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Cyanide does more to inhibit heme enzymes, than merely serving as an active-site ligand.
Parashar, Abhinav; Venkatachalam, Avanthika; Gideon, Daniel Andrew; Manoj, Kelath Murali.
Afiliación
  • Parashar A; Center for Biomedical Research, VIT University, Vellore, Tamil Nadu, 632014 India.
  • Venkatachalam A; REDOx Lab, PSG Institute of Advanced Studies, Avinashi Road, Peelamedu, Coimbatore, Tamil Nadu, 641004, India.
  • Gideon DA; Center for Biomedical Research, VIT University, Vellore, Tamil Nadu, 632014 India.
  • Manoj KM; REDOx Lab, PSG Institute of Advanced Studies, Avinashi Road, Peelamedu, Coimbatore, Tamil Nadu, 641004, India. Electronic address: satyamjayatu@yahoo.com.
Biochem Biophys Res Commun ; 455(3-4): 190-3, 2014 Dec 12.
Article en En | MEDLINE | ID: mdl-25449264
The toxicity of cyanide is hitherto attributed to its ability to bind to heme proteins' active site and thereby inhibit their activity. It is shown herein that the long-held interpretation is inadequate to explain several observations in heme-enzyme reaction systems. Generation of cyanide-based diffusible radicals in heme-enzyme reaction milieu could shunt electron transfers (by non-active site processes), and thus be detrimental to the efficiency of oxidative outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cianuros / Hemo Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cianuros / Hemo Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article