InteracTor: Feature engineering and explainable AI for profiling protein structure-interaction-function relationships

Characterizing protein families' structural and functional diversity is essential for understanding their biological roles. Traditional analyses often focus on primary and secondary structures, which may not fully capture complex protein interactions. Here we introduce InteracTor, a novel toolkit that extracts multimodal features from protein three-dimensional (3D) structures, including interatomic interactions like hydrogen bonds, van der Waals forces, and hydrophobic contacts. By integrating eXplainable Artificial Intelligence (XAI) techniques, we quantified the importance of the extracted features in the classification of protein structural and functional families. InteracTor's interpref features enable mechanistic insights into the determinants of protein structure, function, and dynamics, offering a transparent means to assess their predictive power within machine learning models. Interatomic interaction features extracted by InteracTor demonstrated superior predictive power for protein family classification compared to features based solely on primary or secondary structure, revealing the importance of considering specific tertiary contacts in computational protein analysis. This work provides a robust framework for future studies aiming to enhance the capabilities of models for protein function prediction and drug discovery.

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Publication Details

Journal
PLoS Computational Biology
Published
2025-10-13
DOI
https://doi.org/10.1371/journal.pcbi.1013038
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

InteracTor: Feature engineering and explainable AI for profiling protein structure-interaction-function relationships

Melissa Erdem, José Cleydson F. Silva, Layla Schuster, Matias Kirst et al.
PLoS Computational Biology
Computational Drug Discovery Methods
article

InteracTor: Feature engineering and explainable AI for profiling protein structure-interaction-function relationships

Melissa Erdem, José Cleydson F. Silva, Layla Schuster, Matias Kirst, Márcio F. R. Resende, Nick Sexson, Raquel Dias, Ryan Hulke
article en

Abstract

Characterizing protein families' structural and functional diversity is essential for understanding their biological roles. Traditional analyses often focus on primary and secondary structures, which may not fully capture complex protein interactions. Here we introduce InteracTor, a novel toolkit that extracts multimodal features from protein three-dimensional (3D) structures, including interatomic interactions like hydrogen bonds, van der Waals forces, and hydrophobic contacts. By integrating eXplainable Artificial Intelligence (XAI) techniques, we quantified the importance of the extracted features in the classification of protein structural and functional families. InteracTor's interpref features enable mechanistic insights into the determinants of protein structure, function, and dynamics, offering a transparent means to assess their predictive power within machine learning models. Interatomic interaction features extracted by InteracTor demonstrated superior predictive power for protein family classification compared to features based solely on primary or secondary structure, revealing the importance of considering specific tertiary contacts in computational protein analysis. This work provides a robust framework for future studies aiming to enhance the capabilities of models for protein function prediction and drug discovery.

PLoS Computational BiologyVol. 21(10)
University of Florida (US)
Openalex Percentile: Top 70%
Computational Drug Discovery Methods
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