Evidence map›Paper›PMID 19390620›Full record

ArticlePLoS pathogens2009

Accurate prediction of secreted substrates and identification of a conserved putative secretion signal for type III secretion systems.

Ram Samudrala, Fred Heffron, Jason E McDermott

Abstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
–field-weighted citation impact
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

123 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Protein Sorting Prediction.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Article
  7. Type III Secretion inMicrobiology and molecular biology reviews : MMBR · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Application of aJournal of bacteriology · 2021
    Article
  16. Article
  17. Article
  18. Computational prediction of secreted proteins in gram-negative bacteria.Computational and structural biotechnology journal · 2021
    Review
  19. AIMS microbiology · 2021
    Review
  20. Interesting Biochemistries in the Structure and Function of Bacterial Effectors.Frontiers in cellular and infection microbiology · 2021
    Review

63 more citing papers are in PubMed but not listed here.

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

3 authors.

Ram SamudralaDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Fred Heffron
Jason E McDermott

Funding

SALMONELLA GENES REQUIRED FOR SURVIVAL IN THE MACROPHAGER01AI022933 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI HEFFRON, FRED L · 1987 to 2013
$4.6M
Protein structure from theory and experimentR33GM068152 · NIGMS · UNIVERSITY OF WASHINGTON · PI SAMUDRALA, RAM · 2003 to 2005
$901k
NIAID NIH HHS R01 AI022933NIAID NIH HHS Y1-AI-4894-01NIGMS NIH HHS GM068152NIGMS NIH HHS R33 GM068152
6 · The paper itself

Abstract

The type III secretion system is an essential component for virulence in many Gram-negative bacteria. Though components of the secretion system apparatus are conserved, its substrates--effector proteins--are not. We have used a novel computational approach to confidently identify new secreted effectors by integrating protein sequence-based features, including evolutionary measures such as the pattern of homologs in a range of other organisms, G+C content, amino acid composition, and the N-terminal 30 residues of the protein sequence. The method was trained on known effectors from the plant pathogen Pseudomonas syringae and validated on a set of effectors from the animal pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) after eliminating effectors with detectable sequence similarity. We show that this approach can predict known secreted effectors with high specificity and sensitivity. Furthermore, by considering a large set of effectors from multiple organisms, we computationally identify a common putative secretion signal in the N-terminal 20 residues of secreted effectors. This signal can be used to discriminate 46 out of 68 total known effectors from both organisms, suggesting that it is a real, shared signal applicable to many type III secreted effectors. We use the method to make novel predictions of secreted effectors in S. Typhimurium, some of which have been experimentally validated. We also apply the method to predict secreted effectors in the genetically intractable human pathogen Chlamydia trachomatis, identifying the majority of known secreted proteins in addition to providing a number of novel predictions. This approach provides a new way to identify secreted effectors in a broad range of pathogenic bacteria for further experimental characterization and provides insight into the nature of the type III secretion signal.

Indexed as

Amino Acid SequenceArtificial IntelligenceBacterial ProteinsChlamydia trachomatisComputational BiologyDatabases, ProteinEvolution, MolecularGram-Negative BacteriaProtein Sorting SignalsPseudomonas syringaeSalmonella entericaBacterial ProteinsProtein Sorting Signals

Identifiers

PMID19390620
PMCPMC2668754

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Registered trials

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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.