Dual Ser and Thr phosphorylation of CPI-17, an inhibitor of myosin phosphatase, by MYPT-associated kinase

Citation
Ja. Macdonald et al., Dual Ser and Thr phosphorylation of CPI-17, an inhibitor of myosin phosphatase, by MYPT-associated kinase, FEBS LETTER, 493(2-3), 2001, pp. 91-94
Citations number
29
Categorie Soggetti
Biochemistry & Biophysics
Journal title
FEBS LETTERS
ISSN journal
00145793 → ACNP
Volume
493
Issue
2-3
Year of publication
2001
Pages
91 - 94
Database
ISI
SICI code
0014-5793(20010330)493:2-3<91:DSATPO>2.0.ZU;2-N
Abstract
Phosphorylation of CPI-17 and PHI-1 by the MYPT1-associated kinase (M110 ki nase) was investigated. M110 kinase is a recently identified serine/threoni ne kinase with a catalytic domain that is homologous to that of ZIP kinase (ZIPK, GST-rN-ZIPk, a constitutively active GST fusion fragment, phosphoryl ates CPI-17 (but not PHI-1) to a stoichiometry of 1.7 mol/mol, Phosphoamino acid analysis revealed phosphorylation of both Ser and Thr residues, Phosp horylation sites in CPI-17 were identified as Thr 38 and Ser 12 using Edman sequencing with P-32 release and a point mutant of Thr 38, (C) 2001 Publis hed by Elsevier Science B.V. on behalf of the Federation of European Bioche mical Societies.