Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis
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Summary
It is concluded that mammals depend on two distinct mitochondrial ferredoxins for the specific production of either steroid hormones or heme A and Fe/S proteins.
- Type
- article
- Published
- 2010-06-14
- Cited by
- 376
- References
- 48
- Access
- Open access
- OpenAlex
- https://openalex.org/W1987704635
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:33907561
Keywords
Adrenodoxin, Ferredoxin, Biochemistry, Iron–sulfur cluster, Heme
References
- The Heme Synthesis Defect of Mutants Impaired in Mitochondrial Iron-Sulfur Protein Biogenesis Is Caused by Reversible Inhibition of Ferrochelatase*
- Analysis of iron–sulfur protein maturation in eukaryotes
- Iron acquisition and transcriptional regulation.
- Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
- Purification and functional characterization of human 11β hydroxylase expressed in Escherichia coli
- Distribution of iron in reticulocytes after inhibition of heme synthesis with succinylacetone: examination of the intermediates involved in iron metabolism.
- Chapter 12 Controlled expression of iron-sulfur cluster assembly components for respiratory chain complexes in mammalian cells.
- Ferredoxin reductase affects p53-dependent, 5-fluorouracil–induced apoptosis in colorectal cancer cells
- The ubiquitous roles of cytochrome P450 proteins
- Overview of iron--sulfur proteins.
- Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia
- Iron-sulfur proteins in health and disease.
- Adrenodoxin: Structure, stability, and electron transfer properties
- Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy.
- A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins.
- New aspects of electron transfer revealed by the crystal structure of a truncated bovine adrenodoxin, Adx(4-108).
- Characterization of Iron-Sulfur Protein Assembly in Isolated Mitochondria
- Pattern of Expression and Substrate Specificity of Chloroplast Ferredoxins from Chlamydomonas reinhardtii*
- Molecular evolution before the origin of species.
- Iron transport in K562 cells: a kinetic study using native gel electrophoresis and 59Fe autoradiography.
Cited by
- Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.
- Etude de la voie du coenzyme Q¦ chez la levure Saccharomyces cerevisiae
- The mitochondrial redox regulation of steroidogenesis
- Frataxin Accelerates [2Fe-2S] Cluster Formation on the Human Fe–S Assembly Complex
- New Methodology for Measuring Semantic Functional Similarity Based on Bidirectional Integration
- Functional reconstitution of mitochondrial Fe/S cluster synthesis on Isu1 reveals the involvement of ferredoxin
- Optimierung der Identifizierungsstrategie von Proteinsignaturen aus Gewebe und Plasma: Proteomanalyse von Conn-Tumoren und Rektumkarzinom
- Early steps in steroidogenesis: intracellular cholesterol trafficking
- ISC-like [2Fe–2S] ferredoxin (FdxB) dimer from Pseudomonas putida JCM 20004: structural and electron–nuclear double resonance characterization
- Adrenodoxin: the archetype of vertebrate-type [2Fe-2S] cluster ferredoxins.
- Mammalian iron metabolism and its control by iron regulatory proteins
- Human CIA2A (FAM96A) and CIA2B (FAM96B) integrate maturation of different subsets of cytosolic-nuclear iron-sulfur proteins and iron homeostasis
- Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in disease.
- Human Ferredoxin-2 Displays a Unique Conformational Change
- Functional characterization of Fdx1: evidence for an evolutionary relationship between P450-type and ISC-type ferredoxins.
- Coenzyme Q biosynthesis: Coq6 is required for the C5-hydroxylation reaction and substrate analogs rescue Coq6 deficiency.
- Transcriptional regulation of human ferredoxin reductase through an intronic enhancer in steroidogenic cells.
- The Long History of Iron in the Universe and in Health and Disease
- [2Fe-2S]-Ferredoxin Binds Directly to Cysteine Desulfurase and Supplies an Electron for Iron–Sulfur Cluster Assembly but Is Displaced by the Scaffold Protein or Bacterial Frataxin
- Adrenodoxin—A versatile ferredoxin
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