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Crystal structure of an organic hydroperoxide resistance protein from burkholderia cenocepacia

Analyse Crystal structure of an organic hydroperoxide resistance protein from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4NOZ
Type
protein
Length
290 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Organic hydroperoxide resistance protein
UniProt
B4EPK2
Pockets
3 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AOrganic hydroperoxide resistance proteinprotein14233% helix, 33% strandB4EPK2
BOrganic hydroperoxide resistance proteinprotein14832% helix, 32% strandB4EPK2

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 7 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12370.660.8329EDO
22340.640.8230EDO
3730.340.7616EDO

Interfaces

1 interface between chains.

  • A–B · 3339 Ų buried · 54 hydrogen bonds · protein-protein

Compared structures

  • 4NOZ · Crystal Structure of an Organic Hydroperoxide Resistance Protein from Burkholderia… · the same entry in another collection · chain A against A, TM-score 1.00

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