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.
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.
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 employ our advanced, specialised process to create targeted 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P20337
UPID:
RAB3B_HUMAN
Alternative names:
-
Alternative UPACC:
P20337; Q5VUL2; Q9BSI1
Background:
Ras-related protein Rab-3B plays a crucial role in protein transport, facilitating vesicular traffic within cells. This protein is part of the Rab family, known for its significance in intracellular transport mechanisms.
Therapeutic significance:
Understanding the role of Ras-related protein Rab-3B could open doors to potential therapeutic strategies. Its involvement in cellular transport processes makes it a candidate for research in diseases where these pathways are disrupted.