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一组经修订的蛋白质中β-转角形成的势能。

A revised set of potentials for beta-turn formation in proteins.

作者信息

Hutchinson E G, Thornton J M

机构信息

Department of Biochemistry and Molecular Biology, University College, London, United Kingdom.

出版信息

Protein Sci. 1994 Dec;3(12):2207-16. doi: 10.1002/pro.5560031206.

Abstract

Three thousand eight hundred ninety-nine beta-turns have been identified and classified using a nonhomologous data set of 205 protein chains. These were used to derive beta-turn positional potentials for turn types I' and II' for the first time and to provide updated potentials for formation of the more common types I, II, and VIII. Many of the sequence preferences for each of the 4 positions in turns can be rationalized in terms of the formation of stabilizing hydrogen bonds, preferences for amino acids to adopt a particular conformation in phi, psi space, and the involvement of turn types I' and II' in beta-hairpins. Only 1,632 (42%) of the turns occur in isolation; the remainder have at least 1 residue in common with another turn and have hence been classified as multiple turns. Several types of multiple turn have been identified and analyzed.

摘要

利用包含205条蛋白质链的非同源数据集,已识别并分类出3899个β-转角。首次利用这些数据推导了I'型和II'型转角的β-转角位置势,并为更常见的I型、II型和VIII型转角的形成提供了更新的势。转角中4个位置各自的许多序列偏好都可以通过形成稳定氢键、氨基酸在φ、ψ空间中采用特定构象的偏好以及I'型和II'型转角参与β-发夹结构来解释。只有1632个(42%)转角是孤立出现的;其余转角至少有1个残基与另一个转角共用,因此被归类为多重转角。已识别并分析了几种类型的多重转角。

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引用本文的文献

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Satisfying hydrogen bonding potential in proteins.满足蛋白质中的氢键形成潜力。
J Mol Biol. 1994 May 20;238(5):777-93. doi: 10.1006/jmbi.1994.1334.
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Analysis of two-residue turns in proteins.蛋白质中双残基转角的分析。
J Mol Biol. 1994 May 20;238(5):733-47. doi: 10.1006/jmbi.1994.1332.
3
Characterization of multiple bends in proteins.蛋白质中多个弯曲的表征。
Biopolymers. 1980 Jun;19(6):1183-210. doi: 10.1002/bip.1980.360190607.
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The anatomy and taxonomy of protein structure.蛋白质结构的解剖学与分类学。
Adv Protein Chem. 1981;34:167-339. doi: 10.1016/s0065-3233(08)60520-3.

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