Evidence map›Paper›PMID 34840080›Full record

ReviewSeminars in cell & developmental biology2022

Fast friends - Ubiquitin-like modifiers as engineered fusion partners.

Evrydiki Asimaki, Kirill Petriukov, Christian Renz, Cindy Meister, Helle D Ulrich

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors at 1 institution in 1 country.

Evrydiki AsimakiInstitute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, D-55128 Mainz, Germany.
Kirill PetriukovInstitute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, D-55128 Mainz, Germany.
Christian RenzInstitute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, D-55128 Mainz, Germany.
Cindy MeisterInstitute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, D-55128 Mainz, Germany.
Helle D UlrichInstitute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, D-55128 Mainz, Germany. Electronic address: h.ulrich@imb-mainz.de.
Institute of Molecular Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ubiquitin and its relatives are major players in many biological pathways, and a variety of experimental tools based on biological chemistry or protein engineering is available for their manipulation. One popular approach is the use of linear fusions between the modifier and a protein of interest. Such artificial constructs can facilitate the understanding of the role of ubiquitin in biological processes and can be exploited to control protein stability, interactions and degradation. Here we summarize the basic design considerations and discuss the advantages as well as limitations associated with their use. Finally, we will refer to several published case studies highlighting the principles of how they provide insight into pathways ranging from membrane protein trafficking to the control of epigenetic modifications.

Indexed as

Small Ubiquitin-Related Modifier ProteinsUbiquitinEpigenesis, GeneticHumansProtein StabilitySmall Ubiquitin-Related Modifier ProteinsUbiquitinDegron technologyEndocytosisGenome maintenanceMitophagyProtein engineeringProtein stabilitySUMOTranscriptional regulationUbiquitinUFD

Identifiers

PMID34840080
PMCPMC9703124
OpenAlexW3215205932

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.