Reaction Details |
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Target | Pyridoxal kinase |
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Ligand | BDBM207992 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1636780 (CHEMBL3879678) |
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IC50 | >10000±n/a nM |
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Citation | Won, SJ; Eschweiler, JD; Majmudar, JD; Chong, FS; Hwang, SY; Ruotolo, BT; Martin, BR Affinity-Based Selectivity Profiling of an In-Class Selective Competitive Inhibitor of Acyl Protein Thioesterase 2. ACS Med Chem Lett8:215-220 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Pyridoxal kinase |
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Name: | Pyridoxal kinase |
Synonyms: | C21orf124 | C21orf97 | PDXK | PDXK_HUMAN | PKH | PNK | Pyridoxine kinase |
Type: | PROTEIN |
Mol. Mass.: | 35099.40 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_103125 |
Residue: | 312 |
Sequence: | MEEECRVLSIQSHVIRGYVGNRAATFPLQVLGFEIDAVNSVQFSNHTGYAHWKGQVLNSD
ELQELYEGLRLNNMNKYDYVLTGYTRDKSFLAMVVDIVQELKQQNPRLVYVCDPVLGDKW
DGEGSMYVPEDLLPVYKEKVVPLADIITPNQFEAELLSGRKIHSQEEALRVMDMLHSMGP
DTVVITSSDLPSPQGSNYLIVLGSQRRRNPAGSVVMERIRMDIRKVDAVFVGTGDLFAAM
LLAWTHKHPNNLKVACEKTVSTLHHVLQRTIQCAKAQAGEGVRPSPMQLELRMVQSKRDI
EDPEIVVQATVL
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BDBM207992 |
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n/a |
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Name | BDBM207992 |
Synonyms: | ML349 |
Type | Small organic molecule |
Emp. Form. | C23H22N2O4S2 |
Mol. Mass. | 454.562 |
SMILES | COc1ccc(cc1)N1CCN(CC1)C(=O)c1cc2CS(=O)(=O)c3ccccc3-c2s1 |
Structure |
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