Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced activity, selectivity, and safety.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q8NEZ3
UPID:
WDR19_HUMAN
Alternative names:
Intraflagellar transport 144 homolog
Alternative UPACC:
Q8NEZ3; B5MEF2; Q8N5B4; Q9H5S0; Q9HCD4
Background:
WD repeat-containing protein 19, also known as Intraflagellar transport 144 homolog, plays a crucial role in ciliary function and assembly. It is a key component of the IFT complex A, essential for retrograde ciliary transport and the entry of G protein-coupled receptors into cilia. This protein's association with the BBSome complex further underscores its significance in mediating ciliary transport.
Therapeutic significance:
Given its involvement in a spectrum of genetic disorders, including Cranioectodermal dysplasia 4, Short-rib thoracic dysplasia 5, Nephronophthisis 13, Senior-Loken syndrome 8, and Spermatogenic failure 72, WD repeat-containing protein 19 represents a promising target for therapeutic intervention. Understanding its role could open doors to potential therapeutic strategies for these ciliopathies and male infertility disorders.