Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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.
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
Q9C0B2
UPID:
CFA74_HUMAN
Alternative names:
-
Alternative UPACC:
Q9C0B2; A4VCI2; H7C4E1; Q5T2D9; Q5T2E0; Q69YW0; Q6ZSJ4
Background:
Cilia- and flagella-associated protein 74 plays a crucial role in the movement of cilia and flagella, essential for cell motility and fluid flow across cell surfaces. This protein is integral to the central apparatus of the cilium axoneme, contributing to the precise architecture and function of sperm, as well as respiratory cilia.
Therapeutic significance:
Given its pivotal role in primary ciliary dyskinesia, particularly Ciliary dyskinesia, primary, 49, without situs inversus, understanding the function and mechanisms of Cilia- and flagella-associated protein 74 could pave the way for innovative treatments. Targeting the protein's function may offer new therapeutic avenues for managing respiratory infections and infertility associated with this condition.