Structural genomics projects aim to solve the experimental structures of al
l possible protein folds. Such projects entail a conceptual shift from trad
itional structural biology in which structural information is obtained on k
nown proteins to one in which the structure of a protein is determined firs
t and the function assigned only later. Whereas the goal of converting prot
ein structure into function can be accomplished by traditional sequence mot
if-based approaches, recent studies have shown that assignment of a protein
's biochemical function can also be achieved by scanning its structure for
a match to the geometry and chemical identity of a known active site. Impor
tantly, this approach can use tow-resolution structures provided by contemp
orary structure prediction methods. When applied to genomes, structural inf
ormation (either experimental or predicted) is likely to play an important
role in high-throughput function assignment.