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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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 utilise our cutting-edge, exclusive workflow to develop focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The method includes detailed molecular simulations of the catalytic and allosteric binding pockets, along with ensemble virtual screening that considers their conformational flexibility. In the design of modulators, structural changes induced by reaction intermediates are taken into account to enhance activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q8TE96
UPID:
DQX1_HUMAN
Alternative names:
DEAQ box polypeptide 1
Alternative UPACC:
Q8TE96; Q6B017; Q8NAM8
Background:
ATP-dependent RNA helicase DQX1, also known as DEAQ box polypeptide 1, plays a crucial role in RNA metabolism, impacting processes such as RNA splicing, ribosome biogenesis, and the initiation of translation. Its ability to remodel RNA-RNA, DNA-RNA, and protein-RNA complexes underlines its importance in cellular homeostasis and gene expression regulation.
Therapeutic significance:
Understanding the role of ATP-dependent RNA helicase DQX1 could open doors to potential therapeutic strategies. Its pivotal function in RNA metabolism suggests that modulation of its activity could have far-reaching implications for diseases where RNA processing is disrupted.