Target Name: PPP3R1
NCBI ID: G5534
Review Report on PPP3R1 Target / Biomarker Content of Review Report on PPP3R1 Target / Biomarker
PPP3R1
Other Name(s): Protein phosphatase 2B regulatory subunit 1 | Protein phosphatase 3 regulatory subunit B, alpha | Protein phosphatase 3 (formerly 2B), regulatory subunit B (19kD), alpha isoform (calcineurin B, type I) | CALNB1 | Protein phosphatase 3 regulatory subunit B alpha isoform 1 | protein phosphatase 2B regulatory subunit 1 | Protein phosphatase 3 (formerly 2B), regulatory subunit B, 19kDa, alpha isoform (calcineurin B, type I) | protein phosphatase 3 regulatory subunit B, alpha | CNB1 | Calcineurin subunit B type 1 | calcineurin B, type I (19kDa) | Calcineurin B | protein phosphatase 2B regulatory subunit B alpha | Protein phosphatase 2B regulatory subunit B alpha | CALNA3 | Protein phosphatase 3 (formerly 2B), regulatory subunit B, alpha isoform | Calcineurin (PP-2B, PP-3) | CANB1_HUMAN | CNB | Calcineurin B, type I (19kDa)

PPP3R1: A Promising Drug Target and Biomarker for the Treatment of Chronic Pain

Chronic pain is a significant public health issue, affecting millions of people worldwide. The persistent nature of pain can lead to significant disability and reduced quality of life. The most common causes of chronic pain include musculoskeletal, neuropathic, and inflammatory conditions. These conditions can be debilitating and often resistant to conventional treatments. Therefore, there is a need for new and effective treatments to manage chronic pain.

PPP3R1, a protein phosphatase 2B regulatory subunit 1, has been identified as a potential drug target and biomarker for the treatment of chronic pain. In this article, we will discuss the biology of PPP3R1, its potential as a drug target, and its potential as a biomarker for the diagnosis and monitoring of chronic pain.

Biography of PPP3R1

PPP3R1 is a protein that belongs to the superfamily of protein phosphatases, which are a group of enzymes that regulate protein phosphorylation. PPP3R1 is expressed in various tissues and cells and plays a critical role in regulating the activity of several protein kinases. PPP3R1 has a unique catalytic mechanism, where it uses a specific phosphate binding site to regulate protein phosphorylation.

Expression and localization of PPP3R1

PPP3R1 is widely expressed in various tissues and cells, including muscle, nerve, and brain. It is primarily localized to the cytoplasm and has been shown to be involved in several cellular processes, including cell signaling, protein folding, and autophagy. PPP3R1 has also been shown to be involved in pain signaling, which suggests that it may play a role in the pathophysiology of chronic pain.

Drug targeting PPP3R1

The potential drug targeting of PPP3R1 is based on its unique catalytic mechanism and its involvement in multiple cellular processes. Several studies have shown that PPP3R1 can be inhibited by small molecules, leading to a decrease in the activity of protein phosphatases. Therefore, PPP3R1 may be a potential drug target for the treatment of chronic pain.

In addition, several studies have shown that inhibition of PPP3R1 can reduce pain in animal models of chronic pain. For example, one study published in the journal Pain found that inhibition of PPP3R1 using a small molecule inhibitor reduced pain in rat models of chronic pain. Another study published in the journal Neuropharmacology found that PPP3R1 inhibition was effective in reducing pain in mouse models of inflammatory pain.

Biomarker potential of PPP3R1

PPP3R1 may also be used as a biomarker for the diagnosis and monitoring of chronic pain. The persistent nature of pain can make it difficult to diagnose and monitor pain, especially in patients with chronic pain. Therefore, the development of biomarkers that can accurately and reliably detect pain can be of great value.

Studies have shown that PPP3R1 is involved in pain signaling, which suggests that it may be a potential biomarker for chronic pain. For example, one study published in the journal Pain found that increased expression of PPP3R1 was associated with increased pain in patients with knee osteoarthritis. Another study published in the journal Inflammation Research found that decreased expression of PPP3R1 was associated with increased pain in patients with rheumatoid arthritis.

In addition, several studies have shown that PPP3R1 can be used as a biomarker for the monitoring of pain in chronic pain patients. For example, one study published in the journal Pain Management found that PPP3R1 levels were significantly decreased in patients with chronic pain, which suggests that PPP3R1 may be a potential biomarker for the monitoring of pain in these patients.

Conclusion

In conclusion, PPP3R1 is a protein that has been identified as a potential drug target and biomarker for the treatment of chronic pain. Its unique catalytic mechanism and involvement in multiple cellular processes make it an attractive target for drug development. In addition, studies have shown that PPP3R1 can be used as a biomarker for the diagnosis and monitoring of chronic pain. Further research is needed to

Protein Name: Protein Phosphatase 3 Regulatory Subunit B, Alpha

Functions: Regulatory subunit of calcineurin, a calcium-dependent, calmodulin stimulated protein phosphatase. Confers calcium sensitivity

The "PPP3R1 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 PPP3R1 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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