Target Name: RPL5P4
NCBI ID: G643343
Review Report on RPL5P4 Target / Biomarker Content of Review Report on RPL5P4 Target / Biomarker
RPL5P4
Other Name(s): RPL5_1_31 | ribosomal protein L5 pseudogene 4 | Ribosomal protein L5 pseudogene 4

RPL5 Gene as A Drug Target Forplasmid Replication and Disease

RPL5P4 (RPL5_1_31) is a gene that encodes for a protein known as RPL5, which is a key regulator of the plasmid replication process in bacteria. The RPL5 gene is located on chromosome 1 and encodes for a protein that is essential for the growth and replication of plasmids in E. coli. The protein encoded by RPL5 functions as a scaffold to form a complex structure on the outer membrane of E. coli plasmids, allowing them to replicate their genetic material.

The RPL5 gene is a promising drug target due to its involvement in the replication of plasmids, which are often used in genetic engineering and gene therapy. Many diseases are caused by the failure of normal cell replication, including cancer, and the development of drug resistance. Therefore, targeting the RPL5 gene could potentially lead to the development of new treatments for these diseases.

Expression of RPL5

RPL5 is a 16-kDa protein that is expressed in E. coli cells. It is composed of a catalytic active center, a transmembrane region, and a cytoplasmic tail. The catalytic active center is the region where the protein functions as a scaffold, while the transmembrane region is responsible for its stability and cytoplasmic tail is involved in its stability and localization.

The RPL5 gene is expressed in E. coli cells, and its expression is regulated by various factors, including the cytosine concentration and the availability of growth factors. Once transcribed into RNA, RPL5 is translated into protein and is located in the cytoplasm.

The role of RPL5 in plasmid replication

RPL5 plays a crucial role in the replication of plasmids in E. coli. It functions as a scaffold to form a complex structure on the outer membrane of plasmids, allowing them to replicate their genetic material. The RPL5-complex structure is composed of several subunits, including RPL5 itself, RPL5b, RPL5c, and RPL5d.

The RPL5 protein is involved in the formation of the RPL5-complex by interacting with the bacterial outer membrane protein OmpA. OmpA is a transmembrane protein that is involved in the regulation of bacterial outer membrane structure and is composed of multiple domains, including a transmembrane region, a cytoplasmic tail, and a catalytic active center.

The RPL5 protein interacts with OmpA through its amino acid residues, allowing it to form a stable complex with the outer membrane protein. The RPL5-OmpA complex is then involved in the formation of a more stable structure that allows plasmids to replicate their genetic material.

The failure of RPL5 to function properly can result in the failure of plasmid replication and the development of drug resistance. Therefore, targeting the RPL5 gene could potentially lead to the development of new treatments for diseases caused by the failure of normal cell replication, such as cancer and the development of drug resistance.

Drug targeting RPL5

Drug targeting RPL5 is a promising strategy for the development of new treatments for diseases caused by the failure of normal cell replication. By inhibiting the function of RPL5, drugs can reduce the replication of plasmids and potentially lead to the death of bacteria.

One approach to drug targeting RPL5 is to use small molecules that inhibit the activity of RPL5. Many small molecules have been shown to inhibit the activity of RPL5, including inhibitors of the DNA-binding domain, the catalytic active center, and the cytoplasmic tail.

Another approach to drug targeting RPL5 is to use antibodies that recognize and label RPL5. Antibodies are

Protein Name: Ribosomal Protein L5 Pseudogene 4

The "RPL5P4 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 RPL5P4 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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