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One rbd-up 1 of pre-fusion SARS-cov-2 delta variant spike protein

Analyse One rbd-up 1 of pre-fusion SARS-cov-2 delta variant spike protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7SBL
Type
protein
Length
3,286 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG, MAN, FUC
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 3 distinct chains · 23% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein110223% helix, 30% strandP0DTC2
BSpike glycoproteinprotein108124% helix, 31% strandP0DTC2
CSpike glycoproteinprotein110323% helix, 30% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 83 copies · chains A, B, C
  • MAN · alpha-D-mannopyranose · sugar · 10 copies · chains B
  • FUC · alpha-L-fucopyranose · sugar · 3 copies

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
18710.860.88100empty
26560.820.8781empty
33600.800.9043empty
42520.800.9340empty
55430.780.8579empty

Interfaces

3 interfaces between chains.

  • B–C · 6356 Ų buried · 56 hydrogen bonds · protein-protein
  • A–C · 6289 Ų buried · 50 hydrogen bonds · protein-protein
  • A–B · 5209 Ų buried · 36 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 54 glycan, 43 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7SBL · One RBD-up 1 of pre-fusion SARS-CoV-2 Delta variant spike protein · the same entry in another collection · chain A against A, TM-score 1.00

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