HS3ST3A1: A Potential Drug Target for Hematological Diseases (G9955)
HS3ST3A1: A Potential Drug Target for Hematological Diseases
HS3ST3A1, also known as H3-OST-3A, is a protein that is expressed in various tissues throughout the body. It is a key regulator of the hematopoietic stem cell (HSC) lineage and has been identified as a potential drug target in the field of hematological diseases.
The HSC is a specialized type of stem cell that gives rise to all blood cells, including red blood cells, white blood cells, and platelets. HSCs have the ability to self-renew and differentiate into different cell types, making them a promising source of cancer therapies. However, the development and maintenance of HSCs is a complex process that is not fully understood.
HS3ST3A1 is a non-coding RNA molecule that has been shown to regulate the self-renewal and differentiation of HSCs. It is a key regulator of the p53 gene, which is a well-known tumor suppressor gene that plays a critical role in preventing the development and progression of cancer.
studies have shown that HS3ST3A1 can inhibit the self-renewal ability of HSCs by targeting the p53 gene. This can lead to a reduction in the number of HSCs that have the ability to divide and multiply, which can potentially lead to a reduction in the risk of developing cancer.
Additionally, HS3ST3A1 has also been shown to play a role in the regulation of cell survival and the transition of cells to apoptosis. This is important because the regulation of cell survival and apoptosis is a critical aspect of the immune system and has been implicated in a number of diseases, including cancer.
In conclusion, HS3ST3A1 is a protein that has the potential to be a drug target in the field of hematological diseases. Further research is needed to fully understand its role in the regulation of HSCs and its potential as a therapeutic agent.
Protein Name: Heparan Sulfate-glucosamine 3-sulfotransferase 3A1
Functions: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) to catalyze the transfer of a sulfo group to an N-unsubstituted glucosamine linked to a 2-O-sulfo iduronic acid unit on heparan sulfate (PubMed:10520990, PubMed:9988768, PubMed:10608887, PubMed:15304505). Catalyzes the O-sulfation of glucosamine in IdoUA2S-GlcNS and also in IdoUA2S-GlcNH2 (PubMed:10520990, PubMed:9988768, PubMed:15304505). The substrate-specific O-sulfation generates an enzyme-modified heparan sulfate which acts as a binding receptor to Herpes simplex virus-1 (HSV-1) and permits its entry (PubMed:10520990). Unlike HS3ST1/3-OST-1, does not convert non-anticoagulant heparan sulfate to anticoagulant heparan sulfate (PubMed:10520990)
More Common Targets
HS3ST3B1 | HS3ST4 | HS3ST5 | HS3ST6 | HS6ST1 | HS6ST2 | HS6ST3 | HSBP1 | HSBP1L1 | HSCB | HSD11B1 | HSD11B1-AS1 | HSD11B1L | HSD11B2 | HSD17B1 | HSD17B1-AS1 | HSD17B10 | HSD17B11 | HSD17B12 | HSD17B13 | HSD17B14 | HSD17B1P1 | HSD17B2 | HSD17B3 | HSD17B4 | HSD17B6 | HSD17B7 | HSD17B7P1 | HSD17B7P2 | HSD17B8 | HSD3B1 | HSD3B2 | HSD3B7 | HSD3BP4 | HSD3BP5 | HSD52 | HSDL1 | HSDL2 | HSDL2-AS1 | HSF1 | HSF2 | HSF2BP | HSF4 | HSF5 | HSFX1 | HSFX2 | HSFX3 | HSFY1 | HSFY1P1 | HSFY2 | HSH2D | HSP90AA1 | HSP90AA2P | HSP90AA3P | HSP90AA4P | HSP90AA5P | HSP90AA6P | HSP90AB1 | HSP90AB2P | HSP90AB3P | HSP90AB4P | HSP90B1 | HSP90B2P | HSP90B3P | HSPA12A | HSPA12B | HSPA13 | HSPA14 | HSPA1A | HSPA1B | HSPA1L | HSPA2 | HSPA2-AS1 | HSPA4 | HSPA4L | HSPA5 | HSPA5-DT | HSPA5P1 | HSPA6 | HSPA7 | HSPA8 | HSPA8P1 | HSPA8P19 | HSPA9 | HSPA9P1 | HSPB1 | HSPB11 | HSPB2 | HSPB2-C11orf52 | HSPB3 | HSPB6 | HSPB7 | HSPB8 | HSPB9 | HSPBAP1 | HSPBP1 | HSPC102 | HSPC324 | HSPD1 | HSPD1P11