Fundación Instituto Leloir. Av. Patricias Argentinas 435 - Ciudad Autónoma de Buenos Aires, Argentina. CP C1405BWE.
Nucleic Acids Res. 2018 Jul 2;46(W1):W323-W328. doi: 10.1093/nar/gky419.
Correlated mutations between residue pairs in evolutionarily related proteins arise from constraints needed to maintain a functional and stable protein. Identifying these inter-related positions narrows down the search for structurally or functionally important sites. MISTIC is a server designed to assist users to calculate covariation in protein families and provide them with an interactive tool to visualize the results. Here, we present MISTIC2, an update to the previous server, that allows to calculate four covariation methods (MIp, mfDCA, plmDCA and gaussianDCA). The results visualization framework has been reworked for improved performance, compatibility and user experience. It includes a circos representation of the information contained in the alignment, an interactive covariation network, a 3D structure viewer and a sequence logo. Others components provide additional information such as residue annotations, a roc curve for assessing contact prediction, data tables and different ways of filtering the data and exporting figures. Comparison of different methods is easily done and scores combination is also possible. A newly implemented web service allows users to access MISTIC2 programmatically using an API to calculate covariation and retrieve results. MISTIC2 is available at: https://mistic2.leloir.org.ar.
进化相关蛋白质中残基对之间的相关突变是由于维持功能和稳定蛋白质所需的约束条件引起的。确定这些相互关联的位置可以缩小寻找结构或功能重要位点的范围。MISTIC 是一个旨在帮助用户计算蛋白质家族中的共变并为他们提供可视化结果的交互式工具的服务器。在这里,我们介绍了 MISTIC2,这是对之前服务器的更新,它允许计算四种共变方法(MIp、mfDCA、plmDCA 和 gaussianDCA)。结果可视化框架经过重新设计,以提高性能、兼容性和用户体验。它包括对齐信息的 circos 表示、交互式共变网络、3D 结构查看器和序列 logo。其他组件提供了其他信息,如残基注释、用于评估接触预测的 ROC 曲线、数据表以及过滤数据和导出图形的不同方法。可以轻松比较不同的方法,并且还可以组合得分。新实现的 Web 服务允许用户使用 API 以编程方式访问 MISTIC2 来计算共变并检索结果。MISTIC2 可在以下网址获得:https://mistic2.leloir.org.ar。