The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
IntEnzyDB: an Integrated Structure-Kinetics Enzymology Database
Open accessPreprint — published as 10.1021/acs.jcim.2c01139 · Paper page
Abstract
Data-driven modeling has emerged as a new paradigm for biocatalyst design and discovery. Biocatalytic databases that integrate enzyme structure and function data are in urgent need. Here, we described IntEnzyDB as an integrated structure-kinetics database for facile statistical modeling and machine learning. IntEnzyDB employs a relational architecture with flattened data structure, which allows rapid data operation. This architecture also makes it easy for IntEnzyDB to incorporate more types of enzyme function data. IntEnzyDB contains enzyme kinetics and structure data from six enzyme commission classes. Using 1019 enzyme structure-kinetics pairs, we investigated the efficiency-perturbing propensity for mutations that are close or distal to the active site. The statistical results show that efficiency-enhancing mutations are globally encoded; deleterious mutations are much more likely to occur in close mutations than in distal mutations. Finally, we described a web interface that allows public users to access enzymology data stored in IntEnzyDB. IntEnzyDB will provide a computational facility for data-driven modeling in biocatalysis and molecular evolution.
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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
Deep learning-based kcat prediction enables improved enzyme-constrained model reconstruction
Li, F., Yuan, L., Lu, H., Li, G., Chen, Y., Engqvist, M. K. M., Kerkhoven, E. J., & Nielsen, J. (2022) · Nature Catalysis · doi:10.1038/s41929-022-00798-z · Cited by 466
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Metadata
- Authors
- Yan, B., Ran, X., Gollu, A., Cheng, Z., Zhou, X., Chen, Y., & Yang, Z.
- Affiliations
- Vanderbilt University (US)
- Corresponding author
- Yang, Zhongyue
- Venue
- Journal of Chemical Information and Modeling
- Publisher
- American Chemical Society (ACS)
- Published
- 2022-07-05
- Volume
- 62
- Issue
- 22
- Pages
- 5841-5848
- ISSN
- 1549-9596 (ISSN-L)
- PMC
- PMC10335264
- OpenAlex
- W4307291940
- Cited by
- 23
- References
- 2
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 2 · 2023: 7 · 2022: 1
- FWCI
- 1.31
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Journal of Chemical Information and Modeling (publishedVersion)
- ChemRxiv (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation (BIO200057, TG-BIO200057)
- Vanderbilt University (FF_300061)
- National Institutes of Health
- Department of Chemistry, Vanderbilt University (FF_300061)
- National Institute of General Medical Sciences (R35GM146982)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme Catalysis and Immobilization
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Keywords
- enzyme kinetics, enzyme structure, biocatalyst design, mutation efficiency, active site mutations, deleterious mutations, web interface, molecular evolution, data-driven modeling
- MeSH terms
- Kinetics, Databases, Factual, Catalytic Domain, Biocatalysis
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