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Nitroreductase from E-COLI in complex with the dinitrobenzamide prodrug SN23862

Analyse Nitroreductase from E-COLI in complex with the dinitrobenzamide prodrug SN23862 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1OO6
Type
protein
Length
434 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Oxygen-insensitive NAD(P)H nitroreductase
EC
1.6.99.7
UniProt
P38489
Ligands
FMN, SN2
Pockets
4 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 55% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BOxygen-insensitive NAD(P)H nitroreductase (EC 1.6.99.7)protein21755% helix, 15% strandP38489

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B
  • SN2 · 5-[bis-2(chloro-ethyl)-amino]-2,4-dintro-benzamide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14330.740.8342FMN, SN2
25090.720.8145SN2, FMN
31970.510.7725empty
41860.500.7723empty

Interfaces

1 interface between chains.

  • A–B · 3785 Ų buried · 61 hydrogen bonds · protein-protein

Compared structures

  • 1OO6 · Nitroreductase from e-coli in complex with the dinitrobenzamide prodrug SN23862 · the same entry in another collection · chain A against A, TM-score 1.00
  • P38489 · AlphaFold monomer V2.0 prediction for oxygen-insensitive NAD(P)H nitroreductase (P38489) · a predicted model of the same protein · chain A against A, TM-score 0.99

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