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MDM-TASK-web:用于分析蛋白质动力学的MD-TASK和MODE-TASK网络服务器。

MDM-TASK-web: MD-TASK and MODE-TASK web server for analyzing protein dynamics.

作者信息

Sheik Amamuddy Olivier, Glenister Michael, Tshabalala Thulani, Tastan Bishop Özlem

机构信息

Research Unit in Bioinformatics (RUBi), Department of Biochemistry and Microbiology, Rhodes University, Makhanda 6140, South Africa.

出版信息

Comput Struct Biotechnol J. 2021 Sep 2;19:5059-5071. doi: 10.1016/j.csbj.2021.08.043. eCollection 2021.

Abstract

The web server, MDM-TASK-web, combines the MD-TASK and MODE-TASK software suites, which are aimed at the coarse-grained analysis of static and all-atom MD-simulated proteins, using a variety of non-conventional approaches, such as dynamic residue network analysis, perturbation-response scanning, dynamic cross-correlation, essential dynamics and normal mode analysis. Altogether, these tools allow for the exploration of protein dynamics at various levels of detail, spanning single residue perturbations and weighted contact network representations, to global residue centrality measurements and the investigation of global protein motion. Typically, following molecular dynamic simulations designed to investigate intrinsic and extrinsic protein perturbations (for instance induced by allosteric and orthosteric ligands, protein binding, temperature, pH and mutations), this selection of tools can be used to further describe protein dynamics. This may lead to the discovery of key residues involved in biological processes, such as drug resistance. The server simplifies the set-up required for running these tools and visualizing their results. Several scripts from the tool suites were updated and new ones were also added and integrated with 2D/3D visualization via the web interface. An embedded work-flow, integrated documentation and visualization tools shorten the number of steps to follow, starting from calculations to result visualization. The Django-powered web server (available at https://mdmtaskweb.rubi.ru.ac.za/) is compatible with all major web browsers. All scripts implemented in the web platform are freely available at https://github.com/RUBi-ZA/MD-TASK/tree/mdm-task-web and https://github.com/RUBi-ZA/MODE-TASK/tree/mdm-task-web.

摘要

网络服务器MDM-TASK-web整合了MD-TASK和MODE-TASK软件套件,其旨在使用多种非常规方法对静态和全原子分子动力学模拟的蛋白质进行粗粒度分析,这些方法包括动态残基网络分析、扰动响应扫描、动态交叉相关、主成分动力学分析和简正模式分析。总之,这些工具能够在不同细节层面探索蛋白质动力学,范围涵盖单个残基扰动和加权接触网络表示,到全局残基中心性测量以及全局蛋白质运动研究。通常,在设计用于研究蛋白质内在和外在扰动(例如由变构和正构配体、蛋白质结合、温度、pH值和突变引起的扰动)的分子动力学模拟之后,可使用这一系列工具进一步描述蛋白质动力学。这可能会发现参与生物过程(如耐药性)的关键残基。该服务器简化了运行这些工具及其结果可视化所需的设置。工具套件中的几个脚本已更新,还添加了新脚本,并通过网络界面与二维/三维可视化集成。从计算到结果可视化,嵌入式工作流程、集成文档和可视化工具缩短了所需的步骤数量。由Django驱动的网络服务器(可在https://mdmtaskweb.rubi.ru.ac.za/获取)与所有主流网络浏览器兼容。网络平台中实现的所有脚本均可在https://github.com/RUBi-ZA/MD-TASK/tree/mdm-task-web和https://github.com/RUBi-ZA/MODE-TASK/tree/mdm-task-web上免费获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceaa/8455658/2e9cc8dbdc5e/gr1.jpg

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