Focused On-demand Library for Tyrosine--tRNA ligase, mitochondrial

Focused On-demand Libraries - Receptor.AI Collaboration


Explore the Potential with AI-Driven Innovation

The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher activity, selectivity, and safety.


We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Reaxense helps in synthesizing and delivering these compounds.


The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.


Our high-tech, dedicated method is applied to construct targeted libraries for enzymes.


 

Fig. 1. The screening workflow of Receptor.AI

It includes comprehensive molecular simulations of the catalytic and allosteric binding pockets and the ensemble virtual screening accounting for their conformational mobility. In the case of designing modulators, the structural changes induced by reaction intermediates are taken into account to leverage activity and selectivity.


Our library is unique due to several crucial aspects:


  • Receptor.AI compiles all relevant data on the target protein, such as past experimental results, literature findings, known ligands, and structural data, thereby enhancing the likelihood of focusing on the most significant compounds.

  • By utilizing advanced molecular simulations, the platform is adept at locating potential binding sites, rendering the compounds in the focused library well-suited for unearthing allosteric inhibitors and binders for hidden pockets.

  • The platform is supported by more than 50 highly specialized AI models, all of which have been rigorously tested and validated in diverse drug discovery and research programs. Its design emphasizes efficiency, reliability, and accuracy, crucial for producing focused libraries.

  • Receptor.AI extends beyond just creating focused libraries; it offers a complete spectrum of services and solutions during the preclinical drug discovery phase, with a success-dependent pricing strategy that reduces risk and fosters shared success in the project.


PARTNER
Receptor.AI
 
UPACC
Q9Y2Z4

UPID:
SYYM_HUMAN

ALTERNATIVE NAMES:
Tyrosyl-tRNA synthetase

ALTERNATIVE UPACC:
Q9Y2Z4; D3DUW8; Q9H817

BACKGROUND:
The mitochondrial enzyme Tyrosine--tRNA ligase, also known as Tyrosyl-tRNA synthetase, is essential for the synthesis of proteins. It ensures the proper attachment of tyrosine to tRNA(Tyr), a critical step in translating genetic information into functional proteins.

THERAPEUTIC SIGNIFICANCE:
Understanding the role of Tyrosine--tRNA ligase could open doors to potential therapeutic strategies, especially considering its involvement in Myopathy with lactic acidosis and sideroblastic anemia 2. This disease link offers a unique opportunity for developing targeted treatments.

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