9O4F
Pre-fusion Stabilized HERV-K Envelope Trimer Ectodomain
9O4F の概要
| エントリーDOI | 10.2210/pdb9o4f/pdb |
| 関連するPDBエントリー | 9MLA 9MLK |
| EMDBエントリー | 70098 |
| 分子名称 | Surface protein, Transmembrane protein,Fibritin, alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total) |
| 機能のキーワード | human endogenous retrovirus k, glycoprotein, herv-k, envelope, pre-fusion, viral protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 224303.05 |
| 構造登録者 | |
| 主引用文献 | Shek, J.,Sun, C.,Wilson, E.M.,Moadab, F.,Hastie, K.M.,Rajamanickam, R.R.,Penalosa, P.J.,Harkins, S.S.,Parekh, D.,Hariharan, C.,Zyla, D.S.,Yu, C.,Shaffer, K.C.L.,Lewis, V.I.,Avalos, R.D.,Mustelin, T.,Saphire, E.O. Human endogenous retrovirus K (HERV-K) envelope structures in pre- and postfusion by cryo-EM. Sci Adv, 11:eady8168-eady8168, 2025 Cited by PubMed Abstract: Human endogenous retroviruses (HERVs) are remnants of ancient infections that comprise ~8% of the human genome. The HERV-K envelope glycoprotein (Env) is aberrantly expressed in cancers, autoimmune disorders, and neurodegenerative diseases, and is targeted by patients' own antibodies. However, a lack of structural information has limited molecular and immunological studies of the roles of HERVs in disease. Here, we present cryo-electron microscopy structures of stabilized HERV-K Env in the prefusion conformation, revealing a distinct fold and architecture compared to HIV and simian immunodeficiency virus. We also generated and characterized a panel of monoclonal antibodies with subunit and conformational specificity, serving as valuable research tools. These antibodies enabled structure determination of the postfusion conformation of HERV-K Env, including its unique "tether" helix, and antibody-bound prefusion Env. Together, these results provide a structural framework that opens the door to mechanistic studies of HERV-K Env and tools for its evaluation as a potential therapeutic target. PubMed: 40864726DOI: 10.1126/sciadv.ady8168 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.24 Å) |
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