| BioPerl documentation | Contained in the BioPerl distribution. |
Bio::Tools::Analysis::Protein::ELM - a wrapper around the ELM server which predicts short functional motifs on amino acid sequences
# get a Bio::Seq object to start with, or a Bio::PrimaryI object.
my $tool = Bio::Tools::Analysis::Protein::ELM->
new(seq => $seqobj->primary_seq() );
$tool->compartment(['ER', 'Golgi']);
$tool->species(9606);
$tool->run;
my @fts = $tool->Result('Bio::SeqFeatureI');
$seqobj->addSeqFeature(@fts);
This module is a wrapper around the ELM server http://elm.eu.org/ which predicts short functional motifs on amino acid sequences.
False positives can be limited by providing values for the species and cellular compartment of the protein. To set the species attribute, use either a Bio::Species object or an NCBI taxon ID number. To set the cell compartment attribute (any number of compartments can be chosen) use an array reference to a list of compartment names.
Results can be obtained either as raw text output, parsed into a data structure, or as Bio::SeqFeature::Generic objects.
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
Please direct usage questions or support issues to the mailing list:
bioperl-l@bioperl.org
rather than to the module maintainer directly. Many experienced and reponsive experts will be able look at the problem and quickly address it. Please include a thorough description of the problem with code and data examples if at all possible.
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:
https://redmine.open-bio.org/projects/bioperl/
Richard Adams, Richard.Adams@ed.ac.uk,
The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _
name : compartment
usage : $elm->compartment(['golgi', 'er']);
purpose : get/setter for cell compartment specifications
arguments : None, single compartment string or ref to array of
compartment names.
returns : Array of compartment names (default if not previously set).
name : species
usage : $tool->species('9606');
purpose : get/setter for species selction for ELM server
arguments : none, taxon_id or Bio::Species object
returns : a string of the ncbi taxon_id
name : result
usage : $tool->result('Bio::SeqFeatureI');
purpose : parse results into sequence features or basic data format
arguments : 1. none (retrieves raw text without html)
2. a value (retrieves data structure)
3. 'Bio::SeqFeatureI' (returns array of sequence features)
tag names are : {method => 'ELM', motif => motifname,
peptide => seqeunce of match,
concensus => regexp of match}.
returns : see arguments.
| BioPerl documentation | Contained in the BioPerl distribution. |
# # BioPerl module for Bio::Tools::Analysis::Protein::ELM # # Please direct questions and support issues to <bioperl-l@bioperl.org> # # 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
use strict; package Bio::Tools::Analysis::Protein::ELM; use vars qw(%cc); use HTML::HeadParser; use Bio::SeqFeature::Generic; use HTTP::Request::Common qw(POST); use IO::String; use base qw(Bio::Tools::Analysis::SimpleAnalysisBase); ## valid cell compartments ## %cc = ( all => 1, nucleus => 'GO:0005634', extracellular => 'GO:0005576', cytoplasm => 'GO:0005737', peroxisome => 'GO:0005777', glycosome => 'GO:0020015', glyoxisome => 'GO:0009514', golgi => 'GO:0005794', er => 'GO:0005783', lysosome => 'GO:0005764', endosome => 'GO:0005768', plasma_membrane=> 'GO:0005886', ); my $URL = 'http://elm.eu.org/basicELM/cgimodel.py'; my $ANALYSIS_NAME = 'ELM'; my $INPUT_SPEC = [ { 'mandatory' => 'true', 'type' => 'Bio::PrimarySeqI', 'name' => 'seq', }, { 'mandatory' => 'false', 'type' => 'taxon_id or Bio::Species object', 'name' => 'species', 'default' => '9606', }, { 'mandatory' => 'false', 'type' => 'string', 'name' => 'compartment', 'default' => [1], }, ]; my $RESULT_SPEC = { '' => 'bulk', # same as undef 'Bio::SeqFeatureI' => 'ARRAY of Bio::SeqFeature::Generic', 'parsed' => '{motif1_name=>{locus=>[], peptide=>[], regexp=>[] }, }', }; my $ANALYSIS_SPEC= {name => 'ELM', type => 'Protein', version => 'n/a', supplier =>'BioComputing Unit, EMBL', description =>'Prediction of linear functional motifs in proteins', reference => 'NAR, 31:3625-3630'}; 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_NAME; return $self; }
