Evidence map›Paper›PMID 39261563›Full record

ArticleScientific reports2024

Analysis of phosphofructokinase-1 activity as affected by pH and ATP concentration.

Chengcheng Wang, Mackenzie J Taylor, Chandler D Stafford, David S Dang, Sulaiman K Matarneh, David E Gerrard, Jinglu Tan

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  9. Is the vLamax for Glycolysis What theSports medicine (Auckland, N.Z.) · 2025
    Review
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  11. Article
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

7 authors.

Chengcheng WangDepartment of Chemical and Biomedical Engineering, University of Missouri, Columbia, MO, USA.
Mackenzie J TaylorDepartment of Nutrition, Dietetics and Food Sciences, Utah State University, Logan, UT, USA.
Chandler D StaffordDepartment of Nutrition, Dietetics and Food Sciences, Utah State University, Logan, UT, USA.
David S DangDepartment of Nutrition, Dietetics and Food Sciences, Utah State University, Logan, UT, USA.
Sulaiman K MatarnehDepartment of Nutrition, Dietetics and Food Sciences, Utah State University, Logan, UT, USA.
David E GerrardSchool of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Jinglu TanDepartment of Chemical and Biomedical Engineering, University of Missouri, Columbia, MO, USA. tanj@missouri.edu.

Funding

National Institute of Food and Agriculture 2017-67017-26470
6 · The paper itself

Abstract

A key player in energy metabolism is phosphofructokinase-1 (PFK1) whose activity and behavior strongly influence glycolysis and thus have implications in many areas. In this research, PFK1 assays were performed to convert F6P and ATP into F-1,6-P and ADP for varied pH and ATP concentrations. PFK1 activity was assessed by evaluating F-1,6-P generation velocity in two ways: (1) directly calculating the time slope from the first two or more datapoints of measured product concentration (the initial-velocity method), and (2) by fitting all the datapoints with a differential equation explicitly representing the effects of ATP and pH (the modeling method). Similar general trends of inhibition were shown by both methods, but the former gives only a qualitative picture while the modeling method yields the degree of inhibition because the model can separate the two simultaneous roles of ATP as both a substrate of reaction and an inhibitor of PFK1. Analysis based on the model suggests that the ATP affinity is much greater to the PFK1 catalytic site than to the inhibitory site, but the inhibited ATP-PFK1-ATP complex is much slower than the uninhibited PFK1-ATP complex in product generation, leading to reduced overall reaction velocity when ATP concentration increases. The initial-velocity method is simple and useful for general observation of enzyme activity while the modeling method has advantages in quantifying the inhibition effects and providing insights into the process.

Indexed as

Adenosine TriphosphatePhosphofructokinase-1Adenosine DiphosphateFructosephosphatesGlycolysisHydrogen-Ion ConcentrationKineticsAdenosine DiphosphateAdenosine Triphosphatefructose-6-phosphateFructosephosphatesPhosphofructokinase-1ATPEnzyme activityInitial-velocity methodKinetic modelingPFK1pHSubstrate inhibition

Identifiers

PMID39261563
PMCPMC11390725

What OpenQuestion holds

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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.