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Crystal structure of human kynurenine aminotransferase I in complex with L-phe

Analyse Crystal structure of human kynurenine aminotransferase I in complex with L-phe in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1W7M
Type
protein
Length
415 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kynurenine--oxoglutarate transaminase I
EC
4.4.1.13
UniProt
Q16773
Ligands
PHE, PLP
Pockets
3 · best druggability 0.59

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AKynurenine--oxoglutarate transaminase I (EC 4.4.1.13)protein41546% helix, 15% strandQ16773

Ligands and binding sites

  • PHE · Phenylalanine · ligand · chains A
  • PLP · Pyridoxal-5'-phosphate · ligand · 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
12220.590.8031PHE, PLP
21980.500.7622empty
31530.450.7524empty

Modifications

Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 1W7M · Crystal structure of human kynurenine aminotransferase I in complex with L-Phe · the same entry in another collection · chain A against A, TM-score 1.00
  • Q16773 · AlphaFold monomer V2.0 prediction for kynurenine--oxoglutarate transaminase 1 (Q16773) · a predicted model of the same protein · chain A against A, TM-score 1.00

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