8p0i

X-ray diffraction
3.5Å resolution

Crystal structure of the open conformation of insulin-regulated aminopeptidase in complex with a small-MW inhibitor

Released:

Function and Biology Details

Reaction catalysed:
Release of an N-terminal amino acid, Cys-|-Xaa-, in which the half-cystine residue is involved in a disulfide loop, notably in oxytocin or vasopressin. Hydrolysis rates on a range of aminoacyl arylamides exceed that for the cystinyl derivative, however.
Biochemical function:
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
monomeric (preferred)
PDBe Complex ID:
PDB-CPX-193794 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecules (4 distinct):
Leucyl-cystinyl aminopeptidase, pregnancy serum form Chains: A, B
Molecule details ›
Chains: A, B
Length: 871 amino acids
Theoretical weight: 100.14 KDa
Source organism: Homo sapiens
Expression system: Homo sapiens
UniProt:
  • Canonical: Q9UIQ6 (Residues: 155-1025; Coverage: 85%)
Gene names: LNPEP, OTASE
Sequence domains:

Ligands and Environments

Carbohydrate polymer : NEW Components: NAG, BMA
Carbohydrate polymer : NEW Components: NAG, BMA, MAN
Carbohydrate polymer : NEW Components: NAG
3 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: PETRA III, EMBL c/o DESY BEAMLINE P13 (MX1)
Spacegroup: P21
Unit cell:
a: 68.229Å b: 255.121Å c: 73.274Å
α: 90° β: 110° γ: 90°
R-values:
R R work R free
0.24 0.24 0.277
Expression system: Homo sapiens