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柠檬酸合酶与草酰乙酸和S-丙酮基辅酶A复合物的晶体结构分析及分子模型

Crystal structure analysis and molecular model of a complex of citrate synthase with oxaloacetate and S-acetonyl-coenzyme A.

作者信息

Wiegand G, Remington S, Deisenhofer J, Huber R

出版信息

J Mol Biol. 1984 Mar 25;174(1):205-19. doi: 10.1016/0022-2836(84)90373-5.

Abstract

The crystal structure of the complex of pig heart citrate synthase and oxaloacetate in the presence of the potent inhibitor S-acetonyl coenzyme A has been determined at a nominal resolution of 2.9 A by Patterson search techniques and refined by restrained crystallographic refinement. The complex crystallizes in the presence of polyvinylpyrrolidone in space group P4(3)2(1)2 with a = 101.5 A and c = 224.6 A, with one dimeric molecule of molecular weight 100,000 in the asymmetric unit. The crystallographic R factor is 0.194 for the 14,332 unique reflections between 6.0 and 2.9 A resolution. The structures of two forms of citrate synthase in the presence and absence of product molecules have been determined recently and shown to differ in the relative arrangement of the large and small domains ("closed" and "open" forms). The third crystal form described here is also closed, but there is substantial rearrangement within the small domain relative to either of the other crystal forms. We conclude that this is a third structural state of the enzyme, and catalytic activity of the enzyme depends on structural changes during the course of the reaction affecting domain conformation also. The three structures are compared, and it is shown that the large domain is considerably more rigid than the small domain. The conformation of the small domain adapts to the ligand. The inhibitor, and the "coenzyme-A-binding segment" of the enzyme are disordered. No electron density is observed for the inhibitor, and only weak density for the coenzyme-A-binding segment. Electron density for oxaloacetate is well defined. It binds in a very similar manner to citrate.

摘要

在强效抑制剂S-乙酰丙酮辅酶A存在的情况下,利用帕特森搜索技术以2.9埃的名义分辨率测定了猪心柠檬酸合酶与草酰乙酸复合物的晶体结构,并通过约束晶体学精修进行了优化。该复合物在聚乙烯吡咯烷酮存在下结晶,空间群为P(4)(3)2(1)2,a = 101.5埃,c = 224.6埃,不对称单位中有一个分子量为100,000的二聚体分子。在6.0至2.9埃分辨率之间的14,332个独立反射中,晶体学R因子为0.194。最近已经确定了存在和不存在产物分子时柠檬酸合酶的两种形式的结构,结果表明它们在大结构域和小结构域的相对排列上有所不同(“封闭”和“开放”形式)。这里描述的第三种晶体形式也是封闭的,但相对于其他两种晶体形式,小结构域内有大量重排。我们得出结论,这是该酶的第三种结构状态,并且酶的催化活性取决于反应过程中影响结构域构象的结构变化。对这三种结构进行了比较,结果表明大结构域比小结构域刚性大得多。小结构域的构象适应配体。抑制剂以及酶的“辅酶A结合片段”无序。未观察到抑制剂的电子密度,辅酶A结合片段只有微弱的密度。草酰乙酸的电子密度定义明确。它与柠檬酸的结合方式非常相似。

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