ACOT11B
Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
---|---|---|---|---|---|---|
Zebrafish | ACOT11B-3556Z | Recombinant Zebrafish ACOT11B | Mammalian Cell | His |
- Involved Pathway
- Protein Function
- Interacting Protein
ACOT11B involved in several pathways and played different roles in them. We selected most pathways ACOT11B participated on our site, such as Fatty Acyl-CoA Biosynthesis, Fatty acid, triacylglycerol, and ketone body metabolism, Metabolism, which may be useful for your reference. Also, other proteins which involved in the same pathway with ACOT11B were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
Pathway Name | Pathway Related Protein |
---|---|
Fatty Acyl-CoA Biosynthesis | SLC25A1;ACOT10;ELOVL1A;ACSF2;SLC25A1A;ACOT11A;ACOT6;ACOT2;ACOT12 |
Fatty acid, triacylglycerol, and ketone body metabolism | MED6;YAP1;ACOT2;ACOT8;ACOT7;MED26;ANKRD1;MED16;MED25 |
Metabolism | FTCD;DSEL;FABP12;AMD2;FAAH2B;SIN3B;ELOVL1A;ACER1;ARV1 |
Metabolism of lipids and lipoproteins | YAP1;MED21;CYP2N13;APOA4A;SACM1L;SLC27A5;COQ7;CPNE1;CPNE7 |
Triglyceride Biosynthesis | ACOT7;ACOT10;ACOT6;ACOT12;SLC25A1;ELOVL1A;THEM5;ACOT11A;ACOT9.2 |
ACOT11B has several biochemical functions, for example, lipid binding. Some of the functions are cooperated with other proteins, some of the functions could acted by ACOT11B itself. We selected most functions ACOT11B had, and list some proteins which have the same functions with ACOT11B. You can find most of the proteins on our site.
Function | Related Protein |
---|---|
lipid binding | APOL1;COQ9;APOA4A;C3;APODA.2;PPP5C;CYP21A1;DOK7;CPTP |
ACOT11B has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with ACOT11B here. Most of them are supplied by our site. Hope this information will be useful for your research of ACOT11B.
- Q&As
- Reviews
Q&As (15)
Ask a questionLipid metabolism and energy balance are complex processes that involve multiple proteins, enzymes, receptors, and signaling pathways. Some other proteins that have been studied in relation to metabolic disorders include AMP-activated protein kinase (AMPK), peroxisome proliferator-activated receptor gamma (PPARγ), and adiponectin. Future research may identify additional targets for the development of new therapies.
ACOT11B can be studied in humans using a variety of methods, including genetic studies, transcriptomic analyses, proteomic analyses, and metabolic profiling. In animal models, ACOT11B activity can also be modulated using genetic manipulations or pharmacological interventions. However, any research involving human subjects would need to be approved by an ethics committee and follow appropriate guidelines for protecting privacy, confidentiality, and informed consent.
It is possible that ACOT11B-targeted therapies could be used in combination with other treatments for metabolic disorders, such as lifestyle modifications, pharmacological interventions, or surgical procedures. However, more research is needed to determine which combinations of therapies would be most effective and safe.
ACOT11B protein has potential applications in the development of therapies for metabolic disorders such as obesity, type 2 diabetes, and cardiovascular disease. It has been proposed as a target for the development of new drugs that could modulate lipid metabolism and improve energy balance.
The potential risks and side effects of modulating ACOT11B activity are not yet fully understood, as this area of research is still in its early stages. However, any new drug or therapy that targets ACOT11B would need to undergo rigorous safety and efficacy testing before it could be approved for clinical use.
The potential risks and concerns associated with ACOT11B-targeted therapies are not yet fully understood and would depend on the specific targeting strategy used. For example, small molecule inhibitors can have off-target effects and may interact with other drugs, while biologics can have immunogenicity and other safety concerns. Additionally, long-term effects of targeting ACOT11B are still unclear and require further research.
Some studies have explored the use of natural compounds such as polyunsaturated fatty acids and resveratrol to modulate ACOT11B activity and improve metabolic function. Other studies have investigated the development of synthetic compounds that could specifically target ACOT11B or related proteins. However, more research is needed before ACOT11B-targeted therapies can be developed and tested in humans.
Targeting ACOT11B could have potential applications in the treatment of metabolic disorders, such as obesity, type 2 diabetes, and fatty liver disease. Additionally, ACOT11B may play a role in the development of certain types of cancer, so targeting this protein could have applications in cancer therapy as well.
ACOT11A and ACOT11B are both members of the acyl-CoA thioesterase family and play a role in lipid metabolism. ACOT11A is primarily expressed in the liver and has been associated with systemic metabolic function, while ACOT11B is expressed in multiple tissues and has been shown to play a role in regulating lipid metabolism in adipose tissue. The function of ACOT11B in metabolic disorders is less well understood than ACOT11A, but both proteins may have potential applications as therapeutic targets.
The expression and activity of ACOT11B have been shown to be altered in animal models and human studies of obesity, type 2 diabetes, and other metabolic disorders. However, more research is needed to determine whether ACOT11B could be used as a reliable biomarker for these conditions in clinical settings.
There are currently no known clinical trials of ACOT11B-targeted therapies. However, as this area of research continues to develop, it is possible that clinical trials may be initiated in the future.
One challenge for developing ACOT11B-targeted therapies is that the function and regulation of this protein are not fully understood. Additionally, any new therapy would need to undergo rigorous testing for safety and efficacy before it could be approved for clinical use. However, the potential benefits of developing new treatments for metabolic disorders are substantial, given the growing prevalence and impact of these conditions on global health.
ACOT11B could potentially be targeted with small molecule inhibitors or activators, as well as with biologics such as monoclonal antibodies or RNA-based therapeutics. However, more research is needed to identify the most effective and specific targeting strategies for this protein.
It is possible that ACOT11B-targeted therapies could be used as preventive measures for metabolic disorders, especially in at-risk populations. However, more research is needed to determine the optimal timing and dosing of these therapies for maximum benefit.
One challenge to the use of ACOT11B as a therapeutic target is that its functions and mechanisms are not fully understood. Additionally, targeting a single protein such as ACOT11B is unlikely to provide a complete solution to complex metabolic disorders. More research is needed to identify the most effective and safe ways to modulate ACOT11B activity.
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