Target Name: HIVEP2
NCBI ID: G3097
Review Report on HIVEP2 Target / Biomarker Content of Review Report on HIVEP2 Target / Biomarker
HIVEP2
Other Name(s): OTTHUMP00000017322 | SHN2 | ZAS2 | ZEP2_HUMAN | MRD43 | MBP-2 | MHC-binding protein 2 | Transcription factor HIVEP2 | c-myc intron binding protein 1 | MHC binding protein-2 | Human immunodeficiency virus type I enhancer-binding protein 2 | c-myc intron-binding protein 1 | MIBP1 | ZNF40B | human immunodeficiency virus type I enhancer binding protein 2 | HIV-EP2 | HIVEP zinc finger 2 | Schnurri-2 | OTTHUMP00000017321

Hivep2: A Potential Drug Target and Biomarker

Hivesp2, also known as human hepcidin-like peptide 2, is a 24 amino acid protein that is expressed in various tissues throughout the body. It is a potential drug target and biomarker for various diseases, including diabetes, cardiovascular disease, and neurodegenerative disorders.

Hivesp2 functions as a negative regulator of the insulin/IGF-1 signaling pathway. It inhibits the activity of the transcription factor, NF-kappa-B, which is responsible for transcriptional activity of genes involved in inflammation and stress responses. This results in decreased inflammation and improved insulin sensitivity.

Hivesp2 has been shown to have a positive impact on various biological processes, including glucose metabolism, insulin sensitivity, and inflammation. Studies have also shown that Hivesp2 has a potential role in treating various diseases, including diabetes, cardiovascular disease, and neurodegenerative disorders.

One of the potential benefits of Hivesp2 as a drug target is its ability to improve insulin sensitivity in both humans and obese rats. Insulin sensitivity is a key factor in the development and progression of type 2 diabetes. By improving insulin sensitivity, Hivesp2 has the potential to be a useful tool in the treatment of this disease.

Another potential benefit of Hivesp2 is its ability to protect against neurodegenerative disorders. Neurodegenerative disorders, such as Alzheimer's disease and Parkinson's disease, are characterized by the progressive loss of brain cells and the development of neurofibrillary tangles. Hivesp2 has been shown to have a positive impact on the development and progression of these disorders.

In addition to its potential benefits for insulin sensitivity and neurodegenerative disorders, Hivesp2 has also been shown to have a positive impact on inflammation. Chronic inflammation is a key factor in the development and progression of various diseases, including cardiovascular disease and neurodegenerative disorders. By reducing inflammation, Hivesp2 has the potential to be a useful tool in the treatment of these diseases.

Hivesp2 has also been shown to have a positive impact on glucose metabolism. Glucose metabolism is a key factor in the development and progression of type 2 diabetes. By improving glucose metabolism, Hivesp2 has the potential to be a useful tool in the treatment of this disease.

In conclusion, Hivesp2 is a potential drug target and biomarker with a positive impact on various biological processes. Its ability to improve insulin sensitivity, protect against neurodegenerative disorders, reduce inflammation, and improve glucose metabolism make it an attractive candidate for further research. Further studies are needed to fully understand the potential of Hivesp2 as a drug target and biomarker.

Protein Name: HIVEP Zinc Finger 2

Functions: This protein specifically binds to the DNA sequence 5'-GGGACTTTCC-3' which is found in the enhancer elements of numerous viral promoters such as those of SV40, CMV, or HIV1. In addition, related sequences are found in the enhancer elements of a number of cellular promoters, including those of the class I MHC, interleukin-2 receptor, somatostatin receptor II, and interferon-beta genes. It may act in T-cell activation

The "HIVEP2 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 HIVEP2 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

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 | HLA-DQB1 | HLA-DQB1-AS1 | HLA-DQB2 | HLA-DRA | HLA-DRB1 | HLA-DRB2 | HLA-DRB3 | HLA-DRB4 | HLA-DRB5 | HLA-DRB6 | HLA-DRB7 | HLA-DRB8 | HLA-DRB9 | HLA-E | HLA-F | HLA-F-AS1 | HLA-G | HLA-H | HLA-J | HLA-K | HLA-L | HLA-N | HLA-P | HLA-U | HLA-V | HLA-W | HLCS | HLF | HLTF | HLX | HM13 | HMBOX1 | HMBS | HMCES | HMCN1 | HMCN2 | HMG20A | HMG20B | HMGA1 | HMGA1P2 | HMGA1P4 | HMGA1P7 | HMGA1P8 | HMGA2 | HMGA2-AS1 | HMGB1 | HMGB1P1 | HMGB1P10 | HMGB1P19 | HMGB1P37 | HMGB1P38 | HMGB1P46 | HMGB1P5 | HMGB1P6 | HMGB2 | HMGB2P1 | HMGB3 | HMGB3P1 | HMGB3P14 | HMGB3P15 | HMGB3P19 | HMGB3P2 | HMGB3P22 | HMGB3P24 | HMGB3P27 | HMGB3P30 | HMGB3P6 | HMGB4 | HMGCL