BIRC6: A Potential Drug Target for Various Diseases (G57448)
BIRC6: A Potential Drug Target for Various Diseases
Baculoviral IAP repeat containing 6 (BIRC6) is a non-coding RNA molecule that has been identified as a potential drug target in various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. BIRC6 is a repeat of the Baculovirus IAP gene, which is known to be involved in the replication of several viruses, including H7N1 flu virus, SARS-CoV-2, and Zika virus. The IAP gene has four splice variants, which result in the production of different isoforms of the gene. BIRC6 is one of these isoforms, and it has been shown to have unique functions in various cellular processes.
Disease-relevant functions of BIRC6
BIRC6 has been shown to be involved in several diseases and disorders, including cancer, neurodegenerative diseases, and autoimmune disorders. Its functions in these diseases have been attributed to its unique structure and the specific way it interacts with other molecules.
BIRC6 as a drug target
BIRC6 has been identified as a potential drug target due to its unique structure and the functions it is involved in. Several studies have shown that BIRC6 can interact with various molecules and have been shown to play a role in several cellular processes. This makes it an attractive drug target for researchers to explore and develop new treatments for various diseases.
One of the potential benefits of targeting BIRC6 is its ability to inhibit the activity of other molecules, such as cancer cells, neurodegenerative diseases, and autoimmune disorders. This is because BIRC6 has been shown to interact with multiple molecules, including cell signaling pathways, which can lead to the inhibition of critical cellular processes that contribute to the development and progression of these diseases.
Another potential benefit of targeting BIRC6 is its ability to enhance the effectiveness of existing treatments. BIRC6 has been shown to interact with multiple molecules, including proteins that are involved in cell signaling pathways. By targeting these molecules, researchers may be able to enhance the effectiveness of existing treatments and improve the overall health and wellbeing of patients.
Preclinical studies
Preclinical studies have shown that targeting BIRC6 may be an effective way to treat various diseases. In cancer cells, BIRC6 has been shown to inhibit the growth and survival of cancer cells, which may lead to the inhibition of critical cellular processes that contribute to the development and progression of cancer.
In neurodegenerative diseases, BIRC6 has been shown to interact with proteins involved in the development and progression of neurodegenerative diseases. This may lead to the inhibition of critical cellular processes that contribute to the development and progression of these diseases.
In autoimmune disorders, BIRC6 has been shown to interact with proteins involved in the development and progression of autoimmune disorders. This may lead to the inhibition of critical cellular processes that contribute to the development and progression of these diseases.
Conclusion
Baculoviral IAP repeat containing 6 (BIRC6) has been identified as a potential drug target due to its unique structure and the functions it is involved in. BIRC6 has been shown to interact with various molecules and have been associated with the development and progression of several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Further research is needed to fully understand the potential of BIRC6 as a drug target and to develop new treatments for various diseases.
Protein Name: Baculoviral IAP Repeat Containing 6
Functions: Anti-apoptotic protein which can regulate cell death by controlling caspases and by acting as an E3 ubiquitin-protein ligase. Has an unusual ubiquitin conjugation system in that it could combine in a single polypeptide, ubiquitin conjugating (E2) with ubiquitin ligase (E3) activity, forming a chimeric E2/E3 ubiquitin ligase. Its targets include CASP9 and DIABLO/SMAC. Acts as an inhibitor of CASP3, CASP7 and CASP9. Important regulator for the final stages of cytokinesis. Crucial for normal vesicle targeting to the site of abscission, but also for the integrity of the midbody and the midbody ring, and its striking ubiquitin modification
More Common Targets
BIRC7 | BIRC8 | BISPR | BIVM | BIVM-ERCC5 | BLACAT1 | BLACE | BLCAP | BLID | BLK | BLM | BLMH | BLNK | BLOC-1 (biogenesis of lysosome-related organelles complex 1) | BLOC1S1 | BLOC1S1-RDH5 | BLOC1S2 | BLOC1S3 | BLOC1S4 | BLOC1S5 | BLOC1S5-TXNDC5 | BLOC1S6 | BLTP1 | BLTP2 | BLTP3A | BLTP3B | BLVRA | BLVRB | BLZF1 | BMAL1 | BMAL2 | BMAL2-AS1 | BMERB1 | BMF | BMI1 | BMP1 | BMP10 | BMP15 | BMP2 | BMP2K | BMP3 | BMP4 | BMP5 | BMP6 | BMP7 | BMP8A | BMP8B | BMPER | BMPR1A | BMPR1B | BMPR1B-DT | BMPR2 | BMS1 | BMS1P1 | BMS1P10 | BMS1P14 | BMS1P15 | BMS1P17 | BMS1P18 | BMS1P2 | BMS1P20 | BMS1P21 | BMS1P22 | BMS1P4 | BMS1P7 | BMS1P8 | BMT2 | BMX | BNC1 | BNC2 | BNC2-AS1 | BNIP1 | BNIP2 | BNIP3 | BNIP3L | BNIP5 | BNIPL | BOC | BOD1 | BOD1L1 | BOD1L2 | BOK | BOK-AS1 | BOLA1 | BOLA2 | BOLA2B | BOLA3 | BOLA3-DT | BOLL | Bombesin receptor | Bone morphogenetic protein (BMP) | Bone Morphogenetic Protein Receptor | Bone Morphogenetic Protein Receptor Type I | BOP1 | BORA | BORCS5 | BORCS6 | BORCS7 | BORCS7-ASMT | BORCS8