Evidence map›Paper›PMID 42435408›Full record

ArticleBioinformatics (Oxford, England)2026

WILDkCAT: extract, retrieve, and predict enzyme turnover numbers of constraint-based metabolic models.

Hugues Escoffier, Carole L Linster, Thomas Sauter

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Hugues EscoffierDepartment of Health, Medicine and Life Sciences (DHML), University of Luxembourg, Esch-sur-Alzette L-4362, Luxembourg.ORCID 0000-0002-3525-7661
Carole L LinsterLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Esch-sur-Alzette L-4362, Luxembourg.ORCID 0000-0001-7143-0719
Thomas SauterDepartment of Health, Medicine and Life Sciences (DHML), University of Luxembourg, Esch-sur-Alzette L-4362, Luxembourg.ORCID 0000-0001-8225-2954

Funding

the Luxembourg National Research Fund PRIDE21/16763386/CANBIO2
6 · The paper itself

Abstract

summaryAccurate enzyme turnover numbers are essential for building enzyme-constrained genome-scale metabolic models. However, collecting and curating these parameters remains a major bottleneck. Indeed, kcat values are scattered across multiple databases, reported under varying experimental conditions, and often missing for many enzymes. To address this challenge, we present WILDkCAT, a Python-based pipeline that enables the retrieval of kcat values from wild-type enzyme measured under user-specified pH and temperature ranges for a given metabolic model. The application to Escherichia coli (iML1515) and Homo sapiens (Human-GEM) models demonstrated the ability of WILDkCAT to retrieve substantial kcat coverage and its applicability across diverse genome-scale models. AVAILABILITY AND IMPLEMENTATION: WILDkCAT is available at https://github.com/sysbiolux/WILDkCAT and from PyPI. WILDkCAT works on all major operating systems and computer architectures. The documentation is available at https://sysbiolux.github.io/WILDkCAT.

Indexed as

Computational BiologyEnzymesModels, BiologicalSoftwareEscherichia coliHumansEnzymes

Identifiers

PMID42435408
PMCPMC13450424

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.