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MolNFT v1 · #177211 · protein

Cryo-EM structure of SARS-cov-2 spike D614G variant, one rbd-up conformation 3

7EB3 · Spike glycoprotein: “Cryo-EM structure of SARS-cov-2 spike D614G variant, one rbd-up conformation 3”. Electron microscopy, 2 ligands (NAG, BMA), 20 pockets (best druggability 0.87). MolNFT v1 #177211 on GenesisL1: 3D structure…

PDB
7EB3
Type
protein
Length
3,041 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 0.87

Structure

electron microscopy · 3 distinct chains · 21% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein101021% helix, 28% strandP0DTC2
BSpike glycoproteinprotein101621% helix, 26% strandP0DTC2
CSpike glycoproteinprotein101521% helix, 28% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 78 copies · chains A, C, B
  • BMA · beta-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
111460.870.88131empty
29680.830.8480empty
35630.820.8870empty
49850.810.8273empty
511950.790.8193empty

Interfaces

3 interfaces between chains.

  • B–C · 4441 Ų buried · 42 hydrogen bonds · protein-protein
  • A–C · 4321 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 4163 Ų buried · 26 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 48 glycan, 34 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7EB3 · Cryo-EM structure of SARS-CoV-2 Spike D614G variant, one RBD-up conformation 3 · the same entry in another collection · chain A against A, TM-score 1.00

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