Design of potent and selective human cathepsin K inhibitors that span the active site.
Thompson, S.K., Halbert, S.M., Bossard, M.J., Tomaszek, T.A., Levy, M.A., Zhao, B., Smith, W.W., Abdel-Meguid, S.S., Janson, C.A., D'Alessio, K.J., McQueney, M.S., Amegadzie, B.Y., Hanning, C.R., DesJarlais, R.L., Briand, J., Sarkar, S.K., Huddleston, M.J., Ijames, C.F., Carr, S.A., Garnes, K.T., Shu, A., Heys, J.R., Bradbeer, J., Zembryki, D., Lee-Rykaczewski, L., James, I.E., Lark, M.W., Drake, F.H., Gowen, M., Gleason, J.G., Veber, D.F.
Proc.Natl.Acad.Sci.USA
