LAUSR

Phylogenetic inference from protein data is traditionally based on empirical substitution models of evolution that assume that protein sites evolve independently of each other and under the same substitution process. However, it is well known that the structural properties of a protein site in the native state affect its evolution, in particular the sequence entropy and the substitution rate. Starting from the seminal proposal by Halpern and Bruno, where structural properties are incorporated in the evolutionary model through site-specific amino acid frequencies, several models have been developed to tackle the influence of protein structure on sequence evolution. Here we describe stability-constrained substitution (SCS) models that explicitly consider the stability of the native state against both unfolded and misfolded states. One of them, the mean-field model, provides an independent sites approximation that can be readily incorporated in maximum likelihood methods of phylogenetic inference, including ancestral sequence reconstruction. Next, we describe its validation with simulated and real proteins and its limitations and advantages with respect to empirical models that lack site specificity. We finally provide guidelines and recommendations to analyze protein data accounting for stability constraints, including computer simulations and inferences of protein evolution based on maximum likelihood. Some practical examples are included to illustrate these procedures.