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.
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.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We employ our advanced, specialised process to create 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P14678
UPID:
RSMB_HUMAN
Alternative names:
Sm protein B/B'
Alternative UPACC:
P14678; Q15490; Q6IB35; Q9UIS5
Background:
Small nuclear ribonucleoprotein-associated proteins B and B', also known as Sm protein B/B', play a crucial role in pre-mRNA splicing. They are core components of the spliceosomal U1, U2, U4, and U5 small nuclear ribonucleoproteins (snRNPs), essential for the spliceosome's assembly and function. These proteins are involved in the splicing of U12-type introns and in histone pre-mRNA 3'-end processing, highlighting their importance in RNA metabolism.
Therapeutic significance:
The association of Small nuclear ribonucleoprotein-associated proteins B and B' with Cerebrocostomandibular syndrome, a condition marked by severe micrognathia, rib defects, and intellectual disability, underscores their potential as targets for therapeutic intervention. Understanding the role of these proteins could open doors to potential therapeutic strategies.