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Snapshots of enzymatic baeyer-villiger catalysis: oxygen activation and intermediate stabilization: ARG337LYS mutant reduced state with NADP

Analyse Snapshots of enzymatic baeyer-villiger catalysis: oxygen activation and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2YM2
Type
protein
Length
531 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phenylacetone monooxygenase
EC
1.14.13.92
UniProt
Q47PU3
Ligands
FAD, NAP
Pockets
4 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhenylacetone monooxygenase (EC 1.14.13.92)protein53135% helix, 18% strandQ47PU3

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · chains A
  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111960.870.88116FAD, NAP
2600.410.8117empty
3560.380.8018empty
4530.320.7714empty

Compared structures

  • 2YM2 · SNAPSHOTS OF ENZYMATIC BAEYER-VILLIGER CATALYSIS: OXYGEN ACTIVATION AND INTERMEDIATE… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q47PU3 · AlphaFold monomer V2.0 prediction for phenylacetone monooxygenase (Q47PU3) · a predicted model of the same protein · chain A against A, TM-score 1.00

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