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Crystal structure of COXYL43, GH43 beta-XYLOSIDASE/ALPHA- arabinofuranosidase from a compostmicrobial metagenome in complex with xylotriose, calcium-bound form

Analyse Crystal structure of COXYL43, GH43 beta-XYLOSIDASE/ALPHA- arabinofuranosidase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5GLN
Type
protein
Length
655 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycoside hydrolase family 43
UniProt
A0A0H5BL38
Ligands
XYP, XYS, CA, NA
Pockets
6 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 4% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlycoside hydrolase family 43protein3304% helix, 42% strandA0A0H5BL38
BGlycoside hydrolase family 43protein3254% helix, 42% strandA0A0H5BL38

Ligands and binding sites

  • XYP · beta-D-xylopyranose · sugar · 11 copies · chains A, B
  • XYS · alpha-D-xylopyranose · sugar · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11230.710.9226XYP, XYS
21630.680.8832XYP, XYS
37120.670.7573XYP, NA, ACT
42100.560.7923empty
52170.560.7823empty

Interfaces

1 interface between chains.

  • A–B · 620 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5GLN · Crystal structure of CoXyl43, GH43 beta-xylosidase/alpha-arabinofuranosidase from a… · the same entry in another collection · chain A against A, TM-score 1.00

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