We present a model of amino acid sequence evolution based on a hidden Marko
v model that extends to transmembrane proteins previous methods that incorp
orate protein structural information into phylogenetics. Our model aims to
give a better understanding of processes of molecular evolution and to extr
act structural information from multiple alignments of transmembrane sequen
ces and use such information to improve phylogenetic analyses. This should
be of value in phylogenetic studies of transmembrane proteins: for example,
mitochondrial proteins have acquired a special importance in phylogenetics
and are mostly transmembrane proteins. The improvement in fit to example d
ata sets of our new model relative to less complex models of amino acid seq
uence evolution is statistically tested. To further illustrate the potentia
l utility of our method, phylogeny estimation is performed on primate CCR5
receptor sequences, sequences of l and m subunits of the light reaction cen
ter in purple bacteria, guinea pig sequences with respect to lagomorph and
rodent sequences of calcitonin receptor and K-substance receptor, and cetac
ean sequences of cytochrome b.