PED in 2024: improving the community deposition of structural ensembles for intrinsically disordered proteins

被引:18
|
作者
Ghafouri, Hamidreza [1 ]
Lazar, Tamas [2 ,3 ]
Del Conte, Alessio [1 ]
Ku, Luiggi G. Tenorio [1 ]
Tompa, Peter [2 ,3 ,4 ]
Tosatto, Silvio C. E. [1 ]
Monzon, Alexander Miguel [5 ]
机构
[1] Univ Padua, Dept Biomed Sci, Padua, Italy
[2] VIB VUB Ctr Struct Biol, Vlaams Inst Biotechnol VIB, Brussels, Belgium
[3] Vrije Univ Brussel VUB, Dept Bioengn, Struct Biol Brussels, Brussels, Belgium
[4] Inst Enzymol, Res Ctr Nat Sci RCNS, Budapest, Hungary
[5] Univ Padua, Dept Informat Engn, Padua, Italy
关键词
CONFORMATIONAL ENSEMBLES; FORCE-FIELD; DATABASE; SPACE;
D O I
10.1093/nar/gkad947
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Protein Ensemble Database (PED) (URL: https://proteinensemble.org) is the primary resource for depositing structural ensembles of intrinsically disordered proteins. This updated version of PED reflects advancements in the field, denoting a continual expansion with a total of 461 entries and 538 ensembles, including those generated without explicit experimental data through novel machine learning (ML) techniques. With this significant increment in the number of ensembles, a few yet-unprecedented new entries entered the database, including those also determined or refined by electron paramagnetic resonance or circular dichroism data. In addition, PED was enriched with several new features, including a novel deposition service, improved user interface, new database cross-referencing options and integration with the 3D-Beacons network-all representing efforts to improve the FAIRness of the database. Foreseeably, PED will keep growing in size and expanding with new types of ensembles generated by accurate and fast ML-based generative models and coarse-grained simulations. Therefore, among future efforts, priority will be given to further develop the database to be compatible with ensembles modeled at a coarse-grained level. Graphical Abstract
引用
收藏
页码:D536 / D544
页数:9
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