WebThe gene underlying this phenotype was found to encode a protein containing a putative membrane-localized domain of unknown function (DUF21) and a cystathionine-β-synthase domain. The cbs1 mutants had defective infection threads that were sometimes devoid of rhizobia and formed small nodules with greatly reduced numbers of symbiosomes. WebMar 26, 2024 · Definition. Die Cystathionin-beta-Synthase, kurz CBS, kondensiert im Methioninstoffwechsel die Aminosäuren Homocystein und Serin zu Cystathionin. Der …
Homocystinuria due to Cystathionine Beta-Synthase Deficiency
WebDescription. An enzymatic deficiency resulting in altered sulfur metabolism and homocystinuria. The clinical features of untreated homocystinuria due to CBS deficiency include myopia, ectopia lentis, intellectual disability, skeletal anomalies resembling Marfan syndrome, and thromboembolic events. Light skin and hair can also be present. WebCystathionine β-synthase (CBS)1 (EC 4.2.1.22) catalyzes the pyridoxal 5′-phosphate (PLP)-dependent β-replacement reaction in which the thiolate of l-homocysteine … how many followers does shintoism have
CBS gene: MedlinePlus Genetics
WebThe CBS gene provides instructions for making an enzyme called cystathionine beta-synthase. This enzyme acts in a chemical pathway and is responsible for using vitamin B6 to convert building block of proteins (amino acid) called homocysteine and serine to a molecule called cytathionine. Another enzyme then converts cystathionine to the amino ... http://www.csi.org.cn/article/1373 WebSep 9, 2024 · As mentioned above, cystathionine-β-synthase is an enzyme involved in the transsulfuration pathway, which is how the body regulates its levels of sulfur-containing … how many followers do hinduism have