New structural data have emerged for the ligand-binding sites of C-type lec
tin domains and C-type lectin-like domains of receptors of the immune syste
m. These include binding sites for oligosaccharide or polypeptide ligands,
or both oligosaccharide and polypeptide ligands. The structural basis for t
he binding of a lectin domain of the beta -trefoil family to different sulf
o-oligosaccharide sequences has been revealed. Lectin activity has been doc
umented for a beta/alpha, TIM barrel fold that does not have the chitinase
activity of the prototype enzyme with this fold.