Target Name: PTPN13
NCBI ID: G5783
Review Report on PTPN13 Target / Biomarker Content of Review Report on PTPN13 Target / Biomarker
PTPN13
Other Name(s): PTPN13 variant 4 | Tyrosine-protein phosphatase non-receptor type 13 (isoform 2) | PTPL1 | PTP1E | Fas-associated phosphatase-1 | Protein tyrosine phosphatase 1E | Tyrosine-protein phosphatase non-receptor type 13 (isoform 4) | hPTP1E | PTP-BL | PTPN13 variant 2 | PTN13_HUMAN | Protein-tyrosine phosphatase 1E | FAP1 | PNP1 | Protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) | protein-tyrosine phosphatase 1E | Protein tyrosine phosphatase non-receptor type 13, transcript variant 2 | PTP-BAS | protein-tyrosine phosphatase PTPL1 | PTPLE | fas-associated protein-tyrosine phosphatase 1 | PTP-E1 | protein tyrosine phosphatase non-receptor type 13 | Fas-associated protein-tyrosine phosphatase 1 | protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) | Protein tyrosine phosphatase non-receptor type 13, transcript variant 4 | Tyrosine-protein phosphatase non-receptor type 13 | Protein-tyrosine phosphatase PTPL1 | hPTPE1 | PTP-1E | APO-1/CD95 (Fas)-associated phosphatase | Protein tyrosine phosphatase, non-receptor type 13 (PTPN13) | FAP-1

PTPN13: A Promising Drug Target and Biomarker for the Treatment of Paralytic-Spastic Disabilities

Introduction

Paralytic-spastic disabilities are a group of chronic conditions characterized by muscle stiffness, stiffness, and reduced muscle mobility. These conditions can significantly impact an individual's quality of life, making them a significant public health burden. The most common form of paralytic-spastic disabilities is multiple sclerosis, a progressive neuroimmune disorder that causes muscle weakness, stiffness, and loss of function. While there are currently several medications available to treat these conditions, the management of these disorders remains a clinical challenge.

The protein PTPN13, located on the protein kinase C (PKC) gene, is a potential drug target and biomarker for the treatment of paralytic-spastic disabilities. PTPN13 is a 12-kDa protein that plays a crucial role in the regulation of actin dynamics and cell signaling. It is a non-catalytic subunit of the PKC enzyme, which is responsible for regulating the activity of various cellular signaling pathways.

Expression of PTPN13 in human tissues

Studies have shown that PTPN13 is expressed in various human tissues, including muscle, brain, and heart. In muscle tissue, PTPN13 is predominantly expressed in the satellite cells, which are responsible for muscle fiber fusion and regeneration. In brain tissue, PTPN13 is expressed in the endoplasmic reticulum (ER) and is involved in the regulation of synaptic plasticity and neurotransmitter release. In heart tissue, PTPN13 is expressed in the cardiac muscle cells and pericardial cells, where it plays a role in the regulation of contractility and cardiac fibrosis.

Functional characterization of PTPN13

The functions of PTPN13 have been extensively investigated, and several studies have demonstrated its involvement in various cellular signaling pathways. PTPN13 is a key regulator of the PKC signaling pathway, which is involved in the regulation of cell growth, differentiation, and survival. Studies have shown that PTPN13 plays a critical role in the regulation of actin dynamics and protein-protein interactions, which are crucial for the proper functioning of actin-based structures.

In addition to its role in PKC signaling, PTPN13 is also involved in the regulation of several other cellular signaling pathways, including TGF-β, NF-kappa-B, and Hedgehog. These signaling pathways are involved in the regulation of cell growth, differentiation, and survival, and are crucial for the development and maintenance of various tissues and organs.

Drug targeting PTPN13

Several drugs have been developed to target PTPN13 and treat paralytic-spastic disabilities. These drugs act by modulating the activity of PTPN13 or its downstream targets. One of the most promising drugs currently in development is a small molecule inhibitor of PTPN13, known as PTPN13 inhibitor . This drug is designed to specifically bind to PTPN13 and inhibit its activity, which should lead to the relaxation of muscle stiffness and improved muscle mobility.

Another approach to targeting PTPN13 is the use of monoclonal antibodies (mAbs). These antibodies are designed to specifically bind to PTPN13 and can be used to treat paralytic-spastic disabilities by blocking the activity of PTPN13. Several studies have shown that the use of mAbs Targeting PTPN13 has been effective in animal models of paralytic-spastic disabilities.

Biomarker analysis

While drug targeting PTPN13 is an exciting new approach to treating paralytic-spastic disabilities, it is important to

Protein Name: Protein Tyrosine Phosphatase Non-receptor Type 13

Functions: Tyrosine phosphatase which regulates negatively FAS-induced apoptosis and NGFR-mediated pro-apoptotic signaling (PubMed:15611135). May regulate phosphoinositide 3-kinase (PI3K) signaling through dephosphorylation of PIK3R2 (PubMed:23604317)

The "PTPN13 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 PTPN13 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

More Common Targets

PTPN14 | PTPN18 | PTPN2 | PTPN20 | PTPN20A | PTPN20CP | PTPN21 | PTPN22 | PTPN23 | PTPN3 | PTPN4 | PTPN5 | PTPN6 | PTPN7 | PTPN9 | PTPRA | PTPRB | PTPRC | PTPRCAP | PTPRD | PTPRE | PTPRF | PTPRG | PTPRH | PTPRJ | PTPRK | PTPRM | PTPRN | PTPRN2 | PTPRN2-AS1 | PTPRO | PTPRQ | PTPRR | PTPRS | PTPRT | PTPRU | PTPRVP | PTPRZ1 | PTRH1 | PTRH2 | PTRHD1 | PTS | PTTG1 | PTTG1IP | PTTG2 | PTTG3P | PTX3 | PTX4 | PUDP | PUDPP2 | PUF60 | PUM1 | PUM2 | PUM3 | PURA | PURB | PURG | PURPL | PUS1 | PUS10 | PUS3 | PUS7 | PUS7L | PUSL1 | Putative POM121-like protein 1 | Putative uncharacterized protein C12orf63 | PVALB | PVALEF | PVR | PVRIG | PVT1 | PWAR1 | PWAR4 | PWAR5 | PWAR6 | PWARSN | PWP1 | PWP2 | PWRN1 | PWRN2 | PWRN3 | PWWP2A | PWWP2B | PWWP3A | PWWP3B | PXDC1 | PXDN | PXDNL | PXK | PXMP2 | PXMP4 | PXN | PXN-AS1 | PXT1 | PXYLP1 | PYCARD | PYCR1 | PYCR2 | PYCR3 | PYDC1