sub compartment { my ($self, $arg) = @_; if ($arg) { # convert to array ref if not one already if (ref ($arg) ne 'ARRAY') { $arg = [$arg]; } ## now add params if valid for my $param (@$arg) { if (exists($cc{lc($param)})) { push @{$self->{'_compartment'}} , $cc{$param}; } else { $self->warn("invalid argument ! Must be one of " . join "\n", keys %cc ); } } #end of for loop } #endif $arg return defined($self->{'_compartment'})? $self->{'_compartment'} : $self->input_spec()->[2]{'default'}; }
sub species { my ($self, $arg) = @_; if ($arg) { if (ref($arg) && $arg->isa('Bio::Species')) { $self->{'_species'} = $arg->ncbi_taxid(); } elsif ($arg =~ /^\d+$/) { $self->{'_species'} = $arg; } else { $self->warn("Argument must be a Bio::Species object or ". " an integer NCBI taxon id. "); } } #end if $arg return defined($self->{'_species'})?$self->{'_species'} :$self->input_spec()->[1]{'default'}; } sub _run { my $self = shift; $self->delay(1); # delay repeated calls by default by 3 sec, set delay() to change #$self->sleep; $self->status('TERMINATED_BY_ERROR'); #### this deals with being able to submit multiple checkboxed #### slections #1st of all make param array my @cc_str; my @cmpts = @{$self->compartment()}; for (my $i = 0; $i <= $#cmpts ; $i++) { splice @cc_str, @cc_str, 0, 'userCC',$cmpts[$i]; } my %h = (swissprotId => "", sequence => $self->seq->seq, userSpecies => $self->species, typedUserSpecies => '', fun => "Submit"); splice (@cc_str, @cc_str,0, ( map{$_, $h{$_}} keys %h)); my $request = POST $self->url(), Content_Type => 'form-data', Content => \@cc_str; $self->debug( $request->as_string); my $r1 = $self->request($request); if ( $r1->is_error ) { $self->warn(ref($self)." Request Error:\n".$r1->as_string); return; } my $text = $r1->content; my ($url) = $text =~ /URL=\S+(fun=\S+r=\d)/s; #$url =~ s/amp;//g ; my ($resp2); $url = $URL . "?" .$url; while (1) { my $req2 = HTTP::Request->new(GET=>$url); my $r2 = $self->request ($req2); if ( $r2->is_error ) { $self->warn(ref($self)." Request Error:\n".$r2->as_string); return; } $resp2 = $r2->content(); if ($resp2 !~ /patient/s) { $self->status('COMPLETED'); $resp2=~ s/<[^>]+>/ /sg; $self->{'_result'} = $resp2; return; } else { print "." if $self->verbose > 0; $self->sleep(1); } } }
sub result { my ($self, $val) = @_; if ($val) { if (!exists($self->{'_parsed'}) ) { $self->_parse_raw(); } if ($val eq 'Bio::SeqFeatureI') { my @fts; for my $motif (keys %{$self->{'_parsed'}}) { for (my $i = 0; $i< scalar @{$self->{'_parsed'}{$motif}{'locus'}};$i++) { my ($st, $end) = split /\-/, $self->{'_parsed'}{$motif}{'locus'}[$i]; push @fts, Bio::SeqFeature::Generic->new ( -start => $st, -end => $end, -primary_tag => 'Domain', -source => 'ELM', -tag => { method => 'ELM', motif => $motif, peptide => $self->{'_parsed'}{$motif}{'peptide'}[$i], concensus => $self->{'_parsed'}{$motif}{'regexp'}[0], }); } } return @fts; } #end if BioSeqFeature return $self->{'_parsed'}; } #endif ($val) return $self->{'_result'}; } ## internal sub to parse raw data into internal data structure which is cached. sub _parse_raw { my $self = shift; my $result = IO::String->new($self->{'_result'}); my $in_results = 0; my $name; my %results; my $last; while (my $l = <$result>) { next unless $in_results > 0 ||$l =~ /^\s+Elm\s+Name\s+Instances/; $in_results++; #will be set whnstart of results reached. last if $l =~ /List of excluded/; next unless $in_results >1; my @line_parts = split /\s+/, $l; shift @line_parts; ## if result has motif name on 1 line if (scalar @line_parts == 1 && $line_parts[0]=~ /^\s*(\w+_\w+)/) { $name = $1; next; } ## else if is line with loci /seq matches elsif (@line_parts > 1) { my $index = 0; ## array index my $read_loci = 0; ## flag to know that loci are being read while ($index <= $#line_parts) { my $word = $line_parts[$index++]; if ($read_loci ==0 && $word =~/_/) { $name = $word; } elsif ($read_loci == 0 && $word =~ /^\w+$/ ) { push @{$results{$name}{'peptide'}}, $word; } elsif ($word =~ /\d+\-\d+/) { $read_loci = 1; push @{$results{$name}{'locus'}}, $word; } else { ## only get here if there are elements last; } } #end of while push @{$results{$name}{'regexp'}}, $line_parts[$#line_parts]; } #end of elsif } #end of while $self->{'_parsed'} = \%results; } 1;