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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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Detalhes bibliográficos
Publicado no:Virology
Main Authors: Leone, Gustavo, Duncan, Roy, Mah, David C.W., Price, Angela, Cashdollar, L.William, Lee, Patrick W.K.
Formato: Artigo
Idioma:Inglês
Publicado em: Published by Elsevier Inc. 1991
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7130816/
https://ncbi.nlm.nih.gov/pubmed/2024469
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/0042-6822(91)90677-4
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