A minimal region in the NTPase/helicase domain of the TGBp1 plant virus movement protein is responsible for ATPase activity and cooperative RNA binding

Journal of General Virology

Volumn 87, Issue 10, 2006, Pages 3087-3095

  Leshchiner, Anna D ^a   Solovyev, Andrey G ^a   Morozov, Sergey Yu ^a   Kalinina, Natalia O ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; AMINO ACID; MUTANT PROTEIN; RNA HELICASE; VIRUS PROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; GENE DELETION; HYDROLYSIS; IN VITRO STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; PLANT VIRUS; POINT MUTATION; POTEXVIRUS; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; RNA BINDING; VIRUS GENOME;

ADENOSINE TRIPHOSPHATASES; AMINO ACID MOTIFS; MOVEMENT; PLANT VIRUSES; PROTEIN BINDING; RNA; RNA HELICASES; RNA-BINDING PROTEINS;

HORDEIVIRUS; POA SEMILATENT VIRUS; POTATO VIRUS X; POTEXVIRUS;

EID: 33749064607     PISSN: 00221317     EISSN: None     Source Type: Journal    
DOI: 10.1099/vir.0.81971-0     Document Type: Article

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