Brand  (β version)

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
9RQ [2-oxidanylidene-7-[oxidanyl-[(1~{S})-1-phenylethyl]phosphoryl]oxy-chromen-4-yl]methanesulfonic acid
GOL Glycerol
ZN Zinc ion
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 5OD1   PDBj   RCSB PDB   PDBe
Header : De Novo Protein/Hydrolase
Title : Structure of the engineered metalloesterase MID1sc10 complexed with a phosphonate transition state analogue
Release Data : 2018-12-12
Compound :
mol_id molecule chains
1 MID1sc10 A
Source :
mol_id organism_scientific expression_system
1 Synthetic construct  (taxid:32630) Escherichia coli  (taxid:562)
Authors : Mittl, P.R.E., Studer, S., Hansen, D.A., Hilvert, D.
Keywords : directed evolution, engineered Metalloenzyme, DE NOVO PROTEIN-HYDROLASE, De Novo Protein-Hydrolase complex
Exp. method : X-RAY DIFFRACTION ( 1.34 Å )
Citation :

Evolution of a highly active and enantiospecific metalloenzyme from short peptides.

Studer, S.,Hansen, D.A.,Pianowski, Z.L.  et al.
(2018)  Science  362 : 1285 - 1288

PubMed: 30545884
DOI: 10.1126/science.aau3744