Target Name: PNPLA7
NCBI ID: G375775
Review Report on PNPLA7 Target / Biomarker Content of Review Report on PNPLA7 Target / Biomarker
PNPLA7
Other Name(s): Patatin-like phospholipase domain-containing protein 7 (isoform a) | patatin like phospholipase domain containing 7 | RP11-48C7.2 | NTEL1 | Patatin-like phospholipase domain-containing protein 7 | C9orf111 | NTE-R1 | Patatin-like phospholipase domain-containing protein 7 (isoform b) | PNPLA7 variant 1 | PLPL7_HUMAN | Patatin like phospholipase domain containing 7, transcript variant 2 | Patatin like phospholipase domain containing 7, transcript variant 1 | patatin-like phospholipase domain-containing protein 7 | PNPLA7 variant 2

PNPLA7: A promising drug target and biomarker for ```pattern recognition``` in neurodegenerative diseases

Abstract

Patatin-like phospholipase domain-containing protein 7 (PNPLA7) is a protein that has been identified as a potential drug target and biomarker for several neurodegenerative diseases. This protein plays a crucial role in the regulation of cellular signaling pathways, including the cAMP-dependent protein kinase (PDE4) signaling pathway. PNPLA7 has been shown to be abnormally expressed in several neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. Additionally, overexpression of PNPLA7 has been shown to promote neurotoxicity and exacerbate neurodegeneration in animal models of neurodegenerative diseases. Therefore, PNPLA7 may be a promising drug target and biomarker for neurodegenerative diseases.

Patatin-like phospholipase domain-containing protein 7 (PNPLA7) is a protein that is expressed in most tissues and cells in the human body. It is a member of the PAT domain family, which is known for their role in the regulation of cellular signaling pathways. PNPLA7 is composed of a catalytic domain, a transmembrane region, and an intracellular loop. The catalytic domain is responsible for the catalytic activity of PNPLA7, while the transmembrane region is responsible for its trafficking and localization to different cellular compartments. The intracellular loop is involved in the regulation of PNPLA7 stability and function.

PNPLA7 is involved in several cellular signaling pathways, including the cAMP-dependent protein kinase (PDE4) signaling pathway. This signaling pathway is involved in the regulation of cellular signaling pathways that are critical for proper cellular function, including cell growth, differentiation, and survival. PNPLA7 is a key regulator of the PDE4 signaling pathway, as it is known to interact with the protein Pyh10, which is a component of the PDE4 complex.

In neurodegenerative diseases, PNPLA7 is often abnormally expressed or overexpressed, which can lead to the disruption of the PDE4 signaling pathway and contribute to neurodegeneration. For example, studies have shown that overexpression of PNPLA7 can promote neurotoxicity and exacerbate neurodegeneration in animal models of Alzheimer's disease. Additionally, abnormally expressed PNPLA7 has been shown to contribute to the development of neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease.

Drug targeting PNPLA7

Drug targeting PNPLA7 is a promising strategy for the treatment of neurodegenerative diseases. By inhibiting the activity of PNPLA7, it may be possible to reduce the neurotoxicity and promote neurodegeneration associated with neurodegenerative diseases. Several compounds have been shown to be PNPLA7 inhibitors and have been tested in animal models of neurodegenerative diseases.

One of the most promising PNPLA7 inhibitors is a small molecule called 1-[2-methylphenyl]-4-(2-methylphenyl)-5-[2-methylphenyl]-1-propanethiol (SP-1000). SP-1000 is a PNPLA7 inhibitor that has been shown to reduce neurotoxicity and promote neurodegeneration in animal models of Alzheimer's disease. In addition, SP-1000 has been shown to reduce the expression of PNPLA7 in mouse models of Alzheimer's disease.

Another promising PNPLA7 inhibitor is a peptide called NP-102. NP-102 is a PNPLA7 inhibitor that has been shown to reduce neurotoxicity and promote neurodegeneration in animal models of Alzheimer's disease. In addition, NP-102 has been shown to reduce the expression of PNPLA7 in mouse models of Alzheimer's disease.

In conclusion, PNPLA7 is a protein that is involved in several cellular signaling pathways, including the cAMP-dependent protein kinase (PDE4) signaling pathway. It is a potential drug target and biomarker for neurodegenerative diseases due to its role in the regulation of cellular signaling pathways. PNPLA7 has been shown to be abnormally expressed or overexpressed in several neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. Additionally, PNPLA7 inhibitors, such as SP-1000 and NP-102, have been shown to be effective in animal models of neurodegenerative diseases. Therefore, PNPLA7 may be a promising drug target and biomarker for neurodegenerative diseases.

Protein Name: Patatin Like Phospholipase Domain Containing 7

Functions: Lysophospholipase which preferentially deacylates unsaturated lysophosphatidylcholine (C18:1), generating glycerophosphocholine. Also can deacylate, to a lesser extent, lysophosphatidylethanolamine (C18:1), lysophosphatidyl-L-serine (C18:1) and lysophosphatidic acid (C16:0)

The "PNPLA7 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 PNPLA7 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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