Evidence map›Paper›PMID 38612889›Full record

ReviewInternational journal of molecular sciences2024

Domains in Action: Understanding Ddi1's Diverse Functions in the Ubiquitin-Proteasome System.

Artur Fabijan, Bartosz Polis, Agnieszka Zawadzka-Fabijan, Izabela Korabiewska, Krzysztof Zakrzewski, Emilia Nowosławska, Michał Chojnacki

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

7 authors at 3 institutions in 1 country.

Artur FabijanDepartment of Neurosurgery, Polish-Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.ORCID 0000-0002-0998-4435
Bartosz PolisDepartment of Neurosurgery, Polish-Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Agnieszka Zawadzka-FabijanDepartment of Rehabilitation Medicine, Faculty of Health Sciences, Medical University of Lodz, 90-419 Lodz, Poland.ORCID 0000-0002-4031-0930
Izabela KorabiewskaDepartment of Rehabilitation, Faculty of Dental Medicine, Medical University of Warsaw, 02-091 Warsaw, Poland.
Krzysztof ZakrzewskiDepartment of Neurosurgery, Polish-Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Emilia NowosławskaDepartment of Neurosurgery, Polish-Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.
Michał ChojnackiDepartment of Medical Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Polish Mother’s Memorial Hospital Research Institute · PLMedical University of Lodz · PLMedical University of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitin-proteasome system (UPS) is a pivotal cellular mechanism responsible for the selective degradation of proteins, playing an essential role in proteostasis, protein quality control, and regulating various cellular processes, with ubiquitin marking proteins for degradation through a complex, multi-stage process. The shuttle proteins family is a very unique group of proteins that plays an important role in the ubiquitin-proteasome system. Ddi1, Dsk2, and Rad23 are shuttle factors that bind ubiquitinated substrates and deliver them to the 26S proteasome. Besides mediating the delivery of ubiquitinated proteins, they are also involved in many other biological processes. Ddi1, the least-studied shuttle protein, exhibits unique physicochemical properties that allow it to play non-canonical functions in the cells. It regulates cell cycle progression and response to proteasome inhibition and defines MAT type of yeast cells. The Ddi1 contains UBL and UBA domains, which are crucial for binding to proteasome receptors and ubiquitin respectively, but also an additional domain called RVP. Additionally, much evidence has been provided to question whether Ddi1 is a classical shuttle protein. For many years, the true nature of this protein remained unclear. Here, we highlight the recent discoveries, which shed new light on the structure and biological functions of the Ddi1 protein.

Indexed as

Proteasome Endopeptidase ComplexUbiquitinCell DivisionCytoplasmSaccharomyces cerevisiaeUbiquitinated ProteinsProteasome Endopeptidase ComplexUbiquitinUbiquitinated ProteinsDNA-damage inducible protein 1 (Ddi1)retroviral-like protease domain (RVP)ubiquitin associated domain (UBA)ubiquitin-like domain (UBL)ubiquitin-proteasome system (UPS)ubiquitin (Ub)

Identifiers

PMID38612889
PMCPMC11012796
OpenAlexW4394568442

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.