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W W Smith

Showing results (51-60 of 65) with videos related to

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Cell|June 3, 1994
Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyproteinD A Matthews, W W Smith, R A Ferre, et al.
Journal of Medicinal Chemistry|March 6, 1992
Design and synthesis of novel 6,7-imidazotetrahydroquinoline inhibitors of thymidylate synthase using iterative protein crystal structure analysisS H Reich, M A Fuhry, D Nguyen, et al.
International Journal of Obesity (2005)|December 14, 2011
A novel obesity model: synphilin-1-induced hyperphagia and obesity in miceX Li, K L K Tamashiro, Z Liu, et al.
Biochemistry|December 31, 1997
Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complexS S Hoog, W W Smith, X Qiu, et al.
Nature Structural Biology|February 1, 1997
Crystal structure of human osteoclast cathepsin K complex with E-64B Zhao, C A Janson, B Y Amegadzie, et al.
Journal of Medicinal Chemistry|November 7, 1998
Use of papain as a model for the structure-based design of cathepsin K inhibitors: crystal structures of two papain-inhibitor complexes demonstrate binding to S'-subsitesJ M LaLonde, B Zhao, W W Smith, et al.
Protein Science : a Publication of the Protein Society|September 22, 2001
Crystal structure of Staphylococcus aureus tyrosyl-tRNA synthetase in complex with a class of potent and specific inhibitorsX Qiu, C A Janson, W W Smith, et al.
Journal of Medicinal Chemistry|October 10, 1998
Structure-based design of cathepsin K inhibitors containing a benzyloxy-substituted benzoyl peptidomimeticS K Thompson, W W Smith, B Zhao, et al.
Journal of Medicinal Chemistry|September 11, 1998
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin KR W Marquis, D S Yamashita, Y Ru, et al.
Bioorganic & Medicinal Chemistry|June 3, 1999
Potent dipeptidylketone inhibitors of the cysteine protease cathepsin KR W Marquis, Y Ru, D S Yamashita, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Cell|June 3, 1994
Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyproteinD A Matthews, W W Smith, R A Ferre, et al.
Journal of Medicinal Chemistry|March 6, 1992
Design and synthesis of novel 6,7-imidazotetrahydroquinoline inhibitors of thymidylate synthase using iterative protein crystal structure analysisS H Reich, M A Fuhry, D Nguyen, et al.
International Journal of Obesity (2005)|December 14, 2011
A novel obesity model: synphilin-1-induced hyperphagia and obesity in miceX Li, K L K Tamashiro, Z Liu, et al.
Biochemistry|December 31, 1997
Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complexS S Hoog, W W Smith, X Qiu, et al.
Nature Structural Biology|February 1, 1997
Crystal structure of human osteoclast cathepsin K complex with E-64B Zhao, C A Janson, B Y Amegadzie, et al.
Journal of Medicinal Chemistry|November 7, 1998
Use of papain as a model for the structure-based design of cathepsin K inhibitors: crystal structures of two papain-inhibitor complexes demonstrate binding to S'-subsitesJ M LaLonde, B Zhao, W W Smith, et al.
Protein Science : a Publication of the Protein Society|September 22, 2001
Crystal structure of Staphylococcus aureus tyrosyl-tRNA synthetase in complex with a class of potent and specific inhibitorsX Qiu, C A Janson, W W Smith, et al.
Journal of Medicinal Chemistry|October 10, 1998
Structure-based design of cathepsin K inhibitors containing a benzyloxy-substituted benzoyl peptidomimeticS K Thompson, W W Smith, B Zhao, et al.
Journal of Medicinal Chemistry|September 11, 1998
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin KR W Marquis, D S Yamashita, Y Ru, et al.
Bioorganic & Medicinal Chemistry|June 3, 1999
Potent dipeptidylketone inhibitors of the cysteine protease cathepsin KR W Marquis, Y Ru, D S Yamashita, et al.
Pageof 7