Entry of vaccinia virus and cell-cell fusion require a highly conserved cysteine-rich membrane protein encoded by the A16L gene

Journal of Virology

Volumn 80, Issue 1, 2006, Pages 51-61

  Ojeda, Suany ^a   Senkevich, Tatiana G ^a   Moss, Bernard ^a,b  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; MEMBRANE PROTEIN; PROTEIN A21; PROTEIN A28; PROTEIN H2; PROTEIN L5; UNCLASSIFIED DRUG; VIRUS DNA; VIRUS PROTEIN; VIRUS PROTEIN A16;

A16L GENE; AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL FUSION; CONTROLLED STUDY; DISULFIDE BOND; ESCHERICHIA COLI; GENE DELETION; GENE REPRESSION; GENETIC CONSERVATION; NONHUMAN; OPEN READING FRAME; OXIDATION REDUCTION REACTION; PHENOTYPE; POXVIRUS; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; VACCINIA VIRUS; VIRUS CELL INTERACTION; VIRUS GENE; VIRUS ISOLATION; VIRUS MUTATION; VIRUS PARTICLE; VIRUS PURIFICATION;

AMINO ACID SEQUENCE; CELL FUSION; CELL LINE; CYSTEINE; MEMBRANE FUSION; MOLECULAR SEQUENCE DATA; OPEN READING FRAMES; VACCINIA VIRUS; VIRAL FUSION PROTEINS; VIRUS REPLICATION;

ANIMALIA; DNA VIRUSES; ESCHERICHIA COLI; POXVIRIDAE; VACCINIA VIRUS;

EID: 29444454707     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.80.1.51-61.2006     Document Type: Article

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