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Crystal structure of the ivr-165 (H3N2) influenza virus hemagglutinin in complex with 3'-slnln

Analyse Crystal structure of the ivr-165 (H3N2) influenza virus hemagglutinin in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6NSA
Type
protein
Length
486 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin HA1 chain; Hemagglutinin HA2 chain
UniProt
L0HR89
Ligands
NAG, MAN, BMA, GAL, SIA
Pockets
5 · best druggability 0.56

Structure

x-ray diffraction · 2 distinct chains · 25% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin HA1 chainprotein31710% helix, 41% strandL0HR89
BHemagglutinin HA2 chainprotein16954% helix, 14% strandL0HR89

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 14 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 4 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 3 copies
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A
  • SIA · N-acetyl-alpha-neuraminic acid · sugar · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1570.560.8920empty
21020.370.7518empty
3560.290.7517empty
4610.290.7416SIA
5520.230.7212empty

Interfaces

1 interface between chains.

  • A–B · 2986 Ų buried · 52 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 glycan, 6 disulfide (N-glycosylation, disulfide).

Compared structures

  • 6NSA · Crystal structure of the IVR-165 (H3N2) influenza virus hemagglutinin in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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