scispace - formally typeset
Open AccessJournal ArticleDOI

A community-driven global reconstruction of human metabolism

Ines Thiele, +53 more
- 01 May 2013 - 
- Vol. 31, Iss: 5, pp 419-425
Reads0
Chats0
TLDR
Recon 2, a community-driven, consensus 'metabolic reconstruction', is described, which is the most comprehensive representation of human metabolism that is applicable to computational modeling and has improved topological and functional features.
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/.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Primordial Krebs-cycle-like non-enzymatic reactions detected by mass spectrometry and nuclear magnetic resonance

TL;DR: These results strengthen previous conclusions about the existence of unifying reaction conditions that enables a series of co-occurring metabolism-like non-enzymatic Krebs cycle reactions, and discuss why constraints applying to metabolism disentangle concentration from importance of any reaction intermediates.
Journal ArticleDOI

Metabolic Modeling to Interrogate Microbial Disease: A Tale for Experimentalists.

TL;DR: The role of metabolic interactions among microbial species cannot easily be resolved by current experimental approaches such as 16S rRNA gene sequencing, metagenomics and/or metabolomics.
Journal ArticleDOI

Supporting novel biomedical research via multilayer collaboration networks.

TL;DR: In this article, the authors propose a tool that helps to resolve the tension between safe/fundable research vs high-risk/potentially transformational research by identifying hidden overlapping interests around novel molecular research topics.
Posted ContentDOI

Advances in the integration of transcriptional regulatory information into genome-scale metabolic models

TL;DR: Here, a review of the existing methods to integrate transcriptional regulatory information into constraint-based models of metabolic networks in order to increase the predictive capabilities of computational models and understand the regulation of cellular metabolism.
References
More filters
Journal ArticleDOI

What is flux balance analysis

TL;DR: This primer covers the theoretical basis of the approach, several practical examples and a software toolbox for performing the calculations.
Journal ArticleDOI

The systems biology markup language (SBML): a medium for representation and exchange of biochemical network models.

TL;DR: This work summarizes the Systems Biology Markup Language (SBML) Level 1, a free, open, XML-based format for representing biochemical reaction networks, a software-independent language for describing models common to research in many areas of computational biology.
Journal ArticleDOI

DrugBank: a knowledgebase for drugs, drug actions and drug targets

TL;DR: The latest version of DrugBank (release 2.0) has been expanded significantly over the previous release and contains 60% more FDA-approved small molecule and biotech drugs including 10% more ‘experimental’ drugs.
Journal ArticleDOI

Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites

TL;DR: A broad, drug-like phase II metabolic response of the host to metabolites generated by the microbiome was observed, suggesting that the gut microflora has a direct impact on the drug metabolism capacity of theHost.
Journal ArticleDOI

Towards a knowledge-based Human Protein Atlas

TL;DR: The analysis here suggests that state stem cell funding programs are sufficiently large and established that simply ending the programs, at least in the absence of substantial investment in the field by other funding sources, could have deleterious effects.
Related Papers (5)