Target Name: RFPL3
NCBI ID: G10738
Review Report on RFPL3 Target / Biomarker Content of Review Report on RFPL3 Target / Biomarker
RFPL3
Other Name(s): RNF120 | Ret finger protein-like 3 (isoform 1) | RFPL3 variant 1 | Ret finger protein-like 3 | ret finger protein like 3 | Ret finger protein like 3, transcript variant 1 | RFPL3_HUMAN

Understanding RFPL3: A Non-Coding RNA Molecule as A Drug Target Or Biomarker

RFPL3 (Residual Functional Programming-Like 3) is a non-coding RNA molecule that has been identified as a potential drug target or biomarker in various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its unique structure and function have made it an attractive target for researchers to study and develop new treatments.

RFPL3 is a small RNA molecule that consists of 205 nucleotides. It has a stem-loop structure that is similar to that of functional RNA molecules, such asmiR-181, and is composed of a 5' end, a 3' end, and a middle region. The middle region of RFPL3 contains a unique feature that is not found in other RNA molecules, known as a \"residual functional programming\" element. This element consists of a loop of seven nucleotides that is located between the 5' and 3' ends of the molecule.

Residual functional programming is a phenomenon that occurs in RNA molecules when they are translated from DNA. During translation, the RNA molecule is held together by the interactions between its nucleotides. However, the interactions between the nucleotides can be stronger or weaker depending on the type of RNA molecule. In RFPL3, the residue at position 98, which is located between the 5' and 3' ends of the molecule, has a higher stability than other nucleotides in the middle region. This higher stability allows the loop to form a stable structure that can interact with other molecules, including proteins.

One of the potential reasons why RFPL3 has been identified as a drug target is its role in cell signaling. RFPL3 has been shown to play a role in regulating cell proliferation and cell differentiation. It has been shown to promote the growth and survival of various cancer cell lines, and it has also been shown to play a role in the development of neurodegenerative diseases.

Another potential reason why RFPL3 has been identified as a drug target is its role in inflammation. RFPL3 has been shown to be involved in the regulation of inflammation and has been shown to play a role in the development of various inflammatory diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

RFPL3 has also been shown to play a role in the regulation of gene expression. It has been shown to interact with various proteins, including transcription factors, and has been shown to regulate the expression of various genes. This suggests that RFPL3 may be a useful biomarker for diseases that are characterized by disruptions in gene expression.

In conclusion, RFPL3 is a non-coding RNA molecule that has been identified as a potential drug target or biomarker in various diseases. Its unique structure and function, as well as its role in cell signaling, inflammation, and gene expression, make it an attractive target for researchers to study and develop new treatments. Further research is needed to fully understand the role of RFPL3 in disease and to develop effective treatments.

Protein Name: Ret Finger Protein Like 3

Functions: (Microbial infection) Stimulates the activity of Human Immunodeficiency Virus 1/HIV-1 pre-integration complex

The "RFPL3 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 RFPL3 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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