Cited by 177Bacterial Genetics and BiotechnologyDrug Transport and Resistance MechanismsHeat shock proteins research

The DOI matches its Crossref record; 402 of the 402 references it cites were found in a registry or an index.

Protein translocation across the inner membrane of Gram-negative bacteria: the Sec and Tat dependent protein transport pathways.

Open access
Kudva, Renuka, Denks, Kärt, Kuhn, Patrick, Vogt, Andreas, Müller, Matthias, Koch, Hans-Georg·2013·Research in Microbiology

Abstract

Gram negative bacteria possess a large variety of protein transport systems, by which proteins that are synthesised in the cytosol are exported to destinations in the cell envelope or entirely secreted into the extracellular environment. The inner membrane (IM) contains three major transport systems for the translocation and insertion of signal sequence containing proteins: the Sec translocon, the YidC insertase, and the Tat system. The heterotrimeric SecYEG translocon forms a narrow channel in the membrane that serves a dual function; it allows the translocation of unfolded proteins across the pore and the integration of α-helical proteins into the IM. The YidC insertase is a multi-spanning membrane protein that cooperates with the SecYEG translocon during the integration of membrane proteins but also functions as an independent insertase. Depending upon the type of protein cargo that needs to be transported, the Signal Recognition Particle (SRP), the SRP receptor, SecA and chaperones are required to coordinate translation with transport and to target and energise the different transport systems. The Tat system consists of three membrane proteins (TatA, TatB and TatC) which in a still unknown manner accomplish the transmembrane passage of completely folded proteins and protein complexes.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.resmic.2013.03.016

Cites

402 of 402 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Items 401–402 of 402

Research works printed but not linked: 2

  1. de Cock, 1991, Conservation of components of the Escherichia coli export machinery in prokaryotes, FEMS Microbiol. Lett., 59, 249
  2. Yen, 2002, Sequence and phylogenetic analyses of the twin-arginine targeting (Tat) protein export system, Arch. Microbiol., 177, 441, 10.1007/s00203-002-0408-4 · DOI

Cited by

Sorted by citations

See all 177

Metadata

Authors
Kudva, R., Denks, K., Kuhn, P., Vogt, A., Müller, M., & Koch, H.-G.
Affiliations
University of Freiburg (DE)
Corresponding author
  • Müller, Matthias
  • Koch, Hans-Georg
Venue
Research in Microbiology
Publisher
Elsevier BV
Published
2013-07
Volume
164
Issue
6
Pages
505-534
ISSN
  • 0769-2609 (ISSN-L)
  • 0923-2508
OpenAlex
W1979649414
Cited by
177
References
402
Citations by year
2026: 5 · 2025: 9 · 2024: 6 · 2023: 10 · 2022: 13 · 2021: 12 · 2020: 14 · 2019: 14 · 2018: 11 · 2017: 14 · 2016: 16 · 2015: 29 · 2014: 18 · 2013: 6
FWCI
15.26
Type
journal article
Language
en
Open access
Locations
  • Research in Microbiology (publishedVersion)
  • PubMed (publishedVersion)
Funders
Deutsche Forschungsgemeinschaft (GSC‐4, FOR 967, SFB-746, FOR 929)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
Keywords
protein translocation, Gram-negative bacteria, inner membrane, Sec translocon, Tat system, SecYEG translocon, signal recognition particle, SecA, molecular chaperones, membrane protein insertion, protein secretion, TatA, TATB, TatC
MeSH terms
Bacterial Proteins, Cell Membrane, Gram-Negative Bacteria, Protein Transport, Bacterial Secretion Systems

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review