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The BM3 mutant wifi-wc heme domain in complex with testosterone

Analyse The BM3 mutant wifi-wc heme domain in complex with testosterone in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5OG9
Type
protein
Length
908 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional cytochrome P450/NADPH--P450 reductase
EC
1.14.14.1, 1.6.2.4
UniProt
F2Q7T0
Ligands
TES, HEM, ZN, CL
Pockets
5 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 55% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional cytochrome P450/NADPH--P450 reductase (EC 1.14.14.1, 1.6.2.4)protein45455% helix, 11% strandF2Q7T0
BBifunctional cytochrome P450/NADPH--P450 reductase (EC 1.14.14.1, 1.6.2.4)protein45455% helix, 11% strandF2Q7T0

Ligands and binding sites

  • TES · Testosterone · ligand · 4 copies · chains A, B
  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · chains A, B
  • CL · Chloride ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111560.880.88110HEM, TES
211700.870.88101HEM, TES
35510.720.8167empty
42080.470.7429empty
51930.450.7429empty

Interfaces

1 interface between chains.

  • A–B · 512 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 5OG9 · The BM3 mutant WIFI-WC heme domain in complex with testosterone · the same entry in another collection · chain A against A, TM-score 1.00

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