5ndz

X-ray diffraction
3.6Å resolution

Crystal structure of a thermostabilised human protease-activated receptor-2 (PAR2) in complex with AZ3451 at 3.6 angstrom resolution

Released:

Function and Biology Details

Reaction catalysed:
Hydrolysis of (1->4)-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in a peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrins
Biochemical function:
Cellular component:

Structure analysis Details

Assembly composition:
monomeric (preferred)
PDBe Complex ID:
PDB-CPX-132959 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Endolysin; Proteinase-activated receptor 2, alternate cleaved 2; Soluble cytochrome b562 Chain: A
Molecule details ›
Chain: A
Length: 619 amino acids
Theoretical weight: 69.56 KDa
Source organisms: Expression system: Spodoptera frugiperda
UniProt:
  • Canonical: P00720 (Residues: 2-161; Coverage: 98%)
  • Canonical: P55085 (Residues: 59-269, 276-377; Coverage: 84%)
  • Canonical: P0ABE7 (Residues: 23-127; Coverage: 99%)
Gene names: E, F2RL1, GPR11, PAR2, cybC
Sequence domains:

Ligands and Environments

2 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: DIAMOND BEAMLINE I24
Spacegroup: P1
Unit cell:
a: 37.099Å b: 62.599Å c: 86.467Å
α: 104.38° β: 91.66° γ: 96.4°
R-values:
R R work R free
0.246 0.244 0.291
Expression system: Spodoptera frugiperda