Literature DB >> 3930292

Glycogen synthase (casein) kinase-1: tissue distribution and subcellular localization.

T J Singh, K P Huang.   

Abstract

The distribution of glycogen synthase (casein) kinase-1 (CK-1) among different rat tissues and subcellular fractions was investigated. Using casein, glycogen synthase and phosphorylase kinase as substrates, CK-1 activity was detected in kidney, spleen, liver, testis, lung, brain, heart, skeletal muscle and adipose tissue. The distribution of CK-1 among different subcellular fractions of rat liver was; cytosol (72.1%), microsome (17.6%), mitochondria (9.6%) and nuclei (0.7%). CK-1 from rat tissues was shown to have a similarly wide substrate specificity as highly purified CK-1 from rabbit skeletal muscle. Such wide substrate specificity and distribution among different mammalian tissues and subcellular organelles indicate that CK-1 may be involved in the regulation of diverse cellular functions.

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Year:  1985        PMID: 3930292     DOI: 10.1016/0014-5793(85)80433-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  12 in total

1.  Selective knockout of the casein kinase 2 in d1 medium spiny neurons controls dopaminergic function.

Authors:  Heike Rebholz; Mingming Zhou; Angus C Nairn; Paul Greengard; Marc Flajolet
Journal:  Biol Psychiatry       Date:  2013-01-03       Impact factor: 13.382

2.  Association of protein kinase CK2 with eukaryotic translation initiation factor eIF-2 and with grp94/endoplasmin.

Authors:  M Riera; N Roher; F Miró; C Gil; R Trujillo; J Aguilera; M Plana; E Itarte
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

3.  CK2 negatively regulates Galphas signaling.

Authors:  Heike Rebholz; Akinori Nishi; Sabine Liebscher; Angus C Nairn; Marc Flajolet; Paul Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-03       Impact factor: 11.205

4.  Microsomal casein kinase II in endoplasmic reticulum- and Golgi apparatus-rich fractions of ROS 17/2.8 osteoblast-like cells: an enzyme that modifies osteopontin.

Authors:  C B Wu; Y M Pan; Y Simizu
Journal:  Calcif Tissue Int       Date:  1995-10       Impact factor: 4.333

5.  Two genes in Saccharomyces cerevisiae encode a membrane-bound form of casein kinase-1.

Authors:  P C Wang; A Vancura; T G Mitcheson; J Kuret
Journal:  Mol Biol Cell       Date:  1992-03       Impact factor: 4.138

6.  The p53 tumour suppressor protein is phosphorylated at serine 389 by casein kinase II.

Authors:  D W Meek; S Simon; U Kikkawa; W Eckhart
Journal:  EMBO J       Date:  1990-10       Impact factor: 11.598

7.  Comparison of the phosphorylation of microtubule-associated protein tau by non-proline dependent protein kinases.

Authors:  T J Singh; I Grundke-Iqbal; B McDonald; K Iqbal
Journal:  Mol Cell Biochem       Date:  1994-02-23       Impact factor: 3.396

8.  A majority of casein kinase II alpha subunit is tightly bound to intranuclear components but not to the beta subunit.

Authors:  J Stigare; N Buddelmeijer; A Pigon; E Egyhazi
Journal:  Mol Cell Biochem       Date:  1993-12-08       Impact factor: 3.396

9.  Molecular cloning of casein kinase II alpha subunit from Dictyostelium discoideum and its expression in the life cycle.

Authors:  U Kikkawa; S K Mann; R A Firtel; T Hunter
Journal:  Mol Cell Biol       Date:  1992-12       Impact factor: 4.272

10.  Evidence for the induction of casein kinase II in bovine lymphocytes transformed by the intracellular protozoan parasite Theileria parva.

Authors:  O K ole-MoiYoi; W C Brown; K P Iams; A Nayar; T Tsukamoto; M D Macklin
Journal:  EMBO J       Date:  1993-04       Impact factor: 11.598

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