Evidence map›Paper›PMID 34460869›Full record

ArticlePLoS pathogens2021

A kinase-independent function of PAK is crucial for pathogen-mediated actin remodelling.

Anthony Davidson, Joe Tyler, Peter Hume, Vikash Singh, Vassilis Koronakis

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. PAK2-driven cytoskeleton-endosome dynamics control macrophage hyperphagia and SIRPA engagement.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. iScience · 2023
    Article
  8. 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

5 authors at 1 institution in 1 country.

Anthony DavidsonDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Joe TylerDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Peter HumeDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-4064-4519
Vikash SinghDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Vassilis KoronakisDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-1353-1092
University of Cambridge · GB

Funding

Medical Research Council MR/L008122/1Medical Research Council MR/N000994/1Wellcome Trust 101828/Z/13/Z
6 · The paper itself

Abstract

The p21-activated kinase (PAK) family regulate a multitude of cellular processes, including actin cytoskeleton remodelling. Numerous bacterial pathogens usurp host signalling pathways that regulate actin reorganisation in order to promote Infection. Salmonella and pathogenic Escherichia coli drive actin-dependent forced uptake and intimate attachment respectively. We demonstrate that the pathogen-driven generation of both these distinct actin structures relies on the recruitment and activation of PAK. We show that the PAK kinase domain is dispensable for this actin remodelling, which instead requires the GTPase-binding CRIB and the central poly-proline rich region. PAK interacts with and inhibits the guanine nucleotide exchange factor β-PIX, preventing it from exerting a negative effect on cytoskeleton reorganisation. This kinase-independent function of PAK may be usurped by other pathogens that modify host cytoskeleton signalling and helps us better understand how PAK functions in normal and diseased eukaryotic cells.

Indexed as

ActinsCytoskeletonHumansMembrane Proteinsp21-Activated KinasesPhosphorylationRho Guanine Nucleotide Exchange FactorsSalmonella entericaSalmonella InfectionsTumor Suppressor ProteinsActinsARHGEF7 protein, humanMembrane Proteinsp21-Activated KinasesRho Guanine Nucleotide Exchange FactorsSCRIB protein, humanTumor Suppressor Proteins

Identifiers

PMID34460869
PMCPMC8432889
OpenAlexW3198377032

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.