Target Name: AP5M1
NCBI ID: G55745
Review Report on AP5M1 Target / Biomarker Content of Review Report on AP5M1 Target / Biomarker
AP5M1
Other Name(s): MUDENG | putative HIV-1 infection-related protein | Adaptor-related protein complex 5 subunit mu-1 | MU-2/AP1M2 domain containing, death-inducing | AP-5 complex subunit mu | Adaptor related protein complex 5 subunit mu 1, transcript variant 1 | Mu-2 related death-inducing | FLJ10813 | adapter-related protein complex 5 subunit mu-1 | AP5M1_HUMAN | Mu5 | MHD domain-containing death-inducing protein | MuD | AP5M1 variant 1 | C14orf108 | AP-5 complex subunit mu-1 | OTTHUMP00000179018 | mu-2-related death-inducing protein | Mu-2-related death-inducing protein | Putative HIV-1 infection-related protein | adaptor related protein complex 5 subunit mu 1 | adaptor related protein complex 5 mu 1 subunit | adapter-related protein complex 5 mu subunit

Unlocking the Potential of AP5M1 (MUDENG) as a Drug Target and Biomarker

Apoptosis, the process of natural cell death, is a crucial aspect of cell biology that regulates growth, development, and maintenance. The apoptosis-mediated regulation of neural networks has been the focus of extensive research in the past decade, with a growing understanding of the molecular mechanisms underlying this process. One of the key proteins involved in this regulation is AP5M1 (MUDENG), which has been identified as a potential drug target and biomarker for various neurological and psychiatric disorders.

In this article, we will explore the AP5M1 protein, its functions, and its potential as a drug target and biomarker. We will discuss the current research on AP5M1 and its potential therapeutic applications, as well as the challenges and opportunities in the development of new treatments for neurodegenerative diseases.

The AP5M1 Protein

AP5M1, also known as PDZ/ZPK-MEDIator, is a member of the PDZ/ZPK family of proteins. This family is known for their role in regulating cell survival and proliferation through the inhibition of the pro-apoptotic protein, p53. PDZ/ZPK signaling pathways have been implicated in a wide range of physiological processes, including cell survival, cell migration, and neurotransmission.

AP5M1 is a 21-kDa protein that is expressed in various tissues, including brain, heart, and pancreas. It is highly conserved, with a calculated pI of 6.4, which makes it a potential protein-based drug candidate. Several studies have demonstrated that AP5M1 is involved in various cellular processes, including cell survival, proliferation, migration, and neurotransmission.

AP5M1 as a Potential Drug Target

The identification of AP5M1 as a potential drug target is based on several factors. Firstly, its involvement in cell survival and proliferation, as well as its role in the regulation of neurotransmission, make it an attractive target for small molecules. Secondly, its high conservation and the lack of known cross-reactions with other proteins make it a promising candidate for drug targeting.

Several studies have demonstrated that AP5M1 can be targeted by small molecules, including inhibitors of its activity as a protein- kinase modulator. These studies have led to the development of several potential drug candidates, including inhibitors of the PI3K/AKT signaling pathway, which is known to be involved in the regulation of cell survival and proliferation.

AP5M1 as a Potential Biomarker

The detection of AP5M1 as a potential biomarker for neurodegenerative diseases has also been shown in several studies. Neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, are characterized by the progressive loss of brain cells and the development of neurofibrillary tangles and neurogenic criteria. The dysfunction of AP5M1 has been implicated in the development and progression of these diseases.

Studies have shown that the expression of AP5M1 is decreased in the brains of individuals with neurodegenerative diseases, and that its levels are highly correlated with the severity of the disease. Additionally, several studies have demonstrated that inhibitors of AP5M1 can protect against the neurotoxicity of various neurodegenerative drugs, suggesting that it may be a useful biomarker for the evaluation of the efficacy of these drugs.

Challenges and Opportunities in the Development of New Treatments

The development of new treatments for neurodegenerative diseases is a major goal in modern medicine. The identification of AP5M1 as a potential drug target and biomarker has great promise for the development of new treatments for these diseases. However, several challenges must be overcome before such treatments can be developed.

Firstly, the development of new treatments for neurodegenerative diseases

Protein Name: Adaptor Related Protein Complex 5 Subunit Mu 1

Functions: As part of AP-5, a probable fifth adaptor protein complex it may be involved in endosomal transport. According to PubMed:18395520, it may play a role in cell death

The "AP5M1 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 AP5M1 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

AP5S1 | AP5Z1 | APAF1 | APBA1 | APBA2 | APBA3 | APBB1 | APBB1IP | APBB2 | APBB3 | APC | APC2 | APCDD1 | APCDD1L | APCDD1L-DT | APCS | APEH | APELA | APEX1 | APEX2 | APH1A | APH1B | API5 | APIP | APLF | APLN | APLNR | APLP1 | APLP2 | APMAP | APOA1 | APOA1-AS | APOA2 | APOA4 | APOA5 | APOB | APOBEC1 | APOBEC2 | APOBEC3A | APOBEC3A_B | APOBEC3B | APOBEC3B-AS1 | APOBEC3C | APOBEC3D | APOBEC3F | APOBEC3G | APOBEC3H | APOBEC4 | APOBR | APOC1 | APOC1P1 | APOC2 | APOC3 | APOC4 | APOC4-APOC2 | APOD | APOE | APOF | APOH | APOL1 | APOL2 | APOL3 | APOL4 | APOL5 | APOL6 | APOLD1 | Apolipoprotein B mRNA editing complex | APOM | APOO | APOOL | APOOP2 | APOOP5 | APP | APPAT | APPBP2 | APPL1 | APPL2 | APRG1 | APRT | APTR | APTX | AQP1 | AQP10 | AQP11 | AQP12A | AQP12B | AQP2 | AQP3 | AQP4 | AQP4-AS1 | AQP5 | AQP6 | AQP7 | AQP7P1 | AQP7P2 | AQP7P3 | AQP7P5 | AQP8 | AQP9 | AQR