HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase
Diketo acids such as L-731,988 are potent inhibitors of HIV-1 integrase that inhibit integration and viral replication in cells. These compounds exhibit the unique ability to inhibit the strand transfer activity of integrase in the absence of an effect on 3′ end processing. To understand the reasons...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2000
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC17185/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11016953/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.200139397 |
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