Evidence map›Paper›PMID 16374509›Full record

ArticleEMBO reports2006

Identification of preferred protein interactions by phage-display of the human Src homology-3 proteome.

Satu Kärkkäinen, Marita Hiipakka, Jing-Huan Wang, Iivari Kleino, Marika Vähä-Jaakkola, G Herma Renkema, Michael Liss, Ralf Wagner, Kalle Saksela

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 117 citations in OpenAlex.

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  7. Functional selection in SH3-mediated activation of the PI3 kinase.bioRxiv : the preprint server for biology · 2024
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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

9 authors at 5 institutions in 2 countries.

Satu KärkkäinenInstitute of Medical Technology, University of Tampere and Tampere University Hospital, Biokatu 8, Tampere 33014, Finland.
Marita Hiipakka
Jing-Huan Wang
Iivari Kleino
Marika Vähä-Jaakkola
G Herma Renkema
Michael Liss
Ralf Wagner
Kalle Saksela
Tampere University · FITampere University Hospital · FIUniversity Hospital Regensburg · DETampere University · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have determined the human genome to contain 296 different Src homology-3 (SH3) domains and cloned them into a phage-display vector. This provided a powerful and unbiased system for simultaneous assaying of the complete human SH3 proteome for the strongest binding to target proteins of interest, without the limitations posed by short linear peptide ligands or confounding variables of more indirect methods for protein interaction screening. Studies involving three ligand proteins, human immunodeficiency virus-1 Nef, p21-activated kinase (PAK)2 and ADAM15, showed previously reported as well as novel SH3 partners with nanomolar affinities specific for them. This argues that SH3 domains may have a more dominant role in directing cellular protein interactions than has been assumed. Besides showing potentially important new SH3-directed interactions, these studies also led to the discovery of novel signalling proteins, such as the PAK2-binding adaptor protein POSH2 and the ADAM15-binding sorting nexin family member SNX30.

Indexed as

Peptide LibraryProteomeADAM ProteinsCarrier ProteinsGene Products, nefGenetic VectorsGlutathione TransferaseHumansLigandsMembrane Proteinsp21-Activated KinasesProtein BindingProteinsProtein Serine-Threonine KinasesRecombinant Fusion Proteinssrc Homology DomainsADAM15 protein, humanADAM ProteinsCarrier ProteinsGene Products, nefGlutathione TransferaseLigandsMembrane Proteinsp21-Activated KinasesPAK2 protein, humanPeptide LibraryProteinsProtein Serine-Threonine KinasesProteomeRecombinant Fusion ProteinsSH3RF1 protein, humanUbiquitin-Protein LigasesVesicular Transport Proteins

Identifiers

PMID16374509
PMCPMC1369250
OpenAlexW2116022941

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.