Difference between revisions of "Task 3 - Sequence-based predictions"

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In contrast to the vast amount of known protein sequences, information about structure and function is available for only very few proteins. Sequence-based predictions of protein features aim to decrease this gap. Many sequence-based preditiction methods use evolutionary information, i.e. sequence similiarity. Sequence alignments are therefore often a prerequisite for the predictions.
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In contrast to the vast amount of known protein sequences, information about structure and function is available for only very few proteins. Sequence-based predictions of protein features aim to decrease this gap. Many sequence-based preditiction methods use evolutionary information. Sequence alignments are therefore often a prerequisite for the predictions.
   
 
== Theoretical background talks ==
 
== Theoretical background talks ==
The introductory talks will give an introduction to sequence-based protein predictions. In particular:
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The talks will give an introduction to sequence-based protein predictions. In particular:
 
* secondary structure
 
* secondary structure
 
* disorder
 
* disorder

Revision as of 02:16, 8 May 2012

In contrast to the vast amount of known protein sequences, information about structure and function is available for only very few proteins. Sequence-based predictions of protein features aim to decrease this gap. Many sequence-based preditiction methods use evolutionary information. Sequence alignments are therefore often a prerequisite for the predictions.

Theoretical background talks

The talks will give an introduction to sequence-based protein predictions. In particular:

  • secondary structure
  • disorder
  • transmembrane helices
  • GO terms

Where to run the jobs

  • You can log in to the student computer pool: i12k-biolab??.informatik.tu-muenchen.de, where ?? goes from 01 to 10.
  • Work in the student computer pool.
  • You can also install the programs on your own computer.

Secondary structure

Use ReProf to predict secondary structure for your protein. Apply ReProf also to these proteins (given are UniProt IDs):

  • P10775
  • Q9X0E6
  • Q08209

Use fasta sequences for the prediction. You can find out about Reprof usage by running reprof or reading the man page (man reprof). Peter Hoenigschmig (hoenigschmid@rostlab.org) would like to hear about anything that would improve the description or if anything seems unclear. For help, you can always ask us first.

Compare the ReProf results to PsiPred and [ http://mrs.cmbi.ru.nl/hsspsoap/ DSSP_server] (DSSP). Before you use DSSP, find out more about the example proteins (and yours) using UniProt and the PDB.

Disorder

Use IUPred to predict disorder for your protein. Apply IUPred to the example proteins given above, too (run iupred). You can find a README here: /opt/iupred/README.

Compare the results to the DisProt database.

Transmembrane helices

Use PolyPhobius to predict transmembrane helices for your protein and for the follwoing proteins:

  • P35462

PolyPhobius is installed in /mnt/project/pracstrucfunc12/polyphobius.

In contrast to its precursor Phobius, PolyPhobius uses homology information for the prediction. First, you have to execute a blast search. PolyPhobius distributed its own perl script for this purpose: blastget (/mnt/project/pracstrucfunc12/polyphobius/blastget). Usage: blastget -h. Use only the -db and -ix parameters. Input is the fasta sequence of the above given proteins. Use SwissProt (/mnt/project/pracstrucfunc12/data/swissprot/uniprot_sprot) as database and /mnt/project/pracstrucfunc12/data/index_pp/uniprot_sprot.idx as index.

Use the blastget output to create a MSA using Kalign (/mnt/opt/T-Coffee/bin//kalign).


   Give a brief description of the theory and the algorithm, if possible
   What is predicted? Describe the features in some detail
   What information is required for the predictions?
   Apply the prediction methods to your protein and explain how to do this
   You may try out other protein sequences (this is required when specified)
   Present, describe and discuss the results
   Look for other methods, for example here: http://expasy.org/tools/
   You may try out more methods