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首页> 外文期刊>Journal of Virology >The 55K protein on the 5' termini of adenovirus type 2 DNA is unrelated to virus-coded candidate transformation proteins (E1-53K, E1-40K-50K) and DNA-binding proteins (E2-42K/47K/73K).
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The 55K protein on the 5' termini of adenovirus type 2 DNA is unrelated to virus-coded candidate transformation proteins (E1-53K, E1-40K-50K) and DNA-binding proteins (E2-42K/47K/73K).

机译:腺病毒2型DNA的5'末端的55k蛋白与病毒编码候选转化蛋白(E1-53K,E1-40K-50K)和DNA结合蛋白(E2-42K / 47K / 73K)无关。

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摘要

A polypeptide of 55,000 daltons (55K) is linked, probably covalently, to the K' termini of adenovirus type 2 DNA. The 55K polypeptide is synthesized during early stages of infection (T. Yamashita, M. Arens, and M. Green, J. Virol. 30: 497-507, 1979) and thus may function in viral DNA replication, gene regulation, or cell transformation. Several virus-coded early polypeptides have been identified that could correspond to the terminal 55K, including the E1-40K-50K and E1-53K candidate transformation polypeptides and the E2-42K/47K/73K single-stranded DNA-binding polypeptide. We show here that two-dimensional tryptic [35S]methionine-peptide maps of the terminal 55K differ completely from [35S]methionine-peptide maps of four related E1-40K-50K polypeptides, the E1-53K, and the related E2-42K, E2-47K, and E2-73K polypeptides. We conclude that the terminal 55K polypeptide does not correspond to any of the known virus-coded early polypeptides.
机译:将55,000道尔顿(55k)的多肽连接,可能与腺病毒2型DNA的K'末端连接。 55k多肽在感染的早期阶段合成(T. Yamashita,M. Arens和M. Green,J.Virol。30:497-507,1979),因此可以在病毒DNA复制,基因调控或细胞中起作用转型。已经鉴定了几种病毒编码的早期多肽,其可以对应于终端55K,包括E1-40K-50K和E1-53K候选转化多肽和E2-42K / 47K / 73K单链DNA结合多肽。在这里,在这里展示终端55K的二维胰蛋白酶[35s]甲硫氨酸肽图谱完全不同于四种相关的E1-40K-50K多肽,E1-53K和相关的E2-42K相关的甲硫氨酸 - 肽图谱,E2-47K和E2-73K多肽。我们得出结论,终端55K多肽不对应于任何已知的病毒编码的早期多肽。

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