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http://purl.uniprot.org/citations/31291580http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31291580http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31291580http://www.w3.org/2000/01/rdf-schema#comment"To ensure a successful infection, herpesviruses have developed elegant strategies to counterbalance the host anti-viral responses. Sterile alpha motif and HD domain 1 (SAMHD1) was recently identified as an intrinsic restriction factor for a variety of viruses. Aside from HIV-2 and the related simian immunodeficiency virus (SIV) Vpx proteins, the direct viral countermeasures against SAMHD1 restriction remain unknown. Using Epstein-Barr virus (EBV) as a primary model, we discover that SAMHD1-mediated anti-viral restriction is antagonized by EBV BGLF4, a member of the conserved viral protein kinases encoded by all herpesviruses. Mechanistically, we find that BGLF4 phosphorylates SAMHD1 and thereby inhibits its deoxynucleotide triphosphate triphosphohydrolase (dNTPase) activity. We further demonstrate that the targeting of SAMHD1 for phosphorylation is a common feature shared by beta- and gamma-herpesviruses. Together, our findings uncover an immune evasion mechanism whereby herpesviruses exploit the phosphorylation of SAMHD1 to thwart host defenses."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.org/dc/terms/identifier"doi:10.1016/j.celrep.2019.04.020"xsd:string
http://purl.uniprot.org/citations/31291580http://purl.org/dc/terms/identifier"doi:10.1016/j.celrep.2019.04.020"xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Li R."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Li R."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Zhang K."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Zhang K."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Lv D.W."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/author"Lv D.W."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/name"Cell Rep."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/name"Cell Rep."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/pages"449-459"xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/pages"449-459"xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/title"Conserved Herpesvirus Protein Kinases Target SAMHD1 to Facilitate Virus Replication."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/title"Conserved Herpesvirus Protein Kinases Target SAMHD1 to Facilitate Virus Replication."xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/volume"28"xsd:string
http://purl.uniprot.org/citations/31291580http://purl.uniprot.org/core/volume"28"xsd:string
http://purl.uniprot.org/citations/31291580http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31291580
http://purl.uniprot.org/citations/31291580http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31291580
http://purl.uniprot.org/citations/31291580http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31291580
http://purl.uniprot.org/citations/31291580http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31291580