————# $Id: Scansite.pm,v 1.16.4.1 2006/10/02 23:10:32 sendu Exp $
#
# BioPerl module for Bio::Tools::Analysis::Protein::Scansite
#
# Cared for by Richard Adams <richard.adams@ed.ac.uk>
#
# Copyright Richard Adams
#
# You may distribute this module under the same terms as perl itself
# POD documentation - main docs before the code
=head1 NAME
Bio::Tools::Analysis::Protein::Scansite - a wrapper around the Scansite server
=head1 SYNOPSIS
use Bio::Tools::Analysis::Protein::Scansite;
my $seq; # a Bio::PrimarySeqI object
my $tool = Bio::Tools::Analysis::Protein::Scansite->new
( -seq => $seq->primary_seq );
# run Scansite prediction on a sequence
$tool->run();
# alternatively you can say
$tool->seq($seq->primary_seq)->run;
die "Could not get a result" unless $tool->status =~ /^COMPLETED/;
print $tool->result; # print raw prediction to STDOUT
foreach my $feat ( $tool->result('Bio::SeqFeatureI') ) {
# do something to SeqFeature
# e.g. print as GFF
print $feat->gff_string, "\n";
# or store within the sequence - if it is a Bio::RichSeqI
$seq->add_SeqFeature($feat);
}
=head1 DESCRIPTION
This class is a wrapper around the Scansite 2.0 server which produces
predictions for serine, threonine and tyrosine phosphorylation sites
in eukaryotic proteins. At present this is a basic wrapper for the
"Scan protein by input sequence" functionality, which takes a sequence
and searches for motifs, with the option to select the search
stringency. At present, searches for specific phosphorylation
sites are not supported; all predicted sites are returned.
=head2 Return formats
The Scansite results can be obtained in several formats:
=over 3
=item 1.
By calling
my $res = $tool->result('');
$res holds a string of the predicted sites in tabular format.
=item 2.
By calling
my $data_ref = $tool->result('value')
$data_ref is a reference to an array of hashes. Each element in the
array represents a predicted phosphorylation site. The hash keys are
the names of the data fields,i.e.,
'motif' => 'Casn_Kin1' # name of kinase
'percentile' => 0.155 # see Scansite docs
'position' => 9 # position in protein
'protein' => 'A1' # protein id
'score' => 0.3696 # see Scansite docs
'sequence' => 'ASYFDTASYFSADAT' # sequence surrounding site
'site' => 'S9' # phosphorylated residue
'zscore' => '-3.110' # see Scansite docs
=item 3.
By calling
my @fts = $tool->Result('Bio::SeqFeatureI');
which returns an array of L<Bio::SeqFeatureI> compliant objects with
primary tag value 'Site' and tag names of 'motif', 'score',
'sequence', 'zscore' as above.
=back
See L<http://scansite.mit.edu/>.
This inherits Bio::SimpleAnalysisI which hopefully makes it easier to
write wrappers on various services. This class uses a web resource and
therefore inherits from L<Bio::WebAgent>.
=head1 SEE ALSO
L<Bio::SimpleAnalysisI>,
L<Bio::WebAgent>
=head1 FEEDBACK
=head2 Mailing Lists
User feedback is an integral part of the evolution of this and other
Bioperl modules. Send your comments and suggestions preferably to one
of the Bioperl mailing lists. Your participation is much appreciated.
bioperl-l@bioperl.org - General discussion
http://bioperl.org/wiki/Mailing_lists - About the mailing lists
=head2 Reporting Bugs
Report bugs to the Bioperl bug tracking system to help us keep track
the bugs and their resolution. Bug reports can be submitted via the
web:
