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Engineering the active site of a GH43 glycoside hydrolase generates a biotechnologically significant enzyme that displays both endo- xylanase and exo-arabinofuranosidase activity

Analyse Engineering the active site of a GH43 glycoside hydrolase generates a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ZXL
Type
protein
Length
1,063 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIAXHD3
EC
3.2.1.55
Pockets
8 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 4% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIAXHD3 (EC 3.2.1.55)protein5304% helix, 47% strand—
BHIAXHD3 (EC 3.2.1.55)protein5334% helix, 47% strand—

Ligands and binding sites

  • B3P · 2-[3-(2-hydroxy-1,1-dihydroxymethyl-ethylamino)-propylamino]-2-hydroxymethyl-propane-1,3-diol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15510.650.7678empty
23180.570.7634empty
32160.560.7921empty
42130.560.7922empty
52370.550.7730B3P

Interfaces

1 interface between chains.

  • A–B · 354 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 3ZXL · Engineering the active site of a GH43 glycoside hydrolase generates a biotechnologically… · the same entry in another collection · chain A against A, TM-score 1.00

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