Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better activity, selectivity, and safety.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q9UI30
UPID:
TR112_HUMAN
Alternative names:
tRNA methyltransferase 112 homolog
Alternative UPACC:
Q9UI30; B2R539; J3KNG5; Q3MHC7; Q8N2Z4
Background:
The Multifunctional methyltransferase subunit TRM112-like protein, also known as tRNA methyltransferase 112 homolog, plays a pivotal role in cellular processes through its involvement in the methylation of rRNA, tRNA, and proteins. This protein acts as an activator for both rRNA/tRNA and protein methyltransferases, participating in critical methylation reactions that include the N(7) position of guanine in 18S rRNA, N5-methylation of ETF1, monomethylation of 'Lys-12' of histone H4, and the formation of N(2)-methylguanosine in tRNA. Its activities are essential for the pre-rRNA processing steps leading to small-subunit rRNA production.
Therapeutic significance:
Understanding the role of Multifunctional methyltransferase subunit TRM112-like protein could open doors to potential therapeutic strategies.