7USB
CCoV-HuPn-2018 S in the swung out conformation (local refinement of domain 0)
7USB の概要
エントリーDOI | 10.2210/pdb7usb/pdb |
EMDBエントリー | 26731 |
分子名称 | Spike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total) |
機能のキーワード | human coronavirus, coronavirus, ccov-hupn-2018, spike glycoprotein, alpha-coronaviruses, structural genomics, seattle structural genomics center for infectious disease, ssgcid, viral protein |
由来する生物種 | unidentified human coronavirus |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 38712.61 |
構造登録者 | Tortorici, M.A.,Veesler, D.,Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2022-04-23, 公開日: 2022-08-24, 最終更新日: 2024-11-13) |
主引用文献 | Tortorici, M.A.,Walls, A.C.,Joshi, A.,Park, Y.J.,Eguia, R.T.,Miranda, M.C.,Kepl, E.,Dosey, A.,Stevens-Ayers, T.,Boeckh, M.J.,Telenti, A.,Lanzavecchia, A.,King, N.P.,Corti, D.,Bloom, J.D.,Veesler, D. Structure, receptor recognition, and antigenicity of the human coronavirus CCoV-HuPn-2018 spike glycoprotein. Cell, 185:2279-2291.e17, 2022 Cited by PubMed Abstract: The isolation of CCoV-HuPn-2018 from a child respiratory swab indicates that more coronaviruses are spilling over to humans than previously appreciated. We determined the structures of the CCoV-HuPn-2018 spike glycoprotein trimer in two distinct conformational states and showed that its domain 0 recognizes sialosides. We identified that the CCoV-HuPn-2018 spike binds canine, feline, and porcine aminopeptidase N (APN) orthologs, which serve as entry receptors, and determined the structure of the receptor-binding B domain in complex with canine APN. The introduction of an oligosaccharide at position N739 of human APN renders cells susceptible to CCoV-HuPn-2018 spike-mediated entry, suggesting that single-nucleotide polymorphisms might account for viral detection in some individuals. Human polyclonal plasma antibodies elicited by HCoV-229E infection and a porcine coronavirus monoclonal antibody inhibit CCoV-HuPn-2018 spike-mediated entry, underscoring the cross-neutralizing activity among ɑ-coronaviruses. These data pave the way for vaccine and therapeutic development targeting this zoonotic pathogen representing the eighth human-infecting coronavirus. PubMed: 35700730DOI: 10.1016/j.cell.2022.05.019 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.1 Å) |
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