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Crystal structure of 2009 pandemic H1N1 neuraminidase complexed with laninamivir

Analyse Crystal structure of 2009 pandemic H1N1 neuraminidase complexed with laninamivir in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TI3
Type
protein
Length
774 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Neuraminidase
UniProt
C3W5S3
Ligands
LNV, NAG, CA
Pockets
5 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 3% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BNeuraminidaseprotein3873% helix, 46% strandC3W5S3

Ligands and binding sites

  • LNV · 5-acetamido-2,6-anhydro-4-carbamimidamido-3,4,5-trideoxy-7-O-methyl-D-glycero-D-galacto-non-2-enonic acid · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • CA · Calcium ion · metal · 5 copies · chains A, B
  • GOL · Glycerol · additive · 3 copies · chains A, B
  • ACT · Acetate ion · additive · 3 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12570.650.8340LNV, ACT
22820.630.8139LNV, GOL
31980.570.8027GOL
41170.390.7423empty
5530.290.7615empty

Interfaces

1 interface between chains.

  • A–B · 1576 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 3TI3 · Crystal structure of 2009 pandemic H1N1 neuraminidase complexed with laninamivir · the same entry in another collection · chain A against A, TM-score 1.00

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