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Crystal structure of a bacterial fucosidase with iminocyclitol (2S,3S, 4R,5S)-3,4-dihydroxy-2-ethynyl-5-methylpyrrolidine

Analyse Crystal structure of a bacterial fucosidase with iminocyclitol (2S,3S… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5I5R
Type
protein
Length
1,761 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-L-fucosidase
UniProt
Q8A3I4
Ligands
68F, SO4
Pockets
8 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, DAlpha-L-fucosidaseprotein44032% helix, 23% strandQ8A3I4
CAlpha-L-fucosidaseprotein44132% helix, 22% strandQ8A3I4

Ligands and binding sites

  • 68F · (2S,3S,4R,5S,2'S,3'S,4'R,5'S)-2,2'-(butane-1,4-diyl)bis(5-methylpyrrolidine-3,4-diol) · ligand · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 8 copies · chains A, B, C, D
  • IMD · Imidazole · additive · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18690.700.7571empty
25580.660.7755empty
33940.630.7851empty
4610.410.801768F
5640.410.801768F

Interfaces

3 interfaces between chains.

  • C–D · 383 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 329 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 107 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5I5R · Crystal structure of a bacterial fucosidase with iminocyclitol… · the same entry in another collection · chain A against A, TM-score 1.00

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