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。

An enzyme without its cofactor is termed an apoenzyme.

没有助因子的酶叫做脱酶。

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.

与脱基蛋白结合松弛、易于与之分离的基因子。

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。

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。

An enzyme without its cofactor is termed an apoenzyme.

没有助子叫做脱。

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.

与脱基蛋白结合松弛、易于与之分离基子称为。

When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.

蛋白和助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。

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。

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.

与脱辅基白结、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.

酶白和辅助因子两者结成完整分子时，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。

An enzyme without its cofactor is termed an apoenzyme.

没有辅助的叫做脱辅。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一全是高度复杂的，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称为辅。

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。

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。

An enzyme without its cofactor is termed an apoenzyme.

没有助因子的叫做。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一全复杂的，如丙酮酸氢。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与基蛋白结合松弛、易于与之分离的基因子称为。

When a catalytically active enzyme forms a complex with a cofactor a holoenzyme is produced.

蛋白和助因子两者结合成完整分子时，形成具有活力的全。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症由于甲基丙二酰A变位或其腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

An enzyme without its cofactor is termed an apoenzyme.

没有辅助因子的酶辅酶。

Some holoenzymes, such as pyruvate dehydrogenase, are highly compex, with several cofactors.

有一全酶是高的，如丙酮酸氢酶。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与辅基蛋白结合松弛、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。

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。