Evidence map›Paper›PMID 42469205›Full record

ArticleNature communications2026

An enzyme-specific protein language model for catalytic property prediction.

Chong Wang, Mengyao Li, Shaolei Geng, Weidong Li, Xuezhi Zhou, Yu Guang Wang, Yi Yu, Tianyun Wang, Yiqing Shen

Abstract read
In one paragraph

Article in Nature communications, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chong WangSchool of Medical Engineering, Henan Medical University, Xinxiang, China.
Mengyao LiSchool of Medical Engineering, Henan Medical University, Xinxiang, China.
Shaolei GengHenan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, China.
Weidong LiHenan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, China.
Xuezhi ZhouEngineering Technology Research Center of Neurosense and Control of Henan Province, Xinxiang, China.
Yu Guang WangInstitute of Natural Sciences, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0002-7450-0273
Yi YuSchool of Medical Engineering, Henan Medical University, Xinxiang, China. yuyi@xxmu.edu.cn.
Tianyun WangHenan Key Laboratory of Neurorestoratology and Protein Modification, The First Affiliated Hospital of Henan Medical University, Xinxiang, China. wtianyuncn@126.com.ORCID http://orcid.org/0000-0002-0793-1006
Yiqing ShenDepartment of Computer Science, Johns Hopkins University, Baltimore, MD, USA. yshen92@jhu.edu.ORCID http://orcid.org/0000-0001-7866-3339

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enzymes drive cellular metabolism, yet predicting catalytic properties from amino acid sequences remains challenging. Existing protein language models (PLMs) provide powerful general-purpose representations but are often inefficient for high-throughput screening and insufficiently adapted to enzyme-specific tasks. Here, we propose EnzGFM, an enzyme-specific PLM based on a Mamba-Transformer hybrid architecture with hierarchical pre-training to capture enzyme-specific patterns. Across enzyme property prediction benchmarks, EnzGFM consistently outperforms Transformer-based PLMs with 2-5-fold acceleration, achieving relative improvements of 16.67% in kinetic parameter prediction, 15.69% in enzyme-reaction mapping, 13.19% in EC number classification, and 20.04% in mutation effect assessment. Building on EnzGFM, we develop EnzGFM-Agent, an enzyme-focused agentic pipeline. Experimental validation further suggests that EnzGFM-Agent can enrich beneficial variants within small candidate pools. Together, these results demonstrate that EnzGFM captures enzyme-specific sequence-function patterns, while EnzGFM-Agent translates these predictions into experimentally actionable candidates and can help reduce wet-lab screening burden for practical enzyme engineering.

Indexed as

EnzymesAmino Acid SequenceCatalysisKineticsLarge Language ModelsPrediction AlgorithmsPredictive Learning ModelsEnzymes

Identifiers

PMID42469205
PMCPMC13494029

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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.