Endonuclease substrate selectivity characterized with full-length PA of influenza A virus polymerase

Virology

Volumn 433, Issue 1, 2012, Pages 27-34

  Noble, Erin ^a   Cox, Andrew ^a   Deval, Jerome ^b   Kim, Baek ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b AliosBiopharma   (United States)

Author keywords

Endonuclease; Influenza A Virus; Polymerase

Indexed keywords

DIVALENT CATION; PA ENDONUCLEASE; PA PROTEIN; RNA POLYMERASE; UNCLASSIFIED DRUG; VIRUS DNA; VIRUS PROTEIN; VIRUS RNA;

ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME SUBSTRATE; FLUORESCENCE; IN VITRO STUDY; INFLUENZA VIRUS A; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN SECONDARY STRUCTURE; RNA BINDING; RNA CLEAVAGE; RNA SYNTHESIS;

BIOLOGICAL ASSAY; CATIONS, DIVALENT; COENZYMES; ENDONUCLEASES; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMANS; INFLUENZA A VIRUS; MAGNESIUM; MANGANESE; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT PROTEINS; RNA CAPS; RNA REPLICASE; RNA, VIRAL; SUBSTRATE SPECIFICITY; VIRAL PROTEINS;

INFLUENZA A VIRUS;

EID: 84866166327     PISSN: 00426822     EISSN: 10960341     Source Type: Journal    
DOI: 10.1016/j.virol.2012.07.008     Document Type: Article

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