mlsanityData to 7 Oct 2026

Interpretable Enzyme Function Prediction via Residue-Level Detection

arXiv 2501.05644 ↗First posted 10 Jan 2025q-bio.BM cs.LGcited by 2

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Abstract (arXiv)

Predicting multiple functions labeled with Enzyme Commission (EC) numbers from the enzyme sequence is of great significance but remains a challenge due to its sparse multi-label classification nature, i.e., each enzyme is typically associated with only a few labels out of more than 6000 possible EC numbers. However, existing machine learning algorithms generally learn a fixed global representation for each enzyme to classify all functions, thereby they lack interpretability and the fine-grained information of some function-specific local residue fragments may be overwhelmed. Here we present an attention-based framework, namely ProtDETR (Protein Detection Transformer), by casting enzyme function prediction as a detection problem. It uses a set of learnable functional queries to adaptatively extract different local representations from the sequence of residue-level features for predicting different EC numbers. ProtDETR not only significantly outperforms existing deep learning-based enzyme function prediction methods, but also provides a new interpretable perspective on automatically detecting different local regions for identifying different functions through cross-attentions between queries and residue-level features. Code is available at https://github.com/yangzhao1230/ProtDETR.

Key facts. Cited by 2 papers in the map (data through 7 Oct 2026). Builds on 10 of its 37 references that are in the map. First posted on arXiv 10 Jan 2025.

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10 of 37 references.

References · 10

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  9. 2022Exploring evolution-aware & -free protein language models as protein function predictorscited by 20
  10. 2022ECRECer: Enzyme Commission Number Recommendation and Benchmarking based on Multiagent Dual-core Learningcited by 3

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Citing papers per year: 2025: 2.

2 papers.