Evidence map›Paper›PMID 28448471›Full record

ReviewInternational journal of molecular sciences2017

Regulation of G Protein-Coupled Receptors by Ubiquitination.

Kamila Skieterska, Pieter Rondou, Kathleen Van Craenenbroeck

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 57 citations in OpenAlex.

  1. Proteasomal-dependent endothelial P2YPurinergic signalling · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Neddylation steers the fate of cellular receptors.Experimental & molecular medicine · 2024
    Review
  6. Review
  7. Beneath the surface: endosomal GPCR signaling.Trends in biochemical sciences · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. GPharmacological reviews · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. 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

3 authors at 2 institutions in 1 country.

Kamila SkieterskaLaboratory of GPCR Expression and Signal Transduction (L-GEST), Ghent University, Proeftuinstraat 86, 9000 Ghent, Belgium. k.skieterska@gmail.com.
Pieter RondouLaboratory of GPCR Expression and Signal Transduction (L-GEST), Ghent University, Proeftuinstraat 86, 9000 Ghent, Belgium. Pieter.rondou@ugent.be.
Kathleen Van CraenenbroeckLaboratory of GPCR Expression and Signal Transduction (L-GEST), Ghent University, Proeftuinstraat 86, 9000 Ghent, Belgium. kathleen.vancraenenbroeck@ugent.be.
Ghent University · BEGhent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) comprise the largest family of membrane receptors that control many cellular processes and consequently often serve as drug targets. These receptors undergo a strict regulation by mechanisms such as internalization and desensitization, which are strongly influenced by posttranslational modifications. Ubiquitination is a posttranslational modification with a broad range of functions that is currently gaining increased appreciation as a regulator of GPCR activity. The role of ubiquitination in directing GPCRs for lysosomal degradation has already been well-established. Furthermore, this modification can also play a role in targeting membrane and endoplasmic reticulum-associated receptors to the proteasome. Most recently, ubiquitination was also shown to be involved in GPCR signaling. In this review, we present current knowledge on the molecular basis of GPCR regulation by ubiquitination, and highlight the importance of E3 ubiquitin ligases, deubiquitinating enzymes and β-arrestins. Finally, we discuss classical and newly-discovered functions of ubiquitination in controlling GPCR activity.

Indexed as

Animalsbeta-ArrestinsDeubiquitinating EnzymesHumansLysosomesProteasome Endopeptidase ComplexReceptors, G-Protein-CoupledSignal TransductionUbiquitinationUbiquitin-Protein Ligasesbeta-ArrestinsDeubiquitinating EnzymesProteasome Endopeptidase ComplexReceptors, G-Protein-CoupledUbiquitin-Protein Ligasesdeubiquitinating enzymeE3 ubiquitin ligaseG protein-coupled receptors (GPCR)ubiquitinationβ-arrestin

Identifiers

PMID28448471
PMCPMC5454836
OpenAlexW2608635043

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.