血清(浆)脂类及 - docin.com豆丁网 LPL)作用,可以水解为甘 油和游离脂肪酸(free fatty acid,FFA),甘油在ATP 和甘油激酶(glycerokinase,GK)的作用下, 生成3-磷酸甘油,再经磷酸甘油氧化酶(glycerophosphate oxidase,
基于4个网页-相关网页
血清(浆)脂类及 - docin.com豆丁网 LPL)作用,可以水解为甘 油和游离脂肪酸(free fatty acid,FFA),甘油在ATP 和甘油激酶(glycerokinase,GK)的作用下, 生成3-磷酸甘油,再经磷酸甘油氧化酶(glycerophosphate oxidase,
基于2个网页-相关网页
和酵母磷酸甘油激酶 PGK
甘油激酶缺乏症(GKD)是一种少见的X染色体隐性遗传性代谢缺陷病,可分为单纯型和复合型。
Glycerol kinase deficiency (GKD), a rare X-linked recessive disorder, is classified into two types: isolated and complex.
ATP在糖酵解的收获阶段经过两个反应生成,由磷酸甘油酸激酶和丙酮酸激酶催化。
ATP is formed in the payoff phase of glycolysis by two reactions, promoted by phosphoglycerate kinase and pyruvate kinase.
应用推荐