Williams-Beuren Syndrome Related Methyltransferase WBSCR27: From Structure to Possible Function

Williams-Beuren Syndrome Related Methyltransferase WBSCR27: From Structure to Possible Function

Williams-Beuren syndrome (WBS) is a genetic disorder associated with the hemizygous deletion of several genes in chromosome 7, encoding 26 proteins. Malfunction of these proteins induce multisystemic failure in an organism. While biological functions of most proteins are more or less established, th...

Full description

Bibliographic Details
Main Authors: Sofia S. Mariasina, Chi-Fon Chang, Tsimafei L. Navalayeu, Anastasia A. Chugunova, Sergey V. Efimov, Viktor G. Zgoda, Vasily A. Ivlev, Olga A. Dontsova, Petr V. Sergiev, Vladimir I. Polshakov
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Molecular Biosciences
Subjects:
Williams-Beuren syndrome (WBS)
methyltransferase (MTase)
NMR
protein structure in solution
protein dynamics
S-adenosyl-L-homocysteine (SAH)
Online Access:https://www.frontiersin.org/articles/10.3389/fmolb.2022.865743/full

Internet

https://www.frontiersin.org/articles/10.3389/fmolb.2022.865743/full

Similar Items