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MolNFT v1 · #83548 · protein

Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in complex with octyl-O-glucoside

3WLM · Beta-D-glucan exohydrolase isoenzyme exoi: “Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in complex with octyl-O-glucoside”. X-ray diffraction, 3 ligands (NAG, BMA, FUC), 2 pockets (best druggability…

PDB
3WLM
Type
protein
Length
602 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-D-glucan exohydrolase isoenzyme exoi
EC
3.2.1.-
UniProt
Q9XEI3
Ligands
NAG, BMA, FUC
Pockets
2 · best druggability 0.51

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-D-glucan exohydrolase isoenzyme exoi (EC 3.2.1.-)protein60238% helix, 13% strandQ9XEI3

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • FUC · alpha-L-fucopyranose · sugar
  • BOG · octyl beta-D-glucopyranoside · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1860.510.8319BOG
2590.310.7616empty

Modifications

Observed in the structure: 3 glycan, 2 disulfide (N-glycosylation, disulfide).

Compared structures

  • 3WLM · Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme exo1 in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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