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Alpha-keto acid dehydrogenase complexes. 13. Reaction of sulfhydryl groups in pyruvate dehydrogenase with organic mercurials.

作者信息

Schwartz E R, Reed L J

出版信息

J Biol Chem. 1970 Jan 10;245(1):183-7.

PMID:4904089
Abstract
摘要

相似文献

1
Alpha-keto acid dehydrogenase complexes. 13. Reaction of sulfhydryl groups in pyruvate dehydrogenase with organic mercurials.α-酮酸脱氢酶复合体。13. 丙酮酸脱氢酶中巯基与有机汞的反应。
J Biol Chem. 1970 Jan 10;245(1):183-7.
2
Reaction of the sulphydryl groups of lobster-muscle glyceraldehyde-3-phosphate dehydrogenase with organic mercurials.龙虾肌肉磷酸甘油醛脱氢酶的巯基与有机汞的反应。
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3
Studies on Escherichia coli pyruvate dehydrogenase complex. I. Effect of bromopyruvate on the catalytic activities of the complex.
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Studies on methionyl transfer RNA synthetase from Escherichia coli K12. Amino acid composition and relation of sulfhydryl groups to enzyme activities.
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Studies on the nature of the binding of thiamine pyrophosphate to enzymes.硫胺素焦磷酸与酶结合性质的研究。
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On the reactivity of the sulfhydryl groups of ferredoxin nicotinamide adenine dinucleotide phosphate reductase.关于铁氧化还原蛋白烟酰胺腺嘌呤二核苷酸磷酸还原酶巯基的反应活性
J Biol Chem. 1969 Sep 10;244(17):4757-60.
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The mechanism of 6-deoxyhexose synthesis. V. The relation of pyridine nucleotide to the structure of the deoxythymidine diphosphate-glucose oxidoreductase.6-脱氧己糖的合成机制。V. 吡啶核苷酸与脱氧胸苷二磷酸葡萄糖氧化还原酶结构的关系。
J Biol Chem. 1970 Dec 25;245(24):6599-606.
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Regulatroy properties of the pyruvate-dehydrogenase complex from Escherichia coli. Thiamine pyrophosphate as an effector.大肠杆菌丙酮酸脱氢酶复合体的调节特性。硫胺素焦磷酸作为效应物。
Eur J Biochem. 1974 Oct 2;48(2):377-87. doi: 10.1111/j.1432-1033.1974.tb03779.x.
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Mechanism of coupled electron and group transfer in Escherichia coli pyruvate dehydrogenase.大肠杆菌丙酮酸脱氢酶中电子与基团偶联转移的机制。
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The sulfhydryl groups of rabbit muscle adenosine triphosphate-adenosine monophosphate phosphotransferase. Activity of enzyme treated with mercurials.兔肌三磷酸腺苷-单磷酸腺苷磷酸转移酶的巯基。用汞制剂处理后的酶活性。
J Biol Chem. 1966 May 25;241(10):2293-300.

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Syndromic progressive neurodegenerative disease of infancy caused by novel variants in HIBCH: Report of two cases in Colombia.由HIBCH基因新变异引起的婴儿期综合征性进行性神经退行性疾病：哥伦比亚两例报告
Intractable Rare Dis Res. 2019 Aug;8(3):187-193. doi: 10.5582/irdr.2019.01014.
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Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency.病例报告和短链烯酰基辅酶 A 水合酶缺乏症所致常染色体隐性 Leigh 综合征的新型治疗方法。
Am J Med Genet A. 2019 May;179(5):803-807. doi: 10.1002/ajmg.a.61074. Epub 2019 Mar 7.
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HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase.
HIBCH 突变可导致类似 Leigh 病的疾病，伴有多种线粒体呼吸链酶和丙酮酸脱氢酶的联合缺乏。
Orphanet J Rare Dis. 2013 Dec 4;8:188. doi: 10.1186/1750-1172-8-188.
4
Pyruvate dehydrogenase complex from higher plant mitochondria and proplastids.高等植物线粒体和前质体中的丙酮酸脱氢酶复合物。
Plant Physiol. 1977 May;59(5):842-8. doi: 10.1104/pp.59.5.842.
5
Molecular structure of the pyruvate dehydrogenase complex from Escherichia coli K-12.来自大肠杆菌K-12的丙酮酸脱氢酶复合体的分子结构。
Proc Natl Acad Sci U S A. 1972 Jun;69(6):1615-9. doi: 10.1073/pnas.69.6.1615.
6
Kinetic properties of the partially purified pyruvate dehydrogenase complex of ox brain.牛脑部分纯化丙酮酸脱氢酶复合体的动力学特性
Biochem J. 1973 Jan;131(1):31-7. doi: 10.1042/bj1310031.
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Partial purification and characterization of a pyruvate dehydrogenase-complex-inactivating enzyme from rat liver.大鼠肝脏丙酮酸脱氢酶复合体失活酶的部分纯化及特性研究
Biochem J. 1978 Feb 1;169(2):321-28. doi: 10.1042/bj1690321.