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Crystal structure of the GH1 beta-glucosidase from exiguobacterium antarcticum B7 in space group C2221

Analyse Crystal structure of the GH1 beta-glucosidase from exiguobacterium antarcticum… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5DT7
Type
protein
Length
1,776 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-glucosidase
EC
3.2.1.21
UniProt
K0A8J9
Ligands
SO4
Pockets
7 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 44% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-glucosidase (EC 3.2.1.21)protein44445% helix, 17% strandK0A8J9
BBeta-glucosidase (EC 3.2.1.21)protein44244% helix, 16% strandK0A8J9
C, DBeta-glucosidase (EC 3.2.1.21)protein44544% helix, 17% strandK0A8J9

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 7 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 5 copies · chains A, B, C, D
  • CXS · 3-cyclohexyl-1-propylsulfonic acid · additive · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110240.800.81104CXS
24250.700.8145empty
34580.690.8048CXS
4790.320.7425GOL
5620.300.7412empty

Interfaces

2 interfaces between chains.

  • C–D · 881 Ų buried · 16 hydrogen bonds · protein-protein
  • A–B · 625 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 5DT7 · Crystal structure of the GH1 beta-glucosidase from Exiguobacterium antarcticum B7 in… · the same entry in another collection · chain A against A, TM-score 1.00

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