Sequence-Based Mutation Analysis Hemochromatosis

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Revision as of 16:52, 13 June 2012 by Bernhoferm (talk | contribs) (Amino acid features)

Hemochromatosis>>Task 6: Sequence-based mutation analysis


Riddle of the Task

Coming soon...


Short task description

Detailed description: Sequence-based mutation analysis


Protocol

A protocol with a description of the data acquisition and other scripts used for this task is available here.


SNPs

From MSUD: M35T V53M G93R Q127H A162S L183P T217I R224W E277K C282S


Amino acid features

<figtable id="TODO_ID">

Mutation Hydrophobicity (wt) Hydrophobicity (mt) Polarity (wt) Polarity (mt) pI (wt) pI (mt) v.d.W. volume (wt) v.d.W. volume (mt)
M35T 1.9 -0.7 nonpolar polar 5.74 5.60 124 93
V53M 4.2 1.9 nonpolar nonpolar 6.00 5.74 105 124
G93R -0.4 -4.5 nonpolar polar 6.06 10.76 48 148
Q127H -3.5 -3.2 polar polar 5.65 7.60 114 118
A162S 1.8 -0.8 nonpolar polar 6.01 5.68 67 73
L183P 3.8 -1.6 nonpolar nonpolar 6.01 6.30 124 90
T217I -0.7 4.5 polar nonpolar 5.60 6.05 93 124
R224W -4.5 -0.9 polar nonpolar 10.76 5.89 148 163
E277K -3.5 -3.9 polar polar 3.15 9.60 109 135
C282S 2.5 -0.8 polar polar 5.05 5.68 86 73
TODO: description.

</figtable>


PyMol visualization


Secondary structure


DUMMY


References