二氫硫辛酰胺脫氫酶

二氫硫辛酰胺脫氫酶
命名
系統命名
縮寫
識別碼
EC編號	1.8.1.4
CAS號	9001-18-7
數據庫
IntEnz	IntEnz瀏覽
BRENDA	BRENDA入口
ExPASy	NiceZyme瀏覽
KEGG	KEGG入口
MetaCyc	代謝路徑
PRIAM	概述
PDB	RCSB PDB PDBe PDBsum
基因本體	AmiGO / EGO
搜索
PMC	相關文獻
PubMed	相關文獻

二氫硫辛酰胺脫氫酶
	; PDB渲染的1zy8
有效結構
PDB	直系同源檢索：PDBe, RCSB
PDB查詢代碼列表
	1ZMC, 1ZMD, 1ZY8, 2F5Z
標識
代號	DLD; DLDH; E3; GCSL; LAD; PHE3
擴展標識	遺傳學：238331 鼠基因：107450 同源基因：84 GeneCards: DLD Gene
EC編號	1.8.1.4
基因本體論描述
分子功能	· dihydrolipoyl dehydrogenase activity; · electron carrier activity; · oxidoreductase activity; · lipoamide binding; · flavin adenine dinucleotide binding; · NAD binding;
細胞成分	· cytoplasm; · mitochondrion; · mitochondrial matrix; · flagellum; · acrosomal matrix; · oxoglutarate dehydrogenase complex; · pyruvate dehydrogenase complex;
生物過程	· pyruvate metabolic process; · tricarboxylic acid cycle; · 2-oxoglutarate metabolic process; · mitochondrial electron transport, NADH to ubiquinone; · proteolysis; · lysine catabolic process; · gastrulation; · aging; · branched chain family amino acid catabolic process; · lipoate metabolic process; · regulation of acetyl-CoA biosynthetic process from pyruvate; · cellular nitrogen compound metabolic process; · regulation of membrane potential; · cell redox homeostasis; · sperm capacitation; · dihydrolipoamide metabolic process;
	Sources: Amigo / QuickGO
直系同源體
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A+醫學百科 >> 二氫硫辛酰胺脫氫酶

二氫硫辛酰胺脫氫酶（EC 1.8.1.4，英語：Dihydrolipoamide dehydrogenase，縮寫DLD，又稱為線粒體二氫硫辛酸脫氫酶，dihydrolipoyl dehydrogenase, mitochondrial）是一種由人類基因DLD^[1]^[2]^[3]^[4]所編碼的黃素蛋白，其作用是將二氫硫辛酰胺脫氫從而轉化為氧化型硫辛酰胺。

DLD作為一種線粒體蛋白質，在真核生物的能量代謝中起到重要作用，它至少參與了五種多酶復合體，且為復合體完成反應所必需的組份^[5]。另外，DLD作為一種黃素蛋白氧化還原酶，以FAD為輔基接受質子與電子催化二硫鍵的形成。

DLD是大小為51千道爾頓亞基的同二聚體，其中每個亞基都與一分子的FAD以共價鍵的形式相連^[6]。

硫辛酰胺

二氫硫辛酰胺

功能

在哺乳動物的線粒體三羧酸循環中，該酶與丙酮酸脫氫酶和二氫硫辛酰基乙酰基轉基酶一起組成中丙酮酸脫氫酶復合體，同時該酶亦是α-酮戊二酸脫氫酶復合體中的一個組分。二氫硫辛酰胺脫氫酶的主要任務是負責將復合物中另一組分硫辛酰胺轉乙酰基酶（或二氫硫辛酰琥珀酰轉移酶）的輔基二氫硫辛酰胺脫氫從而轉化為氧化型硫辛酰胺，該酶也是線粒體甘氨酸剪切體系的組分。

參考文獻

↑ Entrez Gene: dihydrolipoamide dehydrogenase.
↑ Otulakowski G, Robinson BH. Isolation and sequence determination of cDNA clones for porcine and human lipoamide dehydrogenase. Homology to other disulfide oxidoreductases. J. Biol. Chem.. December 1987, 262 (36): 17313–8. PMID 3693355.
↑ Pons G, Raefsky-Estrin C, Carothers DJ, Pepin RA, Javed AA, Jesse BW, Ganapathi MK, Samols D, Patel MS. [http//www.ncbi.nlm.nih.gov/pmc/articles/PMC279783/ Cloning and cDNA sequence of the dihydrolipoamide dehydrogenase component human alpha-ketoacid dehydrogenase complexes]. Proc. Natl. Acad. Sci. U.S.A.. March 1988, 85 (5): 1422–6. doi:10.1073/pnas.85.5.1422. PMID 3278312. PMC 279783.
↑ Scherer SW, Otulakowski G, Robinson BH, Tsui LC. Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31----q32. Cytogenet. Cell Genet.. 1991, 56 (3-4): 176–7. doi:10.1159/000133081. PMID 2055113.
↑ Babady NE, Pang YP, Elpeleg O, Isaya G. [http//www.ncbi.nlm.nih.gov/pmc/articles/PMC1851069/ Cryptic proteolytic activity of dihydrolipoamide dehydrogenase]. Proceedings of the National Academy of Sciences of the United States of America. 2007, 104 (15): 6158–63. doi:10.1073/pnas.0610618104. PMID 17404228. PMC 1851069.
↑ Ciszak EM, Makal A, Hong YS, Vettaikkorumakankauv AK, Korotchkina LG, Patel MS. How dihydrolipoamide dehydrogenase-binding protein binds dihydrolipoamide dehydrogenase in the human pyruvate dehydrogenase complex. The Journal of Biological Chemistry. 2006, 281 (1): 648–55. doi:10.1074/jbc.M507850200. PMID 16263718.

深入閱讀

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