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

Analyse One rbd-up 1 of pre-fusion SARS-cov-2 gamma 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
7SBS
Type
protein
Length
3,330 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 0.85

Structure

electron microscopy · 3 distinct chains · 23% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein111622% helix, 31% strandP0DTC2
BSpike glycoproteinprotein109724% helix, 33% strandP0DTC2
CSpike glycoproteinprotein111723% helix, 32% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 85 copies · chains A, B, C
  • MAN · alpha-D-mannopyranose · sugar · 6 copies
  • 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
19510.850.86103empty
22810.830.9435empty
36410.820.8678empty
46720.810.8693empty
55810.790.8560empty

Interfaces

3 interfaces between chains.

  • B–C · 6335 Ų buried · 49 hydrogen bonds · protein-protein
  • A–C · 6317 Ų buried · 47 hydrogen bonds · protein-protein
  • A–B · 5000 Ų buried · 36 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 57 glycan, 43 disulfide (N-glycosylation, disulfide).

Compared structures

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

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