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SARS-cov-2 S B.1.1.529 omicron variant (rbd + S309 local refinement)

Analyse SARS-cov-2 S B.1.1.529 omicron variant (rbd + S309 local refinement) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TLY
Type
protein
Length
408 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S309 Fab heavy chain; S309 Fab light chain; Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG, BMA, FUC
Pockets
3 · best druggability 0.51

Structure

electron microscopy · 3 distinct chains · 10% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AS309 Fab heavy chainprotein1267% helix, 50% strand—
BS309 Fab light chainprotein1013% helix, 47% strand—
ISpike glycoproteinprotein18115% helix, 30% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A, B, I
  • BMA · beta-D-mannopyranose · sugar
  • FUC · alpha-L-fucopyranose · sugar · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12740.510.7440NAG, FUC
2620.380.7916empty
3870.340.7521empty

Interfaces

3 interfaces between chains.

  • A–B · 735 Ų buried · 6 hydrogen bonds · protein-protein
  • A–I · 659 Ų buried · 8 hydrogen bonds · protein-protein
  • B–I · 180 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 5 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 7TLY · SARS-CoV-2 S B.1.1.529 Omicron variant (RBD + S309 Local Refinement) · the same entry in another collection · chain A against A, TM-score 1.00

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