The serine/threonine protein kinase PKB (also known as Akt) is thought to b
e a key mediator of signal transduction processes. The identification of PK
B substrates and the role PKB phosphorylation plays in regulating these mol
ecules have been a major focus of research in recent years. A recently deve
loped motif-profile scoring algorithm that can be used to scan the genome f
or potential PKB substrates is therefore a useful tool, although additional
considerations, such as the evolutionary conservation of the phosphorylati
on site, must also be taken into account. Recent evidence indicates that PK
B plays a key role in cancer progression by stimulating cell proliferation
and inhibiting apoptosis and is also probably a key mediator of insulin sig
nalling. These findings indicate that PKB is likely to be a hot drug target
for the treatment of cancer, diabetes and stroke. There are, however, a nu
mber of pitfalls of methodologies currently employed to study PKB function,
and therefore caution should be used in interpretation of such experiments
.