6svy

X-ray diffraction
2.6Å resolution

Crystal structure of Neprilysin in complex with Sampatrilat-ASP.

Released:

Function and Biology Details

Reaction catalysed:
Preferential cleavage of polypeptides between hydrophobic residues, particularly with Phe or Tyr at P1'.
Biochemical function:
Cellular component:

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-140129 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Neprilysin Chain: A
Molecule details ›
Chain: A
Length: 699 amino acids
Theoretical weight: 79.92 KDa
Source organism: Homo sapiens
Expression system: Komagataella pastoris
UniProt:
  • Canonical: P08473 (Residues: 52-750; Coverage: 93%)
Gene names: EPN, MME
Sequence domains:

Ligands and Environments

3 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: DIAMOND BEAMLINE I04
Spacegroup: P3221
Unit cell:
a: 108.164Å b: 108.164Å c: 112.955Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.211 0.208 0.254
Expression system: Komagataella pastoris