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.
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.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our high-tech, dedicated method is applied to construct targeted 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
O43924
UPID:
PDE6D_HUMAN
Alternative names:
Protein p17
Alternative UPACC:
O43924; O43250
Background:
Protein p17, also known as Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta, plays a crucial role in cellular processes through the modulation of prenylated or palmitoylated Ras family members. It is instrumental in promoting the release of target proteins from cellular membranes, thereby influencing their subcellular localization. This protein is vital for the proper targeting of farnesylated proteins to cilia, exemplified by its interaction with INPP5E.
Therapeutic significance:
Joubert syndrome 22, a disorder characterized by cerebellar ataxia, oculomotor apraxia, and other neurological symptoms, is linked to variants affecting this protein's gene. Understanding the role of Protein p17 could open doors to potential therapeutic strategies for this and related ciliopathies.