Literature DB >> 3157375

Structural analogies between protein kinase C activators.

R Brasseur, V Cabiaux, P Huart, M Castagna, S Baztar, J M Ruysschaert.   

Abstract

Phorbol esters and diacylglycerols activate protein kinase C but specific structural parameters appear to be required for the enzyme activation. We have analyzed the conformation of potent and not potent diacylglycerols and phorbol esters. The orientation of the CH20H group at C3 of 1,2 diolein is remarkably similar to that of the same group at C-20 of 4 beta phorbol didecanoate and crucial for potency in activating the enzyme. Our data suggest that the new conformational approach here described could be used to rationally design specific inhibitors preventing the effects of tumor promoters and to predict the structure of potential tumor promoters.

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Year:  1985        PMID: 3157375     DOI: 10.1016/s0006-291x(85)80039-5

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

Review 1.  Activation and regulation of protein kinase C enzymes.

Authors:  G L Nelsestuen; M D Bazzi
Journal:  J Bioenerg Biomembr       Date:  1991-02       Impact factor: 2.945

Review 2.  Regulation of protein kinase C activity by various lipids.

Authors:  A A Farooqui; T Farooqui; A J Yates; L A Horrocks
Journal:  Neurochem Res       Date:  1988-06       Impact factor: 3.996

3.  Derivatives of di-O-octanoylglycerol and mono-O-octylglycerol as modulators of protein kinase C and diacylglycerol kinase activities.

Authors:  J Goddat; H Coste; I Vilgrain; E Chambaz; H Driguez
Journal:  Lipids       Date:  1992-05       Impact factor: 1.880

4.  Inhibition of high-affinity gamma-aminobutyric acid uptake in primary astrocyte cultures by phorbol esters and phospholipase C.

Authors:  J Gomeza; M Casado; C Gimenez; C Aragon
Journal:  Biochem J       Date:  1991-04-15       Impact factor: 3.857

  4 in total

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