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Complex of SARS-cov-2 spike and CR3022 Fab (non-uniform refinement)

Analyse Complex of SARS-cov-2 spike and CR3022 Fab (non-uniform refinement) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7A5R
Type
protein
Length
1,358 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CR3022 Fab heavy chain; CR3022 Fab light chain; Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.65

Structure

electron microscopy · 3 distinct chains · 5% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H, ICR3022 Fab heavy chainprotein2131% helix, 49% strand—
L, MCR3022 Fab light chainprotein2023% helix, 50% strand—
A, BSpike glycoproteinprotein2649% helix, 26% strandP0DTC2

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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11460.650.8737empty
21060.570.8525empty
32380.530.7632empty
42440.520.7632empty
51360.450.7722empty

Interfaces

8 interfaces between chains.

  • H–L · 1669 Ų buried · 11 hydrogen bonds · protein-protein
  • M–I · 1637 Ų buried · 11 hydrogen bonds · protein-protein
  • L–A · 661 Ų buried · 3 hydrogen bonds · protein-protein
  • B–M · 645 Ų buried · 2 hydrogen bonds · protein-protein
  • B–I · 644 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 7A5R · Complex of SARS-CoV-2 spike and CR3022 Fab (Non-Uniform Refinement) · the same entry in another collection · chain H against H, TM-score 1.00

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