Target Name: MNAT1
NCBI ID: G4331
Review Report on MNAT1 Target / Biomarker Content of Review Report on MNAT1 Target / Biomarker
MNAT1
Other Name(s): MNAT1 variant 1 | CAP35 | RING finger protein MAT1 | p35 | CDK-activating kinase assembly factor MAT1 (isoform 2) | menage a trois 1 (CAK assembly factor) | MNAT1 variant 2 | Cyclin-G1-interacting protein | CDK7/cyclin-H assembly factor | CDK-activating kinase assembly factor MAT1 | RING finger protein 66 | MNAT1 component of CDK activating kinase | MNAT1, CDK activating kinase assembly factor | MAT1 | RNF66 | menage a trois homolog 1, cyclin H assembly factor | TFB3 | p36 | Menage a trois | cyclin G1 interacting protein | Cyclin G1 interacting protein | MNAT1 component of CDK activating kinase, transcript variant 1 | cyclin-G1-interacting protein | Menage a trois 1 (CAK assembly factor) | MNAT CDK-activating kinase assembly factor 1 | CDK-activating kinase assembly factor MAT1 (isoform 1) | menage a trois-like protein 1 cyclin H assembly factor | MAT1_HUMAN | MNAT1 component of CDK activating kinase, transcript variant 2

MNAT1 as A Drug and Biomarker Target for Neurodegenerative Diseases

Molecular neurodegenerative diseases (MNDs) are a group of progressive brain disorders that are characterized by the progressive loss of neurons and their associated proteins. These diseases, including MNAT1 (MNAT1 variant 1), are often treated with drugs that aim to slow down or halt the progression of neurodegeneration. However, the development and progression of MND can also be influenced by various genetic and environmental factors. Therefore, identifying potential drug targets and biomarkers for MND is crucial for the development of new treatments. In this article, we will discuss MNAT1 as a drug target and its potential as a biomarker for MND.

MNAT1: Background and Function

MNAT1 is a gene that encodes the 伪-helical domain (伪-helix) at the N-terminus of the protein. It is one of the main components of neuronal cell membranes and plays a vital role in the survival and function of neurons. Studies have shown that the 伪-helical domain of MNAT1 plays an important role in neuronal death and neurodegenerative diseases.

The 伪-helical domain of MNAT1 contains a special domain called the core 伪-helix. This domain is composed of two interacting helices, including an 伪-helix and a new 尾-helix. Research shows that the secondary structure of the core 伪-helix is 鈥嬧?媍ritical to the survival and function of neurons.

In addition, the 伪-helical domain of MNAT1 is also related to neuronal apoptosis. Studies have shown that the 伪-helical domain of MNAT1 can inhibit neuronal apoptosis and thereby extend the lifespan of neurons.

MNAT1 as a drug target

The properties of the 伪-helical domain of MNAT1 make it a potential drug target. Since the 伪-helical domain of MNAT1 plays an important role in neuronal death and neurodegenerative diseases, studying the drug targets of the 伪-helical domain of MNAT1 is of great significance for the development of new drugs to treat these diseases.

Currently, some studies are exploring the possibility of the 伪-helical domain of MNAT1 as a drug target. For example, some researchers are studying whether the 伪-helical domain of MNAT1 could serve as a new drug target for treating neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease.

MNAT1 as a biomarker

In addition to being a drug target, MNAT1 can also serve as a potential biomarker for neurodegenerative diseases. Neurodegenerative diseases, such as Parkinson's disease and Alzheimer's disease, often lead to neuronal death and neuronal loss. Therefore, studying protein markers in neurodegenerative diseases, such as MNAT1, is of great significance for the diagnosis and treatment of these diseases.

Some studies have shown that MNAT1 can serve as a potential biomarker for neurodegenerative diseases. For example, some researchers have found that MNAT1 expression levels can be increased and are overexpressed in some patients with neurodegenerative diseases. In addition, some researchers have also found that MNAT1 can interact with other proteins in neurodegenerative diseases, thereby increasing its possibility as a potential biomarker for neurodegenerative diseases.

Conclusion

MNAT1 is a gene that plays an important role in neuronal survival and function. By studying the 伪-helical domain of MNAT1, new drug targets can be discovered to treat neurodegenerative diseases. At the same time, MNAT1 can also serve as a potential biomarker for neurodegenerative diseases, providing new clues for the diagnosis and treatment of these diseases. In the future, we will further study the 伪-helical domain of MNAT1 in order to provide new treatments and diagnostic methods for neurodegenerative diseases.

Protein Name: MNAT1 Component Of CDK Activating Kinase

Functions: Stabilizes the cyclin H-CDK7 complex to form a functional CDK-activating kinase (CAK) enzymatic complex. CAK activates the cyclin-associated kinases CDK1, CDK2, CDK4 and CDK6 by threonine phosphorylation. CAK complexed to the core-TFIIH basal transcription factor activates RNA polymerase II by serine phosphorylation of the repetitive C-terminal domain (CTD) of its large subunit (POLR2A), allowing its escape from the promoter and elongation of the transcripts. Involved in cell cycle control and in RNA transcription by RNA polymerase II

The "MNAT1 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 MNAT1 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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MND1 | MNDA | MNS1 | MNT | MNX1 | MNX1-AS1 | MOAP1 | MOB1A | MOB1B | MOB2 | MOB3A | MOB3B | MOB3C | MOB4 | MOBP | MOCOS | MOCS1 | MOCS2 | MOCS2-DT | MOCS3 | MOG | MOGAT1 | MOGAT2 | MOGAT3 | MOGS | MOK | MON1A | MON1B | MON2 | Monoamine oxidase (MAO) | Monoamine Transporter (MAT) | MORC1 | MORC2 | MORC2-AS1 | MORC3 | MORC4 | MORF4 | MORF4L1 | MORF4L1P1 | MORF4L1P3 | MORF4L1P7 | MORF4L2 | MORF4L2-AS1 | MORN1 | MORN2 | MORN3 | MORN4 | MORN5 | MOS | MOSMO | MOSPD1 | MOSPD2 | MOSPD3 | MOV10 | MOV10L1 | MOXD1 | MOXD2P | MPC1 | MPC2 | MPDU1 | MPDU1-AS1 | MPDZ | MPEG1 | MPG | MPHOSPH10 | MPHOSPH10P1 | MPHOSPH6 | MPHOSPH8 | MPHOSPH9 | MPI | MPIG6B | MPL | MPLKIP | MPND | MPO | MPP1 | MPP2 | MPP3 | MPP4 | MPP7 | MPPE1 | MPPED1 | MPPED2 | MPPED2-AS1 | MPRIP | MPST | MPTX1 | MPV17 | MPV17L | MPV17L2 | MPZ | MPZL1 | MPZL2 | MPZL3 | MR1 | MRAP | MRAP2 | MRAS | MRC1 | MRC2