TY - JOUR
T1 - Characterization and purification of kinase activities against Arabidopsis COP9 signalosome subunit 7
AU - Malec, Przemyslaw
AU - Chamovitz, Daniel A.
PY - 2006
Y1 - 2006
N2 - The COP9 signalosome (CSN) is a multisubunit protein complex that intersects the ubiquitin (Ub)-proteasome pathway at several junctions. The CSN associates with several protein kinases that target key regulatory proteins that themselves are targets for Ub-dependent degradation, and several subunits themselves are phosphoproteins. We previously reported that Arabidopsis CSN7 is a phosphoprotein. To identify the kinases responsible for CSN7 phosphorylation, we biochemically purified CSN7-kinsae activities from cauliflower through a four-step purification procedure that resulted in a ca. 300-fold enrichment. One of these activities is Ca2+ dependent, while the second is not. Peptide fingerprint analysis of the purified proteins identified three putative CSN7 kinases.
AB - The COP9 signalosome (CSN) is a multisubunit protein complex that intersects the ubiquitin (Ub)-proteasome pathway at several junctions. The CSN associates with several protein kinases that target key regulatory proteins that themselves are targets for Ub-dependent degradation, and several subunits themselves are phosphoproteins. We previously reported that Arabidopsis CSN7 is a phosphoprotein. To identify the kinases responsible for CSN7 phosphorylation, we biochemically purified CSN7-kinsae activities from cauliflower through a four-step purification procedure that resulted in a ca. 300-fold enrichment. One of these activities is Ca2+ dependent, while the second is not. Peptide fingerprint analysis of the purified proteins identified three putative CSN7 kinases.
UR - http://www.scopus.com/inward/record.url?scp=33845678681&partnerID=8YFLogxK
U2 - 10.1560/D63A-QF35-RGEB-NRMQ
DO - 10.1560/D63A-QF35-RGEB-NRMQ
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AN - SCOPUS:33845678681
SN - 0021-2148
VL - 46
SP - 239
EP - 246
JO - Israel Journal of Chemistry
JF - Israel Journal of Chemistry
IS - 2
ER -