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.
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.
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 top-notch dedicated system is used to design specialised libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
This approach involves comprehensive molecular simulations of the catalytic and allosteric binding pockets and ensemble virtual screening that accounts for their conformational flexibility. In the case of designing modulators, the structural adjustments caused by reaction intermediates are considered to improve activity and selectivity.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
O15357
UPID:
SHIP2_HUMAN
Alternative names:
Inositol polyphosphate phosphatase-like protein 1; Protein 51C; SH2 domain-containing inositol 5'-phosphatase 2
Alternative UPACC:
O15357; B2RTX5; Q13577; Q13578
Background:
Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2, also known as Inositol polyphosphate phosphatase-like protein 1, plays a pivotal role in cellular processes including mitotic spindle orientation, insulin signaling, and actin cytoskeleton remodeling. It acts by hydrolyzing PtdIns(3,4,5)P3 to PtdIns(3,4)P2, regulating the PI3K pathways and affecting various signaling pathways crucial for cell function.
Therapeutic significance:
Given its central role in insulin signaling and actin cytoskeleton remodeling, this protein is implicated in Type 2 diabetes mellitus and Opsismodysplasia. Understanding its function could lead to novel therapeutic strategies for these conditions, highlighting its potential as a target for drug discovery.