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Structure of the Quorum Quenching lactonase from Parageobacillus caldoxylosilyticus bind to substrate C4-AHL

Analyse Structure of the Quorum Quenching lactonase from Parageobacillus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6N9Q
Type
protein
Length
554 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.35
Source
Parageobacillus caldoxylosilyticus NBRC 107762
Molecule
Lactonase GcL
UniProt
A0A023DFE8
Ligands
HL4, CO, FE, SO4
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · resolution 2.35 · 1 distinct chain · 27% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
P, DLactonase GcLprotein27727% helix, 29% strandA0A023DFE8

Ligands and binding sites

  • HL4 · N-[(3S)-2-oxotetrahydrofuran-3-yl]butanamide · ligand · 2 copies · chains P, D
  • CO · Cobalt (II) ion · metal · 2 copies · chains P, D
  • FE · Fe (III) ion · metal · 2 copies · chains P, D
  • SO4 · Sulfate ion · ion · 5 copies · chains P, D
  • EDO · 1,2-ethanediol · additive · 15 copies · chains P, D
  • 1PE · Pentaethylene glycol · additive · 4 copies · chains P, D
  • PGE · Triethylene glycol · additive · 4 copies · chains P, D
  • ACT · Acetate ion · additive · 3 copies · chains P, D

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

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14160.650.7852HL4, EDO
22070.620.8228HL4, EDO

Interfaces

1 interface between chains.

  • P–D · 749 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 6N9Q · Structure of the quorum quenching lactonase from parageobacillus caldoxylosilyticus bind… · the same entry in another collection · chain D against D, TM-score 1.00

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