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・ Alpha-2 blocker
・ Alpha-2-HS-glycoprotein
・ Alpha-2-Macroglobulin
・ Alpha-2A adrenergic receptor
・ Alpha-2B adrenergic receptor
・ Alpha-2C adrenergic receptor
・ Alpha-3 beta-2 nicotinic receptor
・ Alpha-3 beta-4 nicotinic receptor
・ Alpha-4 beta-2 nicotinic receptor
・ Alpha-5 beta-1
・ Alpha-7 nicotinic receptor
・ Alpha-adrenergic agonist
・ Alpha-agarase
・ Alpha-Amanitin
・ Alpha-amino-acid esterase
Alpha-aminoadipate pathway
・ Alpha-Aminoadipic acid
・ Alpha-aminoadipic and alpha-ketoadipic aciduria
・ Alpha-aminoadipic semialdehyde synthase, mitochondrial
・ Alpha-Aminobutyric acid
・ Alpha-amylase
・ Alpha-amyrin synthase
・ Alpha-bisabolene synthase
・ Alpha-Bits
・ Alpha-Bungarotoxin
・ Alpha-Cadinol
・ Alpha-Carotene
・ Alpha-Chlorocodide
・ Alpha-copaene synthase
・ Alpha-Cyano-4-hydroxycinnamic acid


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Alpha-aminoadipate pathway : ウィキペディア英語版
Alpha-aminoadipate pathway

The α-aminoadipate pathway is a biochemical pathway for the synthesis of the amino acid L-lysine. In the eukaryotes, this pathway is unique to the higher fungi (containing chitin in their cell walls) and the euglenids. It has also been reported from bacteria of the genus ''Thermus''.
==Pathway overview==

Homocitrate is initially synthesised from acetyl-CoA and 2-oxoglutarate by homocitrate synthase. This is then converted to homoaconitate by homoaconitase and then to homoisocitrate by homoisocitrate dehydrogenase. A nitrogen atom is added from glutamate by aminoadipate aminotransferase to form the α-aminoadipate from which this pathway gets its name. This is then reduced by aminoadipate reductase via an acyl-enzyme intermediate to a semialdehyde. Reaction with glutamate by one class of saccharopine dehydrogenase yields saccharopine which is then cleaved by a second saccharopine dehydrogenase to yield lysine and oxoglutarate.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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