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MolNFT v1 · #138144 · protein

MERS S ectodomain trimer in complex with variable domain of neutralizing antibody G4

5W9O · Spike glycoprotein: “MERS S ectodomain trimer in complex with variable domain of neutralizing antibody G4”. Electron microscopy, 20 pockets (best druggability 0.86). MolNFT v1 #138144 on GenesisL1: 3D structure, binding sites and…

PDB
5W9O
Type
protein
Length
4,257 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spike glycoprotein; G4 vh; G4 vl
UniProt
W5ZZF5
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 4 distinct chains · 19% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, GSpike glycoproteinprotein46340% helix, 18% strandW5ZZF5
B, E, HG4 vhprotein1198% helix, 58% strand—
C, F, IG4 vlprotein1113% helix, 48% strand—
J, K, LSpike glycoproteinprotein72610% helix, 36% strandW5ZZF5

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19650.860.87114empty
27270.840.8885empty
38930.840.8689empty
410560.820.83101empty
51230.800.9725empty

Interfaces

21 interfaces between chains.

  • A–L · 2083 Ų buried · 19 hydrogen bonds · protein-protein
  • G–K · 2081 Ų buried · 23 hydrogen bonds · protein-protein
  • D–J · 1708 Ų buried · 24 hydrogen bonds · protein-protein
  • D–G · 1603 Ų buried · 14 hydrogen bonds · protein-protein
  • A–D · 1556 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 54 disulfide (disulfide).

Compared structures

  • 5W9O · MERS S ectodomain trimer in complex with variable domain of neutralizing antibody G4 · the same entry in another collection · chain A against A, TM-score 1.00

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