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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed 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.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9Y272
UPID:
RASD1_HUMAN
Alternative names:
Activator of G-protein signaling 1
Alternative UPACC:
Q9Y272; B2R709; B4DFF4; Q9NYB4
Background:
Dexamethasone-induced Ras-related protein 1, also known as Activator of G-protein signaling 1, plays a pivotal role in cellular processes by negatively regulating the transcription regulation activity of the APBB1/FE65-APP complex through its interaction with APBB1/FE65. This small GTPase's function is crucial for understanding cellular signaling pathways and their regulation.
Therapeutic significance:
Understanding the role of Dexamethasone-induced Ras-related protein 1 could open doors to potential therapeutic strategies. Its involvement in key cellular signaling pathways suggests that targeting this protein could offer new avenues for intervention in diseases where these pathways are dysregulated.