| Literature DB >> 22723302 |
Christopher J Challis1, Scott C Schmidler.
Abstract
We present a stochastic process model for the joint evolution of protein primary and tertiary structure, suitable for use in alignment and estimation of phylogeny. Indels arise from a classic Links model, and mutations follow a standard substitution matrix, whereas backbone atoms diffuse in three-dimensional space according to an Ornstein-Uhlenbeck process. The model allows for simultaneous estimation of evolutionary distances, indel rates, structural drift rates, and alignments, while fully accounting for uncertainty. The inclusion of structural information enables phylogenetic inference on time scales not previously attainable with sequence evolution models. The model also provides a tool for testing evolutionary hypotheses and improving our understanding of protein structural evolution.Mesh:
Substances:
Year: 2012 PMID: 22723302 PMCID: PMC3697813 DOI: 10.1093/molbev/mss167
Source DB: PubMed Journal: Mol Biol Evol ISSN: 0737-4038 Impact factor: 16.240