Evidence map›Paper›PMID 41617688›Full record

ArticleNature communications2026

Trustworthy prediction of enzyme commission numbers using a hierarchical interpretable transformer.

Louis Dumontet, So-Ra Han, Jun Hyuck Lee, Tae-Jin Oh, Mingon Kang

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Artificial Intelligence Powers Protein Functional Annotation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Louis Dumontet *Department of Computer Science, University of Nevada, Las Vegas, 4505 S Maryland Pkwy, Las Vegas, NV, USA.ORCID http://orcid.org/0009-0009-8569-768X
So-Ra Han *Genome-based BioIT Convergence Institute, 70, Sunmoon-ro 221beon-gil, Tangjeong-myeon, Asan-si, Republic of Korea.ORCID http://orcid.org/0000-0003-2649-1795
Jun Hyuck LeeDivision of Life Sciences, Korea Polar Research Institute, 26 Songdomirae-ro, Yeonsu-gu, Incheon, Republic of Korea.
Tae-Jin OhGenome-based BioIT Convergence Institute, 70, Sunmoon-ro 221beon-gil, Tangjeong-myeon, Asan-si, Republic of Korea. tjoh3782@sunmoon.ac.kr.ORCID http://orcid.org/0000-0002-8407-5039
Mingon KangDepartment of Computer Science, University of Nevada, Las Vegas, 4505 S Maryland Pkwy, Las Vegas, NV, USA. mingon.kang@unlv.edu.ORCID http://orcid.org/0000-0002-9565-9523

Funding

National Research Foundation of Korea (NRF) RS-2024-00354012National Research Foundation of Korea (NRF) RS-2024-00441423National Science Foundation (NSF) 2117941
6 · The paper itself

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 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 learning strategy to handle samples associated with 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 is assessed by multiple experiments: a cross-validation with a large dataset, a validation with external data, and a species-based performance evaluation. HIT-EC shows statistically significant improvement in predictive performance when compared to the current state-of-the-art benchmark models. HIT-EC's robust interpretability is further validated by identifying well-known conserved motifs and functional regions. HIT-EC is a robust, interpretable, and reliable solution for EC number prediction, with significant implications for enzymology, drug discovery, and metabolic engineering.

Indexed as

EnzymesBacteriaClassificationComputational BiologyDatabases, ProteinDeep LearningPrediction AlgorithmsEnzymes

Identifiers

PMID41617688
PMCPMC12858967

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.