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TargetProteasome subunit beta type-5
LigandBDBM50600766
Substrate/Competitorn/a
Meas. Tech.IC50 Determination
IC50 7060±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:
BDBM50600766
n/a
NameBDBM50600766
Synonyms:CHEMBL5193963 | US20240043470, Compound 3-10
TypeSmall organic molecule
Emp. Form.C31H38F2N4O5
Mol. Mass.584.654
SMILESFC(F)CNC(=O)[C@@H]1CCCCOc2cccc(C[C@H](N3CCCC3=O)C(=O)N[C@@H](CCc3ccccc3)C(=O)N1)c2 |r|
Structure
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