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Crystal structure of the A/PUERTO RICO/8/1934 (H1N1) influenza virus hemagglutinin in complex with cyclic peptide CP141046 (P3)

Analyse Crystal structure of the A/PUERTO RICO/8/1934 (H1N1) influenza virus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5W6I
Type
protein
Length
504 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin; ACE-PH8-orn-leu-glu-tyr-phe-glu-TRP-leu-ser-bal
UniProt
P03452
Ligands
ACE, NAG
Pockets
4 · best druggability 0.56

Structure

x-ray diffraction · 3 distinct chains · 23% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutininprotein3227% helix, 41% strandP03452
BHemagglutininprotein17156% helix, 15% strandP03452
DACE-PH8-orn-leu-glu-tyr-phe-glu-TRP-leu-ser-balprotein110% helix, 0% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains B, D
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1570.560.9017empty
21500.430.7519empty
3890.390.7721empty
4620.340.7717empty

Interfaces

3 interfaces between chains.

  • A–B · 2794 Ų buried · 48 hydrogen bonds · protein-protein
  • B–D · 484 Ų buried · 4 hydrogen bonds · protein-protein
  • A–D · 197 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 6 disulfide, 5 glycan, 3 modified, 1 covalent (disulfide, N-glycosylation, nonstandard, covalent ligand).

Compared structures

  • 5W6I · Crystal structure of the A/Puerto Rico/8/1934 (H1N1) influenza virus hemagglutinin in… · the same entry in another collection · chain A against A, TM-score 1.00

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