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

Analyse MERS S ectodomain trimer in complex with variable domain of neutralizing… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5W9N
Type
protein
Length
4,021 residues
Chains
10
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MERS S; G4 vh; G4 vl
UniProt
W5ZZF5
Pockets
20 · best druggability 0.85

Structure

electron microscopy · 5 distinct chains · 24% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DMERS Sprotein46340% helix, 18% strandW5ZZF5
B, EG4 vhprotein1198% helix, 54% strand—
C, FG4 vlprotein1113% helix, 53% strand—
GMERS Sprotein45739% helix, 17% strandW5ZZF5
H, I, JMERS Sprotein72611% helix, 37% strandW5ZZF5

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19710.850.8696empty
210850.840.85120empty
310330.840.8594empty
411320.830.84104empty
511670.830.84137empty

Interfaces

18 interfaces between chains.

  • A–J · 2064 Ų buried · 23 hydrogen bonds · protein-protein
  • G–I · 2011 Ų buried · 22 hydrogen bonds · protein-protein
  • D–H · 1726 Ų buried · 27 hydrogen bonds · protein-protein
  • D–G · 1651 Ų buried · 17 hydrogen bonds · protein-protein
  • A–D · 1631 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 53 disulfide (disulfide).

Compared structures

  • 5W9N · MERS S ectodomain trimer in complex with variable domain of neutralizing antibody G4 · the same entry in another collection · chain I against I, TM-score 1.00

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