AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Type 2 DNA topoisomerase 6 subunit B-like

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

Explore the Potential with AI-Driven Innovation

The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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.

Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.

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

Q8N6T0

UPID:

TO6BL_HUMAN

Alternative names:

TOP6B like initiator of meiotic double strand breaks; Type 2 DNA topoisomerase VI subunit B-like

Alternative UPACC:

Q8N6T0; Q9H677

Background:

Type 2 DNA topoisomerase 6 subunit B-like, also known as TOP6B like initiator of meiotic double strand breaks, plays a crucial role in meiotic recombination. It is a component of a topoisomerase 6 complex that, alongside SPO11, mediates DNA cleavage forming double-strand breaks essential for initiating meiotic recombination. This process facilitates the relaxation and decatenation of DNA through cleavage and ligation cycles.

Therapeutic significance:

The protein's involvement in Hydatidiform mole, recurrent, 4, a disorder characterized by abnormal pregnancies, underscores its potential as a target for therapeutic intervention. Understanding the role of Type 2 DNA topoisomerase 6 subunit B-like could open doors to potential therapeutic strategies.

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