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A general substitution matrix for structural phylogenetics.

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Garg,  Sriram
Max Planck Research Group Evolutionary Biochemistry, Max Planck Institute for Terrestrial Microbiology, Max Planck Society;

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Hochberg,  Georg K. A.       
Max Planck Research Group Evolutionary Biochemistry, Max Planck Institute for Terrestrial Microbiology, Max Planck Society;

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Citation

Garg, S., & Hochberg, G. K. A. (2024). A general substitution matrix for structural phylogenetics. bioRxiv: the preprint server for biology, 2024.09.19.613819. doi:10.1101/2024.09.19.613819.


Cite as: https://hdl.handle.net/21.11116/0000-000F-DDA7-C
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