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The complex structure of hemagglutinin-esterase-fusion mutant protein from the influenza D virus with receptor analog 9-N-ac-sia

Analyse The complex structure of hemagglutinin-esterase-fusion mutant protein from the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5E66
Type
protein
Length
573 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin-esterase
UniProt
K9LG83
Ligands
5KQ, NAG, MAN, BMA
Pockets
2 · best druggability 0.31

Structure

x-ray diffraction · 2 distinct chains · 18% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin-esteraseprotein42413% helix, 32% strandK9LG83
BHemagglutinin-esteraseprotein14934% helix, 10% strandK9LG83

Ligands and binding sites

  • 5KQ · (6R)-5-acetamido-6-[(1S,2S)-3-acetamido-1,2-dihydroxypropyl]-3,5-dideoxy-beta-L-threo-hex-2-ulopyranosonic acid · ligand · 2 copies · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 9 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 3 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · chains A
  • CAC · Cacodylate ion · additive · chains A

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1700.310.7412empty
2530.300.7513empty

Interfaces

1 interface between chains.

  • A–B · 3261 Ų buried · 54 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 5 glycan (disulfide, N-glycosylation).

Compared structures

  • 5E66 · The complex structure of Hemagglutinin-esterase-fusion mutant protein from the influenza… · the same entry in another collection · chain A against A, TM-score 1.00

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