Knopf C W
J Gen Virol. 1987 May;68 ( Pt 5):1429-33. doi: 10.1099/0022-1317-68-5-1429.
By comparative sequence analysis of the herpes simplex virus type 1 DNA polymerase gene of strain Angelotti and a phosphonoacetic acid-resistant (PAAr) derivative, the site of the PAAr mutation was identified as a single nucleotide (C----T) conversion within the mapping limits of the known PAAr mutations of strains KOS and 17. The conservative amino acid change at residue 719 from alanine to valine results in a radical change in the properties of the polymerase, rendering the mutant enzyme resistant to PAA and various antiviral compounds. Amino acid homologies as well as secondary structure analysis reveal that the PAAr mutation is contained in a 14 amino acid sequence which is highly conserved, and detected in the central domain of prokaryotic and eukaryotic DNA polymerases.
通过对安杰洛蒂株单纯疱疹病毒1型DNA聚合酶基因与耐膦甲酸(PAAr)衍生物进行比较序列分析,确定PAAr突变位点为在KOS株和17株已知PAAr突变的定位范围内的单个核苷酸(C→T)转换。第719位氨基酸从丙氨酸到缬氨酸的保守性氨基酸变化导致聚合酶性质发生根本改变,使突变酶对膦甲酸和各种抗病毒化合物具有抗性。氨基酸同源性以及二级结构分析表明,PAAr突变包含在一个高度保守的14个氨基酸序列中,并且在原核和真核DNA聚合酶的中央结构域中检测到。