Department of Biotechnology and Biosciences, University of Milano-Bicocca, P.zza della Scienza 2, 20126 Milan, Italy.
J Chem Inf Model. 2012 Jul 23;52(7):1865-74. doi: 10.1021/ci300213c. Epub 2012 Jul 5.
A versatile method to directly identify and analyze short- or long-range coupled or communicating residues in a protein conformational ensemble is of extreme relevance to achieve a complete understanding of protein dynamics and structural communication routes. Here, we present xPyder, an interface between one of the most employed molecular graphics systems, PyMOL, and the analysis of dynamical cross-correlation matrices (DCCM). The approach can also be extended, in principle, to matrices including other indexes of communication propensity or intensity between protein residues, as well as the persistence of intra- or intermolecular interactions, such as those underlying protein dynamics. The xPyder plugin for PyMOL 1.4 and 1.5 is offered as Open Source software via the GPL v2 license, and it can be found, along with the installation package, the user guide, and examples, at http://linux.btbs.unimib.it/xpyder/.
一种通用的方法,可以直接识别和分析蛋白质构象集合中的短程或长程偶联或通讯残基,对于全面了解蛋白质动力学和结构通讯途径至关重要。在这里,我们介绍了 xPyder,它是最常用的分子图形系统之一 PyMOL 与动态互相关矩阵 (DCCM) 分析之间的接口。该方法原则上也可以扩展到包括其他残基之间通讯倾向或强度指标的矩阵,以及分子内或分子间相互作用的持久性,例如蛋白质动力学的基础。xPyder 是为 PyMOL 1.4 和 1.5 版本提供的插件,采用 GPL v2 许可证作为开源软件发布,可在 http://linux.btbs.unimib.it/xpyder/ 上找到,包括安装包、用户指南和示例。