Suplatov Dmitry, Kirilin Evgeny, Takhaveev Vakil, Svedas Vytas
a Faculty of Bioengineering and Bioinformatics , Belozersky Institute of Physicochemical Biology, Lomonosov Moscow State University , Vorobjev hills, 1-40, Moscow , 119991 , Russia .
J Biomol Struct Dyn. 2014;32(11):1752-8. doi: 10.1080/07391102.2013.834514. Epub 2013 Sep 13.
During evolution of proteins from a common ancestor, one functional property can be preserved while others can vary leading to functional diversity. A systematic study of the corresponding adaptive mutations provides a key to one of the most challenging problems of modern structural biology - understanding the impact of amino acid substitutions on protein function. The subfamily-specific positions (SSPs) are conserved within functional subfamilies but are different between them and, therefore, seem to be responsible for functional diversity in protein superfamilies. Consequently, a corresponding method to perform the bioinformatic analysis of sequence and structural data has to be implemented in the common laboratory practice to study the structure-function relationship in proteins and develop novel protein engineering strategies. This paper describes Zebra web server - a powerful remote platform that implements a novel bioinformatic analysis algorithm to study diverse protein families. It is the first application that provides specificity determinants at different levels of functional classification, therefore addressing complex functional diversity of large superfamilies. Statistical analysis is implemented to automatically select a set of highly significant SSPs to be used as hotspots for directed evolution or rational design experiments and analyzed studying the structure-function relationship. Zebra results are provided in two ways - (1) as a single all-in-one parsable text file and (2) as PyMol sessions with structural representation of SSPs. Zebra web server is available at http://biokinet.belozersky.msu.ru/zebra .
在蛋白质从共同祖先进化的过程中,一种功能特性可以保留,而其他特性则可能发生变化,从而导致功能多样性。对相应适应性突变的系统研究为现代结构生物学最具挑战性的问题之一——理解氨基酸取代对蛋白质功能的影响——提供了关键线索。亚家族特异性位点(SSPs)在功能亚家族内是保守的,但在不同亚家族之间存在差异,因此似乎是蛋白质超家族功能多样性的原因。因此,必须在常规实验室实践中实施一种相应的方法来对序列和结构数据进行生物信息学分析,以研究蛋白质的结构-功能关系并开发新的蛋白质工程策略。本文介绍了Zebra网络服务器——一个强大的远程平台,它实现了一种新颖的生物信息学分析算法来研究不同的蛋白质家族。它是第一个在不同功能分类水平上提供特异性决定因素的应用程序,因此能够解决大型超家族复杂的功能多样性问题。通过实施统计分析来自动选择一组高度显著的SSPs,将其用作定向进化或合理设计实验的热点,并用于分析研究结构-功能关系。Zebra的结果以两种方式提供——(1)作为一个单一的、一体化的可解析文本文件,(2)作为具有SSPs结构表示的PyMol会话。Zebra网络服务器可在http://biokinet.belozersky.msu.ru/zebra上获取。