%0 Journal Article %1 Ma2007Edinburgh %A Ma, Hongwu %A Sorokin, Anatoly %A Mazein, Alexander %A Selkov, Alex %A Selkov, Evgeni %A Demin, Oleg %A Goryanin, Igor %C Computational Systems Biology, School of Informatics, The University of Edinburgh, Edinburgh, UK. %D 2007 %I Nature Publishing Group %J Molecular systems biology %K genome-scale human metabolic-networks reconstruction %N 1 %R 10.1038/msb4100177 %T The Edinburgh human metabolic network reconstruction and its functional analysis. %U http://dx.doi.org/10.1038/msb4100177 %V 3 %X A better understanding of human metabolism and its relationship with diseases is an important task in human systems biology studies. In this paper, we present a high-quality human metabolic network manually reconstructed by integrating genome annotation information from different databases and metabolic reaction information from literature. The network contains nearly 3000 metabolic reactions, which were reorganized into about 70 human-specific metabolic pathways according to their functional relationships. By analysis of the functional connectivity of the metabolites in the network, the bow-tie structure, which was found previously by structure analysis, is reconfirmed. Furthermore, the distribution of the disease related genes in the network suggests that the IN (substrates) subset of the bow-tie structure has more flexibility than other parts.

@article{Ma2007Edinburgh, abstract = { A better understanding of human metabolism and its relationship with diseases is an important task in human systems biology studies. In this paper, we present a high-quality human metabolic network manually reconstructed by integrating genome annotation information from different databases and metabolic reaction information from literature. The network contains nearly 3000 metabolic reactions, which were reorganized into about 70 human-specific metabolic pathways according to their functional relationships. By analysis of the functional connectivity of the metabolites in the network, the bow-tie structure, which was found previously by structure analysis, is reconfirmed. Furthermore, the distribution of the disease related genes in the network suggests that the {IN} (substrates) subset of the bow-tie structure has more flexibility than other parts. }, added-at = {2018-12-02T16:09:07.000+0100}, address = {Computational Systems Biology, School of Informatics, The University of Edinburgh, Edinburgh, UK.}, author = {Ma, Hongwu and Sorokin, Anatoly and Mazein, Alexander and Selkov, Alex and Selkov, Evgeni and Demin, Oleg and Goryanin, Igor}, biburl = {https://www.bibsonomy.org/bibtex/25b33f3315d7af7d49995a7c50e49edc2/karthikraman}, citeulike-article-id = {1695367}, citeulike-linkout-0 = {http://dx.doi.org/10.1038/msb4100177}, citeulike-linkout-1 = {http://dx.doi.org/10.1038/msb4100177}, citeulike-linkout-2 = {http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2013923/}, citeulike-linkout-3 = {http://view.ncbi.nlm.nih.gov/pubmed/17882155}, citeulike-linkout-4 = {http://www.hubmed.org/display.cgi?uids=17882155}, day = 18, doi = {10.1038/msb4100177}, interhash = {3d7d757dd439d28e99c05b96b1e21053}, intrahash = {5b33f3315d7af7d49995a7c50e49edc2}, issn = {1744-4292}, journal = {Molecular systems biology}, keywords = {genome-scale human metabolic-networks reconstruction}, month = sep, number = 1, pmcid = {PMC2013923}, pmid = {17882155}, posted-at = {2010-07-19 17:15:12}, priority = {2}, publisher = {Nature Publishing Group}, timestamp = {2018-12-02T16:09:07.000+0100}, title = {The Edinburgh human metabolic network reconstruction and its functional analysis.}, url = {http://dx.doi.org/10.1038/msb4100177}, volume = 3, year = 2007 }