Evidence map›Paper›PMID 41806044›Full record

ReviewArchives of microbiology2026

Bacterial β-carbonic anhydrases: a six-step prioritization framework for antibacterial target validation.

Mariia Y Stoliarskaia

Abstract readReview
PubMed Publisher
In one paragraph

Review in Archives of microbiology, 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

1 author.

Mariia Y StoliarskaiaInstitute of Protein Research, Russian Academy of Sciences, Pushchino, Moscow Region, Russian Federation. stomayar98@gmail.com.ORCID http://orcid.org/0009-0008-6467-6321

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial β-carbonic anhydrases (β-CAs) are actively studied as potential targets for next-generation antibacterial agents. Despite extensive biochemical and structural characterization, their validation as isoform-specific therapeutic targets remains incomplete. Here, we developed and applied a six-filter validation framework-encompassing genetic essentiality, physiological relevance, biochemical feasibility, structural rationale, cellular target engagement, and therapeutic context-to integrate disparate data into a strategic prioritization map across representative pathogens (Escherichia coli, Mycobacterium tuberculosis, Pseudomonas aeruginosa, and Streptococcus pneumoniae). Application of this framework reveals that none of the analyzed β-CA isoforms currently qualifies as a ready therapeutic candidate (Group A), with most falling into context-dependent (Group C) or high-risk (Group D) categories due to specific validation gaps. By systematically defining these gaps, the framework provides a prioritized, target-driven roadmap for future experimental design and antibacterial drug discovery targeting bacterial β-carbonic anhydrases.

Indexed as

Anti-Bacterial AgentsBacteriaCarbonic Anhydrase InhibitorsCarbonic AnhydrasesDrug DiscoveryMycobacterium tuberculosisAnti-Bacterial AgentsCarbonic Anhydrase InhibitorsCarbonic AnhydrasesAllosteric regulationAntimicrobial targetsAntimicrobial target validationCO2/HCO3⁻ homeostasisEscherichia coliInhibitor selectivityIsoform specificityMycobacterium tuberculosispH-dependent activitypH-dependent regulationβ-carbonic anhydrase

Identifiers

PMID41806044

What OpenQuestion holds

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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.