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TitleHighly Potent and Oral Macrocyclic Peptides as a HIV-1 Protease Inhibitor: mRNA Display-Derived Hit-to-Lead Optimization.
Journal, issue, pagesAcs Med. Chem. Lett., Vol. 13, Page 1634-1641, Year 2022
Publish dateJul 7, 2022 (structure data deposition date)
AuthorsKusumoto, Y. / Hayashi, K. / Sato, S. / Yamada, T. / Kozono, I. / Nakata, Z. / Asada, N. / Mitsuki, S. / Watanabe, A. / Wakasa-Morimoto, C. ...Kusumoto, Y. / Hayashi, K. / Sato, S. / Yamada, T. / Kozono, I. / Nakata, Z. / Asada, N. / Mitsuki, S. / Watanabe, A. / Wakasa-Morimoto, C. / Uemura, K. / Arita, S. / Miki, S. / Mizutare, T. / Mikamiyama, H.
External linksAcs Med. Chem. Lett. / PubMed:36262395
MethodsX-ray diffraction
Resolution2.01 Å
Structure data

PDB-7yf6:
Crystal structure of HIV-1 protease in complex with macrocyclic peptide
Method: X-RAY DIFFRACTION / Resolution: 2.01 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus 1
  • synthetic construct (others)
KeywordsVIRAL PROTEIN/INHIBITOR / VIRAL PROTEIN-INHIBITOR COMPLEX

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