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Omicron spike bitrimer with 6M6 antibody

Analyse Omicron spike bitrimer with 6M6 antibody in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7WJZ
Type
protein
Length
8,886 residues
Chains
18
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein; 6M6 heavy chain; 6M6 light chain
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 3 distinct chains · 13% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B, I, J, K, L, MSpike glycoproteinprotein104518% helix, 24% strandP0DTC2
A, D, E, F, G, H6M6 heavy chainprotein2261% helix, 31% strand—
C, N, O, P, Q, R6M6 light chainprotein2101% helix, 35% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 49 copies · chains B, J, I, K, L, M

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19620.860.87118empty
28820.860.88106empty
36260.850.9072empty
49960.820.8398empty
53230.810.9142empty

Interfaces

39 interfaces between chains.

  • L–M · 4736 Ų buried · 50 hydrogen bonds · protein-protein
  • K–L · 4736 Ų buried · 50 hydrogen bonds · protein-protein
  • K–M · 4729 Ų buried · 50 hydrogen bonds · protein-protein
  • B–J · 4727 Ų buried · 51 hydrogen bonds · protein-protein
  • B–I · 4709 Ų buried · 50 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 102 disulfide, 49 glycan (disulfide, N-glycosylation).

Compared structures

  • 7WJZ · Omicron Spike bitrimer with 6m6 antibody · the same entry in another collection · chain B against B, TM-score 1.00

Analyse

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