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1,5-二磷酸核酮糖羧化酶、Mg(II)和激活剂CO2三元复合物在2.3埃分辨率下的晶体结构。

Crystal structure of the ternary complex of ribulose-1,5-bisphosphate carboxylase, Mg(II), and activator CO2 at 2.3-A resolution.

作者信息

Lundqvist T, Schneider G

机构信息

Department of Molecular Biology, Swedish University of Agricultural Sciences, Uppsala.

出版信息

Biochemistry. 1991 Jan 29;30(4):904-8. doi: 10.1021/bi00218a004.

Abstract

The activated ternary complex, enzyme-CO2-Mg(II), of the dimeric ribulose-1,5-bisphosphate carboxylase/oxygenase from Rhodospirillum rubrum can be prepared in the same crystal form that was used for the crystallographic structure determination of the native nonactivated enzyme (Schneider, G., Bränden, C.-I., & Lorimer, G. (1986) J. Mol. Biol. 187, 141-143). The three-dimensional structure of the activated enzyme has been determined to a nominal resolution of 2.3 A by protein crystallographic methods. The activator CO2 forms a carbamate with Lys191, located at the bottom of the funnel-shaped active site. In both subunits, this labile adduct is stabilized by a Mg(II) ion, bound to the carbamate and the side chains of Asp193 and Glu194. One solvent molecule was found within the first coordination sphere of the metal ion. The metal-binding site in ribulose-1,5-bisphosphate carboxylase consists thus of at least three protein ligands, all located on loop 2 of the beta/alpha barrel. One additional metal ligand, the side chain of the conserved Asn111, was observed close to the Mg(II) ion in the B-subunit. Other structural differences at the active site between the activated and nonactivated enzyme are limited to side-chain positions. Nevertheless, it is obvious that the hydrogen-bonding pattern in the vicinity of the activator site is completely altered.

摘要

来自红螺菌的二聚体核酮糖-1,5-二磷酸羧化酶/加氧酶的活化三元复合物,即酶-CO₂-Mg(II),可以以与用于天然非活化酶晶体结构测定相同的晶体形式制备(施奈德,G.,布伦登,C.-I.,&洛里默,G.(1986年)《分子生物学杂志》187卷,141 - 143页)。已通过蛋白质晶体学方法将活化酶的三维结构测定到名义分辨率为2.3埃。活化剂CO₂与位于漏斗形活性位点底部的赖氨酸191形成氨基甲酸盐。在两个亚基中,这种不稳定的加合物通过一个Mg(II)离子稳定,该离子与氨基甲酸盐以及天冬氨酸193和谷氨酸194的侧链结合。在金属离子的第一配位球内发现了一个溶剂分子。因此,核酮糖-1,5-二磷酸羧化酶中的金属结合位点由至少三个蛋白质配体组成,它们都位于β/α桶的环2上。在B亚基中,靠近Mg(II)离子观察到另一个金属配体,即保守的天冬酰胺111的侧链。活化酶和非活化酶在活性位点的其他结构差异仅限于侧链位置。然而,很明显活化剂位点附近的氢键模式完全改变了。

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