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 pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal 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
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
O43665
UPID:
RGS10_HUMAN
Alternative names:
-
Alternative UPACC:
O43665; A8K408; B1AMR8; Q6IAZ6; Q96GN0
Background:
Regulator of G-protein signaling 10 (RGS10) plays a pivotal role in modulating G protein-coupled receptor (GPCR) signaling pathways. Specifically, it regulates signaling cascades downstream of the muscarinic acetylcholine receptor CHRM2 by enhancing the GTPase activity of G protein alpha subunits, leading to their inactivation. Additionally, RGS10 modulates potassium channel activity in response to CHRM2 signaling, highlighting its intricate role in cellular signaling mechanisms.
Therapeutic significance:
Understanding the role of Regulator of G-protein signaling 10 could open doors to potential therapeutic strategies. Its involvement in critical signaling pathways suggests that modulating its activity could offer new avenues for treating diseases linked to GPCR dysregulation.