2viz: Difference between revisions

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[[Image:2viz.jpg|left|200px]]
{{Seed}}
[[Image:2viz.png|left|200px]]


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{{STRUCTURE_2viz|  PDB=2viz  |  SCENE=  }}  
{{STRUCTURE_2viz|  PDB=2viz  |  SCENE=  }}  


'''HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)-1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(2-OXO-1-PYRROLIDINYL)-5-(PROPYLOXY) BENZAMIDE'''
===HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)-1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(2-OXO-1-PYRROLIDINYL)-5-(PROPYLOXY) BENZAMIDE===




==Overview==
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Inhibition of the aspartyl protease BACE-1 has the potential to deliver a disease-modifying therapy for Alzheimer's disease. Herein, is described the lead generation effort which resulted, with the support of X-ray crystallography, in the discovery of potent inhibitors based on a hydroxy ethylamine (HEA) transition-state mimetic. These inhibitors were capable of lowering amyloid production in a cell-based assay.
The line below this paragraph, {{ABSTRACT_PUBMED_18171614}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 18171614 is the PubMed ID number.
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{{ABSTRACT_PUBMED_18171614}}


==About this Structure==
==About this Structure==
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[[Category: Transmembrane]]
[[Category: Transmembrane]]
[[Category: Zymogen]]
[[Category: Zymogen]]
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