Reaction Details |
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Target | Proteasome subunit beta type-5 |
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Ligand | BDBM388323 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Determination of Beta5 Activity |
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IC50 | 275±n/a nM |
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Citation | Klein, M; Schadt, O; Haselmayer, P; Busch, M Substituted boronic acids and boronate esters as immunoproteasome inhibitors US Patent US10294246 Publication Date 5/21/2019 |
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More Info.: | Get all data from this article, Assay Method |
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Proteasome subunit beta type-5 |
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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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BDBM388323 |
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n/a |
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Name | BDBM388323 |
Synonyms: | US10294246, Compound No. 20 |
Type | Small organic molecule |
Emp. Form. | C16H16BN3O4 |
Mol. Mass. | 325.127 |
SMILES | OB(O)[C@H](Cc1coc2ccccc12)NC(=O)Cc1ncccn1 |r| |
Structure |
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