HIT-EC: Trustworthy prediction of enzyme commission numbers using a hierarchical interpretable transformer
Dumontet, L.; Han, S.-R.; Oh, T.-J.; Kang, M.
Show abstract
Accurate and trustworthy prediction of Enzyme Commission (EC) numbers is critical for understanding enzyme functions and their roles in biological processes. Despite the success of recently proposed deep learning-based models, there remain limitations, such as low performance in underrepresented EC numbers, lack of learning strategy with incomplete annotations, and limited interpretability. To address these challenges, we propose a novel hierarchical interpretable transformer model, HIT-EC, for trustworthy EC number prediction. HIT-EC employs a four-level transformer architecture that aligns with the hierarchical structure of EC numbers, and leverages both local and global dependencies within protein sequences for this multi-label classification task. We also propose a novel learning strategy to handle incomplete EC numbers. HIT-EC, as an evidential deep learning model, produces trustworthy predictions by providing domain-specific evidence through a biologically meaningful interpretation scheme. The predictive performance of HIT-EC was assessed by multiple experiments: a cross-validation with a large dataset, a validation with external data, and a species-based performance evaluation. HIT-EC showed statistically significant improvement in predictive performance when compared to the current state-of-the-art benchmark models. HIT-ECs robust interpretability was further validated by identifying well-known conserved motifs and functional regions in the CYP106A2 enzyme family. HIT-EC would be a robust, interpretable, and reliable solution for EC number prediction, with significant implications for enzymology, drug discovery, and metabolic engineering. The open-source code is publicly available at: https://github.com/datax-lab/HIT-EC.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- FAPM: Functional Annotation of Proteins using Multi-Modal Models Beyond Structural Modeling 97%
- Pair-EGRET: enhancing the prediction of protein-proteininteraction sites through graph attention networks and protein language models 96%
- Prediction of bacterial protein-compound interactions with only positive samples 96%
Similar papers in this journal
- SAINT-Angle: self-attention augmented inception-inside-inception network and transfer learning improve protein backbone torsion angle prediction 96%
- Improving protein function prediction by learning and integrating representations of protein sequences and function labels 96%
- KSMoFinder - Knowledge graph embedding of proteins and motifs for predicting kinases of human phosphosites 95%
Similar papers in this journal
- Paying Attention to Attention: High Attention Sites as Indicators of Protein Family and Function in Language Models 95%
- MoCETSE: A mixture-of-convolutional experts and transformer-based model for predicting Gram-negative bacterial secreted effectors 95%
- Designing diverse and high-performance proteins with a large language model in the loop 94%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.