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A general substitution matrix for structural phylogenetics
Open accessPreprint — published as 10.1093/molbev/msaf124 · Paper page
Abstract
Sequence-based maximum likelihood (ML) phylogenetics is a widely used method for inferring evolutionary relationships, which has illuminated the evolutionary histories of proteins and the organisms that harbour them. But modern implementations with sophisticated models of sequence evolution struggle to resolve deep evolutionary relationships, which can be obscured by excessive sequence divergence and substitution saturation. Structural phylogenetics has emerged as a promising alternative, because protein structure evolves much more slowly than protein sequences. Recent developments protein structure prediction using AI have made it possible to predict protein structures for entire protein families, and then to translate these structures into a sequence representation - the 3Di structural alphabet - that can in theory be directly fed into existing sequence based phylogenetic software. To unlock the full potential of this idea, however, requires the inference of a general substitution matrix for structural phylogenetics, which has so far been missing. Here we infer this matrix from large datasets of protein structures and show that it results in a better fit to empirical datasets that previous approaches. We then use this matrix to re-visit the question of the root of the tree of life. Using structural phylogenies of universal paralogs, we provide the first unambiguous evidence for a root between and archaea and bacteria. Finally, we discuss some practical and conceptual limitations of structural phylogenetics. Our 3Di substitution matrix provides a starting point for revisiting many deep phylogenetic problems that have so far been extremely difficult to solve.
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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
Varadi, M., Bertoni, D., Magana, P., Paramval, U., Pidruchna, I., Radhakrishnan, M., Tsenkov, M., Nair, S., Mirdita, M., Yeo, J., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkad1011 · Cited by 2,052
Flagged first, then by citations
Research works printed but not linked: 48
- 10.1093/protein/14.4.219 · DOI
- 10.1093/nar/29.1.61 · DOI
- 10.1073/pnas.93.15.7749 · DOI
- 10.1073/pnas.92.7.2441 · DOI
- 10.1093/bioinformatics/btp348 · DOI
- 10.1002/pro.4353 · DOI · Paper page
- 10.1126/science.1260031 · DOI · Paper page
- 10.1016/j.febslet.2004.08.065 · DOI · Paper page
- 10.1093/sysbio/19.1.83 · DOI
- 10.1007/BF01734359 · DOI · Paper page
- 1971, Toward defining the course of evolution: minimum change for a specific tree topology, Syst. Zoöl, 20, 406, 10.2307/2412116 · DOI
- Gilchrist CLM , Mirdita M , Steinegger M. 2024. Multiple protein structure alignment at scale with FoldMason. bioRxiv:2024.08.01.606130. · DOI · Paper page
- 10.1038/s41594-020-00555-5 · DOI
- 1989, Evolution of the vacuolar H+-ATPase: implications for the origin of eukaryotes, Proc. Natl. Acad. Sci. USA, 17, 6661
- 10.1098/rstb.2014.0329 · DOI · Paper page
- 2001, Structure–function relationships of A-, F- and V-ATPases, J. Exp. Biol, 204, 2597, 10.1242/jeb.204.15.2597 · DOI
- Heinzinger M , Weissenow K , Sanchez JG , Henkel A , Steinegger M , Rost B . 2023. ProstT5: bilingual language model for protein sequence and structure. bioRxiv:2023.07.23.550085. · DOI · Paper page
- 2011, Evolution of photosynthesis, Plant Biol, 62, 515, 10.1146/annurev-arplant-042110-103811 · DOI · Paper page
- 10.1073/pnas.86.23.9355 · DOI · Paper page
- 10.1016/0076-6879(90)83044-A · DOI
