Seq2Topt: a sequence-based deep learning predictor of enzyme optimal temperature

An accurate deep learning predictor is needed for enzyme optimal temperature (${T}_{opt}$), which quantitatively describes how temperature affects the enzyme catalytic activity. In comparison with existing models, a new model developed in this study, Seq2Topt, reached a superior accuracy on ${T}_{opt}$ prediction just using protein sequences (RMSE = 12.26°C and R2 = 0.57), and could capture key protein regions for enzyme ${T}_{opt}$ with multi-head attention on residues. Through case studies on thermophilic enzyme selection and predicting enzyme ${T}_{opt}$ shifts caused by point mutations, Seq2Topt was demonstrated as a promising computational tool for enzyme mining and in-silico enzyme design. Additionally, accurate deep learning predictors of enzyme optimal pH (Seq2pHopt, RMSE = 0.88 and R2 = 0.42) and melting temperature (Seq2Tm, RMSE = 7.57 °C and R2 = 0.64) were developed based on the model architecture of Seq2Topt, suggesting that the development of Seq2Topt could potentially give rise to a useful prediction platform of enzymes.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-03-01
DOI
https://doi.org/10.1093/bib/bbaf114
Citations
10
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
8.06

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article

Seq2Topt: a sequence-based deep learning predictor of enzyme optimal temperature

Sizhe Qiu, Bozhen Hu, Aidong Yang, XU Wei-ren et al.
10 citations
Briefings in Bioinformatics
Protein Structure and Dynamics
8.06
article

Seq2Topt: a sequence-based deep learning predictor of enzyme optimal temperature

Sizhe Qiu, Bozhen Hu, Aidong Yang, XU Wei-ren, Jing Zhao
article en
10 citations

Abstract

An accurate deep learning predictor is needed for enzyme optimal temperature (${T}_{opt}$), which quantitatively describes how temperature affects the enzyme catalytic activity. In comparison with existing models, a new model developed in this study, Seq2Topt, reached a superior accuracy on ${T}_{opt}$ prediction just using protein sequences (RMSE = 12.26°C and R2 = 0.57), and could capture key protein regions for enzyme ${T}_{opt}$ with multi-head attention on residues. Through case studies on thermophilic enzyme selection and predicting enzyme ${T}_{opt}$ shifts caused by point mutations, Seq2Topt was demonstrated as a promising computational tool for enzyme mining and in-silico enzyme design. Additionally, accurate deep learning predictors of enzyme optimal pH (Seq2pHopt, RMSE = 0.88 and R2 = 0.42) and melting temperature (Seq2Tm, RMSE = 7.57 °C and R2 = 0.64) were developed based on the model architecture of Seq2Topt, suggesting that the development of Seq2Topt could potentially give rise to a useful prediction platform of enzymes.

Briefings in BioinformaticsVol. 26(2)
Westlake University (CN), University of Oxford (GB), Tianjin Institute of Pharmaceutical Research (China) (CN), Hubei University (CN), Zhejiang University (CN)
University of Oxford
Openalex Percentile: Top 2%
Protein Structure and Dynamics
8.06
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