APA

Dohnálek J., Hasek J., Dusková J., Petroková H., Hradilek M., Soucek M., Konvalinka J., Brynda J., Sedlácek J. & Fábry M. (20020429). Hydroxyethylamine isostere of an HIV-1 protease inhibitor prefers its amine to the hydroxy group in binding to catalytic aspartates. A synchrotron study of HIV-1 protease in complex with a peptidomimetic inhibitor. : Journal of medicinal chemistry.

Chicago

Dohnálek Jan, Hasek Jindrich, Dusková Jarmila, Petroková Hana, Hradilek Martin, Soucek Milan, Konvalinka Jan, Brynda Jirí, Sedlácek Juraj and Fábry Milan. 20020429. Hydroxyethylamine isostere of an HIV-1 protease inhibitor prefers its amine to the hydroxy group in binding to catalytic aspartates. A synchrotron study of HIV-1 protease in complex with a peptidomimetic inhibitor. : Journal of medicinal chemistry.

Harvard

Dohnálek J., Hasek J., Dusková J., Petroková H., Hradilek M., Soucek M., Konvalinka J., Brynda J., Sedlácek J. and Fábry M. (20020429). Hydroxyethylamine isostere of an HIV-1 protease inhibitor prefers its amine to the hydroxy group in binding to catalytic aspartates. A synchrotron study of HIV-1 protease in complex with a peptidomimetic inhibitor. : Journal of medicinal chemistry.

MLA

Dohnálek Jan, Hasek Jindrich, Dusková Jarmila, Petroková Hana, Hradilek Martin, Soucek Milan, Konvalinka Jan, Brynda Jirí, Sedlácek Juraj and Fábry Milan. Hydroxyethylamine isostere of an HIV-1 protease inhibitor prefers its amine to the hydroxy group in binding to catalytic aspartates. A synchrotron study of HIV-1 protease in complex with a peptidomimetic inhibitor. : Journal of medicinal chemistry. 20020429.