Literature DB >> 10721890

Long-chain acyl-CoA as a multi-effector ligand in cellular metabolism.

E Shrago1.   

Abstract

Fatty acyl-CoA esters have the ability to bind at specific sites on certain proteins through their CoA moiety, thereby acting as modulators of cellular metabolism. In some cases at least, the acyl-CoA competes with cofactors (nucleotides) for binding to the proteins and results in either their activation or inhibition of catalytic activity. Photolabeling derivatives of acyl-CoA permit covalent binding of the esters to the proteins, which should lead to determination of amino acid residues required for ligand binding, if a common binding motif exists. On the basis of the accumulation of published results, there is now evidence to implicate acyl-CoA esters in the regulation of a variety of biological processes, ranging from mitochondrial metabolism to gene transcription to insulin secretion and signaling.

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Year:  2000        PMID: 10721890     DOI: 10.1093/jn/130.2.290S

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  4 in total

1.  Cloning and characterization of a hormonally regulated rat long chain acyl-CoA synthetase.

Authors:  P Z Tang; C H Tsai-Morris; M L Dufau
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-29       Impact factor: 11.205

2.  Human intestinal acyl-CoA synthetase 5 is sensitive to the inhibitor triacsin C.

Authors:  Elke Kaemmerer; Anne Peuscher; Andrea Reinartz; Christian Liedtke; Ralf Weiskirchen; Jürgen Kopitz; Nikolaus Gassler
Journal:  World J Gastroenterol       Date:  2011-11-28       Impact factor: 5.742

3.  5-Hydroxydecanoate is metabolised in mitochondria and creates a rate-limiting bottleneck for beta-oxidation of fatty acids.

Authors:  Peter J Hanley; Stefan Dröse; Ulrich Brandt; Rachel A Lareau; Abir L Banerjee; D K Srivastava; Leonard J Banaszak; Joseph J Barycki; Paul P Van Veldhoven; Jürgen Daut
Journal:  J Physiol       Date:  2004-10-28       Impact factor: 5.182

4.  Single residue (K332A) substitution in Kir6.2 abolishes the stimulatory effect of long-chain acyl-CoA esters: indications for a long-chain acyl-CoA ester binding motif.

Authors:  R Bränström; I B Leibiger; B Leibiger; G Klement; J Nilsson; P Arhem; C A Aspinwall; B E Corkey; O Larsson; P-O Berggren
Journal:  Diabetologia       Date:  2007-05-24       Impact factor: 10.122

  4 in total

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