=head1 AUTHORS
Richard Adams, Richard.Adams@ed.ac.uk,
=head1 APPENDIX
The rest of the documentation details each of the object
methods. Internal methods are usually preceded with a _
=cut
# Let the code begin...
use
strict;
use
IO::String;
use
Bio::SeqIO;
$FLOAT
=
'[+-]?\d*\.\d*'
;
@STRINGENCY
=
qw(High Medium Low)
;
my
$ANALYSIS_SPEC
=
{
'name'
=>
'Scansite'
,
'type'
=>
'Protein'
,
'version'
=>
'2.0'
,
'supplier'
=>
'Massachusetts Institute of Technology'
,
'description'
=> 'Prediction of serine, threonine and tyrosine
phosphorylation sites in eukaryotic proteins',
};
my
$INPUT_SPEC
=
[
{
'mandatory'
=>
'true'
,
'type'
=>
'Bio::PrimarySeqI'
,
'name'
=>
'seq'
,
},
{
'mandatory'
=>
'false'
,
'type'
=>
'text'
,
'name'
=>
'protein_id'
,
'default'
=>
'unnamed'
,
},
{
'mandatory'
=>
'false'
,
'type'
=>
'text'
,
'name'
=>
'stringency'
,
'default'
=>
'High'
,
},
];
my
$RESULT_SPEC
=
{
''
=>
'bulk'
,
# same as undef
'Bio::SeqFeatureI'
=>
'ARRAY of Bio::SeqFeature::Generic'
,
'raw'
=> 'Array of {
motif
=>,
percentile
=>,
position
=>,
protein
=>,
score
=>,
site
=>,
zscore
=>
sequence
=>
}',
};
=head2 result
Name : result
Usage : $job->result (...)
Returns : a result created by running an analysis
Args : none (but an implementation may choose
to add arguments for instructions how to process
the raw result)
The method returns a scalar representing a result of an executed
job. If the job was terminated by an error, the result may contain
an error message instead of the real data.
This implementation returns differently processed data depending on
argument:
=over 3
=item undef
Returns the raw ASCII data stream but without HTML tags
=item 'Bio::SeqFeatureI'
The argument string defined the type of bioperl objects returned in an
array. The objects are L<Bio::SeqFeature::Generic>.
=item 'parsed'
Returns a reference to an array of hashes containing the data of one
phosphorylation site prediction. Key values are:
motif, percentile, position, protein, score, site, zscore, sequence.
=back
=cut
sub
result {
my
(
$self
,
$value
) =
@_
;
if
( !
exists
(
$self
->{
'_result'
}) ||
$self
->status ne
'COMPLETED'
){
$self
->throw(
"Cannot get results, analysis not run!"
);
}
my
@fts
;
if
(
$value
) {
if
(
$value
eq
'Bio::SeqFeatureI'
) {
for
my
$hit
(@{
$self
->{
'_parsed'
}}) {
push
@fts
, Bio::SeqFeature::Generic->new(
-start
=>
$hit
->{
'position'
},
-end
=>
$hit
->{
'position'
},
-primary_tag
=>
'Site'
,
-source
=>
'Scansite'
,
-tag
=> {
score
=>
$hit
->{
'score'
},
zscore
=>
$hit
->{
'zscore'
},
motif
=>
$hit
->{
'motif'
},
site
=>
$hit
->{
'site'
},
sequence
=>
$hit
->{
'sequence'
},
},
);
}
return
@fts
;
}
elsif
(
$value
eq
'meta'
) {
$self
->throw(
"No meta sequences available in this analysis!"
);
}
## else get here
return
$self
->{
'_parsed'
};
}
return
$self
->{
'_result'
};
}
=head2 stringency
Usage : $job->stringency(...)
Returns : The significance stringency of a prediction
Args : None (retrieves value) or 'High', 'Medium' or 'Low'.
Purpose : Get/setter of the stringency to be sumitted for analysis.
=cut
sub
stringency {
my
(
$self
,
$value
) =
@_
;
if
(
$value
) {
if
(!
grep
{
$_
=~ /
$value
/i}
@STRINGENCY
) {
$self
->throw(
"I need a stringency of ["
.
join
" "
,
@STRINGENCY
.
"], not [$value]"
);
}
$self
->{
'_stringency'
} =
$value
;
return
$self
;
}
return
$self
->{
'_stringency'
} ||
$self
->input_spec->[2]{
'default'
} ;
}
=head2 protein_id
Usage : $job->protein_id(...)
Returns : The sequence id of the protein or 'unnamed' if not set.
Args : None
Purpose : Getter of the seq_id. Returns the display_id of the sequence
object.
=cut
sub
protein_id {
my
$self
=
shift
;
return
defined
(
$self
->seq())?
