Title of article :
β-Secretase (BACE-1) inhibitors: Accounting for 10s loop flexibility using rigid active sites
Author/Authors :
Georgia B. McGaughey، نويسنده , , Dennis Colussi، نويسنده , , Samuel L. Graham، نويسنده , , Ming-Tain Lai، نويسنده , , Sanjeev K. Munshi، نويسنده , , Philippe G. Nantermet، نويسنده , , Beth Pietrak، نويسنده , , Hemaka A. Rajapakse، نويسنده , , Harold G. Selnick، نويسنده , , Shaun R. Stauffer، نويسنده , , M. Katharine Holloway، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
5
From page :
1117
To page :
1121
Abstract :
BACE-1 is a flexible enzyme with experimentally determined motion in the flap region, the catalytic aspartates, and the 10s loop. Four in-house crystallographically determined complexes of tertiary carbinamine inhibitors revealed 10s loop motion in the S3 pocket. These X-ray structures were used to correlate Ki values, which span over five orders of magnitude, with the calculated interaction energy, using the Merck Molecular Force Field for a series of 19 tertiary carbinamine inhibitors.
Keywords :
BACE , Scoring functions , Molecular modeling , molecular mechanics , Tertiary carbinamine inhibitors
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2007
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
797803
Link To Document :
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