Difference between revisions of "Talk:Canavan Task 2 - Sequence alignments"
From Bioinformatikpedia
(→Review) |
m (→Review) |
||
Line 19: | Line 19: | ||
A few things in addition to what alice said |
A few things in addition to what alice said |
||
− | * The |
+ | * The red markings in the sequence at the beginning are explained only towards the very end |
* What does this figure signify? http://i12r-studfilesrv.informatik.tu-muenchen.de/wiki/index.php/File:Seq_overlap.png |
* What does this figure signify? http://i12r-studfilesrv.informatik.tu-muenchen.de/wiki/index.php/File:Seq_overlap.png |
||
* I do not agree with your reasoning that it is unlikely to find another structure for a class of proteins, once one structure has been solved for them. In fact the knowledge of how to solve the structure gained from the first experiment might lead to a higher probability, that more structures e.g. of homologs in another species or mutants, will be solved |
* I do not agree with your reasoning that it is unlikely to find another structure for a class of proteins, once one structure has been solved for them. In fact the knowledge of how to solve the structure gained from the first experiment might lead to a higher probability, that more structures e.g. of homologs in another species or mutants, will be solved |
||
− | * |
Revision as of 09:04, 8 May 2012
- Your PSI-Blast search seems to have hit the reporting limits. Please increase the cutoffs, so you can really compare the results. andrea 10:32, 3 May 2012 (UTC)
Review
- Some figures are not referenced properly in the text, tables are not referenced or mentioned at all
- Your cutoff for the blast searches seems very low, and I think you didn't increase the number of results like andrea wrote. My guess is that you consequently can not really compare the number of hits.
- Agreed, this might also solve you problem of no pdb structures -jonas
- You could have tried to use the whole big database for PSI-Blast and PDB for HHBlits to make the results more comparable.
- You could elaborate a little bit more, e.g. on the MSA's.
- I like your figures, very nice, just get rid of the ??.
- Making the link to 3D structure is very interesting but I would have enjoyed reading more about it :)
I did not have the time to really rethink your approach in detail, but you worked nicely and especially very efficiently.
Best, Alice
A few things in addition to what alice said
- The red markings in the sequence at the beginning are explained only towards the very end
- What does this figure signify? http://i12r-studfilesrv.informatik.tu-muenchen.de/wiki/index.php/File:Seq_overlap.png
- I do not agree with your reasoning that it is unlikely to find another structure for a class of proteins, once one structure has been solved for them. In fact the knowledge of how to solve the structure gained from the first experiment might lead to a higher probability, that more structures e.g. of homologs in another species or mutants, will be solved