Target Name: Fucosyltransferase
NCBI ID: P48426
Review Report on Fucosyltransferase Target / Biomarker Content of Review Report on Fucosyltransferase Target / Biomarker
Fucosyltransferase
Other Name(s): FUT

FUTs: Metabolism-Controlled Diseases and Potential Drug Targets

Fucosyltransferase (FUT) is a protein that plays a crucial role in cellular metabolism and metabolism-controlled diseases. FUTs are a subtype of the Fucosyltransferase enzyme, which is involved in the transfer of fucose units from the extracellular matrix to various cellular organelles, including the endoplasmic reticulum, mitochondria, and the cytosol.

FUTs are widely expressed in various tissues and cells throughout the body, and they are involved in the metabolism of a wide range of macromolecules, including proteins, nucleic acids, and lipids. They are also involved in the regulation of cellular processes such as cell growth , apoptosis, and autophagy.

One of the unique features of FUTs is their ability to transfer fucose units to different cellular organelles. This is accomplished through a specific active site on the enzyme that allows for the transfer of fucose units from the extracellular matrix to the endoplasmic reticulum, where it can be processed and then to the cytosol, where it can be used for energy metabolism.

FUTs are also involved in the regulation of cellular processes that are critical for the survival of cells, such as cell growth, apoptosis, and autophagy. In cell growth, FUTs play a role in the regulation of cell size and in the development of cancer. FUTs are also involved in the regulation of apoptosis, which is the process by which cells die, and in the regulation of autophagy, which is the process by which cells break down and recycle their own damaged or unnecessary components.

FUTs are also involved in the regulation of various cellular signaling, including the TGF-β pathway. This pathway is involved pathways in the regulation of cell growth, differentiation, and apoptosis, and it is a key factor in the development and maintenance of tissues and organs.

FUTs have also been shown to be involved in the regulation of cellular adhesion and adhesion. This is important for various cellular processes, including the development of tissues and organs and the regulation of embryonic development.

In addition to their role in cellular metabolism and signaling pathways, FUTs are also potential drug targets. For example, FUTs have been shown to be involved in the regulation of various cellular processes that are critical for the survival of cancer cells, and therefore they may be a useful target for cancer therapies.

FUTs are also involved in the regulation of cellular stress responses, which are critical for the survival of cells in response to various stressors, such as oxidative stress, radiation, and chemicals.

FUTs are also involved in the regulation of the transport of various macromolecules across the endoplasmic reticulum. This is important for the delivery of macromolecules to the cytosol, where they can be used for energy metabolism.

In conclusion, FUTs are a subtype of the Fucosyltransferase enzyme that plays a crucial role in cellular metabolism and signaling pathways. They are involved in the transfer of fucose units from the extracellular matrix to various cellular organelles and they are also involved in the regulation of cellular processes that are critical for the survival of cells, such as cell growth, apoptosis, and autophagy. FUTs are also involved in the regulation of various cellular signaling pathways and they have been shown to be potential drug targets. Further research is needed to fully understand the role of FUTs in cellular metabolism and their potential as drug targets.

Protein Name: Fucosyltransferase (nonspecified Subtype)

The "Fucosyltransferase 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 Fucosyltransferase 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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FUNDC1 | FUNDC2 | FUNDC2P2 | FUNDC2P3 | FUOM | FURIN | FUS | FUT1 | FUT10 | FUT11 | FUT2 | FUT3 | FUT4 | FUT5 | FUT6 | FUT7 | FUT8 | FUT8-AS1 | FUT9 | FUZ | FXN | FXR1 | FXR2 | FXYD1 | FXYD2 | FXYD3 | FXYD4 | FXYD5 | FXYD6 | FXYD6-FXYD2 | FXYD7 | FYB1 | FYB2 | FYCO1 | FYN | FYTTD1 | FZD1 | FZD10 | FZD10-AS1 | FZD2 | FZD3 | FZD4 | FZD4-DT | FZD5 | FZD6 | FZD7 | FZD8 | FZD9 | FZR1 | G protein-Coupled Inwardly-Rectifying Potassium Channel (GIRK) | G Protein-Coupled Receptor Kinases (GRKs) | G0S2 | G2E3 | G2E3-AS1 | G3BP1 | G3BP2 | G6PC1 | G6PC2 | G6PC3 | G6PD | GA-binding protein | GAA | GAB1 | GAB2 | GAB3 | GAB4 | GABA(A) receptor | GABARAP | GABARAPL1 | GABARAPL2 | GABARAPL3 | GABBR1 | GABBR2 | GABPA | GABPAP | GABPB1 | GABPB1-AS1 | GABPB1-IT1 | GABPB2 | GABRA1 | GABRA2 | GABRA3 | GABRA4 | GABRA5 | GABRA6 | GABRB1 | GABRB2 | GABRB3 | GABRD | GABRE | GABRG1 | GABRG2 | GABRG3 | GABRG3-AS1 | GABRP | GABRQ | GABRR1 | GABRR2 | GABRR3 | GACAT1