Resistance of HIV-1 reverse transcriptase against [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro-5''-(4''-amino-1'',2''- oxathiole-2'',2''-dioxide)] (TSAO) derivatives is determined by the mutation Glu138-->Lys on the p51 subunit. [electronic resource]
Producer: 19941117Description: 25255-8 p. digitalISSN:- 0021-9258
- Antiviral Agents -- chemistry
- Base Sequence
- Benzodiazepines -- pharmacology
- Binding Sites -- genetics
- Deoxyguanine Nucleotides -- pharmacology
- Dideoxynucleotides
- Drug Resistance -- genetics
- Escherichia coli -- genetics
- HIV Reverse Transcriptase
- Imidazoles -- pharmacology
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Mutation
- Protein Conformation
- RNA-Directed DNA Polymerase -- genetics
- Recombinant Proteins -- metabolism
- Reverse Transcriptase Inhibitors
- Sequence Analysis, DNA
- Spiro Compounds
- Thymidine -- analogs & derivatives
- Uridine -- analogs & derivatives
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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