4be2
PFV intasome with inhibitor XZ-259PFV intasome with inhibitor XZ-259
Structural highlights
Publication Abstract from PubMedBased on a series of lactam and phthalimide derivatives that inhibit HIV-1 integrase, we developed a new derivative, XZ-259, with biochemical and antiviral activities comparable to raltegravir. We determined the crystal structures of XZ-259 and four other derivatives in complex with the prototype foamy virus intasome. The compounds bind at the integrase-Mg2+-DNA interface of the integrase active site. In biochemical and antiviral assays, XZ-259 inhibits raltegravir-resistant HIV-1 integrases harboring the Y143R mutation. Molecular modeling is also presented suggesting that XZ-259 can bind in the HIV-1 intasome with its dimethyl sulfonamide group adopting two opposite orientations. Molecular dynamics analyses of the HIV-1 intasome highlight the importance of the viral DNA in drug potency. Activities, crystal structures and molecular dynamics of dihydro-1H-isoindole derivatives, inhibitors of HIV-1 integrase.,Metifiot M, Maddali K, Johnson BC, Hare S, Smith SJ, Zhao XZ, Marchand C, Burke TR, Hughes SH, Cherepanov P, Pommier Y ACS Chem Biol. 2012 Oct 17. PMID:23075516[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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OCA- Human spumaretrovirus
- Cherepanov, P
- Hare, S
- Dna integration
- Dna-binding
- Endonuclease
- Hhcc motif
- Inhibitor
- Metal-binding
- Multifunctional enzyme
- Nuclease
- Nucleotidyltransferase
- Nucleus
- Recombination
- Recombination-inhibitor-dna complex
- Transferase
- Transferase-dna complex
- Viral nucleoprotein
- Viral protein
- Virion
- Zinc binding