Difference between revisions of "Sequence-based predictions HEXA"

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(Prediction of GO terms)
(Prediction of disordered regions)
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== Secondary Structure Prediction ==
 
== Secondary Structure Prediction ==
 
== Prediction of disordered regions ==
 
 
* DISOPRED
 
Authors: Ward JJ, Sodhi JS, McGuffin LJ, Buxton BF, Jones DT.
 
 
Year: 2004
 
 
Source: [[http://www.ncbi.nlm.nih.gov/pubmed/15019783 Prediction and functional analysis of native disorder in proteins from the three kingdoms of life.]]
 
 
Description:
 
 
This method is based on a neuronal network which was trained on high resolution X-ray structures from PDB. Disordered regions are regions, which appears in the sequence record, but their electrons are missing from electronic density map. This approach can also failed, because missing electrons can also arise because of the cristallization process.
 
The method runs first a PsiBlast search against a filtered sequence database. Next, a profile for each residue is calculated and classified by using the trained neuronal network.
 
 
Prediction:
 
 
As a prediction result you get a file with the predicted disordered region, the precision and recall. Furthermore you can a more detailed output. There you see the sequence, and the predictions and also numbers above the sequence (from 0 to 9 which shows you how likly your prediction is)
 
 
Input:
 
 
If you run disopred on the console, you have to define the location of your database. The program needs as input your sequence in a file with fasta format.
 
 
 
*POODLE
 
Prediction of order and disorder by machine-learning
 
 
Authors: S. Hirose, K. Shimizu, S. Kanai, Y. Kuroda and T. Noguchi
 
 
Year: 2007
 
 
There exist three different variants of POODLE.
 
 
The first variant is called POODLE-L which predicts mainly long disorder region with a length more than 40.
 
 
Source: [[http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSearch=17545177&ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum POODLE-L: a two-level SVM prediction system for reliably predicting long disordered regions.]]
 
 
The next variant is called POODLE-S, which predicts mainly short disorder regions.
 
 
Source: [[http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSearch=17599940&ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum POODLE-S: web application for predicting protein disorder by using physicochemical features and reduced amino acid set of a position-specific scoring matrix.]]
 
 
The last variant is called POODLE-I, which integrates structal information predictors.
 
 
Source: [[http://www.bioinfo.de/isb/2010/10/0015/ POODLE-I: Disordered region prediction by integrating POODLE series and structural information predictors based on a workflow approach]]
 
 
There exists als another variant called POODLE-W, which compares different sequences and predicts which sequence is the most disordered one, but this method wasn't used in our analysis.
 
 
Description:
 
 
POODLE is also a machine learning based method. This method based on a 2-level SVM (Support Vector Machine).
 
 
We describe here the POODLE-L in detail, but all POODLE variants use the same principle.
 
The method was trained on disordered proteins and proteins with no disoredered regions. On the first level, the SVM predicts the probability of a 40-residue sequence segment to be disordered. If the algorithm found such a disordered regions, the second level of the SVM use the output from the first level and predicts the probability to be disordered for each amino acid.
 
 
Output:
 
 
The result of this method is a file with the single amino acids, the prediction if it is ordered or not and the probability for the state. Furtheremore, you get a graphical view of the result.
 
 
Input:
 
 
We used the POODLE webserver for our analysis. We paste our sequence in fasta format in the input window and chose the POODLE variant.
 
   
 
== Prediction of transmembrane alpha-helices and signal peptides ==
 
== Prediction of transmembrane alpha-helices and signal peptides ==

Revision as of 15:31, 27 May 2011

General Information

Secondary Structure Prediction

Prediction of transmembrane alpha-helices and signal peptides

Prediction of GO terms

Secondary Structure prediction

Prediction of disordered regions

  • Disopred

Disopred predicts two disordered regions in our protein. The first region is at the beginning of the protein (first two residues) and the second region is at the end (last three regions). This prediction is probably wrong, because it is normal, that the electrons from the first and the last amino acids lack in the electron density map. So, our protein Hexosamidase A has no disordered regions.

Result of the Disopred prediction. * shows that this amino acid belongs to a disordered regions, whereas . signs for a non-disordered region.


  • POODLE

We decided to test several POODLE variants and to compare the results.

POODLE-I

POODLE-I predicted five disordered regions:

start position end position length
1 2 2
14 19 6
83 89 7
105 109 5
527 529 3


POODLE-L

POODLE-L found no disordered regions. Therefore, there is no disordered region with a length more than 40aa in our protein.


POODLE-S (High B-factor residues)

TODO

POODLE-S predicted five disordered regions:

start position end position length
0 2 2
13 19 7
83 88 6
105 109 5
526 529 4


POODLE-S (missing residues)

POODLE-S (missing residues) predicts regions as disordered, if there is a amino acid in the sequence record, but not on the electron density map.

Poodle-S found 6 disordered regions.

start position end position length
17 18 2
53 61 9
78 109 33
153 153 1
280 280 1
345 345 1


Graphical Output:

Prediction of POODLE-I
Prediction of POODLE-L
Prediction of POODLE-S (High B-factor residues)
Prediction of POODLE-S (missing residues)


TODO Comparison!!!

Prediction of transmembrane alpha-helices and signal peptides

Prediction of GO terms