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Crystal structure of epoxide hydrolase VREH1 from vigna radiata

Analyse Crystal structure of epoxide hydrolase VREH1 from vigna radiata in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5XMD
Type
protein
Length
1,255 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Epoxide hydrolase a
UniProt
E5L4L1
Pockets
8 · best druggability 0.83

Structure

x-ray diffraction · 4 distinct chains · 45% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEpoxide hydrolase aprotein32044% helix, 16% strandE5L4L1
BEpoxide hydrolase aprotein32244% helix, 16% strandE5L4L1
CEpoxide hydrolase aprotein30545% helix, 16% strandE5L4L1
DEpoxide hydrolase aprotein30845% helix, 17% strandE5L4L1

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111910.830.8490empty
28700.810.8371empty
38810.800.8268empty
47700.800.8360empty
52540.480.7429empty

Interfaces

3 interfaces between chains.

  • A–C · 412 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 259 Ų buried · 3 hydrogen bonds · protein-protein
  • C–D · 170 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 5XMD · Crystal structure of epoxide hydrolase VrEH1 from Vigna radiata · the same entry in another collection · chain A against A, TM-score 1.00

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