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TargetProteasome subunit beta type-5
LigandBDBM50199450
Substrate/Competitorn/a
Meas. Tech.ChEMBL_413589 (CHEMBL853870)
IC50>10000±n/a nM
Citation Adsule, SBarve, VChen, DAhmed, FDou, QPPadhye, SSarkar, FH Novel Schiff base copper complexes of quinoline-2 carboxaldehyde as proteasome inhibitors in human prostate cancer cells. J Med Chem49:7242-6 (2006) [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:
BDBM50199450
n/a
NameBDBM50199450
Synonyms:1-(quinolin-2-ylmethylene)thiosemicarbazide | 2-(quinolin-2-ylmethylene)hydrazinecarbothioamide | CHEMBL215065
TypeSmall organic molecule
Emp. Form.C11H10N4S
Mol. Mass.230.289
SMILESNC(=S)NN=Cc1ccc2ccccc2n1 |w:5.5|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: