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 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.
We employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q9NRR6
UPID:
INP5E_HUMAN
Alternative names:
72 kDa inositol polyphosphate 5-phosphatase; Inositol polyphosphate-5-phosphatase E; Phosphatidylinositol 4,5-bisphosphate 5-phosphatase; Phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase
Alternative UPACC:
Q9NRR6; Q15734; Q6PIV5
Background:
The Phosphatidylinositol polyphosphate 5-phosphatase type IV, known by alternative names such as 72 kDa inositol polyphosphate 5-phosphatase, plays a pivotal role in lipid signaling pathways. It specifically hydrolyzes the 5-phosphate groups of various phosphatidylinositols, crucial for cellular processes. Its activity is essential for controlling ciliary growth and stability, highlighting its significance in cellular signaling and structure.
Therapeutic significance:
Linked to Joubert syndrome 1 and a disorder characterized by intellectual disability, truncal obesity, and retinal dystrophy, this protein's dysfunction underscores its potential as a therapeutic target. Understanding the role of Phosphatidylinositol polyphosphate 5-phosphatase type IV could open doors to potential therapeutic strategies for these conditions.