抄録
Rho-kinase is a main player in the regulation of cytoskeletal events and a promising drug target in the treatment of both vascular and neurological disorders. Here we report the crystal structure of the Rho-kinase catalytic domain in complex with the specific inhibitor Y-27632. Comparison with the structure of PKA bound to this inhibitor revealed a potential induced-fit binding mode that can be accommodated by the phosphate binding loop. This binding mode resembles to that observed in the Rho-kinase-fasudil complex. A structural database search indicated that a pocket underneath the phosphate-binding loop is present that favors binding to a small aromatic ring. Introduction of such a ring group might spawn a new modification scheme of pre-existing protein kinase inhibitors for improved binding capability.
本文言語 | 英語 |
---|---|
ページ(範囲) | 305-311 |
ページ数 | 7 |
ジャーナル | Journal of Biochemistry |
巻 | 140 |
号 | 3 |
DOI | |
出版ステータス | 出版済み - 09-2006 |
外部発表 | はい |
All Science Journal Classification (ASJC) codes
- 生化学
- 分子生物学