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Structure of sybody SR31 in complex with the SARS-cov-2 S receptor binding domain (rbd)

Analyse Structure of sybody SR31 in complex with the SARS-cov-2 S receptor binding… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7D2Z
Type
protein
Length
329 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SR31 against SARS-cov-2 rbd, non neutralizing; Spike protein S1
UniProt
P0DTC2
Ligands
NAG, MAN, FUC, BMA
Pockets
1 · best druggability 0.63

Structure

x-ray diffraction · 2 distinct chains · 15% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASR31 against SARS-cov-2 rbd, non neutralizingprotein1178% helix, 54% strand—
BSpike protein S1protein21219% helix, 27% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains B, A
  • MAN · alpha-D-mannopyranose · sugar · 2 copies · chains A
  • FUC · alpha-L-fucopyranose · sugar · 2 copies · chains B
  • BMA · beta-D-mannopyranose · sugar
  • FMT · Formic acid · additive · 13 copies · chains A, B
  • GOL · Glycerol · additive · 5 copies · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11380.630.8629GOL, FMT

Interfaces

1 interface between chains.

  • A–B · 1478 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 7D2Z · Structure of sybody SR31 in complex with the SARS-CoV-2 S Receptor Binding domain (RBD) · the same entry in another collection · chain A against A, TM-score 1.00

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