2oah: Difference between revisions

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{{STRUCTURE_2oah|  PDB=2oah  |  SCENE=  }}  
{{STRUCTURE_2oah|  PDB=2oah  |  SCENE=  }}  


'''Crystal Structure of Human Beta Secretase Complexed with inhibitor'''
===Crystal Structure of Human Beta Secretase Complexed with inhibitor===




==Overview==
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A series of low-molecular weight 2,6-diamino-isonicotinamide BACE-1 inhibitors containing an amine transition-state isostere were synthesized and shown to be highly potent in both enzymatic and cell-based assays. These inhibitors contain a trans-S,S-methyl cyclopropane P(3) which bind BACE-1 in a 10s-loop down conformation giving rise to highly potent compounds with favorable molecular weight and moderate to high susceptibility to P-glycoprotein (P-gp) efflux.
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{{ABSTRACT_PUBMED_17257835}}


==About this Structure==
==About this Structure==
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[[Category: Bace]]
[[Category: Bace]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]
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