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Rat cypor D632F mutant

Analyse Rat cypor D632F mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5URG
Type
protein
Length
1,214 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NADPH--cytochrome P450 reductase
EC
1.6.2.4
UniProt
P00388
Ligands
FMN, FAD, NAP, PO4
Pockets
13 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANADPH--cytochrome P450 reductase (EC 1.6.2.4)protein61038% helix, 21% strandP00388
BNADPH--cytochrome P450 reductase (EC 1.6.2.4)protein60438% helix, 21% strandP00388

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B
  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B

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

Pockets

13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111530.790.8194empty
27950.760.8090FMN
38750.740.7887FMN, FAD
44780.670.7958FAD
53910.660.7938NAP

Interfaces

1 interface between chains.

  • A–B · 737 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 5URG · rat CYPOR D632F mutant · the same entry in another collection · chain A against A, TM-score 1.00
  • P00388 · AlphaFold monomer V2.0 prediction for NADPH--cytochrome P450 reductase (P00388) · a predicted model of the same protein · chain A against A, TM-score 0.99

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