Evidence map›Paper›PMID 24033479›Full record

ArticleMolecular microbiology2013

Secretion of atypical protein substrates by the ESAT-6 secretion system of Staphylococcus aureus.

Mark Anderson, Khaled A Aly, Yi-Hsing Chen, Dominique Missiakas

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  9. Type VII secretion system extracellular protein B targets STING to evade host anti-Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Review
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  12. Article
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  15. Article
  16. Article
  17. Review
  18. Comparative Genomic Analysis of Type VII Secretion System inFrontiers in cellular and infection microbiology · 2022
    Article
  19. Article
  20. The Type VII Secretion System ofAnnual review of microbiology · 2021
    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

4 authors at 1 institution in 1 country.

Mark AndersonDepartment of Microbiology, The University of Chicago, Chicago, IL, 60637, USA.
Khaled A Aly
Yi-Hsing Chen
Dominique Missiakas
University of Chicago · US

Funding

ESAT-6 Secretion in Staphylococcus AureusR01AI075258 · NIAID · UNIVERSITY OF CHICAGO · PI MISSIAKAS, DOMINIQUE M. · 2009 to 2013
$1.9M
Biodefense Training in Host-Pathogen InteractionsT32AI065382 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2005 to 2009
$688k
NIAID NIH HHS AI75258NIAID NIH HHS R01 AI075258NIAID NIH HHS T32 AI065382
6 · The paper itself

Abstract

Staphylococcus aureus encodes the specialized ESAT-6 Secretion System (ESS). EsxA and EsxB are secreted by the ESS pathway, and share sequence features of ESAT-6 and CFP-10 of the Type VII Secretion System (T7SS) of Mycobacterium tuberculosis. Unlike ESAT-6 and CFP-10, EsxA and EsxB do not interact. Instead, EsxB associates with a novel substrate, EsxD, and EsxA dimerizes with itself or EsxC (EsaC). Unlike EsxA and EsxB, EsxC and EsxD do not share obvious sequence features of WXG100 proteins nor PE/PPE and Esp families of proteins, all of which belong to the pfam EsxAB clan of mycobacterial T7SS. EsxD carries the C-terminal motif YxxxD/E that has been proposed to target T7 substrates for secretion in mycobacteria. Here, we find that deletion, but not amino acid substitutions, in this motif prevent secretion of EsxA and EsxC but not EsxB or EsxD. This is unlike the genetic inactivation of esxA, esxB, esxC or esxD that leads to loss of secretion of all four substrates. Thus, substrate secretion can be uncoupled by deleting the last six amino acids of EsxD. The physical association of EsxC and EsxD with canonical WXG100 proteins suggests that these proteins belong to the EsxAB clan.

Indexed as

Secretory PathwayAmino Acid MotifsBacterial ProteinsConsensus SequenceGene Expression Regulation, BacterialGenes, BacterialMultigene FamilyMycobacterium tuberculosisProtein MultimerizationSequence DeletionStaphylococcal InfectionsStaphylococcus aureusBacterial Proteins

Identifiers

PMID24033479
PMCPMC3951145
OpenAlexW2136858660

What OpenQuestion holds

Textmetadata
LicenceTDM
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.