Please use this identifier to cite or link to this item: https://doi.org/10.1007/s11306-016-1051-4
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dc.titleRecon 2.2: from reconstruction to model of human metabolism
dc.contributor.authorSwainston, N
dc.contributor.authorSmallbone, K
dc.contributor.authorHefzi, H
dc.contributor.authorDobson, P.D
dc.contributor.authorBrewer, J
dc.contributor.authorHanscho, M
dc.contributor.authorZielinski, D.C
dc.contributor.authorAng, K.S
dc.contributor.authorGardiner, N.J
dc.contributor.authorGutierrez, J.M
dc.contributor.authorKyriakopoulos, S
dc.contributor.authorLakshmanan, M
dc.contributor.authorLi, S
dc.contributor.authorLiu, J.K
dc.contributor.authorMartínez, V.S
dc.contributor.authorOrellana, C.A
dc.contributor.authorQuek, L.-E
dc.contributor.authorThomas, A
dc.contributor.authorZanghellini, J
dc.contributor.authorBorth, N
dc.contributor.authorLee, D.-Y
dc.contributor.authorNielsen, L.K
dc.contributor.authorKell, D.B
dc.contributor.authorLewis, N.E
dc.contributor.authorMendes, P.
dc.date.accessioned2020-09-04T02:03:52Z
dc.date.available2020-09-04T02:03:52Z
dc.date.issued2016
dc.identifier.citationSwainston, N, Smallbone, K, Hefzi, H, Dobson, P.D, Brewer, J, Hanscho, M, Zielinski, D.C, Ang, K.S, Gardiner, N.J, Gutierrez, J.M, Kyriakopoulos, S, Lakshmanan, M, Li, S, Liu, J.K, Martínez, V.S, Orellana, C.A, Quek, L.-E, Thomas, A, Zanghellini, J, Borth, N, Lee, D.-Y, Nielsen, L.K, Kell, D.B, Lewis, N.E, Mendes, P. (2016). Recon 2.2: from reconstruction to model of human metabolism. Metabolomics 12 (7) : 109. ScholarBank@NUS Repository. https://doi.org/10.1007/s11306-016-1051-4
dc.identifier.issn15733882
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174252
dc.description.abstractIntroduction: The human genome-scale metabolic reconstruction details all known metabolic reactions occurring in humans, and thereby holds substantial promise for studying complex diseases and phenotypes. Capturing the whole human metabolic reconstruction is an on-going task and since the last community effort generated a consensus reconstruction, several updates have been developed. Objectives: We report a new consensus version, Recon 2.2, which integrates various alternative versions with significant additional updates. In addition to re-establishing a consensus reconstruction, further key objectives included providing more comprehensive annotation of metabolites and genes, ensuring full mass and charge balance in all reactions, and developing a model that correctly predicts ATP production on a range of carbon sources. Methods: Recon 2.2 has been developed through a combination of manual curation and automated error checking. Specific and significant manual updates include a respecification of fatty acid metabolism, oxidative phosphorylation and a coupling of the electron transport chain to ATP synthase activity. All metabolites have definitive chemical formulae and charges specified, and these are used to ensure full mass and charge reaction balancing through an automated linear programming approach. Additionally, improved integration with transcriptomics and proteomics data has been facilitated with the updated curation of relationships between genes, proteins and reactions. Results: Recon 2.2 now represents the most predictive model of human metabolism to date as demonstrated here. Extensive manual curation has increased the reconstruction size to 5324 metabolites, 7785 reactions and 1675 associated genes, which now are mapped to a single standard. The focus upon mass and charge balancing of all reactions, along with better representation of energy generation, has produced a flux model that correctly predicts ATP yield on different carbon sources. Conclusion: Through these updates we have achieved the most complete and best annotated consensus human metabolic reconstruction available, thereby increasing the ability of this resource to provide novel insights into normal and disease states in human. The model is freely available from the Biomodels database (http://identifiers.org/biomodels.db/MODEL1603150001). © 2016, The Author(s).
dc.publisherSpringer New York LLC
dc.sourceUnpaywall 20200831
dc.subjectalgorithm
dc.subjectArticle
dc.subjectbiological model
dc.subjectcarbon source
dc.subjectcomputer program
dc.subjectdata base
dc.subjectfatty acid metabolism
dc.subjectmetabolism
dc.subjectmetabolite
dc.subjectoxidative phosphorylation
dc.subjectprediction
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1007/s11306-016-1051-4
dc.description.sourcetitleMetabolomics
dc.description.volume12
dc.description.issue7
dc.description.page109
dc.published.statePublished
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