Evidence map›Paper›PMID 20404072›Full record

ReviewMolecular pharmacology2010

Heterotrimeric G protein signaling outside the realm of seven transmembrane domain receptors.

Caroline Marty, Richard D Ye

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Receptor tyrosine kinases activate heterotrimeric G proteins via phosphorylation within the interdomain cleft of Gαi.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Update onCancers · 2020
    Review
  6. αFrontiers in cell and developmental biology · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Heterotrimeric G protein signaling via GIV/Girdin: Breaking the rules of engagement, space, and time.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Review
  14. Review
  15. Article
  16. Therapeutic effects of cell-permeant peptides that activate G proteins downstream of growth factors.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  17. Multimodular biosensors reveal a novel platform for activation of G proteins by growth factor receptors.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  18. Article
  19. Contribution of each Trp residue toward the intrinsic fluorescence of the Giα1 protein.Protein science : a publication of the Protein Society · 2014
    Article
  20. 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

2 authors at 1 institution in 1 country.

Caroline MartyInstitut National de la Santé et de la Recherche Médicale, Université Paris XI, Institut Gustave Roussy, Villejuif, France.
Richard D Ye
Inserm · FR

Funding

MOLECULAR MECHANISMS OF LEUKOCYTE ACTIVATIONR01AI033503 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI YE, RICHARD D · 1993 to 2014
$4.5M
Pharmacological Study of G-proteins in Gene RegulationR01GM066182 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI YE, RICHARD D · 2004 to 2007
$1.0M
Molecular Mechanisms of Leukocyte ActivationR56AI033503 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI YE, RICHARD D · 2009 to 2009
$393k
NIAID NIH HHS AI033503NIAID NIH HHS R01 AI033503NIAID NIH HHS R56 AI033503NIGMS NIH HHS GM066182NIGMS NIH HHS R01 GM066182
6 · The paper itself

Abstract

Heterotrimeric G proteins, consisting of the guanine nucleotide-binding Galpha subunits with GTPase activity and the closely associated Gbeta and Ggamma subunits, are important signaling components for receptors with seven transmembrane domains (7TMRs). These receptors, also termed G protein-coupled receptors (GPCRs), act as guanine nucleotide exchange factors upon agonist stimulation. There is now accumulating evidence for noncanonical functions of heterotrimeric G proteins independent of 7TMR coupling. Galpha proteins belonging to all 4 subfamilies, including G(s), G(i), G(q), and G(12) are found to play important roles in receptor tyrosine kinase signaling, regulation of oxidant production, development, and cell migration, through physical and functional interaction with proteins other than 7TMRs. Association of Galpha with non-7TMR proteins also facilitates presentation of these G proteins to specific cellular microdomains. This Minireview aims to summarize our current understanding of the noncanonical roles of Galpha proteins in cell signaling and to discuss unresolved issues including regulation of Galpha activation by proteins other than the 7TMRs.

Indexed as

Signal TransductionAnimalsHeterotrimeric GTP-Binding ProteinsHumansReceptor Protein-Tyrosine KinasesHeterotrimeric GTP-Binding ProteinsReceptor Protein-Tyrosine Kinases

Identifiers

PMID20404072
PMCPMC2912057
OpenAlexW2111535188

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.