TopEC: prediction of Enzyme Commission classes by 3D graph neural networks and localized 3D protein descriptor

Tools available for inferring enzyme function from general sequence, fold, or evolutionary information are generally successful. However, they can lead to misclassification if a deviation in local structural features influences the function. Here, we present TopEC, a 3D graph neural network based on a localized 3D descriptor to learn chemical reactions of enzymes from enzyme structures and predict Enzyme Commission (EC) classes. Using message-passing frameworks, we include distance and angle information to significantly improve the predictive performance for EC classification (F-score: 0.72) compared to regular 2D graph neural networks. We trained networks without fold bias that can classify enzyme structures for a vast functional space (>800 ECs). Our model is robust to uncertainties in binding site locations and similar functions in distinct binding sites. We observe that TopEC networks learn from an interplay between biochemical features and local shape-dependent features. TopEC is available as a repository on GitHub: https://github.com/IBG4-CBCLab/TopEC and https://doi.org/10.25838/d5p-66 .

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Publication Details

Journal
Nature Communications
Published
2025-03-20
DOI
https://doi.org/10.1038/s41467-025-57324-5
Citations
13
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
10.48
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article

TopEC: prediction of Enzyme Commission classes by 3D graph neural networks and localized 3D protein descriptor

Marie Piraud, Karel van der Weg, Erinç Merdivan, Holger Gohlke
13 citations
Nature Communications
Protein Structure and Dynamics
10.48
article

TopEC: prediction of Enzyme Commission classes by 3D graph neural networks and localized 3D protein descriptor

Marie Piraud, Karel van der Weg, Erinç Merdivan, Holger Gohlke
article en
13 citations

Abstract

Tools available for inferring enzyme function from general sequence, fold, or evolutionary information are generally successful. However, they can lead to misclassification if a deviation in local structural features influences the function. Here, we present TopEC, a 3D graph neural network based on a localized 3D descriptor to learn chemical reactions of enzymes from enzyme structures and predict Enzyme Commission (EC) classes. Using message-passing frameworks, we include distance and angle information to significantly improve the predictive performance for EC classification (F-score: 0.72) compared to regular 2D graph neural networks. We trained networks without fold bias that can classify enzyme structures for a vast functional space (>800 ECs). Our model is robust to uncertainties in binding site locations and similar functions in distinct binding sites. We observe that TopEC networks learn from an interplay between biochemical features and local shape-dependent features. TopEC is available as a repository on GitHub: https://github.com/IBG4-CBCLab/TopEC and https://doi.org/10.25838/d5p-66 .

Nature CommunicationsVol. 16(1)
Forschungszentrum Jülich (DE), Institute of Bioinformatics and Systems Biology (DE), Heinrich Heine University Düsseldorf (DE)
Openalex Percentile: Top 1%
Protein Structure and Dynamics
10.48
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