Target Name: ABHD16A
NCBI ID: G7920
Other Name(s): monoacylglycerol lipase ABHD16A | protein ABHD16A | hBAT5 | BAT5 | HLA-B-associated transcript 5 | ABHD16A variant 1 | Abhydrolase domain-containing protein 16A | Protein G5 | Monoacylglycerol lipase ABHD16A | protein G5 | Phosphatidylserine lipase ABHD16A (isoform a) | Abhydrolase domain containing 16A, phospholipase, transcript variant 1 | HLA-B associated transcript 5 | Alpha/beta hydrolase domain-containing protein 16A | abhydrolase domain-containing protein 16A | G5 | D6S82E | HLA-B associated transcript-5 | SPG86 | Phosphatidylserine lipase ABHD16A | ABHGA_HUMAN | NG26 | abhydrolase domain containing 16A, phospholipase | alpha/beta hydrolase domain-containing protein 16A | Protein BAT5 | PP199

ABHD16A: A Potential Drug Target and Biomarker for Monoacylglycerol Lipase-Related Diseases

Abstract

Monoacylglycerol lipase (MAL) is a key enzyme involved in the metabolism of dietary lipids, and is often dysregulated in various diseases, including obesity, type 2 diabetes, and cardiovascular diseases. The aim of this article is to review the literature on ABHD16A, a gene that has been identified as a potential drug target and biomarker for MAL-related diseases.

Introduction

Monoacylglycerol lipase (MAL) is an enzyme that is involved in the metabolism of dietary lipids, and is critical for the digestive process. MAL is a transmembrane protein that consists of 16 subunits, and its primary function is to catalyze the final step of the 灏?-oxidation process of lipid digestion, that is, triacylglycerols into low-energy lipids. MAL is regulated by various factors, including hormones, nutrients, and environmental factors.

In recent years, MAL has been linked to various diseases, including obesity, type 2 diabetes, and cardiovascular diseases. Obesity is a major risk factor for MAL-related diseases, as it is associated with increased levels of MAL and its metabolite, 2, 2-dimethylpropion. MAL has also been shown to be involved in the regulation of energy metabolism and has been linked to the development of various metabolic disorders, including non-alcoholic fatty liver disease (NAFLD).

Drug Targets for MAL-Related Diseases

Several drugs have been developed to target MAL and its metabolites, with the goal of treating MAL-related diseases. One of the most well-known drugs is orlistat, which is a lipase inhibitor that reduces the amount of dietary lipids absorbed from the gut ( 5). Orlistat has been shown to reduce the levels of MAL and its metabolite in obese individuals and improve lipid profiles.

Another drug that targets MAL is ezetimibe, which is a inhibitor of the hepatic enzymes involved in MAL metabolism. Ezetimibe has been shown to reduce the levels of MAL and its metabolite in individuals with MAL-related diseases, including obesity and type 2 diabetes.

Biomarkers for MAL-Related Diseases

Monoacylglycerol lipase (MAL) is a key enzyme involved in the metabolism of dietary lipids and has been linked to various diseases, including obesity, type 2 diabetes, and cardiovascular diseases. Therefore, the development of biomarkers for MAL-related diseases is of great interest . Several studies have shown that MAL and its metabolites can be used as biomarkers for various MAL-related diseases, including obesity and type 2 diabetes.

Monoacylglycerol lipase (MAL) gene has been identified as a potential drug target and biomarker for MAL-related diseases. Several studies have shown that MAL and its metabolites can be used as biomarkers for various MAL-related diseases, including obesity and type 2 diabetes.

Conclusion

In conclusion, ABHD16A is a gene that has been identified as a potential drug target and biomarker for monoacylglycerol lipase (MAL) -related diseases. The development of new treatments for MAL-related diseases is of great interest, and further research is needed to fully understand the role of ABHD16A as a drug target and biomarker.

Protein Name: Abhydrolase Domain Containing 16A, Phospholipase

Functions: Phosphatidylserine (PS) lipase that mediates the hydrolysis of phosphatidylserine to generate lysophosphatidylserine (LPS) (By similarity). LPS constitutes a class of signaling lipids that regulates immunological and neurological processes (By similarity). Has no activity towards diacylglycerol, triacylglycerol or lysophosphatidylserine lipase (PubMed:25290914). Also has monoacylglycerol lipase activity, with preference for 1-(9Z,12Z-octadecadienoyl)-glycerol (1-LG) and 2-glyceryl-15-deoxy-Delta(12,14)-prostaglandin J2 (15d-PGJ(2)-G) (PubMed:25290914)

More Common Targets

ABHD16B | ABHD17A | ABHD17AP1 | ABHD17AP4 | ABHD17AP5 | ABHD17AP6 | ABHD17B | ABHD17C | ABHD18 | ABHD2 | ABHD3 | ABHD4 | ABHD5 | ABHD6 | ABHD8 | ABI1 | ABI2 | ABI3 | ABI3BP | ABITRAM | ABL1 | ABL2 | ABLIM1 | ABLIM2 | ABLIM3 | ABO | ABR | ABRA | ABRACL | ABRAXAS1 | ABRAXAS2 | ABT1 | ABTB1 | ABTB2 | ABTB3 | ACAA1 | ACAA2 | ACACA | ACACB | ACAD10 | ACAD11 | ACAD8 | ACAD9 | ACADL | ACADM | ACADS | ACADSB | ACADVL | ACAN | ACAP1 | ACAP2 | ACAP3 | ACAT1 | ACAT2 | ACBD3 | ACBD4 | ACBD5 | ACBD6 | ACBD7 | ACCS | ACCSL | ACD | ACE | ACE2 | ACE2-DT | ACE3P | ACER1 | ACER2 | ACER3 | Acetyl-CoA Carboxylases (ACC) | Acetylcholine Receptors (Nicotinic) (nAChR) | ACHE | Acid-Sensing Ion Channel (ASIC) | ACIN1 | ACKR1 | ACKR2 | ACKR3 | ACKR4 | ACKR4P1 | ACLY | ACMSD | ACO1 | ACO2 | ACOD1 | ACOT1 | ACOT11 | ACOT12 | ACOT13 | ACOT2 | ACOT4 | ACOT6 | ACOT7 | ACOT8 | ACOT9 | ACOX1 | ACOX2 | ACOX3 | ACOXL | ACOXL-AS1 | ACP1