Literature DB >> 25449264

Cyanide does more to inhibit heme enzymes, than merely serving as an active-site ligand.

Abhinav Parashar1, Avanthika Venkatachalam2, Daniel Andrew Gideon1, Kelath Murali Manoj3.   

Abstract

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.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cyanide; Dose-response; Heme-enzymes; Inhibition; Peroxidation

Mesh:

Substances:

Year:  2014        PMID: 25449264     DOI: 10.1016/j.bbrc.2014.10.137

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


  3 in total

1.  The proton pumping bo oxidase from Vitreoscilla.

Authors:  Simone Graf; Peter Brzezinski; Christoph von Ballmoos
Journal:  Sci Rep       Date:  2019-03-18       Impact factor: 4.379

2.  Functioning of Microsomal Cytochrome P450s: Murburn Concept Explains the Metabolism of Xenobiotics in Hepatocytes.

Authors:  Kelath Murali Manoj; Abhinav Parashar; Sudeep K Gade; Avanthika Venkatachalam
Journal:  Front Pharmacol       Date:  2016-06-23       Impact factor: 5.810

3.  Murburn Concept: A Molecular Explanation for Hormetic and Idiosyncratic Dose Responses.

Authors:  Abhinav Parashar; Daniel Andrew Gideon; Kelath Murali Manoj
Journal:  Dose Response       Date:  2018-05-09       Impact factor: 2.658

  3 in total

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