Methods and Websites

Websites with useful information or software

RCSB Protein Database: PDB

Structural Classification of Proteins: SCOP

Structural Comparison of Proteins: Dali, CE

Multiple Structure Alignment: CEMC

Protein families database: Pfam at St Louis Pfam at Sanger

Clusters of Orthologous groups: COG

Domain prediction: InterPro

Webserver that converts sequence identifiers into species names.

The website lets you change the sequence identifiers to organism taxonomies. You need to upload the original FASTA file with all sequences and a second file (e.g. the Newick tree file, but could be any other (text) format). The result you get back from the web page will have replaced identifiers by taxonomies where possible in the second file.

ProteinPredictionServers

DeepEvolutionaryAnalysis

blast clustalx muscle seaview phylip-3.36 treeview rasmol pymol

Blast

Call up a command prompt (accessories), it should be H: (your student directory)

E:lastlastall -p blastp -d e:lastdatabasesimg_bacteria -i yourfile.fasta -o usefuloutputname.blast

-p the blast program to use: blastp, blastn

-d the database to use: =img_bacteria img_archaea img_eukaryota= You can search several databases by putting quotes around them: =-d "img_archaea img_bacteria"=

-i input, query sequence (in FastaFormat)

-o output file to write blast results to.

Psi-blast =

Psi-blast is very similar, but you need to use "blastpgp" and be aware of -j and -h options. Also remember that psi-blast will generally be slower because it has to do normal blast first, and then build profiles and do later rounds of searching with the profiles.

E:lastlastpgp -d e:lastdatabasesimg_bacteria -i yourfile.fasta -o usefuloutputname.blast -j 3 -h 0.000001

-j maximum number of rounds to do (it will stop earlier, once the searches don't find more matches)

-h significance level cut-off

The documentation with all possible options is on the CD/DVD under blastdoc.

Obtaining FastaFormat files of the sequences found with blast: =

Call up a command prompt.

E:lastastacmd -d e:lastdatabasesimg_bacteria -i filewith_img_numbers -o newsequences.fasta

-i the input file should be a line-by-line listing of the "accession numbers" from the same img database you used in the blast search. Each number needs to have =lcl|= in front of it:

<verbatim>

lcl|1234567

lcl|1234589

lcl|1456789

</verbatim>

[[%ATTACHURL%/ExtractIDs.doc][ExtractIDs.doc]] shows a fast, painless way to prepare the input file from your blast result.

The complete fastacmd document is [[1][here]].

Clustal

Click on the clustalx.exe icon in the clustal folder. Load sequences (you can use "browse" to go to your student area files) in FastaFormat.

Select options from the various clustal menu items.

Alignment output defaults to =.aln= (which can be loaded back into clustal later); select phylip output format also (=.phy=) for phylip analysis.

Remember to change the output format options from branch to NODE before bootstrapping in clustal. If not, you will not be able to see the reliability of the branches in treeview (shown with the internal edge labels).

Phylip

Click on the icon for the appropriate program in the phylip *exe* folder. Type in the input file name eg =H:BIOL3004mydata.phy=. Most phylip programs take =.phy= input files; *neighbor* takes a distance matrix produced by *protdist*, *dnadist* or similar.

PhylipBootstrapping is a multi-stage process (details to come).

Complete phylip documentation is also on the DVD: click on the phylip.html document in the phylip folder, it has links to documentation for specific programs. Or, on the web, you can find it [[2][here]].

Treeview

Click on treev32.exe in the Treeview folder. The input file should be a tree in NewHampshire format.

From clustal: =filename.ph filename.phb=

From phylip: =outtree= (renamed appropriately)

Rasmol

Click on rasmol.exe in the Rasmol folder. The input is a protein structure file, such as a PDB file.