Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
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
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q9P2L0
UPID:
WDR35_HUMAN
Alternative names:
Intraflagellar transport protein 121 homolog
Alternative UPACC:
Q9P2L0; B3KVI5; Q4ZG01; Q8NE11
Background:
WD repeat-containing protein 35, also known as Intraflagellar transport protein 121 homolog, plays a crucial role in ciliogenesis and ciliary protein trafficking. It is a part of the IFT complex A, essential for retrograde ciliary transport and the entry of G protein-coupled receptors into cilia. This protein's involvement in CASP3 activation and TNF-stimulated apoptosis highlights its multifaceted role in cellular processes.
Therapeutic significance:
WD repeat-containing protein 35 is implicated in several genetic disorders, including Cranioectodermal dysplasia 2 and Short-rib thoracic dysplasia 7, both characterized by skeletal and ectodermal abnormalities. Understanding the role of this protein could open doors to potential therapeutic strategies for these ciliopathies, emphasizing the importance of targeted research in this area.