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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner 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.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q53GS7
UPID:
GLE1_HUMAN
Alternative names:
GLE1 RNA export mediator; GLE1-like protein; Nucleoporin GLE1
Alternative UPACC:
Q53GS7; O75458; Q53GT9; Q5VVU1; Q8NCP6; Q9UFL6
Background:
The mRNA export factor GLE1, also known as GLE1 RNA export mediator or Nucleoporin GLE1, plays a crucial role in cellular function by facilitating the export of mRNAs with poly(A) tails from the nucleus to the cytoplasm. This process is vital for the proper expression of genes and the functioning of the cell.
Therapeutic significance:
GLE1's involvement in lethal congenital contracture syndrome 1 and congenital arthrogryposis with anterior horn cell disease highlights its potential as a target for therapeutic intervention. Understanding the role of mRNA export factor GLE1 could open doors to potential therapeutic strategies for these devastating conditions.