GL1X · GenesisL1 explorer

Research workbench

Crystal structure of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase, reduced form

Analyse Crystal structure of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ALJ
Type
protein
Length
369 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase
EC
1.14.12.4
UniProt
Q988D3
Ligands
FAD
Pockets
2 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (EC 1.14.12.4)protein36935% helix, 28% strandQ988D3

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · chains A
  • GOL · Glycerol · additive · 7 copies · chains A
  • BME · Beta-mercaptoethanol · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19230.810.8384FAD, BME, GOL
2950.370.7517empty

Modifications

Observed in the structure: 2 covalent (additive adduct).

Compared structures

  • 3ALJ · Crystal structure of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase, reduced form · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.