AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Adapter SH3BGRL

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

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 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.

The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.

Our top-notch dedicated system is used to design specialised libraries.

 Fig. 1. The sreening workflow of Receptor.AI

Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.

Our library stands out due to several important features:

  • The Receptor.AI platform compiles comprehensive data on the target protein, encompassing previous experiments, literature, known ligands, structural details, and more, leading to a higher chance of selecting the most relevant compounds.
  • Advanced molecular simulations on the platform help pinpoint potential binding sites, making the compounds in our focused library ideal for finding allosteric inhibitors and targeting cryptic pockets.
  • Receptor.AI boasts over 50 tailor-made AI models, rigorously tested and proven in various drug discovery projects and research initiatives. They are crafted for efficacy, dependability, and precision, all of which are key in creating our focused libraries.
  • Beyond creating focused libraries, Receptor.AI offers comprehensive services and complete solutions throughout the preclinical drug discovery phase. Our success-based pricing model minimises risk and maximises the mutual benefits of the project's success.

partner

Reaxense

upacc

O75368

UPID:

SH3L1_HUMAN

Alternative names:

SH3 domain-binding glutamic acid-rich-like protein 1

Alternative UPACC:

O75368; Q3SYL1; Q5JT50; Q6FIE8; Q9H0N8

Background:

Adapter SH3BGRL, also known as SH3 domain-binding glutamic acid-rich-like protein 1, plays a crucial role in cellular processes. It acts as an adapter protein, facilitating interactions between proteins or proteins and mRNAs, as evidenced by research findings (PubMed:34331014). Furthermore, SH3BGRL is implicated in ubiquitin ligase-substrate adapter activity and associates with cytoplasmic ribosomes to enhance the expression of specific mRNAs (PubMed:34331014, PubMed:34870550).

Therapeutic significance:

Understanding the role of Adapter SH3BGRL could open doors to potential therapeutic strategies.

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