研究协同进化信号的统计条件,使算法预测蛋白质伙伴。

IF 5.6 2区 化学 Q1 CHEMISTRY, MEDICINAL
José Fiorote,João Alves,Letícia Stock,Werner Treptow
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引用次数: 0

摘要

本研究考察了协同进化信号的统计条件,该信号允许基于氨基酸序列而不是3D结构的蛋白质伴侣的算法预测。引入了一个基于共同进化信息的马尔可夫随机模型来预测正确蛋白质伴侣的数量。该模型使用泊松混合正态分布来定义状态概率,关键参数包括蛋白质序列总数M、共同进化信息间隙α和方差σ02。该模型表明,最大化共同进化信息的算法方法不能有效地解决大量序列M≥100的蛋白质家族中的伙伴。该模型表明,忽略相似序列之间的不匹配可以提高真阳性(TP)率。根据{α, σ02},这种方法可以区分具有微小误差的优化解和其他退化解。我们的发现使得蛋白质家族的先验分类能够通过忽略相似序列之间的微小误差来可靠地预测伴侣,从而促进了对大型蛋白质数据集的共同进化模型的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating Statistical Conditions of Coevolutionary Signals that Enable Algorithmic Predictions of Protein Partners.
This study examines the statistical conditions of coevolutionary signals that allow algorithmic predictions of protein partners based on amino acid sequences rather than 3D structures. It introduces a Markov stochastic model that predicts the number of correct protein partners based on coevolutionary information. The model defines state probabilities using a Poisson mixture of normal distributions, with key parameters including the total number of protein sequences M, the coevolutionary information gap α, and variance σ02. The model suggests that algorithmic approaches that maximize coevolutionary information cannot effectively resolve partners in protein families with a large number of sequences M ≥ 100. The model shows that true-positive (TP) rates can be enhanced by disregarding mismatches among similar sequences. This approach allows a distinction, in terms of {α, σ02}, between optimized solutions with trivial errors and other degenerate solutions. Our findings enable the a priori classification of protein families where partners can be reliably predicted by ignoring trivial errors between similar sequences, advancing the understanding of coevolutionary models for large protein data sets.
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来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
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