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SARS-cov-2 SPIKE:5A6 Fab complex I focused refinement

Analyse SARS-cov-2 SPIKE:5A6 Fab complex I focused refinement in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7M71
Type
protein
Length
852 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein; Antibody 5A6 Fab heavy chain; Antibody 5A6 Fab light chain
UniProt
P0DTC2
Ligands
NAG
Pockets
8 · best druggability 0.61

Structure

electron microscopy · 3 distinct chains · 9% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BSpike glycoproteinprotein20915% helix, 27% strandP0DTC2
HAntibody 5A6 Fab heavy chainprotein2208% helix, 47% strand—
LAntibody 5A6 Fab light chainprotein2145% helix, 37% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12140.610.8240empty
23480.570.7536empty
31760.500.7739empty
41790.450.7421empty
5720.380.7816empty

Interfaces

4 interfaces between chains.

  • H–L · 2183 Ų buried · 23 hydrogen bonds · protein-protein
  • A–H · 725 Ų buried · 7 hydrogen bonds · protein-protein
  • B–L · 393 Ų buried · 5 hydrogen bonds · protein-protein
  • A–L · 281 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 13 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 7M71 · SARS-CoV-2 Spike:5A6 Fab complex I focused refinement · the same entry in another collection · chain A against A, TM-score 1.00

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