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传染性法氏囊病病毒小双链RNA基因组片段序列及其推导的90 kDa产物

Sequence of the small double-stranded RNA genomic segment of infectious bursal disease virus and its deduced 90-kDa product.

作者信息

Morgan M M, Macreadie I G, Harley V R, Hudson P J, Azad A A

机构信息

CSIRO, Division of Biotechnology, Parkville, Australia.

出版信息

Virology. 1988 Mar;163(1):240-2. doi: 10.1016/0042-6822(88)90258-9.

Abstract

The smaller dsRNA segment of the genome of infectious bursal disease virus (IBDV) encodes a single polypeptide of approximately 90 kDa (VP1). The consensus nucleotide sequence, derived from independent and overlapping cDNA clones, contains a single open reading frame which begins with an exact Kozak sequence and could encode a polypeptide of 878 amino acid residues. It has been suggested that VP1 could be the viral RNA-dependent RNA polymerase. A comparison of the predicted amino acid sequence of this protein with those of other DNA-dependent and ssRNA-dependent RNA polymerases has failed to reveal any homology between VP1 and the conserved regions in these enzymes. It is possible that the polypeptide encoded by the IBDV virus may represent a new class of polymerases which are involved in the replication of double-stranded RNA genomes.

摘要

传染性法氏囊病病毒(IBDV)基因组中较小的双链RNA片段编码一种约90 kDa的单一多肽(VP1)。从独立且重叠的cDNA克隆推导得到的共有核苷酸序列包含一个单一的开放阅读框,其起始于一个精确的科扎克序列,可编码一个由878个氨基酸残基组成的多肽。有人提出VP1可能是病毒RNA依赖性RNA聚合酶。将该蛋白的预测氨基酸序列与其他DNA依赖性和单链RNA依赖性RNA聚合酶的序列进行比较,未发现VP1与这些酶的保守区域之间存在任何同源性。IBDV病毒编码的多肽有可能代表一类参与双链RNA基因组复制的新型聚合酶。

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