EC Number   |
General Information  |
Reference |
|---|
    6.4.1.3 | malfunction |
gene knockout/complementation demonstrates that the enzyme consists of a fusion protein of a biotin carboxylase and a biotin-carboxyl carrier protein (PccA, HFX_2490), a carboxyltransferase component (PccB, HFX_2478), and an essential small subunit (PccX, HFX_2479). Knockout of pccBX leads to an inability to utilize propionate and a higher intracellular propionyl-CoA level, indicating that the enzyme is indispensable for propionyl-CoA utilization. the pccBX-deleted strain displays multiple phenotypic changes, including retarded cell growth, decreased glucose consumption, impaired PHBV biosynthesis, and wrinkled cells. Genome-wide microarray analysis shows that many genes for glycolysis, pyruvate oxidation, PHBV accumulation, electron transport, and stress responses are affected in the pccBX-deleted strain |
729050 |
| 6.4.1.3 | metabolism |
methylmalonyl-CoA mutase and PCC are key enzmyes in the catabolic pathway of propionate metabolism in the developing and adult rat central nervous system |
705936 |
| 6.4.1.3 | metabolism |
PCC is essential for the catabolism of the amino acids L-Thr, L-Val, L-Ile and L-Met, cholesterol and fatty acids with an odd number of carbon atoms |
716328 |
| 6.4.1.3 | metabolism |
the enzyme is indispensability for propionyl-CoA assimilation und the global metabolism of Haloferax mediterranei |
729050 |
| 6.4.1.3 | physiological function |
animal lifespan is significantly reduced relative to wild-type worms in mutant strains lacking either subunit PccA or PccB. Mitochondrial oxidative phosphorylation capacity and efficiency of isolated mitochondria are also significantly reduced in both mutant strains. In vivo quantitation of mitochondrial physiology is normal in PccB-1 mutants, but PccA-1 deletion mutants have significantly increased mitochondrial matrix oxidant burden as well as significantly decreased mitochondrial membrane potential and mitochondrial content. Both deletion strains have decreased accumulation of malate, isotopic enrichment in citrate, and increased lactate accumulation |
745501 |
| 6.4.1.3 | physiological function |
the PCC pathway is the dominant route for the supply of methylmalonyl-CoA for rapamycin production in Streptomyces hygroscopicus UV2-2 strain |
-, 713913 |
