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・ Proliga (Portugal)
・ Proligestone
・ Prolimacodes badia
・ Prolimacodes lilalia
・ Prolimnophila
・ Proline
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・ Proline (disambiguation)
・ Proline 3-hydroxylase
・ Proline aminopeptidase
・ Proline dehydrogenase
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Proline oxidase
・ Proline racemase
・ Proline rich protein
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・ Proline-Rich Coiled Coil 1
・ Proline-rich protein 21
・ Proline-rich protein haeiii subfamily 2
・ Proline—tRNA ligase
・ PROLINNOVA
・ Prolinol
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・ Prolisky
・ Prolistrophorus bakeri
・ Prolistrophorus grassii


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Proline oxidase : ウィキペディア英語版
Proline oxidase

Proline dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ''PRODH'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5625 )
The protein encoded by this gene is a mitochondrial proline dehydrogenase which catalyzes the first step in proline catabolism. Deletion of this gene has been associated with type I hyperprolinemia. The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes: DiGeorge syndrome and CATCH22 syndrome.〔
== Function ==

Proline oxidase, or proline dehydrogenase, functions as the initiator of the proline cycle. Proline metabolism is especially important in nutrient stress because proline is readily available from the breakdown of extracellular matrix (ECM), and the degradation of proline through the proline cycle initiated by proline oxidase (PRODH), a mitochondrial inner membrane enzyme, can generate ATP. This degradative pathway generates glutamate and alpha-ketoglutarate, products that can play an anaplerotic role for the TCA cycle.The proline cycle is also in a metabolic interlock with the pentose phosphate pathway providing another bioenergetic mechanism. The induction of stress either by glucose withdrawal or by treatment with rapamycin, stimulated degradation of proline and increased PRODH catalytic activity. Under these conditions PRODH was responsible, at least in part, for maintenance of ATP levels. Activation of AMP-activated protein kinase (AMPK), the cellular energy sensor, by 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), also markedly upregulated PRODH and increased PRODH-dependent ATP levels, further supporting its role during stress. Glucose deprivation increased intracellular proline levels, and expression of PRODH activated the pentose phosphate pathway. Therefore, the induction of the proline cycle under conditions of nutrient stress may be a mechanism by which cells switch to a catabolic mode for maintaining cellular energy levels.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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