Evidence map›Paper›PMID 42509841›Full record

ArticleBiomolecules2026

AUKAT: Conditional VAE-Driven Augmentation and Neural Modeling of Enzyme Turnover Numbers.

Mengmeng Liu, Xialong Ni, Michal Brylinski

Abstract read
In one paragraph

Article in Biomolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mengmeng LiuCenter for Computation and Technology, Louisiana State University, Baton Rouge, LA 70803, USA.ORCID 0000-0002-8475-2319
Xialong NiDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.ORCID 0000-0003-3410-103X
Michal BrylinskiCenter for Computation and Technology, Louisiana State University, Baton Rouge, LA 70803, USA.ORCID 0000-0002-6204-2869

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate prediction of enzyme turnover numbers (kcat) is essential for applications in systems biology, metabolic engineering, and drug discovery, yet remains challenging due to the limited availability and uneven distribution of experimental data. Here, we present AUKAT, an integrated framework that combines conditional generative modeling with deep neural prediction to improve kcat estimation. A conditional variational autoencoder generates synthetic training instances in embedding space, followed by a selection pipeline that retains samples with strong agreement across independent evaluators, thereby ensuring data reliability. A hybrid convolutional neural network and transformer-based architecture is then used to predict kcat from substrate, enzyme functional, and species embeddings. Incorporating synthetic data improved predictive performance for both random forest and neural network models in five-fold cross-validation, with larger gains observed for the neural network architecture. Benchmarking against DLKcat demonstrated comparable predictive accuracy on the standard test set, while evaluation on stricter unseen subsets indicated improved generalization for low-similarity substrates and enzymes. Feature importance analysis further showed that AUKAT leverages substrate, enzyme functional, and species information in a more balanced manner rather than relying predominantly on a single feature source. In addition, AUKAT-human, a specialized model trained using a pre-training and fine-tuning strategy, achieved improved prediction accuracy for human enzyme kinetics. Overall, AUKAT provides a scalable approach for enzyme kinetics prediction and offers a practical solution to data scarcity in biochemical modeling.

Indexed as

EnzymesNeural Networks, ComputerAutoencoderGenerative Artificial IntelligenceKineticsEnzymesconditional variational autoencoderdeep learningenzyme kineticskcat predictionsynthetic data augmentationtransformer models

Identifiers

PMID42509841
PMCPMC13406586

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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.