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Crystal structure of pyrococcus horikoshii kynurenine aminotransferase in complex with pmp, kyn as substrates and kya as products

Analyse Crystal structure of pyrococcus horikoshii kynurenine aminotransferase in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3AV7
Type
protein
Length
808 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative uncharacterized protein PH0207
EC
2.6.1.7
UniProt
O57946
Ligands
PMP, KYN, KYA
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CPutative uncharacterized protein PH0207 (EC 2.6.1.7)protein40449% helix, 16% strandO57946

Ligands and binding sites

  • PMP · 4'-deoxy-4'-aminopyridoxal-5'-phosphate · ligand · 2 copies · chains A, C
  • KYN · (2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid · ligand · 2 copies · chains A, C
  • KYA · 4-hydroxyquinoline-2-carboxylic acid · ligand · 2 copies · chains A, C

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
18130.800.8369PMP, KYN, KYA
29680.800.8285PMP, KYN, KYA
31090.520.8223empty
4610.310.7618empty
5690.300.7417empty

Interfaces

1 interface between chains.

  • A–C · 3697 Ų buried · 61 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 3AV7 · Crystal structure of Pyrococcus horikoshii kynurenine aminotransferase in complex with… · the same entry in another collection · chain C against C, TM-score 1.00

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