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The crystal structure of hemagglutinin from a H3N8 influenza virus isolated from new england harbor seals

Analyse The crystal structure of hemagglutinin from a H3N8 influenza virus isolated… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4WA1
Type
protein
Length
2,946 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin
UniProt
I6NNE1
Ligands
NAG, BMA
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 25% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FHemagglutininprotein49125% helix, 32% strandI6NNE1

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 28 copies · chains A, B, D, C, E, F
  • BMA · beta-D-mannopyranose · sugar · 2 copies

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111600.870.88136empty
22510.840.9631empty
37170.730.7960empty
49330.720.7675empty
55170.710.8151empty

Interfaces

6 interfaces between chains.

  • E–F · 2462 Ų buried · 30 hydrogen bonds · protein-protein
  • C–D · 2451 Ų buried · 30 hydrogen bonds · protein-protein
  • B–D · 2409 Ų buried · 34 hydrogen bonds · protein-protein
  • B–C · 2375 Ų buried · 30 hydrogen bonds · protein-protein
  • A–C · 425 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 36 disulfide, 18 glycan (disulfide, N-glycosylation).

Compared structures

  • 4WA1 · The crystal structure of hemagglutinin from a H3N8 influenza virus isolated from New… · the same entry in another collection · chain A against A, TM-score 1.00

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