Target Name: GMPR2
NCBI ID: G51292
Other Name(s): guanosine monophosphate reductase isolog | GMPR2_HUMAN | Guanosine 5'-monophosphate oxidoreductase 2 | GMPR2 variant 1 | Guanosine monophosphate reductase 2, transcript variant 1 | Guanosine monophosp

GMPR2: A Potential Drug Target and Biomarker for Guanosine Monophosphate Reductase

Guanosine monophosphate (GMP) is a crucial molecule in many biological processes, including DNA replication, RNA transcription, and cellular signaling. It is an essential precursor for the synthesis of other important molecules, such as nucleotides and nucleosides. However, abnormalities in GMP metabolism can Causes a variety of diseases, including cardiovascular, neurodegenerative, and reproductive disorders. The guanosine monophosphate reductase (GMPred) enzyme is a key player in the GMP metabolic pathway, and its dysfunction has been implicated in numerous diseases. Therefore, targeting GMPred has the potential to develop new treatments for a variety of conditions.

GMPred is an enzyme that catalyzes the conversion of GMP to GDP. This conversion is critical for the regulation of various cellular processes, including cell signaling, DNA replication, and RNA transcription. GMPred is a member of the SMT family, which includes enzymes involved in the transfer of phosphate groups. The SMT family is a conserved group of enzymes that have been identified as potential drug targets in various diseases.

GMPred is expressed in many different tissues and cells, including the brain, heart, liver, and kidneys. It is also highly expressed in the placenta, which plays a critical role in fetal development and growth. Therefore, targeting GMPred may have therapeutic implications for a variety of conditions.

One potential mechanism by which GMPred could be targeted is by its role in the regulation of DNA replication. In DNA replication, GMPred is involved in the repair of DNA double-strand breaks.double-strand breaks are a common type of genetic mutation that can occur during DNA replication. These mutations can lead to the development of cancer, as they can alter the structure and function of the replicated DNA. Therefore, targeting GMPred may be a promising strategy for the development of cancer therapies.

Another potential mechanism by which GMPred could be targeted is by its role in neurodegenerative diseases. GMPred is involved in the regulation of synaptic plasticity, which is the ability of the brain to change and adapt over time. Therefore, alterations in GMPred function have been implicated in the development of neurodegenerative diseases, such as Alzheimer's and Parkinson's disease. Therefore, targeting GMPred may be a promising strategy for the development of neurodegenerative disease therapies.

In addition to its role in DNA replication and neurodegenerative diseases, GMPred is also involved in the regulation of cellular signaling. GMPred is a negative regulator of the protein kinase CKAP, which is involved in a variety of cellular signaling pathways. Therefore, alterations in GMPred function have been implicated in the development of many cellular signaling pathways. Targeting GMPred may be a promising strategy for the development of new therapies for a variety of cellular signaling pathways.

GMPred is also involved in the regulation of cell signaling pathways that are important for the development and maintenance of tissues and organs. For example, GMPred is involved in the regulation of the Wnt signaling pathway, which is involved in the development and maintenance of tissues and organs. Therefore, alterations in GMPred function have been implicated in the development of diseases that are characterized by the loss of tissues and organs, such as cancer and neurodegenerative diseases.

In conclusion, GMPred is a crucial enzyme involved in the regulation of various cellular processes. Its dysfunction has been implicated in a variety of diseases, including cardiovascular, neurodegenerative, and reproductive disorders. Therefore, targeting GMPred may have therapeutic implications for the development of new treatments for a variety of conditions. Further research is needed to determine the full spectrum of therapeutic targets for GMPred and to develop effective therapies that can

Protein Name: Guanosine Monophosphate Reductase 2

Functions: Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides (PubMed:12009299, PubMed:12669231, PubMed:16359702, PubMed:22037469). Plays a role in modulating cellular differentiation (PubMed:12669231)

More Common Targets

GMPS | GNA11 | GNA12 | GNA13 | GNA14 | GNA15 | GNAI1 | GNAI2 | GNAI3 | GNAL | GNAO1 | GNAO1-DT | GNAQ | GNAS | GNAS-AS1 | GNAT1 | GNAT2 | GNAT3 | GNAZ | GNB1 | GNB1L | GNB2 | GNB3 | GNB4 | GNB5 | GNE | GNG10 | GNG11 | GNG12 | GNG12-AS1 | GNG13 | GNG2 | GNG3 | GNG4 | GNG5 | GNG5P5 | GNG7 | GNG8 | GNGT1 | GNGT2 | GNL1 | GNL2 | GNL3 | GNL3L | GNLY | GNMT | GNPAT | GNPDA1 | GNPDA2 | GNPNAT1 | GNPTAB | GNPTG | GNRH1 | GNRH2 | GNRHR | GNRHR2 | GNS | GOLGA1 | GOLGA2 | GOLGA2P10 | GOLGA2P11 | GOLGA2P2Y | GOLGA2P5 | GOLGA2P7 | GOLGA3 | GOLGA4 | GOLGA5 | GOLGA6A | GOLGA6B | GOLGA6C | GOLGA6D | GOLGA6EP | GOLGA6FP | GOLGA6L1 | GOLGA6L10 | GOLGA6L2 | GOLGA6L22 | GOLGA6L3P | GOLGA6L4 | GOLGA6L5P | GOLGA6L6 | GOLGA6L9 | GOLGA7 | GOLGA7B | GOLGA8A | GOLGA8B | GOLGA8CP | GOLGA8DP | GOLGA8EP | GOLGA8F | GOLGA8G | GOLGA8H | GOLGA8IP | GOLGA8J | GOLGA8K | GOLGA8M | GOLGA8N | GOLGA8O | GOLGA8Q | GOLGA8R