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Beta-secretase (BACE-1) inhibitors: accounting for 10s loop flexibility using rigid active sites.

Authors :
McGaughey GB
Colussi D
Graham SL
Lai MT
Munshi SK
Nantermet PG
Pietrak B
Rajapakse HA
Selnick HG
Stauffer SR
Holloway MK
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2007 Feb 15; Vol. 17 (4), pp. 1117-21. Date of Electronic Publication: 2006 Nov 06.
Publication Year :
2007

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 S(3) pocket. These X-ray structures were used to correlate K(i) 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.

Details

Language :
English
ISSN :
0960-894X
Volume :
17
Issue :
4
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
17112725
Full Text :
https://doi.org/10.1016/j.bmcl.2006.11.003