Evidence map›Paper›PMID 29168745›Full record

ReviewToxins2017

Interaction of Cholesterol with Perfringolysin O: What Have We Learned from Functional Analysis?

Sergey N Savinov, Alejandro P Heuck

Open access · goldAbstract readReview
In one paragraph

Review in Toxins, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
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  7. Review
  8. Article
  9. NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Host Lipid Rafts as the Gates forFrontiers in immunology · 2020
    Review
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Sergey N SavinovDepartment of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, USA. ssavinov@umass.edu.
Alejandro P HeuckDepartment of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, USA. heuck@umass.edu.ORCID 0000-0002-7786-3109
University of Massachusetts Amherst · US

Funding

Molecular Mechanism of Translocon Assembly into Cell Plasma MembranesR01GM097414 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI HEUCK, ALEJANDRO PABLO · 2012 to 2016
$1.5M
NIGMS NIH HHS R01 GM097414
6 · The paper itself

Abstract

Cholesterol-dependent cytolysins (CDCs) constitute a family of pore-forming toxins secreted by Gram-positive bacteria. These toxins form transmembrane pores by inserting a large β-barrel into cholesterol-containing membranes. Cholesterol is absolutely required for pore-formation. For most CDCs, binding to cholesterol triggers conformational changes that lead to oligomerization and end in pore-formation. Perfringolysin O (PFO), secreted by

Indexed as

Bacterial ToxinsCholesterolHemolysin ProteinsHumansBacterial ToxinsCholesterolClostridium perfringens theta-toxinHemolysin Proteinscholesterolcholesterol-bindingcholesterol-dependent cytolysinsPerfringolysin O

Identifiers

PMID29168745
PMCPMC5744101
OpenAlexW2768872932

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.