AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Polycomb group RING finger protein 2

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 use our state-of-the-art dedicated workflow for designing focused 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:

  • The Receptor.AI platform integrates all available data about the target protein, including past experiments, literature data, known ligands, structural information and more. This consolidated approach maximises the probability of prioritising highly relevant compounds.
  • The platform uses sophisticated molecular simulations to identify possible binding sites so that the compounds in the focused library are suitable for discovering allosteric inhibitors and the binders for cryptic pockets.
  • The platform integrates over 50 highly customisable AI models, which are thoroughly tested and validated on a multitude of commercial drug discovery programs and research projects. It is designed to be efficient, reliable and accurate. All this power is utilised when producing the focused libraries.
  • In addition to producing the focused libraries, Receptor.AI provides services and end-to-end solutions at every stage of preclinical drug discovery. The pricing model is success-based, which reduces your risks and leverages the mutual benefits of the project's success.

partner

Reaxense

upacc

P35227

UPID:

PCGF2_HUMAN

Alternative names:

DNA-binding protein Mel-18; RING finger protein 110; Zinc finger protein 144

Alternative UPACC:

P35227; A6NGD8

Background:

Polycomb group RING finger protein 2, also known as Mel-18 and RING finger protein 110, plays a pivotal role in transcriptional repression, binding specifically to DNA sequences to regulate cell proliferation and neural development. It is a key component of the Polycomb group (PcG) multiprotein PRC1-like complex, crucial for maintaining genes in a transcriptionally repressive state through chromatin remodeling and histone modification.

Therapeutic significance:

The protein's involvement in Turnpenny-Fry syndrome, characterized by a spectrum of developmental anomalies, underscores its clinical relevance. Understanding the role of Polycomb group RING finger protein 2 could open doors to potential therapeutic strategies for managing this syndrome and related developmental disorders.

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