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Biochemical mechanisms of biotin and thiamin action and relationships to genetic disease.

作者信息

Utter M F, Sheu K F

出版信息

Birth Defects Orig Artic Ser. 1980;16(1):289-304.

PMID:7448358
Abstract
摘要

相似文献

1
Biochemical mechanisms of biotin and thiamin action and relationships to genetic disease.
Birth Defects Orig Artic Ser. 1980;16(1):289-304.
2
The involvement of biotin in preventing the fatty liver and kidney syndrome in chicks.生物素在预防雏鸡脂肪肝和肾综合征中的作用。
Res Vet Sci. 1976 Mar;20(2):180-4.
3
Letter: Pyruvate decarboxylase deficiency in liver.信件:肝脏中的丙酮酸脱羧酶缺乏症
N Engl J Med. 1974 Feb 14;290(7):406-7.
4
Clinical signs of fatty liver and kidney syndrome in broilers and their alleviation by the short-term use of biotin or animal tallow.肉鸡脂肪肝和肾综合征的临床症状及其通过短期使用生物素或动物脂肪的缓解情况。
Br Poult Sci. 1977 Nov;18(6):749-53. doi: 10.1080/00071667708416430.
5
Structural basis for flip-flop action of thiamin pyrophosphate-dependent enzymes revealed by human pyruvate dehydrogenase.人丙酮酸脱氢酶揭示硫胺素焦磷酸依赖性酶翻转作用的结构基础。
J Biol Chem. 2003 Jun 6;278(23):21240-6. doi: 10.1074/jbc.M300339200. Epub 2003 Mar 21.
6
Elucidation of the chemistry of enzyme-bound thiamin diphosphate prior to substrate binding: defining internal equilibria among tautomeric and ionization states.底物结合前酶结合硫胺素二磷酸的化学性质阐释:确定互变异构体和电离状态之间的内部平衡。
Biochemistry. 2007 Sep 18;46(37):10739-44. doi: 10.1021/bi700838q. Epub 2007 Aug 23.
7
Characterization of point mutations in patients with pyruvate dehydrogenase deficiency: role of methionine-181, proline-188, and arginine-349 in the alpha subunit.丙酮酸脱氢酶缺乏症患者点突变的特征:α亚基中蛋氨酸-181、脯氨酸-188和精氨酸-349的作用
Arch Biochem Biophys. 1999 Jul 1;367(1):39-50. doi: 10.1006/abbi.1999.1231.
8
Reaction mechanisms of thiamin diphosphate enzymes.硫胺素二磷酸酶的反应机制。
FEBS J. 2009 May;276(9):2431. doi: 10.1111/j.1742-4658.2009.06963.x. Epub 2009 Mar 16.
9
[Theory of the thiamine pyrophosphate action. 12. Participation of the 4'-NH2 group, the S-atom and 2'-alkylic residue in the binding of functional mechanism of thiamine pyrophosphate].[硫胺素焦磷酸作用理论。12. 4'-氨基、硫原子和2'-烷基残基在硫胺素焦磷酸功能机制结合中的参与]
Acta Biol Med Ger. 1973;31(4):525-35.
10
Binding of thiamin thiazolone pyrophosphate to mammalian pyruvate dehydrogenase and its effects of kinase and phosphatase activities.硫胺噻唑酮焦磷酸与哺乳动物丙酮酸脱氢酶的结合及其对激酶和磷酸酶活性的影响。
Biochem Biophys Res Commun. 1977 Feb 21;74(4):1667-74. doi: 10.1016/0006-291x(77)90636-2.

引用本文的文献

1
Pyruvate dehydrogenase complex activity in normal and deficient fibroblasts.正常和成纤维细胞缺陷型中的丙酮酸脱氢酶复合物活性
J Clin Invest. 1981 May;67(5):1463-71. doi: 10.1172/jci110176.
2
The biotin-dependent carboxylase deficiencies.生物素依赖性羧化酶缺乏症
Am J Hum Genet. 1982 Sep;34(5):699-716.
3
Deficiency of the pyruvate dehydrogenase component in pyruvate dehydrogenase complex-deficient human fibroblasts. Immunological identification.丙酮酸脱氢酶复合体缺乏的人类成纤维细胞中丙酮酸脱氢酶成分的缺乏。免疫学鉴定。
J Clin Invest. 1986 Sep;78(3):844-7. doi: 10.1172/JCI112651.
4
Defective gene in lactic acidosis: abnormal pyruvate dehydrogenase E1 alpha-subunit caused by a frame shift.乳酸酸中毒中的缺陷基因:由移码导致的丙酮酸脱氢酶E1α亚基异常
Am J Hum Genet. 1989 Mar;44(3):358-64.