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Crystal structure of A/VICTORIA/361/2011 (H3N2) influenza virus hemagglutinin

Analyse Crystal structure of A/VICTORIA/361/2011 (H3N2) influenza virus hemagglutinin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4O5N
Type
protein
Length
490 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin HA1 chain; Hemagglutinin HA2 chain
UniProt
R9U684
Ligands
NAG, BMA
Pockets
5 · best druggability 0.60

Structure

x-ray diffraction · 2 distinct chains · 25% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin HA1 chainprotein31710% helix, 40% strandR9U684
BHemagglutinin HA2 chainprotein17353% helix, 15% strandR9U684

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar
  • GOL · Glycerol · additive · 8 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.600.9218empty
2570.560.8919empty
3900.370.7617empty
4710.330.7515GOL
5530.280.7516empty

Interfaces

1 interface between chains.

  • A–B · 3010 Ų buried · 45 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 4O5N · Crystal structure of A/Victoria/361/2011 (H3N2) influenza virus hemagglutinin · the same entry in another collection · chain A against A, TM-score 1.00

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