Phosphorylation of human polyomavirus BK agnoprotein at Ser-11 is mediated by PKC and has an important regulative function

Virology

Volumn 379, Issue 1, 2008, Pages 97-109

  Johannessen, Mona ^a   Myhre, Marit Renée ^a   Dragset, Marte ^a   Tümmler, Conny ^a   Moens, Ugo ^a  

^a UNIVERSITY OF TROMSØ   (Norway)

Author keywords

Agnoprotein; Agnoprotein deletion mutant; BK virus; Gene expression; Kinase; Phosphorylation; PKC; Protein stability; Subcellular localization

Indexed keywords

AGNOPROTEIN; ALANINE; ASPARTIC ACID; PHOSPHOPROTEIN; PROTEIN KINASE C; PROTEIN VP1; PROTEIN VP3; SERINE;

ARTICLE; ENZYME INHIBITION; HUMAN; HUMAN CELL; POLYOMA VIRUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN STABILITY; VIRUS INFECTION; WILD TYPE;

AMINO ACID SUBSTITUTION; ANIMALS; BK VIRUS; CELL LINE; CERCOPITHECUS AETHIOPS; HUMANS; MUTAGENESIS, SITE-DIRECTED; PHOSPHORYLATION; PROTEIN KINASE C; VIRAL PROTEINS; VIRAL REGULATORY AND ACCESSORY PROTEINS; VIRUS REPLICATION;

BK POLYOMAVIRUS; MIRIDAE;

EID: 48949097511     PISSN: 00426822     EISSN: 10960341     Source Type: Journal    
DOI: 10.1016/j.virol.2008.06.007     Document Type: Article

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