Target Name: MRPL1
NCBI ID: G65008
Review Report on MRPL1 Target / Biomarker Content of Review Report on MRPL1 Target / Biomarker
MRPL1
Other Name(s): mitochondrial ribosomal protein L1 | L1mt | mitochondrial large ribosomal subunit protein uL1m | BM022 | L1MT | Mitochondrial large ribosomal subunit protein uL1m | Mitochondrial ribosomal protein L1 | MRP-L1 | 39S ribosomal protein L1, mitochondrial | RM01_HUMAN

Mitochondrial Ribosomal Protein L1 in Protein Synthesis, Potential as A Drug Target

Mitochondrial Ribosomal Protein L1 (MRPL1) is a protein that plays a crucial role in the structure and function of the mitochondria, which are organelles responsible for generating energy in the form of ATP in cells throughout the body. Ribosomal proteins are large proteins that are synthesized in the mitochondria and help to synthesize the DNA and RNA necessary for gene expression.

MRPL1 is a member of the ribosomal protein family 1 (RPL1) and is the protein responsible for catalyzing the first step of protein synthesis in the mitochondria, known as initiation. This protein functions as a nucleotide-binding protein, using its active site to bind to and translocate nucleotides into the synthesizing 23S rRNA.

The structure and function of MRPL1 are highly conserved across different species, and similar studies have identified conserved secondary structure elements within the protein. One of these conserved elements is a unique farnesylated cysteine 鈥嬧?媟esidue, which is known as cysteine-215. This cysteine 鈥嬧?媟esidue is involved in the stability and function of MRPL1 and has been shown to play a role in its stability and stability in the mitochondria.

Another important structural feature of MRPL1 is its ability to interact with various co-factors, which help to regulate its stability and function. These co-factors include the amino acids lysine and acetyl groups, as well as the nucleotides GTP and AUG. These interactions are important for maintaining the stability of MRPL1 and for regulating its function in the mitochondria.

Due to its role in the first step of protein synthesis in the mitochondria, MRPL1 has been shown to be a potential drug target in the treatment of various diseases. Studies have shown that modulating the activity of MRPL1 can be an effective way to treat a variety of conditions, including cancer, neurodegenerative diseases, and respiratory diseases.

One of the main advantages of targeting MRPL1 is its potential to affect a wide range of cellular processes that are affected by disruptions in protein synthesis in the mitochondria. This is because MRPL1 is involved in the initiation of protein synthesis in the mitochondria, and many cellular processes rely on the availability of these processes to function properly.

Another potential benefit of targeting MRPL1 is its potential to be a more targeted and less invasive treatment option compared to some other treatments. Because MRPL1 is primarily localized to the mitochondria, targeting it may be less likely to cause unintended effects in other parts of the cell . This can be especially important in the treatment of neurodegenerative diseases, where unintended effects can be devastating.

In conclusion, MRPL1 is a protein that plays a crucial role in the structure and function of the mitochondria, and has been identified as a potential drug target due to its involvement in the initiation of protein synthesis in the mitochondria and its potential to affect a wide range of cellular processes. Further research is needed to fully understand the potential benefits and risks of targeting MRPL1 for various diseases.

Protein Name: Mitochondrial Ribosomal Protein L1

The "MRPL1 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 MRPL1 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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MRPL10 | MRPL11 | MRPL12 | MRPL13 | MRPL14 | MRPL15 | MRPL16 | MRPL17 | MRPL18 | MRPL19 | MRPL2 | MRPL20 | MRPL20-AS1 | MRPL20P1 | MRPL21 | MRPL22 | MRPL23 | MRPL23-AS1 | MRPL24 | MRPL27 | MRPL28 | MRPL3 | MRPL30 | MRPL33 | MRPL34 | MRPL35 | MRPL35P2 | MRPL37 | MRPL38 | MRPL39 | MRPL4 | MRPL40 | MRPL41 | MRPL42 | MRPL42P5 | MRPL43 | MRPL44 | MRPL45 | MRPL45P1 | MRPL45P2 | MRPL46 | MRPL47 | MRPL48 | MRPL49 | MRPL50 | MRPL51 | MRPL52 | MRPL53 | MRPL54 | MRPL55 | MRPL57 | MRPL57P1 | MRPL57P8 | MRPL58 | MRPL9 | MRPL9P1 | MRPS10 | MRPS10P2 | MRPS11 | MRPS12 | MRPS14 | MRPS15 | MRPS16 | MRPS17 | MRPS18A | MRPS18B | MRPS18C | MRPS18CP2 | MRPS18CP4 | MRPS18CP7 | MRPS2 | MRPS21 | MRPS22 | MRPS23 | MRPS24 | MRPS25 | MRPS26 | MRPS27 | MRPS28 | MRPS30 | MRPS30-DT | MRPS31 | MRPS31P2 | MRPS31P4 | MRPS31P5 | MRPS33 | MRPS33P4 | MRPS34 | MRPS35 | MRPS35-DT | MRPS36 | MRPS36P4 | MRPS5 | MRPS6 | MRPS7 | MRPS9 | MRRF | MRS2 | MRS2P2 | MRTFA