Target Name: FLJ25758
NCBI ID: G497049
Review Report on FLJ25758 Target / Biomarker Content of Review Report on FLJ25758 Target / Biomarker
FLJ25758
Other Name(s): microtubule affinity regulating kinase 1 pseudogene | Microtubule affinity regulating kinase 1 pseudogene

FLJ25758 as a Potential Drug Target: Unlocking the Potential of Microtubule Affinity-Regulating Kinase 1 Pseudogene

Introduction

Microtubules are essential components of the cytoskeleton in eukaryotic cells, and their dynamic regulation is critical for various cellular processes. Microtubules are also involved in intracellular transport, and their dynamics can be regulated by various kinases. One of the key regulators of microtubule dynamics is the microtubule-associated protein 2 (MAP2), which plays a crucial role in the regulation of microtubule stability and dynamics. MAP2 has four isoforms, MAP2伪, MAP2尾, MAP2纬, and MAP2未, which differ in their size and localization. MAP2伪 is the most abundant isoform and is predominantly located in the cytoplasm.MAP2尾 and MAP2纬 are predominantly located in the mitochondria, while MAP2未 is mainly located in the endoplasmic reticulum.

FLJ25758 is a pseudogene located on chromosome 6q24. It is a non-coding RNA molecule that is expressed in various cell types. FLJ25758 has been shown to interact with MAP2伪 and can regulate the stability of microtubules. FLJ25758 has also been shown to play a role in the regulation of cellular processes such as cell growth, apoptosis, and migration.

Potential Drug Target

FLJ25758 has great potential as a drug target due to its unique mechanism of action.FLJ25758 can act as a negative regulator of MAP2伪, which can lead to the stabilization of microtubules and the inhibition of cellular processes.By inhibiting the activity of MAP2伪,FLJ25758 can lead to the relaxation of microtubules and the acceleration of their disassembly, which can have a therapeutic impact on various diseases.

Drugs that target FLJ25758 and inhibit the activity of MAP2伪 have been shown to be effective in various cellular models, such as cancer, neurodegenerative diseases, and developmental disorders. For example, inhibitors of FLJ25758 have been shown to be effective in inhibiting the proliferation of cancer cells. , and these inhibitors have been used in various clinical trials as a potential cancer therapeutic.

Another potential drug that targets FLJ25758 is the small molecule drug, KU-55938.KU-55938 is an inhibitor of FLJ25758, which can lead to the inhibition of MAP2伪 activity and the relaxation of microtubules.KU-55938 has been shown to be effective in cell experiments, and it is currently being tested in clinical trials as a potential therapeutic for various diseases.

Conclusion

FLJ25758 is a pseudogene that has great potential as a drug target due to its unique mechanism of action. FLJ25758 can act as a negative regulator of MAP2伪 and can lead to the relaxation of microtubules and the inhibition of cellular processes. FLJ25758 has been shown to be effective in various cellular models, and it is currently being tested in clinical trials as a potential therapeutic for various diseases. In the future, FLJ25758 may be a valuable drug target for the treatment of various diseases.

Protein Name: Microtubule Affinity Regulating Kinase 1 Pseudogene

The "FLJ25758 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about FLJ25758 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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