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Crystal structure of endoglycosidase E GH18 domain from enterococcus faecalis in complex with MAN5 product

Analyse Crystal structure of endoglycosidase E GH18 domain from enterococcus faecalis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7PUK
Type
protein
Length
847 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-N-acetylhexosaminidase
EC
3.2.1.52
UniProt
Q6U890
Ligands
MAN, NAG, BMA
Pockets
7 · best druggability 0.52

Structure

x-ray diffraction · 2 distinct chains · 51% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-N-acetylhexosaminidase (EC 3.2.1.52)protein42551% helix, 11% strandQ6U890
CBeta-N-acetylhexosaminidase (EC 3.2.1.52)protein42250% helix, 11% strandQ6U890

Ligands and binding sites

  • MAN · alpha-D-mannopyranose · sugar · 8 copies · chains A, C
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A, C
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13120.520.7347NAG, BMA, MAN
2590.450.8317empty
3550.430.8317empty
41250.410.7527NAG, BMA, MAN
5620.310.7517empty

Interfaces

1 interface between chains.

  • A–C · 105 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 7PUK · Crystal structure of Endoglycosidase E GH18 domain from Enterococcus faecalis in complex… · the same entry in another collection · chain A against A, TM-score 1.00

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