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JAIL:一个基于结构的大分子接口库。

JAIL: a structure-based interface library for macromolecules.

作者信息

Günther Stefan, von Eichborn Joachim, May Patrick, Preissner Robert

机构信息

Institute of Molecular Biology and Bioinformatics, Charité-University Medicine Berlin, Arnimallee 22, 14195 Berlin, Germany.

出版信息

Nucleic Acids Res. 2009 Jan;37(Database issue):D338-41. doi: 10.1093/nar/gkn599. Epub 2008 Oct 2.

Abstract

The increasing number of solved macromolecules provides a solid number of 3D interfaces, if all types of molecular contacts are being considered. JAIL annotates three different kinds of macromolecular interfaces, those between interacting protein domains, interfaces of different protein chains and interfaces between proteins and nucleic acids. This results in a total number of about 184,000 database entries. All the interfaces can easily be identified by a detailed search form or by a hierarchical tree that describes the protein domain architectures classified by the SCOP database. Visual inspection of the interfaces is possible via an interactive protein viewer. Furthermore, large scale analyses are supported by an implemented sequential and by a structural clustering. Similar interfaces as well as non-redundant interfaces can be easily picked out. Additionally, the sequential conservation of binding sites was also included in the database and is retrievable via Jmol. A comprehensive download section allows the composition of representative data sets with user defined parameters. The huge data set in combination with various search options allow a comprehensive view on all interfaces between macromolecules included in the Protein Data Bank (PDB). The download of the data sets supports numerous further investigations in macromolecular recognition. JAIL is publicly available at http://bioinformatics.charite.de/jail.

摘要

如果考虑所有类型的分子接触,已解析的大分子数量不断增加,这就提供了大量的三维界面。JAIL对三种不同类型的大分子界面进行注释,即相互作用的蛋白质结构域之间的界面、不同蛋白质链的界面以及蛋白质与核酸之间的界面。这导致数据库条目总数约为184,000个。所有界面都可以通过详细的搜索表单或通过描述由SCOP数据库分类的蛋白质结构域架构的层次树轻松识别。通过交互式蛋白质查看器可以对界面进行可视化检查。此外,通过已实现的序列分析和结构聚类支持大规模分析。可以轻松挑选出相似的界面以及非冗余界面。此外,结合位点的序列保守性也包含在数据库中,可通过Jmol检索。全面的下载部分允许使用用户定义的参数组成代表性数据集。庞大的数据集与各种搜索选项相结合,可以全面了解蛋白质数据库(PDB)中包含的大分子之间的所有界面。数据集的下载支持对大分子识别进行大量进一步研究。JAIL可在http://bioinformatics.charite.de/jail上公开获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6944/2686555/a4544f621513/gkn599f1.jpg

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