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Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in complex with 2-deoxy-2-fluoro-alpha-D-glucoside

Analyse Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1IEW
Type
protein
Length
602 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-D-glucan glucohydrolase isoenzyme EXO1
EC
3.2.1.58
Ligands
G2F, NAG, BMA, MAN, FUL
Pockets
2 · best druggability 0.50

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-D-glucan glucohydrolase isoenzyme EXO1 (EC 3.2.1.58)protein60239% helix, 12% strand—

Ligands and binding sites

  • G2F · 2-deoxy-2-fluoro-alpha-D-glucopyranose · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains A
  • MAN · alpha-D-mannopyranose · sugar · chains A
  • FUL · beta-L-fucopyranose · sugar

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
1860.500.8318G2F
2620.320.7616empty

Modifications

Observed in the structure: 3 glycan, 2 disulfide, 1 covalent (N-glycosylation, disulfide, covalent ligand).

Compared structures

  • 1IEW · 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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