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10.1016/j.gde.2016.03.006

http://scihub22266oqcxt.onion/10.1016/j.gde.2016.03.006
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C5055408!5055408!27061491
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suck abstract from ncbi


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pmid27061491      Curr+Opin+Genet+Dev 2016 ; 38 (ä): 45-51
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  • Roles of Fe-S clusters: From cofactor synthesis to iron homeostasis to protein synthesis #MMPMID27061491
  • Pain D; Dancis A
  • Curr Opin Genet Dev 2016[Jun]; 38 (ä): 45-51 PMID27061491show ga
  • Fe-S cluster assembly is an essential process for all cells. Impairment of Fe-S cluster assembly creates diseases in diverse and surprising ways. In one scenario, the loss of function of lipoic acid synthase, an enzyme with Fe-S cluster cofactor in mitochondria, impairs activity of various lipoamide-dependent enzymes with drastic consequences for metabolism. In a second scenario, the heme biosynthetic pathway in red cell precursors is specifically targeted, and iron homeostasis is perturbed, but lipoic acid is unaffected. In a third scenario, tRNA modifications arising from action of the cysteine desulfurase and/or Fe-S cluster proteins are lost, which may lead to impaired protein synthesis. This can then result in cancer, neurologic dysfunction or type 2 diabetes.
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