Analysis of N-terminal nucleotide sequence of NDV fusion protein

Wen Bing Wang; Ping Ji; Jia Lu He; Xiang Fu Wu

Analysis of N-terminal nucleotide sequence of NDV fusion protein

Wen Bing Wang, Ping Ji, Jia Lu He, Xiang Fu Wu

Research output: Contribution to journal › Article › peer-review

Abstract

Fusion protein of Newcastle disease virus is a glycoprotein with antigenicity. The cDNA of fusion gene of NDV strain F48E8 was cloned by RT-PCR, and the sequence of F48E8 was compared with other two virulent strains, Australia-victoria and Italien. Results show that the sequences of N-terminus are very similar, and cysteine residues and the potential glycosylation sites are relatively conserved. However, there are a few differences in the region of signal peptides.

Original language	English (US)
Pages (from-to)	458
Number of pages	1
Journal	Acta Biochimica et Biophysica Sinica
Volume	31
Issue number	4
State	Published - 1999
Externally published	Yes

Keywords

Analysis
Fusion protein
NDV
Sequence

ASJC Scopus subject areas

Biophysics
Biochemistry

Cite this

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keywords = "Analysis, Fusion protein, NDV, Sequence",

author = "Wang, {Wen Bing} and Ping Ji and He, {Jia Lu} and Wu, {Xiang Fu}",

year = "1999",

language = "English (US)",

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journal = "Acta Biochimica et Biophysica Sinica",

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T1 - Analysis of N-terminal nucleotide sequence of NDV fusion protein

AU - Wang, Wen Bing

AU - Ji, Ping

AU - He, Jia Lu

AU - Wu, Xiang Fu

PY - 1999

Y1 - 1999

N2 - Fusion protein of Newcastle disease virus is a glycoprotein with antigenicity. The cDNA of fusion gene of NDV strain F48E8 was cloned by RT-PCR, and the sequence of F48E8 was compared with other two virulent strains, Australia-victoria and Italien. Results show that the sequences of N-terminus are very similar, and cysteine residues and the potential glycosylation sites are relatively conserved. However, there are a few differences in the region of signal peptides.

AB - Fusion protein of Newcastle disease virus is a glycoprotein with antigenicity. The cDNA of fusion gene of NDV strain F48E8 was cloned by RT-PCR, and the sequence of F48E8 was compared with other two virulent strains, Australia-victoria and Italien. Results show that the sequences of N-terminus are very similar, and cysteine residues and the potential glycosylation sites are relatively conserved. However, there are a few differences in the region of signal peptides.

KW - Analysis

KW - Fusion protein

KW - NDV

KW - Sequence

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M3 - Article

AN - SCOPUS:20444415351

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VL - 31

SP - 458

JO - Acta Biochimica et Biophysica Sinica

JF - Acta Biochimica et Biophysica Sinica

IS - 4

ER -

Analysis of N-terminal nucleotide sequence of NDV fusion protein

Abstract

Keywords

ASJC Scopus subject areas

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