Evidence map›Paper›PMID 38270169›Full record

ArticleeLife2024

Comparative interactome analysis of α-arrestin families in human and

Kyung-Tae Lee, Inez K A Pranoto, Soon-Young Kim, Hee-Joo Choi, Ngoc Bao To, Hansong Chae, Jeong-Yeon Lee, Jung-Eun Kim, Young V Kwon, Jin-Wu Nam

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 1 institution in 2 countries.

Kyung-Tae Lee *Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-5354-6910
Inez K A Pranoto *Department of Biochemistry, University of Washington, Seattle, United States.ORCID https://orcid.org/0000-0002-0709-5642
Soon-Young KimDepartment of Molecular Medicine, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.ORCID https://orcid.org/0009-0001-5132-7797
Hee-Joo ChoiBio-BigData Center, Hanyang Institute for Bioscience and Biotechnology, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-6432-8193
Ngoc Bao ToDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Hansong ChaeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Jeong-Yeon LeeBio-BigData Center, Hanyang Institute for Bioscience and Biotechnology, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-1298-7466
Jung-Eun KimDepartment of Molecular Medicine, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Young V KwonDepartment of Biochemistry, University of Washington, Seattle, United States.ORCID https://orcid.org/0000-0002-8937-3182
Jin-Wu NamDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-0047-3687
University of Washington · US

Funding

The Molecular Basis of Basal Cell Extrusion in Drosophila Intestinal EpitheliumR35GM128752 · NIGMS · UNIVERSITY OF WASHINGTON · PI Young Kwon · 2018 to 2026
$3.4M
NIGMS NIH HHS R35 GM128752NIH HHS R35GM128752
6 · The paper itself

Abstract

The α-arrestins form a large family of evolutionally conserved modulators that control diverse signaling pathways, including both G-protein-coupled receptor (GPCR)-mediated and non-GPCR-mediated pathways, across eukaryotes. However, unlike β-arrestins, only a few α-arrestin targets and functions have been characterized. Here, using affinity purification and mass spectrometry, we constructed interactomes for 6 human and 12

Indexed as

ArrestinVacuolar Proton-Translocating ATPasesAnimalsArrestinsDrosophilaHistonesHumansMammalsArrestinArrestinsHistonesVacuolar Proton-Translocating ATPasesAP/MSATAC-seqcomparative interactomescomputational biologyD. melanogastergeneticsgenomicshumanPPIsystems biologyTXNIPα-arrestin

Identifiers

PMID38270169
PMCPMC10945707
OpenAlexW4385271022

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.