Showing Protein Methylmalonyl-CoA epimerase, mitochondrial (HMDBP00256)

• 5488
• HMDBP03172

1. DL-methylmalonyl-CoA racemase

• 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-Ketothiolase Deficiency
• Glyoxylate and dicarboxylate metabolism
• Isobutyryl-coa dehydrogenase deficiency
• Isovaleric acidemia
• Isovaleric Aciduria
• Malonic Aciduria
• Malonyl-coa decarboxylase deficiency
• Maple Syrup Urine Disease
• Methylmalonate Semialdehyde Dehydrogenase Deficiency
• Methylmalonic Aciduria
• Methylmalonic Aciduria Due to Cobalamin-Related Disorders
• Propanoate metabolism
• Propanoate metabolism
• Propionic Acidemia
• Threonine and 2-Oxobutanoate Degradation
• Valine, leucine and isoleucine degradation
• Valine, leucine and isoleucine degradation

1. Cytoplasm
2. Mitochondrion (Probable)

>531 bp
ATGGCGCGGGTGCTGAAGGCTGCAGCCGCGAATGCCGTAGGGCTTTTTTCCAGACTTCAA
GCTCCCATTCCAACAGTAAGAGCTTCTTCCACATCACAGCCCTTGGATCAAGTGACAGGT
TCTGTGTGGAACCTGGGTCGACTCAACCATGTAGCCATAGCAGTGCCAGATTTGGAAAAG
GCTGCAGCATTTTATAAGAATATTCTGGGGGCCCAGGTAAGTGAAGCGGTCCCTCTTCCT
GAACATGGAGTATCTGTTGTTTTTGTCAACCTGGGAAATACCAAGATGGAACTGCTTCAT
CCATTGGGACGTGACAGTCCAATTGCAGGTTTTCTGCAGAAAAACAAGGCTGGAGGAATG
CATCACATCTGCATCGAGGTGGATAATATTAATGCAGCTGTGATGGATTTGAAAAAAAAG
AAGATCCGCAGTCTAAGTGAAGAGGTCAAAATAGGAGCACATGGAAAACCAGTGATTTTT
CTCCATCCTAAAGACTGTGGTGGAGTCCTTGTGGAACTGGAGCAAGCTTGA

• Glyoxalase (PF00903 )

>Methylmalonyl-CoA epimerase, mitochondrial
MARVLKAAAANAVGLFSRLQAPIPTVRASSTSQPLDQVTGSVWNLGRLNHVAIAVPDLEK
AAAFYKNILGAQVSEAVPLPEHGVSVVFVNLGNTKMELLHPLGRDSPIAGFLQKNKAGGM
HHICIEVDNINAAVMDLKKKKIRSLSEEVKIGAHGKPVIFLHPKDCGGVLVELEQA

• 3RMU

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3. Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M: Lysine acetylation targets protein complexes and co-regulates major cellular functions. Science. 2009 Aug 14;325(5942):834-40. doi: 10.1126/science.1175371. Epub 2009 Jul 16. [PubMed:19608861 ]
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5. Bikker H, Bakker HD, Abeling NG, Poll-The BT, Kleijer WJ, Rosenblatt DS, Waterham HR, Wanders RJ, Duran M: A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria. Hum Mutat. 2006 Jul;27(7):640-3. [PubMed:16752391 ]