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烯醇化酶的作用机制:分辨率为2.2埃的烯醇化酶-Mg2(+)-2-磷酸甘油酸/磷酸烯醇丙酮酸复合物的晶体结构

Mechanism of enolase: the crystal structure of enolase-Mg2(+)-2-phosphoglycerate/phosphoenolpyruvate complex at 2.2-A resolution.

作者信息

Lebioda L, Stec B

机构信息

Department of Chemistry, University of South Carolina, Columbia 29208.

出版信息

Biochemistry. 1991 Mar 19;30(11):2817-22. doi: 10.1021/bi00225a012.

Abstract

Enolase in the presence of Mg2+ catalyzes the elimination of H2O from 2-phosphoglyceric acid (PGA) to form phosphoenolpyruvate (PEP) and the reverse reaction, the hydration of PEP to PGA. The structure of the ternary complex yeast enolase-Mg2(+)-PGA/PEP has been determined by X-ray diffraction and refined by crystallographic restrained least-squares to an R = 16.9% for those data with I/sigma (I) greater than or equal to 2 to 2.2-A resolution with a good geometry of the model. The structure indicates the substrate molecule in the active site has its hydroxyl group coordinated to the Mg2+ ion. The carboxylic group interacts with the side chains of His373 and Lys396. The phosphate group is H-bonded to the guanidinium group of Arg374. A water molecule H-bonded to the carboxylic groups of Glu168 and Glu211 is located at a 2.6-A distance from carbon-2 of the substrate in the direction of its proton. We propose that this cluster functions as the base abstracting the proton in the catalytic process. The proton is probably transferred, first to the water molecule, then to Glu168, and further to the substrate hydroxyl to form a water molecule. Some analogy is apparent between the initial stages of the enolase reverse reaction, the hydration of PEP, and the proteolytic mechanism of the metallohydrolases carboxypeptidase A and thermolysin. The substrate/product binding is accompanied by large movements of loops Ser36-His43 and Ser158-Gly162. The role of these conformational changes is not clear at this time.

摘要

在Mg2+存在的情况下,烯醇化酶催化2-磷酸甘油酸(PGA)脱去H2O形成磷酸烯醇式丙酮酸(PEP),以及逆反应,即PEP水合生成PGA。通过X射线衍射确定了酵母烯醇化酶-Mg2(+)-PGA/PEP三元复合物的结构,并通过晶体学约束最小二乘法进行精修,对于I/σ(I)大于或等于2至2.2 Å分辨率且模型几何结构良好的数据,R值为16.9%。该结构表明活性位点中的底物分子其羟基与Mg2+离子配位。羧基与His373和Lys396的侧链相互作用。磷酸基团通过氢键与Arg374的胍基相连。一个与Glu168和Glu211的羧基形成氢键的水分子在底物碳-2质子方向距离底物2.6 Å处。我们提出这个簇在催化过程中作为夺取质子的碱起作用。质子可能首先转移到水分子,然后到Glu168,再进一步到底物羟基形成一个水分子。烯醇化酶逆反应的初始阶段,即PEP的水合作用,与金属水解酶羧肽酶A和嗜热菌蛋白酶的蛋白水解机制之间存在一些明显的相似之处。底物/产物结合伴随着Ser36-His43和Ser158-Gly162环的大幅移动。目前这些构象变化的作用尚不清楚。

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