2v16
From Proteopedia
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==Reference== | ==Reference== | ||
Structure-based drug design: the discovery of novel nonpeptide orally active inhibitors of human renin., Rahuel J, Rasetti V, Maibaum J, Rueger H, Goschke R, Cohen NC, Stutz S, Cumin F, Fuhrer W, Wood JM, Grutter MG, Chem Biol. 2000 Jul;7(7):493-504. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10903938 10903938] | Structure-based drug design: the discovery of novel nonpeptide orally active inhibitors of human renin., Rahuel J, Rasetti V, Maibaum J, Rueger H, Goschke R, Cohen NC, Stutz S, Cumin F, Fuhrer W, Wood JM, Grutter MG, Chem Biol. 2000 Jul;7(7):493-504. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10903938 10903938] | ||
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| + | The crystal structures of recombinant glycosylated human renin alone and in complex with a transition state analog inhibitor., Rahuel J, Priestle JP, Grutter MG, J Struct Biol. 1991 Dec;107(3):227-36. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/1807356 1807356] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Renin]] | [[Category: Renin]] | ||
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[[Category: Zymogen]] | [[Category: Zymogen]] | ||
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Revision as of 10:22, 27 July 2008
CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 3
Template:ABSTRACT PUBMED 10903938
About this Structure
2V16 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structure-based drug design: the discovery of novel nonpeptide orally active inhibitors of human renin., Rahuel J, Rasetti V, Maibaum J, Rueger H, Goschke R, Cohen NC, Stutz S, Cumin F, Fuhrer W, Wood JM, Grutter MG, Chem Biol. 2000 Jul;7(7):493-504. PMID:10903938
The crystal structures of recombinant glycosylated human renin alone and in complex with a transition state analog inhibitor., Rahuel J, Priestle JP, Grutter MG, J Struct Biol. 1991 Dec;107(3):227-36. PMID:1807356
Page seeded by OCA on Sun Jul 27 13:22:21 2008
Categories: Homo sapiens | Renin | Single protein | Cohen, N C. | Cumin, F. | Fuhrer, W. | Goschke, R. | Grutter, M G. | Maibaum, J. | Rahuel, J. | Rasetti, V. | Rueger, H. | Stutz, S. | Wood, J M. | Alternative splicing | Aspartyl protease | Cleavage on pair of basic residue | Glycoprotein | Hydrolase | Inhibitor-complex | Polymorphism | Protease | Zymogen
