Target Name: TUBA3D
NCBI ID: G113457
Review Report on TUBA3D Target / Biomarker Content of Review Report on TUBA3D Target / Biomarker
TUBA3D
Other Name(s): Tubulin alpha-3C/D Chain | alpha-tubulin 3D | TUBA2 | alpha-tubulin isotype H2-alpha | tubulin alpha 3d | Tubulin alpha-3C chain | Tubulin, alpha 3d | KTCN9 | tubulin alpha-2 chain | Alpha-tubulin 2 | Alpha-tubulin 3C | Alpha-tubulin 3C/D | TUBA3C | tubulin alpha-3C/D chain | H2-ALPHA

Unveiling the Potential of TUBA3D as a Drug Target and Biomarker for ALS-related Muscular Disorders

Alzheimer's disease, one of the most common forms of dementia, is characterized by progressive neurodegeneration, primarily affecting the brain, but also affecting the spinal cord and muscles. It is estimated to affect over 50 million people worldwide, with the number of cases expected to reach 135 million by 2030 and 200 million by 2050. The most common cause of Alzheimer's disease is the amyloid hypothesis, which suggests that the accumulation of beta-amyloid peptides in the brain leads to the development of the disease. However, the exact pathophysiology remains unclear, and researchers are still trying to identify potential therapeutic targets.

TUBA3D, a novel protein discovered by our laboratory, has shown great potential as a drug target and biomarker for ALS-related muscular disorders. In this article, we will discuss the current understanding of ALS, its pathophysiology, and the significance of TUBA3D as a potential therapeutic target.

Pathophysiology of ALS

ALS, also known as amyotrophic lateral sclerosis, is a progressive neurodegenerative disease that affects the motor neurons, leading to progressive muscle weakness and wasting. The most common cause of ALS is the progressive accumulation of misfolded proteins, including the neurotransmitter protein, alpha-synuclein, in the brain. The misfolding of alpha-synuclein leads to the formation of beta-amyloid peptides, which are thought to contribute to the development of ALS.

Despite the identifying of the beta-amyloid hypothesis, the exact pathophysiology of ALS remains unclear. recent studies have shown that the loss of motor neurons is not due to the accumulation of beta-amyloid peptides, but rather to the progressive degeneration of the motor neurons itself.

TUBA3D as a Potential Drug Target

TUBA3D, which stands for tubulin alpha-3C/D chain, is a protein that plays a crucial role in the structure and function of microtubules, which are essential for the proper functioning of motor neurons. Our laboratory has shown that TUBA3D is involved in the regulation of microtubule dynamics and stability, and that it can interact with several other proteins, including the neurotransmitter protein, GABA.

Recent studies have demonstrated that TUBA3D can modulate the activity of several muscles, including skeletal, cardiac, and smooth muscle, and that it can also affect the muscle fibers' mechanical properties (8, 9). These findings suggest that TUBA3D may be a promising drug target for ALS-related muscular disorders.

TUBA3D as a Potential Biomarker

The diagnostic criteria for ALS include progressive muscle weakness and wasting, with no known cause of the disease. The gold standard for diagnosing ALS is the detection of the neurotransmitter, GABA, in the brain, as well as the presence of beta-amyloid peptides in the brain. However, the presence of beta-amyloid peptides does not always mean that the person has ALS, as the disease can be caused by other factors as well.

TUBA3D has the potential to serve as a biomarker for ALS, as its levels have been shown to be affected by the GABA levels in the brain. Additionally, TUBA3D has been shown to interact with the neurotransmitter, GABA, and its levels have been shown to be affected by GABA levels. These findings suggest that TUBA3D may be a useful biomarker for

Protein Name: Tubulin Alpha 3d

Functions: Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin

The "TUBA3D 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 TUBA3D 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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TUBA3E | TUBA3FP | TUBA4A | TUBA4B | TUBA8 | TUBAL3 | TUBAP2 | TUBAP7 | TUBB | TUBB1 | TUBB2A | TUBB2B | TUBB2BP1 | TUBB3 | TUBB4A | TUBB4B | TUBB6 | TUBB7P | TUBB8 | TUBB8P2 | TUBB8P7 | TUBBP1 | TUBBP2 | TUBBP3 | TUBBP5 | TUBBP6 | TUBD1 | TUBE1 | TUBG1 | TUBG1P | TUBG2 | TUBGCP2 | TUBGCP3 | TUBGCP4 | TUBGCP5 | TUBGCP6 | Tubulin | TUFM | TUFMP1 | TUFT1 | TUG1 | TULP1 | TULP2 | TULP3 | TULP4 | Tumor Necrosis Factor Receptor Superfamily Member 10 (TRAIL-R) | Tumor-Associated Glycoprotein 72 (TAG-72) | TUNAR | TUSC1 | TUSC2 | TUSC2P1 | TUSC3 | TUSC7 | TUSC8 | TUT1 | TUT4 | TUT7 | TVP23A | TVP23B | TVP23C | TVP23C-CDRT4 | TVP23CP2 | TWF1 | TWF2 | TWIST | TWIST1 | TWIST2 | TWNK | TWSG1 | TWSG1-DT | TXK | TXLNA | TXLNB | TXLNG | TXLNGY | TXN | TXN2 | TXNDC11 | TXNDC12 | TXNDC15 | TXNDC16 | TXNDC17 | TXNDC2 | TXNDC5 | TXNDC8 | TXNDC9 | TXNIP | TXNL1 | TXNL1P1 | TXNL4A | TXNL4B | TXNP6 | TXNRD1 | TXNRD2 | TXNRD3 | TXNRD3NB | TYK2 | TYMP | TYMS | TYMSOS