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TitleDesign and synthesis of pyridone inhibitors of non-nucleoside reverse transcriptase.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 7344-7350, Year 2011
Publish dateAug 4, 2011 (structure data deposition date)
AuthorsGomez, R. / Jolly, S. / Williams, T. / Tucker, T. / Tynebor, R. / Vacca, J. / McGaughey, G. / Lai, M.T. / Felock, P. / Munshi, V. ...Gomez, R. / Jolly, S. / Williams, T. / Tucker, T. / Tynebor, R. / Vacca, J. / McGaughey, G. / Lai, M.T. / Felock, P. / Munshi, V. / DeStefano, D. / Touch, S. / Miller, M. / Yan, Y. / Sanchez, R. / Liang, Y. / Paton, B. / Wan, B.L. / Anthony, N.
External linksBioorg. Med. Chem. Lett. / PubMed:22071300
MethodsX-ray diffraction
Resolution2.51 Å
Structure data

PDB-3tam:
Crystal structure of HIV-1 reverse transcriptase (K103N mutant) in complex with inhibitor M06
Method: X-RAY DIFFRACTION / Resolution: 2.51 Å

Chemicals

ChemComp-M06:
3-chloro-5-{[4-methyl-2-oxo-1-(2H-pyrazolo[3,4-b]pyridin-3-ylmethyl)-1,2-dihydropyridin-3-yl]oxy}benzonitrile

ChemComp-HOH:
WATER

Source
  • hiv-1 m:b_hxb2r (virus)
KeywordsTransferase/transferase Inhibitor / HIV-1 reverse transcriptase / non-nucleoside inhibition / nucleotidyltranferase / K103N / HIV-1 / Transferase-transferase Inhibitor complex

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