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2.3 a resolution crystal structure of the ornithine aminotransferase from toxoplasma gondii ME49

Analyse 2.3 a resolution crystal structure of the ornithine aminotransferase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4ZWM
Type
protein
Length
844 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ornithine aminotransferase, mitochondrial, putative
EC
2.6.1.13
UniProt
S8EY38
Ligands
PLP, SO4
Pockets
5 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AOrnithine aminotransferase, mitochondrial, putative (EC 2.6.1.13)protein42141% helix, 18% strandS8EY38
BOrnithine aminotransferase, mitochondrial, putative (EC 2.6.1.13)protein42341% helix, 18% strandS8EY38

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 12 copies · 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14620.780.8662SO4, PLP
24870.760.8469PLP, SO4
31040.610.8823empty
41550.590.8328empty
5610.290.7411empty

Interfaces

1 interface between chains.

  • A–B · 5902 Ų buried · 82 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 4ZWM · 2.3 A resolution crystal structure of the ornithine aminotransferase from Toxoplasma… · the same entry in another collection · chain A against A, TM-score 1.00

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