RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/30092200http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30092200http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30092200http://www.w3.org/2000/01/rdf-schema#comment"Herpes simplex virus 1 (HSV-1) establishes infections in humans and mice, but some non-human primates exhibit resistance via unknown mechanisms. Innate immune recognition pathways are highly conserved but are pivotal in determining susceptibility to DNA virus infections. We report that variation of a single amino acid residue in the innate immune sensor cGAS determines species-specific inactivation by HSV-1. The HSV-1 UL37 tegument protein deamidates human and mouse cGAS. Deamidation impairs the ability of cGAS to catalyze cGAMP synthesis, which activates innate immunity. HSV-1 with deamidase-deficient UL37 promotes robust antiviral responses and is attenuated in mice in a cGAS- and STING-dependent manner. Mutational analyses identified a single asparagine in human and mouse cGAS that is not conserved in many non-human primates. This residue underpins UL37-mediated cGAS deamidation and species permissiveness of HSV-1. Thus, HSV-1 mediates cGAS deamidation for immune evasion and exploits species sequence variation to disarm host defenses."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.org/dc/terms/identifier"doi:10.1016/j.chom.2018.07.004"xsd:string
http://purl.uniprot.org/citations/30092200http://purl.org/dc/terms/identifier"doi:10.1016/j.chom.2018.07.004"xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Chen L."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Chen L."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"He S."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"He S."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Liu T."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Liu T."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Lee K."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Lee K."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Feng P."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Feng P."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Huang C."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Huang C."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Seo G.J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Seo G.J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Zhao J."xsd:string
http://purl.uniprot.org/citations/30092200http://purl.uniprot.org/core/author"Zhao J."xsd:string