Artículo

PED in 2021: A major update of the protein ensemble database for intrinsically disordered proteins

Lazar, Tamas ; Martinez Perez, Elizabeth Icon; Quaglia, Federica ; Hatos, András ; Chemes, Lucia Beatriz Icon; Iserte, Javier Alonso Icon; Méndez, Nicolás Agustín Icon; Garrone, Nicolás Agustín Icon; Saldaño, Tadeo Enrique Icon; Marchetti, Julia Icon; Velez Rueda, Ana Julia Icon; Bernadó, Pau ; Blackledge, Martin ; Cordeiro, Tiago N. ; Fagerberg, Eric ; Forman Kay, Julie D ; Fornasari, Maria Silvina Icon; Gibson, Toby James Icon; Gomes, Gregory Neal W ; Gradinaru, Claudiu C. ; Head Gordon, Teresa ; Jensen, Malene Ringkjøbing ; Lemke, Edward A ; Longhi, Sonia ; Marino Buslje, Cristina Icon; Minervini, Giovanni ; Mittag, Tanja ; Monzon, Alexander Miguel ; Pappu, Rohit V. ; Parisi, Gustavo Daniel Icon

Otros responsables

Fecha

2021-01-08

Editorial

Oxford University Press

Revista

Nucleic Acids Research

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

1362-4962

eISSN

0305-1048

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

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.

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