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Structure of wild type Bt4394, a GH20 family sulfoglycosidase, in complex with 6S-GlcNAc

Analyse Structure of wild type Bt4394, a GH20 family sulfoglycosidase, in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DVA
Type
protein
Length
1,045 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.55
Source
Bacteroides thetaiotaomicron
Molecule
Beta-N-acetylhexosaminidase
EC
3.2.1.52
UniProt
A0A0P0FIE8
Ligands
NGS
Pockets
6 · best druggability 0.82

Structure

x-ray diffraction · resolution 1.55 · 2 distinct chains · 37% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BBeta-N-acetylhexosaminidase (EC 3.2.1.52)protein52237% helix, 19% strandA0A0P0FIE8
ABeta-N-acetylhexosaminidase (EC 3.2.1.52)protein52336% helix, 20% strandA0A0P0FIE8

Ligands and binding sites

  • NGS · 2-acetamido-2-deoxy-6-O-sulfo-beta-D-glucopyranose · sugar · 2 copies · chains B, A
  • GOL · Glycerol · additive · 5 copies · chains B, A

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19590.820.8391GOL, NGS
22770.770.8938empty
31340.520.8019NGS, GOL
41210.480.7925empty
5940.320.7322empty

Interfaces

1 interface between chains.

  • B–A · 1020 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 7DVA · A complex of a new GH20 enzyme from bacteroides thetaiotaomicron · the same entry in another collection · chain A against A, TM-score 1.00

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