Target Name: Calcium channel
NCBI ID: P6009
Review Report on Calcium channel Target / Biomarker Content of Review Report on Calcium channel Target / Biomarker
Calcium channel
Other Name(s): Calcium channel

Calcium Channel Subtype as a Drug Target: Unlocking the Potential of Calcium Signaling in Neurodegenerative Disorders

Introduction

Calcium homeostasis is a critical signaling pathway that regulates various cellular processes in the body. It plays a central role in neuronal communication and learning, and dysregulation of calcium homeostasis has been implicated in numerous neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and Huntington's disease . The Calcium channel, also known as the Calcium channel subtype (Ca2+ channel), is a critical protein that enables calcium homeostasis in neurons. In this article, we will explore the calcium channel as a drug target and its potential in the treatment of neurodegenerative disorders.

The Calcium Channel Subtype: Structure and Function

The Calcium channel subtype is a family of proteins that belong to the Ca2+-ATPase superfamily. These proteins share a conserved catalytic core and share a common transmembrane domain. The Ca2+ channel subtype is composed of two main subunits, alpha and beta subunits, which are held together by ionic bonds.

The alpha subunit is responsible for the channel's opening and closing, while the beta subunit is responsible for the channel's conductivity. The Ca2+ channel subtype has a unique property where the alpha subunit is extracellular, while the beta subunit is intracellular. This unique structure allows the Ca2+ channel subtype to regulate the concentration of calcium ions in the cell without crossing the membrane.

The Ca2+ channel subtype plays a critical role in neuronal communication and learning. When calcium ions are released from the intracellular store, they can activate the alpha subunit, which in turn opens the channel, allowing calcium ions to enter the cell. This increase in calcium ions can then trigger a variety of downstream signaling pathways that regulate neuronal function.

Dysregulation of the Ca2+ channel subtype has been implicated in numerous neurodegenerative disorders. For example, studies have shown that individuals with Alzheimer's disease have reduced levels of the Ca2+ channel subtype in their brains, which may contribute to the dysfunction of the neuronal network in this disease . Similarly, individuals with Parkinson's disease have increased levels of the Ca2+ channel subtype in their brains, which may also contribute to the dysfunction of the neuronal network in this disease.

Calcium Channel as a Drug Target: The Potential for Treating Neurodegenerative Disorders

The calcium channel subtype has emerged as a promising drug target for the treatment of neurodegenerative disorders. By targeting the Ca2+ channel subtype, researchers can potentially improve neuronal function and slow the progression of neurodegenerative disorders.

One approach to targeting the Ca2+ channel subtype is through the use of small molecules that can modulate the activity of the channel. These small molecules can act on the alpha or beta subunits of the Ca2+ channel subtype to alter the conductivity of the channel. For example , inhibitors of the Ca2+ channel subtype have been shown to improve neuronal function in individuals with Alzheimer's disease and Parkinson's disease.

Another approach to targeting the Ca2+ channel subtype is through the use of antibodies that can specifically bind to the channel and prevent it from functioning. These antibodies can be used to treat neurodegenerative disorders by reducing the activity of the Ca2+ channel subtype and improving neuronal function.

In conclusion, the calcium channel subtype is a promising drug target for the treatment of neurodegenerative disorders. By targeting the Ca2+ channel subtype, researchers can potentially improve neuronal function and slow the progression of these disorders. Further research is needed to

Protein Name: Calcium Channel (nonspecified Subtype)

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•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
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•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
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•   advantages and risks of development, etc.
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Calcium release-activated channel (CRAC) | Calcium-activated chloride channel regulators | Calcium-Activated K(Ca) Potassium Channel | CALCOCO1 | CALCOCO2 | CALCR | CALCRL | CALCRL-AS1 | CALD1 | CALHM1 | CALHM2 | CALHM3 | CALHM4 | CALHM5 | CALHM6 | CALM1 | CALM2 | CALM2P1 | CALM2P2 | CALM3 | CALML3 | CALML3-AS1 | CALML4 | CALML5 | CALML6 | Calmodulin | CALN1 | Calpain | Calpain-13 | Calprotectin | CALR | CALR3 | CALU | CALY | CAMK1 | CAMK1D | CAMK1G | CAMK2A | CAMK2B | CAMK2D | CAMK2G | CAMK2N1 | CAMK2N2 | CAMK4 | CAMKK1 | CAMKK2 | CAMKMT | CAMKV | CAMLG | CAMP | cAMP Phosphodiesterase | cAMP Responsive Element Binding Protein (CREB) | cAMP-Dependent protein kinase (PKA) | CAMSAP1 | CAMSAP2 | CAMSAP3 | CAMTA1 | CAMTA2 | CAND1 | CAND1.11 | CAND2 | Cannabinoid receptor | CANT1 | CANX | Cap-binding complex | CAP1 | CAP2 | CAPG | CAPN1 | CAPN10 | CAPN10-DT | CAPN11 | CAPN12 | CAPN13 | CAPN14 | CAPN15 | CAPN2 | CAPN3 | CAPN5 | CAPN6 | CAPN7 | CAPN8 | CAPN9 | CAPNS1 | CAPNS2 | CAPRIN1 | CAPRIN2 | CAPS | CAPS2 | CAPSL | CAPZA1 | CAPZA2 | CAPZA3 | CAPZB | Carbonic Anhydrase | Carbonic Anhydrase V | Carboxylesterase | Carboxypeptidase A | Carboxypeptidase B | Carboxypeptidase N