Evidence map›Paper›PMID 40193588›Full record

ArticleJournal of proteome research2025

NA_mCNN: Classification of Sodium Transporters in Membrane Proteins by Integrating Multi-Window Deep Learning and ProtTrans for Their Therapeutic Potential.

Muhammad Shahid Malik, Van The Le, Yu-Yen Ou

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Muhammad Shahid MalikDepartment of Computer Science and Engineering, Yuan Ze University, Chung-Li 32003, Taiwan.ORCID 0000-0001-5615-9000
Van The LeDepartment of Computer Science and Engineering, Yuan Ze University, Chung-Li 32003, Taiwan.ORCID 0009-0000-5239-2075
Yu-Yen OuDepartment of Computer Science and Engineering, Yuan Ze University, Chung-Li 32003, Taiwan.ORCID 0000-0002-9894-926X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium transporters maintain cellular homeostasis by transporting ions, minerals, and nutrients across the membrane, and Na+/K+ ATPases facilitate the cotransport of solutes in neurons, muscle cells, and epithelial cells. Sodium transporters are important for many physiological processes, and their dysfunction leads to diseases such as hypertension, diabetes, neurological disorders, and cancer. The NA_mCNN computational method highlights the functional diversity and significance of sodium transporters in membrane proteins using protein language model embeddings (PLMs) and multiple-window scanning deep learning models. This work investigates PLMs that include Tape, ProtTrans, ESM-1b-1280, and ESM-2-128 to achieve more accuracy in sodium transporter classification. Five-fold cross-validation and independent testing demonstrate ProtTrans embedding robustness. In cross-validation, ProtTrans achieved an AUC of 0.9939, a sensitivity of 0.9829, and a specificity of 0.9889, demonstrating its ability to distinguish positive and negative samples. In independent testing, ProtTrans maintained a sensitivity of 0.9765, a specificity of 0.9991, and an AUC of 0.9975, which indicates its high level of discrimination. This study advances the understanding of sodium transporter diversity and function, as well as their role in human pathophysiology. Our goal is to use deep learning techniques and protein language models for identifying sodium transporters to accelerate identification and develop new therapeutic interventions.

Indexed as

Deep LearningMembrane ProteinsMembrane Transport ProteinsHumansSodiumMembrane ProteinsMembrane Transport ProteinsSodiumdrug targetspredictive modelingpretrained protein language models (PLMs)protein sequence classificationsodium transporters

Identifiers

PMID40193588
PMCPMC12053934

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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.