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MolNFT v1 · #10047 · protein

Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in complex with cyclohexitol

1IEV: “Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 in complex with cyclohexitol”. X-ray diffraction, 5 ligands (INS, NAG, BMA), 3 pockets (best druggability 0.50). MolNFT v1 #10047 on GenesisL1: 3D structure…

PDB
1IEV
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
INS, NAG, BMA, MAN, FUC
Pockets
3 · best druggability 0.50

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-D-glucan glucohydrolase isoenzyme EXO1 (EC 3.2.1.58)protein60238% helix, 12% strand—

Ligands and binding sites

  • INS · 1,2,3,4,5,6-hexahydroxy-cyclohexane · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A
  • BMA · beta-D-mannopyranose · sugar
  • MAN · alpha-D-mannopyranose · sugar · chains A
  • FUC · alpha-L-fucopyranose · sugar · chains A

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1860.500.8318INS
2650.330.7616empty
3510.240.7214empty

Modifications

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

Compared structures

  • 1IEV · 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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