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Structures of omicron spike complexes illuminate broad-spectrum neutralizing antibody development

Analyse Structures of omicron spike complexes illuminate broad-spectrum neutralizing… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7WS6
Type
protein
Length
451 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike protein S1; 510A5 light chain; 510A5 heavy chain
UniProt
P0DTC2
Pockets
3 · best druggability 0.58

Structure

electron microscopy · 3 distinct chains · 6% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
CSpike protein S1protein21811% helix, 23% strandP0DTC2
H510A5 light chainprotein1080% helix, 44% strand—
I510A5 heavy chainprotein1252% helix, 44% strand—

Pockets

3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13480.580.7635empty
2960.400.7721empty
3650.310.7515empty

Interfaces

3 interfaces between chains.

  • H–I · 878 Ų buried · 8 hydrogen bonds · protein-protein
  • C–I · 562 Ų buried · 8 hydrogen bonds · protein-protein
  • C–H · 248 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 7WS6 · Structures of Omicron Spike complexes illuminate broad-spectrum neutralizing antibody… · the same entry in another collection · chain C against C, TM-score 1.00

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