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TargetUrease [D459Y,K653P]
LigandBDBM123720
Substrate/Competitorn/a
Meas. Tech.Urease Inhibition Assay
Temperature303.15±0 K
IC50 4.10e+4± 1.3e+3 nM
Citation Akhtar, TKhan, MAIqbal, JJones, PGHameed, S A facile one-pot synthesis of 2-arylamino-5-aryloxylalkyl-1,3,4-oxadiazoles and their urease inhibition studies. Chem Biol Drug Des84:92-8 (2014) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Urease [D459Y,K653P]
Name:Urease [D459Y,K653P]
Synonyms:UREA_CANEN | Urea amidohydrolase | Urease
Type:Protein
Mol. Mass.:90763.23
Organism:Canavalia ensiformis (Jack bean)
Description:P07374[D459Y,K653P]
Residue:840
Sequence:
MKLSPREVEKLGLHNAGYLAQKRLARGVRLNYTEAVALIASQIMEYARDGEKTVAQLMCL
GQHLLGRRQVLPAVPHLLNAVQVEATFPDGTKLVTVHDPISRENGELQEALFGSLLPVPS
LDKFAETKEDNRIPGEILCEDECLTLNIGRKAVILKVTSKGDRPIQVGSHYHFIEVNPYL
TFDRRKAYGMRLNIAAGTAVRFEPGDCKSVTLVSIEGNKVIRGGNAIADGPVNETNLEAA
MHAVRSKGFGHEEEKDASEGFTKEDPNCPFNTFIHRKEYANKYGPTTGDKIRLGDTNLLA
EIEKDYALYGDECVFGGGKVIRDGMGQSCGHPPAISLDTVITNAVIIDYTGIIKADIGIK
DGLIASIGKAGNPDIMNGVFSNMIIGANTEVIAGEGLIVTAGAIDCHVHYICPQLVYEAI
SSGITTLVGGGTGPAAGTRATTCTPSPTQMRLMLQSTDYLPLNFGFTGKGSSSKPDELHE
IIKAGAMGLKLHEDWGSTPAAIDNCLTIAEHHDIQINIHTDTLNEAGFVEHSIAAFKGRT
IHTYHSEGAGGGHAPDIIKVCGIKNVLPSSTNPTRPLTSNTIDEHLDMLMVCHHLDREIP
EDLAFAHSRIRKKTIAAEDVLNDIGAISIISSDSQAMGRVGEVISRTWQTADPMKAQTGP
LKCDSSDNDNFRIRRYIAKYTINPAIANGFSQYVGSVEVGKLADLVMWKPSFFGTKPEMV
IKGGMVAWADIGDPNASIPTPEPVKMRPMYGTLGKAGGALSIAFVSKAALDQRVNVLYGL
NKRVEAVSNVRKLTKLDMKLNDALPEITVDPESYTVKADGKLLCVSEATTVPLSRNYFLF
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  Blast E-value cutoff:
BDBM123720
n/a
NameBDBM123720
Synonyms:2-(4-Methylphenyl)amino-5-(1-(3,4-dichlorophenoxy)ethyl)-1,3,4-oxadiazole (3d)
TypeSmall organic molecule
Emp. Form.C17H15Cl2N3O2
Mol. Mass.364.226
SMILESCC(Oc1ccc(Cl)c(Cl)c1)c1nnc(Nc2ccc(C)cc2)o1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: