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West nile virus NS1 in complex with neutralizing 22NS1 antibody Fab

Analyse West nile virus NS1 in complex with neutralizing 22NS1 antibody Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OII
Type
protein
Length
1,214 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Non-structural protein NS1; Light chain of Fab fragment of 22NS1 antibody; Heavy chain of…
UniProt
U3N977
Pockets
13 · best druggability 0.76

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BNon-structural protein NS1protein1775% helix, 32% strandU3N977
L, MLight chain of Fab fragment of 22NS1 antibodyprotein2137% helix, 54% strand—
H, IHeavy chain of Fab fragment of 22NS1 antibodyprotein2176% helix, 54% strand—

Pockets

13 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110610.760.78105empty
21660.710.9028empty
34500.580.7462empty
44020.560.7455empty
5990.480.8121empty

Interfaces

12 interfaces between chains.

  • L–H · 1817 Ų buried · 9 hydrogen bonds · protein-protein
  • M–I · 1810 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 761 Ų buried · 15 hydrogen bonds · protein-protein
  • A–H · 714 Ų buried · 13 hydrogen bonds · protein-protein
  • B–I · 678 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 4OII · West Nile Virus NS1 in complex with neutralizing 22NS1 antibody Fab · the same entry in another collection · chain A against A, TM-score 1.00

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