In this review we demonstrate how the interplay of genomics, bioinformatics
and genomic technologies has enabled an in-depth analysis of the component
enzymes of the bacterial fatty-acid biosynthesis pathway as a source of no
vel antibacterial targets. This evaluation has revealed that many of the en
zymes are potentially selective, broad-spectrum antibacterial targets. We a
lso illustrate the suitability of some of these targets for HTS. Furthermor
e, we discuss how the availability of a robust selectivity assay, mode-of-a
ction assays and numerous crystal structures provide an excellent set of to
ols with which to initiate integrated programs of research to identify nove
l antibiotics targeted at these enzymes.