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8XNK

Cryo-EM structure of SARS-CoV-2 Omicron HV.1 spike protein(6P) in complex with human ACE2

Summary for 8XNK
Entry DOI10.2210/pdb8xnk/pdb
EMDB information38505
DescriptorAngiotensin-converting enzyme 2, Spike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
Functional Keywordssars-cov-2, omicron, hv.1, spike protein, human ace2, viral protein, hydrolase-viral protein complex, hydrolase/viral protein
Biological sourceHomo sapiens (human)
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Total number of polymer chains4
Total formula weight485684.52
Authors
Li, L.J.,Gu, Y.H.,Shi, K.Y.,Qi, J.X.,Gao, G.F. (deposition date: 2023-12-30, release date: 2024-07-03, Last modification date: 2024-11-27)
Primary citationLi, L.,Shi, K.,Gu, Y.,Xu, Z.,Shu, C.,Li, D.,Sun, J.,Cong, M.,Li, X.,Zhao, X.,Yu, G.,Hu, S.,Tan, H.,Qi, J.,Ma, X.,Liu, K.,Gao, G.F.
Spike structures, receptor binding, and immune escape of recently circulating SARS-CoV-2 Omicron BA.2.86, JN.1, EG.5, EG.5.1, and HV.1 sub-variants.
Structure, 32:1055-1067.e6, 2024
Cited by
PubMed Abstract: The recently emerged BA.2.86, JN.1, EG.5, EG.5.1, and HV.1 variants have a growth advantage. In this study, we explore the structural bases of receptor binding and immune evasion for the Omicron BA.2.86, JN.1, EG.5, EG.5.1, and HV.1 sub-variants. Our findings reveal that BA.2.86 exhibits strong receptor binding, whereas its JN.1 sub-lineage displays a decreased binding affinity to human ACE2 (hACE2). Through complex structure analyses, we observed that the reversion of R493Q in BA.2.86 receptor binding domain (RBD) plays a facilitating role in receptor binding, while the L455S substitution in JN.1 RBD restores optimal affinity. Furthermore, the structure of monoclonal antibody (mAb) S309 complexed with BA.2.86 RBD highlights the importance of the K356T mutation, which brings a new N-glycosylation motif, altering the binding pattern of mAbs belonging to RBD-5 represented by S309. These findings emphasize the importance of closely monitoring BA.2.86 and its sub-lineages to prevent another wave of SARS-CoV-2 infections.
PubMed: 39013463
DOI: 10.1016/j.str.2024.06.012
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.78 Å)
Structure validation

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