Evidence map›Paper›PMID 39873491›Full record

ArticlemSystems2025

Allosteric regulation of pyruvate kinase enables efficient and robust gluconeogenesis by preventing metabolic conflicts and carbon overflow.

Fukang She, Brent W Anderson, Daven B Khana, Shenwei Zhang, Wieland Steinchen, Danny K Fung, Nathalie G Lesser, Lauren N Lucas, David M Stevenson, Theresa J Astmann and 4 more

Abstract read
In one paragraph

Article in mSystems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Glyceraldehyde-3-phosphate dehydrogenase homologs as bifunctional gatekeepers of metabolic segregation inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Staying in the loop to make ends meet: roles and regulation of GlmR inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Unraveling metabolic reprogramming inFrontiers in molecular biosciences · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Fukang SheDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0009-0008-8633-252X
Brent W AndersonDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Daven B KhanaDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Shenwei ZhangDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Wieland SteinchenPhilipps-University-Marburg, Center for Synthetic Microbiology (SYNMIKRO) & Faculty of Chemistry, Marburg, Germany.
Danny K FungDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Nathalie G LesserDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Lauren N LucasDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
David M StevensonDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Theresa J AstmannDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Gert BangePhilipps-University-Marburg, Center for Synthetic Microbiology (SYNMIKRO) & Faculty of Chemistry, Marburg, Germany.
Jan-Peter van PijkerenDepartment of Food Science, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0003-4649-5726
Daniel Amador-NoguezDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-3568-3070
Jue D WangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0003-1503-170X

Funding

The critical roles of (p)ppGpp in homeostasis and antibiotic tolerance in Gram positive bacteriaR35GM127088 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Jue D. Wang · 2018 to 2026
$3.9M
Deutsche Forschungsgemeinschaft (DFG) SPP1879HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM127088National Science Foundation (NSF) 1715710NIGMS NIH HHS R35 GM127088NSF | National Science Foundation Graduate Research Fellowship Program (GRFP) DGE-1256259
6 · The paper itself

Abstract

Gluconeogenesis, the reciprocal pathway of glycolysis, is an energy-consuming process that generates glycolytic intermediates from non-carbohydrate sources. In this study, we demonstrate that robust and efficient gluconeogenesis in bacteria relies on the allosteric inactivation of pyruvate kinase, the enzyme responsible for the irreversible final step of glycolysis. Using the model bacterium

Indexed as

Bacillus subtilisCarbonGluconeogenesisPyruvate KinaseAllosteric RegulationBacterial ProteinsGlycineGlycolysisGlyphosatePhosphoenolpyruvateBacterial ProteinsCarbonGlycineGlyphosatePhosphoenolpyruvatePyruvate Kinaseallosteric regulationgluconeogenesisoverflow metabolismpyruvate kinase

Identifiers

PMID39873491
PMCPMC11834443

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.