GL1X · GenesisL1 explorer

MolNFT v1 · #10042 · protein

Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1

1IEQ: “Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1”. X-ray diffraction, 5 ligands (NAG, BMA, MAN), 2 pockets (best druggability 0.51). MolNFT v1 #10042 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
1IEQ
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
NAG, BMA, MAN, FUC, BGC
Pockets
2 · best druggability 0.51

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

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains A
  • MAN · alpha-D-mannopyranose · sugar · chains A
  • FUC · alpha-L-fucopyranose · sugar · chains A
  • BGC · beta-D-glucopyranose · sugar · 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
1810.510.8417BGC
2550.310.7615empty

Modifications

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

Compared structures

  • 1IEQ · Crystal structure of barley beta-D-glucan glucohydrolase isoenzyme EXO1 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.