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MolNFT v1 · #88306 · protein

Crystal structure of H5 (VN1194) SER227ASN/GLN196ARG mutant haemagglutinin

4CQP · Hemagglutinin HA1: “Crystal structure of H5 (VN1194) SER227ASN/GLN196ARG mutant haemagglutinin”. X-ray diffraction, 3 ligands (NAG, MAN, BMA), 5 pockets (best druggability 0.49). MolNFT v1 #88306 on GenesisL1: 3D structure, binding…

PDB
4CQP
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
5 · best druggability 0.49

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin HA1protein32110% helix, 41% strandQ6DQ34
BHemagglutinin HA2protein16253% 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11890.490.7626empty
21260.480.7930empty
3690.430.8115empty
4680.300.7420empty
5540.280.7413empty

Interfaces

1 interface between chains.

  • A–B · 2466 Ų buried · 37 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 4CQP · Crystal Structure of H5 (VN1194) Ser227Asn/Gln196Arg Mutant Haemagglutinin · the same entry in another collection · chain A against A, TM-score 1.00

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