5arc

X-ray diffraction
1.1Å resolution

Cooperative bio-metallic selectivity in a tailored protease enables creation of a C-C cross-coupling Heckase

Released:
Source organism: Lederbergia lenta
Entry authors: Sharma M, Diaz-Rodriguez A, Offen WA, Palm-Espling ME, Pordea A, Wormald MR, Mcdonough M, Davies GJ, Davis BG

Function and Biology Details

Reaction catalysed:
Hydrolysis of proteins with broad specificity for peptide bonds, and a preference for a large uncharged residue in P1. Hydrolyzes peptide amides.
Biochemical function:
Cellular component:

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-151551 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Subtilisin Savinase Chain: A
Molecule details ›
Chain: A
Length: 269 amino acids
Theoretical weight: 26.71 KDa
Source organism: Lederbergia lenta
Expression system: Bacillus subtilis
UniProt:
  • Canonical: P29600 (Residues: 1-269; Coverage: 100%)
Sequence domains: Subtilase family
Structure domains: Peptidase S8/S53 domain

Ligands and Environments

No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: DIAMOND BEAMLINE I04
Spacegroup: P212121
Unit cell:
a: 52.461Å b: 61.005Å c: 74.729Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.109 0.109 0.123
Expression system: Bacillus subtilis