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Structure of the hemagglutinin-neuraminidase from human parainfluenza virus type III: complex with NEU5AC2EN

Analyse Structure of the hemagglutinin-neuraminidase from human parainfluenza virus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1V3D
Type
protein
Length
862 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.28
Source
Human parainfluenza virus 3
Molecule
hemagglutinin-neuraminidase glycoprotein
EC
3.2.1.18
Ligands
NAG, DAN, CA, SO4
Pockets
11 · best druggability 0.77

Structure

x-ray diffraction · resolution 2.28 · 1 distinct chain · 6% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, Bhemagglutinin-neuraminidase glycoprotein (EC 3.2.1.18)protein4316% helix, 45% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B
  • DAN · 2-deoxy-2,3-dehydro-N-acetyl-neuraminic acid · sugar · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1960.770.9829empty
24220.750.8566SO4
33730.650.7932DAN
43760.650.7931SO4, DAN
51700.600.8226empty

Interfaces

1 interface between chains.

  • A–B · 1669 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 14 disulfide, 6 glycan (disulfide, N-glycosylation).

Compared structures

  • 1V3D · Structure of the hemagglutinin-neuraminidase from human parainfluenza virus type III… · the same entry in another collection · chain A against A, TM-score 1.00

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