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.
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
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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q9BQA9
UPID:
CYBC1_HUMAN
Alternative names:
Essential for reactive oxygen species protein
Alternative UPACC:
Q9BQA9; E1B6X3; Q96NR1
Background:
Cytochrome b-245 chaperone 1, alternatively known as Essential for reactive oxygen species protein, plays a pivotal role in innate immunity. It functions as a chaperone, ensuring the stable expression of the CYBA and CYBB subunits of the cytochrome b-245 heterodimer. This protein is crucial for controlling the phagocyte respiratory burst, a key defense mechanism against pathogens.
Therapeutic significance:
The protein is linked to Granulomatous disease, chronic, autosomal recessive, 5 (CGD5), characterized by severe recurrent infections and chronic granulomatous inflammation. Understanding the role of Cytochrome b-245 chaperone 1 in CGD5 could open doors to potential therapeutic strategies, offering hope for patients suffering from this debilitating condition.