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Cryo-EM structure of SARS-cov-2 spike D614G variant, one rbd-up conformation 2

Analyse Cryo-EM structure of SARS-cov-2 spike D614G variant, one rbd-up conformation 2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7EB0
Type
protein
Length
3,055 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG, BMA
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 3 distinct chains · 22% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein101322% helix, 27% strandP0DTC2
BSpike glycoproteinprotein101521% helix, 25% strandP0DTC2
CSpike glycoproteinprotein102722% helix, 27% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 77 copies · chains A, C, B
  • BMA · beta-D-mannopyranose · 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
18750.840.8695empty
210310.830.8472empty
35560.820.8775empty
411690.800.8298empty
510970.790.8196empty

Interfaces

3 interfaces between chains.

  • B–C · 4282 Ų buried · 41 hydrogen bonds · protein-protein
  • A–C · 4204 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 3924 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 47 glycan, 35 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7EB0 · Cryo-EM structure of SARS-CoV-2 Spike D614G variant, one RBD-up conformation 2 · the same entry in another collection · chain A against A, TM-score 1.00

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