ELOVL6: A Potential Drug Target and Biomarker for 3-Keto Acyl-CoA Synthesis
ELOVL6: A Potential Drug Target and Biomarker for 3-Keto Acyl-CoA Synthesis
The 3-keto acyl-CoA (3-keto-CoA) synthesis pathway is a critical metabolic pathway that plays a crucial role in the development and treatment of various diseases, including obesity, diabetes, and cardiovascular diseases. Mutations in the genes involved in this pathway have been implicated in the development of these diseases, and thus, targeting these genes has the potential to develop new treatments. One such gene is ELOVL6, which encodes the enzyme 3-keto acyl-CoA synthase ELOVL6. In this article, we will discuss ELOVL6 as a potential drug target and biomarker for the treatment of diseases associated with 3-keto acyl-CoA synthesis pathway disorders.
ELOVL6: Structure and Function
The 3-keto acyl-CoA synthesis pathway is a critical pathway for the production of essential fatty acids, which are vital for maintaining various physiological functions. The pathway involves the following steps:
1. Acetyl-CoA (acetyl-CoA) + FAT 鈫? 3-keto acyl-CoA (3-keto-CoA) + FAT
2. 3-keto acyl-CoA + CoA 鈫? 3-acetyl-CoA + CO2
3. 3-acetyl-CoA + 3-keto acyl-CoA + NADPH + FAT 鈫? CoA + NADPH + 3-keto acyl-CoA
ELOVL6 is a gene that encodes the 3-keto acyl-CoA synthase enzyme ELOVL6. The primary function of ELOVL6 is to catalyze the conversion of 3-keto acyl-CoA to 3-acetyl-CoA. This enzyme plays a crucial role in the production of essential fatty acids and is expressed in various tissues, including liver, muscle, and fat cells.
Mutations in the ELOVL6 gene have been implicated in the development of various diseases, including obesity, diabetes, and cardiovascular diseases. For example, a study published in the journal Nature Communications found that individuals with the ELOVL6 gene had a higher risk of developing obesity compared to individuals without the gene. Additionally, a study published in the journal Molecular Metabolism found that mutations in the ELOVL6 gene were associated with an increased risk of developing cardiovascular diseases.
Targeting ELOVL6 as a Drug Target
Targeting ELOVL6 as a drug target has the potential to treat various diseases associated with 3-keto acyl-CoA synthesis pathway disorders. One potential mechanism by which targeting ELOVL6 could be effective is by inhibiting the activity of this enzyme. By inhibiting the activity of ELOVL6 , it is possible to reduce the production of 3-acetyl-CoA, which is a crucial step in the 3-keto acyl-CoA synthesis pathway.
There are several potential strategies that could be used to target ELOVL6 as a drug target. One approach is to use small molecules, such as drugs, to inhibit the activity of ELOVL6. For example, a study published in the journal Biochimica et Biophysica Acta found that a compound called TAT-3012 inhibited the activity of ELOVL6 with high affinity. Additionally, a study published in the journal Molecular Metabolism found that a compound called SIRT1 inhibited the activity of ELOVL6 in cell culture.
Another approach to targeting ELOVL6 is to use antibodies to block the activity of this enzyme. For example, a study published in the journal Scientific Reports found that antibodies specific for ELOVL6 were able to inhibit the activity of ELOVL6 in cell culture. Additionally, a study published in the journal PLoS One found that specific antibodies for ELOVL6 were able to reduce the production of 3-acetyl-CoA in obese rats.
ELOVL6 as a Biomarker
In addition to its potential as a drug target, ELOVL6 has also been identified as a potential biomarker for the treatment of diseases associated with 3-keto acyl-CoA synthesis pathway disorders. The 3-keto acyl-CoA synthesis pathway is involved in the production of essential fatty acids, which are vital for various physiological functions. Therefore
Protein Name: ELOVL Fatty Acid Elongase 6
Functions: Catalyzes the first and rate-limiting reaction of the four reactions that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids (VLCFAs) per cycle. Condensing enzyme that elongates fatty acids with 12, 14 and 16 carbons with higher activity toward C16:0 acyl-CoAs. Catalyzes the synthesis of unsaturated C16 long chain fatty acids and, to a lesser extent, C18:0 and those with low desaturation degree. May participate in the production of saturated and monounsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators
More Common Targets
ELOVL7 | ELP1 | ELP2 | ELP3 | ELP4 | ELP5 | ELP6 | ELSPBP1 | EMB | EMBP1 | EMC1 | EMC1-AS1 | EMC10 | EMC2 | EMC3 | EMC3-AS1 | EMC4 | EMC6 | EMC7 | EMC8 | EMC9 | EMCN | EMD | EME1 | EME2 | EMG1 | EMID1 | EMILIN1 | EMILIN2 | EML1 | EML2 | EML2-AS1 | EML3 | EML4 | EML4-AS1 | EML5 | EML6 | EMP1 | EMP2 | EMP2P1 | EMP3 | EMSLR | EMSY | EMX1 | EMX2 | EMX2OS | EN1 | EN2 | ENAH | ENAM | ENC1 | ENDOD1 | ENDOG | Endogenous Retrovirus group K Env polyprotein (ERVK) | Endogenous retrovirus group K member 25 Pol protein-like, transcript variant X1 | EndoGlyx-1 | Endoplasmic reticulum collagen prolyl 3-hydroxylation complex | Endothelin receptor | Endothelin-Converting Enzymes (ECE) | Endothiapepsin | ENDOU | ENDOV | ENG | ENGASE | ENHO | ENKD1 | ENKUR | ENO1 | ENO1-AS1 | ENO1P1 | ENO1P4 | ENO2 | ENO3 | ENO4 | ENOPH1 | eNoSC Complex | ENOSF1 | ENOX1 | ENOX1-AS2 | ENOX2 | ENPEP | ENPP1 | ENPP2 | ENPP3 | ENPP4 | ENPP5 | ENPP6 | ENPP7 | ENPP7P10 | ENPP7P12 | ENPP7P7 | ENSA | ENSAP2 | ENTHD1 | ENTPD1 | ENTPD1-AS1 | ENTPD2 | ENTPD3 | ENTPD3-AS1 | ENTPD4