acad8造句
例句與造句
- ACAD8 functions in catabolism of the branched-chain amino acid valine.
- Mutations in ACAD8 have been linked to isobutyryl-CoA dehydrogenase deficiency.
- Defects in the " ACAD8 " gene cause isobutyryl-coenzyme A dehydrogenase deficiency.
- The " ACAD8 " gene provides instructions for making an enzyme that plays an essential role in breaking down proteins from the diet.
- If a mutation in the ACAD8 gene reduces or eliminates the activity of this enzyme, the body is unable to break down valine properly.
- It's difficult to find acad8 in a sentence. 用acad8造句挺難的
- The protein encoded by ACAD8 is a mitochondrial protein belongs to the acyl-CoA dehydrogenase family of enzymes, which function to catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branched-chain amino acids.
- ACAD8 is an isobutyryl-CoA dehydrogenase that functions in the catabolism of branched-chain amino acids including valine, and shows high reactivity toward isobutyryl-CoA . ACAD8 is responsible for the third step in the breakdown of valine and converts isobutyryl-CoA into methylacrylyl-CoA.
- ACAD8 is an isobutyryl-CoA dehydrogenase that functions in the catabolism of branched-chain amino acids including valine, and shows high reactivity toward isobutyryl-CoA . ACAD8 is responsible for the third step in the breakdown of valine and converts isobutyryl-CoA into methylacrylyl-CoA.