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TargetPyridoxal kinase
LigandBDBM207992
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1636780 (CHEMBL3879678)
IC50>10000±n/a nM
Citation Won, SJEschweiler, JDMajmudar, JDChong, FSHwang, SYRuotolo, BTMartin, 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
More Info.:Get all data from this article,  Assay Method
 
Pyridoxal kinase
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM207992
n/a
NameBDBM207992
Synonyms:ML349
TypeSmall organic molecule
Emp. Form.C23H22N2O4S2
Mol. Mass.454.562
SMILESCOc1ccc(cc1)N1CCN(CC1)C(=O)c1cc2CS(=O)(=O)c3ccccc3-c2s1
Structure
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