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.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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
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
Q3MUY2
UPID:
PIGY_HUMAN
Alternative names:
Phosphatidylinositol-glycan biosynthesis class Y protein
Alternative UPACC:
Q3MUY2
Background:
The Phosphatidylinositol N-acetylglucosaminyltransferase subunit Y, also known as Phosphatidylinositol-glycan biosynthesis class Y protein, plays a crucial role in the glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex. This complex is responsible for the transfer of N-acetylglucosamine to phosphatidylinositol, marking the first step in GPI biosynthesis, essential for cell surface molecule anchoring.
Therapeutic significance:
Linked to Hyperphosphatasia with impaired intellectual development syndrome 6, this protein's dysfunction underscores the importance of GPI biosynthesis in human health. Understanding its role could pave the way for innovative treatments targeting GPI-anchor related disorders.