4wme

X-ray diffraction
1.55Å resolution

Crystal structure of catalytically inactive MERS-CoV 3CL Protease (C148A) in spacegroup C2

Released:

Function and Biology Details

Reaction catalysed:
Thiol-dependent hydrolysis of ester, thioester, amide, peptide and isopeptide bonds formed by the C-terminal Gly of ubiquitin (a 76-residue protein attached to proteins as an intracellular targeting signal).
Biochemical function:
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo dimer (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-197770 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
ORF1a Chains: A, B, C, D
Molecule details ›
Chains: A, B, C, D
Length: 306 amino acids
Theoretical weight: 33.32 KDa
Source organism: Middle East respiratory syndrome-related coronavirus
Expression system: Escherichia coli
UniProt:
  • Canonical: W6A941 (Residues: 3248-3553; Coverage: 7%)
Sequence domains: Coronavirus endopeptidase C30
Structure domains:

Ligands and Environments

1 bound ligand:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 22-BM
Spacegroup: C2
Unit cell:
a: 131.695Å b: 91.447Å c: 120.339Å
α: 90° β: 106.64° γ: 90°
R-values:
R R work R free
0.187 0.185 0.216
Expression system: Escherichia coli