Evidence map›Paper›PMID 42589379›Full record

ReviewInternational journal of molecular sciences2026

The Origins of GPCRs.

Vsevolod V Gurevich

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. 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
–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

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

1 author.

Vsevolod V GurevichDepartment of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA.ORCID 0000-0002-3950-5351

Funding

STRUCTURE/FUNCTION STUDIES OF VISUAL ARRESTINR01EY011500 · NEI · VANDERBILT UNIVERSITY · PI T M Iverson · 1997 to 2026
$12.3M
NEI NIH HHS 2R01EY011500-29NEI NIH HHS R01 EY011500
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are present in all kingdoms of life. GPCRs are the largest family of signaling proteins in animals, including humans. Numerous lines of indirect evidence suggest that eukaryotic light-sensitive rhodopsins (usually called type II), as well as other structurally similar non-visual GPCRs, trace their origins from prokaryotic rhodopsins (type I), possibly via receptors in unicellular eukaryotes that have a similar transmembrane core, even though existing sequence analysis software cannot detect homology. Bacterial and archaeal rhodopsins share the same overall design with eukaryotic GPCRs: a flexible core consisting of seven transmembrane α-helices with an extracellular N-terminus, an intracellular C-terminus, and three loops on each side of the membrane. Both families include many hundreds of members and apparently have expanded for billions of years, which makes the results of direct comparisons of the sequence and structure of these groups of proteins inconclusive. The distribution of residues with aromatic and ionizable side chains in prokaryotic rhodopsins and eukaryotic GPCRs was found to be similar. Established similarities suggest that shared origins are possible but do not unambiguously prove this hypothesis.

Indexed as

Evolution, MolecularReceptors, G-Protein-CoupledAmino Acid SequenceAnimalsHumansPhylogenyRhodopsinReceptors, G-Protein-CoupledRhodopsineukaryotesevolutionGPCRprokaryotesrhodopsin

Identifiers

PMID42589379
PMCPMC13466386

What OpenQuestion holds

Textmetadata
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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.