Reaction Details |
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Target | Serine/threonine-protein phosphatase 2A activator |
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Ligand | BDBM50127375 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_161790 |
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IC50 | 4000±n/a nM |
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Citation | Liu, W; Sheppeck, JE; Colby, DA; Huang, HB; Nairn, AC; Chamberlin, AR The selective inhibition of phosphatases by natural toxins: the anhydride domain of tautomycin is not a primary factor in controlling PP1/PP2A selectivity. Bioorg Med Chem Lett13:1597-600 (2003) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Serine/threonine-protein phosphatase 2A activator |
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Name: | Serine/threonine-protein phosphatase 2A activator |
Synonyms: | 5.2.1.8 | PPP2R4 | PTPA | PTPA_HUMAN | Phosphotyrosyl phosphatase activator | Protein phosphatase 2A regulatory subunit B | Protein phosphatase 2A regulatory subunit B' | Serine/threonine-protein phosphatase 2A activator | Serine/threonine-protein phosphatase 2A regulatory subunit 4 |
Type: | n/a |
Mol. Mass.: | 40662.53 |
Organism: | Homo sapiens (Human) |
Description: | Q15257 |
Residue: | 358 |
Sequence: | MAEGERQPPPDSSEEAPPATQNFIIPKKEIHTVPDMGKWKRSQAYADYIGFILTLNEGVK
GKKLTFEYRVSEMWNEVHEEKEQAAKQSVSCDECIPLPRAGHCAPSEAIEKLVALLNTLD
RWIDETPPVDQPSRFGNKAYRTWYAKLDEEAENLVATVVPTHLAAAVPEVAVYLKESVGN
STRIDYGTGHEAAFAAFLCCLCKIGVLRVDDQIAIVFKVFNRYLEVMRKLQKTYRMEPAG
SQGVWGLDDFQFLPFIWGSSQLIDHPYLEPRHFVDEKAVNENHKDYMFLECILFITEMKT
GPFAEHSNQLWNISAVPSWSKVNQGLIRMYKAECLEKFPVIQHFKFGSLLPIHPVTSG
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BDBM50127375 |
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n/a |
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Name | BDBM50127375 |
Synonyms: | (E)-(R)-4-Hydroxy-2-methyl-hex-2-enedioic acid 6-{(1R,2S,3R,6S,7S,10R)-10-[(2S,3S,6R,8S,9R)-3,9-dimethyl-8-((S)-3-methyl-4-oxo-pentyl)-1,7-dioxa-spiro[5.5]undec-2-yl]-3,7-dihydroxy-1-isopropyl-2-methoxy-6-methyl-5-oxo-undecyl} ester | CHEMBL295239 |
Type | Small organic molecule |
Emp. Form. | C40H68O12 |
Mol. Mass. | 740.9607 |
SMILES | CO[C@@H]([C@H](O)CC(=O)[C@@H](C)[C@@H](O)CC[C@@H](C)[C@@H]1O[C@]2(CC[C@@H](C)[C@H](CC[C@H](C)C(C)=O)O2)CC[C@@H]1C)[C@H](OC(=O)C[C@@H](O)\C=C(/C)C(O)=O)C(C)C |
Structure |
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