Difference between revisions of "Fabry Disease Selected Mutations"
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Mutations at the amino acid position between 1 and 31 were not included in the selection process, because they are part of the signal peptide (see [http://www.uniprot.org/uniprot/P06280 UniProt entry]) and they are not present in the reference structure ([http://www.rcsb.org/pdb/explore/explore.do?pdbId=1r47 PDB ID 1R47]). |
Mutations at the amino acid position between 1 and 31 were not included in the selection process, because they are part of the signal peptide (see [http://www.uniprot.org/uniprot/P06280 UniProt entry]) and they are not present in the reference structure ([http://www.rcsb.org/pdb/explore/explore.do?pdbId=1r47 PDB ID 1R47]). |
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+ | The visualization of the residues was done by using PyMol. The manual mutagenesis of the residues was performed according to [http://www.pymolwiki.org/index.php/Mutagenesis this tutorial]. The tool-based mutagenesis are used in the task [[Structure-based_mutation_analysis_GLA|structure-based mutation analysis]]. |
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! Wildtype |
! Wildtype |
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! Manual |
! Manual |
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| 1 || 42 || ATG-ACG || Met -> Thr || [[Image:Fabry_Disease_1R47_res42_wt.png|thumb|150px|Close-up of the wildtype residue number 42 of GLA.]] || [[Image:Fabry_Disease_1R47_res42_mut.png|thumb|150px|Close-up of the mutated residue number 42 of GLA.]] ||[[Image:Fabry_Disease_1R47_res42_tool.png|thumb|150px|Close-up of the mutated residue number 42 of GLA.]] |
| 1 || 42 || ATG-ACG || Met -> Thr || [[Image:Fabry_Disease_1R47_res42_wt.png|thumb|150px|Close-up of the wildtype residue number 42 of GLA.]] || [[Image:Fabry_Disease_1R47_res42_mut.png|thumb|150px|Close-up of the mutated residue number 42 of GLA.]] ||[[Image:Fabry_Disease_1R47_res42_tool.png|thumb|150px|Close-up of the mutated residue number 42 of GLA.]] |
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− | The visualization was done by using PyMol and the mutagensis of the residue was performed according to [http://www.pymolwiki.org/index.php/Mutagenesis this] tutorial. The residue of the wildtype is colored green and the mutated residue is colored red. |
Revision as of 04:28, 27 August 2011
We randomly selected ten annotated point mutations of the human gene GLA and they were chosen out of a pool of mutations that consist of two subsets. The first subset contains mutations that are present in HGMD and these mutations were already gathered in the task 4 Mapping SNPs. The second subset are mutations that are present in dbSNP, but not included in HGMD. This was only the case for three mutations.
Mutations at the amino acid position between 1 and 31 were not included in the selection process, because they are part of the signal peptide (see UniProt entry) and they are not present in the reference structure (PDB ID 1R47).
The visualization of the residues was done by using PyMol. The manual mutagenesis of the residues was performed according to this tutorial. The tool-based mutagenesis are used in the task structure-based mutation analysis.
Number | AA-Position | Codon change | Amino acid change | Wildtype | Manual | Tool-based |
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1 | 42 | ATG-ACG | Met -> Thr | |||
2 | 65 | AGT-ACG | Ser -> Thr | |||
3 | 117 | ATT-AGT | Ile -> Ser | |||
4 | 143 | cGCA-ACA | Ala -> Thr | |||
5 | 186 | CAC-CGC | His -> Arg | |||
6 | 205 | gCCT-ACT | Pro -> Thr | |||
7 | 244 | gGAC-CAC | Asp -> His | |||
8 | 283 | CAG-CCG | Gln -> Pro | |||
9 | 321 | tCAG-TAG | Gln -> Glu | |||
10 | 363 | TATa-TAA | Arg -> Cys |