Evidence map›Paper›PMID 36016496›Full record

ArticleBiophysical journal2022

Understanding the separation of timescales in bacterial proteasome core particle assembly.

Pushpa Itagi, Anupama Kante, Leonila Lagunes, Eric J Deeds

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Biophysical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Pushpa ItagiCenter for Computational Biology, University of Kansas, Lawrence, Kansas; Institute for Quantitative and Computational Biosciences, UCLA, Los Angeles, California.
Anupama KanteDepartment of Molecular Biosciences, University of Kansas, Lawrence, Kansas; Department of Integrative Biology and Physiology, UCLA, Los Angeles, California.
Leonila LagunesDepartment of Integrative Biology and Physiology, UCLA, Los Angeles, California.
Eric J DeedsDepartment of Integrative Biology and Physiology, UCLA, Los Angeles, California; Institute for Quantitative and Computational Biosciences, UCLA, Los Angeles, California. Electronic address: deeds@ucla.edu.
University of California, Los Angeles · USUniversity of Kansas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 20S proteasome core particle (CP) is a molecular machine that is a key component of cellular protein degradation pathways. Like other molecular machines, it is not synthesized in an active form but rather as a set of subunits that assemble into a functional complex. The CP is conserved across all domains of life and is composed of 28 subunits, 14 α and 14 β, arranged in four stacked seven-member rings (α

Indexed as

Proteasome Endopeptidase ComplexDimerizationMolecular ConformationProteasome Endopeptidase Complex

Identifiers

PMID36016496
PMCPMC9674962
OpenAlexW4293051373

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.