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The crystal structure of hemagglutinin from 1968 H3N2 influenza virus

Analyse The crystal structure of hemagglutinin from 1968 H3N2 influenza virus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4WE4
Type
protein
Length
493 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin HA1 chain; Hemagglutinin HA2 chain
UniProt
Q91MA7
Ligands
NAG, MAN, BMA
Pockets
4 · best druggability 0.60

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin HA1 chainprotein32110% helix, 40% strandQ91MA7
BHemagglutinin HA2 chainprotein17251% helix, 14% strandQ91MA7

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 11 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 4 copies
  • BMA · beta-D-mannopyranose · sugar · 3 copies
  • PEG · Di(hydroxyethyl)ether · additive · 7 copies · chains A, B
  • PE5 · 3,6,9,12,15,18,21,24-octaoxahexacosan-1-ol · additive · chains A, B

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1600.600.9118PEG
2670.510.8616empty
31470.420.7521PE5
4710.340.7621PEG

Interfaces

1 interface between chains.

  • A–B · 3083 Ų buried · 49 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 6 glycan (disulfide, N-glycosylation).

Compared structures

  • 4WE4 · The crystal structure of hemagglutinin from 1968 H3N2 influenza virus · the same entry in another collection · chain A against A, TM-score 1.00

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