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相關文獻
- Cloning and Sequencing of Glycoprotein H Gene of the Pseudorabies Virus Strain TNL
- Construction and Virulence Test of Genetically Engineered Pseudorabies Virus
- Expression and Functional Analysis of the Pseudorabies Virus Immediate-early Protein IE180
- 假性狂犬病毒之研究
- 豬博德氏菌、巴氏桿菌、放線桿菌、大腸桿菌、沙氏桿菌及假性狂犬病不活化混合菌(疫)苗之研製及田間應用試驗
- Topoisomerases are Involved in the Replication and Gene Expression of Pseudorabies Virus
- Cloning and Characterization of the Pseudorabies Virus Latency-Associated Transcript Promoter
- Establishment and Characterization of the Cell Line with Stable Expression of the Pseudorabies Virus Immediate-early Protein IE180
- Cloning and Sequencing of the ICP0 Homologous Gene of Pseudorabies Virus
- 假性狂犬病毒(臺灣TNL株)封套醣蛋白gp50基因之結構分析
頁籤選單縮合
題名 | Cloning and Sequencing of Glycoprotein H Gene of the Pseudorabies Virus Strain TNL=假性狂犬病毒(TNL株)gH基因的定序 |
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作者姓名(中文) | 王孟亮; 郭舒亭; 張天傑; | 書刊名 | 臺灣畜牧獸醫學會會報 |
卷期 | 65:4 1995.12[民84.12] |
頁次 | 頁317-325 |
分類號 | 437.246 |
關鍵詞 | 假性狂犬病毒; gH基因; Pseudorabies virus; gH gene; |
語文 | 英文(English) |
中文摘要 | 本報告完成假性狂犬病毒(TNL株)的醣蛋白gH基因的定序。實驗結果顯示gH基因共含有2061個核甘酸,預測可轉譯出具有686個胺基酸的蛋白質。與Ka或NIA株相比較,TNL株僅有59號的胺基酸與它們不同。我們也發現五三個可能的醣化位置。另外、實驗結果也顯示gH的RNA大小約為2.3kb。 |
英文摘要 | The gene of glycoprotein gH of pseudorabies virus strain TNL has been isolated and sequenced. Our results show that the gH gene is located at the downstream of viral thymidine kinase gene and contains 2061 nucleotides from the potential translation start codon to stop codon. Predicted from the deduced amino acid sequence, the number of amino acid of gH protein is 686. Comparing the amino acid sequence of strain TNL with that of Ka and NIA strains, the TNL has only one distinctive amino acid at position 59, which is proline in TNL but leucine in Ka or NIA. Three potential N-glycosylation sites are found. The northern blot analysis reveals that the size of transcript of gH gene is 2.3 kb. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。