目的构建汉坦病毒糖基化位点的突变体。
Objective To construct N-linked glycosylation site mutants of hantavirus.
在推导的氨基酸序列中，存在两个跨膜区，但没有潜在的N-联糖基化位点。
There were two transmembrane regions but no N-glycosylation sites in the deduced amino acid sequence.
分析它的主要功能位点表明它具有319位的糖基化位点和完整的抗原位点。
Sequence analysis result indicated GP had a glycosylation site at position 319 and whole antigenic sites.
被编码的蛋白上有多个N 糖基化和蛋白激酶的识别位点，它们可能参与肽转运的调控；
The encoded proteins have a number of potential N-glycosylation as well as protein kinase recognition sites, which may be involved in the regulation of peptide transport;
被编码的蛋白上有多个N 糖基化和蛋白激酶的识别位点，它们可能参与肽转运的调控；
The encoded proteins have a number of potential N-glycosylation as well as protein kinase recognition sites, which may be involved in the regulation of peptide transport;
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