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- W2022356767 abstract "Phosphorylation of one or more viral proteins is probably an essential step in the life cycle of every member of the nonsegmented negative-strand RNA virus (mononegavirales [MNV]) group. Since no virally encoded protein kinases have been discovered in this group, phosphorylation is effected entirely by host cell kinases. The virally encoded P proteins of the MNV are the only ones consistently phosphorylated with a stoichiometry > or =1. The P protein of vesicular stomatitis virus (VSV), and perhaps also of respiratory syncytial virus, are the only ones for which a function of phosphorylation has been established. Phosphorylation by casein kinase 2 at one or more identified sites in the VSV P protein activates transcriptional activity by promoting formation of a homotrimer, which is then capable of binding the RNA polymerase and attaching it to the N protein-RNA template. A second phosphorylation of VSV P protein by a different kinase also occurs, dependent upon prior modification by casein kinase 2, but its function is not definitely known. Phosphorylation of the other MNV P proteins may serve a different purpose. No evidence has been obtained yet for any function for phosphorylation of any other MNV protein." @default.
- W2022356767 created "2016-06-24" @default.
- W2022356767 creator A5054053322 @default.
- W2022356767 date "1999-07-01" @default.
- W2022356767 modified "2023-10-14" @default.
- W2022356767 title "Host cell protein kinases in nonsegmented negative-strand virus (mononegavirales) infection" @default.
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- W2022356767 doi "https://doi.org/10.1016/s0163-7258(99)00016-9" @default.
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