Orotidine 5'-monophosphate: Difference between revisions
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Latest revision as of 21:22, 17 March 2025
Orotidine 5'-monophosphate (OMP), also known as orotidylic acid, is a nucleotide that plays a significant role in the biosynthesis of pyrimidine nucleotides. OMP is an intermediate in the pathway that leads to the formation of uridine 5'-monophosphate (UMP), an essential precursor for the synthesis of RNA and DNA pyrimidine bases. This pathway is crucial for the synthesis and regulation of nucleic acids in all living organisms.
Biosynthesis[edit]
OMP is synthesized from orotic acid and phosphoribosyl pyrophosphate (PRPP) through the action of the enzyme orotate phosphoribosyltransferase (OPRTase), resulting in the formation of OMP and the release of pyrophosphate (PPi). This reaction is part of the de novo synthesis pathway of pyrimidine nucleotides, which is essential for cell growth and division.
Conversion to UMP[edit]
The conversion of OMP to UMP is catalyzed by the enzyme orotidine-5'-phosphate decarboxylase (ODCase). This reaction involves the decarboxylation of OMP to form UMP, a key precursor in the synthesis of other pyrimidine nucleotides such as CTP, TMP, and their respective nucleoside and nucleotide derivatives.
Clinical Significance[edit]
Alterations in the enzymes involved in the OMP synthesis pathway, including OPRTase and ODCase, can lead to disruptions in nucleotide biosynthesis, affecting DNA and RNA synthesis. Such disruptions can result in genetic disorders and have been implicated in certain types of cancer. Understanding the OMP synthesis pathway is also important for the development of antimetabolite drugs that target pyrimidine biosynthesis, which are used in cancer chemotherapy and in the treatment of autoimmune diseases.
See Also[edit]

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