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The Topological Properties of the Protein Universe
Open accessPreprint — published as 10.1038/s41467-025-61108-2 · Paper page
Abstract
Deep learning methods have revolutionized our ability to predict protein structures, allowing us a glimpse into the entire protein universe. As a result, our understanding of how protein structure drives function is now lagging behind our ability to determine and predict protein structure. Here, we describe how topology, the branch of mathematics concerned with qualitative properties of spatial structures, provides a lens through which we can identify fundamental organizing features across the known protein universe. We identify topological determinants that capture global features of the protein universe, such as domain architecture and binding sites. Additionally, our analysis also identified highly specific properties, so-called topological generators, that can be used to provide deeper insights into protein structure-function and evolutionary relationships. We used our approach to determine structural, functional and disease consequences of mutations, explain differences in properties of proteins in mesophiles and thermophiles, and the likely structural and functional consequences of polymorphisms in a protein. Overall, we present a practical methodology for mapping the topology of the known protein universe at scale.
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Metadata
- Authors
- Madsen, C. D., Barbensi, A., Zhang, S. Y., Ham, L., David, A., Pires, D. E. V., & Stumpf, M. P. H.
- Affiliations
- The University of Melbourne (AU)
- Imperial College London (GB)
- Corresponding author
- Pires, Douglas E.V.
- Stumpf, Michael P.H.
- ORCID
- Venue
- Nature Communications
- Publisher
- openRxiv
- Published
- 2023-09-26
- Volume
- 16
- Issue
- 1
- Pages
- 7503-7503
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC12350623
- OpenAlex
- W4413117324
- Cited by
- 7
- References
- 1
- Citations by year
- 2026: 5 · 2025: 2
- FWCI
- 2.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Nature Communications (publishedVersion, cc-by-nc-nd)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Minerva Access (University of Melbourne) (submittedVersion, cc-by-nc-nd)
- Funders
- Wellcome Trust (218242, 218242/Z/19/Z)
- University of Melbourne
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Topological and Geometric Data Analysis
- Keywords
- protein topology, domain architecture, protein binding sites, protein structure-function relationship, protein evolution, polymorphism, pathogenic variants, protein structure prediction
- MeSH terms
- Protein Domains, Deep Learning, Binding Sites, Humans, Models, Molecular, Mutation, Protein Conformation, Proteins
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