BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetProteasome subunit beta type-5
LigandBDBM50600774
Substrate/Competitorn/a
Meas. Tech.IC50 Determination
IC50 9700±n/a nM
Citation LIN, GNATHAN, CKIRKMAN, LZHAN, WMORGAN, TSATO, KHARA, RKAWASAKI, MIMAEDA, TTOITA, AOKAMOTO, RYUKAWA, TASO, KWONG, TGINN, JDFOLEY, MA MACROCYCLIC COMPOUNDS AS PROTEASOME INHIBITORS US Patent US20240043470 Publication Date 2/8/2024
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50600774
n/a
NameBDBM50600774
Synonyms:CHEMBL5200145 | US20240043470, Compound 3-35
TypeSmall organic molecule
Emp. Form.C33H42N4O6
Mol. Mass.590.7098
SMILESO=C(NC1CCCC1)[C@@H]1CCCCOc2cccc(C[C@H](N3CCCC3=O)C(=O)N[C@@H](COc3ccccc3)C(=O)N1)c2 |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: