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Crystal structure of GII.10 P domain in complex with 150MM fucose

Analyse Crystal structure of GII.10 P domain in complex with 150MM fucose in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Z4S
Type
protein
Length
626 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Capsid protein
UniProt
Q5F4T5
Ligands
FUL, NO3
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACapsid proteinprotein3148% helix, 36% strandQ5F4T5
BCapsid proteinprotein3127% helix, 35% strandQ5F4T5

Ligands and binding sites

  • FUL · beta-L-fucopyranose · sugar · 4 copies · chains A, B
  • NO3 · Nitrate ion · ion · chains A
  • EDO · 1,2-ethanediol · additive · 7 copies · chains A, B

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

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110420.800.81117EDO
21460.600.8425empty
31620.510.7926EDO
4520.260.7415empty

Interfaces

1 interface between chains.

  • A–B · 1900 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 4Z4S · Crystal structure of GII.10 P domain in complex with 150mM fucose · the same entry in another collection · chain A against A, TM-score 1.00

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