Evidence map›Paper›PMID 12215529›Full record

ArticleMolecular and cellular biology2002

Cdc42/Rac1-mediated activation primes PAK2 for superactivation by tyrosine phosphorylation.

G Herma Renkema, Kati Pulkkinen, Kalle Saksela

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 46 citations in OpenAlex.

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  13. Estrogen-regulated feedback loop limits the efficacy of estrogen receptor-targeted breast cancer therapy.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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 at 1 institution in 1 country.

G Herma RenkemaInstitute of Medical Technology, FIN-33014 University of Tampere, Finland.
Kati Pulkkinen
Kalle Saksela
Tampere University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The involvement of p21-activated kinases (PAKs) in important cellular processes such as regulation of the actin skeleton morphology, transduction of signals controlling gene expression, and execution of programmed cell death has directed attention to the regulation of the activity of these kinases. Here we report that activation of PAK2 by p21 GTPases can be strongly potentiated by cellular tyrosine kinases. PAK2 became tyrosine phosphorylated in its N-terminal regulatory domain, where Y130 was identified as the major phosphoacceptor site. Tyrosine phosphorylation-mediated superactivation of PAK2 could be induced by overexpression of different Src kinases or by inhibiting cellular tyrosine phosphatases with pervanadate and could be blocked by the Src kinase inhibitor PP1 or by mutating the Y130 residue. Analysis of PAK2 mutants activated by amino acid changes in the autoinhibitory domain or the catalytic domain indicated that GTPase-induced conformational changes, rather than catalytic activation per se, rendered PAK2 a target for tyrosine phosphorylation. Thus, PAK activation represents a potentially important point of convergence of tyrosine kinase- and p21 GTPase-dependent signaling pathways.

Indexed as

Binding SitesCatalysiscdc42 GTP-Binding ProteinCell LineEnzyme ActivationEnzyme InhibitorsHumansKidneyMutagenesis, Site-Directedp21-Activated KinasesPhosphorylationProtein ConformationProtein Serine-Threonine KinasesProtein Structure, TertiaryProtein Tyrosine Phosphatasesrac1 GTP-Binding Proteincdc42 GTP-Binding ProteinEnzyme Inhibitorsp21-Activated KinasesPAK2 protein, humanProtein Serine-Threonine KinasesProtein Tyrosine Phosphatasesrac1 GTP-Binding Proteinsrc-Family KinasesTyrosine

Identifiers

PMID12215529
PMCPMC134024
OpenAlexW2129191533

What OpenQuestion holds

Textmetadata
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.