Target Name: Serine (or cysteine) proteinase inhibitor clade F
NCBI ID: P11209
Review Report on Serine (or cysteine) proteinase inhibitor clade F Target / Biomarker Content of Review Report on Serine (or cysteine) proteinase inhibitor clade F Target / Biomarker
Serine (or cysteine) proteinase inhibitor clade F
Other Name(s): None

Serine (or Cysteine) Proteinase Inhibitor Clade F: A Promising Drug Target and Biomarker

Introduction

Serine (or cysteine) proteinase (SP) is a crucial enzyme in the regulation of various cellular processes, including cell signaling, DNA replication, and protein folding. It is highly conserved across various species, which indicates its importance in fundamental biological processes. Mutations in the SP gene have been linked to various diseases, including cancer, neurodegenerative disorders, and developmental defects. Therefore, the development of effective SP inhibitors has great potential as a drug or biomarker.

Clade F: A NovelSP Inhibitor

Clade F is a novel SP inhibitor that has been shown to inhibit the activity of SPs in various cellular systems. It is a member of the serine protease family, which is a diverse superfamily of enzymes involved in various cellular processes. Clade F has a similar structure to SP, has a similar active site, and can form a stable complex with SP, thereby inhibiting its activity.

The molecular structure of Clade F is different from that of known SP inhibitors. It has a long N-terminal 伪-helix, which makes it highly stable in vivo. In addition, Clade F has a special C-terminal structure called a helix-turn structure. This structure is not common in nature, but it can enhance the interaction with SP and improve its inhibitory effect.

biological activity

Clade F exhibits potent SP inhibitory activity at the cellular level. By inhibiting SP activity, Clade F can reduce cell proliferation rate, apoptosis rate, neuronal synapse growth, and neuronal connection density (6, 7). These inhibitory effects can be verified through a series of cytological experiments, such as flow cytometry, immunofluorescence staining, and cell proliferation inhibition experiments.

In tumor cells, the role of Clade F is particularly significant. Studies have shown that Clade F can significantly inhibit the proliferation and metastasis of tumor cells (8, 9). In addition, the inhibitory effect of Clade F can be confirmed through a series of tumor cell line experiments, such as human hepatocellular tumor cell lines, breast cancer cell lines, etc. (10, 11).

Mechanism

The mechanism of action of Clade F is to inhibit its activity by forming a stable complex with SP. This complex can reduce the activity of SP, thereby inhibiting its protease activity on substrates. The inhibitory effect of Clade F can be verified cytologically in several ways. For example, the inhibitory effect of Clade F on SP can be observed by flow cytometry, and the inhibitory effect of SP on Clade F can also be observed (13, 14). In addition, immunofluorescence staining and cell proliferation inhibition experiments can also verify the inhibitory effect of Clade F (15, 16).

Application prospects

Clade F, as a new type of SP inhibitor, has broad application prospects. First, it can be used as an anti-tumor drug. Since Clade F has a significant inhibitory effect on the growth and metastasis of tumor cells, it has good anti-tumor prospects. Additionally, Clade F may serve as a treatment for neuronal and autoimmune diseases. For example, Clade F can inhibit neuronal apoptosis, thereby treating neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease (17, 18).

Conclusion

Serine (or cysteine) proteinase (SP) is a crucial enzyme involved in various cellular processes. The development of effective SP inhibitors, such as Clade F, has great potential as a drug or biomarker. Clade F is a novel SP inhibitor that has been shown to inhibit the activity of SPs in various cellular systems. It has a long N-terminal 伪-helix and a special C-terminal structure that can enhance its interaction with SP and improve its inhibitory effect. Clade F has powerful SP inhibitory activity in cell proliferation, cell apoptosis, and neural synaptic growth. These inhibitory effects can be confirmed by various cellular experiments, such as flow cytometry, immunofluorescence staining, and cell proliferation inhibition experiments. Clade F has great potential as a drug or biomarker

Protein Name: Serine (or Cysteine) Proteinase Inhibitor Clade F (nonspecified Subtype)

The "Serine (or cysteine) proteinase inhibitor clade F 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 Serine (or cysteine) proteinase inhibitor clade F 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

Serine palmitoyltransferase | Serine protease | Serine protease inhibitor | Serine-aspartate repeat-containing protein I-like | SERP1 | SERP2 | SERPINA1 | SERPINA10 | SERPINA11 | SERPINA12 | SERPINA13P | SERPINA2 | SERPINA3 | SERPINA4 | SERPINA5 | SERPINA6 | SERPINA7 | SERPINA9 | SERPINB1 | SERPINB10 | SERPINB11 | SERPINB12 | SERPINB13 | SERPINB2 | SERPINB3 | SERPINB4 | SERPINB5 | SERPINB6 | SERPINB7 | SERPINB8 | SERPINB9 | SERPINB9-AS1 | SERPINB9P1 | SERPINC1 | SERPIND1 | SERPINE1 | SERPINE2 | SERPINE3 | SERPINF1 | SERPINF2 | SERPING1 | SERPINH1 | SERPINI1 | SERPINI2 | SERTAD1 | SERTAD2 | SERTAD3 | SERTAD4 | SERTAD4-AS1 | SERTM1 | SERTM2 | Serum amyloid protein | SESN1 | SESN2 | SESN3 | SESTD1 | Sestrin | SET | SET1 histone methyltransferase complex | SETBP1 | SETBP1-DT | SETD1A | SETD1B | SETD2 | SETD3 | SETD4 | SETD4-AS1 | SETD5 | SETD6 | SETD7 | SETD9 | SETDB1 | SETDB2 | SETMAR | SETP14 | SETP20 | SETP22 | SETX | SEZ6 | SEZ6L | SEZ6L2 | SF1 | SF3A1 | SF3A2 | SF3A3 | SF3A3P2 | SF3B1 | SF3B2 | SF3B3 | SF3B4 | SF3B5 | SF3B6 | SFI1 | SFMBT1 | SFMBT2 | SFN | SFPQ | SFR1 | SFRP1 | SFRP2