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

Analyse SARS-cov-2 omicron 1-rbd down 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
7TGE
Type
protein
Length
2,677 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
Ligands
NAG
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 3 distinct chains · 24% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein103022% helix, 31% strand—
BSpike glycoproteinprotein84225% helix, 31% strand—
CSpike glycoproteinprotein80524% helix, 31% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 40 copies · chains A, B, C

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
18670.850.8788empty
22430.820.9430empty
35870.810.8784empty
43650.800.9034empty
52990.800.9146empty

Interfaces

3 interfaces between chains.

  • A–B · 5481 Ų buried · 48 hydrogen bonds · protein-protein
  • B–C · 4498 Ų buried · 39 hydrogen bonds · protein-protein
  • A–C · 4451 Ų buried · 37 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 disulfide, 31 glycan (disulfide, N-glycosylation).

Compared structures

  • 7TGE · SARS-CoV-2 Omicron 1-RBD down 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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