Target Name: CR1
NCBI ID: G1378
Review Report on CR1 Target / Biomarker Content of Review Report on CR1 Target / Biomarker
CR1
Other Name(s): complement C3b/C4b receptor 1 (Knops blood group) | complement component (3b/4b) receptor 1 (Knops blood group) | CD35 antigen | Knops blood group antigen | complement receptor 1 | CR1 variant F | C3BR | Complement receptor type 1 | C4BR | C3b/C4b receptor | C3-binding protein | Complement C3b/C4b receptor 1 (Knops blood group), transcript variant F | Complement receptor type 1 (isoform S) | Complement component receptor 1 | Complement C3b/C4b receptor 1 (Knops blood group), transcript variant S | CR1_HUMAN | CD35 | CR1 variant S | Complement receptor type 1 precursor | KN | CR1 protein domain SCR25 | Complement receptor type 1 (isoform F)

CR1: A Potential Drug Target and Biomarker for Platelet Function and Disease

Platelets play a critical role in the immune system and blood clotting mechanisms. Their functions include responding to injured blood vessels, releasing factors that promote blood clotting, and participating in the formation of new blood cells. platelets, also known as platelet cells, are a type of blood cell that plays a vital role in blood clotting and healing. They are responsible for forming the blood clot that helps to stop bleeding when a cut or injury is inflicted on the body. However, when a platelet becomes dysfunctional or abnormal, it can lead to bleeding disorders and other serious health conditions.

The complement component C3b/C4b receptor 1 (CR1) is a protein that is expressed on the surface of platelets. It is one of the six major complement proteins, along with C1, C4, C3, C8, C9, and C13. CR1 is involved in the regulation of platelet function and plays a key role in the immune response. It is also a potential drug target and biomarker for several diseases.

CR1 and its function

CR1 is a transmembrane protein that is expressed on the surface of platelets. It consists of two extracellular domains, a cytoplasmic tail, and an transmembrane domain. The cytoplasmic tail of CR1 contains a region that is involved in the interaction with other plasma proteins, including C3b and C4b. The transmembrane domain contains a unique type of receptor, known as the CR1-C3b or CR1-C4b receptor, which is responsible for the interaction with platelet-derived factors (PDFs).

CR1 is involved in the regulation of platelet function by interacting with PDFs. PDFs are a family of transmembrane proteins that play a critical role in the regulation of platelet function. They include PDF-1, PDF-2, PDF-3, PDF-4, PDF-5, and PDF-6. PDFs can interact with CR1 and other plasma proteins, including C3b and C4b, to regulate the activity of platelets.

CR1 is also involved in the regulation of the immune response. It is a critical receptor for the antigen presentation by dendritic cells, which is the primary site of immune activation. CR1 interacts with the major histocompatibility complex (MHC) class I molecules, which are responsible for presenting antigens to CD8+ T cells. This interaction between CR1 and MHC class I molecules is critical for the regulation of immune responses.

Drug targeting and biomarker

The CR1 protein is a potential drug target for several diseases. One of the main goals of drug targeting is to inhibit the function of a protein and prevent it from causing disease. CR1 is a good candidate for drug targeting because it is involved in the regulation of platelet function and immune responses. This makes it a potential target for diseases that are caused by the dysfunction of platelets or the immune system.

In addition to its potential drug targeting implications, CR1 is also a potential biomarker for several diseases. Biomarkers are proteins that are measured in the body and can be used as indicators of the presence of a particular disease or condition. CR1 is a protein that is expressed in platelets and can be used as a biomarker for several diseases, including cancer, thrombosis, and sepsis.

Conclusion

In conclusion, CR1 is a protein that is expressed on the surface of platelets and is involved in the regulation of platelet function and the immune response. It is a potential drug target and biomarker for several diseases. Further research is needed to fully understand the role of CR1 in disease and to develop effective treatments.

Protein Name: Complement C3b/C4b Receptor 1 (Knops Blood Group)

Functions: Membrane immune adherence receptor that plays a critical role in the capture and clearance of complement-opsonized pathogens by erythrocytes and monocytes/macrophages (PubMed:2963069). Mediates the binding by these cells of particles and immune complexes that have activated complement to eliminate them from the circulation (PubMed:2963069). Acts also in the inhibition of spontaneous complement activation by impairing the formation and function of the alternative and classical pathway C3/C5 convertases, and by serving as a cofactor for the cleavage by factor I of C3b to iC3b, C3c and C3d,g, and of C4b to C4c and C4d (PubMed:2972794, PubMed:8175757). Also plays a role in immune regulation by contributing, upon ligand binding, to the generation of regulatory T cells from activated helper T cells (PubMed:25742728)

The "CR1 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 CR1 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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