Evidence map›Paper›PMID 23549480›Full record

ArticleMolecular systems biology2013

SH3 interactome conserves general function over specific form.

Xiaofeng Xin, David Gfeller, Jackie Cheng, Raffi Tonikian, Lin Sun, Ailan Guo, Lianet Lopez, Alevtina Pavlenco, Adenrele Akintobi, Yingnan Zhang and 19 more

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Analysis ofComputational and structural biotechnology journal · 2024
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  16. Identifying New Substrates and Functions for an Old Enzyme: Calcineurin.Cold Spring Harbor perspectives in biology · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. Network Medicine in Pathobiology.The American journal of pathology · 2019
    Review
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

29 authors at 10 institutions in 3 countries.

Xiaofeng XinThe Donnelly Centre, University of Toronto, Toronto, Ontario, Canada.
David Gfeller
Jackie Cheng
Raffi Tonikian
Lin Sun
Ailan Guo
Lianet Lopez
Alevtina Pavlenco
Adenrele Akintobi
Yingnan Zhang
Jean-François Rual
Bridget Currell
Somasekar Seshagiri
Tong Hao
Xinping Yang
Yun A Shen
Kourosh Salehi-Ashtiani
Jingjing Li
Aaron T Cheng
Dryden Bouamalay
Adrien Lugari
David E Hill
Mark L Grimes
David G Drubin
Barth D Grant
Marc Vidal
Charles Boone
Sachdev S Sidhu
Gary D Bader
University of Toronto · CADana-Farber Cancer Institute · USUniversity of California, Berkeley · USRutgers, The State University of New Jersey · USGene Therapy Laboratory · FRHarvard University · USAix-Marseille Université · FRCell Signaling Technology (United States) · USCenter for Discovery · USUniversity of Montana · US

Funding

TR&D 3 - Network Guided Machine LearningP41GM103504 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI IDEKER, TREY · 2012 to 2024
$17.3M
The C. elegans Interactome ProjectR01HG001715 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI HILL, DAVID E., ROTH, FREDERICK P · 1998 to 2010
$16.5M
Nikon confocal system for improved spatio-dynamic analysis of endocytic trafficking eventsR35GM118149 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DAVID G DRUBIN · 2016 to 2026
$12.0M
Membrane Traffic in C. elegans and MammalsR01GM067237 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI GRANT, BARTH DEMIAN · 2003 to 2019
$6.1M
ENDOCYTIC FUNCTIONS FOR THE MAMMALIAN ACTIN CYTOSKELETONR01GM065462 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DRUBIN, DAVID G · 2002 to 2015
$3.4M
CIHR MOP-84324CIHR MOP-93725NHGRI NIH HHS R01 HG001715NIGMS NIH HHS P41 GM103504NIGMS NIH HHS R01 GM065462NIGMS NIH HHS R01 GM067237NIGMS NIH HHS R01 GM65462NIGMS NIH HHS R35 GM118149
6 · The paper itself

Abstract

Src homology 3 (SH3) domains bind peptides to mediate protein-protein interactions that assemble and regulate dynamic biological processes. We surveyed the repertoire of SH3 binding specificity using peptide phage display in a metazoan, the worm Caenorhabditis elegans, and discovered that it structurally mirrors that of the budding yeast Saccharomyces cerevisiae. We then mapped the worm SH3 interactome using stringent yeast two-hybrid and compared it with the equivalent map for yeast. We found that the worm SH3 interactome resembles the analogous yeast network because it is significantly enriched for proteins with roles in endocytosis. Nevertheless, orthologous SH3 domain-mediated interactions are highly rewired. Our results suggest a model of network evolution where general function of the SH3 domain network is conserved over its specific form.

Indexed as

Amino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsConserved SequenceEndocytosisEvolution, MolecularMolecular Sequence DataProtein Interaction MappingSaccharomyces cerevisiaeSaccharomyces cerevisiae Proteinssrc Homology DomainsStructural Homology, ProteinTwo-Hybrid System TechniquesCaenorhabditis elegans ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID23549480
PMCPMC3658277
OpenAlexW2110311701

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.