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Crystal structure of CV3-25 Fab bound to SARS-cov-2 spike stem helix peptide

Analyse Crystal structure of CV3-25 Fab bound to SARS-cov-2 spike stem helix peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7RAQ
Type
protein
Length
455 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CV3-25 Fab heavy chain; CV3-25 Fab light chain; Spike stem helix peptide
UniProt
P0DTC2
Ligands
SO4
Pockets
5 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HCV3-25 Fab heavy chainprotein2278% helix, 53% strand—
LCV3-25 Fab light chainprotein2136% helix, 52% strand—
PSpike stem helix peptideprotein1533% helix, 0% strandP0DTC2

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 2 copies · chains H, P
  • GOL · Glycerol · additive · 7 copies · chains H, L, P

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.590.9119GOL
24770.580.7362GOL
3930.370.7526GOL
4630.330.7618empty
5680.290.7320empty

Interfaces

3 interfaces between chains.

  • H–L · 2122 Ų buried · 21 hydrogen bonds · protein-protein
  • H–P · 643 Ų buried · 17 hydrogen bonds · protein-protein
  • L–P · 85 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 1 modified (disulfide, cyclization).

Compared structures

  • 7RAQ · Crystal structure of CV3-25 Fab bound to SARS-CoV-2 spike stem helix peptide · the same entry in another collection · chain H against H, TM-score 1.00

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