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GII.10 vietnam 026 norovirus protruding domain in complex with nanobody nano-42

Analyse GII.10 vietnam 026 norovirus protruding domain in complex with nanobody nano-42 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5O05
Type
protein
Length
847 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nanobody (vhh) nano-42; Capsid protein
UniProt
Q5F4T5
Pockets
6 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 6% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
CNanobody (vhh) nano-42protein1163% helix, 56% strand—
DNanobody (vhh) nano-42protein1145% helix, 55% strand—
ACapsid proteinprotein3086% helix, 36% strandQ5F4T5
BCapsid proteinprotein3097% helix, 35% strandQ5F4T5

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 39 copies · chains C, D, A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110840.800.81117EDO
21430.550.8222EDO
3880.450.8121EDO
41190.450.7820EDO
51120.440.7724EDO

Interfaces

3 interfaces between chains.

  • A–B · 1884 Ų buried · 24 hydrogen bonds · protein-protein
  • C–B · 648 Ų buried · 4 hydrogen bonds · protein-protein
  • D–A · 647 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 5O05 · GII.10 Vietnam 026 norovirus protruding domain in complex with Nanobody Nano-42 · the same entry in another collection · chain C against C, TM-score 1.00

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