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TargetDNA dC->dU-editing enzyme APOBEC-3G
LigandBDBM47735
Substrate/Competitorn/a
Meas. Tech.Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay
Temperature298.15±n/a K
IC50 18400±n/a nM
Commentsextracted
Citation PubChem, PC Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay PubChem Bioassay(2011)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
DNA dC->dU-editing enzyme APOBEC-3G
Name:DNA dC->dU-editing enzyme APOBEC-3G
Synonyms:ABC3G_HUMAN | APOBEC3G
Type:Enzyme Catalytic Domain
Mol. Mass.:46419.54
Organism:Homo sapiens (Human)
Description:gi_13399304
Residue:384
Sequence:
MKPHFRNTVERMYRDTFSYNFYNRPILSRRNTVWLCYEVKTKGPSRPPLDAKIFRGQVYS
ELKYHPEMRFFHWFSKWRKLHRDQEYEVTWYISWSPCTKCTRDMATFLAEDPKVTLTIFV
ARLYYFWDPDYQEALRSLCQKRDGPRATMKIMNYDEFQHCWSKFVYSQRELFEPWNNLPK
YYILLHIMLGEILRHSMDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRG
FLCNQAPHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFIS
KNKHVSLCIFTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHCWDTFVDHQGCPFQP
WDGLDEHSQDLSGRLRAILQNQEN
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  Blast E-value cutoff:
BDBM47735
n/a
NameBDBM47735
Synonyms:3-chloranyl-N-(3,3-dimethylbutan-2-yl)-6-nitro-1-benzothiophene-2-carboxamide | 3-chloro-6-nitro-N-(1,2,2-trimethylpropyl)-1-benzothiophene-2-carboxamide | 3-chloro-6-nitro-N-(1,2,2-trimethylpropyl)benzothiophene-2-carboxamide | 3-chloro-N-(3,3-dimethylbutan-2-yl)-6-nitro-1-benzothiophene-2-carboxamide | MLS000583265 | SMR000201101 | cid_2971539
TypeSmall organic molecule
Emp. Form.C15H17ClN2O3S
Mol. Mass.340.825
SMILESCC(NC(=O)c1sc2cc(ccc2c1Cl)[N+]([O-])=O)C(C)(C)C
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: