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Cryo-EM structure of SARS-CoV-2 S-Beta variant (B.1.351), Cleavable form, one RBD-up conformation

Analyse Cryo-EM structure of SARS-CoV-2 S-Beta variant (B.1.351), Cleavable form, one… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7V8C
Type
protein
Length
3,088 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.4
Source
Severe acute respiratory syndrome coronavirus 2
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.87

Structure

electron microscopy · resolution 3.4 · 3 distinct chains · 21% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein102621% helix, 29% strandP0DTC2
BSpike glycoproteinprotein103222% helix, 30% strandP0DTC2
CSpike glycoproteinprotein103021% helix, 30% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 75 copies · chains A, C, B

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
111460.870.88147empty
28160.830.8586empty
311000.820.83112empty
44230.790.8846empty
57520.790.8339empty

Interfaces

3 interfaces between chains.

  • B–C · 4483 Ų buried · 37 hydrogen bonds · protein-protein
  • A–C · 4359 Ų buried · 41 hydrogen bonds · protein-protein
  • A–B · 3864 Ų buried · 36 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 44 glycan, 40 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7V8C · Cryo-EM structure of SARS-cov-2 S-beta variant (B.1.351), cleavable form, one rbd-up… · the same entry in another collection · chain A against A, TM-score 1.00

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