A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合松弛、易于与之分的辅基因
称为辅。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合松弛、易于与之分的辅基因
称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因的
叫做脱辅
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和辅助因
结合成完整分
时,形成具有活力的全
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全是高度复杂的,如丙酮酸脱
。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅A变位
或其辅
腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合松弛、易于与之分辅基因子称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助因子两者结合成完整分子时,形成具有活力全酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全酶是高度,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
脱
蛋白结合松弛、易
分
的
子称为
。
An enzyme without its cofactor is termed an apoenzyme.
没有助
子的酶叫做脱
酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和助
子两者结合成完整分子时,形成具有活力的全酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全酶是高度复杂的,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲丙二酸血症是由
甲
丙二酰
酶A变位酶或其
酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱基蛋白结合松弛、易于与之分
的
基
称为
。
An enzyme without its cofactor is termed an apoenzyme.
没有助
的
叫做脱
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和
助
两者结合成完整分
时,形成具有活力的全
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全是高度复杂的,如丙酮酸脱
。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
基丙二酸血症是由于
基丙二酰
A变位
或其
腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结松弛、易于与之分
的辅基因子称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助因子两者结成完整分子时,形成具有活力的
酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有酶是高度复杂的,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
脱辅
蛋白结合松弛、
之分
的辅
称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助的酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助两者结合成完整分
时,形成具有活力的全酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全酶是高度复杂的,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲丙二酸血症是由
甲
丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结松弛、易于与之分
的辅基因子称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助因子两者结成完整分子时,形成具有活力的
酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有酶是高度复杂的,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基结合松弛、易于与之分
的辅基因子称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的叫做脱辅
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
和辅助因子两者结合成完整分子时,形成具有活力的全
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全是高度复杂的,如丙酮
脱氢
。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二血症是由于甲基丙二酰辅
A变位
或其辅
腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合松弛、易于与之分的辅基因子称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助因子两者结合完整分子
,
具有活力的全酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全酶是高度复杂的,如丙酮酸脱氢酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺缺陷所致的一种遗传性代谢疾病。
声明:以上例句、词性分类均由互联网资源自动生,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。