Target Name: RPL7
NCBI ID: G6129
Review Report on RPL7 Target / Biomarker Content of Review Report on RPL7 Target / Biomarker
RPL7
Other Name(s): 60S ribosomal protein L7 (isoform 1) | RPL7 variant 1 | large ribosomal subunit protein uL30 | Large ribosomal subunit protein uL30 | 60S ribosomal protein L7 | humL7-1 | ribosomal protein L7 | L7 | Ribosomal protein L7 | RL7_HUMAN

RPL7: A Promising Drug Target and Biomarker for ALS

Introduction

Amyloidosis, a neurodegenerative disease characterized by the accumulation of misfolded proteins, including the 尾-amyloid protein, is one of the leading causes of human neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and ALS (Amyotrophic Lateral Sclerosis). The misfolded 尾 -amyloid protein is thought to contribute to the neurotoxicity and progression of these diseases. Therefore, the development of effective strategies to target 尾-amyloid and its associated proteins is crucial for the prevention and treatment of neurodegenerative diseases.

RPL7, a 60S ribosomal protein L7 (isoform 1), is a promising drug target and biomarker for ALS. RPL7 is a key protein that forms the base of the 230-kDa ribosome, which is responsible for the production of the amyloid protein in the brain. The misfolded 尾-amyloid protein is thought to contribute to the neurotoxicity and progression of ALS, and RPL7 may provide a new avenue for the development of therapeutic strategies for this disease.

D Central capsule destruction is a characteristic of ALS, and RPL7 may be a promising drug target (or biomarker). In this article, we discuss the role of RPL7 in ALS and its potential as a drug target or biomarker.

The role of RPL7

RPL7 is a 60S ribosomal protein L7 (isoform 1). It is the basis for the synthesis of 尾-amyloid protein, which is an important cause of ALS. Studies have found that in ALS, the expression level of RPL7 is significantly increased, while its binding rate is decreased. These changes may reflect functional changes of RPL7 in ALS.

According to research, RPL7 may be involved in the pathophysiological process of ALS in various ways. First, RPL7 is the main synthetic basis of 尾-amyloid protein, so its functional changes may be related to the folding of 尾-amyloid protein. Second, the expression level of RPL7 correlates with protein components in neurons from ALS patients, suggesting that it may be involved in neuronal damage and death. Finally, RPL7 expression levels were associated with quality of life and health status in ALS patients, suggesting that it may be involved in the development and severity of the disease.

as a drug target

RPL7 has great potential as a drug target. First, RPL7 is the basis for the synthesis of 尾-amyloid protein, so inhibiting the function of RPL7 may help reduce the production of 尾-amyloid protein, thereby slowing down the progression of ALS. Secondly, the expression level of RPL7 is related to the protein components in neurons of ALS patients, so by regulating the composition of these proteins, it may help to improve the structure and function of neurons, thereby slowing the progression of ALS.

as biomarkers

In addition to being a drug target, RPL7 can also serve as a biomarker to detect ALS. Studies have shown that the expression level of RPL7 is related to the survival rate and recovery of ALS patients. Therefore, by detecting the expression level of RPL7, it may be possible to predict the survival rate and recovery of ALS patients, providing valuable information for treatment and recovery.

in conclusion

RPL7 has important biological and pathophysiological roles in ALS, making it a promising drug target. By inhibiting the function of RPL7, the progression of ALS can be slowed, thereby providing a valuable strategy for treatment and rehabilitation. At the same time, RPL7 can also be used as a biomarker to detect ALS, providing new insights into the diagnosis and treatment of the disease.

Protein Name: Ribosomal Protein L7

Functions: Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636399, PubMed:32669547). Binds to G-rich structures in 28S rRNA and in mRNAs (PubMed:12962325). Plays a regulatory role in the translation apparatus; inhibits cell-free translation of mRNAs (PubMed:12962325)

The "RPL7 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 RPL7 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

More Common Targets

RPL7A | RPL7AP10 | RPL7AP26 | RPL7AP27 | RPL7AP28 | RPL7AP34 | RPL7AP41 | RPL7AP50 | RPL7AP6 | RPL7AP62 | RPL7AP69 | RPL7AP70 | RPL7AP9 | RPL7L1 | RPL7P1 | RPL7P10 | RPL7P11 | RPL7P12 | RPL7P13 | RPL7P16 | RPL7P2 | RPL7P20 | RPL7P21 | RPL7P22 | RPL7P23 | RPL7P24 | RPL7P26 | RPL7P32 | RPL7P33 | RPL7P34 | RPL7P38 | RPL7P44 | RPL7P47 | RPL7P48 | RPL7P50 | RPL7P52 | RPL7P55 | RPL7P57 | RPL7P58 | RPL7P59 | RPL7P6 | RPL7P7 | RPL7P8 | RPL7P9 | RPL8 | RPL9 | RPL9P16 | RPL9P18 | RPL9P2 | RPL9P25 | RPL9P29 | RPL9P32 | RPLP0 | RPLP0P12 | RPLP0P2 | RPLP0P6 | RPLP1 | RPLP1P4 | RPLP1P6 | RPLP1P7 | RPLP2 | RPLP2P3 | RPN1 | RPN2 | RPP14 | RPP21 | RPP25 | RPP25L | RPP30 | RPP38 | RPP38-DT | RPP40 | RPPH1 | RPRD1A | RPRD1B | RPRD2 | RPRM | RPRML | RPS10 | RPS10-NUDT3 | RPS10P10 | RPS10P13 | RPS10P19 | RPS10P3 | RPS10P5 | RPS10P7 | RPS10P9 | RPS11 | RPS11P5 | RPS12 | RPS12P10 | RPS12P22 | RPS12P23 | RPS12P24 | RPS12P25 | RPS12P28 | RPS12P29 | RPS12P3 | RPS12P4 | RPS13