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Crystal structures of clostridium thermocellum xyloglucanase

Analyse Crystal structures of clostridium thermocellum xyloglucanase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2CN3
Type
protein
Length
1,456 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-1,4-xyloglucan hydrolase
EC
3.2.1.151
UniProt
Q70DK5
Ligands
BGC, XYS, GAL, GLC, CA
Pockets
10 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 3% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BBeta-1,4-xyloglucan hydrolase (EC 3.2.1.151)protein7283% helix, 39% strandQ70DK5

Ligands and binding sites

  • BGC · beta-D-glucopyranose · sugar · 12 copies · chains A, B
  • XYS · alpha-D-xylopyranose · sugar · 12 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 5 copies · chains A, B
  • GLC · alpha-D-glucopyranose · sugar · 4 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18630.820.8483CA
25340.810.8745CA
38470.770.8192BGC, XYS, GLC
44180.740.8453empty
54810.660.7846BGC, XYS, GLC

Interfaces

1 interface between chains.

  • A–B · 353 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 2CN3 · Crystal Structures of Clostridium thermocellum Xyloglucanase · the same entry in another collection · chain A against A, TM-score 1.00
  • Q70DK5 · AlphaFold monomer V2.0 prediction for xyloglucanase XGH74A (Q70DK5) · a predicted model of the same protein · chain A against A, TM-score 1.00

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