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SARS-cov-2 omicron 1-rbd up spike protein trimer without the P986-P987 stabilizing mutations (S-gsas-omicron)

Analyse SARS-cov-2 omicron 1-rbd up spike protein trimer without the P986-P987… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TL9
Type
protein
Length
3,083 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG, BMA, MAN
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 3 distinct chains · 22% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein105023% helix, 31% strandP0DTC2
BSpike glycoproteinprotein102822% helix, 29% strandP0DTC2
CSpike glycoproteinprotein100521% helix, 32% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 57 copies · chains A, B, C
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • MAN · alpha-D-mannopyranose · sugar

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
15760.840.9076empty
210930.830.84106empty
35030.830.8956empty
410610.810.83116empty
54230.810.8937empty

Interfaces

3 interfaces between chains.

  • A–C · 6125 Ų buried · 51 hydrogen bonds · protein-protein
  • A–B · 6065 Ų buried · 47 hydrogen bonds · protein-protein
  • B–C · 4155 Ų buried · 35 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 39 disulfide, 38 glycan (disulfide, N-glycosylation).

Compared structures

  • 7TL9 · SARS-CoV-2 Omicron 1-RBD up Spike Protein Trimer without the P986-P987 stabilizing… · the same entry in another collection · chain A against A, TM-score 1.00

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