Robust enzyme discovery and engineering with deep learning using CataPro

Accurate prediction of enzyme kinetic parameters is crucial for enzyme exploration and modification. Existing models face the problem of either low accuracy or poor generalization ability due to overfitting. In this work, we first developed unbiased datasets to evaluate the actual performance of these methods and proposed a deep learning model, CataPro, based on pre-trained models and molecular fingerprints to predict turnover number (k<sub>cat</sub>), Michaelis constant (K<sub>m</sub>), and catalytic efficiency (k<sub>cat</sub>/K<sub>m</sub>). Compared with previous baseline models, CataPro demonstrates clearly enhanced accuracy and generalization ability on the unbiased datasets. In a representational enzyme mining project, by combining CataPro with traditional methods, we identified an enzyme (SsCSO) with 19.53 times increased activity compared to the initial enzyme (CSO2) and then successfully engineered it to improve its activity by 3.34 times. This reveals the high potential of CataPro as an effective tool for future enzyme discovery and modification.

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Publication Details

Journal
Nature Communications
Published
2025-03-20
DOI
https://doi.org/10.1038/s41467-025-58038-4
Citations
57
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
85.75
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article

Robust enzyme discovery and engineering with deep learning using CataPro

Yanmei Yang, Xiaozhou Luo, Weifeng Li, Dongqi Xie et al.
57 citations
Nature Communications
Computational Drug Discovery Methods
85.75
article

Robust enzyme discovery and engineering with deep learning using CataPro

Yanmei Yang, Xiaozhou Luo, Weifeng Li, Dongqi Xie, Liangzhen Zheng, Yangyang Li, Sheng Wang, Di Wu, Zechen Wang
article en
57 citations

Abstract

Accurate prediction of enzyme kinetic parameters is crucial for enzyme exploration and modification. Existing models face the problem of either low accuracy or poor generalization ability due to overfitting. In this work, we first developed unbiased datasets to evaluate the actual performance of these methods and proposed a deep learning model, CataPro, based on pre-trained models and molecular fingerprints to predict turnover number (k<sub>cat</sub>), Michaelis constant (K<sub>m</sub>), and catalytic efficiency (k<sub>cat</sub>/K<sub>m</sub>). Compared with previous baseline models, CataPro demonstrates clearly enhanced accuracy and generalization ability on the unbiased datasets. In a representational enzyme mining project, by combining CataPro with traditional methods, we identified an enzyme (SsCSO) with 19.53 times increased activity compared to the initial enzyme (CSO2) and then successfully engineered it to improve its activity by 3.34 times. This reveals the high potential of CataPro as an effective tool for future enzyme discovery and modification.

Nature CommunicationsVol. 16(1)
Shandong University (CN), Chinese Academy of Sciences (CN), Shandong Normal University (CN), Lifetech Scientific (China) (CN), Ministry of Education (ME), Shenzhen Institutes of Advanced Technology (CN), Viva Biotech (China) (CN)
No poverty
Openalex Percentile: Top 0%
Computational Drug Discovery Methods
85.75
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