埋藏氯立体化学在蛋白质数据库中的应用

IF 2.222 Q3 Biochemistry, Genetics and Molecular Biology
Oliviero Carugo
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引用次数: 45

摘要

尽管氯阴离子参与了基本的生物过程,但它与蛋白质的相互作用却鲜为人知。特别是,我们缺乏对其协调领域的系统调查。对含有至少一个氯阴离子的1739个高分辨率(<2)晶体结构的非冗余集(成对序列同一性)的分析表明,氯化物的第一配位球基本上由氢键供体构成。在带正电的侧链中,精氨酸与氯化物的相互作用比赖氨酸频繁得多。虽然最常见的配位数是4,但当配位数为5时,配位立体化学更接近预期的几何形状,这表明这是氯化物与蛋白质相互作用时倾向的配位数。这些分析的结果在解释、描述和验证含有氯阴离子的新蛋白质晶体结构方面是有用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Buried chloride stereochemistry in the Protein Data Bank

Buried chloride stereochemistry in the Protein Data Bank

Despite the chloride anion is involved in fundamental biological processes, its interactions with proteins are little known. In particular, we lack a systematic survey of its coordination spheres.

The analysis of a non-redundant set (pairwise sequence identity?<?30%) of 1739 high resolution (<2??) crystal structures that contain at least one chloride anion shows that the first coordination spheres of the chlorides are essentially constituted by hydrogen bond donors. Amongst the side-chains positively charged, arginine interacts with chlorides much more frequently than lysine. Although the most common coordination number is 4, the coordination stereochemistry is closer to the expected geometry when the coordination number is 5, suggesting that this is the coordination number towards which the chlorides tend when they interact with proteins.

The results of these analyses are useful in interpreting, describing, and validating new protein crystal structures that contain chloride anions.

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来源期刊
BMC Structural Biology
BMC Structural Biology 生物-生物物理
CiteScore
3.60
自引率
0.00%
发文量
0
期刊介绍: BMC Structural Biology is an open access, peer-reviewed journal that considers articles on investigations into the structure of biological macromolecules, including solving structures, structural and functional analyses, and computational modeling.
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