Evidence map›Paper›PMID 41282416›Full record

ArticleComputational and structural biotechnology journal2025

Evolutionary and structural bioinformatics identifies GPR89 as a conserved member of the LIMR protein superfamily.

Camila A Quercia-Raty, Luka Robeson, Sebastian E Brauchi

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Camila A Quercia-RatyPhysiology Department, Universidad Austral de Chile, Chile.
Luka RobesonPhysiology Department, Universidad Austral de Chile, Chile.
Sebastian E BrauchiPhysiology Department, Universidad Austral de Chile, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Also called the Golgi pH regulator (GPHR), GPR89 is an orphan membrane protein found in nearly all eukaryotic lineages. Despite its broad phylogenetic distribution, the evolutionary history, structural diversity, and function of GPR89 remain poorly understood. In this study, we present a comprehensive bioinformatic analysis of GPR89 in Eukarya by integrating phylogenetic reconstruction, genomic synteny, sequence conservation, and structural modeling. While GPR89 is typically encoded as a single-copy gene, we identified lineage-specific duplications in both vertebrates and vascular plants. In contrast to the large sequence conservation, differences can be observed in whether plants and animals preserve the gene structure flanking GPR89. Structural clustering places GPR89 within the solute carrier (SLC) group, together with LIMR protein family members. Predicted structures reveal a unique intracellular helix hairpin and a conserved transmembrane core compatible with putative transport activity. This work provides a unifying framework for interpreting the existing evidence on the GPR89 function and proposes that GPR89 should be classified within the LIMR superfamily.

Indexed as

COLD1GPHRGTGOrganelleOrphan ReceptorSolute CarrierTransporter

Identifiers

PMID41282416
PMCPMC12639261

What OpenQuestion holds

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Registered trials

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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.