The evolution of proteins and their functions is reviewed from a structural
perspective in the light of the current database. Protein domain families
segregate unequally between the three major classes, the 32 different archi
tectures and almost 700 folds observed to date. We find that the number of
new topologies is still increasing, although 25 new structures are now dete
rmined for each new topology. The corresponding analysis and classification
of-function is only just beginning, fuelled by the genome data. The struct
ural:data revealed unexpected conservations and divergence of function both
within and between families. The next five years will see the compilation
of a definitive dictionary of protein families and their related functions,
based on structural data which reveals relationships hidden at the sequenc
e level. Such information will provide the foundation to build a better und
erstanding of the molecular basis of biological complexity and: hopefully t
o facilitate rational molecular design. (C) 1999 Academic Press.