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:
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.