mutase sentence in Hindi
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- 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.
- Methylmalonyl-CoA mutase catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA, and uses a B12 derived prosthetic group, adenosylcobalamin, in order to accomplish this transfer.
- PurE, " N " 5-carboxyaminoimidazole ribonucleotide mutase, converts N5-CAIR to CAIR, the sixth step of " de novo " purine biosynthesis.
- L-" threo "-3-Methylaspartate "'is an unusual amino acid formed by glutamate mutase and can be metabolised by methylaspartate ammonia-lyase.
- Phosphoglycerate mutase B ( PGM-B ) is one of the latter glycolytic enzymes responsible for the conversion of 3-phosphoglycerate ( 3PG ) to 2-phosphoglycerate ( 2PG ).
- The inherited forms of methylmalonic acidemia cause defects in the metabolic pathway where methylmalonyl-coenzyme A ( CoA ) is converted into succinyl-CoA by the enzyme methylmalonyl-CoA mutase.
- Patients with a complete deletion suffer an inactivation of methylmalonyl CoA mutase and exhibit the most sever symptoms of the deficiency, while patients with a partial mutations have a wide range of symptoms.
- Because phosphoenolpyruvate mutase has the unusual ability to form a new carbon-phosphorus bond, it is essential to the synthesis of phosphonates, such as phosphonolipids and the antibiotics fosfomycin and bialaphos.
- Dysfunction in the activity of phosphoglycerate mutase is a rare autosomal recessive genetic disorder with symptoms ranging from mild to moderate, is not thought life-threatening and can be managed with changes in lifestyle.
- The coenzyme A linked form of methylmalonic acid, methylmalonyl-CoA, is converted into succinyl-CoA by methylmalonyl-CoA mutase, in a reaction that requires vitamin B 12 as a cofactor.
- All these propionyl-CoA substrates are converted to succinyl-CoA following the methylmalonyl pathway For amino acid metabolism, methylmalonyl-CoA mutase works in the degradation pathways of isoleucine, threonine, valine, and methionine.
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