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SARS CoV2 Spike ectodomain with engineered trimerized VH binder

Analyse SARS CoV2 Spike ectodomain with engineered trimerized VH binder in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7JWB
Type
protein
Length
3,289 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.2
Source
Homo sapiens; Severe acute respiratory syndrome coronavirus 2
Molecule
autonomous human heavy chain variable domain; Spike glycoprotein
UniProt
P0DTC2
Pockets
20 · best druggability 0.86

Structure

electron microscopy · resolution 3.2 · 4 distinct chains · 20% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
Dautonomous human heavy chain variable domainprotein3663% helix, 53% strand—
ASpike glycoproteinprotein99122% helix, 33% strandP0DTC2
BSpike glycoproteinprotein98623% helix, 34% strandP0DTC2
CSpike glycoproteinprotein94623% helix, 34% strandP0DTC2

Pockets

20 pockets found on a 1 Å grid, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111260.860.87123empty
211870.860.86117empty
39080.790.8273empty
47020.710.7848empty
58030.700.7664empty

Interfaces

6 interfaces between chains.

  • A–B · 4313 Ų buried · 50 hydrogen bonds · protein-protein
  • B–C · 3953 Ų buried · 51 hydrogen bonds · protein-protein
  • A–C · 3832 Ų buried · 42 hydrogen bonds · protein-protein
  • D–B · 1515 Ų buried · 23 hydrogen bonds · protein-protein
  • D–A · 1001 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 39 disulfide (disulfide).

Compared structures

  • 7JWB · SARS COV2 spike ectodomain with engineered trimerized vh binder · the same entry in another collection · chain A against A, TM-score 1.00

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