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TargetTryptase beta-2
LigandBDBM16307
Substrate/CompetitorBDBM12679
Meas. Tech.Enzyme Inhibition Assay
pH8.2±n/a
Temperature295.15±n/a K
Ki 310±n/a nM
Citation Katz, BAClark, JMFiner-Moore, JSJenkins, TEJohnson, CRRoss, MJLuong, CMoore, WRStroud, RM Design of potent selective zinc-mediated serine protease inhibitors. Nature391:608-12 (1998) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Tryptase beta-2
Name:Tryptase beta-2
Synonyms:TPS2 | TPSB2 | TRYB2_HUMAN | Tryptase | Tryptase II | Tryptase beta-1 | Tryptase-2
Type:PROTEIN
Mol. Mass.:30518.79
Organism:Homo sapiens (Human)
Description:ChEMBL_210702
Residue:275
Sequence:
MLNLLLLALPVLASRAYAAPAPGQALQRVGIVGGQEAPRSKWPWQVSLRVHGPYWMHFCG
GSLIHPQWVLTAAHCVGPDVKDLAALRVQLREQHLYYQDQLLPVSRIIVHPQFYTAQIGA
DIALLELEEPVNVSSHVHTVTLPPASETFPPGMPCWVTGWGDVDNDERLPPPFPLKQVKV
PIMENHICDAKYHLGAYTGDDVRIVRDDMLCAGNTRRDSCQGDSGGPLVCKVNGTWLQAG
VVSWGEGCAQPNRPGIYTRVTYYLDWIHHYVPKKP
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM16307
BDBM12679
NameBDBM16307
Synonyms:2-(pyridin-2-ylmethyl)-1H-1,3-benzodiazole-6-carboximidamide | 2-(pyridin-2-ylmethyl)-1H-benzimidazole-6-carboximidamide | APD-5 | CHEMBL204126
TypeSmall organic molecule
Emp. Form.C14H13N5
Mol. Mass.251.2865
SMILESNC(=N)c1ccc2nc(Cc3ccccn3)[nH]c2c1
Structure
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