Evidence map›Paper›PMID 24987116›Full record

ArticleMolecular systems biology2014

Minimal metabolic pathway structure is consistent with associated biomolecular interactions.

Aarash Bordbar, Harish Nagarajan, Nathan E Lewis, Haythem Latif, Ali Ebrahim, Stephen Federowicz, Jan Schellenberger, Bernhard O Palsson

Abstract read
In one paragraph

Article in Molecular systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

  1. Article
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  6. iScience · 2024
    Article
  7. Article
  8. Article
  9. CsrA Shows Selective Regulation of sRNA-mRNA Networks.bioRxiv : the preprint server for biology · 2023
    Article
  10. Article
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Aarash BordbarDepartment of Bioengineering, University of California San Diego, La Jolla, CA, USA.
Harish NagarajanBioinformatics and Systems Biology Program, University of California San Diego, La Jolla, CA, USA.
Nathan E LewisDepartment of Bioengineering, University of California San Diego, La Jolla, CA, USA Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, CA, USA Wyss Institute for Biologically Inspired Engineering and Department of Genetics, Harvard Medical School, Boston, MA, USA.
Haythem LatifDepartment of Bioengineering, University of California San Diego, La Jolla, CA, USA.
Ali EbrahimDepartment of Bioengineering, University of California San Diego, La Jolla, CA, USA.
Stephen FederowiczBioinformatics and Systems Biology Program, University of California San Diego, La Jolla, CA, USA.
Jan SchellenbergerBioinformatics and Systems Biology Program, University of California San Diego, La Jolla, CA, USA.
Bernhard O PalssonDepartment of Bioengineering, University of California San Diego, La Jolla, CA, USA Bioinformatics and Systems Biology Program, University of California San Diego, La Jolla, CA, USA Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Lyngby, Denmark palsson@ucsd.edu.

Funding

Network-based Analysis of Kinetics and RegulationR01GM068837 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PALSSON, BERNHARD O · 2003 to 2012
$2.4M
NIGMS NIH HHS GM068837NIGMS NIH HHS R01 GM068837
6 · The paper itself

Abstract

Pathways are a universal paradigm for functionally describing cellular processes. Even though advances in high-throughput data generation have transformed biology, the core of our biological understanding, and hence data interpretation, is still predicated on human-defined pathways. Here, we introduce an unbiased, pathway structure for genome-scale metabolic networks defined based on principles of parsimony that do not mimic canonical human-defined textbook pathways. Instead, these minimal pathways better describe multiple independent pathway-associated biomolecular interaction datasets suggesting a functional organization for metabolism based on parsimonious use of cellular components. We use the inherent predictive capability of these pathways to experimentally discover novel transcriptional regulatory interactions in Escherichia coli metabolism for three transcription factors, effectively doubling the known regulatory roles for Nac and MntR. This study suggests an underlying and fundamental principle in the evolutionary selection of pathway structures; namely, that pathways may be minimal, independent, and segregated.

Indexed as

Metabolic Networks and PathwaysAlgorithmsComputational BiologyEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialGenomeHumansModels, GeneticEscherichia coli Proteinsconstraint‐based modelinggenetic interactionspathway analysisprotein‐protein interactionstranscriptional regulatory networks

Identifiers

PMID24987116
PMCPMC4299494

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.