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.
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 use our state-of-the-art dedicated workflow for designing 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 is unique due to several crucial aspects:
partner
Reaxense
upacc
Q9BQ87
UPID:
TBL1Y_HUMAN
Alternative names:
Transducin beta-like protein 1Y; Transducin-beta-like protein 1, Y-linked
Alternative UPACC:
Q9BQ87; A1L4B3
Background:
The F-box-like/WD repeat-containing protein TBL1Y, also known as Transducin beta-like protein 1Y, plays a pivotal role in the recruitment of the ubiquitin/19S proteasome complex to nuclear receptor-regulated transcription units. It is integral in transcription activation mediated by nuclear receptors, facilitating the proteasomal degradation of transcription repressor complexes.
Therapeutic significance:
Given its involvement in Deafness, Y-linked 2, a form of non-syndromic sensorineural hearing loss, understanding the role of TBL1Y could open doors to potential therapeutic strategies for managing this condition.