Insights on the alteration of functionality of a tyrosine kinase 2 variant: a molecular dynamics study
Author(s) -
Nastazia Lesgidou,
Elias Eliopoulos,
George N. Goulielmos,
Metaxia Vlassi
Publication year - 2018
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/bty556
Subject(s) - tyrosine kinase 2 , gene , biology , point mutation , tyrosine , signal transduction , tyrosine kinase , genetics , mechanism (biology) , computational biology , snp , mutation , single nucleotide polymorphism , biochemistry , receptor , genotype , platelet derived growth factor receptor , philosophy , epistemology , growth factor
The tyrosine kinase 2 protein (Tyk2), encoded by the TYK2 gene, has a crucial role in signal transduction and the pathogenesis of many diseases. A single nucleotide polymorphism of the TYK2 gene, SNP rs34536443, is of major importance, since it has been shown to confer protection against various, mainly, autoimmune diseases. This polymorphism results in a Pro to Ala change at amino acid position 1104 of the encoded Tyk2 protein that affects its enzymatic activity. However, the details of the underlined mechanism are unknown. To address this issue, in this study, we used molecular dynamics simulations on the kinase domains of both wild type and variant Tyk2 protein.
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