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First crystal structure of an endo-inulinase, from aspergillus ficuum: structural analysis and comparison with other GH32 enzymes.

Analyse First crystal structure of an endo-inulinase, from aspergillus ficuum… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3RWK
Type
protein
Length
493 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Inulinase
EC
3.2.1.7
UniProt
O94220
Ligands
MAN, NAG, FRU, BMA, NA, SO4
Pockets
4 · best druggability 0.59

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
XInulinase (EC 3.2.1.7)protein4935% helix, 49% strandO94220

Ligands and binding sites

  • MAN · alpha-D-mannopyranose · sugar · 3 copies · chains X
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains X
  • FRU · beta-D-fructofuranose · sugar · 2 copies · chains X
  • BMA · beta-D-mannopyranose · sugar
  • NA · Sodium ion · metal · chains X
  • SO4 · Sulfate ion · ion · chains X
  • ACT · Acetate ion · additive · chains X

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13300.590.7734FRU
22390.520.7634SO4
3850.430.8026ACT
4660.400.7916empty

Modifications

Observed in the structure: 1 glycan (N-glycosylation).

Compared structures

  • 3RWK · First crystal structure of an endo-inulinase, from Aspergillus ficuum: structural… · the same entry in another collection · chain X against X, TM-score 1.00
  • O94220 · AlphaFold monomer V2.0 prediction for extracellular endo-inulinase INU2 (O94220) · a predicted model of the same protein · chain X against A, TM-score 0.99

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