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.
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 strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
P78406
UPID:
RAE1L_HUMAN
Alternative names:
Rae1 protein homolog; mRNA-associated protein mrnp 41
Alternative UPACC:
P78406; A8K882; O15306; Q3SYL7; Q5TCH8; Q6V708; Q9H100; Q9NQM6
Background:
The mRNA export factor RAE1, also known as Rae1 protein homolog and mRNA-associated protein mrnp 41, is pivotal in nucleocytoplasmic transport, as evidenced by its role in mRNA export (PubMed:33849972, PubMed:20498086). Additionally, RAE1 contributes to mitotic bipolar spindle formation and may facilitate the attachment of cytoplasmic mRNPs to the cytoskeleton (PubMed:17172455).
Therapeutic significance:
Understanding the role of mRNA export factor RAE1 could open doors to potential therapeutic strategies.