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7YBM

SARS-CoV-2 C.1.2 variant spike (Close state)

This is a non-PDB format compatible entry.
Summary for 7YBM
Entry DOI10.2210/pdb7ybm/pdb
EMDB information33726
DescriptorSpike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, alpha-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
Functional Keywordssars-cov-2, lambda, spike, viral protein
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
Total number of polymer chains3
Total formula weight446674.92
Authors
Wang, X.,Fu, W. (deposition date: 2022-06-29, release date: 2023-08-09, Last modification date: 2024-11-20)
Primary citationXing, X.,Wang, L.,Cui, Z.,Fu, W.,Zheng, T.,Qin, L.,Ge, P.,Qian, A.,Wang, N.,Yuan, S.
Structures of SARS-CoV-2 spike protein alert noteworthy sites for the potential approaching variants.
Virol Sin, 37:938-941, 2022
Cited by
PubMed Abstract: • Deletion of residues 156–157 warps the neighboring beta-sheet and leads NTD and RBD to shift. • T859N stabilizes the packing of the 630 loop motif to make RBD standing transition more difficult. • The overall structures of the closed state S complex from different variants resemble each other. • Mutations in FPPR may affect the overall structure of the trimeric spike protein.
PubMed: 36368512
DOI: 10.1016/j.virs.2022.11.003
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.45 Å)
Structure validation

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