Biosynfoni: a biosynthesis-informed and interpretable lightweight molecular fingerprint

Natural products provide a rich source of bioactive molecules for a variety of applications. Molecular fingerprints are the tool of choice for systematic large-scale studies of their structures. However, current molecular fingerprints insufficiently represent characteristic features of natural products inherently, decreasing the interpretability of natural product-specific predictions. Here, we show that a natural product-specific molecular fingerprint based on a relatively small set of selected biosynthetic building blocks provides more interpretable predictions of biosynthetic distance and natural product classification. Our fingerprint Biosynfoni outperforms MACCS, Morgan, and Daylight-like fingerprints in biosynthetic distance estimation, using 39 substructure keys. Moreover, Biosynfoni's design, compactness, and concrete substructure definition allow easy visualisation of the detected substructures and their respective biosynthetic pathway origins. Through Biosynfoni, users can gain more insights from predictions and better examine the importance of features within machine learning models. Our results show that a short fingerprint consisting of biologically significant building blocks performs on par with top-performing molecular fingerprints for natural product classification while improving prediction explainability.

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Publication Details

Journal
Journal of Cheminformatics
Published
2025-08-29
DOI
https://doi.org/10.1186/s13321-025-01081-6
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
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article

Biosynfoni: a biosynthesis-informed and interpretable lightweight molecular fingerprint

Justin J. J. van der Hooft, Maria Sorokina, David Meijer, Lucina-May Nollen
Journal of Cheminformatics
Microbial Natural Products and Biosynthesis
article

Biosynfoni: a biosynthesis-informed and interpretable lightweight molecular fingerprint

Justin J. J. van der Hooft, Maria Sorokina, David Meijer, Lucina-May Nollen
article en

Abstract

Natural products provide a rich source of bioactive molecules for a variety of applications. Molecular fingerprints are the tool of choice for systematic large-scale studies of their structures. However, current molecular fingerprints insufficiently represent characteristic features of natural products inherently, decreasing the interpretability of natural product-specific predictions. Here, we show that a natural product-specific molecular fingerprint based on a relatively small set of selected biosynthetic building blocks provides more interpretable predictions of biosynthetic distance and natural product classification. Our fingerprint Biosynfoni outperforms MACCS, Morgan, and Daylight-like fingerprints in biosynthetic distance estimation, using 39 substructure keys. Moreover, Biosynfoni's design, compactness, and concrete substructure definition allow easy visualisation of the detected substructures and their respective biosynthetic pathway origins. Through Biosynfoni, users can gain more insights from predictions and better examine the importance of features within machine learning models. Our results show that a short fingerprint consisting of biologically significant building blocks performs on par with top-performing molecular fingerprints for natural product classification while improving prediction explainability.

Journal of CheminformaticsVol. 17(1)
Leiden University (NL), University of Johannesburg (ZA), Centre for Human Drug Research (NL), Bayer (Germany) (DE), Wageningen University & Research (NL)
Openalex Percentile: Top 74%
Microbial Natural Products and Biosynthesis
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Biosynfoni: a biosynthesis-informed and interpretable lightweight molecular fingerprint — Justin J. J. van der Hooft, Maria Sorokina, et al. · Journal of Cheminformatics (2025) | TGRS Research Map | TGRS