Reaction Details |
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Target | Reverse transcriptase protein |
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Ligand | BDBM50483018 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_677443 (CHEMBL1279436) |
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Kd | 43400±n/a nM |
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Citation | Yang, G; Wang, J; Cheng, Y; Dutschman, GE; Tanaka, H; Baba, M; Cheng, YC Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase by a stavudine analogue, 4'-ethynyl stavudine triphosphate. Antimicrob Agents Chemother52:2035-42 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Reverse transcriptase protein |
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Name: | Reverse transcriptase protein |
Synonyms: | Reverse Transcriptase | Reverse Transcriptase (A62V) | Reverse Transcriptase (F61A) |
Type: | Protein |
Mol. Mass.: | 30203.56 |
Organism: | Human immunodeficiency virus 1 |
Description: | Q9WJQ2 |
Residue: | 259 |
Sequence: | PISPIEPVPVKLKPGMDGPKVKQWPLTEEKIKALVEICTEMEKEGKISKIGPENPYNTPV
FAIKKKDSTRWRKLVDFRELNKRTQDFWEVQLGIPHPAGLKKKRSVTVLDVGDAYFSVPL
DKEFRKYTAFTIPSINNETPGIRYQYNVLPQGWKGSPAIFQSSMTKILEPFRKQNPDIVI
YQYMDDLYVGSDLEIGQHRTKIEELRQHLLKWGFTTPDKKHQKEPPFLWMGYEHHPDKWT
VQPIVLPEKDSWTVNDIQK
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BDBM50483018 |
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n/a |
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Name | BDBM50483018 |
Synonyms: | CHEMBL485651 |
Type | Small organic molecule |
Emp. Form. | C12H15N2O13P3 |
Mol. Mass. | 488.1744 |
SMILES | Cc1cn([C@@H]2O[C@](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)(C=C2)C#C)c(=O)[nH]c1=O |r,c:21| |
Structure |
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