Sugar transport across the plasma membrane is one of the most important tra
nsport processes. The cloning and expression of cDNAs from a superfamily of
related sugar transporters that all adopt a 12-membrane-spanning-domain st
ructure has opened new avenues of investigation, including pre steady-state
kinetic analysis. Structure-function analyses of mammalian and bacterial s
ugar transporters, and comparisons of these transporters with those of para
sitic trypanosomatids, indicate that different environmental pressures have
tailored the evolution of the various members of the sugar-transporter sup
erfamily. Subtle distinctions in the function of these proteins can be rela
ted to particular amino acid residue substitutions.