Evidence map›Paper›PMID 17158657›Full record

ArticleJournal of bacteriology2007

Signal recognition particle-dependent inner membrane targeting of the PulG Pseudopilin component of a type II secretion system.

Olivera Francetic, Nienke Buddelmeijer, Shawn Lewenza, Carol A Kumamoto, Anthony P Pugsley

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 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

43 citing papers in PubMed, 64 citations in OpenAlex.

  1. β-strand addition within tip initiation complexes licenses assembly of diverse type IV filaments.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. PilB fromProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Structure and function of minor pilins of type IV pili.Medical microbiology and immunology · 2020
    Review
  8. Bacterial secretins: Mechanisms of assembly and membrane targeting.Protein science : a publication of the Protein Society · 2020
    Review
  9. Review
  10. Article
  11. Review
  12. Archaeal cell surface biogenesis.FEMS microbiology reviews · 2018
    Article
  13. Reconstitution of a minimal machinery capable of assembling periplasmic type IV pili.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Tracking Proteins Secreted by Bacteria: What's in the Toolbox?Frontiers in cellular and infection microbiology · 2017
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Editorial.FEMS microbiology reviews · 2015
    Article
  20. 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

5 authors at 3 institutions in 2 countries.

Olivera FranceticMolecular Genetics Unit, Institut Pasteur, 25 Rue du Dr. Roux, 75724 Paris Cedex 15, France.
Nienke Buddelmeijer
Shawn Lewenza
Carol A Kumamoto
Anthony P Pugsley
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRTufts University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pseudopilin PulG is an essential component of the pullulanase-specific type II secretion system from Klebsiella oxytoca. PulG is the major subunit of a short, thin-filament pseudopilus, which presumably elongates and retracts in the periplasm, acting as a dynamic piston to promote pullulanase secretion. It has a signal sequence-like N-terminal segment that, according to studies with green and red fluorescent protein chimeras, anchors unassembled PulG in the inner membrane. We analyzed the early steps of PulG inner membrane targeting and insertion in Escherichia coli derivatives defective in different protein targeting and export factors. The beta-galactosidase activity in strains producing a PulG-LacZ hybrid protein increased substantially when the dsbA, dsbB, or all sec genes tested except secB were compromised by mutations. To facilitate analysis of native PulG membrane insertion, a leader peptidase cleavage site was engineered downstream from the N-terminal transmembrane segment (PrePulG*). Unprocessed PrePulG* was detected in strains carrying mutations in secA, secY, secE, and secD genes, including some novel alleles of secY and secD. Furthermore, depletion of the Ffh component of the signal recognition particle (SRP) completely abolished PrePulG* processing, without affecting the Sec-dependent export of periplasmic MalE and RbsB proteins. Thus, PulG is cotranslationally targeted to the inner membrane Sec translocase by SRP.

Indexed as

Amino Acid SequenceCell MembraneEscherichia coliEscherichia coli ProteinsFimbriae ProteinsMolecular Sequence DataProtein Sorting SignalsProtein TransportSignal Recognition ParticleEscherichia coli ProteinsFimbriae ProteinsProtein Sorting SignalsSignal Recognition Particle

Identifiers

PMID17158657
PMCPMC1855701
OpenAlexW2096268195

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.