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Crystal structure of the pce reductive dehalogenase from S. multivorans in complex with iodide

Analyse Crystal structure of the pce reductive dehalogenase from S. multivorans in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4UR2
Type
protein
Length
864 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tetrachloroethene reductive dehalogenase catalytic subunit pcea
EC
1.97.1.8
UniProt
W6EQP0
Ligands
SF4, BVQ, IOD
Pockets
9 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATetrachloroethene reductive dehalogenase catalytic subunit pcea (EC 1.97.1.8)protein44538% helix, 17% strandW6EQP0
BTetrachloroethene reductive dehalogenase catalytic subunit pcea (EC 1.97.1.8)protein41938% helix, 16% strandW6EQP0

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 4 copies · chains A, B
  • BVQ · Norpseudo-B12 · ligand · 2 copies · chains A, B
  • IOD · Iodide ion · ion · 11 copies · chains A, B
  • GOL · Glycerol · additive · 7 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110330.880.8985SF4, BVQ, GOL, IOD
210510.870.8885SF4, BVQ, GOL, IOD
33220.740.8647IOD
42430.700.8633IOD
5690.680.9423empty

Interfaces

1 interface between chains.

  • A–B · 4099 Ų buried · 65 hydrogen bonds · protein-protein

Compared structures

  • 4UR2 · Crystal structure of the PCE reductive dehalogenase from S. multivorans in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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