Evidence map›Paper›PMID 30619111›Full record

ArticleFrontiers in microbiology2018

Advancement of the 5-Amino-1-(Carbamoylmethyl)-1H-1,2,3-Triazole-4-Carboxamide Scaffold to Disarm the Bacterial SOS Response.

Trevor Selwood, Brian J Larsen, Charlie Y Mo, Matthew J Culyba, Zachary M Hostetler, Rahul M Kohli, Allen B Reitz, Simon D P Baugh

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Snapshots ofiScience · 2025
    Article
  4. mLife · 2024
    Review
  5. Article
  6. Article
  7. Integration of molecular modelling andFrontiers in cellular and infection microbiology · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Exploration of inhibitors of the bacterial LexA repressor-protease.Bioorganic & medicinal chemistry letters · 2022
    Article
  12. Article
  13. Review
  14. Targeting evolution of antibiotic resistance by SOS response inhibition.Computational and structural biotechnology journal · 2021
    Review
  15. Review
  16. Article
  17. 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.

Trevor SelwoodDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Brian J LarsenFox Chase Chemical Diversity Center, Inc., Doylestown, PA, United States.
Charlie Y MoDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Matthew J CulybaDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Zachary M HostetlerDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Rahul M KohliDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Allen B ReitzFox Chase Chemical Diversity Center, Inc., Doylestown, PA, United States.
Simon D P BaughFox Chase Chemical Diversity Center, Inc., Doylestown, PA, United States.

Funding

Predoctoral Training at the Chemistry-Biology InterfaceT32GM071339 · NIGMS · WISTAR INSTITUTE · PI MARMORSTEIN, RONEN, SPEICHER, DAVID W. · 2005 to 2019
$3.2M
Predoctoral Training at the Chemistry-Biology InterfaceT32GM133398 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Ronen Marmorstein, Ernest James Petersson · 2020 to 2026
$2.4M
Combating Bacterial Drug Resistance by Targeting the Enzymes of EvolutionDP2GM105444 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI KOHLI, RAHUL MANU · 2012 to 2012
$2.2M
The Molecular Basis for the Bacterial SOS SignalR01GM127593 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI KOHLI, RAHUL MANU, PETERSSON, ERNEST JAMES · 2018 to 2021
$1.2M
NIGMS NIH HHS DP2 GM105444NIGMS NIH HHS R01 GM127593NIGMS NIH HHS T32 GM071339NIGMS NIH HHS T32 GM133398
6 · The paper itself

Abstract

Many antibiotics, either directly or indirectly, cause DNA damage thereby activating the bacterial DNA damage (SOS) response. SOS activation results in expression of genes involved in DNA repair and mutagenesis, and the regulation of the SOS response relies on two key proteins, LexA and RecA. Genetic studies have indicated that inactivating the regulatory proteins of this response sensitizes bacteria to antibiotics and slows the appearance of resistance. However, advancement of small molecule inhibitors of the SOS response has lagged, despite their clear promise in addressing the threat of antibiotic resistance. Previously, we had addressed this deficit by performing a high throughput screen of ∼1.8 million compounds that monitored for inhibition of RecA-mediated auto-proteolysis of

Indexed as

antibiotic resistanceDNA damagePseudomonas aeruginosaSOS responsestructure activity analysis

Identifiers

PMID30619111
PMCPMC6305444

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.