<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(11)</volume><submitter>Malik T</submitter><pubmed_abstract>Mumps virus (MuV) is a neurotropic non-segmented, negative-stranded, enveloped RNA virus in the &lt;i>Paramyxovirus&lt;/i> family. The 15.4 kb genome encodes seven genes, including the V/P, which encodes, among other proteins, the V protein. The MuV V protein has been shown to target the cellular signal transducer and activator of transcription proteins STAT1 and STAT3 for proteasome-mediated degradation. While MuV V protein targeting of STAT1 is generally accepted as a means of limiting innate antiviral responses, the consequence of V protein targeting of STAT3 is less clear. Further, since the MuV V protein targets both STAT1 and STAT3, specifically investigating viral antagonism of STAT3 targeting is challenging. However, a previous study reported that a single amino acid substitution in the </pubmed_abstract><journal>Viruses</journal><pagination>E1016</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6893744</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Single Point Mutation in the Mumps V Protein Alters Targeting of the Cellular STAT Pathways Resulting in Virus Attenuation.</pubmed_title><pmcid>PMC6893744</pmcid><pubmed_authors>Bosma T</pubmed_authors><pubmed_authors>Malik T</pubmed_authors><pubmed_authors>Ngo L</pubmed_authors><pubmed_authors>Rubin S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Single Point Mutation in the Mumps V Protein Alters Targeting of the Cellular STAT Pathways Resulting in Virus Attenuation.</name><description>Mumps virus (MuV) is a neurotropic non-segmented, negative-stranded, enveloped RNA virus in the &lt;i>Paramyxovirus&lt;/i> family. The 15.4 kb genome encodes seven genes, including the V/P, which encodes, among other proteins, the V protein. The MuV V protein has been shown to target the cellular signal transducer and activator of transcription proteins STAT1 and STAT3 for proteasome-mediated degradation. While MuV V protein targeting of STAT1 is generally accepted as a means of limiting innate antiviral responses, the consequence of V protein targeting of STAT3 is less clear. Further, since the MuV V protein targets both STAT1 and STAT3, specifically investigating viral antagonism of STAT3 targeting is challenging. However, a previous study reported that a single amino acid substitution in the </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2026-05-04T08:56:20.24Z</modification><creation>2020-05-21T23:54:24Z</creation></dates><accession>S-EPMC6893744</accession><cross_references><pubmed>31683999</pubmed><doi>10.3390/v11111016</doi></cross_references></HashMap>