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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...

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Kaydedildi:
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2022-06-01
Seri Bilgileri:Frontiers in Molecular Biosciences
Konular:
Williams-Beuren syndrome (WBS)
methyltransferase (MTase)
NMR
protein structure in solution
protein dynamics
S-adenosyl-L-homocysteine (SAH)
Online Erişim:https://www.frontiersin.org/articles/10.3389/fmolb.2022.865743/full
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