Showing Protein Medium-chain specific acyl-CoA dehydrogenase, mitochondrial (HMDBP00104)

• 5336

1. MCAD

• 2-Methyl-3-Hydroxybutryl CoA Dehydrogenase Deficiency
• 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
• 3-hydroxyisobutyric acid dehydrogenase deficiency
• 3-hydroxyisobutyric aciduria
• 3-Methylcrotonyl Coa Carboxylase Deficiency Type I
• 3-Methylglutaconic Aciduria Type I
• 3-Methylglutaconic Aciduria Type III
• 3-Methylglutaconic Aciduria Type IV
• beta-Alanine metabolism
• Beta-Ketothiolase Deficiency
• Carnitine palmitoyl transferase deficiency (I)
• Carnitine palmitoyl transferase deficiency (II)
• Ethylmalonic Encephalopathy
• Fatty acid Metabolism
• fatty acid metabolism
• Glutaric Aciduria Type I
• Isobutyryl-coa dehydrogenase deficiency
• Isovaleric acidemia
• Isovaleric Aciduria
• Long chain acyl-CoA dehydrogenase deficiency (LCAD)
• Malonic Aciduria
• Malonyl-coa decarboxylase deficiency
• Maple Syrup Urine Disease
• Medium chain acyl-coa dehydrogenase deficiency (MCAD)
• Methylmalonate Semialdehyde Dehydrogenase Deficiency
• Methylmalonic Aciduria
• Methylmalonic Aciduria Due to Cobalamin-Related Disorders
• Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids
• mitochondrial fatty acid beta-oxidation
• PPAR signaling pathway
• Propanoate metabolism
• Propanoate metabolism
• Propionic Acidemia
• Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD Deficiency)
• Trifunctional protein deficiency
• Valine, leucine and isoleucine degradation
• Valine, leucine and isoleucine degradation
• Very-long-chain acyl coa dehydrogenase deficiency (VLCAD)

1. Mitochondrion matrix

>1266 bp
ATGGCAGCGGGGTTCGGGCGATGCTGCAGGGTCCTGAGAAGTATTTCTCGTTTTCATTGG
AGATCACAGCATACAAAAGCCAATCGACAACGTGAACCAGGATTAGGATTTAGTTTTGAG
TTCACCGAACAGCAGAAAGAATTTCAAGCTACTGCTCGTAAATTTGCCAGAGAGGAAATC
ATCCCAGTGGCTGCAGAATATGATAAAACTGGTGAATATCCAGTCCCCCTAATTAGAAGA
GCCTGGGAACTTGGTTTAATGAACACACACATTCCAGAGAACTGTGGAGGTCTTGGACTT
GGAACTTTTGATGCTTGTTTAATTAGTGAAGAATTGGCTTATGGATGTACAGGGGTTCAG
ACTGCTATTGAAGGAAATTCTTTGGGGCAAATGCCTATTATTATTGCTGGAAATGATCAA
CAAAAGAAGAAGTATTTGGGGAGAATGACTGAGGAGCCATTGATGTGTGCTTATTGTGTA
ACAGAACCTGGAGCAGGCTCTGATGTAGCTGGTATAAAGACCAAAGCAGAAAAGAAAGGA
GATGAGTATATTATTAATGGTCAGAAGATGTGGATAACCAACGGAGGAAAAGCTAATTGG
TATTTTTTATTGGCACGTTCTGATCCAGATCCTAAAGCTCCTGCTAATAAAGCCTTTACT
GGATTCATTGTGGAAGCAGATACCCCAGGAATTCAGATTGGGAGAAAGGAATTAAACATG
GGCCAGCGATGTTCAGATACTAGAGGAATTGTCTTCGAAGATGTGAAAGTGCCTAAAGAA
AATGTTTTAATTGGTGACGGAGCTGGTTTCAAAGTTGCAATGGGAGCTTTTGATAAAACC
AGACCTGTAGTAGCTGCTGGTGCTGTTGGATTAGCACAAAGAGCTTTGGATGAAGCTACC
AAGTATGCCCTGGAAAGGAAAACTTTCGGAAAGCTACTTGTAGAGCACCAAGCAATATCA
TTTATGCTGGCTGAAATGGCAATGAAAGTTGAACTAGCTAGAATGAGTTACCAGAGAGCA
GCTTGGGAGGTTGATTCTGGTCGTCGAAATACCTATTATGCTTCTATTGCAAAGGCATTT
GCTGGAGATATTGCAAATCAGTTAGCTACTGATGCTGTGCAGATACTTGGAGGCAATGGA
TTTAATACAGAATATCCTGTAGAAAAACTAATGAGGGATGCCAAAATCTATCAGATTTAT
GAAGGTACTTCACAAATTCAAAGACTTATTGTAGCCCGTGAACACATTGACAAGTACAAA
AATTAA

• Acyl-CoA_dh_1 (PF00441 )
• Acyl-CoA_dh_M (PF02770 )
• Acyl-CoA_dh_N (PF02771 )

>Medium-chain specific acyl-CoA dehydrogenase, mitochondrial
MAAGFGRCCRVLRSISRFHWRSQHTKANRQREPGLGFSFEFTEQQKEFQATARKFAREEI
IPVAAEYDKTGEYPVPLIRRAWELGLMNTHIPENCGGLGLGTFDACLISEELAYGCTGVQ
TAIEGNSLGQMPIIIAGNDQQKKKYLGRMTEEPLMCAYCVTEPGAGSDVAGIKTKAEKKG
DEYIINGQKMWITNGGKANWYFLLARSDPDPKAPANKAFTGFIVEADTPGIQIGRKELNM
GQRCSDTRGIVFEDVKVPKENVLIGDGAGFKVAMGAFDKTRPVVAAGAVGLAQRALDEAT
KYALERKTFGKLLVEHQAISFMLAEMAMKVELARMSYQRAAWEVDSGRRNTYYASIAKAF
AGDIANQLATDAVQILGGNGFNTEYPVEKLMRDAKIYQIYEGTSQIQRLIVAREHIDKYK
N

• 1EGC
• 1EGD
• 1EGE
• 1T9G
• 2A1T

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