Journal of General Virology · 1993 · 44 citations · 16 references
Life SciencesBiologyMolecular BiologyGene ExpressionMolecular VirologyVirologyAnimal VirusesViral Protein ProcessingViral StructureVirus Genome OrganizationVirus PurificationVirus-host InteractionsAntiserum PreparationConfocal Laser Scanning MicroscopyGlycosylation Site MappingInsect-specific VirusesPolyacrylamide Gel ElectrophoresisViral Fusion ProteinsViral GlycoproteinsViral Protein Glycosylation
The gene encoding the most abundant protein of purified preparations of Heliothis armigera entomopoxvirus (HaEPV) has been cloned and sequenced. The gene sequence encodes a 40.1K polypeptide with a putative N-terminal 20 amino acid leader peptide, and a single potential N-glycosylation site. Analysis of the protein, which has an apparent M(r) of 50K on polyacrylamide gels, confirmed post-translational loss of the leader peptide, but showed no evidence of glycosylation. The protein is related to others previously described from Choristoneura biennis EPV (63% identity) and Autographa californica nuclear polyhedrosis virus (42% identity). Polyclonal antiserum raised against a bacterial fusion protein containing the majority of the HaEPV protein specifically labelled HaEPV spindle bodies; confocal laser scanning microscopy suggests that the protein is distributed throughout those viral structures.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
A comprehensive set of sequence analysis programs for the VAX
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