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Crystal structure of an inverting family GH156 exosialidase from uncultured bacterium PG7 in complex with N-acetyl-2,3-dehydro-2- deoxyneuraminic acid

Analyse Crystal structure of an inverting family GH156 exosialidase from uncultured… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6S0E
Type
protein
Length
992 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Exosialidase from uncultured bacterium PG7
EC
3.2.1.18
Ligands
DAN
Pockets
6 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 30% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BExosialidase from uncultured bacterium PG7 (EC 3.2.1.18)protein49630% helix, 22% strand—

Ligands and binding sites

  • DAN · 2-deoxy-2,3-dehydro-N-acetyl-neuraminic acid · ligand · 2 copies · chains A, B
  • GOL · Glycerol · additive · 7 copies · chains A, B
  • ACT · Acetate ion · additive · 5 copies · chains A, B
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · 2 copies · chains A, B
  • PG4 · Tetraethylene glycol · additive · chains 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, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17180.860.8980TRS, GOL
24260.690.8138empty
33920.680.8140GOL
42900.620.8030TRS
51620.530.7924GOL, PG4, DAN

Interfaces

1 interface between chains.

  • A–B · 1839 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 6S0E · Crystal structure of an inverting family GH156 exosialidase from uncultured bacterium pG7… · the same entry in another collection · chain A against A, TM-score 1.00

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