So, I've been interested in using the 10,000 human protein assay library 
from swath atlas 
<https://db.systemsbiology.net/sbeams/cgi/PeptideAtlas/GetDIALibs>.  One 
thing that I noticed is that for some assays the peptide sequence is not 
present in one, or more, of the proteins associated with the assay.  For 
example, from the peakview file (phl004_canonical_sall_pv.csv): 
'393.247620674   601.366787076   19.8    2/Q8NFR9/Q8WUD4 light   10000.0 
AIAELIR AIAELIR 2       y       1       5       19.8    2/Q8NFR9/Q8WUD4 
FALSE   3310    1       TRUE'.  AIAELIR is in the Q8WUD4 sequence but not 
in Q8NFR9.  

So, I decided to reprocess the data with tpp to see if that would provide 
any insight.

I downloaded the mzXML files from PRIDE 
<http://www.ebi.ac.uk/pride/archive/projects/PXD000953> and searched with 
comet.  The peptide (AIAELIR) shows up as a hit in 
the YANLIU_K140110_002.mzXML file and is associated with Q8WUD4 as the 
number 1 hit (Q8NFR9 is not in the hit list for the spectrum_query). 
 However, once I run xinteract on the comet search results (xinteract 
-OARPd -dREVERSE_ -Ninteract.comet.pep.xml 
YANLIU_K140110_002.comet.pep.xml) Q8NFR9 now shows up as an 
alternative_protein for the spectrum_query (<alternative_protein 
protein="sp|Q8NFR9|I17RE_HUMAN" protein_descr="Interleukin-17 receptor E 
OS=Homo sapiens GN=IL17RE PE=1 SV=1" num_tol_term="1" peptide_prev_aa="G" 
peptide_next_aa="A"/>)

I'm wondering why this happens?

I've used comet and xinteract from tpp 4.8.0 and the sashimi-code svn 
repository on CENTOS Linux 7.  

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