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SARS-cov-2 D614G 1-rbd up spike protein trimer without the P986-P987 stabilizing mutations (S-gsas-D614G)

Analyse SARS-cov-2 D614G 1-rbd up spike protein trimer without the P986-P987… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7KDL
Type
protein
Length
2,875 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 0.83

Structure

electron microscopy · 3 distinct chains · 24% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpike glycoproteinprotein96625% helix, 33% strandP0DTC2
BSpike glycoproteinprotein94924% helix, 34% strandP0DTC2
CSpike glycoproteinprotein96025% helix, 32% strandP0DTC2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 59 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
110390.830.84105empty
211080.830.84119empty
34680.820.9058empty
49220.800.8284empty
56940.760.8182empty

Interfaces

3 interfaces between chains.

  • A–C · 5131 Ų buried · 45 hydrogen bonds · protein-protein
  • A–B · 4735 Ų buried · 45 hydrogen bonds · protein-protein
  • B–C · 4177 Ų buried · 35 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 47 glycan, 35 disulfide (N-glycosylation, disulfide, glycosylation).

Compared structures

  • 7KDL · SARS-CoV-2 D614G 1-RBD up Spike Protein Trimer without the P986-P987 stabilizing… · the same entry in another collection · chain A against A, TM-score 1.00

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