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Kynurenine aminotransferase II inhibitors

Analyse Kynurenine aminotransferase II inhibitors in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4GE7
Type
protein
Length
856 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
KYNURENINE/ALPHA-aminoadipate aminotransferase, mitochondrial
EC
2.6.1.39, 2.6.1.7
UniProt
Q8N5Z0
Ligands
0K5
Pockets
8 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BKYNURENINE/ALPHA-aminoadipate aminotransferase, mitochondrial (EC 2.6.1.39, 2.6.1.7)protein42843% helix, 17% strandQ8N5Z0

Ligands and binding sites

  • 0K5 · (5-hydroxy-4-{[(1-hydroxy-2-oxo-6-phenoxy-1,2-dihydroquinolin-3-yl)amino]methyl}-6-methylpyridin-3-yl)methyl dihydrogen phosphate · ligand · 2 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16620.760.82770K5
26520.750.81760K5
32820.670.8334empty
41240.460.7822empty
51220.450.7821empty

Interfaces

1 interface between chains.

  • A–B · 4388 Ų buried · 68 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (oxidation).

Compared structures

  • 4GE7 · Kynurenine Aminotransferase II Inhibitors · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8N5Z0 · AlphaFold monomer V2.0 prediction for KYNURENINE/ALPHA-aminoadipate aminotransferase… · a predicted model of the same protein · chain A against A, TM-score 0.98

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