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Crystal structure of barley beta-amylase complexed with 3,4- epoxybutyl alpha-D-glucopyranoside

Analyse Crystal structure of barley beta-amylase complexed with 3,4- epoxybutyl… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2XGI
Type
protein
Length
487 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-amylase
EC
3.2.1.2
UniProt
P16098
Ligands
J5B, EBQ
Pockets
5 · best druggability 0.73

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-amylase (EC 3.2.1.2)protein48738% helix, 12% strandP16098

Ligands and binding sites

  • J5B · (3R)-3-hydroxybutyl alpha-D-glucopyranoside · ligand · chains A
  • EBQ · (3S)-3-hydroxybutyl alpha-D-glucopyranoside · ligand · chains A
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15940.730.8151J5B, EBQ
21620.580.8239empty
3540.340.7814empty
4560.300.7619empty
5530.290.7517empty

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 2XGI · Crystal structure of Barley Beta-Amylase complexed with 3,4- epoxybutyl… · the same entry in another collection · chain A against A, TM-score 1.00
  • P16098 · AlphaFold monomer V2.0 prediction for beta-amylase (P16098) · a predicted model of the same protein · chain A against A, TM-score 0.99

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