[基于结构数据的硫氰酸脱氢酶作用机理]。

Q3 Medicine
K M Polyakov, S Gavryushov
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引用次数: 0

摘要

硫氰酸脱氢酶是一种催化硫氰酸盐离子转化为氰酸盐离子的酶,产生两个电子、两个质子和一个中性的硫原子。从硫酸弧菌悖论硫氰酸脱氢酶的早期结构被解决。尽管结构质量不完美(晶体的孪生和明显的各向异性,铜离子的不完全占据,缺乏与底物类似物的配合物的数据),但有人提出了基于这些结构的酶功能机制。近年来,在原子分辨率上已经解决了甲基营养菌中游离蛋白及其与硫脲络合物的相关酶的基因修饰拷贝的结构。在新结构中,铜离子完全占据活性位点。在这些结构中,可以可靠地识别具有开放和封闭活性位点的蛋白质分子的两种构象。新的结构高分辨率数据也使我们能够确定两种构象中铜离子不同状态叠加的存在。在每种状态下,铜离子具有不同的氧化度,不同的配体和部分占位。根据离子配位来确定离子的电荷。在具有封闭活性位点的蛋白质分子中,观察到与抑制剂(硫脲离子)和分子氧的络合物。与硫脲的配合物使我们能够模拟硫氰酸盐离子与酶分子的结合。结合开放构象和封闭构象结构的变化,提出了一种攻击氧配体活化的机制。讨论了一种新的酶促反应方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Mechanism of Thiocyanate Dehydrogenase Functioning Based on Structural Data].

Thiocyanate dehydrogenase is enzyme catalyzing transformation of a thiocyanate ion into a cyanate ion with outcome of two electrons, two protons and a neutral atom of sulphur. Earlier structures of thiocyanate dehydrogenase from Thioalkalivibrio paradoxus were solved. Despite not perfect quality of the structures (twinning and pronounced anisotropy of the crystals, incomplete occupancy of the copper ions, absence of data for complexes with analogues of the substrate), there was suggested a mechanism of the enzyme functioning based on those structures. Recently at atomic resolution there have been solved structures of a gene-modified copy of relative enzyme from Ptlomicrobium methylotrophicum for free protein and its complex with thiourea. In the new structures copper ions of the active site possess complete occupancy. In these structures it is possible to reliably identify two conformations of the protein molecule with opened and closed active sites. The new structural high resolution data also allowed us to determine the presence of the superposition of different states of the copper ions for each of the two conformations. In each state the copper ions have different oxidation degrees, different corresponding ligands and partial occupancies. The ion charges were determined according to the ions coordination. In the protein molecule with the closed active site the complexes with inhibitor (thiourea ion) and molecular oxygen are observed. The complex with thiourea allows us to model binding of thiocyanate ion to the enzyme molecule. Taking into account the changes of the structures in the opened and closed conformations, a mechanism of the attacking oxygen ligand activation is suggested. A new scheme of the enzymatic reaction is discussed.

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来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
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