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SARS-cov-2 spike in complex with IgG 553-15 (S-553-15 dimer trimer )

Analyse SARS-cov-2 spike in complex with IgG 553-15 (S-553-15 dimer trimer ) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7WO4
Type
protein
Length
9,096 residues
Chains
18
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein; MAB15 vh; MAB15 vl
UniProt
P0DTC2
Ligands
NAG
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 3 distinct chains · 14% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, J, K, LSpike glycoproteinprotein107619% helix, 28% strandP0DTC2
D, F, H, M, O, QMAB15 vhprotein2251% helix, 39% strand—
E, G, I, N, P, RMAB15 vlprotein2153% helix, 29% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 90 copies · chains A, B, C, J, K, L

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
110410.870.88119empty
27230.860.8990empty
310580.850.86107empty
410730.820.8397empty
55940.780.8453empty

Interfaces

33 interfaces between chains.

  • K–L · 4032 Ų buried · 35 hydrogen bonds · protein-protein
  • J–K · 3998 Ų buried · 35 hydrogen bonds · protein-protein
  • B–C · 3993 Ų buried · 36 hydrogen bonds · protein-protein
  • A–B · 3968 Ų buried · 34 hydrogen bonds · protein-protein
  • A–C · 3814 Ų buried · 37 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 104 disulfide, 90 glycan (disulfide, N-glycosylation).

Compared structures

  • 7WO4 · SARS-CoV-2 Spike in complex with IgG 553-15 (S-553-15 dimer trimer ) · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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