The MetaCyc database of metabolic pathways and enzymes and the BioCyc collection of Pathway/Genome Databases

Ron Caspi(SRI International), Tomer Altman(SRI International), Richard Billington(SRI International), Kate Dreher(SRI International), Hartmut Foerster(SRI International), Carol A. Fulcher(SRI International), Timothy A. Holland(SRI International), Ingrid M. Keseler(SRI International), Anamika Kothari(SRI International), Aya Kubo(SRI International), Markus Krummenacker(SRI International), Mario Latendresse(SRI International), Lukas A. Mueller(SRI International), Quang Ong(SRI International), Suzanne Paley(SRI International), Pallavi Subhraveti(SRI International), Daniel Weaver(SRI International), Deepika Weerasinghe(SRI International), Peifen Zhang(SRI International), Peter D. Karp(SRI International)
Nucleic Acids Research
November 12, 2013
Cited by 1,204Open Access
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Abstract

The MetaCyc database (MetaCyc.org) is a comprehensive and freely accessible database describing metabolic pathways and enzymes from all domains of life. MetaCyc pathways are experimentally determined, mostly small-molecule metabolic pathways and are curated from the primary scientific literature. MetaCyc contains >2100 pathways derived from >37,000 publications, and is the largest curated collection of metabolic pathways currently available. BioCyc (BioCyc.org) is a collection of >3000 organism-specific Pathway/Genome Databases (PGDBs), each containing the full genome and predicted metabolic network of one organism, including metabolites, enzymes, reactions, metabolic pathways, predicted operons, transport systems and pathway-hole fillers. Additions to BioCyc over the past 2 years include YeastCyc, a PGDB for Saccharomyces cerevisiae, and 891 new genomes from the Human Microbiome Project. The BioCyc Web site offers a variety of tools for querying and analysis of PGDBs, including Omics Viewers and tools for comparative analysis. New developments include atom mappings in reactions, a new representation of glycan degradation pathways, improved compound structure display, better coverage of enzyme kinetic data, enhancements of the Web Groups functionality, improvements to the Omics viewers, a new representation of the Enzyme Commission system and, for the desktop version of the software, the ability to save display states.


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