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TargetCARBONIC ANHYDRASE
LigandBDBM10888
Substrate/CompetitorBDBM10856
Meas. Tech.CA Inhibition Assay
Ki 231±n/a nM
Citation Nishimori, IMinakuchi, TMorimoto, KSano, SOnishi, STakeuchi, HVullo, DScozzafava, ASupuran, CT Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs. J Med Chem49:2117-26 (2006) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
CARBONIC ANHYDRASE
Name:CARBONIC ANHYDRASE
Synonyms:Carbonic Anhydrase (hpCA) | hpCA
Type:Enzyme
Mol. Mass.:28277.52
Organism:Helicobacter pylori J99
Description:Q9ZK30
Residue:247
Sequence:
MKKTFLIALALTASLIGAENTKWDYKNKENGPHRWDKLHKDFEVCKSGKSQSPINIEHYY
HTQDKADLQFKYAASKPKAVFFTHHTLKASFEPTNHINYRGHDYVLDNVHFHAPMEFLIN
NKTRPLSAHFVHKDAKGRLLVLAIGFEEGKENPNLDPILEGIQKKQNLKEVALDAFLPKS
INYYHFNGSLTAPPCTEGVAWFVIEEPLEVSAKQLAEIKKRMKNSPNQRPVQPDYNTVII
KSSAETR
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  Blast E-value cutoff:
BDBM10888
BDBM10856
NameBDBM10888
Synonyms:1,2-benzoxazol-3-ylmethanesulfonamide | CHEMBL750 | SPR_2 | US10172837, Zonisamide | Zonisamide | Zonisamide (ZNA) | Zonisamide (ZNS) | Zonisamide, 1 | Zonisamide, ZNS
TypeSmall organic molecule
Emp. Form.C8H8N2O3S
Mol. Mass.212.226
SMILESNS(=O)(=O)Cc1noc2ccccc12
Structure
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