ArticleBioinformatics (Oxford, England)2026
Enzyme association for environmental biotransformation reactions through contrastive learning of reaction center-specific fingerprints.
Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
motivationMicrobial biotransformation plays a central role in the environmental degradation of chemical contaminants, driven by the catalytic activities of diverse enzymes. However, linking specific enzymes to contaminant removal and predicting associated transformation products (TPs) under real-world conditions remain a major challenge. In this study, we present a self-supervised, contrastive fine-tuning strategy for reaction fingerprint learning, designed to improve the chemical relevance of BERT-based reaction embeddings for environmental biotransformation reactions. Specifically, we fine-tuned a BERT encoder such that the cosine similarity between its reaction fingerprints aligns with the Tanimoto similarity of traditional structure-based fingerprints.
resultsThe resulting compact, 256-dimensional fingerprints, termed crxnfp, showed an improved ability to cluster reactions according to transformation type and focus attention on chemically meaningful reaction centers. Our crxnfp fingerprints were further validated in reaction classification tasks across multiple datasets, achieving superior or comparable performance relative to existing methods. Importantly, they enabled a similarity-based association of biotransformation rules and reactions from enviPath with enzyme annotations from the Rhea and UniProt databases, offering a scalable approach to enrich environmental biotransformation datasets with enzymatic information. Additionally, crxnfp was employed to identify specific enzyme classes involved in contaminant biotransformation, which were subsequently validated through experiments conducted in this study, achieving 91.3% accuracy at the third-level enzyme classification. The crxnfp fingerprints offer a promising solution to advance the understanding of contaminant biotransformation and guide the development of enzyme-informed strategies for contaminant management across diverse environmental contexts. AVAILABILITY AND IMPLEMENTATION: Code is available at https://github.com/zhangky12/crxnfp and https://github.com/zhangky12/crxnfp_knn.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.