Evidence map›Paper›PMID 30460991›Full record

ArticleImmunology2019

A sequence conserved between CD5 and CD6 binds an FERM domain and exerts a restraint on T-cell activation.

Johannes Breuning, Marion H Brown

Open access · hybridAbstract read
In one paragraph

Article in Immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 10 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

2 authors at 1 institution in 1 country.

Johannes BreuningSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Marion H BrownSir William Dunn School of Pathology, University of Oxford, Oxford, UK.ORCID 0000-0001-5473-4235
University of Oxford · GB

Funding

Medical Research Council G0400808
6 · The paper itself

Abstract

CD5 and CD6 are related surface receptors that limit and promote T-cell responses. Co-stimulatory effects of CD6 depend on binding a cell surface ligand, CD166, and recruitment of the intracellular adaptor proteins GADS and SLP-76 by C-terminal phosphotyrosines. We have continued to identify interactions of CD5 and CD6 to understand their roles in T-cell activation. In a screen to identify binding partners for peptides containing a cytoplasmic sequence, SDSDY conserved between CD5 and CD6, we identified ezrin radixin moesin (ERM) proteins, which link plasma membrane proteins to actin. Purified radixin FERM domain bound directly to CD5 and CD6 SDSDY peptides in a phosphorylation-dependent manner (K

Indexed as

ActinsAnimalsAntibodies, MonoclonalAntigens, CDAntigens, Differentiation, T-LymphocyteCD5 AntigensCell MembraneCytoplasmCytoskeletonDNA-Binding ProteinsHumansLymphocyte ActivationPhosphorylationRatsT-LymphocytesTyrosineActinsAntibodies, MonoclonalAntigens, CDAntigens, Differentiation, T-LymphocyteCD5 AntigensCD6 antigenDNA-Binding ProteinsTyrosineinhibitory/activating receptorssignal transductionT cell

Identifiers

PMID30460991
PMCPMC6376265
OpenAlexW2901141150

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.