Literature DB >> 3022646

Heparin-activated protein kinase from rabbit muscle: relationship to enzymes of the glycogen synthase kinase-3 category.

Z Ahmad, F T Lee, A A DePaoli-Roach, P J Roach.   

Abstract

A heparin-activated protein kinase has been previously identified in rabbit skeletal muscle extracts (Z. Ahmad et al. (1985) FEBS Lett. 179, 96-100). Further study has indicated that this enzyme phosphorylates rabbit muscle glycogen synthase in the same tryptic peptide(s) as the protein kinase FA/GSK-3 (glycogen synthase kinase-3) and is able to activate the ATP-Mg2+-dependent protein phosphatase. These results indicate similarities in properties between the two protein kinases. Exposure of the heparin-activated enzyme to trypsin resulted in loss of heparin activation, from 3-fold to 1.3-fold. One hypothesis suggested by this result is that the enzyme FA/GSK-3 could be a derivative of the heparin-activated enzyme that has lost heparin sensitivity. The conceptual importance of this hypothesis is that it may provide a clue to the mode of regulation of this important class of protein kinases.

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Year:  1986        PMID: 3022646     DOI: 10.1016/0003-9861(86)90734-4

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  2 in total

1.  Heparin binds to Leishmania donovani promastigotes and inhibits protein phosphorylation.

Authors:  N K Mukhopadhyay; K Shome; A K Saha; J R Hassell; R H Glew
Journal:  Biochem J       Date:  1989-12-01       Impact factor: 3.857

2.  Requirement of the self-glucosylating initiator proteins Glg1p and Glg2p for glycogen accumulation in Saccharomyces cerevisiae.

Authors:  C Cheng; J Mu; I Farkas; D Huang; M G Goebl; P J Roach
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

  2 in total

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