来自人胎盘的L-甲基丙二酰辅酶A变位酶。 - Suppr

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超能文献

L-methylmalonyl-CoA mutase from human placenta.

作者信息

Kolhouse J F, Stabler S P, Allen R H

出版信息

Methods Enzymol. 1988;166:407-14. doi: 10.1016/s0076-6879(88)66053-8.

DOI:10.1016/s0076-6879(88)66053-8

PMID:2907367

Abstract

摘要

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L-methylmalonyl-CoA mutase from human placenta.来自人胎盘的L-甲基丙二酰辅酶A变位酶。

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DL-methylmalonyl-CoA racemase from rat liver.来自大鼠肝脏的DL-甲基丙二酰辅酶A消旋酶。

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Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites.正常人成纤维细胞中甲基丙二酰辅酶A变位酶与腺苷钴胺素和甲基丙二酰辅酶A的相互作用：非等效活性位点的证据。

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Purification and properties of methylmalonyl coenzyme A mutase from human liver.人肝脏甲基丙二酰辅酶A变位酶的纯化及性质

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Assay of methylmalonyl CoA mutase with high-performance liquid chromatography.采用高效液相色谱法测定甲基丙二酰辅酶A变位酶

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Isolation and characterization of methylmalonyl-CoA mutase from human placenta.人胎盘甲基丙二酰辅酶A变位酶的分离与鉴定

J Biol Chem. 1980 Apr 10;255(7):2708-12.

Subunit interactions in Propionibacterium shermanii methylmalonyl-CoA mutase studied by analytical ultracentrifugation.通过分析超速离心法研究谢氏丙酸杆菌甲基丙二酰辅酶A变位酶中的亚基相互作用。

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D-methylmalonyl-CoA hydrolase.D-甲基丙二酰辅酶A水解酶

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Purification and characterization of methylmalonyl-CoA mutase from Ascaris lumbricoides.来自蛔虫的甲基丙二酰辅酶A变位酶的纯化与特性分析。

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引用本文的文献

Methylmalonic Acidemia Diagnosis by Laboratory Methods.通过实验室方法诊断甲基丙二酸血症。

Rep Biochem Mol Biol. 2016 Oct;5(1):1-14.

Optimization and validation of a reversed-phase high performance liquid chromatography method for the measurement of bovine liver methylmalonyl-coenzyme a mutase activity.优化和验证反相高效液相色谱法测定牛肝甲基丙二酰辅酶 A 变位酶活性。

BMC Biochem. 2013 Oct 16;14:25. doi: 10.1186/1471-2091-14-25.

Propionyl-CoA and adenosylcobalamin metabolism in Caenorhabditis elegans: evidence for a role of methylmalonyl-CoA epimerase in intermediary metabolism.秀丽隐杆线虫中丙酰辅酶A和腺苷钴胺素的代谢：甲基丙二酰辅酶A差向异构酶在中间代谢中作用的证据

Mol Genet Metab. 2006 Sep-Oct;89(1-2):64-73. doi: 10.1016/j.ymgme.2006.06.001. Epub 2006 Jul 14.

Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.与mut型甲基丙二酸血症相关的甲基丙二酰辅酶A变位酶突变的聚类分析

Am J Hum Genet. 1994 Jul;55(1):42-50.

Genomic structure of murine methylmalonyl-CoA mutase: evidence for genetic and epigenetic mechanisms determining enzyme activity.小鼠甲基丙二酰辅酶A变位酶的基因组结构：决定酶活性的遗传和表观遗传机制的证据。

Biochem J. 1993 Dec 15;296 ( Pt 3)(Pt 3):663-70. doi: 10.1042/bj2960663.

Primary structure and activity of mouse methylmalonyl-CoA mutase.小鼠甲基丙二酰辅酶A变位酶的一级结构与活性

Biochem J. 1990 Oct 15;271(2):449-55. doi: 10.1042/bj2710449.

Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia.甲基丙二酸血症中甲基丙二酰辅酶A变位酶的异质等位基因与表达

Am J Hum Genet. 1990 Mar;46(3):539-47.

Inhibition of cobalamin-dependent enzymes by cobalamin analogues in rats.钴胺素类似物对大鼠体内钴胺素依赖性酶的抑制作用。

J Clin Invest. 1991 Apr;87(4):1422-30. doi: 10.1172/JCI115148.

Differential diagnosis of mut and cbl methylmalonic aciduria by DNA-mediated gene transfer in primary fibroblasts.通过DNA介导的基因转移在原代成纤维细胞中对mut型和cbl型甲基丙二酸尿症进行鉴别诊断。

J Clin Invest. 1991 Mar;87(3):915-8. doi: 10.1172/JCI115098.

Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria.一种导致mut型甲基丙二酸尿症的、钴胺素亲和力改变的突变型甲基丙二酰辅酶A变位酶的克隆与表达

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