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  1. 1.   Structural Insights into the Activation and Inhibition of Histo-Aspartic Protease from Plasmodium falciparum
  2. Bhaumik, P.; Xiao, H. G.; Hidaka, K.; Gustchina, A.; Kiso, Y.; Yada, R. Y.; Wlodawer, A.
  3. Biochemistry. 2011, Oct; 50(41): 8862-8879.
  1. 2.   Amino acid substitutions in Gag protein at non-cleavage sites are indispensable for the development of a high multitude of HIV-1 resistance against protease inhibitors
  2. Gatanaga, H.; Suzuki, Y.; Tsang, H.; Yoshimura, K.; Kavlick, M. F.; Nagashima, K.; Gorelick, R. J.; Mardy, S.; Tang, C.; Summers, M. F.; Mitsuya, H.
  3. Journal of Biological Chemistry. 2002 277(8): 5952-5961.
  1. 3.   JE-2147: A dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1
  2. Yoshimura, K.; Kato, R.; Yusa, K.; Kavlick, M. F.; Maroun, V.; Nguyen, A.; Mimoto, T.; Ueno, T.; Shintani, M.; Falloon, J.; Masur, H.; Hayashi, H.; Erickson, J.; Mitsuya, H.
  3. Proceedings of the National Academy of Sciences of the United States of America. 1999 96(15): 8675-8680.
  1. 4.   Dynamic flexibility of protein-inhibitor complexes: A study of the HIV-1 protease KNI-272 complex
  2. Luo, X. C.; Kato, R. H.; Collins, J. R.
  3. Journal of the American Chemical Society. 1998 120(48): 12410-12418.
  1. 5.   Functional characterization of the protease of human endogenous retrovirus, K10: Can it complement HIV-1 protease?
  2. Towler, E. M.; Gulnik, S. V.; Bhat, T. N.; Xie, D.; Gustschina, E.; Sumpter, T. R.; Robertson, N.; Jones, C.; Sauter, M.; Mueller-Lantzsch, N.; Debouck, C.; Erickson, J. W.
  3. Biochemistry. 1998 37(49): 17137-17144.
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