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Human mitochondrial glycerol phosphate dehydrogenase (GPDm) isozymes.

作者信息

Shaw M A, Edwards Y H, Hopkinson D A

出版信息

Ann Hum Genet. 1982 Jan 1;46(1):11-23. doi: 10.1111/j.1469-1809.1982.tb00690.x.

DOI:10.1111/j.1469-1809.1982.tb00690.x
PMID:6808887
Abstract
  1. A hydrophobic/phospholipid electrophoretic system has been devised which makes possible the analysis of human mitochondrial glycerol phosphate dehydrogenase (E.C. 1.1.99.5. GPDM). 2. GPDM has a wide tissue distribution in both adult and foetal life and is active in cultured lymphoblastoid cells and fibroblasts but is absent from red cells. 3. The solubilization procedure does not significantly alter the kinetic properties of the enzyme (Km alpha-glycerophosphate = 0.04-0.07 M, Km PMS = 0.19-0.35 mM) but the soluble form is less thermostable. 4. Comparisons of physicochemical characteristics, tissue distribution and coenzyme requirement point to a separate genetic determination and low level of evolutionary relatedness between GPDM and its cytosolic counterpart GPDS.
摘要

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引用本文的文献

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The expression of human glycerol-3-phosphate dehydrogenase in human/rodent somatic-cell hybrids.人甘油-3-磷酸脱氢酶在人/啮齿动物体细胞杂种中的表达
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Mitochondrial alpha-glycerol phosphate dehydrogenase activity in IIA fibres of the rat lateral gastrocnemius muscle; the effect of Ca2+ and ATP.
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