Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1989-1-24
pubmed:abstractText
We have obtained antiserum against highly purified vaccinia virus structural protein VP8, a major DNA binding protein present in the viral core particle. The antiserum has been used to monitor the course of the biosynthesis of this protein. The protein can first be detected in extracts of infected cells at 4 hr postinfection (p.i.). Its synthesis increases significantly at 5 hr p.i. and is maintained at about the same level up to 11 hr. The requirement of viral DNA replication for VP8 synthesis indicates that it is a viral late protein. This protein is synthesized in the form of a 28-kDa precursor, which is then processed to a 25-kDa product. The half-life of the precursor is about 2 hr. Comparing the N-terminal amino acid sequence of this purified protein with those derived from the published DNA sequence of the vaccinia viral genome [J.P. Weir and B. Moss (1984) J. Virol. 51, 662-669], it is found that VP8 maps to the HindIII L fragment of the viral genome. The cleavage site at which processing takes place lies between amino acids 32 (Gly) and 33 (Ala) from the N-terminal end of the precursor.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0042-6822
pubmed:author
pubmed:issnType
Print
pubmed:volume
167
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
585-90
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1988
pubmed:articleTitle
Biosynthesis and post-translational cleavage of vaccinia virus structural protein VP8.
pubmed:affiliation
Department of Biochemistry, School of Medicine, State University of New York, Stony Brook 11794.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.