Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior activity, selectivity and safety.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
We use our state-of-the-art dedicated workflow for designing focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes in-depth molecular simulations of both the catalytic and allosteric binding pockets, with ensemble virtual screening focusing on their conformational flexibility. For modulators, the process includes considering the structural shifts due to reaction intermediates to boost activity and selectivity.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q9H7H0
UPID:
MET17_HUMAN
Alternative names:
False p73 target gene protein; Methyltransferase 11 domain-containing protein 1; Protein RSM22 homolog, mitochondrial
Alternative UPACC:
Q9H7H0; Q9BSH1; Q9BZH2; Q9BZH3
Background:
Methyltransferase-like protein 17, mitochondrial, known as Q9H7H0, plays a crucial role in mitochondrial function. It acts as a probable S-adenosyl-L-methionine-dependent RNA methyltransferase, essential for stabilizing the mitochondrial small ribosomal subunit (mt-SSU). This stabilization is vital for protein translation within mitochondria, highlighting its significance in cellular energy production and overall mitochondrial health.
Therapeutic significance:
Understanding the role of Methyltransferase-like protein 17 could open doors to potential therapeutic strategies. Its pivotal function in mitochondrial protein synthesis positions it as a key target for interventions aimed at mitochondrial disorders and diseases with mitochondrial dysfunction components.