Target Name: HFE
NCBI ID: G3077
Review Report on HFE Target / Biomarker Content of Review Report on HFE Target / Biomarker
HFE
Other Name(s): Homeostatic iron regulator, transcript variant 3 | homeostatic iron regulator | TFQTL2 | high Fe | MVCD7 | hereditary hemochromatosis protein HLA-H | HFE variant 3 | High Fe | Homeostatic iron regulator | HLAH | MHC class I-like protein HFE | Hereditary hemochromatosis protein | HFE1 | Hereditary hemochromatosis protein (isoform 1) | Hereditary hemochromatosis protein (isoform 3) | HLA-H | Homeostatic iron regulator, transcript variant 1 | HFE variant 1 | HH | Hereditary hemochromatosis protein HLA-H | HFE_HUMAN

HFE: A Drug Target / Disease Biomarker

Heterofeasibility (HFE) is a term used in the field of drug discovery to describe the ability of a drug to interact with a specific target protein, also known as a biomarker, in the cell. In other words, it refers to the degree to which a drug is able to bind to and stimulate the target protein, which is a key step in the process of drug development.

HFE has been identified as a potential drug target in a number of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. In these conditions, the failure of drugs to interact with their target proteins can be a major reason for their failure in clinical trials.

One of the challenges in identifying and understanding HFE is the complexity of the cell signaling pathways that are involved in protein-protein interactions. Many drugs that are currently in use, such as statins, have been shown to interact with a wide range of proteins, but it is not clear how these interactions are truly relevant to the treatment of disease.

To address this challenge, researchers have developed a number of techniques to study HFE. These techniques include biochemical assays, such as protein-fragment complementation assays, to measure the strength of protein-protein interactions directly. Other techniques include mass spectrometry, which allows researchers to identify the specific proteins that are involved in a given interaction, as well as structural bioinformatics, which can be used to predict the binding of a drug to a protein based on its known structure.

One of the most promising areas of research is the use of machine learning algorithms to analyze large datasets and identify patterns in the data that may be relevant to the development of new drugs. By using techniques such as clustering and association rule mining, researchers have been able to identify a number of potential targets for a variety of diseases.

In addition to its potential as a drug target, HFE is also of interest as a biomarker. The failure of drugs to interact with their target proteins can be an indication of the failure of the drug to effectively treat a given disease. By using HFE as a biomarker, researchers can monitor the effectiveness of a drug and identify potential areas for improvement.

Overall, HFE is a complex and rapidly evolving field of research that has the potential to revolutionize the field of drug discovery. By continued research and development, researchers hope to be able to identify and develop new treatments for a wide range of diseases.

Protein Name: Homeostatic Iron Regulator

Functions: Binds to transferrin receptor (TFR) and reduces its affinity for iron-loaded transferrin

The "HFE 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 HFE 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

HFM1 | HGC6.3 | HGD | HGF | HGFAC | HGH1 | HGS | HGSNAT | HHAT | HHATL | HHEX | HHIP | HHIP-AS1 | HHIPL1 | HHIPL2 | HHLA1 | HHLA2 | HHLA3 | HIBADH | HIBCH | HIC1 | HIC2 | HID1 | HID1-AS1 | HIF1A | HIF1A-AS1 | HIF1A-AS2 | HIF1A-AS3 | HIF1AN | HIF3A | HIGD1A | HIGD1AP1 | HIGD1AP10 | HIGD1B | HIGD1C | HIGD2A | HIGD2B | High affinity cAMP-specif | High Affinity Immunoglobulin Epsilon Fc Receptor | HIKESHI | HILPDA | HILPDA-AS1 | HINFP | HINT1 | HINT1P1 | HINT2 | HINT3 | HIP1 | HIP1R | HIPK1 | HIPK1-AS1 | HIPK2 | HIPK3 | HIPK4 | HIRA | HIRIP3 | HISLA | Histamine Receptor (HR) | Histocompatibility antigen-related | Histone | Histone acetyltransferase (HAT) | Histone deacetylase | Histone H2A | Histone H2B | Histone H3 | Histone Lysine Demethylase | Histone methyltransferase | HIVEP1 | HIVEP2 | HIVEP3 | HJURP | HJV | HK1 | HK2 | HK2P1 | HK3 | HKDC1 | HLA Class II Histocompatibility Antigen DM (HLA-DM) | HLA class II histocompatibility Antigen DO (HLA-DO) | HLA class II histocompatibility antigen DP (HLA-DP) | HLA Class II Histocompatibility Antigen DQ8 | HLA class II histocompatibility antigen DR (HLA-DR) | HLA Class II Histocompatibility Antigen, DQ (HLA-DQ) | HLA class II histocompatibility antigen, DRB1-7 beta chain, transcript variant X1 | HLA complex group 16 (non-protein coding), transcript variant X2 | HLA complex group 8 | HLA-A | HLA-B | HLA-C | HLA-DMA | HLA-DMB | HLA-DOA | HLA-DOB | HLA-DPA1 | HLA-DPA2 | HLA-DPA3 | HLA-DPB1 | HLA-DPB2 | HLA-DQA1 | HLA-DQA2