mutase उदाहरण वाक्य
उदाहरण वाक्य
- Methylmalonyl-CoA mutase is essential to the degradation pathways of many molecules including amino acids, and odd-chain fatty acids.
- For amino acid metabolism, methylmalonyl-CoA mutase works in the degradation pathways of isoleucine, threonine, valine, and methionine.
- While methylmalonic acidemia has a variety of causes, both genetic and dietary, methylmalonyl CoA mutase deficiency is an autosomal recessive genetic disorder.
- In some cases intellectual and developmental disabilities, such as autism, were noted with increased frequency in populations with methylmalonyl-CoA mutase deficiency.
- Mutations in this gene cause muscle phosphoglycerate mutase deficiency, also known as glycogen storage disease X . [ provided by RefSeq, Sep 2009]
- Both phosphate and 2-phosphoglycolate are competitive inhibitors of mutase activity in respect to the substrates 2-phosphoglycerate and 2, 3-bisphosphoglycerate.
- Because the main function of bisphosphoglycerate mutase is the synthesis of 2, 3-BPG, this enzyme is found only in erythrocytes and placental cells.
- The ( " R " )-methylmalonyl-CoA is then converted to succinyl-CoA in a reaction catalyzed by methylmalonyl-CoA mutase.
- In methylmalonyl-CoA mutase the ?-axial ligand is 5-deoxy-5-adenosine and is involved in the free radical chemistry of the reaction.
- Phosphoglycerate mutase ( PGAM ) catalyzes the reversible reaction of 3-phosphoglycerate ( 3-PGA ) to 2-phosphoglycerate ( 2-PGA ) in the glycolytic pathway.