Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced 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.
Our high-tech, dedicated method is applied to construct targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes in-depth molecular simulations of both the catalytic and allosteric binding pockets, with ensemble virtual screening focusing on their conformational flexibility. For modulators, the process includes considering the structural shifts due to reaction intermediates to boost activity and selectivity.
Key features that set our library apart include:
partner
Reaxense
upacc
Q9BVQ7
UPID:
AFG2B_HUMAN
Alternative names:
AFG2 AAA ATPase homolog B; Ribosome biogenesis protein SPATA5L1; Spermatogenesis-associated protein 5-like protein 1
Alternative UPACC:
Q9BVQ7; C9JHR5; Q9H8W7; Q9HA41
Background:
ATPase family gene 2 protein homolog B, also known as AFG2 AAA ATPase homolog B, Ribosome biogenesis protein SPATA5L1, and Spermatogenesis-associated protein 5-like protein 1, is pivotal in the cytoplasmic maturation of pre-60S ribosomal particles. It facilitates the release of RSL24D1/RLP24, working alongside AFG2A, AIRIM, and CINP.
Therapeutic significance:
Linked to Deafness, autosomal recessive, 119, and Neurodevelopmental disorder with hearing loss and spasticity, understanding ATPase family gene 2 protein homolog B's role could unveil new therapeutic strategies.