نتایج جستجو برای: ژن fxn

تعداد نتایج: 16212  

2017
Salvatore Adinolfi Rita Puglisi Jason C. Crack Clara Iannuzzi Fabrizio Dal Piaz Petr V. Konarev Dmitri I. Svergun Stephen Martin Nick E. Le Brun Annalisa Pastore

IscX (or YfhJ) is a protein of unknown function which takes part in the iron-sulfur cluster assembly machinery, a highly specialized and essential metabolic pathway. IscX binds to iron with low affinity and interacts with IscS, the desulfurase central to cluster assembly. Previous studies have suggested a competition between IscX and CyaY, the bacterial ortholog of frataxin, for the same bindin...

2017
Marco Fantini Duccio Malinverni Paolo De Los Rios Annalisa Pastore

Direct coupling analysis (DCA) is a powerful statistical inference tool used to study protein evolution. It was introduced to predict protein folds and protein-protein interactions, and has also been applied to the prediction of entire interactomes. Here, we have used it to analyze three proteins of the iron-sulfur biogenesis machine, an essential metabolic pathway conserved in all organisms. W...

2015
Matija Popovic Domenico Sanfelice Chiara Pastore Filippo Prischi Piero Andrea Temussi Annalisa Pastore

We have exploited the capability of in-cell NMR to selectively observe flexible regions within folded proteins to carry out a comparative study of two members of the highly conserved frataxin family which are found both in prokaryotes and in eukaryotes. They all contain a globular domain which shares more than 50% identity, which in eukaryotes is preceded by an N-terminal tail containing the mi...

Journal: :Human molecular genetics 2002
Geoffrey Duby Françoise Foury Anna Ramazzotti Johannes Herrmann Thomas Lutz

Friedreich's ataxia is caused by a deficit in frataxin, a small mitochondrial protein of unknown function that has been conserved during evolution. Previous studies have pointed out a role for frataxin in mitochondrial iron-sulfur (Fe-S) metabolism. Here, we have analyzed the incorporation of Fe-S clusters into yeast ferredoxin imported into isolated energized mitochondria from cells grown in t...

2010
Filippo Prischi Petr V. Konarev Clara Iannuzzi Chiara Pastore Salvatore Adinolfi Stephen R. Martin Dmitri I. Svergun Annalisa Pastore

Reduced levels of frataxin, an essential protein of as yet unknown function, are responsible for causing the neurodegenerative pathology Friedreich's ataxia. Independent reports have linked frataxin to iron-sulphur cluster assembly through interactions with the two central components of this machinery: desulphurase Nfs1/IscS and the scaffold protein Isu/IscU. In this study, we use a combination...

Journal: :Iranian journal of allergy, asthma, and immunology 2008
Babak Amra Froogh Soltaninejad Mohammad Golshan

The impulse oscillation system (IOS) measures respiratory impedance (Zrs) in terms of resistance (Rrs) and reactance (Xrs) at multiples of 5 Hz. These measurements can be used clinically to help diagnose and monitor respiratory disorders, independent of effort. There is, as yet, no information on reference values for IOS in Iranian adolescents.The predictive equation for resistance and impedanc...

2009
Filippo Prischi Clelia Giannini Salvatore Adinolfi Annalisa Pastore

Frataxin is a highly conserved nuclear-encoded mitochondrial protein whose deficiency is the primary cause of Friedreich's ataxia, an autosomal recessive neurodegenerative disease. The frataxin structure comprises a well-characterized globular domain that is present in all species and is preceded in eukaryotes by a non-conserved N-terminal tail that contains the mitochondrial import signal. Lit...

2017
I-Son Ng You-Jin Yu Ying-Chen Yi Shih-I Tan Bo-Chuan Huang Yin-Lung Han

The proteomics strategy was utilized to analyze and identify the gold adsorption proteins from Tepidimonas fonticaldi AT-A2, due to its outstanding performance in gold-binding and recovery. The results showed that three small proteins, including histidine biosynthesis protein (HisIE), iron donor protein (CyaY) and hypothetical protein_65aa, have a higher ability to adsorb gold ions because of t...

Journal: :The Biochemical journal 2010
Ana R Correia Tao Wang Elizabeth A Craig Cláudio M Gomes

Frataxin is a highly conserved mitochondrial protein whose deficiency in humans results in Friedreich's ataxia (FRDA), an autosomal recessive disorder characterized by progressive ataxia and cardiomyopathy. Although its cellular function is still not fully clear, the fact that frataxin plays a crucial role in Fe-S assembly on the scaffold protein Isu is well accepted. In the present paper, we r...

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