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Crystal structure of the alpha subunit of heme dependent oxidative N- demethylase (hodm) in complex with the dimethylamine substrate

Analyse Crystal structure of the alpha subunit of heme dependent oxidative N… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LTH
Type
protein
Length
334 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heme dependent oxidative N-demethylase
UniProt
A4XXY9
Ligands
HEM, DMN, NA
Pockets
3 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHeme dependent oxidative N-demethylaseprotein33437% helix, 22% strandA4XXY9

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A
  • DMN · Dimethylamine · ligand · chains A
  • NA · Sodium ion · metal · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains A

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
14150.820.9051HEM, DMN
2590.680.9623empty
31070.350.7427PEG

Compared structures

  • 5LTH · Crystal structure of the alpha subunit of heme dependent oxidative N-demethylase (HODM)… · the same entry in another collection · chain A against A, TM-score 1.00

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