Reactive-site cleavage residues confer target specificity to baculovirus P49, a dimeric member of the P35 family of caspase inhibitors

Journal of Virology

Volumn 82, Issue 15, 2008, Pages 7504-7514

  Guy, Michael P ^a   Friesen, Paul D ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE; CASPASE INHIBITOR; CYSTEINE; EFFECTOR CASPASE; INTERLEUKIN 1BETA CONVERTING ENZYME; PROTEIN P35; PROTEIN P49; VIRUS PROTEIN;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; BACULOVIRUS; BIOCHEMISTRY; BIOLOGICAL MONITORING; CELL DEATH; COMPLEX FORMATION; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME DEGRADATION; ENZYME INHIBITION; ENZYME SPECIFICITY; LEPIDOPTERA; MOLECULAR DYNAMICS; MOLECULAR RECOGNITION; MOLECULAR STABILITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN FAMILY; PROTEIN FUNCTION; PROTEIN MOTIF; PROTEIN TARGETING; STOICHIOMETRY; VIRUS INDUCTION; VIRUS INHIBITION;

ANIMALS; BACULOVIRIDAE; BINDING SITES; CASPASES, EFFECTOR; CASPASES, INITIATOR; CELL LINE; DIMERIZATION; INHIBITOR OF APOPTOSIS PROTEINS; SPODOPTERA; SUBSTRATE SPECIFICITY; VIRAL PROTEINS;

HEXAPODA; SPODOPTERA FRUGIPERDA;

EID: 47749123009     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.00231-08     Document Type: Article

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