| Literature DB >> 15196054 |
Ying Wang1, Shuping Liang, Qi-Guang Xie, Ying-Tang Lu.
Abstract
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 IIIS and syntide-2 in a Ca2+-independent manner and the activity was stimulated by several CaM isoforms through its CaM-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.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15196054 PMCID: PMC1134045 DOI: 10.1042/BJ20031907
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857