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SARS-cov-2 S omicron spike B.1.1.529 - rbd down - 1-P2G3 Fab (local)

Analyse SARS-cov-2 S omicron spike B.1.1.529 - rbd down - 1-P2G3 Fab (local) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7QTK
Type
protein
Length
643 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Surface glycoprotein; P2G3 heavy chain; P2G3 light chain
UniProt
A0A8A4XEV3
Ligands
NAG
Pockets
6 · best druggability 0.61

Structure

electron microscopy · 3 distinct chains · 9% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
DSurface glycoproteinprotein20112% helix, 22% strandA0A8A4XEV3
BP2G3 heavy chainprotein2288% helix, 46% strand—
CP2G3 light chainprotein2147% helix, 49% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11250.610.8627empty
24450.570.7461empty
31810.500.7726empty
41320.480.7823empty
5690.310.7513empty

Interfaces

3 interfaces between chains.

  • B–C · 2109 Ų buried · 7 hydrogen bonds · protein-protein
  • D–B · 601 Ų buried · 4 hydrogen bonds · protein-protein
  • D–C · 90 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 7QTK · SARS-CoV-2 S Omicron Spike B.1.1.529 - RBD down - 1-P2G3 Fab (Local) · the same entry in another collection · chain D against D, TM-score 1.00

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