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 effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q8TC44
UPID:
POC1B_HUMAN
Alternative names:
Pix1; Proteome of centriole protein 1B; WD repeat-containing protein 51B
Alternative UPACC:
Q8TC44; G3V1X0
Background:
POC1 centriolar protein homolog B (POC1B) is pivotal in centriole assembly and stability, playing a crucial role in ciliogenesis, centriole duplication, and length control. It works alongside POC1A to maintain centriole integrity, ensuring proper mitotic spindle formation. POC1B is essential for primary cilia formation, ciliary length, cell proliferation, and maintaining retinal integrity.
Therapeutic significance:
POC1B's involvement in Cone-rod dystrophy 20, a retinal dystrophy leading to severe vision loss, underscores its therapeutic potential. Understanding POC1B's role could pave the way for innovative treatments targeting retinal degenerative diseases.