Target Name: UBQLN3
NCBI ID: G50613
Review Report on UBQLN3 Target / Biomarker Content of Review Report on UBQLN3 Target / Biomarker
UBQLN3
Other Name(s): ubiquilin 3 | UBQL3_HUMAN | UBQLN3 variant 2 | OTTHUMP00000069806 | Ubiquilin-3 | Ubiquilin 3 | testicular tissue protein Li 220 | OTTHUMP00000069805 | TUP-1 | Ubiquilin 3, transcript variant 2

UBQLN3: A Potential Drug Target and Biomarker

Uncovering the Potential of UBQLN3 as a Drug Target and Biomarker

Introduction

Unlocking the secrets of protein-coding genes and their potential as drug targets is an attractive area of 鈥嬧?媟esearch. One such gene is UBQLN3, which has been identified as a potential drug target and biomarker. UBQLN3 is a non-coding RNA molecule that plays a crucial role in the regulation of microRNA (miRNA) levels. In recent years, a growing body of research has identified potential drug targets in UBQLN3, which has led to the development of new therapeutics.

The UBQLN3 gene:

UBQLN3 is a non-coding RNA molecule that is approximately 1,800 nucleotides in length. It is located on chromosome 6p21 and has been shown to play a critical role in the regulation of miRNA levels. UBQLN3 is composed of two main functional regions: the first is a 5'-end region that contains a unique GUG repeats sequence, while the second is a 3'-end region that contains a single AUG start codon.

The unique GUG repeats sequence at the 5'-end region of UBQLN3 is a hallmark of the gene and is associated with its function in the regulation of miRNA levels. This region has been shown to interact with several key protein partners, including the RNA- protein complex known as MBP-Bago(Myeloblast Band Protein-Bago). This interaction between UBQLN3 and MBP-Bago has been shown to play a critical role in the regulation of miRNA levels.

The 3'-end region of UBQLN3 contains a single AUG start codon, which is the first amino acid that is translated from the RNA molecule into a protein. This region has been shown to be involved in the regulation of miRNA levels by affecting the translation efficiency of UBQLN3 RNA.

Potential drug targets:

UBQLN3 has several potential drug targets due to its role in the regulation of miRNA levels. One such target is the PI3K/AKT signaling pathway, which is a well-established target for the regulation of cellular signaling pathways. The PI3K/AKT signaling pathway is Involved in the regulation of various cellular processes, including cell survival, angiogenesis, and inflammation.

Recent studies have shown that UBQLN3 plays a critical role in the regulation of miRNA levels in the PI3K/AKT signaling pathway. UBQLN3 has been shown to interact with the protein PDCD1, which is a key component of the PI3K/AKT signaling pathway. This interaction between UBQLN3 and PDCD1 has been shown to play a critical role in the regulation of miRNA levels in the PI3K/AKT signaling pathway.

Another potential drug target for UBQLN3 is the SIRT1 gene, which is a well-established gene involved in the regulation of cellular processes such as DNA repair and stress resistance. The protein encoded by the SIRT1 gene is an important antioxidant that can protect cells from immunity. Damage from free radicals.

Biomarker potential of UBQLN3:

In addition to the above two potential drug targets, UBQLN3 may also have other potential biomarkers.

Protein Name: Ubiquilin 3

The "UBQLN3 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 UBQLN3 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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