Protein Sequence Alignment Using Blast
2
0
Entering edit mode
9.1 years ago
p.s • 0

Hi All,

I am trying to run Blast over protein sequences from two organisms. I downloaded the fasta from NCBI. I am trying to iterate over the list of sequences in the fasta file and do a sequence alignment of each sequence in one file with each sequence in the other. I want to run over local Blast but getting some error, I would greatly appreciate some suggestions.

'''from Bio.Blast.Applications import NcbiblastxCommandline
help(NcbiblastxCommandline)'''

from Bio.Blast.Applications import NcbiblastpCommandline
from StringIO import StringIO
from Bio.Blast import NCBIXML
from Bio.Seq import Seq
from Bio.SeqRecord import SeqRecord
from Bio import SeqIO
from Bio.Blast import NCBIWWW
import cStringIO

def BlastSeq():
SC_Fasta = open("sc.fsa","r")
HS_Fasta = open("hsap.fsa","r")
blastp = "C:\\Program Files\\NCBI\\blast-2.2.29+\\bin\\blastp"

record1 = list(SeqIO.parse(SC_Fasta,"fasta"))
for r1 in record1:
r1.id
r1.seq

record2 = list(SeqIO.parse(HS_Fasta,"fasta"))
for r2 in record2:
r2.id
r2.seq

for r1 in record1:
for r2 in record2:
output = NcbiblastpCommandline(blastp,query= r1.seq, subject=r2.seq, outfmt=5)()[0]

def main():
BlastSeq()

main()

Error: Bio.Application.ApplicationError: Command 'C:\Program Files\NCBI\blast-2.2.29+\bin\blastp -outfmt 5 -query    MVKLTSIAAGVAAIAATASATTTLAQSDERVNLVELGVYVSDIRAHLAQYYMFQAAHPTETYPVEVAEAVFNYGDF -subjectHGLQELKAELDAAVLKATGRQILTLRVRLAGAQLSWLYKEATVQEVDVIPEDGAADVRVIISNSAYGKFRKLFPG' returned non-zero exit status -1073741515


I understand that each seq should be passed as individual fasta file,but I don't understand how to proceed.

biopython blast protein • 4.5k views
1
Entering edit mode
9.1 years ago
Peter 6.0k

The problem is essentially you asked BLAST to do this:

C:\Program Files\NCBI\blast-2.2.29+\bin\blastp -outfmt 5 -query MVKLTSIAAGVAAIAATASATTTLAQSDERVNLVELGVYVSDIRAHLAQYYMFQAAHPTETYPVEVAEAVFNYGDF -subject HGLQELKAELDAAVLKATGRQILTLRVRLAGAQLSWLYKEATVQEVDVIPEDGAADVRVIISNSAYGKFRKLFPG


And that fails (try it directly at the command line). Rather than raw sequence via the command line, you would normally have the sequences on disk in FASTA format, and tell BLAST the filenames.

The larger question is why are you doing lots of pair wise BLAST alignments? Might another tool be better matched? For example, EMBOSS needleall? http://emboss.sourceforge.net/apps/release/6.5/emboss/apps/needleall.html

0
Entering edit mode
9.1 years ago
Zhaorong ★ 1.4k

You are right in saying "I understand that each seq should be passed as individual fasta file". The reason is that you have to pass the filename of the fasta file to BLAST, rather than the sequences inside it.

I modified your code just to pass the filenames to BLAST.

from Bio.Blast.Applications import NcbiblastpCommandline
from Bio.Blast import NCBIXML

def BlastSeq():
SC_Fasta = "sc.fsa"
HS_Fasta = "hsap.fsa"
blastp = "C:\\Program Files\\NCBI\\blast-2.2.29+\\bin\\blastp"

# I would suggest saving the blast output to a file, though you do not have to do this
blast_output = "blast_output.xml"
NcbiblastpCommandline(blastp, query=SC_Fasta, subject=HS_Fasta, outfmt=5, out=blast_output)()
# Now you can read the blast output from the file and process it however you want
blast_result_records = NCBIXML.parse(open(blast_output))

BlastSeq()


Please note that now all the pairwise alignments between the sequences in "sc.fsa" and "hsap.fsa" are stored in a single blast output file.

In your original code, it seems that you intended to call blastp once for each pair of sequences. You don't need to do this, as BLAST can handle multiple sequences in -query and -subject at the same time (thanks, Peter). However, if you insist on doing this, here is the code just to show you how hard it is.

Finally, if you would like to obtain global alignment between the sequences, I would suggest using EMBOSS needle or needleall. You can also call needle in Biopython if you like. A relevant discussion on local and global alignment can be found Is It Possible To Get Near Global Alignment From Blast?.

1
Entering edit mode

Why split the FASTA files? You could try giving BLAST multiple record FASTA files using -query and -subject and it will do pairwise searches (note the e-values will not consider the other sequences, like it would if you used a database search), but the parsing is a little more complicated (loop over the results instead).

0
Entering edit mode

Hi Peter, thank you, you are right. I had the idea in mind that the code could be adapted for using needle rather than BLAST as the alignment tool. I have modified my answers as you suggested.

0
Entering edit mode

Nice. For EMBOSS needle, try "needle all" if you want to do a comparison of many versus many.