Weber J M, Cai F, Horvath J, Guillemette J G
Department of Microbiology, Faculty of Medicine, Université de Sherbrooke, Québec, Canada.
Virus Genes. 1995 Jan;9(2):171-5. doi: 10.1007/BF01702660.
The DNA sequence of a portion of the MAV1 SmaI-D fragment coding for the C-terminal 147 amino acids of the adenoviral DNA-binding protein (DBP) has been determined. A multiple sequence alignment was constructed of the MAV1 fragment and the DBPs of Ad.2, 4, 5, 7, 12, 40, and 41 to examine the degree of conservation of features that have been mapped on the Ad.2 DBP and to identify further conserved features. The less conserved N-terminal segment of the protein contains two nuclear localization signals and two acidic regions, the host range region, and all of the 11 phosphorylation sites. The highly conserved C-terminal segment contains a potential leucine zipper and zinc finger motifs. These sequence features were mapped onto a predicted secondary structure of the Ad.2 DBP.
编码腺病毒DNA结合蛋白(DBP)C端147个氨基酸的MAV1 SmaI-D片段的部分DNA序列已被确定。构建了MAV1片段与Ad.2、4、5、7、12、40和41的DBP的多序列比对,以检查已定位在Ad.2 DBP上的特征的保守程度,并识别其他保守特征。该蛋白保守性较低的N端片段包含两个核定位信号、两个酸性区域、宿主范围区域以及所有11个磷酸化位点。高度保守的C端片段包含一个潜在的亮氨酸拉链和锌指基序。这些序列特征被映射到Ad.2 DBP的预测二级结构上。