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Crystal structure of the hemagglutinin of A/XINJIANG/1/2006 virus

Analyse Crystal structure of the hemagglutinin of A/XINJIANG/1/2006 virus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4KDQ
Type
protein
Length
1,455 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin
UniProt
C5HMM2, Q6J0Q2
Ligands
NAG
Pockets
13 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 22% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, EHemagglutininprotein3219% helix, 41% strandC5HMM2
B, D, FHemagglutininprotein16448% helix, 14% strandQ6J0Q2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 7 copies · chains A, C, E

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

Pockets

13 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18810.870.89132empty
2930.770.9815empty
37920.680.7576empty
43760.650.7947empty
54080.650.7951empty

Interfaces

15 interfaces between chains.

  • A–B · 2577 Ų buried · 33 hydrogen bonds · protein-protein
  • E–F · 2571 Ų buried · 37 hydrogen bonds · protein-protein
  • C–D · 2541 Ų buried · 26 hydrogen bonds · protein-protein
  • B–D · 1456 Ų buried · 16 hydrogen bonds · protein-protein
  • D–F · 1361 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 18 disulfide, 7 glycan (disulfide, N-glycosylation).

Compared structures

  • 4KDQ · Crystal structure of the hemagglutinin of A/Xinjiang/1/2006 virus · the same entry in another collection · chain A against A, TM-score 1.00

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