2h31

X-ray diffraction
2.8Å resolution

Crystal structure of human PAICS, a bifunctional carboxylase and synthetase in purine biosynthesis

Released:

Function and Biology Details

Reactions catalysed:
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylate = 5-amino-1-(5-phospho-D-ribosyl)imidazole + CO(2)
ATP + 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylate + L-aspartate = ADP + phosphate + (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate
Biochemical function:
Cellular component:

Structure analysis Details

Assembly composition:
homo octamer (preferred)
PDBe Complex ID:
PDB-CPX-149557 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Bifunctional phosphoribosylaminoimidazole carboxylase/phosphoribosylaminoimidazole succinocarboxamide synthetase Chain: A
Molecule details ›
Chain: A
Length: 425 amino acids
Theoretical weight: 47.46 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli
UniProt:
  • Canonical: P22234 (Residues: 1-425; Coverage: 100%)
Gene names: ADE2, AIRC, PAICS, PAIS
Sequence domains:
Structure domains: Rossmann fold

Ligands and Environments

1 bound ligand:
1 modified residue:

Experiments and Validation Details

Entry percentile scores
X-ray source: PHOTON FACTORY BEAMLINE BL-5A
Spacegroup: P422
Unit cell:
a: 133.666Å b: 133.666Å c: 60.618Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.245 0.241 0.287
Expression system: Escherichia coli