化提供了基本见解。

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