Sunday, June 9, 2019

The aim of the project is to find a Competitive inhibitor which will Essay

The aim of the project is to find a Competitive appropriateor which will inhibit the methylation of Protein phosphate 2A (PP2A) Via LCMT-1 - Essay ExampleThis means that the methylation of PP2A may be an important regulatory mechanism on the condition that the PP2A methylation is tightly regulated.Tamanoi and Clarke (2006, p. 316) further presents that there atomic number 18 two main levels of regulation of the PP2A. This is may be achieved either through demethylating enzyme LCMT1 or PME-1 or the regulation at the C-terminal tail of PP2AC site (Tamanoi and Clarke, 2006, p. 316). Furthermore, they advance that the methylation of PP2A move also be regulated or deregulated by certain diseases(Sheng 2013). Seshacharyulu, Pandey, Datta and Batra (2013, p.9) elaborates that PP2A serves to regulate the function by dephosphorylating numerous important cellular molecules such as the p53 and Akt. The PP2A is substantive in critical cellular processes including signal transduction, prolife ration and apoptosis.PP2A is structurally multifarious made up of catalytic, support and regulatory subunits. The support and catalytic sub-units of the PP2A comprise of two study isoforms, whereas the regulatory sub-unit has four distinct families of different isoforms. Of these sub-units, the regulatory sub-unit is considered the most diverse in terms of spatial and temporal specificity.The PP2A usually undergoes certain post-translational changes such as methylation and phosphorylation that serve to regulate the enzymatic activity of PP2A. Certain somatic alterations, mutations and aberrant expression of the PP2A support and regulatory sub-units have been common in a build of malignancies in humans including skin, breast and lung cancers. This demonstrates that the role of PP2A as a tumor suppressor (Seshacharyulu et.al 2013). A group of heterogeneous genes encode the individual subunits of the enzyme. This gives rise to a multitude of various PP2A holoenzyme complexes (Schntha l 2013, p.2). Some of the observations that PP2A puts certain stimulatory and

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