GL1X · GenesisL1 explorer

MolNFT v1 · #51761 · protein

Crystal structure of human kynurenine aminotransferase II

2VGZ · KYNURENINE/ALPHA-aminoadipate aminotransferase: “Crystal structure of human kynurenine aminotransferase II”. X-ray diffraction, 2 ligands (PLP, IOD), 5 pockets (best druggability 0.67). MolNFT v1 #51761 on GenesisL1: 3D structure…

PDB
2VGZ
Type
protein
Length
828 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
KYNURENINE/ALPHA-aminoadipate aminotransferase
EC
2.6.1.39, 2.6.1.7
UniProt
Q8N5Z0
Ligands
PLP, IOD
Pockets
5 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BKYNURENINE/ALPHA-aminoadipate aminotransferase (EC 2.6.1.39, 2.6.1.7)protein41441% helix, 18% strandQ8N5Z0

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • IOD · Iodide ion · ion · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13070.670.8239PLP
23130.640.8041PLP
32950.640.8129empty
4720.440.8223empty
5810.440.8023empty

Interfaces

1 interface between chains.

  • A–B · 3789 Ų buried · 58 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 2VGZ · Crystal structure of human kynurenine aminotransferase II · 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 B against A, TM-score 0.99

Analyse

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