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      Rhea, the reaction knowledgebase in 2022

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          Abstract

          Rhea ( https://www.rhea-db.org) is an expert-curated knowledgebase of biochemical reactions based on the chemical ontology ChEBI (Chemical Entities of Biological Interest) ( https://www.ebi.ac.uk/chebi). In this paper, we describe a number of key developments in Rhea since our last report in the database issue of Nucleic Acids Research in 2019. These include improved reaction coverage in Rhea, the adoption of Rhea as the reference vocabulary for enzyme annotation in the UniProt knowledgebase UniProtKB ( https://www.uniprot.org), the development of a new Rhea website, and the designation of Rhea as an ELIXIR Core Data Resource. We hope that these and other developments will enhance the utility of Rhea as a reference resource to study and engineer enzymes and the metabolic systems in which they function.

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          Most cited references50

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          UniProt: the universal protein knowledgebase in 2021

          (2020)
          Abstract The aim of the UniProt Knowledgebase is to provide users with a comprehensive, high-quality and freely accessible set of protein sequences annotated with functional information. In this article, we describe significant updates that we have made over the last two years to the resource. The number of sequences in UniProtKB has risen to approximately 190 million, despite continued work to reduce sequence redundancy at the proteome level. We have adopted new methods of assessing proteome completeness and quality. We continue to extract detailed annotations from the literature to add to reviewed entries and supplement these in unreviewed entries with annotations provided by automated systems such as the newly implemented Association-Rule-Based Annotator (ARBA). We have developed a credit-based publication submission interface to allow the community to contribute publications and annotations to UniProt entries. We describe how UniProtKB responded to the COVID-19 pandemic through expert curation of relevant entries that were rapidly made available to the research community through a dedicated portal. UniProt resources are available under a CC-BY (4.0) license via the web at https://www.uniprot.org/.
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            KEGG: integrating viruses and cellular organisms

            Abstract KEGG (https://www.kegg.jp/) is a manually curated resource integrating eighteen databases categorized into systems, genomic, chemical and health information. It also provides KEGG mapping tools, which enable understanding of cellular and organism-level functions from genome sequences and other molecular datasets. KEGG mapping is a predictive method of reconstructing molecular network systems from molecular building blocks based on the concept of functional orthologs. Since the introduction of the KEGG NETWORK database, various diseases have been associated with network variants, which are perturbed molecular networks caused by human gene variants, viruses, other pathogens and environmental factors. The network variation maps are created as aligned sets of related networks showing, for example, how different viruses inhibit or activate specific cellular signaling pathways. The KEGG pathway maps are now integrated with network variation maps in the NETWORK database, as well as with conserved functional units of KEGG modules and reaction modules in the MODULE database. The KO database for functional orthologs continues to be improved and virus KOs are being expanded for better understanding of virus-cell interactions and for enabling prediction of viral perturbations.
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              The Gene Ontology resource: enriching a GOld mine

              Abstract The Gene Ontology Consortium (GOC) provides the most comprehensive resource currently available for computable knowledge regarding the functions of genes and gene products. Here, we report the advances of the consortium over the past two years. The new GO-CAM annotation framework was notably improved, and we formalized the model with a computational schema to check and validate the rapidly increasing repository of 2838 GO-CAMs. In addition, we describe the impacts of several collaborations to refine GO and report a 10% increase in the number of GO annotations, a 25% increase in annotated gene products, and over 9,400 new scientific articles annotated. As the project matures, we continue our efforts to review older annotations in light of newer findings, and, to maintain consistency with other ontologies. As a result, 20 000 annotations derived from experimental data were reviewed, corresponding to 2.5% of experimental GO annotations. The website (http://geneontology.org) was redesigned for quick access to documentation, downloads and tools. To maintain an accurate resource and support traceability and reproducibility, we have made available a historical archive covering the past 15 years of GO data with a consistent format and file structure for both the ontology and annotations.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                07 January 2022
                10 November 2021
                10 November 2021
                : 50
                : D1
                : D693-D700
                Affiliations
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                EMBL-EBI European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus , Hinxton, Cambridge CB10 1SD, UK
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Swiss-Prot group, SIB Swiss Institute of Bioinformatics, Centre Medical Universitaire , CH-1211 Geneva 4, Switzerland
                Author notes
                To whom correspondence should be addressed. Tel: +41 22 379 41 79; Email: alan.bridge@ 123456sib.swiss
                Correspondence may also be addressed to Parit Bansal. Email: parit.bansal@ 123456sib.swiss
                Correspondence may also be addressed to Anne Morgat. Email: anne.morgat@ 123456sib.swiss

                The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.

                Author information
                https://orcid.org/0000-0002-0875-1680
                https://orcid.org/0000-0002-1216-2969
                https://orcid.org/0000-0003-3889-2879
                https://orcid.org/0000-0002-6850-9888
                https://orcid.org/0000-0001-8314-404X
                https://orcid.org/0000-0003-0943-6401
                https://orcid.org/0000-0001-7855-209X
                https://orcid.org/0000-0003-1829-162X
                https://orcid.org/0000-0002-2890-295X
                https://orcid.org/0000-0003-4543-637X
                https://orcid.org/0000-0002-3080-5243
                https://orcid.org/0000-0002-7474-1499
                https://orcid.org/0000-0002-6083-941X
                https://orcid.org/0000-0001-8890-2268
                https://orcid.org/0000-0003-2148-9135
                Article
                gkab1016
                10.1093/nar/gkab1016
                8728268
                34755880
                7a47c862-d2b1-468b-94e5-0c1b72f87b68
                © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 November 2021
                : 08 October 2021
                : 14 September 2021
                Page count
                Pages: 8
                Funding
                Funded by: Swiss Federal Government;
                Categories
                AcademicSubjects/SCI00010
                Database Issue

                Genetics
                Genetics

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