6ihw

X-ray diffraction
1.55Å resolution

Crystal structure of bacterial serine phosphatase bearing R161K mutation

Released:
Source organism: Staphylococcus aureus

Function and Biology Details

Reaction catalysed:
[a protein]-serine/threonine phosphate + H(2)O = [a protein]-serine/threonine + phosphate
Biochemical function:
Cellular component:

Structure analysis Details

Assembly composition:
monomeric (preferred)
PDBe Complex ID:
PDB-CPX-193196 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
protein-serine/threonine phosphatase Chain: A
Molecule details ›
Chain: A
Length: 266 amino acids
Theoretical weight: 30.11 KDa
Source organism: Staphylococcus aureus
Expression system: Escherichia coli
UniProt:
  • Canonical: Q9RL81 (Residues: 3-247; Coverage: 99%)
Gene names: A6760_05000, BN1321_240063, EP54_08495, EQ90_08165, FAF17_11265, GO793_10355, GO814_06360, GO942_07250, GZ163_05055, NCTC10702_01924, NCTC13131_00423, NCTC7972_00731, SAMEA2078260_01528, SAMEA2078588_01607, SAMEA2080344_01697, SAMEA2081063_01376, SAMEA4008575_01865, SAMEA70146418_01691, SAMEA70245418_01977, prpC, prpC_1
Sequence domains: Protein phosphatase 2C

Ligands and Environments

1 bound ligand:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: SSRF BEAMLINE BL19U1
Spacegroup: P21
Unit cell:
a: 46.578Å b: 38.958Å c: 65.409Å
α: 90° β: 102.08° γ: 90°
R-values:
R R work R free
0.152 0.151 0.174
Expression system: Escherichia coli