Reaction Details |
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Target | Dual specificity protein phosphatase 3 |
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Ligand | BDBM50139372 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_60859 |
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Ki | 290000±n/a nM |
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Citation | Park, J; Fu, H; Pei, D Peptidyl aldehydes as slow-binding inhibitors of dual-specificity phosphatases. Bioorg Med Chem Lett14:685-7 (2004) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Dual specificity protein phosphatase 3 |
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Name: | Dual specificity protein phosphatase 3 |
Synonyms: | DUS3_HUMAN | DUSP3 | Dual specificity protein phosphatase (VHR) | Dual specificity protein phosphatase 3 | Dual specificity protein phosphatase VHR | Protein Tyrosine Phosphatase VHR | Tyrosine-protein phosphatase non-receptor type 1 | VHR |
Type: | Hydrolase |
Mol. Mass.: | 20480.58 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 185 |
Sequence: | MSGSFELSVQDLNDLLSDGSGCYSLPSQPCNEVTPRIYVGNASVAQDIPKLQKLGITHVL
NAAEGRSFMHVNTNANFYKDSGITYLGIKANDTQEFNLSAYFERAADFIDQALAQKNGRV
LVHCREGYSRSPTLVIAYLMMRQKMDVKSALSIVRQNREIGPNDGFLAQLCQLNDRLAKE
GKLKP
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BDBM50139372 |
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n/a |
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Name | BDBM50139372 |
Synonyms: | 4-((S)-(S)-1-Carbamoyl-3-carboxy-propylcarbamoyl)-4-{2-[4-(3-oxo-propenyl)-benzoylamino]-acetylamino}-butyric acid | CHEMBL351423 |
Type | Small organic molecule |
Emp. Form. | C22H26N4O9 |
Mol. Mass. | 490.4632 |
SMILES | NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)c1ccc(\C=C\C=O)cc1 |
Structure |
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