Characterization of a calmodulin-regulated Ca2+-dependent-protein-kinase-related protein kinase, AtCRK1, from Arahidopsis

被引:31
作者
Wang, Y [1 ]
Liang, SP [1 ]
Xie, QG [1 ]
Lu, YT [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, Key Lab Minist Educ Plant Dev Biol, Wuhan 430072, Peoples R China
关键词
Arabidopsis thaliana; autophosphorylation; calmodulin; capillary electrophoresis; Ca2+-dependent protein-kinase (CDPK)-related protein kinase (CRK);
D O I
10.1042/BJ20031907
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An AtCRK1 [Arabidopsis thaliana CDPK (Ca2+-dependent protein kinase)-related protein kinase 1] has been characterized molecularly and biochemically. AtCRK1 contains the kinase catalytic domain and a CaM (calmodulin)-binding site. Our results demonstrated that AtCRK1 could bind CaM in a Ca2+-dependent manner. This kinase phosphorylated itself and substrates such as histone HIS and syntide-2 in a Ca2+-independent manner and the activity was stimulated by several CaM isoforms through its CaN-binding domain. This domain was localized within a stretch of 39 amino acid residues at positions from 403 to 441 with K-d = 67 nM for CaM binding. However, the stimulation amplification of the kinase activity of AtCRK1 by different CaM isoforms was similar.
引用
收藏
页码:73 / 81
页数:9
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