Vaccinia virus D10 protein has mRNA decapping activity, providing a mechanism for control of host and viral gene expression

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 7, 2007, Pages 2139-2144

  Parrish, Susan ^a   Resch, Wolfgang ^a   Moss, Bernard ^a  

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

Author keywords

mRNA metabolism; mRNA turnover; MutT motif; Nudix hydrolase; Poxvirus

Indexed keywords

D10 PROTEIN; HYBRID PROTEIN; HYDROLASE; MESSENGER RNA; UNCLASSIFIED DRUG; VIRUS PROTEIN; VIRUS RNA;

ARTICLE; CAPPING PHENOMENON; CONCENTRATION (PARAMETERS); EUKARYOTIC CELL; GENE EXPRESSION REGULATION; GENE SEQUENCE; GENETIC CODE; GENETIC CONSERVATION; HOST PATHOGEN INTERACTION; METHYLATION; MOLECULAR INTERACTION; MUTT GENE; NONHUMAN; NUDIX GENE; POINT MUTATION; POXVIRUS; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN MOTIF; PROTEIN PURIFICATION; PROTEIN SYNTHESIS; SEQUENCE ANALYSIS; TURNOVER TIME; VACCINIA VIRUS; VIRUS GENE;

BINDING SITES; GENE EXPRESSION REGULATION; GENE EXPRESSION REGULATION, VIRAL; NUCLEOTIDASES; POINT MUTATION; PYROPHOSPHATASES; RECOMBINANT FUSION PROTEINS; RNA CAP ANALOGS; RNA CAPS; RNA-BINDING PROTEINS; SUBSTRATE SPECIFICITY; VACCINIA VIRUS; VIRAL PROTEINS;

EUKARYOTA; POXVIRIDAE; VACCINIA VIRUS;

EID: 33847779501     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0611685104     Document Type: Article

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