|
Mutation Information
|
Mutation Site
|
Y477H |
|
Mutation Type
|
Amino acid level |
|
Gene/Protein/Region Type
|
Gp21 |
|
Viral Reference
|
J02029.1;
U81865–U81869 |
|
Country
|
Brazil |
Literature Information
|
PubMed PMID
|
23800288
|
|
Disease
|
HTLV-1 associated myelopathy/tropical spastic paraparesis
|
|
Published Year
|
2013 |
|
Journal
|
AIDS research and human retroviruses |
|
Title
|
Molecular study of HBZ and gp21 human T cell leukemia virus type 1 proteins isolated from different clinical profile infected individuals. |
|
Author
|
Mota-Miranda AC,Barreto FK,Baptista E,Farre-Vale L,Monteiro-Cunha JP,Galvão-Castro B,Alcantara LC |
|
Evidence
|
From eight gp21-analyzed sequences one amino acid change (Y477H) was associated with the switch of a helix to coil structure at secondary structure prediction.
|
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HTLV1 Mutation Detail Information