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dc.contributor.authorWeaver, Grant
dc.contributor.authorArya, Richa
dc.contributor.authorSchneider, Christine L
dc.contributor.authorHudson, Amy W
dc.contributor.authorStern, Lawrence J
dc.date.accessioned2023-03-02T14:02:42Z
dc.date.available2023-03-02T14:02:42Z
dc.date.issued2022-04-04
dc.identifier.citationWeaver GC, Arya R, Schneider CL, Hudson AW, Stern LJ. Structural Models for Roseolovirus U20 And U21: Non-Classical MHC-I Like Proteins From HHV-6A, HHV-6B, and HHV-7. Front Immunol. 2022 Apr 4;13:864898. doi: 10.3389/fimmu.2022.864898. Erratum in: Front Immunol. 2022 May 23;13:936968. PMID: 35444636; PMCID: PMC9013968.en_US
dc.identifier.eissn1664-3224
dc.identifier.doi10.3389/fimmu.2022.864898en_US
dc.identifier.pmid35444636
dc.identifier.urihttp://hdl.handle.net/20.500.14038/51732
dc.description.abstractHuman roseolovirus U20 and U21 are type I membrane glycoproteins that have been implicated in immune evasion by interfering with recognition of classical and non-classical MHC proteins. U20 and U21 are predicted to be type I glycoproteins with extracytosolic immunoglobulin-like domains, but detailed structural information is lacking. AlphaFold and RoseTTAfold are next generation machine-learning-based prediction engines that recently have revolutionized the field of computational three-dimensional protein structure prediction. Here, we review the structural biology of viral immunoevasins and the current status of computational structure prediction algorithms. We use these computational tools to generate structural models for U20 and U21 proteins, which are predicted to adopt MHC-Ia-like folds with closed MHC platforms and immunoglobulin-like domains. We evaluate these structural models and place them within current understanding of the structural basis for viral immune evasion of T cell and natural killer cell recognition.en_US
dc.language.isoenen_US
dc.relation.ispartofFrontiers in Immunologyen_US
dc.relation.urlhttps://doi.org/10.3389/fimmu.2022.864898en_US
dc.rightsCopyright © 2022 Weaver, Arya, Schneider, Hudson and Stern. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMHC1ben_US
dc.subjecthuman herpesvirusen_US
dc.subjectimmune recognitionen_US
dc.subjectimmunoevasionen_US
dc.subjectmachine learningen_US
dc.subjectmajor histocompatibility proteinen_US
dc.subjectnatural killer cell liganden_US
dc.subjectstructure predictionen_US
dc.titleStructural Models for Roseolovirus U20 And U21: Non-Classical MHC-I Like Proteins From HHV-6A, HHV-6B, and HHV-7en_US
dc.typeJournal Articleen_US
dc.source.journaltitleFrontiers in immunology
dc.source.volume13
dc.source.beginpage864898
dc.source.endpage
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countrySwitzerland
dc.identifier.journalFrontiers in immunology
refterms.dateFOA2023-03-02T14:02:43Z
dc.contributor.departmentBiochemistry and Molecular Biotechnologyen_US
dc.contributor.departmentMorningside Graduate School of Biomedical Sciencesen_US
dc.contributor.departmentPathologyen_US
dc.description.thesisprogramImmunology and Microbiology


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Copyright © 2022 Weaver, Arya, Schneider, Hudson and Stern. This is an open-access
article distributed under the terms of the Creative Commons Attribution License
(CC BY). The use, distribution or reproduction in other forums is permitted, provided
the original author(s) and the copyright owner(s) are credited and that the original
publication in this journal is cited, in accordance with accepted academic practice. No
use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as Copyright © 2022 Weaver, Arya, Schneider, Hudson and Stern. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.