Evidence map›Paper›PMID 37759714›Full record

ArticleBiomolecules2023

Phylogenetic Analysis Guides Transporter Protein Deorphanization: A Case Study of the SLC25 Family of Mitochondrial Metabolite Transporters.

Katie L Byrne, Richard V Szeligowski, Hongying Shen

Abstract read
In one paragraph

Article in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Mitochondrial NADScience advances · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
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.

Katie L ByrneCellular and Molecular Physiology Department, Yale School of Medicine, New Haven, CT 06510, USA.
Richard V SzeligowskiCellular and Molecular Physiology Department, Yale School of Medicine, New Haven, CT 06510, USA.
Hongying ShenCellular and Molecular Physiology Department, Yale School of Medicine, New Haven, CT 06510, USA.ORCID 0000-0002-2115-7037

Funding

A systems approach to decode mitochondrial metabolite transportR35GM150619 · NIGMS · YALE UNIVERSITY · PI Hongying Shen · 2023 to 2026
$1.7M
NIGMS NIH HHS R35 GM150619
6 · The paper itself

Abstract

Homology search and phylogenetic analysis have commonly been used to annotate gene function, although they are prone to error. We hypothesize that the power of homology search in functional annotation depends on the coupling of sequence variation to functional diversification, and we herein focus on the SoLute Carrier (SLC25) family of mitochondrial metabolite transporters to survey this coupling in a family-wide manner. The SLC25 family is the largest family of mitochondrial metabolite transporters in eukaryotes that translocate ligands of different chemical properties, ranging from nucleotides, amino acids, carboxylic acids and cofactors, presenting adequate experimentally validated functional diversification in ligand transport. Here, we combine phylogenetic analysis to profile SLC25 transporters across common eukaryotic model organisms, from

Indexed as

Mitochondrial ProteinsOrganic Anion TransportersAnimalsCaenorhabditis elegansDrosophila melanogasterHumansMitochondriaMitochondrial Membrane Transport ProteinsPhylogenySaccharomyces cerevisiaeMitochondrial Membrane Transport ProteinsMitochondrial ProteinsOrganic Anion TransportersSlc25a1 protein, humandeorphanizationmetabolite transportmitochondriaphylogenetic analysisSLC25

Identifiers

PMID37759714
PMCPMC10526428

What OpenQuestion holds

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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.