Evidence map›Paper›PMID 26055053›Full record

ReviewProgress in molecular biology and translational science2015

Regulation of GPCR Trafficking by Ubiquitin.

Justine E Kennedy, Adriano Marchese

Open access · greenAbstract readReview
In one paragraph

Review in Progress in molecular biology and translational science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Beneath the surface: endosomal GPCR signaling.Trends in biochemical sciences · 2024
    Review
  7. Review
  8. Review
  9. GPCR targeting of E3 ubiquitin ligase MDM2 by inactive β-arrestin.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Review
  11. Article
  12. Mechanisms and Regulation of Neuronal GABACurrent topics in behavioral neurosciences · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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.

Justine E KennedyDepartment of Molecular Pharmacology and Therapeutics, Loyola University Chicago, Health Sciences Division, Maywood, Illinois, USA.
Adriano MarcheseDepartment of Molecular Pharmacology and Therapeutics, Loyola University Chicago, Health Sciences Division, Maywood, Illinois, USA. Electronic address: amarchese@luc.edu.
Loyola University Chicago · US

Funding

Role of beta-arrestins in G protein-coupled receptor sorting and signalingR01GM106727 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI MARCHESE, ADRIANO · 2014 to 2022
$2.9M
NIGMS NIH HHS GM106727NIGMS NIH HHS R01 GM106727
6 · The paper itself

Abstract

G protein-coupled receptor (GPCR)-promoted signaling mediates cellular responses to a variety of stimuli involved in diverse physiological processes. In addition, GPCRs are also the largest class of target for many drugs used to treat a variety of diseases. Despite the role of GPCR signaling in health and disease, the molecular mechanisms governing GPCR signaling remain poorly understanding. Classically, GPCR signaling is tightly regulated by GPCR kinases and β-arrestins, which act in a concerted fashion to govern GPCR desensitization and also GPCR trafficking. Ubiquitination has now emerged as an important posttranslational modification that has multiple roles, either directly or indirectly, in governing GPCR trafficking. Recent studies have revealed a mechanistic link between GPCR phosphorylation, β-arrestins, and ubiquitination. Here, we review recent developments in our understanding of how ubiquitin regulates GPCR trafficking within the endocytic pathway.

Indexed as

Gene Expression RegulationAnimalsArrestinsbeta-ArrestinsCell MembraneEndosomesHumansLysosomesPhosphorylationProtein BindingProtein TransportReceptors, G-Protein-CoupledSignal TransductionUbiquitinUbiquitinationArrestinsbeta-ArrestinsReceptors, G-Protein-CoupledUbiquitinCXCR4DegradationEndosomal sortingEndosomeESCRTGPCRLysosomeMultivesicular bodyReceptor traffickingUbiquitin

Identifiers

PMID26055053
PMCPMC4699176
OpenAlexW329956040

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.