Hi Fred,
I can give you some Ideas regarding this.
step 1:
You can Download GBK files of the particular Genomes / Genes .
step 2:
From the GBK files you can get the UTR regions(sequences) of the genes.
and convert it to fasta format. For this you may have to write a Perl Scripts of your own to do that.
step 3:
To find the motifs in those sequence you can use normal BLASTN (In case you expect bigger motifs). Do blast against each sequence against each...Means you can create a database of those seqs for BLAST. And do BLAST for all the sequences against database.
Otherwise you can load these sequence in "MEME" with stringent e-values. In case if you are searching for KNOWN MOTIFS
you can use SeedTop (comes with BLAST package)
In case if you want to write your own Perl/python/SHELL Script for finding Patterns, you can use Manti Carlo methods to finalise the motifs (cluster) P value.
Hope its helpful...
if you have any questions regarding this dont hesitat eto ask me.
All the best.
Jeevan
--
"The Horse is made ready for the day of battle. But victory rests with the
LORD ". Proverbs 21:31