From: pvtroshin Date: Thu, 16 Jun 2011 16:46:41 +0000 (+0000) Subject: Binaries relocation X-Git-Url: http://source.jalview.org/gitweb/?a=commitdiff_plain;ds=sidebyside;h=2c1c5633a7d1c31008e04136cc4dae6fca1b369e;p=jabaws.git Binaries relocation git-svn-id: link to svn.lifesci.dundee.ac.uk/svn/barton/ptroshin/JABA2@4278 e3abac25-378b-4346-85de-24260fe3988d --- diff --git a/TODO.txt b/TODO.txt index dbd8400..911b957 100644 --- a/TODO.txt +++ b/TODO.txt @@ -1,3 +1,4 @@ +GET rid of binaries/help directory! TODO: Registry 1 week webservices - 1 week diff --git a/binaries/AACon_manual.txt b/binaries/help/AACon_manual.txt similarity index 100% rename from binaries/AACon_manual.txt rename to binaries/help/AACon_manual.txt diff --git a/binaries/clustalw-help.txt b/binaries/help/clustalw-help.txt similarity index 100% rename from binaries/clustalw-help.txt rename to binaries/help/clustalw-help.txt diff --git a/binaries/help/iupred.txt b/binaries/help/iupred.txt new file mode 100644 index 0000000..e023ac9 --- /dev/null +++ b/binaries/help/iupred.txt @@ -0,0 +1,45 @@ +INTERPRETATION OF THE OUTPUT: + +In the case of long and short types of disorder the output gives the +likelihood of disorder for each residue, i.e. it is a value between 0 and 1, +and higher values indicate higher probability of disorder. Residues with values +above 0.5 can be regarded as disordered, and at this cutoff 5% of globular +proteins is expected to be predicted to disordered (false positives). + +For the prediction type of globular domains it gives the number of globular +domains and list their start and end position in the sequence. This is followed +by the submitted sequence with residues of globular domains indicated by +uppercase letters. + + +SHORT SUMMARY OF THE METHOD + +Intrinsically unstructured/disordered proteins have no single well-defined +tertiary structure in their native, functional state. Our server recognizes +such regions from the amino acid sequence based on the estimated pairwise +energy content. The underlying assumption is that globular proteins make a +large number of interresidue interactions, providing the stabilizing energy to +overcome the entropy loss during folding. In contrast, IUPs have special +sequences that do not have the capacity to form sufficient interresidue +interactions. Taking a set of globular proteins with known structure, we have +developed a simple formalism that allows the estimation of the pairwise +interaction energies of these proteins. It uses a quadratic expression in the +amino acid composition, which takes into account that the contribution of an +amino acid to order/disorder depends not only its own chemical type, but also +on its sequential environment, including its potential interaction partners. +Applying this calculation for IUP sequences, their estimated energies are +clearly shifted towards less favorable energies compared to globular proteins, +enabling the predicion of protein disorder on this ground. + + +References + +"The Pairwise Energy Content Estimated from Amino Acid Composition +Discriminates between Folded and Intrinsically Unstructured Proteins" +Zsuzsanna Dosztanyi, Veronika Csizmok, Peter Tompa and Istvan Simon +J. Mol. Biol. (2005) 347, 827-839. + +"IUPred: web server for the prediction of intrinsically unstructured +regions of proteins based on estimated energy content" +Zsuzsanna Dosztanyi, Veronika Csizmok, Peter Tompa and Istvan Simon +Bioinformatics (2005) 21, 3433-3434. diff --git a/binaries/mafft_manual.htm b/binaries/help/mafft_manual.htm similarity index 100% rename from binaries/mafft_manual.htm rename to binaries/help/mafft_manual.htm diff --git a/binaries/muscle3.6.html b/binaries/help/muscle3.6.html similarity index 100% rename from binaries/muscle3.6.html rename to binaries/help/muscle3.6.html diff --git a/binaries/muscle3.7.txt b/binaries/help/muscle3.7.txt similarity index 100% rename from binaries/muscle3.7.txt rename to binaries/help/muscle3.7.txt diff --git a/binaries/probcons.pdf b/binaries/help/probcons.pdf similarity index 100% rename from binaries/probcons.pdf rename to binaries/help/probcons.pdf diff --git a/binaries/t_coffee.htm b/binaries/help/t_coffee.htm similarity index 100% rename from binaries/t_coffee.htm rename to binaries/help/t_coffee.htm diff --git a/binaries/aaconservation.jar b/binaries/windows/aaconservation.jar similarity index 100% rename from binaries/aaconservation.jar rename to binaries/windows/aaconservation.jar diff --git a/binaries/clustalw2.exe b/binaries/windows/clustalw2.exe similarity index 100% rename from binaries/clustalw2.exe rename to binaries/windows/clustalw2.exe diff --git a/binaries/jronn3.1.jar b/binaries/windows/jronn3.1.jar similarity index 100% rename from binaries/jronn3.1.jar rename to binaries/windows/jronn3.1.jar diff --git a/binaries/muscle.exe b/binaries/windows/muscle.exe similarity index 100% rename from binaries/muscle.exe rename to