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The structure of hemagglutinin Q226L-G228S mutant from an avian-origin H4N6 influenza virus in complex with human receptor analog lstc

Analyse The structure of hemagglutinin Q226L-G228S mutant from an avian-origin H4N6… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XLD
Type
protein
Length
982 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin
UniProt
A3KF09
Ligands
NAG, GAL, SIA
Pockets
6 · best druggability 0.58

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHemagglutininprotein3199% helix, 39% strandA3KF09
C, DHemagglutininprotein17254% helix, 15% strandA3KF09

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains B, A
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • SIA · N-acetyl-alpha-neuraminic acid · sugar · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12180.580.8034empty
22020.540.7928empty
31600.500.7824empty
41560.500.7825empty
51010.450.8025empty

Interfaces

3 interfaces between chains.

  • B–D · 2979 Ų buried · 42 hydrogen bonds · protein-protein
  • A–C · 2971 Ų buried · 41 hydrogen bonds · protein-protein
  • C–D · 212 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 5XLD · The structure of hemagglutinin Q226L-G228S mutant from an avian-origin H4N6 influenza… · the same entry in another collection · chain A against A, TM-score 1.00

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