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Hantaan virus gn in complex with Fab nnhtn-GN2

Analyse Hantaan virus gn in complex with Fab nnhtn-GN2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7O9S
Type
protein
Length
770 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab nnhtn-GN2 heavy chain; Fab nnhtn-GN2 light chain; Envelope polyprotein
UniProt
A0A077D153
Ligands
NAG
Pockets
8 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HFab nnhtn-GN2 heavy chainprotein2166% helix, 51% strand—
LFab nnhtn-GN2 light chainprotein2146% helix, 53% strand—
AEnvelope polyproteinprotein34014% helix, 45% strandA0A077D153

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A
  • GOL · Glycerol · additive · 3 copies · chains H, A, L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14800.610.7551GOL
21360.560.8328empty
31370.530.8125empty
41070.520.8219empty
51090.490.8121empty

Interfaces

3 interfaces between chains.

  • H–L · 1942 Ų buried · 23 hydrogen bonds · protein-protein
  • H–A · 587 Ų buried · 12 hydrogen bonds · protein-protein
  • L–A · 425 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 13 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 7O9S · Hantaan virus Gn in complex with Fab nnHTN-Gn2 · the same entry in another collection · chain H against H, TM-score 1.00

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