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<tool id="edu.tamu.cpt.sar.sar_finder" name="SAR Finder" version="1.0"> <description>SAR Domain Finder</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"> </expand> <command detect_errors="aggressive"><![CDATA[ python '$__tool_directory__/SAR_finder.py' '$fa' --sar_min '$sar_min' --sar_max '$sar_max' --out_fa '$out_fa' --out_gff3 '$out_gff3' --out_stat '$out_stat' ]]></command> <inputs> <param label="Multi FASTA File" name="fa" type="data" format="fasta"/> <param label="SAR domain minimal size" name="sar_min" type="integer" value="15"/> <param label="SAR domain maximum size" name="sar_max" type="integer" value="20"/> </inputs> <outputs> <data format="tabular" name="out_stat" label="candidate_SAR_stats.tsv"/> <data format="fasta" name="out_fa" label="candidate_SAR.fa"/> <data format="gff3" name="out_gff3" label="candidate_SAR.gff3"/> </outputs> <tests> <test> <param name="fa" value="simple-proteins.fa"/> <param name="sar_min" value="15"/> <param name="sar_max" value="20"/> <output name="out_stat" file="candidate_SAR_stats.tsv"/> <output name="out_fa" file="candidate_SAR.fa"/> <output name="out_gff3" file="candidate_SAR.gff3"/> </test> </tests> <help><![CDATA[ **What it does** A tool that analyzes the sequence within the first 50 residues of a protein for a weakly hydrophobic domain called Signal-Anchor-Release (aka SAR). The tool finds proteins that contain a stretch (default 15-20 residues) of hydrophobic residues (Ile, Leu, Val, Phe, Tyr, Trp, Met, Gly, Ala, Ser) and calculates the % Gly/Ala/Ser/Thr residues in the hydrophobic stretch. The net charge on the N-terminus is also displayed to aid in determining the SAR orientation in the membrane.[2] Definition: A Signal-Anchor-Release (SAR) domain is an N-terminal, weakly hydrophobic transmembrane region rich in Gly/Ala and/or Ser (and sometimes Thr) residues. The SAR domain is sometimes found in phage lysis proteins, including endolysins and holins. The SAR domain can be released from the membrane in a proton motive force-dependent manner. Known SAR domains in phage endolysins often have >50-60% Gly/Ala/Ser/Thr content. SAR endolysins are expected to have a net positive charge on the N-terminus by the positive-inside rule. **INPUT** --> Protein Multi FASTA **OUTPUT** --> * Multi FASTA with candidate proteins that pass the SAR domain criteria * Tabular summary file that lists every subdomain fitting the criteria for each potential SAR domain-containing protein with the following: protein name/sequence/length, SAR length/start/sequence/end, individual and total GAST% content in SAR, and N-terminal sequence/net charge * Multi GFF3 for unique candidate SAR domain-containing proteins ]]></help> <citations> <citation type="doi">10.1371/journal.pcbi.1008214</citation> <citation type="doi">https://dx.doi.org/10.1016/bs.aivir.2018.09.003</citation> <citation type="bibtex"> @unpublished{galaxyTools, author = {C. Ross}, title = {CPT Galaxy Tools}, year = {2020-}, note = {https://github.com/tamu-cpt/galaxy-tools/} } </citation> </citations> </tool>