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Prefusion 2019-ncov spike glycoprotein with a single receptor-binding domain up

Analyse Prefusion 2019-ncov spike glycoprotein with a single receptor-binding domain up in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VSB
Type
protein
Length
2,905 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 3 distinct chains · 23% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein95923% helix, 29% strandP0DTC2
BSpike glycoproteinprotein97322% helix, 31% strandP0DTC2
CSpike glycoproteinprotein97323% helix, 30% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 61 copies · chains A, B, C

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
110280.860.87122empty
25470.820.8866empty
38110.820.8583empty
45750.810.8779empty
55110.780.8552empty

Interfaces

3 interfaces between chains.

  • B–C · 4992 Ų buried · 41 hydrogen bonds · protein-protein
  • A–C · 4714 Ų buried · 32 hydrogen bonds · protein-protein
  • A–B · 4601 Ų buried · 37 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 44 glycan, 35 disulfide (N-glycosylation, disulfide).

Compared structures

  • 6VSB · Prefusion 2019-nCoV spike glycoprotein with a single receptor-binding domain up · the same entry in another collection · chain A against A, TM-score 1.00

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