$self
->seq->display_id()
:
$self
->input_spec->[1]{
'default'
};
}
sub
_init
{
my
$self
=
shift
;
$self
->url(
$URL
);
$self
->{
'_ANALYSIS_SPEC'
} =
$ANALYSIS_SPEC
;
$self
->{
'_INPUT_SPEC'
} =
$INPUT_SPEC
;
$self
->{
'_RESULT_SPEC'
} =
$RESULT_SPEC
;
$self
->{
'_ANALYSIS_NAME'
} =
$ANALYSIS_SPEC
->{
'name'
};
return
$self
;
}
sub
_run {
my
$self
=
shift
;
# format the sequence into fasta
$self
->delay(1);
# delay repeated calls by default by 3 sec, set delay() to change
$self
->
sleep
;
$self
->status(
'TERMINATED_BY_ERROR'
);
my
$request
= POST
$self
->url,
Content
=> [
sequence
=>
$self
->seq->seq(),
protein_id
=>
$self
->protein_id(),
motif_option
=>
'all'
,
motifs
=>
''
,
motif_groups
=>
''
,
stringency
=>
$self
->stringency(),
domain_flag
=>
''
,
submit
=>
"Submit Request"
,
];
## raw html report,
my
$content
=
$self
->request(
$request
);
my
$text
=
$content
->content;
##access result data from tag in html
my
@parsed_Results
= ();
my
@unwantedParams
=
qw(db source class)
;
my
@results
=
split
/sitestats\.phtml\?/,
$text
;
shift
@results
;
##this module generates 'parsed' output directly from html,
## avoids having toparse twice.
for
my
$hit
(
@results
) {
## get results string
my
(
$res
) =
$hit
=~ /^(.+?)"/;
#get key value pairs
my
%params
=
$res
=~/(\w+)=([^&]+)/g;
##remove unwanted data from hash
map
{
delete
$params
{
$_
}}
@unwantedParams
;
push
@parsed_Results
, \
%params
;
}
## now generate text output in table format
my
$out_Str
=
''
;
$out_Str
.=
$self
->_make_header(\
@parsed_Results
);
$out_Str
.=
$self
->_add_data(\
@parsed_Results
);
$self
->{
'_result'
} =
$out_Str
;
$self
->{
'_parsed'
} = \
@parsed_Results
;
## is successsful if there are results or if there are no results and
## this beacuse there are no matches, not because of parsing errors etc.
$self
->status(
'COMPLETED'
)
if
$text
ne
''
&&
(
scalar
@results
> 0 ||
(
scalar
@results
== 0 &&
$text
=~/No sites found/));
if
(
$text
=~ /server\s+error/i) {
$self
->
warn
(
"There was an internal server error !- text below"
) ;
$self
->
warn
(
$text
);
return
;
}
}
sub
_process_arguments {
# extra checking for sequence length
# mitoprot specific argument testing
my
(
$self
,
$args
) =
@_
;
#use base checking for existence of mandatory fields
$self
->SUPER::_process_arguments(
$args
);
# specific requirements
$self
->throw(
"Sequence must be > 15 amino acids long!"
)
if
$self
->seq->
length
< 15;
$self
->throw(
"Sequence must be protein"
)
unless
$self
->seq->alphabet() eq
'protein'
;
}
sub
_make_header {
my
(
$self
,
$res
) =
@_
;
my
$header
=
''
;
for
my
$k
(
sort
keys
%{
$res
->[0]} ){
next
if
$k
eq
'sequence'
;
$header
.=
$k
;
$header
.=
' '
x(12 -
length
(
$k
));
}
$header
.=
"sequence\n\n"
;
return
$header
;
}
sub
_add_data {
my
(
$self
,
$res
) =
@_
;
my
$outstr
=
''
;
for
my
$hit
(
@$res
) {
for
my
$k
(
sort
keys
%$hit
){
next
if
$k
eq
'sequence'
;
$outstr
.=
$hit
->{
$k
};
$outstr
.=
' '
x(12 -
length
(
$hit
->{
$k
}));
}
$outstr
.=
$hit
->{
'sequence'
}.
"\n"
if
$hit
->{
'sequence'
};
}
return
$outstr
;
}
1;