A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱蛋白结合松弛、易于与之分
的
因子称为
。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱蛋白结合松弛、易于与之分
的
因子称为
。
An enzyme without its cofactor is termed an apoenzyme.
没有助因子的酶叫做脱
酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和助因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.
二酸血症是由于
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。
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.
蛋白和辅助因子两者结合
完整分子时,形
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。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
辅基蛋白结合松弛、易于
之分
辅基因
称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因叫做
辅
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和辅助因
两者结合成完整分
时,形成具有活力
全
。
Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.
有一些全是高度复杂
,如丙酮酸
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。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱基蛋白结
、易于与之分
的
基因子
。
An enzyme without its cofactor is termed an apoenzyme.
没有助因子的酶叫做脱
酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和助因子两者结
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.
甲基丙二酸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。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅蛋白结合松弛、易于与之分
的辅
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.
甲酸血症是由于甲
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、易于与之的辅基因
称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助因的酶叫做脱辅酶。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
酶蛋白和辅助因两者结合成完
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、词性类均由互联网资源自动生成,部
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
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.
与脱辅基蛋白结合松弛、易于与之分的辅基
称为辅。
An enzyme without its cofactor is termed an apoenzyme.
没有辅助的
叫做脱辅
。
When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.
蛋白和辅助
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。