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TitlePotent Inhibitors Active against HIV Reverse Transcriptase with K101P, a Mutation Conferring Rilpivirine Resistance.
Journal, issue, pagesAcs Med. Chem. Lett., Vol. 6, Page 1075-1079, Year 2015
Publish dateJun 17, 2015 (structure data deposition date)
AuthorsGray, W.T. / Frey, K.M. / Laskey, S.B. / Mislak, A.C. / Spasov, K.A. / Lee, W.G. / Bollini, M. / Siliciano, R.F. / Jorgensen, W.L. / Anderson, K.S.
External linksAcs Med. Chem. Lett. / PubMed:26487915
MethodsX-ray diffraction
Resolution3.5 Å
Structure data

PDB-5c42:
Crystal Structure of HIV-1 Reverse Transcriptase (K101P) Variant in Complex with 8-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)ethoxy)phenoxy)indolizine-2-carbonitrile (JLJ555), a non-nucleoside inhibitor
Method: X-RAY DIFFRACTION / Resolution: 3.5 Å

Chemicals

ChemComp-29T:
8-{2-[2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)ethoxy]phenoxy}indolizine-2-carbonitrile

Source
  • human immunodeficiency virus type 1 group m subtype b (isolate bh10)
KeywordsTRANSFERASE / HYDROLASE/INHIBITOR / HIV / reverse transcriptase / polymerase / non-nucleoside inhibitor / resistance / HYDROLASE-INHIBITOR complex

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