Difference between revisions of "Prediction of Disordered Regions"
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=== POODLE-L === |
=== POODLE-L === |
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POODLE-L found no disordered regions. Therefore, there is no disordered region with a length more than 40aa in our protein. |
POODLE-L found no disordered regions. Therefore, there is no disordered region with a length more than 40aa in our protein. |
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=== POODLE-S (High B-factor residues) === |
=== POODLE-S (High B-factor residues) === |
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=== POODLE-S (missing residues) === |
=== POODLE-S (missing residues) === |
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== IUPred == |
== IUPred == |
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As you can see in the picture, IUPred which is focus on short disordered regions found only at the beginning and at the end of the protein a disordered region. This may be wrong, because at the beginning and at the end there are often regions without defined secondary structure, but also without function. |
As you can see in the picture, IUPred which is focus on short disordered regions found only at the beginning and at the end of the protein a disordered region. This may be wrong, because at the beginning and at the end there are often regions without defined secondary structure, but also without function. |
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=== IUPred (long) === |
=== IUPred (long) === |
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Next we take a look to the prediction of the long disordered regions:<br> |
Next we take a look to the prediction of the long disordered regions:<br> |
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The picture above shows the result of this prediction. There is no disordered region predicted, not even at the beginning or at the end of the protein. This prediction is quite good, because the HEXA_HUMAN protein does not posses any disordered regions. |
The picture above shows the result of this prediction. There is no disordered region predicted, not even at the beginning or at the end of the protein. This prediction is quite good, because the HEXA_HUMAN protein does not posses any disordered regions. |
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=== IUPred (with structural information) === |
=== IUPred (with structural information) === |
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As before, the method did not find any disordered regions. Therefore, the method predict three times the right result. Only by the method with focus on short disordered regions was a prediction of two disordered regions, but these regions were located at the beginning and at the end of the protein, which is obviously wrong. |
As before, the method did not find any disordered regions. Therefore, the method predict three times the right result. Only by the method with focus on short disordered regions was a prediction of two disordered regions, but these regions were located at the beginning and at the end of the protein, which is obviously wrong. |
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+ | Back to [[http://i12r-studfilesrv.informatik.tu-muenchen.de/wiki/index.php/Sequence-based_predictions_HEXA Sequence-based prediction]]<br><br> |
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== Meta-Disorder == |
== Meta-Disorder == |
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The result is very good, because HEXA_HUMAN does not have any disordered regions. Therefore, the prediction of Meta-Disorder is right. |
The result is very good, because HEXA_HUMAN does not have any disordered regions. Therefore, the prediction of Meta-Disorder is right. |
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+ | Back to [[http://i12r-studfilesrv.informatik.tu-muenchen.de/wiki/index.php/Sequence-based_predictions_HEXA Sequence-based prediction]]<br><br> |
Revision as of 14:23, 11 August 2011
Contents
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 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.
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 |
Back to [Sequence-based prediction]
POODLE-L
POODLE-L found no disordered regions. Therefore, there is no disordered region with a length more than 40aa in our protein.
Back to [Sequence-based prediction]
POODLE-S (High B-factor residues)
This POODLE-S variant searches for high B-factor values in the crystallography, which implies uncertainty in the assignment of the atom positions.
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 |
Back to [Sequence-based prediction]
POODLE-S (missing residues)
POODLE-S (missing residues) predicts a disordered region, if there is an 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:
Back to [Sequence-based prediction]
IUPred
We tested the three different IUPred variants, which are offered by the webserver.
IUPred (short)
As you can see in the picture, IUPred which is focus on short disordered regions found only at the beginning and at the end of the protein a disordered region. This may be wrong, because at the beginning and at the end there are often regions without defined secondary structure, but also without function.
Back to [Sequence-based prediction]
IUPred (long)
Next we take a look to the prediction of the long disordered regions:
The picture above shows the result of this prediction. There is no disordered region predicted, not even at the beginning or at the end of the protein. This prediction is quite good, because the HEXA_HUMAN protein does not posses any disordered regions.
Back to [Sequence-based prediction]
IUPred (with structural information)
As last, we analysed the prediction of IUPred with the additional usage of structural information.
As before, the method did not find any disordered regions. Therefore, the method predict three times the right result. Only by the method with focus on short disordered regions was a prediction of two disordered regions, but these regions were located at the beginning and at the end of the protein, which is obviously wrong.
Back to [Sequence-based prediction]
Meta-Disorder
Meta-Disorder did not predict any disordered region in our protein. The different methods of which Meta-Disorder consists predicted some disordered regions, but Meta-Disorder build the consensus over all of these methods, and therefore it did not predict any disordered regions.
Graphical representation of the result:
The result is very good, because HEXA_HUMAN does not have any disordered regions. Therefore, the prediction of Meta-Disorder is right.
Back to [Sequence-based prediction]