Target Name: MGAM
NCBI ID: G8972
Review Report on MGAM Target / Biomarker Content of Review Report on MGAM Target / Biomarker
MGAM
Other Name(s): alpha-Glucosidase | Maltase-glucoamylase, intestinal | Alpha-glucosidase | Maltase-glucoamylase (isoform 2) | Glucoamylase | Maltase | MGA_HUMAN | alpha-1,4-glucosidase | maltase-glucoamylase, intestinal | MGAM variant 2 | Maltase-glucoamylase | maltase-glucoamylase | maltase-glucoamylase (alpha-glucosidase) | alpha-D-Glucoside glucohydrolase | Brush border hydrolase | brush border hydrolase | MG | Glucan 1,4-alpha-glucosidase | MGA

MGAM: A Promising Drug Target for Diabetes and Cancer

MGAM, or alpha-glucosidase, is a enzyme that is responsible for breaking down a type of sugar called alpha-glucoside in the body. This sugar is found in a variety of foods, including fruits, vegetables, and whole grains. MGAM is a key player in the immune system and has been shown to play a role in a number of diseases, including diabetes, cancer, and neurodegenerative diseases. As a result, MGAM has become a focus of interest for researchers and pharmaceutical companies looking for new treatments for a variety of diseases.

One of the unique features of MGAM is its ability to be targeted as a drug or biomarker. This is because MGAM is located in the cell's endoplasmic reticulum, which is the part of the cell that transports and stores proteins. This makes it difficult to reach and target the enzyme directly. However, researchers have been able to develop compounds that can interact with MGAM and inhibit its activity, effectively turning it into a drug or biomarker.

One of the most promising applications of MGAM as a drug target is its potential to treat diabetes. Diabetes is a disease in which the body is unable to produce or effectively use insulin, leading to high levels of blood sugar. MGAM is thought to play a role in the immune response, and some studies have suggested that it may be involved in the regulation of insulin sensitivity. As a result, researchers are interested in developing compounds that can inhibit MGAM activity and lower blood sugar levels in people with diabetes.

Another potential application of MGAM as a drug target is its potential to treat cancer. Many studies have suggested that MGAM is involved in the regulation of cell growth and division, which can be a key factor in the development and progression of cancer. As a result, researchers are interested in developing compounds that can inhibit MGAM activity and disrupt these processes. This could lead to new treatments for a variety of cancers.

In addition to its potential as a drug target, MGAM has also been shown to be a potential biomarker for a number of diseases. For example, some studies have suggested that MGAM levels may be elevated in the brains of people with neurodegenerative diseases, such as Alzheimer's and Parkinson's. This could be an indication that MGAM is involved in the development and progression of these diseases. As a result, researchers are interested in developing compounds that can inhibit MGAM activity and lower these brain levels.

Overall, MGAM is a fascinating enzyme that has the potential to be a drug target or biomarker for a variety of diseases. While more research is needed to fully understand its role and potential applications, researchers are excited about the potential of MGAM and are actively working to develop new treatments based on its properties.

Protein Name: Maltase-glucoamylase

Functions: Alpha-(1,4) exo-glucosidase involved in breakdown of dietary starch oligosaccharides in small intestine. Cleaves the non-reducing alpha-(1,4)-linked glucose residue in linear dextrins with retention of anomeric center stereochemistry (PubMed:12547908, PubMed:18356321, PubMed:27480812, PubMed:18036614, PubMed:22058037). Mainly hydrolyzes short length oligomaltoses having two to seven glucose residues (PubMed:12547908, PubMed:18356321, PubMed:27480812, PubMed:18036614, PubMed:22058037). Can cleave alpha-(1,2), alpha-(1,3) and alpha-(1,6) glycosidic linkages with lower efficiency, whereas beta glycosidic linkages are usually not hydrolyzed (PubMed:27480812)

The "MGAM 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 MGAM 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

More Common Targets

MGAM2 | MGARP | MGAT1 | MGAT2 | MGAT3 | MGAT3-AS1 | MGAT4A | MGAT4B | MGAT4C | MGAT4D | MGAT4EP | MGAT4FP | MGAT5 | MGAT5B | MGC12916 | MGC15885 | MGC16025 | MGC16275 | MGC27382 | MGC2889 | MGC32805 | MGC34796 | MGC4859 | MGC70870 | MGLL | MGME1 | MGMT | MGP | MGRN1 | MGST1 | MGST2 | MGST3 | MHRT | MIA | MIA-RAB4B | MIA2 | MIA3 | MIAT | MIATNB | MIB1 | MIB2 | MICA | MICA-AS1 | MICAL1 | MICAL2 | MICAL3 | MICALCL | MICALL1 | MICALL2 | MICB | MICB-DT | MICC | MICD | MICOS10 | MICOS10-NBL1 | MICOS10P1 | MICOS13 | Microfilament-associated triple complex | MicroRNA 1273d | MicroRNA 1273f | MicroRNA 1273g | MicroRNA 3607 | MicroRNA 3653 | MicroRNA 3656 | MicroRNA 4417 | MicroRNA 4419a | MicroRNA 4459 | MicroRNA 4461 | MicroRNA 4532 | MicroRNA 4792 | MicroRNA 5095 | MicroRNA 5096 | MicroRNA 6087 | MicroRNA 6723 | MicroRNA 7641-1 | MicroRNA 7641-2 | Microtubule-Associated Protein | MICU1 | MICU2 | MICU3 | MID1 | MID1IP1 | MID1IP1-AS1 | MID2 | MIDEAS | MIDEAS-AS1 | MIDN | MIEF1 | MIEF2 | MIEN1 | MIER1 | MIER2 | MIER3 | MIF | MIF-AS1 | MIF4GD | MIGA1 | MIGA2 | MIIP | MILIP