| Literature DB >> 25332395 |
Anne Morgat1, Kristian B Axelsen2, Thierry Lombardot2, Rafael Alcántara3, Lucila Aimo2, Mohamed Zerara2, Anne Niknejad4, Eugeni Belda5, Nevila Hyka-Nouspikel2, Elisabeth Coudert2, Nicole Redaschi2, Lydie Bougueleret2, Christoph Steinbeck3, Ioannis Xenarios6, Alan Bridge2.
Abstract
Rhea (http://www.ebi.ac.uk/rhea) is a comprehensive and non-redundant resource of expert-curated biochemical reactions described using species from the ChEBI (Chemical Entities of Biological Interest) ontology of small molecules. Rhea has been designed for the functional annotation of enzymes and the description of genome-scale metabolic networks, providing stoichiometrically balanced enzyme-catalyzed reactions (covering the IUBMB Enzyme Nomenclature list and additional reactions), transport reactions and spontaneously occurring reactions. Rhea reactions are extensively curated with links to source literature and are mapped to other publicly available enzyme and pathway databases such as Reactome, BioCyc, KEGG and UniPathway, through manual curation and computational methods. Here we describe developments in Rhea since our last report in the 2012 database issue of Nucleic Acids Research. These include significant growth in the number of Rhea reactions and the inclusion of reactions involving complex macromolecules such as proteins, nucleic acids and other polymers that lie outside the scope of ChEBI. Together these developments will significantly increase the utility of Rhea as a tool for the description, analysis and reconciliation of genome-scale metabolic models.Entities:
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Year: 2014 PMID: 25332395 PMCID: PMC4384025 DOI: 10.1093/nar/gku961
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971