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Crystal structure of the GH74 xyloglucanase from xanthomonas campestris (XCC1752)

Analyse Crystal structure of the GH74 xyloglucanase from xanthomonas campestris… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7KN8
Type
protein
Length
1,415 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cellulase
UniProt
Q8P9U5
Ligands
BGC, XYS, NA, IOD
Pockets
13 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 4% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACellulaseprotein7074% helix, 40% strandQ8P9U5
BCellulaseprotein7084% helix, 40% strandQ8P9U5

Ligands and binding sites

  • BGC · beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • XYS · alpha-D-xylopyranose · sugar · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B
  • IOD · Iodide ion · ion · 14 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B

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

Pockets

13 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12690.830.9446EDO, NA
22260.830.9636EDO, NA
36880.810.8548empty
46630.800.8546EDO
58840.730.7765BGC, XYS, EDO, IOD

Interfaces

1 interface between chains.

  • A–B · 586 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 7KN8 · Crystal structure of the GH74 xyloglucanase from Xanthomonas campestris (Xcc1752) · the same entry in another collection · chain A against A, TM-score 1.00

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