Evidence map›Paper›PMID 30060171›Full record

ArticleNucleic acids research2018

TraN: A novel repressor of an Enterococcus conjugative type IV secretion system.

Verena Kohler, Nikolaus Goessweiner-Mohr, Andreas Aufschnaiter, Christian Fercher, Ines Probst, Tea Pavkov-Keller, Kristin Hunger, Heimo Wolinski, Sabrina Büttner, Elisabeth Grohmann and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
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  4. Journal of applied crystallography · 2026
    Article
  5. Interactive 3D Objects Enhance Scientific Communication of Structural Data.Chembiochem : a European journal of chemical biology · 2025
    Review
  6. Article
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  9. Article
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  11. Article
  12. Article
  13. Review
  14. Regulation of Gram-Positive Conjugation.Frontiers in microbiology · 2019
    Review
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

11 authors at 5 institutions in 4 countries.

Verena KohlerInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Nikolaus Goessweiner-MohrInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Andreas AufschnaiterInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Christian FercherAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Qld 4072, Australia.
Ines ProbstDivision of Infectious Diseases, University Medical Center Freiburg, Freiburg 79106, Germany.
Tea Pavkov-KellerInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Kristin HungerInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Heimo WolinskiInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Sabrina BüttnerInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
Elisabeth GrohmannDivision of Infectious Diseases, University Medical Center Freiburg, Freiburg 79106, Germany.
Walter KellerInstitute of Molecular Biosciences, University of Graz, Graz 8010, Austria.
University of Graz · ATBerliner Hochschule für Technik · DEJohannes Kepler University of Linz · ATThe University of Queensland · AUUniversity Medical Center Freiburg · DE

Funding

Austrian Science Fund FWF P 27183
6 · The paper itself

Abstract

The dissemination of multi-resistant bacteria represents an enormous burden on modern healthcare. Plasmid-borne conjugative transfer is the most prevalent mechanism, requiring a type IV secretion system that enables bacteria to spread beneficial traits, such as resistance to last-line antibiotics, among different genera. Inc18 plasmids, like the Gram-positive broad host-range plasmid pIP501, are substantially involved in propagation of vancomycin resistance from Enterococci to methicillin-resistant strains of Staphylococcus aureus. Here, we identified the small cytosolic protein TraN as a repressor of the pIP501-encoded conjugative transfer system, since deletion of traN resulted in upregulation of transfer factors, leading to highly enhanced conjugative transfer. Furthermore, we report the complex structure of TraN with DNA and define the exact sequence of its binding motif. Targeting this protein-DNA interaction might represent a novel therapeutic approach against the spreading of antibiotic resistances.

Indexed as

Conjugation, GeneticAmino Acid SequenceAnti-Bacterial AgentsBacterial Outer Membrane ProteinsBinding SitesCrystallography, X-RayDNA, BacterialEnterococcus faecalisEscherichia coliEscherichia coli ProteinsGene DeletionKineticsModels, MolecularNucleic Acid ConformationPlasmidsProtein BindingAnti-Bacterial AgentsBacterial Outer Membrane ProteinsDNA, BacterialEscherichia coli ProteinsProtein IsoformstraN protein, E coliType IV Secretion SystemsVancomycin

Identifiers

PMID30060171
PMCPMC6158623
OpenAlexW2883755263

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.