It is now possible to identify over 30 functional subfamilies among the WD-
repeat-containing proteins found in the completed genomes. The majority of
these subfamilies have at least one member for which experimental data allo
w assignment to a cellular pathway or process. Half of the 63 WD-repeat-con
taining proteins in Saccharomyces cerevisiae. half of the 70 in Caenorhabdi
tis elegans. and a third of the 100 plus predicted in Drosophila can be ass
igned to 23 of these functional subfamilies. Perhaps indicative of the futu
re, 33 WD-repeat-containing proteins from the partial genome of Arabidopsis
thaliana can now be assigned to 18 of these subfamilies. These assignments
have been made possible by combining traditional sequence similarity with
an implied common beta propeller structural context to obtain measures of p
rotein-protein surface similarity. The beta propeller structural context is
represented in the form of a Hidden Markov Model. The procedure is complet
ely automated.