Focused On-demand Library for E3 ubiquitin-protein ligase TRIM68

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 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

The procedure entails thorough molecular simulations of the catalytic and allosteric binding pockets, accompanied by ensemble virtual screening that factors in their conformational flexibility. When developing modulators, the structural modifications brought about by reaction intermediates are factored in to optimize activity and selectivity.

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.







Alternative names:

RING finger protein 137; RING-type E3 ubiquitin transferase TRIM68; SSA protein SS-56; Tripartite motif-containing protein 68

Alternative UPACC:

Q6AZZ1; A6NI19; A8K551; B3KPM5; B4DVK4; Q8WZ70; Q96LE5; Q96PF7; Q9H9C2; Q9NW18


E3 ubiquitin-protein ligase TRIM68, known by alternative names such as RING finger protein 137 and Tripartite motif-containing protein 68, plays a crucial role as a ubiquitin E3 ligase. It functions as a coactivator of the androgen receptor (AR), leveraging its ubiquitin ligase activity to regulate protein stability and function.

Therapeutic significance:

Understanding the role of E3 ubiquitin-protein ligase TRIM68 could open doors to potential therapeutic strategies. Its involvement in protein ubiquitination suggests a pivotal role in cellular processes, making it a target of interest in drug discovery.

Looking for more information on this library or underlying technology? Fill out the form below and we'll be in touch with all the details you need.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
No Spam. Cancel Anytime.