Evidence map›Paper›PMID 40473619›Full record

ArticleNature communications2025

Mechanism of human α3β GlyR regulation by intracellular M3/M4 loop phosphorylation and 2,6-di-tert-butylphenol interaction.

Xiaofen Liu, Malgorzata Krezel, Weiwei Wang

Abstract read
In one paragraph

Article in Nature communications, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Xiaofen LiuDepartments of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-3560-0850
Malgorzata KrezelDepartments of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Weiwei WangDepartments of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX, USA. Weiwei.Wang@UTSouthwestern.edu.ORCID http://orcid.org/0000-0002-0215-9467

Funding

Understanding higher-order glycine receptor assemblies in neurotransmissionR35GM146860 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Weiwei Wang · 2022 to 2026
$2.0M
McKnight Foundation 2022 Scholar AwardNIGMS NIH HHS R35 GM146860U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) 1R35GM146860
6 · The paper itself

Abstract

α3β glycine receptor (GlyR) is a subtype of GlyRs that belongs to the Cys-loop receptor superfamily. It is highly expressed in the spinal dorsal horn where sensory information is integrated. Under inflammatory conditions, the large unstructured intracellular M3/M4 loops of the α3 subunit are phosphorylated through the prostaglandin E2 (PGE

Indexed as

PhenolsReceptors, GlycineAnimalsCryoelectron MicroscopyFluorescence Resonance Energy TransferHEK293 CellsHumansPhosphorylationProtein Bindingglycine receptor alpha3 subunitPhenolsReceptors, Glycine

Identifiers

PMID40473619
PMCPMC12141631

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.