Rigid backbone moiety of KNI-272, a highly selective HIV protease inhibitor: methanol, acetone and dimethylsulfoxide solvated forms of 3-[3-benzyl-2-hydroxy-9-(isoquinolin-5-yloxy)-6-methylsulfanylmethyl-5,8-dioxo-4,7-diazanonanoyl]-N-tert-butyl-1,3-thiazolidine-4-carboxamide

Doi, M.; Kimura, T.; Ishida, T.; Kiso, Y.

doi:10.1107/S0108768104013047

Acta Crystallographica Section B
Acta Crystallographica
Section B STRUCTURAL SCIENCE, CRYSTAL ENGINEERING AND MATERIALS

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Figure 5
Stereoview of the superimposition for four KNI-272 molecules. Molecular fitting was carried out for the four Cα atoms of residues 2–5 with an r.m.s.d. of 0.03–0.08 Å. H atoms are omitted for clarity. The colors cyan, yellow, green, orange and gray represent the ME, AC, DM, MPD and 1HPX forms, respectively. The side chain of Apns³ was disordered to two sites in the MPD form, but only one part is drawn for clarity. This figure is produced using TRUBO-FRODO (Roussel et al., 2002

STRUCTURAL SCIENCE
CRYSTAL ENGINEERING
MATERIALS

ISSN: 2052-5206

Volume 60| Part 4| July 2004| Pages 433-437

doi:10.1107/S0108768104013047

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