Difference between revisions of "Task 8: Sequence-based mutation analysis"

From Bioinformatikpedia
Line 5: Line 5:
 
border: 2px solid black;
 
border: 2px solid black;
 
border-collapse:collapse;
 
border-collapse:collapse;
width: 80%;
+
width: 90%;
 
}
 
}
   

Revision as of 16:25, 22 August 2013

<css> table.colBasic2 { margin-left: auto; margin-right: auto; border: 2px solid black; border-collapse:collapse; width: 90%; }

.colBasic2 th,td { padding: 3px; border: 2px solid black; }

.colBasic2 td { text-align:left; }

.colBasic2 tr th { background-color:#efefef; color: black;} .colBasic2 tr:first-child th { background-color:#adceff; color:black;}

</css>


Lab journal task 8

Mutation selection

<figtable id="mutations">

mutations
nucleotide change amino acid change
Val53Met
His63Asp
Arg67His
Met97Ile
Asn130Ser
Glu168Gln
Leu183Pro
Thr217Ile
Cys282Tyr
Arg330Met
Table 1: List of the 10 selected mutations from HGMD and dbSNP.

</figtable>


Mutation analysis

<figtable id="summary">

reference mutation pyhsicochemical properties strucural properties conservation prediction programms consensus
from to pymol visualisation secondary structure substitution matrix PSSM MSA SIFT Polyphen2 MutationTaster SNAP
Val53Met brached chain, nonpolar, uncharged sulfur containing, nonpolar, neutral
His63Asp
Arg67His
Met97Ile
Asn130Ser
Glu168Gln
Leu183Pro
Thr217Ile
Cys282Tyr
Arg330Met
Table 2: Summary of the results of analysis of all mutations.

</figtable>

Physicochemical properties are given as special property, side chain polarity and charge.