The Protein Data Bank in Europe-Knowledge Base (PDBe-KB, https://pdbe-kb.org) is a community-driven, collaborative resource for literature-derived, manually curated and computationally predicted structural and functional annotations of macromolecular structure data, contained in the Protein Data Bank (PDB). The goal of PDBe-KB is two-fold: (i) to increase the visibility and reduce the fragmentation of annotations contributed by specialist data resources, and to make these data more findable, accessible, interoperable and reusable (FAIR) and (ii) to place macromolecular structure data in their biological context, thus facilitating their use by the broader scientific community in fundamental and applied research. Here, we describe the guidelines of this collaborative effort, the current status of contributed data, and the PDBe-KB infrastructure, which includes the data exchange format, the deposition system for added value annotations, the distributable database containing the assembled data, and programmatic access endpoints. We also describe a series of novel web-pages-the PDBe-KB aggregated views of structure data-which combine information on macromolecular structures from many PDB entries. We have recently released the first set of pages in this series, which provide an overview of available structural and functional information for a protein of interest, referenced by a UniProtKB accession.

Varadi, M., Berrisford, J., Deshpande, M., Nair, S.s., Gutmanas, A., Armstrong, D., et al. (2020). PDBe-KB: a community-driven resource for structural and functional annotations. NUCLEIC ACIDS RESEARCH, 48(D1), D344-D353 [10.1093/nar/gkz853].

PDBe-KB: a community-driven resource for structural and functional annotations

Helmer Citterich, Manuela;
2020-01-01

Abstract

The Protein Data Bank in Europe-Knowledge Base (PDBe-KB, https://pdbe-kb.org) is a community-driven, collaborative resource for literature-derived, manually curated and computationally predicted structural and functional annotations of macromolecular structure data, contained in the Protein Data Bank (PDB). The goal of PDBe-KB is two-fold: (i) to increase the visibility and reduce the fragmentation of annotations contributed by specialist data resources, and to make these data more findable, accessible, interoperable and reusable (FAIR) and (ii) to place macromolecular structure data in their biological context, thus facilitating their use by the broader scientific community in fundamental and applied research. Here, we describe the guidelines of this collaborative effort, the current status of contributed data, and the PDBe-KB infrastructure, which includes the data exchange format, the deposition system for added value annotations, the distributable database containing the assembled data, and programmatic access endpoints. We also describe a series of novel web-pages-the PDBe-KB aggregated views of structure data-which combine information on macromolecular structures from many PDB entries. We have recently released the first set of pages in this series, which provide an overview of available structural and functional information for a protein of interest, referenced by a UniProtKB accession.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/11 - BIOLOGIA MOLECOLARE
English
Con Impact Factor ISI
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943075/pdf/gkz853.pdf
Varadi, M., Berrisford, J., Deshpande, M., Nair, S.s., Gutmanas, A., Armstrong, D., et al. (2020). PDBe-KB: a community-driven resource for structural and functional annotations. NUCLEIC ACIDS RESEARCH, 48(D1), D344-D353 [10.1093/nar/gkz853].
Varadi, M; Berrisford, J; Deshpande, M; Nair, Ss; Gutmanas, A; Armstrong, D; Pravda, L; Al-Lazikani, B; Anyango, S; Barton, Gj; Berka, K; Blundell, T; Borkakoti, N; Dana, J; Das, S; Dey, S; Micco, Pd; Fraternali, F; Gibson, T; Helmer Citterich, M; Hoksza, D; Huang, L; Jain, R; Jubb, H; Kannas, C; Kannan, N; Koca, J; Krivak, R; Kumar, M; Levy, Ed; Madeira, F; Madhusudhan, Ms; Martell, Hj; Macgowan, S; Mcgreig, Je; Mir, S; Mukhopadhyay, A; Parca, L; Paysan-Lafosse, T; Radusky, L; Ribeiro, A; Serrano, L; Sillitoe, I; Singh, G; Skoda, P; Svobodova, R; Tyzack, J; Valencia, A; Fernandez, Ev; Vranken, W; Wass, M; Thornton, J; Sternberg, M; Orengo, C; Velankar, S
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/230386
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