Evidence map›Paper›PMID 42248581›Full record

ArticleBriefings in bioinformatics2026

ProtDML: label-aware representation learning for broad-spectrum protein function prediction.

Yejin Kan, Gangman Yi

Abstract read
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Article in Briefings in bioinformatics, 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yejin KanDepartment of Computer Science and Artificial Intelligence, Dongguk University, 30, Pildong-ro 1-gil, Jung-gu, Seoul 04620, South Korea.ORCID 0000-0002-1653-7764
Gangman YiDepartment of Computer Science and Artificial Intelligence, Dongguk University, 30, Pildong-ro 1-gil, Jung-gu, Seoul 04620, South Korea.ORCID 0000-0003-4664-5325

Funding

Artificial Intelligence Convergence Innovation Human Resources Development IITP-2026-RS-2023-00254592Institute of Information & communications Technology Planning & Evaluation (IITP)Korea government (MSIT)National Research Foundation of Korea RS-2025-23323808
6 · The paper itself

Abstract

Protein function prediction is crucial for narrowing the gap between the rapid growth of protein sequences and the limited availability of experimental annotations. In recent years, protein language models (pLMs) that learn representations from large-scale sequence data have emerged as scalable frameworks for modeling protein function. However, most pLMs rely on self-supervised pretraining and struggle to capture correlations among functional labels, which constrains their applicability to annotation-specific tasks. To address this limitation, we present ProtDML, a protein function prediction framework based on distance metric learning that explicitly models label correlations. ProtDML learns a task-specific distance metric using a similarity-weighted pull-push objective designed to encode co-annotation structure. This approach yields a label-aware feature space with improved intra-class compactness and inter-class separability, thereby enhancing the modeling of protein multifunctionality. Furthermore, we introduce a multi-view strategy that integrates complementary sequence-derived protein representations in sequence-only environments. On Pfam multi-label classification, ProtDML outperforms sequence-based baselines by effectively modeling domain co-occurrence patterns and transforming the embedding space into label-distinct clusters with clearer boundaries. Structural generalization on SCOP-based benchmarks demonstrates that ProtDML's function-informed metric learning can recover latent structural similarities, even without explicit structural supervision. On the CAFA3 benchmark, ProtDML achieves the lowest semantic distance across all ontologies, indicating robust performance in large-scale and imbalanced function prediction. A SARS-CoV-2 case study further illustrates its applicability to real-world viral data. Overall, ProtDML is model-agnostic and complements pretrained pLM embeddings, enabling accurate and scalable sequence-based protein function prediction.

Indexed as

Computational BiologyProteinsPrediction AlgorithmsRepresentation Machine LearningProteinsdistance metric learningmulti-label classificationprotein function predictionprotein representation learning

Identifiers

PMID42248581
PMCPMC13240597

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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.