Entering edit mode
6.8 years ago
maximilian.mayerhofer
▴
30
So,
I have got a multifasta-file
>strain 1
ATCGCTCGACTG
>strain 2
ATGCGCAGCGAC
.....
I translate this to Protein using EMBOSS.
And I have a short Domain sequence of that Protein in AA that I want to align to see if there are any mutations in there.
So i use cat
to align both files in one.
cat multi.fasta shortseq.fasta>combined.fasta
Using MAFFT, I do not get a usable Output (big gaps).
mafft --reorder --adjustdirection combined.fasta>combined.aln
Should I use a different Approach for aligning?
Best Regards,
Max
Try clustal omega, its supposed to work nicely for protein sequences in particular.
Have you checked your fasta file is correct? Make sure the translation has worked properly.
How do I see if the translation was correct?
I mean literally read the fasta file and make sure it's not just ATCG..
Does
more multi.fasta
show properly formatted protein sequence?less is more
;) https://en.wikipedia.org/wiki/Less_(Unix)