Evidence map›Paper›PMID 41273410›Full record

ArticleJournal of molecular evolution2025

Evaluating Pretrained Protein Language Model Embeddings as Proxies for Functional Similarity.

Robert Shaw, Samuel D Love, Claire D McWhite

Abstract read
In one paragraph

Article in Journal of molecular evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Perspectives on Orthology During the Quest for Orthologs.Journal of molecular evolution · 2025
    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

3 authors.

Robert ShawDepartment of Molecular and Cellular Biology, The University of Arizona, Tucson, AZ, USA.ORCID 0009-0003-9810-742X
Samuel D LoveDepartment of Molecular and Cellular Biology, The University of Arizona, Tucson, AZ, USA.ORCID 0009-0007-2597-2016
Claire D McWhiteDepartment of Molecular and Cellular Biology, The University of Arizona, Tucson, AZ, USA. clairemcwhite@arizona.edu.ORCID 0000-0001-7346-3047

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein Language Models (PLMs) have emerged as powerful tools for representing protein sequences. We explore how embeddings (numeric vector representations) from pretrained PLMs can serve as direct numeric proxies for protein structure and function without requiring additional training or fine-tuning. In a proof-of-concept study of 22 cross-species complementation triplets-a gold standard for functional similarity where genes from one species are tested for their ability to rescue gene deletions in another species-we find that ESM-C 600 M embeddings summarized into pooled sliced-Wasserstein embeddings achieved high discrimination of subtle functional differences. This pooling method captures distributional properties of amino acid embeddings by comparing them against reference points using optimal transport theory. While our limited sample size precludes definitive conclusions about whether PLM embeddings systematically outperform sequence-based methods in detecting protein functional similarity, our preliminary results demonstrate the potential of using protein embeddings for functional analysis. Our exploratory analysis of orthology relationships suggests that embedding similarity may correlate with functional conservation, with the least diverged ortholog showing higher embedding similarity in approximately two-thirds of cases. Analyzing the Ortholog Conjecture-that orthologs maintain greater functional similarity than paralogs at equivalent sequence divergence-we do not observe clear differences between one-to-one orthologs and inparalog embedding similarities. Finally, we propose integrating PLMs with phylogenetic methods in a hybrid approach that leverages their complementary strengths: PLM-derived numeric embeddings for rapid homology detection and phylogenetics for evolutionary precision. We introduce embedding-tree versus gene-tree discordance as a potential metric to detect functional divergence between closely related proteins. Integrating protein embeddings with sequence analysis may enable a more nuanced understanding of protein function and evolutionary dynamics.

Indexed as

ProteinsAmino Acid SequenceEvolution, MolecularHumansProteinsFunctional similarityProtein language models

Identifiers

PMID41273410
PMCPMC12756192

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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.