Systems Biology, Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Barcelona 08003, Spain.
Universitat Pompeu Fabra (UPF), Barcelona 08002, Spain.
Bioinformatics. 2020 Aug 15;36(14):4208-4210. doi: 10.1093/bioinformatics/btaa533.
Accurate 3D modelling of protein-protein interactions (PPI) is essential to compensate for the absence of experimentally determined complex structures. Here, we present a new set of commands within the ModelX toolsuite capable of generating atomic-level protein complexes suitable for interface design. Among these commands, the new tool ProteinFishing proposes known and/or putative alternative 3D PPI for a given protein complex. The algorithm exploits backbone compatibility of protein fragments to generate mutually exclusive protein interfaces that are quickly evaluated with a knowledge-based statistical force field. Using interleukin-10-R2 co-crystalized with interferon-lambda-3, and a database of X-ray structures containing interleukin-10, this algorithm was able to generate interleukin-10-R2/interleukin-10 structural models in agreement with experimental data.
ProteinFishing is a portable command-line tool included in the ModelX toolsuite, written in C++, that makes use of an SQL (tested for MySQL and MariaDB) relational database delivered with a template SQL dump called FishXDB. FishXDB contains the empty tables of ModelX fragments and the data used by the embedded statistical force field. ProteinFishing is compiled for Linux-64bit, MacOS-64bit and Windows-32bit operating systems. This software is a proprietary license and is distributed as an executable with its correspondent database dumps. It can be downloaded publicly at http://modelx.crg.es/. Licenses are freely available for academic users after registration on the website and are available under commercial license for for-profit organizations or companies.
javier.delgado@crg.eu or luis.serrano@crg.eu.
Supplementary data are available at Bioinformatics online.
准确的蛋白质-蛋白质相互作用(PPI)三维建模对于补偿缺乏实验确定的复合物结构至关重要。在这里,我们在 ModelX 工具套件中提供了一组新命令,这些命令能够生成适合界面设计的原子级蛋白质复合物。在这些命令中,新工具 ProteinFishing 为给定的蛋白质复合物提出了已知和/或假定的替代 3D PPI。该算法利用蛋白质片段的骨架兼容性生成相互排斥的蛋白质界面,并用基于知识的统计力场快速评估这些界面。该算法使用白细胞介素-10-R2 与干扰素-λ-3 共结晶,以及包含白细胞介素-10 的 X 射线结构数据库,成功生成了与实验数据一致的白细胞介素-10-R2/白细胞介素-10 结构模型。
ProteinFishing 是 ModelX 工具套件中的一个可移植命令行工具,用 C++编写,利用 SQL(针对 MySQL 和 MariaDB 进行了测试)关系数据库,该数据库带有一个名为 FishXDB 的模板 SQL 转储。FishXDB 包含 ModelX 片段的空表和嵌入式统计力场使用的数据。ProteinFishing 针对 Linux-64 位、MacOS-64 位和 Windows-32 位操作系统进行编译。该软件为专有的许可证,并以可执行文件的形式与相应的数据库转储一起分发。它可以在 http://modelx.crg.es/ 上公开下载。注册后,学术用户可以免费获得许可证,并可以根据商业许可证将其用于盈利组织或公司。
javier.delgado@crg.eu 或 luis.serrano@crg.eu。
补充数据可在 Bioinformatics 在线获得。