binaries/windows/muscle.exe diff --git a/conf/Executable.properties b/conf/Executable.properties index 4b75730..b9bdac3 100644 --- a/conf/Executable.properties +++ b/conf/Executable.properties @@ -1,6 +1,6 @@ ### Clustal configuration ### -local.clustalw.bin.windows=binaries/clustalw2.exe +local.clustalw.bin.windows=binaries/windows/clustalw2.exe local.clustalw.bin=binaries/src/clustalw/src/clustalw2 cluster.clustalw.bin=/homes/pvtroshin/workspace/jaba2/binaries/src/clustalw/src/clustalw2 # Parameters names which come from RunnerConfig -> Parameters.xml file ultimately are all lowercased in comparison! @@ -13,7 +13,7 @@ clustalw.limits.file=conf/settings/ClustalLimits.xml clustalw.cluster.settings=-l h_cpu=24:00:00 -l h_vmem=6000M -l ram=6000M ### Muscle configuration ### -local.muscle.bin.windows=binaries/muscle.exe +local.muscle.bin.windows=binaries/windows/muscle.exe local.muscle.bin=binaries/src/muscle/muscle # Beware version of muscle on the cluster older and does not support some # of the newer version attributed thus, will not work with Muscle.java wrapper! @@ -64,7 +64,7 @@ probcons.cluster.settings=-l h_cpu=24:00:00 -l h_vmem=6000M -l ram=6000M local.jronn.bin.windows=D:\\Java\\jdk1.6.0_24\\bin\\java.exe local.jronn.bin=/sw/java/latest/bin/java cluster.jronn.bin=/sw/java/latest/bin/java -jronn.jar.file=binaries/jronn3.1.jar +jronn.jar.file=binaries/windows/jronn3.1.jar # jronn.parameters.file=conf/settings/JronnParameters.xml jronn.limits.file=conf/settings/JronnLimits.xml #TODO jronn.jvm.options=-Xms32M -Xmx512M @@ -89,8 +89,9 @@ globplot.limits.file=conf/settings/GlobPlotLimits.xml globplot.cluster.settings=-l h_cpu=24:00:00 -l h_vmem=6000M -l ram=6000M ### IUPred configuration ### -#local.iupred.bin.windows= +local.iupred.bin.windows=binaries/windows/iupred/iupred.exe local.iupred.bin=binaries/src/iupred/iupred +# This must point to the directory where iupred binary is, with other files it depends on iupred.bin.env=IUPred_PATH#/homes/pvtroshin/workspace/jaba2/binaries/src/iupred cluster.iupred.bin=/homes/pvtroshin/workspace/jaba2/binaries/src/iupred/iupred iupred.parameters.file=conf/settings/IUPredParameters.xml @@ -98,10 +99,12 @@ iupred.limits.file=conf/settings/IUPredLimits.xml iupred.cluster.settings=-l h_cpu=24:00:00 -l h_vmem=6000M -l ram=6000M ### AACon configuration ### +# This is just a path to the standard java executable local.aacon.bin.windows=D:\\Java\\jdk1.6.0_24\\bin\\java.exe local.aacon.bin=/sw/java/latest/bin/java cluster.aacon.bin=/sw/java/latest/bin/java -aacon.jar.file=binaries/aaconservation.jar +# Path to the AACon library +aacon.jar.file=binaries/windows/aaconservation.jar aacon.parameters.file=conf/settings/AAConParameters.xml aacon.presets.file=conf/settings/AAConPresets.xml aacon.limits.file=conf/settings/AAConLimits.xml diff --git a/website/prog_docs/AACon_manual.txt b/website/prog_docs/AACon_manual.txt new file mode 100644 index 0000000..e9b4b53 --- /dev/null +++ b/website/prog_docs/AACon_manual.txt @@ -0,0 +1,94 @@ + +AA Conservation version 1.0b (2 September 2010) + +This program allows calculation of conservation of amino acids in +multiple sequence alignments. +It implements 17 different conservation scores as described by Valdar in +his paper (Scoring Residue Conservation, PROTEINS: Structure, Function +and Bioinformatics 48:227-241 (2002)) and SMERFS scoring algorithm as described +by Manning, Jefferson and Barton (The contrasting properties of conservation +and correlated phylogeny in protein functional residue prediction, +BMC Bioinformatics (2008)). + +The conservation algorithms supported are: + +KABAT, JORES, SCHNEIDER, SHENKIN, GERSTEIN, TAYLOR_GAPS, TAYLOR_NO_GAPS, +ZVELIBIL, KARLIN, ARMON, THOMPSON, NOT_LANCET, MIRNY, WILLIAMSON, +LANDGRAF, SANDER, VALDAR, SMERFS + +Input format is either a FASTA formatted file containing aligned sequences with +gaps or a Clustal alignment. The valid gap characters are *, -, space character, +X and . (a dot). By default program prints the results to the command window. +If the output file is provided the results are printed to the file in two +possible formats with or without an alignment. +If format is not specified, the program outputs conservation scores without +alignment. The scores are not normalized by default but they can be (see below). +SMERFS default parameters are window width of 7, column score is set to +the middle column (MID_SCORE), gap% cutoff of 0.1. Different parameters for SMERFS +can be provided (see below). Details of the program execution can be recorded to +a separate file if an appropriate file path is provided. + +List of command line arguments: + +-m= precedes a comma separated list of method names + EXAMPLE: -m=KABAT,JORES,GERSTEIN + Optional, if no method is specified request for all is assumed. + +-i= precedes a full path to the input FASTA file, required + +-o= precedes a full path to the output file, optional, if no output file is + provided