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.
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.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q15437
UPID:
SC23B_HUMAN
Alternative names:
SEC23-related protein B
Alternative UPACC:
Q15437; D3DW33; Q503A9; Q5W183; Q9BS15; Q9BSI2; Q9H1D7
Background:
Protein transport protein Sec23B, also known as SEC23-related protein B, plays a pivotal role in cellular transport mechanisms. It is a crucial component of the coat protein complex II (COPII), which is instrumental in the formation of transport vesicles from the endoplasmic reticulum (ER). This process is essential for the physical deformation of the ER membrane into vesicles and the selection of cargo molecules for their transport to the Golgi complex.
Therapeutic significance:
Sec23B's involvement in Cowden syndrome 7 and congenital dyserythropoietic anemia type 2 highlights its potential as a target for therapeutic intervention. Understanding the role of Protein transport protein Sec23B could open doors to potential therapeutic strategies, particularly in addressing the underlying genetic variants that contribute to these diseases.