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2oah

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[[Image:2oah.jpg|left|200px]]
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{{STRUCTURE_2oah| PDB=2oah | SCENE= }}
{{STRUCTURE_2oah| PDB=2oah | SCENE= }}
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'''Crystal Structure of Human Beta Secretase Complexed with inhibitor'''
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===Crystal Structure of Human Beta Secretase Complexed with inhibitor===
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==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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(as it appears on PubMed at http://www.pubmed.gov), where 17257835 is the PubMed ID number.
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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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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 10:31:22 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 15:24:28 2008''

Revision as of 12:24, 27 July 2008

Image:2oah.png

Template:STRUCTURE 2oah

Crystal Structure of Human Beta Secretase Complexed with inhibitor

Template:ABSTRACT PUBMED 17257835

About this Structure

2OAH is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Discovery and SAR of isonicotinamide BACE-1 inhibitors that bind beta-secretase in a N-terminal 10s-loop down conformation., Stauffer SR, Stanton MG, Gregro AR, Steinbeiser MA, Shaffer JR, Nantermet PG, Barrow JC, Rittle KE, Collusi D, Espeseth AS, Lai MT, Pietrak BL, Holloway MK, McGaughey GB, Munshi SK, Hochman JH, Simon AJ, Selnick HG, Graham SL, Vacca JP, Bioorg Med Chem Lett. 2007 Mar 15;17(6):1788-92. Epub 2006 Dec 21. PMID:17257835

Page seeded by OCA on Sun Jul 27 15:24:28 2008

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