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A community-driven global reconstruction of human metabolism.

Authors :
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) [research center]
Luxembourg Centre for Systems Biomedicine (LCSB): Molecular Systems Physiology (Thiele Group) [research center]
Thiele, Ines(*)
Swainston, N.(*)
Fleming, Ronan MT
Hoppe, A.
Sahoo, Swagatika
Aurich, Maike Kathrin
Haraldsdottir, Hulda
Mo, M. L.
Rolfsson, O.
Stobbe, M. D.
Thorleifsson, S. G.
Agren, R.
Bölling, C.
Bordel, S.
Chavali, A. K.
Dobson, P.
Dunn, W. B.
Endler, L.
Hala, D.
Hucka, M.
Hull, D.
Jameson, D.
Jamshidi, N.
Jonsson, J. J.
Juty, N.
Keating, S.
Nookaew, I.
Le Novère, N.
Malys, N.
Mazein, A.
Papin, J. A.
Price, N. D.
Selkov, E. Sr
Sigurdsson, M. I.
Simeonidis, Evangelos
Sonnenschein, N.
Smallbone, K.
Sorokin, A.
van Beek, J. H.
Weichart, D.
Goryanin, I.
Nielsen, J.
Westerhoff, H. V.
Kell, D. B.
Mendes, P.
Palsson, B. O.
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) [research center]
Luxembourg Centre for Systems Biomedicine (LCSB): Molecular Systems Physiology (Thiele Group) [research center]
Thiele, Ines(*)
Swainston, N.(*)
Fleming, Ronan MT
Hoppe, A.
Sahoo, Swagatika
Aurich, Maike Kathrin
Haraldsdottir, Hulda
Mo, M. L.
Rolfsson, O.
Stobbe, M. D.
Thorleifsson, S. G.
Agren, R.
Bölling, C.
Bordel, S.
Chavali, A. K.
Dobson, P.
Dunn, W. B.
Endler, L.
Hala, D.
Hucka, M.
Hull, D.
Jameson, D.
Jamshidi, N.
Jonsson, J. J.
Juty, N.
Keating, S.
Nookaew, I.
Le Novère, N.
Malys, N.
Mazein, A.
Papin, J. A.
Price, N. D.
Selkov, E. Sr
Sigurdsson, M. I.
Simeonidis, Evangelos
Sonnenschein, N.
Smallbone, K.
Sorokin, A.
van Beek, J. H.
Weichart, D.
Goryanin, I.
Nielsen, J.
Westerhoff, H. V.
Kell, D. B.
Mendes, P.
Palsson, B. O.
Publication Year :
2013

Abstract

Multiple models of human metabolism have been reconstructed, but each represents only a subset of our knowledge. Here we describe Recon 2, a community-driven, consensus ‘metabolic reconstruction’, which is the most comprehensive representation of human metabolism that is applicable to computational modeling. Compared with its predecessors, the reconstruction has improved topological and functional features, including ~2× more reactions and ~1.7× more unique metabolites. Using Recon 2 we predicted changes in metabolite biomarkers for 49 inborn errors of metabolism with 77% accuracy when compared to experimental data. Mapping metabolomic data and drug information onto Recon 2 demonstrates its potential for integrating and analyzing diverse data types. Using protein expression data, we automatically generated a compendium of 65 cell type–specific models, providing a basis for manual curation or investigation of cell-specific metabolic properties. Recon 2 will facilitate many future biomedical studies and is freely available at http://humanmetabolism.org/.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1346591365
Document Type :
Electronic Resource