Reaction Details Report a problem with these data
Target
Proteasome subunit beta type-8
Ligand
BDBM50332796
Substrate
n/a
Meas. Tech.
ChEMBL_1351341 (CHEMBL3266190)
Ki
7900±n/a nM
Citation
 Fan, H; Angelo, NG; Warren, JD; Nathan, CF; Lin, G Oxathiazolones Selectively Inhibit the Human Immunoproteasome over the Constitutive Proteasome. ACS Med Chem Lett 5:405-10 (2014) [PubMed]  Article 
Target
Name:
Proteasome subunit beta type-8
Synonyms:
26S proteosome | LMP7 | Low molecular mass protein 7 | Macropain subunit C13 | Multicatalytic endopeptidase complex subunit C13 | PSB8_HUMAN | PSMB5i | PSMB8 | Proteasome component C13 | Proteasome subunit beta type-8 | Proteasome subunit beta-5i | RING10 | Y2
Type:
PROTEIN
Mol. Mass.:
30357.49
Organism:
Homo sapiens (Human)
Description:
ChEMBL_1446797
Residue:
276
Sequence:
MALLDVCGAPRGQRPESALPVAGSGRRSDPGHYSFSMRSPELALPRGMQPTEFFQSLGGDGERNVQIEMAHGTTTLAFKFQHGVIAAVDSRASAGSYISALRVNKVIEINPYLLGTMSGCAADCQYWERLLAKECRLYYLRNGERISVSAASKLLSNMMCQYRGMGLSMGSMICGWDKKGPGLYYVDEHGTRLSGNMFSTGSGNTYAYGVMDSGYRPNLSPEEAYDLGRRAIAYATHRDSYSGGVVNMYHMKEDGWVKVESTDVSDLLHQYREANQ
  
Inhibitor
Name:
BDBM50332796
Synonyms:
5-phenyl-1,3,4-oxathiazol-2-one | CHEMBL1632533
Type:
Small organic molecule
Emp. Form.:
C8H5NO2S
Mol. Mass.:
179.196
SMILES:
O=c1oc(ns1)-c1ccccc1
Structure:
Search PDB for entries with ligand similarity: