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利用氨基酸序列指纹图谱预测蛋白质中ADP结合β-α-β折叠的出现。

Prediction of the occurrence of the ADP-binding beta alpha beta-fold in proteins, using an amino acid sequence fingerprint.

作者信息

Wierenga R K, Terpstra P, Hol W G

出版信息

J Mol Biol. 1986 Jan 5;187(1):101-7. doi: 10.1016/0022-2836(86)90409-2.

Abstract

An amino acid sequence "fingerprint" has been derived that can be used to test if a particular sequence will fold into a beta alpha beta-unit with ADP-binding properties. It was deduced from a careful analysis of the known three-dimensional structures of ADP-binding beta alpha beta-folds. This fingerprint is in fact a set of 11 rules describing the type of amino acid that should occur at a specific position in a peptide fragment. The total length of this fingerprint varies between 29 and 31 residues. By checking against all possible sequences in a database, it appeared that every peptide, which exactly follows this fingerprint, does indeed fold into an ADP-binding beta alpha beta-unit.

摘要

已经得出一种氨基酸序列“指纹”,可用于测试特定序列是否会折叠成具有ADP结合特性的β-α-β单元。它是通过对已知的ADP结合β-α-β折叠的三维结构进行仔细分析推导出来的。这个指纹实际上是一组11条规则,描述了在肽片段特定位置应出现的氨基酸类型。这个指纹的总长度在29到31个残基之间变化。通过在数据库中与所有可能的序列进行比对,发现每一个完全符合这个指纹的肽确实会折叠成一个ADP结合β-α-β单元。

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