An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂的,如丙酮酸脱氢酶。
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、易于与之分离的辅基因子称为辅。
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时,形
有活力的全酶。
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一种遗传性代谢疾病。
声明:以上例句、词性分类均由互网资源自动生
,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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂的,如丙酮酸脱氢酶。
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、易于与之分离的辅基因子称为辅。
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。
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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂的,如丙酮酸脱氢酶。
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、易于与之分离的辅基因子称为辅。
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,形成具有的全酶。
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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子脱辅
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全
是高度
,如丙酮酸脱氢
。
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、易于与之分离辅基因子称为辅。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和辅助因子两者结合成完整分子时,形成具有活力
全
。
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
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。
An enzyme without its cofactor is termed an apoenzyme.
没有助
子的酶叫做
酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂的,如丙
氢酶。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与基蛋白结合松弛、易于与之分离的
基
子称为
。
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。
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
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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的叫做脱辅
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有是高度复杂的,如丙酮酸脱氢
。
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、易于与之分离的辅基因子称为辅。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和辅助因子两者结合成完整分子时,形成具有活力的
。
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
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。
An enzyme without its cofactor is termed an apoenzyme.
没有助因子
叫做脱
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全
是高度复杂
,如丙酮酸脱氢
。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱基蛋
结合松弛、易于与之分离
基因子称为
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋
助因子两者结合成完整分子时,形成具有活力
全
。
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A变位
或其
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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子的酶叫做脱辅酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂的,如丙酮
脱氢酶。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合、
于与之分离的辅基因子称为辅。
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,形成具有活力的全酶。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺
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,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。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因子酶叫做脱辅酶。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一全酶是高度复杂
,如丙酮酸脱氢酶。
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、易于与之分离辅基因子称为辅。
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,形成具有全酶。
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。