Evidence map›Paper›PMID 33402750›Full record

ReviewCell death and differentiation2021

Adaptors as the regulators of HECT ubiquitin ligases.

Sonia Shalini Shah, Sharad Kumar

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 11% 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, 38 citations in OpenAlex.

  1. Article
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  4. Review
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  14. Review
  15. Article
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  17. Portrait of WWP1: the current state in human cancer.Frontiers in cell and developmental biology · 2024
    Review
  18. Review
  19. Structure of the human UBR5 E3 ubiquitin ligase.Structure (London, England : 1993) · 2023
    Article
  20. Monitoring HECT Ubiquitination Activity In Vitro.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Sonia Shalini ShahCentre for Cancer Biology, University of South Australia, GPO Box 2471, Adelaide, SA, 5001, Australia. Sonia.Shah@unisa.edu.au.
Sharad KumarCentre for Cancer Biology, University of South Australia, GPO Box 2471, Adelaide, SA, 5001, Australia. Sharad.Kumar@unisa.edu.au.ORCID http://orcid.org/0000-0001-7126-9814
University of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The HECT (homologous to E6AP C-terminus) ubiquitin ligases (E3s) are a small family of highly conserved enzymes involved in diverse cellular functions and pathological conditions. Characterised by a C-terminal HECT domain that accepts ubiquitin from E2 ubiquitin conjugating enzymes, these E3s regulate key signalling pathways. The activity and functional regulation of HECT E3s are controlled by several factors including post-translational modifications, inter- and intramolecular interactions and binding of co-activators and adaptor proteins. In this review, we focus on the regulation of HECT E3s by accessory proteins or adaptors and discuss various ways by which adaptors mediate their regulatory roles to affect physiological outcomes. We discuss common features that are conserved from yeast to mammals, regardless of the type of E3s as well as shed light on recent discoveries explaining some existing enigmas in the field.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCalciumHumansProtein BindingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionUbiquitinUbiquitin-Conjugating EnzymesUbiquitin-Protein LigasesAdaptor Proteins, Signal TransducingCalciumSaccharomyces cerevisiae ProteinsUbiquitinUbiquitin-Conjugating EnzymesUbiquitin-Protein Ligases

Identifiers

PMID33402750
PMCPMC7862271
OpenAlexW3118373671

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.