Evidence map›Paper›PMID 37958899›Full record

ArticleInternational journal of molecular sciences2023

A Protein-Protein Interaction Analysis Suggests a Wide Range of New Functions for the p21-Activated Kinase (PAK) Ste20.

Ifeoluwapo Matthew Joshua, Meng Lin, Ariestia Mardjuki, Alessandra Mazzola, Thomas Höfken

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 69% 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

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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 3 countries.

Ifeoluwapo Matthew JoshuaDivision of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Meng LinInstitute of Biochemistry, Kiel University, 24118 Kiel, Germany.
Ariestia MardjukiDivision of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Alessandra MazzolaDivision of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Thomas HöfkenDivision of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Brunel University of London · GBChristian-Albrechts-Universität zu Kiel · DEUniversity of Palermo · IT

Funding

Deutsche Forschungsgemeinschaft HO 2098/5
6 · The paper itself

Abstract

The p21-activated kinases (PAKs) are important signaling proteins. They contribute to a surprisingly wide range of cellular processes and play critical roles in a number of human diseases including cancer, neurological disorders and cardiac diseases. To get a better understanding of PAK functions, mechanisms and integration of various cellular activities, we screened for proteins that bind to the budding yeast PAK Ste20 as an example, using the split-ubiquitin technique. We identified 56 proteins, most of them not described previously as Ste20 interactors. The proteins fall into a small number of functional categories such as vesicle transport and translation. We analyzed the roles of Ste20 in glucose metabolism and gene expression further. Ste20 has a well-established role in the adaptation to changing environmental conditions through the stimulation of mitogen-activated protein kinase (MAPK) pathways which eventually leads to transcription factor activation. This includes filamentous growth, an adaptation to nutrient depletion. Here we show that Ste20 also induces filamentous growth through interaction with nuclear proteins such as Sac3, Ctk1 and Hmt1, key regulators of gene expression. Combining our observations and the data published by others, we suggest that Ste20 has several new and unexpected functions.

Indexed as

Protein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsHumansMAP Kinase Kinase Kinasesp21-Activated KinasesSaccharomyces cerevisiaeMAP Kinase Kinase Kinasesp21-Activated KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsSTE20 protein, S cerevisiaebudding yeastgene expressionglucose metabolismp21-activated kinase (PAK)protein–protein interactionpseudohyphal growthSaccharomyces cerevisiaesplit-ubiquitinSte20

Identifiers

PMID37958899
PMCPMC10647699
OpenAlexW4388233236

What OpenQuestion holds

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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.