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Citation: Krueger, Tanja and Durmaz, Damla A. and Jimenez Soto, Luisa F.: Exo-Tox: Identifying Exotoxins from secreted bacterial proteins. 2025. Open Data LMU. 10.5282/ubm/data.576

Exo-Tox: Identifying Exotoxins from secreted bacterial proteins
Exo-Tox: Identifying Exotoxins from secreted bacterial proteins

Background: Bacterial exotoxins are secreted proteins able to affect target cells, and associated with diseases. Their accurate identification can enhance drug discovery and ensure the safety of bacteria-based medical applications. How- ever, current toxin predictors prioritize broad coverage by mixing toxins from multiple biological kingdoms and diverse control sets. This general approach has proven sub-optimal for identifying niche toxins, such as bacterial exotoxins. Recent Protein Language Models offer an opportunity to improve toxin prediction by capturing global sequence context and biochemical properties from protein sequences. Results: We introduce Exo-Tox, a specialized predictor trained exclusively on curated datasets of bacterial exotoxins and secreted non-toxic bacterial proteins,represented as embeddings by Protein Language Models. Compared to Basic Local Alignment Search Tool (BLAST)-based methods and generalized toxin predictors, Exo-Tox outperforms across multiple metrics, achieving an Matthews correlation coefficient > 0.9. Notably, Exo-Tox’s performance remains robust regardless of protein length or the presence of signal peptides. We analyze its limited transfer-ability to bacteriophage proteins and non-secreted proteins.

Predictor, bacterial toxins, bacteriophages
Krueger, Tanja
Durmaz, Damla A.
Jimenez Soto, Luisa F.
2025

[thumbnail of Complete files used for the creation and test of the Exo-Tox predictor] Other (Complete files used for the creation and test of the Exo-Tox predictor)
Exo-Tox.zip - Other

1GB
[thumbnail of ReadMe-File to Exo-Tox.zip] Other (ReadMe-File to Exo-Tox.zip)
README_Exo-Tox.md - Additional Metadata

9kB

DOI: 10.5282/ubm/data.576

This dataset is available unter the terms of the following Creative Commons LicenseCC BY-SA 4.0

Abstract

Background: Bacterial exotoxins are secreted proteins able to affect target cells, and associated with diseases. Their accurate identification can enhance drug discovery and ensure the safety of bacteria-based medical applications. How- ever, current toxin predictors prioritize broad coverage by mixing toxins from multiple biological kingdoms and diverse control sets. This general approach has proven sub-optimal for identifying niche toxins, such as bacterial exotoxins. Recent Protein Language Models offer an opportunity to improve toxin prediction by capturing global sequence context and biochemical properties from protein sequences. Results: We introduce Exo-Tox, a specialized predictor trained exclusively on curated datasets of bacterial exotoxins and secreted non-toxic bacterial proteins,represented as embeddings by Protein Language Models. Compared to Basic Local Alignment Search Tool (BLAST)-based methods and generalized toxin predictors, Exo-Tox outperforms across multiple metrics, achieving an Matthews correlation coefficient > 0.9. Notably, Exo-Tox’s performance remains robust regardless of protein length or the presence of signal peptides. We analyze its limited transfer-ability to bacteriophage proteins and non-secreted proteins.

Uncontrolled Keywords

Predictor, bacterial toxins, bacteriophages

Item Type:Other
Contact Person:Jimenez-Soto, Luisa F
E-Mail of Contact:l.jimenez at lmu.de
Subjects:Medicine
Mathematics, Computer Science and Statistics
Biology
Dewey Decimal Classification:500 Natural sciences and mathematics
500 Natural sciences and mathematics > 570 Life sciences
ID Code:576
Deposited By: Dr. Luisa F. Jimenez Soto
Deposited On:18. Mar 2025 12:37
Last Modified:18. Mar 2025 12:37

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