Structure-based mutation analysis ARSA

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Revision as of 08:31, 30 June 2011 by Zacher (talk | contribs) (Visualization with Pymol)

Preparation

Visualization with Pymol

Pymol visualization of ARSA (with closed gaps). The active site is depicted in yellow, metal-binding site in blue, substrate binding sites in green and missense mutations in red.
Nr. mutation position Pymol image Description Effect on function
1 Asp-Asn 29
Arsa29.png
The mutation is located at the position of a metal-binding site. harmful
2 Pro - Ala 136
Arsa136.png
The mutation is located near the active site and a substrate binding site in sequence as well as in structure. harmful
3 Gln-His 153
Arsa153.png
The mutation is located near the active site and a substrate binding site in sequence as well as in structure. harmful
4 Trp-Cys 193
Arsa193.png
The mutation is at moderate distance to all important functional sites of the protein. neutral
5 Thr-Met 274
Arsa274.png
The mutation is located very distant from the active site and a substrate binding site in sequence as well as in structure.
It is located within a beta sheet.
harmful
6 Phe -Val 356
Arsa356.png
The mutation is at moderate distance to all important functional sites of the protein. neutral
7 Thr-Ile 409
Arsa409.png
The mutation is not close to important functional sites. harmful
8 Asn-Ser 440
Arsa440.png
The mutation is very distant from all functional sites. neutral
9 Cys-Gly 489
Arsa489.png
The mutation is very distant from all functional sites. harmful
10 Arg-His 496
Arsa496.png
The mutation is very distant from all functional sites. harmful

Above visualizations indicate, that mutations near functional important sites of the protein are likely to cause a harmful effect. However, for distant mutations no trend can be observed.

SCRWL

BLA


repairPDB arsa_model.pdb -seq > arsa.model.seq
tr '[:upper:]' '[:lower:]' < arsa.model.seq > arsa.model.lower.seq