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Beta-xylosidase, family 43 glycosyl hydrolase from clostridium acetobutylicum

Analyse Beta-xylosidase, family 43 glycosyl hydrolase from clostridium acetobutylicum in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3K1U
Type
protein
Length
314 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-xylosidase, family 43 glycosyl hydrolase
UniProt
Q97IW1
Ligands
MG, NA
Pockets
2 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-xylosidase, family 43 glycosyl hydrolaseprotein3144% helix, 48% strandQ97IW1

Ligands and binding sites

  • MG · Magnesium ion · metal · 3 copies · chains A
  • NA · Sodium ion · metal · chains A
  • EDO · 1,2-ethanediol · additive · 6 copies · chains A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12160.700.8629TRS
22760.570.7726MG

Modifications

Observed in the structure: 7 modified (engineered).

Compared structures

  • 3K1U · Beta-xylosidase, family 43 glycosyl hydrolase from Clostridium acetobutylicum · the same entry in another collection · chain A against A, TM-score 1.00

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