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SARS cov-2 spike protein, bristol uk deletion variant, closed conformation, C3 symmetry

Analyse SARS cov-2 spike protein, bristol uk deletion variant, closed conformation, C3… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7OD3
Type
protein
Length
3,036 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
EIC, NAG
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 1 distinct chain · 22% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CSpike glycoproteinprotein101222% helix, 32% strandP0DTC2

Ligands and binding sites

  • EIC · Linoleic acid · ligand · 3 copies · chains A, C, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 33 copies · chains A, C, 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, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111020.850.86132empty
22970.850.9536EIC
310380.850.8578empty
47760.840.8785empty
53030.840.9436EIC

Interfaces

3 interfaces between chains.

  • A–C · 6137 Ų buried · 49 hydrogen bonds · protein-protein
  • B–C · 6109 Ų buried · 49 hydrogen bonds · protein-protein
  • A–B · 6091 Ų buried · 51 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 33 disulfide, 33 glycan (disulfide, N-glycosylation).

Compared structures

  • 7OD3 · SARS CoV-2 Spike protein, Bristol UK Deletion variant, Closed conformation, C3 symmetry · the same entry in another collection · chain A against A, TM-score 1.00

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