EP-pred: A Machine Learning Tool for Bioprospecting Promiscuous Ester Hydrolases
Open accessPreprint — published as 10.3390/biom12101529 · Paper page
Abstract
When bioprospecting for novel industrial enzymes, substrate promiscuity is a desirable property that increases the reusability of the enzyme. Among industrial enzymes, ester hydrolases have great relevance for which the demand has not ceased to increase. However, the search for new substrate promiscuous ester hydrolases is not trivial since the mechanism behind this property is greatly influenced by the active site's structural and physicochemical characteristics. These characteristics must be computed from the 3D structure, which is rarely available, and expensive to measure, hence the need for a method that can predict promiscuity from a sequence alone. Here we report such a method called EP-pred, an ensemble binary classifier, that combines three machine learning algorithms: SVM, KNN, and a Linear model. EP-pred has been evaluated against the Lipase Engineering Database together with a hidden Markov approach leading to a final set of 10 sequences predicted to encode promiscuous esterases. Experimental results confirmed the validity of our method since all ten proteins were found to exhibit a broad substrate ambiguity.
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
Machine learning modeling of family wide enzyme-substrate specificity screens
Goldman, S., Das, R., Yang, K. K., & Coley, C. W. (2022) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1009853 · Cited by 120 · see citing works
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- Authors
- Xiang, R., Fernandez-Lopez, L., Robles-Martin, A., Ferrer, M., & Guallar, V.
- Affiliations
- Barcelona Supercomputing Center (ES)
- Consejo Superior de Investigaciones Científicas (ES)
- Venue
- Preprints.org
- Publisher
- MDPI AG
- Published
- 2022-09-07
- OpenAlex
- W4297825892
- Cited by
- 5
- References
- 2
- Citations by year
- 2026: 2 · 2024: 1 · 2023: 1 · 2022: 1
- Type
- posted content
- Language
- en
- Open access
- green
- doi.org
- Locations
- Preprints.org (acceptedVersion, cc-by)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, cc-by)
- Funders
- European Commission (10.13039/501100011033, 101000607, 13039/501100011033, 501100011033, HORIZON2020, /AEI/10.13039/501100011033, 101000327)
- Ministerio de Ciencia e Innovación (PDC2021-121534-I00, .13039/501100011033, 10.13039, / AEI/10, PID2020-112758RB-I00, PID2019, 10.13039/501100011033/, PID2019-106370RB-I00/AEI/10.13039/501100011033, 501100011033, PID2020, I00/AEI/10.13039, PID2019-106370RB-I00, /AEI/10.13039/ 501100011033)
- European Regional Development Fund (10.13039/501100011033, 13039/501100011033, AEI/10.13039/501100011033, 501100011033)
- Agencia Estatal de Investigación (AEI//10.13039/501100011033/, PDC2021-121534-I00, 501100011033, 10.13039/501100011033, 13039, .13039/501100011033, 10.13039, PID2020-112758RB-I00, AEI/10, PID2019-106370RB-I00, I00/AEI/10.13039/501100011033, PID2019)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme Catalysis and Immobilization
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Enzyme Production and Characterization
- Keywords
- ester hydrolase, substrate promiscuity, support vector machine, k-nearest neighbors, industrial enzymes
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