Evidence map›Paper›PMID 17434972›Full record

ArticleJournal of bacteriology2007

Membrane association and multimerization of TcpT, the cognate ATPase ortholog of the Vibrio cholerae toxin-coregulated-pilus biogenesis apparatus.

Shital A Tripathi, Ronald K Taylor

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Vibrio Pathogenicity Island-1: The Master Determinant of Cholera Pathogenesis.Frontiers in cellular and infection microbiology · 2020
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Editorial.FEMS microbiology reviews · 2015
    Article
  9. Review
  10. Type IV pili in Gram-positive bacteria.Microbiology and molecular biology reviews : MMBR · 2013
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Type IV pili: paradoxes in form and function.Current opinion in structural biology · 2008
    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

2 authors at 1 institution in 1 country.

Shital A TripathiDepartment of Microbiology and Immunology, Dartmouth Medical School, HB7550, Hanover, NH 03755, USA.
Ronald K Taylor
Dartmouth College · US

Funding

Genetic Determinants of Virulence in Vibrio choleraeR37AI025096 · NIAID · DARTMOUTH COLLEGE · PI TAYLOR, RONALD K · 2007 to 2015
$4.3M
GENTICS DETERMINATION OF VIRULENCE OF VIBRIO CHOLERAER01AI025096 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SKORUPSKI, KAREN A · 1989 to 2016
$3.1M
GENETIC DETERMINANTS OF VIRULENCE IN VIBRIO CHOLERAER22AI025096 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TAYLOR, RONALD K · 1987 to 1991
–
NIAID NIH HHS AI25096NIAID NIH HHS R01 AI025096NIAID NIH HHS R37 AI025096
6 · The paper itself

Abstract

The toxin-coregulated pilus (TCP) is one of the major virulence factors of Vibrio cholerae. Biogenesis of this type 4 pilus (Tfp) requires a number of structural components encoded by the tcp operon. TcpT, the cognate putative ATPase, is required for TCP biogenesis and all TCP-mediated functions. We studied the stability and localization of TcpT in cells containing in-frame deletions in each of the tcp genes. TcpT was detectable in each of the biogenesis mutants except the DeltatcpT strain. TcpT was localized to the inner membrane (IM) in a TcpR-dependent manner. TcpR is a predicted bitopic inner membrane protein of the TCP biogenesis apparatus. Using metal affinity pull-down experiments, we demonstrated interaction between TcpT and TcpR. Using Escherichia coli as a heterologous system, we investigated direct interaction between TcpR and TcpT. We report that TcpR is sufficient for TcpT IM localization per se; however, stable IM localization of TcpT requires an additional V. cholerae-specific factor(s). A LexA-based two-hybrid system was utilized to define interaction domains of the two proteins. We demonstrate a strong interaction between the cytoplasmic domain of TcpR and the N-terminal 100 amino acid residues of TcpT. We also demonstrated the ability of the C-terminal domain of TcpT to multimerize.

Indexed as

Adenosine TriphosphatasesBacterial ProteinsCell MembraneDimerizationEscherichia coliFimbriae, BacterialGene DeletionGenes, BacterialMembrane ProteinsOperonProtein BindingProtein Interaction MappingTwo-Hybrid System TechniquesVibrio choleraeVirulence FactorsAdenosine TriphosphatasesBacterial ProteinsMembrane ProteinsVirulence Factors

Identifiers

PMID17434972
PMCPMC1913367
OpenAlexW2168840243

What OpenQuestion holds

Textmetadata
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.