Target
Proteasome subunit beta type-5
Ligand
BDBM50021350
Substrate
n/a
Meas. Tech.
ChEMBL_1366689 (CHEMBL3296840)
Ki
51±n/a nM
Citation
 Troiano, VScarbaci, KEttari, RMicale, NCerchia, CPinto, ASchirmeister, TNovellino, EGrasso, SLavecchia, AZappalą, M Optimization of peptidomimetic boronates bearing a P3 bicyclic scaffold as proteasome inhibitors. Eur J Med Chem 83:1-14 (2014) [PubMed]  Article 
Target
Name:
Proteasome subunit beta type-5
Synonyms:
20S proteasome chymotrypsin-like | 26S proteosome | LMPX | MB1 | PSB5_HUMAN | PSMB5 | Proteasome Macropain subunit MB1 | Proteasome subunit beta type-1/beta type-5 | X
Type:
Protein
Mol. Mass.:
28480.96
Organism:
Homo sapiens (Human)
Description:
n/a
Residue:
263
Sequence:
MALASVLERPLPVNQRGFFGLGGRADLLDLGPGSLSDGLSLAAPGWGVPEEPGIEMLHGTTTLAFKFRHGVIVAADSRATAGAYIASQTVKKVIEINPYLLGTMAGGAADCSFWERLLARQCRIYELRNKERISVAAASKLLANMVYQYKGMGLSMGTMICGWDKRGPGLYYVDSEGNRISGATFSVGSGSVYAYGVMDRGYSYDLEVEQAYDLARRAIYQATYRDAYSGGAVNLYHVREDGWIRVSSDNVADLHEKYSGSTP
  
Inhibitor
Name:
BDBM50021350
Synonyms:
CHEMBL3287940
Type:
Small organic molecule
Emp. Form.:
C17H23BN2O4
Mol. Mass.:
330.187
SMILES:
CC(C)C[C@H](NC(=O)CCn1ccc2ccccc2c1=O)B(O)O |r|
Structure:
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