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SARS-cov-2 spike in complex with the S2A4 neutralizing antibody Fab fragment (local refinement of the receptor-binding domain and Fab variable domains)

Analyse SARS-cov-2 spike in complex with the S2A4 neutralizing antibody Fab fragment… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7JVA
Type
protein
Length
420 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S2A4 Fab heavy chain; S2A4 Fab light chain; Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG, BMA
Pockets
4 · best druggability 0.57

Structure

electron microscopy · 3 distinct chains · 10% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HS2A4 Fab heavy chainprotein1178% helix, 53% strand—
LS2A4 Fab light chainprotein1105% helix, 44% strand—
ASpike glycoproteinprotein19313% helix, 29% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A, H
  • BMA · beta-D-mannopyranose · sugar · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11970.570.8024empty
21280.480.7930empty
31380.400.7425empty
4790.360.7624empty

Interfaces

3 interfaces between chains.

  • H–L · 832 Ų buried · 7 hydrogen bonds · protein-protein
  • L–A · 511 Ų buried · 8 hydrogen bonds · protein-protein
  • H–A · 415 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 7JVA · SARS-CoV-2 spike in complex with the S2A4 neutralizing antibody Fab fragment (local… · the same entry in another collection · chain H against H, TM-score 1.00

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