AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Phosphatidylinositol polyphosphate 5-phosphatase type IV

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

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:

  • Receptor.AI compiles all relevant data on the target protein, such as past experimental results, literature findings, known ligands, and structural data, thereby enhancing the likelihood of focusing on the most significant compounds.
  • By utilizing advanced molecular simulations, the platform is adept at locating potential binding sites, rendering the compounds in the focused library well-suited for unearthing allosteric inhibitors and binders for hidden pockets.
  • The platform is supported by more than 50 highly specialized AI models, all of which have been rigorously tested and validated in diverse drug discovery and research programs. Its design emphasizes efficiency, reliability, and accuracy, crucial for producing focused libraries.
  • Receptor.AI extends beyond just creating focused libraries; it offers a complete spectrum of services and solutions during the preclinical drug discovery phase, with a success-dependent pricing strategy that reduces risk and fosters shared success in the project.

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.

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