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Artículo

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

Lazar, Tamas; Martinez Perez, ElizabethIcon ; Quaglia, Federica; Hatos, András; Chemes, Lucia BeatrizIcon ; Iserte, Javier AlonsoIcon ; Méndez, Nicolás AgustínIcon ; Garrone, Nicolás AgustínIcon ; Saldaño, Tadeo EnriqueIcon ; Marchetti, JuliaIcon ; Velez Rueda, Ana JuliaIcon ; Bernadó, Pau; Blackledge, Martin; Cordeiro, Tiago N.; Fagerberg, Eric; Forman Kay, Julie D; Fornasari, Maria SilvinaIcon ; Gibson, Toby James; Gomes, Gregory Neal W; Gradinaru, Claudiu C.; Head Gordon, Teresa; Jensen, Malene Ringkjøbing; Lemke, Edward A; Longhi, Sonia; Marino Buslje, Cristina; Minervini, Giovanni; Mittag, Tanja; Monzon, Alexander Miguel; Pappu, Rohit V.; Parisi, Gustavo DanielIcon
Fecha de publicación: 08/01/2021
Editorial: Oxford University Press
Revista: Nucleic Acids Research
ISSN: 1362-4962
e-ISSN: 0305-1048
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Otras Ciencias Biológicas

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.
Palabras clave: ENSEMBLE , DISORDER , PROTEINS , IDP
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial 2.5 Unported (CC BY-NC 2.5)
Identificadores
URI: http://hdl.handle.net/11336/164928
URL: https://academic.oup.com/nar/article/49/D1/D404/6030232
DOI: http://dx.doi.org/10.1093/nar/gkaa1021
Colecciones
Articulos (IIBIO)
Articulos de INSTITUTO DE INVESTIGACIONES BIOTECNOLOGICAS
Articulos(IIB-INTECH)
Articulos de INST.DE INVEST.BIOTECNOLOGICAS - INSTITUTO TECNOLOGICO CHASCOMUS
Articulos(IIBBA)
Articulos de INST.DE INVEST.BIOQUIMICAS DE BS.AS(I)
Articulos(SEDE CENTRAL)
Articulos de SEDE CENTRAL
Citación
Lazar, Tamas; Martinez Perez, Elizabeth; Quaglia, Federica; Hatos, András; Chemes, Lucia Beatriz; et al.; PED in 2021: A major update of the protein ensemble database for intrinsically disordered proteins; Oxford University Press; Nucleic Acids Research; 49; D1; 8-1-2021; D404-D411
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