標題: | Zinc ion acts as a cofactor for serine/threonine kinase MST3 and has a distinct role in autophosphorylation of MST3 |
作者: | Lu, TJ Huang, CYF Yuan, CJ Lee, YC Leu, TH Chang, WC Lu, TL Jeng, WY Lai, MD 生物科技學系 Department of Biological Science and Technology |
關鍵字: | MST3;zinc;cofactor;kinase;cobalt;autophosphorylation |
公開日期: | 1-六月-2005 |
摘要: | We examined the metal ion cofactor preference for MST3 (mammalian Ste20-like kinase 3) of the Ste20 serine/threonine kinase family. Four metal ions (Mg+2, Mn+2, Zn2+, and Co2+) activate endogenous, exogenous, and baculovirus-expressed recombinant MST3 within the physiological concentration range. In contrast, Fe+2 and Ca+2 do not function as MST3 cofactors. Mn2+, Co2+, and Mg2+-dependent autophosphorylation of MST3 is mainly on threonine residue while Zn2+-stimulated MST3 autophosphorylation is on both serine and threonine residues. The distinct autophosphorylation pattern on MST3 suggests that MST3 may exert various types of kinase reactions depending on the type of metal ion cofactor used. To our knowledge, this is the first report showing Zn2+ as the metal ion cofactor of a recombinant serine/threonine kinase. (C) 2005 Elsevier Inc. All rights reserved. |
URI: | http://dx.doi.org/10.1016/j.jinorgbio.2005.03.003 http://hdl.handle.net/11536/13589 |
ISSN: | 0162-0134 |
DOI: | 10.1016/j.jinorgbio.2005.03.003 |
期刊: | JOURNAL OF INORGANIC BIOCHEMISTRY |
Volume: | 99 |
Issue: | 6 |
起始頁: | 1306 |
結束頁: | 1313 |
顯示於類別: | 期刊論文 |