Functional studies of Fe-S cluster biogenesis machinery in L. donovani
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1
Functional studies of Fe-S cluster biogenesis machinery in L. donovani
DE NW
ISBN: 3330023341 bzw. 9783330023345, in Deutsch, neu.
Functional studies of Fe-S cluster biogenesis machinery in L. donovani ab 69.9 EURO A study of the sulfur donor, IscS, and Fe-S cluster scaffold, IscU, proteins of L. donovani.
2
Functional studies of Fe-S cluster biogenesis machinery in L. donovani
~EN NW
ISBN: 3330023341 bzw. 9783330023345, vermutlich in Englisch, neu.
Functional studies of Fe-S cluster biogenesis machinery in L. donovani ab 69.9 EURO A study of the sulfur donor IscS and Fe-S cluster scaffold IscU proteins of L. donovani.
3
Functional studies of Fe-S cluster biogenesis machinery in L. donovani
DE NW
ISBN: 9783330023345 bzw. 3330023341, in Deutsch, neu.
Lieferung aus: Vereinigtes Königreich Grossbritannien und Nordirland, Lieferzeit: 11 Tage, zzgl. Versandkosten.
The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages.
The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages.
4
Functional studies of Fe-S cluster biogenesis machinery in L. donovani - A study of the sulfur donor, IscS, and Fe-S cluster scaffold, IscU, proteins of L. donovani
DE PB NW
ISBN: 9783330023345 bzw. 3330023341, in Deutsch, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
Functional studies of Fe-S cluster biogenesis machinery in L. donovani: The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages. Englisch, Taschenbuch.
Functional studies of Fe-S cluster biogenesis machinery in L. donovani: The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages. Englisch, Taschenbuch.
5
Functional studies of Fe-S cluster biogenesis machinery in L. donovani
DE HC NW
ISBN: 9783330023345 bzw. 3330023341, in Deutsch, Lap Lambert Academic Publishing, gebundenes Buch, neu.
Lieferung aus: Deutschland, Versandkostenfrei innerhalb von Deutschland.
The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages. Lieferzeit 1-2 Werktage.
The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of The pathogenicity of protozoan parasites, including Leishmania, is frequently attributed to their ability to circumvent the deleterious effects of ROS and Fe-S clusters are amongst their susceptible targets with paramount importance for parasite survival. However, the mechanism of Fe-S clusters biogenesis in Leishmania spp. is unknown impending our knowledge about its potential role in drug resistance, parasite survival and pathogenesis. So, in this study, we characterized the core components of Fe-S cluster biogenesis machinery of L. donovani i.e. IscS and IscU proteins, investigated the interaction between them and tried to identify their correlation with Fe-S proteins activity and drug resistance in L. donovani, the causative agent of the fatal human disease visceral leishmaniasis. For the first time among protozoan parasites, our study showed the biochemical properties of scaffold protein IscU and demonstrated the conservation of IscS-IscU interaction in L. donovani. Additionally, this study revealed a mechanism for regulation of LdIscS and LdIscU expression that may help parasites survival under oxidative stress conditions encountered during infection of macrophages. Lieferzeit 1-2 Werktage.
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Functional studies of Fe-S cluster biogenesis mach (2017)
DE PB NW
ISBN: 9783330023345 bzw. 3330023341, in Deutsch, Taschenbuch, neu.
Lieferung aus: Deutschland, Next Day, Versandkostenfrei.
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Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
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