Evidence map›Paper›PMID 42602309›Full record

ArticleComputational and structural biotechnology journal2026

UNKAI: A Protein Functional Identity Prediction Model Based on ESM-C Latent Representations and the Attention Mechanism.

Kotaro Ukai, Suguru Fujita, Tohru Terada

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Kotaro UkaiDepartment of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.
Suguru FujitaDepartment of Animal Resource Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.ORCID https://orcid.org/0000-0001-7488-0045
Tohru TeradaDepartment of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan.ORCID https://orcid.org/0000-0002-7091-0646

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid advancement of genome sequencing technologies has led to the accumulation of a vast number of protein sequences in public databases. However, a substantial proportion of these proteins remain functionally uncharacterized. Concurrently, the expansion of protein sequence data has enabled the development of protein language models (pLMs). By distilling billions of years of evolutionary history into a latent representational space, these models have acquired an unprecedented capacity to predict both the tertiary structures and functions of proteins. In this study, we developed a deep learning-based method to predict whether 2 proteins catalyze the same enzymatic reaction. Our approach leverages latent representations generated by ESM Cambrian (ESM-C), a state-of-the-art pLM, which are then processed through a neural network architecture integrating an attention mechanism. Our method outperformed existing approaches, including those based solely on full-length sequence similarity. Notably, it also surpassed our previous LightGBM-based model, which relied on structural similarity scores derived from AlphaFold-predicted models. Analysis of the attention weights reveals that our model autonomously highlights biologically significant sites, such as catalytic and binding residues. This demonstrates that integrating pLMs with attention mechanisms can enhance the accuracy and interpretability of protein function prediction while eliminating the need for manual feature engineering.

Identifiers

PMID42602309
PMCPMC13473713

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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.