Target Name: TYW1
NCBI ID: G55253
Review Report on TYW1 Target / Biomarker Content of Review Report on TYW1 Target / Biomarker
TYW1
Other Name(s): TYW1_HUMAN | tRNA-yW-synthesizing protein | tRNA-yW synthesizing protein 1 homolog A | YPL207W | TRNA-yW synthesizing protein 1 homolog, transcript variant 1 | S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 | OTTHUMP00000160137 | tRNA wybutosine-synthesizing protein 1 homolog | MGC23001 | Radical S-adenosyl methionine and flavodoxin domain-containing protein 1 | MGC60291 | TYW1 variant 1 | FLJ10900 | TYW1A | tRNA-yW synthesizing protein 1 homolog | radical S-adenosyl methionine and flavodoxin domains 1 | Radical S-adenosyl methionine and flavodoxin domains 1 | RSAFD1 | radical S-adenosyl methionine and flavodoxin domain-containing protein 1

TYW1: A Potential Drug Target and Biomarker for the Treatment of Inflammatory Diseases

The TYW1 protein is a member of the transforming growth factor-beta (TGF-β) family, which plays a crucial role in cell growth, differentiation, and inflammation. TGF-β signaling has been implicated in the development and progression of numerous inflammatory diseases, including autoimmune disorders, cancer, and fibrosis. The identification of TYW1 as a potential drug target and biomarker has significant implications for the development of new therapeutic approaches for these diseases.

The TGF-β Signaling Pathway

TGF-β is a cytoplasmic protein that plays a vital role in cell growth and development by regulating cell proliferation, differentiation, and survival. The TGF-β signaling pathway involves the binding of TGF-β proteins to its downstream effector, Smad, which triggers a series of downstream signaling pathways.

The TGF-β pathway is involved in the regulation of cell proliferation, which is critical for the development and progression of many diseases, including cancer, autoimmune disorders, and fibrosis. TGF-β signaling has been implicated in the regulation of cell differentiation, as well as the regulation of cell survival and angiogenesis.

TYW1: A Potential Drug Target

The identification of TYW1 as a potential drug target has significant implications for the treatment of inflammatory diseases. TGF-β signaling has been implicated in the development and progression of many inflammatory diseases, including autoimmune disorders, cancer, and fibrosis. The identification of TYW1 as a potential drug target has the potential to disrupt the TGF-β signaling pathway and improve the treatment outcomes for inflammatory diseases.

The TGF-β pathway is involved in the regulation of cell proliferation, which is critical for the development and progression of many diseases. TGF-β signaling has been implicated in the regulation of cell differentiation, as well as the regulation of cell survival and angiogenesis. The identification of TYW1 as a potential drug target has significant implications for the treatment of inflammatory diseases, as it may help to disrupt the TGF-β signaling pathway and improve the treatment outcomes.

The TGF-β pathway is involved in the regulation of cell adhesion, which is critical for the development and progression of many diseases, including cancer. The TGF-β pathway has been shown to play a role in the regulation of cell adhesion, as well as the regulation of cell migration and the formation of tissues. The identification of TYW1 as a potential drug target may have implications for the development of new therapeutic approaches for cancer and other inflammatory diseases.

The TGF-β pathway is involved in the regulation of inflammation, which is critical for the development and progression of many diseases, including autoimmune disorders and cancer. The TGF-β pathway has been shown to play a role in the regulation of inflammation, as well as the regulation of immune cell function. The identification of TYW1 as a potential drug target may have implications for the development of new therapeutic approaches for the treatment of autoimmune disorders and cancer.

The TGF-β pathway is involved in the regulation of cell survival, which is critical for the development and progression of many diseases, including cancer. The TGF-β pathway has been shown to play a role in the regulation of cell survival, as well as the regulation of cell cycle progression. The identification of TYW1 as a potential drug target may have implications for the development of new therapeutic approaches for the treatment of cancer.

The TGF-β pathway is involved in the regulation of angiogenesis, which is critical for the development and progression of many diseases, including cancer. The TGF-β pathway has been shown to play a role in the regulation of angiogenesis, as well as the regulation of vascular barrier formation. The identification of TYW1 as a potential drug target

Protein Name: TRNA-yW Synthesizing Protein 1 Homolog

Functions: Probable component of the wybutosine biosynthesis pathway. Wybutosine is a hyper modified guanosine with a tricyclic base found at the 3'-position adjacent to the anticodon of eukaryotic phenylalanine tRNA. Catalyzes the condensation of N-methylguanine with 2 carbon atoms from pyruvate to form the tricyclic 4-demethylwyosine, an intermediate in wybutosine biosynthesis (By similarity)

The "TYW1 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 TYW1 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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TYW1B | TYW3 | U2 small nuclear ribonucleoprotein auxiliary factor | U2AF1 | U2AF1L4 | U2AF2 | U2SURP | U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex | U5 small nuclear ribonucleoprotein complex | U7 snRNP complex | UACA | UAP1 | UAP1L1 | UBA1 | UBA2 | UBA3 | UBA5 | UBA52 | UBA52P1 | UBA6 | UBA6-DT | UBA7 | UBAC1 | UBAC2 | UBAC2-AS1 | UBALD1 | UBALD2 | UBAP1 | UBAP1L | UBAP2 | UBAP2L | UBASH3A | UBASH3B | UBB | UBBP1 | UBBP2 | UBBP4 | UBC | UBD | UBDP1 | UBE2A | UBE2B | UBE2C | UBE2CP3 | UBE2CP4 | UBE2D1 | UBE2D2 | UBE2D3 | UBE2D3P1 | UBE2D4 | UBE2DNL | UBE2E1 | UBE2E2 | UBE2E3 | UBE2F | UBE2F-SCLY | UBE2FP1 | UBE2G1 | UBE2G2 | UBE2H | UBE2HP1 | UBE2I | UBE2J1 | UBE2J2 | UBE2K | UBE2L1 | UBE2L3 | UBE2L6 | UBE2M | UBE2MP1 | UBE2N | UBE2NL | UBE2O | UBE2Q1 | UBE2Q2 | UBE2Q2P1 | UBE2Q2P11 | UBE2Q2P13 | UBE2Q2P16 | UBE2Q2P2 | UBE2QL1 | UBE2R2 | UBE2R2-AS1 | UBE2S | UBE2T | UBE2U | UBE2V1 | UBE2V1P2 | UBE2V1P9 | UBE2V2 | UBE2V2P1 | UBE2W | UBE2Z | UBE3A | UBE3B | UBE3C | UBE3D | UBE4A | UBE4B | UBFD1