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Crystal structure of alpha-glucosidase from weissella cibaria BKK1 in complex with maltose

Analyse Crystal structure of alpha-glucosidase from weissella cibaria BKK1 in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7EHH
Type
protein
Length
588 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-glucosidase
EC
3.2.1.20
Ligands
GLC, CA, SO4
Pockets
6 · best druggability 0.61

Structure

x-ray diffraction · 1 distinct chain · 31% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-glucosidase (EC 3.2.1.20)protein58831% helix, 25% strand—

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A
  • CA · Calcium ion · metal · chains A
  • SO4 · Sulfate ion · ion · 6 copies · chains A
  • GOL · Glycerol · additive · 3 copies · chains A
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12860.610.7939GLC
22660.580.7832empty
3720.410.8016empty
4510.330.7814empty
5530.310.7713empty

Compared structures

  • 7EHH · Crystal structure of alpha-glucosidase from Weissella cibaria BKK1 in complex with maltose · the same entry in another collection · chain A against A, TM-score 1.00

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