Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/26434
Title: Aminopyrazine inhibitors binding to an unusual inactive conformation of the mitotic kinase Nek2: SAR and structural characterization.
Authors: Whelligan, DK
Solanki, S
Taylor, D
Thomson, DW
Cheung, KM
Boxall, K
Mas-Droux, C
Barillari, C
Burns, S
Grummitt, CG
Collins, I
van Montfort RL
Aherne, GW
Bayliss, R
Hoelder, S
First Published: 11-Nov-2010
Citation: J MED CHEM, 2010, 53 (21), pp. 7682-7698
Abstract: We report herein the first systematic exploration of inhibitors of the mitotic kinase Nek2. Starting from HTS hit aminopyrazine 2, compounds with improved activity were identified using structure-based design. Our structural biology investigations reveal two notable observations. First, 2 and related compounds bind to an unusual, inactive conformation of the kinase which to the best of our knowledge has not been reported for other types of kinase inhibitors. Second, a phenylalanine residue at the center of the ATP pocket strongly affects the ability of the inhibitor to bind to the protein. The implications of these observations are discussed, and the work described here defines key features for potent and selective Nek2 inhibition, which will aid the identification of more advanced inhibitors of Nek2.
DOI Link: 10.1021/jm1008727
eISSN: 1520-4804
Links: http://hdl.handle.net/2381/26434
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Biochemistry

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