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CLEAN-Contact: Contrastive Learning-enabled Enzyme Functional Annotation Prediction with Structural Inference
Open accessPreprint — published as 10.1038/s42003-024-07359-z · Paper page
Abstract
Recent years have witnessed the remarkable progress of deep learning within the realm of scientific disciplines, yielding a wealth of promising outcomes. A prominent challenge within this domain has been the task of predicting enzyme function, a complex problem that has seen the development of numerous computational methods, particularly those rooted in deep learning techniques. However, the majority of these methods have primarily focused on either amino acid sequence data or protein structure data, neglecting the potential synergy of combining of both modalities. To address this gap, we propose a novel C ontrastive L earning framework for E nzyme functional AN notation prediction combined with protein amino acid sequences and Contact maps (CLEAN-Contact). We rigorously evaluated the performance of our CLEAN-Contact framework against the state-of-the-art enzyme function prediction model using multiple benchmark datasets. Our findings convincingly demonstrate the substantial superiority of our CLEAN-Contact framework, marking a significant step forward in enzyme function prediction accuracy.
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Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
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Metadata
- Authors
- Guan, Q., Yang, Y., Jerger, A., Feng, S., Wang, Z., Cheung, M., & Zucker, J.
- Affiliations
- Kent State University (US)
- Cleveland Clinic (US)
- Pacific Northwest National Laboratory (US)
- Corresponding author
- Guan, Qiang
- Zucker, Jeremy
- Venue
- Communications Biology
- Published
- 2024-06-10
- Volume
- 7
- Issue
- 1
- Pages
- 1690-1690
- ISSN
- 2399-3642 (ISSN-L)
- PMC
- PMC11666736
- OpenAlex
- W4405702281
- Cited by
- 24
- References
- 1
- Citations by year
- 2026: 13 · 2025: 11
- FWCI
- 3.27
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Communications Biology (publishedVersion, cc-by-nc-nd)
- Research Square (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- National Science Foundation (2311950, 2217104, 2212465, 2238734, 2230111, 76RL01830, 2217021)
- U.S. Department of Energy (DE-AC05–76RL01830, 10.46936/expl.proj.2022.60535/60008718, 76RL01830, DE-AC05?, 76RLO 1830, FWP 81832, DE‐AC05‐76RLO1830)
- Battelle (DE- AC05-76RL01830, DE-AC05, DE‐AC05‐76RLO 1830)
- Office of Science (DE-AC05-76RLO 1830)
- Biological and Environmental Research (FWP 81832, DE-AC05-76RLO-1830, 76RL01830)
- Laboratory Directed Research and Development (DE-AC05-76RLO 1830, 76RL01830)
- Pacific Northwest National Laboratory (DE-AC05-76RLO 1830, 76RL01830)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Keywords
- enzyme function prediction, contrastive learning, contact maps, protein structure, amino acid sequence, multimodal fusion
- MeSH terms
- Deep Learning, Amino Acid Sequence, Enzymes, Computational Biology, Proteome, Databases, Protein, Prochlorococcus, Molecular Sequence Annotation
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