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7TN0

SARS-CoV-2 Omicron RBD in complex with human ACE2 and S304 Fab and S309 Fab

7TN0 の概要
エントリーDOI10.2210/pdb7tn0/pdb
関連するPDBエントリー7TLY 7TLZ 7TM0 7TNO
EMDBエントリー25990 25991 25992 25993
分子名称S309 light chain, 2-acetamido-2-deoxy-beta-D-glucopyranose, S309 heavy chain, ... (11 entities in total)
機能のキーワードcovid-19, sars-cov-2, neutralizing monoclonal antibody, sars-cov-2 receptor human ace2, viral protein-immune system complex, structural genomics, seattle structural genomics center for infectious disease, ssgcid, viral protein/immune system
由来する生物種Homo sapiens
詳細
タンパク質・核酸の鎖数12
化学式量合計382458.66
構造登録者
主引用文献McCallum, M.,Czudnochowski, N.,Rosen, L.E.,Zepeda, S.K.,Bowen, J.E.,Walls, A.C.,Hauser, K.,Joshi, A.,Stewart, C.,Dillen, J.R.,Powell, A.E.,Croll, T.I.,Nix, J.,Virgin, H.W.,Corti, D.,Snell, G.,Veesler, D.
Structural basis of SARS-CoV-2 Omicron immune evasion and receptor engagement.
Science, 375:864-868, 2022
Cited by
PubMed Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant of concern evades antibody-mediated immunity that comes from vaccination or infection with earlier variants due to accumulation of numerous spike mutations. To understand the Omicron antigenic shift, we determined cryo-electron microscopy and x-ray crystal structures of the spike protein and the receptor-binding domain bound to the broadly neutralizing sarbecovirus monoclonal antibody (mAb) S309 (the parent mAb of sotrovimab) and to the human ACE2 receptor. We provide a blueprint for understanding the marked reduction of binding of other therapeutic mAbs that leads to dampened neutralizing activity. Remodeling of interactions between the Omicron receptor-binding domain and human ACE2 likely explains the enhanced affinity for the host receptor relative to the ancestral virus.
PubMed: 35076256
DOI: 10.1126/science.abn8652
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.85 Å)
構造検証レポート
Validation report summary of 7tn0
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-04-16に公開中

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