Evidence map›Paper›PMID 40170302›Full record

ArticleACS infectious diseases2025

Time-Dependent Inhibition of Leucyl-tRNA-Synthetase (LeuRS): Insight into Target Vulnerability.

Mingqian Wang, YongLe He, Siobhan A Cohen, Amanda R Strohm, John D Haley, Stephen G Walker, M R K Alley, Peter J Tonge

Abstract read
In one paragraph

Article in ACS infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Selectivity of the Time-DependentACS chemical biology · 2025
    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

8 authors.

Mingqian WangCenter for Advanced Study of Drug Action, and Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.
YongLe HeCenter for Advanced Study of Drug Action, and Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.
Siobhan A CohenCenter for Advanced Study of Drug Action, and Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.
Amanda R StrohmCenter for Advanced Study of Drug Action, and Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.ORCID 0009-0003-2334-9504
John D HaleyDepartment of Pathology, Stony Brook University, Stony Brook, New York 11794-8691, United States.
Stephen G WalkerDepartment of Oral Biology and Pathology, Stony Brook University, Stony Brook, New York 11794-8702, United States.
M R K AlleyAN2 Therapeutics, Menlo Park, California 94027, United States.
Peter J TongeCenter for Advanced Study of Drug Action, and Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.ORCID 0000-0003-1606-3471

Funding

Chemical Biology Training InterfaceT32GM136572 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI ELIZABETH M BOON, Jessica Chuang Seeliger · 2020 to 2026
$2.9M
SBU Chemistry-Biology Interface Training ProgramT32GM092714 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI SAMPSON, NICOLE S, TONGE, PETER J · 2010 to 2019
$1.7M
Mechanism of Slow Onset Enzyme Inhibition and Translation to Time-Dependent Drug ActivityR35GM149297 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI PETER J TONGE · 2023 to 2026
$1.6M
Scholars in BioMedical Sciences (SBMS) Training ProgramT32GM148331 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Styliani-Anna (Stella) E Tsirka · 2024 to 2026
$695k
NIGMS NIH HHS R35 GM149297NIGMS NIH HHS T32 GM092714NIGMS NIH HHS T32 GM136572NIGMS NIH HHS T32 GM148331
6 · The paper itself

Abstract

The postantibiotic effect (PAE) is the persistent suppression of microbial growth following the removal of antimicrobial therapy. In general, antibiotics that generate a PAE are dosed less frequently, and thus, the PAE has important implications for dosing regimens. PAEs can arise through several mechanisms, including the extended occupancy of the drug target following drug elimination, and the correlation between drug-target residence time and PAE provides insight into target vulnerability. To assess the vulnerability of

Indexed as

Anti-Bacterial AgentsEnzyme InhibitorsEscherichia coliLeucine-tRNA LigaseBoron CompoundsEscherichia coli ProteinsTime FactorsAnti-Bacterial AgentsBoron CompoundsEnzyme InhibitorsEscherichia coli ProteinsLeucine-tRNA Ligaseepetraboroleleucyl-tRNA-synthetasepostantibiotic effectpSILACresidence timetarget vulnerability

Identifiers

PMID40170302
PMCPMC12117471

What OpenQuestion holds

Textmetadata
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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.