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CYP106A2 with substrate abietic acid

Analyse CYP106A2 with substrate abietic acid in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IKI
Type
protein
Length
782 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.4
Source
Bacillus megaterium
Molecule
Cytochrome P450(MEG)
EC
1.14.99.-, 1.14.15.8
UniProt
Q06069
Ligands
HEM, A9H
Pockets
8 · best druggability 0.84

Structure

x-ray diffraction · resolution 2.4 · 2 distinct chains · 53% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACytochrome P450(MEG) (EC 1.14.99.-, 1.14.15.8)protein38354% helix, 10% strandQ06069
BCytochrome P450(MEG) (EC 1.14.99.-, 1.14.15.8)protein39952% helix, 10% strandQ06069

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • A9H · Abietic acid · ligand · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17070.840.8856HEM, A9H
27610.770.8158HEM
32080.480.7525empty
4740.470.8317empty
5590.440.8318empty

Interfaces

1 interface between chains.

  • A–B · 895 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 5IKI · CYP106A2 with substrate abietic acid · the same entry in another collection · chain A against A, TM-score 1.00
  • Q06069 · AlphaFold monomer V2.0 prediction for cytochrome P450(MEG) (Q06069) · a predicted model of the same protein · chain B against A, TM-score 0.98

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