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H5 (VN1194) ASN186LYS mutant haemagglutinin in complex with avian receptor analogue 3'SLN

Analyse H5 (VN1194) ASN186LYS mutant haemagglutinin in complex with avian receptor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4CQS
Type
protein
Length
483 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin HA1; Hemagglutinin HA2
UniProt
Q6DQ34
Ligands
NAG, MAN, BMA
Pockets
3 · best druggability 0.58

Structure

x-ray diffraction · 2 distinct chains · 23% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin HA1protein3219% helix, 40% strandQ6DQ34
BHemagglutinin HA2protein16251% helix, 14% strandQ6DQ34

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 2 copies
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • MPO · 3[N-morpholino]propane sulfonic acid · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13000.580.7741empty
2580.420.8213empty
3580.300.7513empty

Interfaces

1 interface between chains.

  • A–B · 2492 Ų buried · 36 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 5 glycan (disulfide, N-glycosylation).

Compared structures

  • 4CQS · H5 (VN1194) Asn186Lys Mutant Haemagglutinin in Complex with Avian Receptor Analogue 3'SLN · the same entry in another collection · chain A against A, TM-score 1.00

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