3-羟酰辅酶A脱氢酶(3-Hydroxyacyl-CoA dehydrogenase)是一种参与脂肪酸代谢的酶。长链3-羟酰辅酶A脱氢酶缺乏是一种遗传性代谢疾病,也被称为长链脂肪酸氧化缺陷(long-chain fatty acid oxidation disorder)。该疾病是由于基因突变导致3-羟酰辅酶A脱氢酶的功能缺陷,进而影响脂肪酸的正常代谢。 长链3-羟酰辅酶A脱氢...
3-羟酰辅酶A脱氢酶缺乏症的英文名字是3-Hydroxyacyl-CoA Dehydrogenase Deficiency。基因解码表明:3-羟酰辅酶A脱氢酶缺乏症是一种遗传性代谢疾病,主要由HADH基因的突变引起。HADH基因位于人类染色体4q25-q26区域。 已经发现多种HADH基因的突变与3-羟酰辅酶A脱氢酶缺乏症相关。这些突变导致3-羟酰辅酶A脱氢酶的功能...
SCHADD代表“中/短链 3-羟酰基 CoA 脱氢酶缺乏症”,这种疾病其他名称:短链 3-羟酰辅酶 A 脱氢酶缺乏导致的高胰岛素性低血糖;SCHAD 缺乏导致的高胰岛素血症;由于谷氨酰胺脱氢酶缺乏而导致的高胰岛素血症 研究人员Clayton 等人首次报道了由 HADH 基因隐性突变引起的高胰岛素血症。2001年。先证者是一对非近亲结婚...
网友 2 最佳答案 回答者:网友 3-hydroxyacyl-coa dehydrogenase 羟酰基辅酶A脱氢酶 双语对照 词典结果: 3-hydroxyacyl-CoA dehydrogenase [医]3-羟酰基-辅酶A脱氢酶; 以上结果来自金山词霸推荐: 丙二酸二乙酯 Cas No: 105-53-3 对溴苯酚 Cas No: 106-41-2 对氨基苯酚 Cas No: 123-30-8 肉桂酸 C...
TheC-terminal part of the enzyme harbors enoyl-CoA hydratase activity and is able to convert trans-crotonyl-CoA to3-hydroxybutyryl-CoA. The N-terminal part of FadB’ comprises an NAD+binding site and is responsible for3-hydroxyacyl-CoA dehydrogenase activity converting (S)-3-hydroxybutyryl-CoA ...
In enzymology, a 3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35) is an enzyme that catalyzes the chemical reaction. (S)-3-hydroxyacyl-CoA + NAD+ rightleftharpoons 3-oxoacyl-CoA + NADH + H+. Thus, the two substrates of this enzyme are (S)-3-hydroxyacyl-CoA and NAD+, whereas its 3 ...
别名 HAD; HADH; HADH1; HADHSC; HCDH; HCDH_HUMAN; HHF4; Hydroxyacyl CoA dehydrogenase; Hydroxyacyl-coenzyme A dehydrogenase; hydroxyacyl-coenzyme A dehydrogenase, mitochondrial; L 3 hydroxyacyl Coenzyme A dehydrogenase short chain; M SCHAD; Medium and short chain L 3 hydroxyacyl coenzyme A dehydr...
别名HAD; HADH; HADH1; HADHSC; HCDH; HCDH_HUMAN; HHF4; Hydroxyacyl CoA dehydrogenase; Hydroxyacyl-coenzyme A dehydrogenase; hydroxyacyl-coenzyme A dehydrogenase, mitochondrial; L 3 hydroxyacyl Coenzyme A dehydrogenase short chain; M SCHAD; Medium and short chain L 3 hydroxyacyl coenzyme A dehydrog...
长链3-羟酰基辅酶A 脱氢酶缺乏症的英文名字是Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency。基因解码表明:长链3-羟酰基辅酶A脱氢酶缺乏症是一种遗传性代谢疾病,主要由基因突变引起。这种疾病是由于长链3-羟酰基辅酶A脱氢酶(LCHAD)基因的突变导致该酶的功能缺陷或有效缺失。 LCHAD基因位于人类染色体2q23-24...
长链3-羟酰基辅酶A脱氢酶缺乏症的英文名字是Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency。基因解码表明:长链3-羟酰基辅酶A脱氢酶缺乏症是一种遗传性代谢疾病,由于基因突变导致长链3-羟酰基辅酶A脱氢酶(LCHAD)的功能缺失。这种疾病通常由HADHA基因的突变引起,该基因位于人类染色体2上。