MRC Laboratory of Molecular Biology, Cambridge, UK.
Genomics England, London, UK.
Nat Struct Mol Biol. 2018 Feb;25(2):185-194. doi: 10.1038/s41594-017-0019-z. Epub 2018 Jan 15.
Visualizations of biomolecular structures empower us to gain insights into biological functions, generate testable hypotheses, and communicate biological concepts. Typical visualizations (such as ball and stick) primarily depict covalent bonds. In contrast, non-covalent contacts between atoms, which govern normal physiology, pathogenesis, and drug action, are seldom visualized. We present the Protein Contacts Atlas, an interactive resource of non-covalent contacts from over 100,000 PDB crystal structures. We developed multiple representations for visualization and analysis of non-covalent contacts at different scales of organization: atoms, residues, secondary structure, subunits, and entire complexes. The Protein Contacts Atlas enables researchers from different disciplines to investigate diverse questions in the framework of non-covalent contacts, including the interpretation of allostery, disease mutations and polymorphisms, by exploring individual subunits, interfaces, and protein-ligand contacts and by mapping external information. The Protein Contacts Atlas is available at http://www.mrc-lmb.cam.ac.uk/pca/ and also through PDBe.
生物分子结构的可视化使我们能够深入了解生物功能,生成可测试的假设,并交流生物学概念。典型的可视化(如球棒)主要描述共价键。相比之下,原子之间的非共价相互作用,它们控制着正常的生理、发病机制和药物作用,很少被可视化。我们提出了蛋白质接触图谱,这是一个来自超过 100,000 个 PDB 晶体结构的非共价接触的交互式资源。我们开发了多种表示方法,用于在不同的组织层次上可视化和分析非共价接触:原子、残基、二级结构、亚基和整个复合物。蛋白质接触图谱使来自不同学科的研究人员能够在非共价接触的框架内研究各种问题,包括变构的解释、疾病突变和多态性,通过探索单个亚基、界面和蛋白-配体相互作用,并映射外部信息。蛋白质接触图谱可在 http://www.mrc-lmb.cam.ac.uk/pca/ 获得,也可通过 PDBe 获得。