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Influenza virus hemagglutinin, (escape) mutant with thr 131 replaced by ile, complexed with a neutralizing antibody

Analyse Influenza virus hemagglutinin, (escape) mutant with thr 131 replaced by ile… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VIS
Type
protein
Length
698 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Immunoglobulin (IGG1, lambda); Hemagglutinin
UniProt
P03437
Ligands
NAG, ZN
Pockets
5 · best druggability 0.64

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AImmunoglobulin (IGG1, lambda)protein2108% helix, 52% strand—
BImmunoglobulin (IGG1, lambda)protein2215% helix, 50% strand—
CHemagglutininprotein26712% helix, 41% strandP03437

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains C
  • ZN · Zinc ion · metal · 3 copies · chains A, B, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14240.640.7856empty
24880.590.7452empty
32430.540.7726empty
4610.390.8019empty
5650.310.7516empty

Interfaces

3 interfaces between chains.

  • A–B · 1857 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 680 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 54 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 2VIS · Influenza virus hemagglutinin, (escape) mutant with thr 131 replaced by ile, complexed… · the same entry in another collection · chain A against A, TM-score 1.00

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