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A multimodal Transformer Network for protein-small molecule interactions enhances predictions of kinase inhibition and enzyme-substrate relationships.
- Source :
-
PLoS computational biology [PLoS Comput Biol] 2024 May 20; Vol. 20 (5), pp. e1012100. Date of Electronic Publication: 2024 May 20 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- The activities of most enzymes and drugs depend on interactions between proteins and small molecules. Accurate prediction of these interactions could greatly accelerate pharmaceutical and biotechnological research. Current machine learning models designed for this task have a limited ability to generalize beyond the proteins used for training. This limitation is likely due to a lack of information exchange between the protein and the small molecule during the generation of the required numerical representations. Here, we introduce ProSmith, a machine learning framework that employs a multimodal Transformer Network to simultaneously process protein amino acid sequences and small molecule strings in the same input. This approach facilitates the exchange of all relevant information between the two molecule types during the computation of their numerical representations, allowing the model to account for their structural and functional interactions. Our final model combines gradient boosting predictions based on the resulting multimodal Transformer Network with independent predictions based on separate deep learning representations of the proteins and small molecules. The resulting predictions outperform recently published state-of-the-art models for predicting protein-small molecule interactions across three diverse tasks: predicting kinase inhibitions; inferring potential substrates for enzymes; and predicting Michaelis constants KM. The Python code provided can be used to easily implement and improve machine learning predictions involving arbitrary protein-small molecule interactions.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2024 Kroll et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Subjects :
- Protein Kinase Inhibitors pharmacology
Protein Kinase Inhibitors chemistry
Substrate Specificity
Small Molecule Libraries chemistry
Small Molecule Libraries pharmacology
Proteins metabolism
Proteins chemistry
Amino Acid Sequence
Deep Learning
Protein Binding
Protein Kinases metabolism
Protein Kinases chemistry
Humans
Computational Biology
Machine Learning
Subjects
Details
- Language :
- English
- ISSN :
- 1553-7358
- Volume :
- 20
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- PLoS computational biology
- Publication Type :
- Academic Journal
- Accession number :
- 38768223
- Full Text :
- https://doi.org/10.1371/journal.pcbi.1012100