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TargetProteasome subunit beta type-5
LigandBDBM50432549
Substrate/Competitorn/a
Meas. Tech.ChEMBL_949940 (CHEMBL2352040)
IC50 3500±n/a nM
Citation Ozcan, SKazi, AMarsilio, FFang, BGuida, WCKoomen, JLawrence, HRSebti, SM Oxadiazole-isopropylamides as potent and noncovalent proteasome inhibitors. J Med Chem56:3783-805 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Proteasome subunit beta type-5
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:
MALASVLERPLPVNQRGFFGLGGRADLLDLGPGSLSDGLSLAAPGWGVPEEPGIEMLHGT
TTLAFKFRHGVIVAADSRATAGAYIASQTVKKVIEINPYLLGTMAGGAADCSFWERLLAR
QCRIYELRNKERISVAAASKLLANMVYQYKGMGLSMGTMICGWDKRGPGLYYVDSEGNRI
SGATFSVGSGSVYAYGVMDRGYSYDLEVEQAYDLARRAIYQATYRDAYSGGAVNLYHVRE
DGWIRVSSDNVADLHEKYSGSTP
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  Blast E-value cutoff:
BDBM50432549
n/a
NameBDBM50432549
Synonyms:CHEMBL2346860 | PI-1833
TypeSmall organic molecule
Emp. Form.C22H25N3O3
Mol. Mass.379.4522
SMILESCC(C)N(Cc1nc(no1)-c1ccc(C)cc1)C(=O)COc1ccc(C)cc1
Structure
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