Literature DB >> 15527509

Computation of elementary modes: a unifying framework and the new binary approach.

Julien Gagneur1, Steffen Klamt.   

Abstract

BACKGROUND: Metabolic pathway analysis has been recognized as a central approach to the structural analysis of metabolic networks. The concept of elementary (flux) modes provides a rigorous formalism to describe and assess pathways and has proven to be valuable for many applications. However, computing elementary modes is a hard computational task. In recent years we assisted in a multiplication of algorithms dedicated to it. We require a summarizing point of view and a continued improvement of the current methods.
RESULTS: We show that computing the set of elementary modes is equivalent to computing the set of extreme rays of a convex cone. This standard mathematical representation provides a unified framework that encompasses the most prominent algorithmic methods that compute elementary modes and allows a clear comparison between them. Taking lessons from this benchmark, we here introduce a new method, the binary approach, which computes the elementary modes as binary patterns of participating reactions from which the respective stoichiometric coefficients can be computed in a post-processing step. We implemented the binary approach in FluxAnalyzer 5.1, a software that is free for academics. The binary approach decreases the memory demand up to 96% without loss of speed giving the most efficient method available for computing elementary modes to date.
CONCLUSIONS: The equivalence between elementary modes and extreme ray computations offers opportunities for employing tools from polyhedral computation for metabolic pathway analysis. The new binary approach introduced herein was derived from this general theoretical framework and facilitates the computation of elementary modes in considerably larger networks.

Entities:  

Mesh:

Year:  2004        PMID: 15527509      PMCID: PMC544875          DOI: 10.1186/1471-2105-5-175

Source DB:  PubMed          Journal:  BMC Bioinformatics        ISSN: 1471-2105            Impact factor:   3.169


  24 in total

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Journal:  Genome Res       Date:  2002-12       Impact factor: 9.043

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7.  The genome-scale metabolic extreme pathway structure in Haemophilus influenzae shows significant network redundancy.

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8.  Combinatorial complexity of pathway analysis in metabolic networks.

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9.  Determination of redundancy and systems properties of the metabolic network of Helicobacter pylori using genome-scale extreme pathway analysis.

Authors:  Nathan D Price; Jason A Papin; Bernhard Ø Palsson
Journal:  Genome Res       Date:  2002-05       Impact factor: 9.043

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Authors:  S Schuster; C Hilgetag; J H Woods; D A Fell
Journal:  J Math Biol       Date:  2002-08       Impact factor: 2.259

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  63 in total

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Journal:  Algorithms Mol Biol       Date:  2012-05-29       Impact factor: 1.405

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Review 3.  Analyzing molecular reaction networks: from pathways to chemical organizations.

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5.  Subnetwork analysis reveals dynamic features of complex (bio)chemical networks.

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-27       Impact factor: 11.205

6.  Elementary Growth Modes provide a molecular description of cellular self-fabrication.

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Journal:  PLoS Comput Biol       Date:  2020-01-27       Impact factor: 4.475

7.  Robust simplifications of multiscale biochemical networks.

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Journal:  BMC Syst Biol       Date:  2008-10-14

8.  The logic of EGFR/ErbB signaling: theoretical properties and analysis of high-throughput data.

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9.  In silico approaches to study mass and energy flows in microbial consortia: a syntrophic case study.

Authors:  Reed Taffs; John E Aston; Kristen Brileya; Zackary Jay; Christian G Klatt; Shawn McGlynn; Natasha Mallette; Scott Montross; Robin Gerlach; William P Inskeep; David M Ward; Ross P Carlson
Journal:  BMC Syst Biol       Date:  2009-12-10

10.  ON/OFF and beyond--a boolean model of apoptosis.

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Journal:  PLoS Comput Biol       Date:  2009-12-11       Impact factor: 4.475

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