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Cryo-EM structure of SARS-CoV-2 Delta (B.1.617.2) spike protein

Analyse Cryo-EM structure of SARS-CoV-2 Delta (B.1.617.2) spike protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TEY
Type
protein
Length
2,703 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.25
Source
Severe acute respiratory syndrome coronavirus 2
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.86

Structure

electron microscopy · resolution 2.25 · 2 distinct chains · 22% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BSpike glycoproteinprotein83424% helix, 36% strandP0DTC2
CSpike glycoproteinprotein103521% helix, 34% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 56 copies · chains A, B, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 13 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19320.860.88129empty
26840.860.9086empty
35270.810.8766empty
44120.770.8654empty
55820.740.8245empty

Interfaces

3 interfaces between chains.

  • A–C · 4641 Ų buried · 53 hydrogen bonds · protein-protein
  • A–B · 4203 Ų buried · 40 hydrogen bonds · protein-protein
  • B–C · 4177 Ų buried · 34 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 38 glycan, 34 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7TEY · Cryo-EM structure of SARS-cov-2 delta (B.1.617.2) spike protein · the same entry in another collection · chain A against A, TM-score 1.00

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