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TargetCarbonic anhydrase 6 (CA-VI)
LigandBDBM50137675
Substrate/Competitorn/a
Meas. Tech.Enzyme Inhbition Assay
pH7.5±0
Temperature293.15±0 K
Ki 0.56±0 nM
Citation Winum JYMontero JLVullo DSupuran CT Carbonic anhydrase inhibitors: glycosylsulfanilamides act as subnanomolar inhibitors of the human secreted isoform VI. Chem Biol Drug Des 74:636-9 (2009) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Carbonic anhydrase 6 (CA-VI)
Name:Carbonic anhydrase 6 (CA-VI)
Synonyms:CA-VI | Carbonate dehydratase VI | Carbonic Anhydrase VI | Carbonic anhydrase 6 | Carbonic anhydrase 6 (CA VI) | Carbonic anhydrase VI (CA VI) | Salivary carbonic anhydrase | Secreted carbonic anhydrase
Type:Enzyme
Mol. Mass.:35371.40
Organism:Homo sapiens (Human)
Description:P23280
Residue:308
Sequence:
MRALVLLLSLFLLGGQAQHVSDWTYSEGALDEAHWPQHYPACGGQRQSPINLQRTKVRYN
PSLKGLNMTGYETQAGEFPMVNNGHTVQISLPSTMRMTVADGTVYIAQQMHFHWGGASSE
ISGSEHTVDGIRHVIEIHIVHYNSKYKSYDIAQDAPDGLAVLAAFVEVKNYPENTYYSNF
ISHLANIKYPGQRTTLTGLDVQDMLPRNLQHYYTYHGSLTTPPCTENVHWFVLADFVKLS
RTQVWKLENSLLDHRNKTIHNDYRRTQPLNHRVVESNFPNQEYTLGSEFQFYLHKIEEIL
DYLRRALN
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  Blast E-value cutoff:
BDBM50137675
n/a
NameBDBM50137675
Synonyms:4-(3,4,5-Trihydroxy-tetrahydro-pyran-2-ylamino)-benzenesulfonamide | CHEMBL308495 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 4 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 5 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 6
TypeSmall organic molecule
Emp. Form.C11H16N2O6S
Mol. Mass.304.32
SMILESNS(=O)(=O)c1ccc(NC2OCC(O)C(O)C2O)cc1
Structure
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