Target Name: KIF20A
NCBI ID: G10112
Review Report on KIF20A Target / Biomarker Content of Review Report on KIF20A Target / Biomarker
KIF20A
Other Name(s): OTTHUMP00000159481 | mitotic kinesin-like protein 2 | RCM6 | RAB6KIFL | Kinesin family member 20A | rabkinesin-6 | kinesin family member 20A | Rabkinesin-6 | GG10_2 | OTTHUMP00000223777 | Mitotic kinesin-like protein 2 | MKlp2 | Rab6-interacting kinesin-like protein | MKLP2 | rab6-interacting kinesin-like protein | FLJ21151 | Kinesin-like protein KIF20A | KI20A_HUMAN | RAB6 interacting, kinesin-like (rabkinesin6)

KIF20A: A Potential Drug Target and Biomarker

Kallikrein-related peptidases (KrPs) are a family of enzymes that regulate proteolytic enzymes, which are responsible for breaking down other proteins into smaller peptides. In recent years, the discovery of new KrPs has led to a growing interest in their potential functions and potential as drug targets. One such protein is KIF20A, which is a member of the Kallikrein-related peptidases family and has been shown to play a critical role in various physiological processes in the body.

KIF20A: Structure and Function

KIF20A is a 21-kDa protein that is expressed in various tissues and organs, including the liver, heart, kidneys, and intestines. It is characterized by a catalytic active site, a distinct N-terminus, and a C-terminus that is involved in its interactions with other proteins. KIF20A has a unique fold, with a distinct N-terminal alpha-helix and a N-tail that is involved in its stability and interactions with other proteins.

KIF20A has been shown to regulate the activity of several proteases, including the 尾-glucanases, which are involved in the degradation of extracellular matrix (ECM) components. In addition, KIF20A has also been shown to regulate the activity of other enzymes, including the proteases that break down extracellular vesicles, which are released by cells as a means of signaling and communication.

KIF20A is also involved in the regulation of cellular signaling pathways, including the TGF-β pathway, which is involved in cell growth, differentiation, and survival. KIF20A has been shown to play a critical role in the regulation of TGF-β signaling by interacting with the transcription factor, Smad2.

KIF20A: Potential Drug Target

The discovery of KIF20A as a potential drug target has significant implications for the development of new treatments for a variety of diseases. Given its involvement in several important cellular processes, KIF20A is a promising target for the treatment of diseases that are characterized by the over-activation of proteolytic enzymes, including cancer, neurodegenerative diseases, and autoimmune disorders.

One potential approach to targeting KIF20A is to use small molecules that can inhibit its activity. Such molecules have been shown to be effective in blocking the activity of KIF20A, including inhibitors of the proteases that it regulates. Additionally, drugs that can modulate the activity of KIF20A have been shown to be effective in treating a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

KIF20A: Biomarker

The discovery of KIF20A as a potential drug target has also led to a growing interest in its potential as a biomarker for the diagnosis and treatment of various diseases. Given its involvement in several important cellular processes, KIF20A has been shown to be a potential biomarker for a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

One potential approach to using KIF20A as a biomarker is to use techniques such as protein array analysis or mass spectrometry to measure the expression and activity of KIF20A in a variety of tissues and fluids. This can provide valuable information about the underlying biology of the disease and the effectiveness of potential treatments. Additionally, the use of KIF20A as a biomarker can also serve as a basis for the development of new diagnostic tests for diseases associated with KIF20A over-activation.

Conclusion

In conclusion, KIF20A is a promising protein that has significant implications for the development of new treatments for a variety of diseases. Its unique structure and function, as well as its involvement in several important cellular processes, make it an attractive target for small molecules and other therapies. Additionally, the discovery of KIF20A as a potential biomarker for a variety of diseases has significant implications for the development of new diagnostic tests and therapies for diseases associated with KIF20A over-activation. Further research is needed to fully understand the role of KIF20A in the regulation of cellular processes and its potential as a drug target and biomarker.

Protein Name: Kinesin Family Member 20A

Functions: Mitotic kinesin required for chromosome passenger complex (CPC)-mediated cytokinesis. Following phosphorylation by PLK1, involved in recruitment of PLK1 to the central spindle. Interacts with guanosine triphosphate (GTP)-bound forms of RAB6A and RAB6B. May act as a motor required for the retrograde RAB6 regulated transport of Golgi membranes and associated vesicles along microtubules. Has a microtubule plus end-directed motility

The "KIF20A 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 KIF20A 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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KIF20B | KIF21A | KIF21B | KIF22 | KIF23 | KIF23-AS1 | KIF24 | KIF25 | KIF25-AS1 | KIF26A | KIF26B | KIF27 | KIF28P | KIF2A | KIF2B | KIF2C | KIF3A | KIF3B | KIF3C | KIF4A | KIF4B | KIF5A | KIF5B | KIF5C | KIF6 | KIF7 | KIF9 | KIF9-AS1 | KIFAP3 | KIFBP | KIFC1 | KIFC2 | KIFC3 | Killer Cell Immunoglobulin-Like Receptor (KIR) | Killer cell immunoglobulin-like receptor 2DS1, transcript variant X1 | KIN | Kinesin-like protein KIF16B (isoform 1) | KIR2DL1 | KIR2DL2 | KIR2DL3 | KIR2DL4 | KIR2DL5A | KIR2DL5B | KIR2DP1 | KIR2DS1 | KIR2DS2 | KIR2DS3 | KIR2DS4 | KIR2DS5 | KIR3DL1 | KIR3DL2 | KIR3DL3 | KIR3DP1 | KIR3DS1 | KIR3DX1 | KIRREL1 | KIRREL1-IT1 | KIRREL2 | KIRREL3 | KIRREL3-AS2 | KIRREL3-AS3 | KISS1 | KISS1R | KIT | KITLG | KIZ | KIZ-AS1 | KL | KLB | KLC1 | KLC2 | KLC3 | KLC4 | KLF1 | KLF10 | KLF11 | KLF12 | KLF13 | KLF14 | KLF15 | KLF16 | KLF17 | KLF17P1 | KLF2 | KLF3 | KLF3-AS1 | KLF4 | KLF5 | KLF6 | KLF7 | KLF8 | KLF9 | KLHDC1 | KLHDC10 | KLHDC2 | KLHDC3 | KLHDC4 | KLHDC7A | KLHDC7B | KLHDC7B-DT