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Crystal structures of the nipah G attachment glycoprotein

Analyse Crystal structures of the nipah G attachment glycoprotein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3D11
Type
protein
Length
427 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemagglutinin-neuraminidase
EC
3.2.1.18
UniProt
Q9IH62
Ligands
NAG, BMA, MAN, IOD
Pockets
4 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemagglutinin-neuraminidase (EC 3.2.1.18)protein4275% helix, 47% strandQ9IH62

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 7 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • MAN · alpha-D-mannopyranose · sugar
  • IOD · Iodide ion · ion · 19 copies · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1600.700.9726empty
24570.670.7941IOD
3530.420.8312empty
4810.360.7622IOD

Modifications

Observed in the structure: 7 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 3D11 · Crystal Structures of the Nipah G Attachment Glycoprotein · the same entry in another collection · chain A against A, TM-score 1.00

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