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.
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 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.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q4LDG9
UPID:
DNAL1_HUMAN
Alternative names:
-
Alternative UPACC:
Q4LDG9; B2RD38; Q5JPB7; Q9BS43
Background:
Dynein axonemal light chain 1 plays a crucial role in ciliary motility, essential for respiratory health and embryonic development. It is a key component of the outer arm dynein, which drives the force for cilia movement. This protein's function is vital for the airways' ciliary operation and for establishing the body's left-right asymmetry.
Therapeutic significance:
Mutations in Dynein axonemal light chain 1 are linked to Primary Ciliary Dyskinesia 16, a condition marked by respiratory infections and potential fertility issues. Understanding its role could lead to novel treatments for this and related ciliary disorders.