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蛋白质结构中金属离子与主链羰基相互作用的系统研究。

Systematics in the interaction of metal ions with the main-chain carbonyl group in protein structures.

作者信息

Chakrabarti P

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles 90024.

出版信息

Biochemistry. 1990 Jan 23;29(3):651-8. doi: 10.1021/bi00455a009.

Abstract

An analysis of the geometry of metal binding by peptide carbonyl groups in proteins is presented. Such metal ions are predominantly calcium in known protein structures. Cations tend to be located in the peptide plane, near the C = O bond direction. This distribution differs from that observed for water molecules bound to carbonyl oxygens. Most metal ions are bound to carbonyl oxygens of peptides in turns or in regions with no regular secondary structure. More infrequent binding interactions occur at the C-terminal end of alpha-helices or at the edges and sides of beta-sheets, where the geometrical preferences of the metal-carbonyl interaction may be satisfied. In many proteins carbonyl groups that are one, two, or three residues apart along the polypeptide chain bind to the same cation; these structures show a limited number of main-chain conformations around the metal center.

摘要

本文对蛋白质中肽羰基与金属结合的几何结构进行了分析。在已知的蛋白质结构中,此类金属离子主要为钙。阳离子倾向于位于肽平面内,靠近C=O键的方向。这种分布与结合在羰基氧上的水分子的分布不同。大多数金属离子与肽的羰基氧在转角处或无规则二级结构的区域结合。在α-螺旋的C末端或β-折叠的边缘和侧面发生的结合相互作用较少,在这些位置金属-羰基相互作用的几何偏好可能得到满足。在许多蛋白质中,沿着多肽链相隔一个、两个或三个残基的羰基与同一个阳离子结合;这些结构在金属中心周围显示出有限数量的主链构象。

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