Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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.
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 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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q5TAX3
UPID:
TUT4_HUMAN
Alternative names:
Zinc finger CCHC domain-containing protein 11
Alternative UPACC:
Q5TAX3; A2RRP0; B7Z8J5; D3DQ35; Q12764; Q5TAX2; Q5TAX4; Q86XZ3
Background:
Terminal uridylyltransferase 4, also known as Zinc finger CCHC domain-containing protein 11, plays a pivotal role in mRNA decay, oocyte maturation, fertility, and microRNA (miRNA) regulation. It facilitates the degradation of mRNAs with short poly(A) tails and is involved in miRNA-induced gene silencing. This protein is essential for sculpting the maternal transcriptome by eliminating transcripts during oocyte growth and acts as a suppressor of miRNA biogenesis by mediating the terminal uridylation of some miRNA precursors.
Therapeutic significance:
Understanding the role of Terminal uridylyltransferase 4 could open doors to potential therapeutic strategies.