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Crystal structure of the modified fructosyl peptide oxidase from aspergillus nidulans, seleno-methionine derivative

Analyse Crystal structure of the modified fructosyl peptide oxidase from aspergillus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6A6R
Type
protein
Length
431 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fructosyl amine: oxygen oxidoreductase
Ligands
D1D, FAD, SO4
Pockets
3 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFructosyl amine: oxygen oxidoreductaseprotein43129% helix, 26% strand—

Ligands and binding sites

  • D1D · (4S,5S)-1,2-dithiane-4,5-diol · ligand · 2 copies · chains A
  • FAD · Flavin-adenine dinucleotide · ligand · chains A
  • SO4 · Sulfate ion · ion · 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
111310.830.84107FAD
22090.570.8025empty
3710.310.7420empty

Modifications

Observed in the structure: 8 modified, 1 cofactor (engineered, flavinylation, oxidation).

Compared structures

  • 6A6R · Crystal structure of the modified fructosyl peptide oxidase from Aspergillus nidulans… · the same entry in another collection · chain A against A, TM-score 1.00

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