ArticleBioinformatics (Oxford, England)2023
Hierarchical graph transformer with contrastive learning for protein function prediction.
Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.
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47 citing papers in PubMed.
- Structure-based virulence factor classification using a dual-driven graph transformer with a pretrained language model.Briefings in bioinformatics · 2026Article
- GPCR-GO: Relation-aware graph learning for predicting Gene Ontology terms of G protein-coupled receptors.PLoS computational biology · 2026Article
- Advancing generative large language models toward discriminative performance in protein function prediction.Genome biology · 2026Article
- Out-of-distribution generalization enhances protein function annotation for low-homology sequences.Briefings in bioinformatics · 2026Article
- SSAS-GO: structure-sequence adaptive synergy network for protein function prediction.Briefings in bioinformatics · 2026Article
- From machine learning to multimodal models: The AI revolution in enzyme engineering.Biodesign research · 2026Review
- Research Progress in Artificial Intelligence-Assisted Preparation of High-Quality Biomaterials.ACS omega · 2026Review
- Graph Learning in Bioinformatics: A Survey of Graph Neural Network Architectures, Biological Graph Construction and Bioinformatics Applications.Biomolecules · 2026Review
- S2DA-GO: enhancing protein function prediction via gradient-decoupled cross-attention and semantic priors.Frontiers in genetics · 2026Article
- Protein Design Enters the Artificial Intelligence Era: Foundations, Tools, and Emerging Paradigms.Computational and structural biotechnology journal · 2026Review
- IMAGO: An Improved Model Based on Attention Mechanism for Enhanced Protein Function Prediction.Biomolecules · 2025Article
- ProGraphTrans: multimodal dynamic collaborative framework for protein representation learning.BMC biology · 2025Article
- Bioactivity Deep Learning for Complex Structure-Free Compound-Protein Interaction Prediction.Journal of chemical information and modeling · 2025Article
- DeepProtein: deep learning library and benchmark for protein sequence learning.Bioinformatics (Oxford, England) · 2025Article
- Structure-sensitive transformer and multi-view graph contrastive learning enhanced prediction of drug-related microbes.BMC bioinformatics · 2025Article
- Utilizing protein structure graph embeddings to predict the pathogenicity of missense variants.NAR genomics and bioinformatics · 2025Article
- Structure-guided sequence representation learning for generalizable protein function prediction.Bioinformatics (Oxford, England) · 2025Article
- Integrating ESM‑2 and Graph Neural Networks with AlphaFold‑2 Structures for Enhanced Protein Function Prediction.ACS omega · 2025Article
- GS-DTI: a graph-structure-aware framework leveraging large language models for drug-target interaction prediction.Bioinformatics (Oxford, England) · 2025Article
- GOBeacon: An ensemble model for protein function prediction enhanced by contrastive learning.Protein science : a publication of the Protein Society · 2025Article
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5 authors.
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Abstract
motivationIn recent years, high-throughput sequencing technologies have made large-scale protein sequences accessible. However, their functional annotations usually rely on low-throughput and pricey experimental studies. Computational prediction models offer a promising alternative to accelerate this process. Graph neural networks have shown significant progress in protein research, but capturing long-distance structural correlations and identifying key residues in protein graphs remains challenging.
resultsIn the present study, we propose a novel deep learning model named Hierarchical graph transformEr with contrAstive Learning (HEAL) for protein function prediction. The core feature of HEAL is its ability to capture structural semantics using a hierarchical graph Transformer, which introduces a range of super-nodes mimicking functional motifs to interact with nodes in the protein graph. These semantic-aware super-node embeddings are then aggregated with varying emphasis to produce a graph representation. To optimize the network, we utilized graph contrastive learning as a regularization technique to maximize the similarity between different views of the graph representation. Evaluation of the PDBch test set shows that HEAL-PDB, trained on fewer data, achieves comparable performance to the recent state-of-the-art methods, such as DeepFRI. Moreover, HEAL, with the added benefit of unresolved protein structures predicted by AlphaFold2, outperforms DeepFRI by a significant margin on Fmax, AUPR, and Smin metrics on PDBch test set. Additionally, when there are no experimentally resolved structures available for the proteins of interest, HEAL can still achieve better performance on AFch test set than DeepFRI and DeepGOPlus by taking advantage of AlphaFold2 predicted structures. Finally, HEAL is capable of finding functional sites through class activation mapping. AVAILABILITY AND IMPLEMENTATION: Implementations of our HEAL can be found at https://github.com/ZhonghuiGu/HEAL.
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