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Influenza hemagglutinin in complex with CH67 Fab

Analyse Influenza hemagglutinin in complex with CH67 Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4HKX
Type
protein
Length
639 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin HA1; CH67 heavy chain; CH67 light chain
UniProt
A7UPX0
Ligands
NAG
Pockets
8 · best druggability 0.66

Structure

x-ray diffraction · 3 distinct chains · 10% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
EHemagglutinin HA1protein21213% helix, 38% strandA7UPX0
ACH67 heavy chainprotein2268% helix, 49% strand—
BCH67 light chainprotein2018% helix, 51% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17220.660.7571empty
21670.650.8539empty
31550.630.8524empty
41290.460.7826empty
5720.440.8114empty

Interfaces

3 interfaces between chains.

  • A–B · 1881 Ų buried · 10 hydrogen bonds · protein-protein
  • E–A · 604 Ų buried · 11 hydrogen bonds · protein-protein
  • E–B · 317 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 4HKX · Influenza hemagglutinin in complex with CH67 Fab · the same entry in another collection · chain B against B, TM-score 1.00

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