The N-terminal heptad repeat region of reovirus cell attachment protein σ1 is responsible for σ1 oligomer stability and possesses intrinsic oligomerization function

The oligomerization domain of the reovirus cell attachment protein (σ1) was probed using the type 3 reovirus of synthesized in vitro. Trypsin cleaved the α1 protein (49K molecular weight) approximately in the middle and yielded a 26K N-terminal fragment and a 23K C-terminal fragment. Under condition...

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Detalles Bibliográficos
Autores principales: Leone, Gustavo, Duncan, Roy, Mah, David C.W., Price, Angela, Cashdollar, L.William, Lee, Patrick W.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 1991
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130816/
https://www.ncbi.nlm.nih.gov/pubmed/2024469
http://dx.doi.org/10.1016/0042-6822(91)90677-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130816/
https://www.ncbi.nlm.nih.gov/pubmed/2024469
http://dx.doi.org/10.1016/0042-6822(91)90677-4

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