Evidence map›Paper›PMID 40313980›Full record

ArticlemLife2025

Identification of a phenyl ester covalent inhibitor of caseinolytic protease and analysis of the ClpP1P2 inhibition in mycobacteria.

Genhui Xiao, Yumeng Cui, Liangliang Zhou, Chuya Niu, Bing Wang, Jinglan Wang, Shaoyang Zhou, Miaomiao Pan, Chi Kin Chan, Yan Xia and 3 more

Abstract read
In one paragraph

Article in mLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Proteostasis-targeted antibacterial strategies.Journal of microbiology (Seoul, Korea) · 2026
    Review
  4. 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

13 authors.

Genhui XiaoGlobal Health Drug Discovery Institute Beijing China.
Yumeng CuiGlobal Health Drug Discovery Institute Beijing China.
Liangliang ZhouGlobal Health Drug Discovery Institute Beijing China.
Chuya NiuGlobal Health Drug Discovery Institute Beijing China.
Bing WangBeijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, and Beijing Chest Hospital Capital Medical University Beijing China.
Jinglan WangGlobal Health Drug Discovery Institute Beijing China.
Shaoyang ZhouGlobal Health Drug Discovery Institute Beijing China.
Miaomiao PanGlobal Health Drug Discovery Institute Beijing China.
Chi Kin ChanGlobal Health Drug Discovery Institute Beijing China.
Yan XiaGlobal Health Drug Discovery Institute Beijing China.
Lan XuGlobal Health Drug Discovery Institute Beijing China.
Yu LuBeijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, and Beijing Chest Hospital Capital Medical University Beijing China.
Shawn ChenGlobal Health Drug Discovery Institute Beijing China.ORCID 0000-0002-6678-3293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The caseinolytic protease complex ClpP1P2 is crucial for protein homeostasis in mycobacteria and stress response and virulence of the pathogens. Its role as a potential drug target for combating tuberculosis (TB) has just begun to be substantiated in drug discovery research. We conducted a biochemical screening targeting the ClpP1P2 using a library of compounds phenotypically active against

Indexed as

caseinolytic proteasechemical–genetic interactiondrug combinationenzyme inhibitormycobacteria

Identifiers

PMID40313980
PMCPMC12042115

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.