Astell C R, Mol C D, Anderson W F
J Gen Virol. 1987 Mar;68 ( Pt 3):885-93. doi: 10.1099/0022-1317-68-3-885.
We have compared the sequences of the putative polypeptides of the human pathogenic B19 parvovirus with protein sequences in the National Bethesda Research Foundation Library, and have discovered a significant homology between a B19 parvovirus non-structural (NS) protein and the T antigens of polyomaviruses and simian virus 40 (SV40) and the putative E1 proteins of papillomaviruses. The region of highest homology with the papovavirus proteins corresponds to the region that is most highly conserved in the NS1 proteins of several other parvoviruses. Studies with the T antigen of both polyomaviruses and SV40 have implicated this region as having an ATPase activity and nucleotide-binding function.
我们已将人类致病性B19细小病毒推定多肽的序列与美国国立贝塞斯达研究基金会图书馆中的蛋白质序列进行了比较,并且发现B19细小病毒的一种非结构(NS)蛋白与多瘤病毒和猿猴病毒40(SV40)的T抗原以及乳头瘤病毒的推定E1蛋白之间存在显著的同源性。与乳多空病毒蛋白同源性最高的区域对应于其他几种细小病毒的NS1蛋白中保守性最高的区域。对多瘤病毒和SV40的T抗原的研究表明,该区域具有ATP酶活性和核苷酸结合功能。