VIB-VUB Center for Structural Biology, Flanders Institute for Biotechnology, Brussels 1050, Belgium.
Structural Biology Brussels, Bioengineering Sciences Department, Vrije Universiteit Brussel, Brussels 1050, Belgium.
Nucleic Acids Res. 2021 Jan 8;49(D1):D404-D411. doi: 10.1093/nar/gkaa1021.
The Protein Ensemble Database (PED) (https://proteinensemble.org), which holds structural ensembles of intrinsically disordered proteins (IDPs), has been significantly updated and upgraded since its last release in 2016. The new version, PED 4.0, has been completely redesigned and reimplemented with cutting-edge technology and now holds about six times more data (162 versus 24 entries and 242 versus 60 structural ensembles) and a broader representation of state of the art ensemble generation methods than the previous version. The database has a completely renewed graphical interface with an interactive feature viewer for region-based annotations, and provides a series of descriptors of the qualitative and quantitative properties of the ensembles. High quality of the data is guaranteed by a new submission process, which combines both automatic and manual evaluation steps. A team of biocurators integrate structured metadata describing the ensemble generation methodology, experimental constraints and conditions. A new search engine allows the user to build advanced queries and search all entry fields including cross-references to IDP-related resources such as DisProt, MobiDB, BMRB and SASBDB. We expect that the renewed PED will be useful for researchers interested in the atomic-level understanding of IDP function, and promote the rational, structure-based design of IDP-targeting drugs.
蛋白质集合数据库(PED)(https://proteinensemble.org),它保存了无序蛋白质(IDP)的结构集合,自 2016 年最后一次发布以来,已经得到了显著的更新和升级。新版本 PED 4.0 完全重新设计和实现,采用了最先进的技术,现在的数据量大约增加了六倍(162 个条目对 24 个条目,242 个结构集合对 60 个结构集合),并且比上一版本更全面地代表了最新的集合生成方法。该数据库具有完全更新的图形界面,具有基于区域注释的交互式特征查看器,并提供了一系列有关集合定性和定量特性的描述符。通过新的提交流程保证了数据的高质量,该流程结合了自动和手动评估步骤。一组生物注释员整合了描述集合生成方法、实验约束和条件的结构化元数据。一个新的搜索引擎允许用户构建高级查询,并搜索所有条目字段,包括对 IDP 相关资源(如 DisProt、MobiDB、BMRB 和 SASBDB)的交叉引用。我们希望更新后的 PED 将对有兴趣从原子水平理解 IDP 功能的研究人员有用,并促进基于结构的 IDP 靶向药物的合理设计。