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TargetReverse transcriptase/RNaseH
LigandBDBM50183194
Substrate/Competitorn/a
Meas. Tech.ChEMBL_355438 (CHEMBL868998)
IC50 165±n/a nM
Citation Muraglia, EKinzel, ODLaufer, RMiller, MDMoyer, GMunshi, VOrvieto, FPalumbi, MCPescatore, GRowley, MWilliams, PDSumma, V Tetrazole thioacetanilides: potent non-nucleoside inhibitors of WT HIV reverse transcriptase and its K103N mutant. Bioorg Med Chem Lett16:2748-52 (2006) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Reverse transcriptase/RNaseH
Name:Reverse transcriptase/RNaseH
Synonyms:HIV-1 Reverse Transcriptase RNase H | Human immunodeficiency virus type 1 reverse transcriptase | Reverse transcriptase/RNaseH
Type:PROTEIN
Mol. Mass.:65229.15
Organism:Human immunodeficiency virus 1
Description:ChEMBL_1473730
Residue:566
Sequence:
PISPIETVPVKLKPGMDGPKVKQWPLTEEKIKALVEICTEMEKEGKISKIGPENPYNTPV
FAIKKKDSTKWRKLVDFRELNKRTQDFWEVQLGIPHPAGLKKRKSVTVLDVGDAYFSVPL
DEDFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVI
YQYMDDLYVGSDLEIGQHRTKIEELRQHLLRWGLTTPDKKHQKEPPFLWMGYELHPDKWT
VQPIVLPEKDSWTVNDIQKLVGKLNWASQIYPGIRVRQLCKLLRGTKALTEVIPLTEEAE
LELAENREILKEPVHGVYYDPSKDLIAEIQKQGQGQWTYQIYQEPFKNLRTGKYARMRGA
HTNDVKQLTEAVQKITTESIVIWGKTPKFKLPIQKETWETWWTEYWQATWIPEWEFVNTP
PLVKLWYQLEKEPIVGAETFYVDGAANRETKLGKAGYVTNRGRQKVVTLTDTTNQKTELQ
AIYLALQDSGLEVNIVTDSQYALGIIQAQPDQSESELVNQIIEQLIKKEKVYLAWVPAHK
GIGGNEQVDKLVSAGIRKVLFLDGID
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50183194
n/a
NameBDBM50183194
Synonyms:2-(1-mesityl-1H-tetrazol-5-ylthio)-N-(2-methyl-4-nitrophenyl)acetamide | CHEMBL377310
TypeSmall organic molecule
Emp. Form.C19H20N6O3S
Mol. Mass.412.465
SMILESCc1cc(C)c(c(C)c1)-n1nnnc1SCC(=O)Nc1ccc(cc1C)[N+]([O-])=O |(-7.4,-3.06,;-7.06,-1.55,;-8.2,-.51,;-7.87,.99,;-9.01,2.03,;-6.4,1.46,;-5.26,.43,;-3.8,.9,;-5.59,-1.09,;-6.08,2.97,;-7.11,4.12,;-6.33,5.45,;-4.83,5.13,;-4.67,3.59,;-3.34,2.82,;-2,3.59,;-.67,2.82,;-.67,1.28,;.66,3.58,;2,2.81,;1.99,1.27,;3.32,.5,;4.66,1.27,;4.65,2.81,;3.32,3.58,;3.32,5.12,;5.99,.49,;5.99,-1.05,;7.33,1.26,)|
Structure
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