- 10.1007/BF02102452 · DOI
- 10.1038/nmeth.4285 · DOI · Paper page
- 10.1093/molbev/msn067 · DOI · Paper page
- 10.1101/gr.8.12.1233 · DOI
- 10.1093/oxfordjournals.molbev.a003973 · DOI
- 2021, Robustness of phylogenetic inference to model misspecification caused by pairwise epistasis, Mol. Biol. Evol, 38, 4603, 10.1093/molbev/msab163 · DOI
- 2023, ATP synthase evolution on a cross-braced dated tree of life, Nat. Commun, 14, 7456, 10.1038/s41467-023-42924-w · DOI · Paper page
- 2018, A physiological perspective on the origin and evolution of photosynthesis, FEMS Microbiol. Rev, 2, 205
- 10.2307/1390728 · DOI
- 2009, Why neighbor-joining works, Algorithmica, 54, 1, 10.1007/s00453-007-9116-4 · DOI
- 1972, Elongation factors EF Tu and EF G interact at related sites on ribosomes, Proc. Natl. Acad. Sci. USA, 3, 752
- 2021, QMaker: Fast and accurate method to estimate empirical models of protein evolution, Syst. Biol, 70, syab010
- Moi D , Bernard C , Steinegger M , Nevers Y , Langleib M , Dessimoz C . 2023. Structural phylogenetics unravels the evolutionary diversification of communication systems in gram-positive bacteria and their viruses. bioRxiv:2023.09.19.558401. · DOI
- Mutti G , Ocaña-Pallarés E , Gabaldón T. 2024. Newly developed structure-based methods do not outperform standard sequence-based methods for large-scale phylogenomics. bioRxiv:2024.08.02.606352 · DOI
- 10.1371/journal.pbio.1000602 · DOI · Paper page
- 10.1007/PL00006573 · DOI · Paper page
- 2021, Felsenstein phylogenetic likelihood, J. Mol. Evol, 89, 134, 10.1007/s00239-020-09982-w · DOI
- Puente-Lelievre C , Malik AJ , Douglas J , Ascher D , Baker M , Allison J , Poole A , Lundin D , Fullmer M , Bouckert R , et al. 2024. Tertiary-interaction characters enable fast, model-based structural phylogenetics beyond the twilight zone. bioRxiv:2023.12.12.571181. · DOI
- 10.1007/BF02338839 · DOI
- 10.1093/oxfordjournals.molbev.a040454 · DOI
- 10.1016/j.sbi.2023.102645 · DOI · Paper page
- 10.1111/nph.16249 · DOI
- 10.1002/pro.2897 · DOI
- 2024, Anoxygenic phototroph of the Chloroflexota uses a type I reaction centre, Nature, 627, 915, 10.1038/s41586-024-07180-y · DOI
- 10.1093/nar/gky427 · DOI
- Wayment-Steele HK , Ojoawo A , Otten R , Apitz JM , Pitsawong W , Hömberger M , Ovchinnikov S , Colwell L , Kern D . 2023. Predicting multiple conformations via sequence clustering and AlphaFold2. Nature:1–3. · DOI
- 10.1016/S0168-9525(01)02272-7 · DOI
- 2023, Crowded environments tune the fold-switching in metamorphic proteins, Commun. Chem, 6, 117, 10.1038/s42004-023-00909-2 · DOI
Metadata
- Authors
- Garg, S. G., & Hochberg, G. K.
- Affiliations
- Max Planck Institute for Terrestrial Microbiology (DE)
- Philipps University of Marburg (DE)
- Corresponding author
- Garg, Sriram G
- Hochberg, Georg KA
- Venue
- Molecular Biology and Evolution
- Publisher
- openRxiv
- Published
- 2024-09-19
- Volume
- 42
- Issue
- 6
- ISSN
- 0737-4038 (ISSN-L)
- PMC
- PMC12198762
- OpenAlex
- W4411095222
- Cited by
- 29
- References
- 2
- Citations by year
- 2026: 15 · 2025: 14
- FWCI
- 8.72
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecular Biology and Evolution (publishedVersion, cc-by-nc)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- Human Frontier Science Program (RGP0028)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Keywords
- substitution matrices, protein structure, deep phylogenetic relationships, protein structure prediction
- MeSH terms
- Archaea, Models, Genetic, Phylogeny, Protein Conformation, Proteins, Software, Evolution, Molecular
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