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Complex of 6-hydroxy-L-nicotine oxidase with final ketone product formed during catalytic turnover

Analyse Complex of 6-hydroxy-L-nicotine oxidase with final ketone product formed during… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3NH3
Type
protein
Length
425 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
6-hydroxy-L-nicotine oxidase
EC
1.5.3.5
UniProt
Q93NH4
Ligands
HNL, FAD, GP7, HNM
Pockets
4 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
X6-hydroxy-L-nicotine oxidase (EC 1.5.3.5)protein42534% helix, 21% strandQ93NH4

Ligands and binding sites

  • HNL · 5-[(2S)-1-methylpyrrolidin-2-yl]pyridin-2-ol · ligand · chains X
  • FAD · Flavin-adenine dinucleotide · ligand · chains X
  • GP7 · (1R)-2-{[(S)-(2-aminoethoxy)(hydroxy)phosphoryl]oxy}-1-[(pentadecanoyloxy)methyl]ethyl (12E)-hexadeca-9,12-dienoate · ligand · chains X
  • HNM · 1-(6-hydroxypyridin-3-yl)-4-(methylamino)butan-1-one · ligand · chains X

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14410.860.9365HNL, FAD
23540.740.8440GP7, HNM
31230.470.7818empty
4670.350.7714empty

Compared structures

  • 3NH3 · Complex of 6-hydroxy-L-nicotine oxidase with final ketone product formed during catalytic… · the same entry in another collection · chain X against X, TM-score 1.00

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