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Enterovirus D68 in complex with human monoclonal antibody EV68-159

Analyse Enterovirus D68 in complex with human monoclonal antibody EV68-159 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6WDS
Type
protein
Length
1,025 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
EV68-159 light chain; Viral protein 1; Viral protein 2; Viral protein 3; Viral protein 4…
UniProt
A0A097BW12, A0A0A7X639, A0A126D252
Pockets
13 · best druggability 0.76

Structure

electron microscopy · 6 distinct chains · 8% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LEV68-159 light chainprotein1060% helix, 42% strand—
AViral protein 1protein2919% helix, 32% strandA0A097BW12
BViral protein 2protein23813% helix, 37% strandA0A0A7X639
CViral protein 3protein2458% helix, 30% strandA0A097BW12
DViral protein 4protein3013% helix, 10% strandA0A126D252
HEV68-159 heavy chainprotein1153% helix, 32% strand—

Pockets

13 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13310.760.8755empty
22310.700.8738empty
33370.640.7944empty
43300.630.7929empty
51960.520.7733empty

Interfaces

12 interfaces between chains.

  • A–C · 4623 Ų buried · 69 hydrogen bonds · protein-protein
  • A–B · 2102 Ų buried · 39 hydrogen bonds · protein-protein
  • B–C · 1822 Ų buried · 26 hydrogen bonds · protein-protein
  • A–D · 896 Ų buried · 13 hydrogen bonds · protein-protein
  • L–H · 853 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 6WDS · Enterovirus D68 in complex with human monoclonal antibody EV68-159 · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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