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Crystal Structure of stachydrine demethylase in complex with cyanide, oxygen, and N-methyl proline in a new orientation

Analyse Crystal Structure of stachydrine demethylase in complex with cyanide, oxygen… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4QUR
Type
protein
Length
415 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.759
Source
Sinorhizobium meliloti 1021
Molecule
monoxygenase; demethylase
EC
1.-.-.-
UniProt
Q92ZP9
Ligands
FES, NCO, 3BY, FE, OXY, CYN
Pockets
3 · best druggability 0.78

Structure

x-ray diffraction · resolution 1.759 · 1 distinct chain · 33% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
Amonoxygenase; demethylase (EC 1.-.-.-)protein41533% helix, 24% strandQ92ZP9

Ligands and binding sites

  • FES · Fe2/s2 (inorganic) cluster · ligand · chains A
  • NCO · Cobalt hexammine(iii) · ligand · chains A
  • 3BY · 1-methyl-L-proline · ligand · chains A
  • FE · Fe (III) ion · metal · chains A
  • OXY · Oxygen molecule · ion · chains A
  • CYN · Cyanide ion · ion · chains A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11070.780.98283BY, OXY, CYN
21010.440.7930empty
31230.430.7718empty

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 4QUR · Crystal structure of stachydrine demethylase in complex with cyanide, oxygen, and… · the same entry in another collection · chain A against A, TM-score 1.00

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