Evidence map›Paper›PMID 33860801›Full record

ReviewBiochemical Society transactions2021

Regulation of MST complexes and activity via SARAH domain modifications.

Sofiia Karchugina, Dorothy Benton, Jonathan Chernoff

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical Society transactions, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Sofiia KarchuginaCancer Signaling and Epigenetics Program, Fox Chase Cancer Center, Philadelphia, PA, U.S.A.
Dorothy BentonBiochemistry Department, Drexel University College of Medicine, 245 N 15th St, Philadelphia, PA, U.S.A.
Jonathan ChernoffCancer Signaling and Epigenetics Program, Fox Chase Cancer Center, Philadelphia, PA, U.S.A.
Fox Chase Cancer Center · USDrexel University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
The Role of p21-Activated Kinases in Malignant MesotheliomaR01CA148805 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHERNOFF, JONATHAN, TESTA, JOSEPH R. · 2011 to 2020
$4.0M
NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA148805
6 · The paper itself

Abstract

Three elements of the Hippo tumor suppressor pathway - MST1/2, SAV1, and RASSF1-6 - share in common a C-terminal interaction motif termed the SARAH domain. Proteins containing this domain are capable of self-association as homodimers and also of trans-association with other SARAH domain containing proteins as well as selected additional proteins that lack this domain. Recently, the association of MST1/2 with itself or with other proteins has been shown to be regulated by phosphorylation at sites near or within the SARAH domain. In this review, we focus on recent findings regarding the regulation of such MST1/2 interactions, with an emphasis on the effects of these events on Hippo pathway activity.

Indexed as

Gene Expression RegulationAmino Acid SequenceAnimalsBinding SitesCell Cycle ProteinsHippo KinasesHippo Signaling PathwayHumansIntracellular Signaling Peptides and ProteinsMultiprotein ComplexesProtein DomainsProtein MultimerizationProtein Serine-Threonine KinasesSequence Homology, Amino AcidSerine-Threonine Kinase 3Tumor Suppressor ProteinsCell Cycle ProteinsHippo KinasesIntracellular Signaling Peptides and ProteinsMultiprotein ComplexesProtein Serine-Threonine KinasesSAV1 protein, humanSerine-Threonine Kinase 3STK3 protein, humanSTK4 protein, humanTumor Suppressor Proteinscancerdimerizationhippo pathwayprotein kinasesSARAH domainsignal transduction

Identifiers

PMID33860801
PMCPMC9540434
OpenAlexW3155199974

What OpenQuestion holds

Textmetadata
LicenceTDM
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.