Explainability of Protein Deep Learning Models

Protein embeddings are the new main source of information about proteins, producing state-of-the-art solutions to many problems, including protein interaction prediction, a fundamental issue in proteomics. Understanding the embeddings and what causes the interactions is very important, as these models lack transparency due to their black-box nature. In the first study of its kind, we investigate the inner workings of these models using XAI (explainable AI) approaches. We perform extensive testing (3.3 TB of total data) involving nine of the best-known XAI methods on two problems: (i) the prediction of protein interaction sites using the current top method, Seq-InSite, and (ii) the production of protein embedding vectors using three methods, ProtBERT, ProtT5, and Ankh. The results are evaluated in terms of their ability to correlate with six basic amino acid properties-aromaticity, acidity/basicity, hydrophobicity, molecular mass, van der Waals volume, and dipole moment-as well as the propensity for interaction with other proteins, the impact of distant residues, and the infidelity scores of the XAI methods. The results are unexpected. Some XAI methods are much better than others at discovering essential information. Simple methods can be as good as advanced ones. Different protein embedding vectors can capture distinct properties, indicating significant room for improvement in embedding quality.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-05-29
DOI
https://doi.org/10.3390/ijms26115255
Citations
2
Primary Topic
Cell Image Analysis Techniques
Type
article
Field-Weighted Citation Impact
3.27
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article

Explainability of Protein Deep Learning Models

Zahra Fazel, G. Brian Golding, Lucian Ilie, Camila P. E. de Souza
2 citations
International Journal of Molecular Sciences
Cell Image Analysis Techniques
3.27
article

Explainability of Protein Deep Learning Models

Zahra Fazel, G. Brian Golding, Lucian Ilie, Camila P. E. de Souza
article en
2 citations

Abstract

Protein embeddings are the new main source of information about proteins, producing state-of-the-art solutions to many problems, including protein interaction prediction, a fundamental issue in proteomics. Understanding the embeddings and what causes the interactions is very important, as these models lack transparency due to their black-box nature. In the first study of its kind, we investigate the inner workings of these models using XAI (explainable AI) approaches. We perform extensive testing (3.3 TB of total data) involving nine of the best-known XAI methods on two problems: (i) the prediction of protein interaction sites using the current top method, Seq-InSite, and (ii) the production of protein embedding vectors using three methods, ProtBERT, ProtT5, and Ankh. The results are evaluated in terms of their ability to correlate with six basic amino acid properties-aromaticity, acidity/basicity, hydrophobicity, molecular mass, van der Waals volume, and dipole moment-as well as the propensity for interaction with other proteins, the impact of distant residues, and the infidelity scores of the XAI methods. The results are unexpected. Some XAI methods are much better than others at discovering essential information. Simple methods can be as good as advanced ones. Different protein embedding vectors can capture distinct properties, indicating significant room for improvement in embedding quality.

International Journal of Molecular SciencesVol. 26(11)
Western University (CA), McMaster University (CA)
Openalex Percentile: Top 8%
Cell Image Analysis Techniques
3.27
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Explainability of Protein Deep Learning Models — Zahra Fazel, G. Brian Golding, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS