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Immunogen sequence: EERLETPSA KKLTDIGIRR IFSPEHDIFR KSVRKFFQEE VIPHHSEWEK AGEVSREVWE KAGKQGLLGV NIAEHLGGIG GDLYSAAIVW EEQAYSNCSG PGFSIHSGIV MSYITNHGSE EQIKHFIPQM TAGKCIGAIA MTEPGAGSDL QGIKTNAKKD GSDWILNGSK VFISNGSLSD VVIVVAVTNH EAPSPAHGIS LFLVENGMKG FIKGRKLHKM GLKAQDTAEL FFEDIRLPAS ALLGEENKGF YYIMKELPQE RLLIADVAIS ASEFMFEETR NYVKQRKAFG KTVAHLQTVQ HKLAELKTHI CVTRAFVDNC LQLHEAKRLD SATACMAKYW ASELQNSVAY DCVQLHGGWG YMWEYPIAKA YVDARVQPIY GGTNEIMKEL IAREIVFDK (33-430 aa encoded by BC039063)
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
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Protein Aliases: acetyl-Coenzyme A dehydrogenase, long-chain; Acyl Coenzyme A dehydrogenase, long chain; acyl-Coenzyme A dehydrogenase, long chain; acyl-Coenzyme A dehydrogenase, long-chain; LCAD; LCAD long chain acyl-CoA dehydrogenase; long-chain acyl-CoA dehydrogenase; Long-chain specific acyl-CoA dehydrogenase, mitochondrial
Gene Aliases: AA960361; ACAD4; ACADL; ACOADA; AU018452; C79855; LCAD
UniProt ID: (Human) P28330, (Mouse) P51174, (Rat) P15650
Entrez Gene ID: (Human) 33, (Mouse) 11363, (Rat) 25287
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