Target Name: HAVCR1
NCBI ID: G26762
Review Report on HAVCR1 Target / Biomarker Content of Review Report on HAVCR1 Target / Biomarker
HAVCR1
Other Name(s): Hepatitis A virus cellular receptor 1 (TIM-1) | Hepatitis A virus cellular receptor 1 | CD365 | TIMD-1 | Hepatitis A virus cellular receptor 1, transcript variant 4 | KIM-1 | HAVCR1 variant 4 | hepatitis A virus cellular receptor 1 | HAVcr-1 | TIM-1 | T-cell membrane protein 1 | KIM1 | HAVCR | T cell immunoglobin domain and mucin domain protein 1 | T-cell immunoglobulin and mucin domain-containing protein 1 | T-cell immunoglobulin mucin receptor 1 | TIMD1 | TIM-1 (T cell immunoglobin domain and mucin domain protein 1) | KIM-1 extracellular domain | Hepatitis A virus cellular receptor 1 (isoform b) | Kidney injury molecule 1 | T-cell immunoglobulin mucin family member 1 | Hepatitis A virus cellular receptor 1 (isoform a) | TIM1 | soluble form of Hepatitis A virus cellular receptor 1 | sHAVR1_(HUMAN) | kidney injury molecule 1 | HAVCR1 variant 1 | Hepatitis A virus cellular receptor 1, transcript variant 1 | HAVR1_HUMAN | TIM | HAVCR-1

HAVCR1: A Potential Drug Target for Hepatitis A

Hepatitis A virus (HAV) is a highly infectious and sometimes serious disease that affects the liver and causes symptoms such as nausea, vomiting, loss of appetite, dark urine, and a low-grade fever. It is estimated that over 1.4 million people worldwide are affected by HAV, and the incidence is increasing.

Hepatitis A virus is a member of the A virus family, which includes other viruses such as hepatitis B and C. The virus is transmitted through contaminated food and water, and people can also contract it through sexual contact. It is often associated with heavy drinking , unprotected sex, and sharing needles or other injection equipment.

HAV has a large genome size, with over 120,000 nucleotides, and its genetic material is highly conserved across different strains. It consists of a core RNA molecule that is surrounded by a protein envelope. The virus uses a type of protein called NS-1 to infect host cells and replicate.

The viral genome contains several open reading frames (ORFs) that encode different proteins that are essential for the virus's replication and infection. One of these ORFs is called HAVCR1, which is a protein that is highly conserved across different strains of HAV.

HAVCR1 is a 14-kDa protein that is expressed in the cytoplasm of HAV-infected cells. It is involved in the virus's replication and has been shown to play a role in the virus's pathogenesis. HAVCR1 is also a potential drug target or biomarker, and its study could have implications for the treatment of hepatitis A.

HAVCR1 functions as a receptor for the virus's envelope protein, which is known as NS-1. The NS-1 protein has four transmembrane domains, including an N-terminal alpha-helix, a middle transmembrane domain, and two C-terminal alpha- helices. It is involved in the formation of the viral envelope and is a key factor in the virus's replication.

HAVCR1 is a critical regulator of the NS-1 protein, and it has been shown to interact with the virus's NS-1 protein in a number of ways. For example, HAVCR1 has been shown to physically interact with NS-1 and to modulate its activity. This interaction between HAVCR1 and NS-1 is important for the virus's replication, as changes in the activity of NS-1 have been shown to affect the levels of viral genome expression in HAV-infected cells.

Another way that HAVCR1 interacts with NS-1 is through a process called tyrosination. Tyrosination is a post-translational modification that involves the addition of a tyrosine molecule to a protein. HAVcr1 has been shown to tyrosinate NS-1, which is known to modulate its activity and to play a role in the production of infectious copies of the virus.

HAVcr1 is also involved in the regulation of the host cell's immune response to the virus. For example, it has been shown to suppress the production of interferon, a protein that is involved in the immune response. This suppression of interferon production by HAVcr1 allows the virus to evade the host's immune system and to continue to replicate.

In conclusion, HAVCR1 is a protein that is highly conserved across different strains of HAV and is involved in the virus's replication. Its interaction with NS-1 and its regulation of the host cell's immune response make it a potential drug target or biomarker for the treatment of hepatitis A. Further research is needed to fully understand the role of HAVcr1 in the virus's replication and to explore its potential as a therapeutic approach.

Protein Name: Hepatitis A Virus Cellular Receptor 1

Functions: Phosphatidylserine receptor that plays an important functional role in regulatory B-cells homeostasis including generation, expansion and suppressor functions (By similarity). As P-selectin/SELPLG ligand, plays a specialized role in activated but not naive T-cell trafficking during inflammatory responses (PubMed:24703780). Controls thereby T-cell accumulation in the inflamed central nervous system (CNS) and the induction of autoimmune disease (PubMed:24703780). Regulates also expression of various anti-inflammatory cytokines and co-inhibitory ligands including IL10 (By similarity). Acts as regulator of T-cell proliferation (By similarity). May play a role in kidney injury and repair (PubMed:17471468)

The "HAVCR1 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 HAVCR1 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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