Koener J F, Passavant C W, Kurath G, Leong J
J Virol. 1987 May;61(5):1342-9. doi: 10.1128/JVI.61.5.1342-1349.1987.
The nucleotide sequence of the mRNA encoding the glycoprotein of infectious hematopoietic necrosis virus was determined from a cDNA clone containing the entire coding region. The G-protein cDNA is 1,609 nucleotides long (excluding the polyadenylic acid) and encodes a protein of 508 amino acids. The predicted amino acid sequence was compared with that of the glycoprotein of the Indiana and New Jersey serotypes of vesicular stomatitis virus and with the glycoprotein of rabies virus, using a computer program which determined optimal alignment. An amino acid identity of approximately 20% was found between infectious hematopoietic necrosis virus and the two vesicular stomatitis virus serotypes and between infectious hematopoietic necrosis virus and rabies virus. The positions and sizes of the signal sequence and transmembrane domain and the possible glycosylation sites were determined.
从一个包含完整编码区的 cDNA 克隆中确定了编码传染性造血坏死病毒糖蛋白的 mRNA 的核苷酸序列。G 蛋白 cDNA 长 1609 个核苷酸(不包括聚腺苷酸),编码一个由 508 个氨基酸组成的蛋白质。使用一个确定最佳比对的计算机程序,将预测的氨基酸序列与水疱性口炎病毒印第安纳和新泽西血清型的糖蛋白以及狂犬病病毒的糖蛋白进行了比较。在传染性造血坏死病毒与两种水疱性口炎病毒血清型之间以及传染性造血坏死病毒与狂犬病病毒之间发现了约 20% 的氨基酸同一性。确定了信号序列和跨膜结构域的位置和大小以及可能的糖基化位点。