Target Name: CHKA
NCBI ID: G1119
Review Report on CHKA Target / Biomarker Content of Review Report on CHKA Target / Biomarker
CHKA
Other Name(s): ethanolamine kinase | CKI | CHETK-alpha | CHKA_HUMAN | Ethanolamine kinase (phosphorylating) | CHKA variant 1 | choline kinase alpha | Ethanolamine kinase | Ethanolamine phosphokinase | Choline kinase alpha | NEDMIMS | Choline kinase alpha (isoform a) | EK | CHK | CK

CHKA: A Potential Drug Target and Biomarker for Ethanolamine Kinase

Ethanolamine kinase (CHKA) is a enzyme that is involved in the metabolism of ethanolamines, which are naturally occurring compounds found in many organisms. Ethanolamines have been shown to have a variety of roles in cellular processes, including modulating cell signaling pathways and participating in cellular signaling cascades. CHKA is a key enzyme in the metabolism of these compounds, and its function has been the subject of extensive research in the past few decades.

Recent studies have identified CHKA as a potential drug target for a variety of diseases, including cancer, neurodegenerative diseases, and mental disorders. This is because CHKA plays a crucial role in the metabolism of many of the drugs that are currently used to treat these conditions, and its inhibition could lead to a reduction in drug resistance and improved treatment outcomes.

One of the key reasons for the potential drug-targeting of CHKA is its involvement in the production of key metabolites, such as ethylamine, which have been shown to have a variety of roles in cellular signaling pathways. These metabolites are often used as targets for drugs that aim to modify the expression of genes involved in cellular signaling pathways. For example, inhibition of CHKA has been shown to reduce the production of ethylamine, which can lead to a reduction in the activity of genes involved in cell signaling pathways and a decrease in cellular signaling.

Another potential mechanism by which CHKA may be targeted by drugs is its role in the metabolism of other drugs. Many drugs are metabolized by enzymes in the liver, and CHKA is involved in the metabolism of many of these drugs. For example, inhibition of CHKA has been shown to reduce the metabolism of a variety of drugs, including chemotherapy drugs, which can lead to increased drug levels and reduced efficacy of the treatments.

In addition to its potential as a drug target, CHKA is also a potential biomarker for a variety of diseases. Its involvement in the metabolism of ethanolamines makes it a useful tool for the diagnosis and treatment of conditions that involve changes in the levels of these compounds in the body. For example, CHKA has been shown to be involved in the metabolism of many neurotransmitters, including dopamine, which is involved in the treatment of Parkinson's disease.

In conclusion, CHKA is a potential drug target and biomarker for a variety of diseases. Its involvement in the metabolism of ethanolamines and its potential as a target for drugs that modify gene expression make it an attractive target for researchers and clinicians. Further research is needed to fully understand the role of CHKA in the treatment of these conditions and to develop safe and effective drugs that can target this enzyme.

Protein Name: Choline Kinase Alpha

Functions: Plays a key role in phospholipid biosynthesis by catalyzing the phosphorylation of free choline to phosphocholine, the first step in phosphatidylcholine biosynthesis (PubMed:19915674, PubMed:34077757, PubMed:17007874). Also phosphorylates ethanolamine, thereby contributing to phosphatidylethanolamine biosynthesis (PubMed:19915674, PubMed:17007874). Has higher activity with choline (PubMed:19915674, PubMed:17007874). May contribute to tumor cell growth (PubMed:19915674)

The "CHKA 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 CHKA 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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CHKB | CHKB-CPT1B | CHKB-DT | CHL1 | CHL1-AS2 | Chloride channel | CHM | CHML | CHMP1A | CHMP1B | CHMP1B2P | CHMP2A | CHMP2B | CHMP3 | CHMP4A | CHMP4B | CHMP4BP1 | CHMP4C | CHMP5 | CHMP6 | CHMP7 | CHN1 | CHN2 | CHN2-AS1 | CHODL | Cholesterol Epoxide Hydrolase (ChEH) | Cholesterol esterase | Choline transporter-like protein | CHORDC1 | CHORDC1P4 | CHP1 | CHP1P2 | CHP2 | CHPF | CHPF2 | CHPT1 | CHRAC1 | CHRD | CHRDL1 | CHRDL2 | CHRFAM7A | CHRM1 | CHRM2 | CHRM3 | CHRM3-AS2 | CHRM4 | CHRM5 | CHRNA1 | CHRNA10 | CHRNA2 | CHRNA3 | CHRNA4 | CHRNA5 | CHRNA6 | CHRNA7 | CHRNA9 | CHRNB1 | CHRNB2 | CHRNB3 | CHRNB4 | CHRND | CHRNE | CHRNG | Chromobox protein homolog | Chromodomain Helicase DNA Binding Protein | Chromosome 10 open reading frame 115 | Chromosome 16 open reading frame 47 | Chromosome 17 open reading frame 47 | Chromosome 6 open reading frame 183 | CHROMR | CHST1 | CHST10 | CHST11 | CHST12 | CHST13 | CHST14 | CHST15 | CHST2 | CHST3 | CHST4 | CHST5 | CHST6 | CHST7 | CHST8 | CHST9 | CHSY1 | CHSY3 | CHTF18 | CHTF8 | CHTOP | CHUK | CHURC1 | CHURC1-FNTB | Chymotrypsin | CIAO1 | CIAO2A | CIAO2AP2 | CIAO2B | CIAO3 | CIAPIN1