the program will output to the standard out. + +-t= precedes the number of CPUs (CPU cores more precisely) to use. Optional, + defaults to all processors available on the machine. + +-f= precedes the format of the results in the output file + two different formats are possible: + RESULT_WITH_ALIGNMENT + RESULT_NO_ALIGNMENT + Optional, if not specified RESULT_NO_ALIGNMENT is assumed + +-d= precedes a full path to a file where program execution details are to be + listed. Optional, if not provided, no execution statistics is produced. + +-g= precedes comma separated list of gap characters provided by the user, if + you're using an unusual gap character (not a -,., ,*,X) you have to + provide it. If you you provide this list you have to list all the gaps + accepted. Including those that were previously treated as a default. + Optional. + +-n using this key causes the results to be normalized. + Normalized results have values between 0 and 1. Please note however, that + some results cannot be normalized. In such a case, the system returns not + normalized value, and log the issue to the standard error stream. + The following formula is used for normalization + n = (d - dmin)/(dmax - dmin) + Negative results first converted to positive by adding an absolute value of + the most negative result. Optional. + +SMERFS Only Parameters: + +-smerfsGT= precedes SMERFS Gap Treshold - a gap percentage cutoff - + a float greater than 0 and smaller or equal 1. Optional defaults + to 0.1 + +-smerfsCS= precedes SMERFS Column Score algorithm defines the window scores to + columns allocation , two methods are possible: + MID_SCORE - gives the window score to the middle column + MAX_SCORE - gives the column the highest score of all the windows it + belongs to. Optional defaults to MID_SCORE. + +-smerfsWW= precedes Window Width parameter - an integer and an odd number. + Optional, defaults to 7 + + +EXAMPLE HOW TO RUN THE PROGRAM: +java -jar -m=KABAT,SMERFS -i=prot1 -o=prot1_results -n + +As a result of the execution KABAT and SMERFS scores will be calculated. +Input comes form prot1 file and an output without an alignment is recorded to +prot1_results file. + +Authors: Peter Troshin, Agnieszka Golicz, David Martin and Geoff Barton. +Please visit http://www.compbio.dundee.ac.uk/aacon for further information. + \ No newline at end of file diff --git a/website/prog_docs/iupred.txt b/website/prog_docs/iupred.txt new file mode 100644 index 0000000..e023ac9 --- /dev/null +++ b/website/prog_docs/iupred.txt @@ -0,0 +1,45 @@ +INTERPRETATION OF THE OUTPUT: + +In the case of long and short types of disorder the output gives the +likelihood of disorder for each residue, i.e. it is a value between 0 and 1, +and higher values indicate higher probability of disorder. Residues with values +above 0.5 can be regarded as disordered, and at this cutoff 5% of globular +proteins is expected to be predicted to disordered (false positives). + +For the prediction type of globular domains it gives the number of globular +domains and list their start and end position in the sequence. This is followed +by the submitted sequence with residues of globular domains indicated by +uppercase letters. + + +SHORT SUMMARY OF THE METHOD + +Intrinsically unstructured/disordered proteins have no single well-defined +tertiary structure in their native, functional state. Our server recognizes +such regions from the amino acid sequence based on the estimated pairwise +energy content. The underlying assumption is that globular proteins make a +large number of interresidue interactions, providing the stabilizing energy to +overcome the entropy loss during folding. In contrast, IUPs have special +sequences that do not have the capacity to form sufficient interresidue +interactions. Taking a set of globular proteins with known structure, we have +developed a simple formalism that allows the estimation of the pairwise +interaction energies of these proteins. It uses a quadratic expression in the +amino acid composition, which takes into account that the contribution of an +amino acid to order/disorder depends not only its own chemical type, but also +on its sequential environment, including its potential interaction partners. +Applying this calculation for IUP sequences, their estimated energies are +clearly shifted towards less favorable energies compared to globular proteins, +enabling the predicion of protein disorder on this ground. + + +References + +"The Pairwise Energy Content Estimated from Amino Acid Composition +Discriminates between Folded and Intrinsically Unstructured Proteins" +Zsuzsanna Dosztanyi, Veronika Csizmok, Peter Tompa and Istvan Simon +J. Mol. Biol. (2005) 347, 827-839. + +"IUPred: web server for the prediction of intrinsically unstructured +regions of proteins based on estimated energy content" +Zsuzsanna Dosztanyi, Veronika Csizmok, Peter Tompa and Istvan Simon +Bioinformatics (2005) 21, 3433-3434.