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.
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.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q10570
UPID:
CPSF1_HUMAN
Alternative names:
Cleavage and polyadenylation specificity factor 160 kDa subunit
Alternative UPACC:
Q10570; Q96AF0
Background:
The Cleavage and polyadenylation specificity factor subunit 1, also known as the 160 kDa subunit, plays a pivotal role in pre-mRNA 3'-end formation. It recognizes the AAUAAA signal sequence, interacting with poly(A) polymerase and other factors for cleavage and poly(A) addition. This subunit is crucial in the RNA recognition step of the polyadenylation reaction, with implications in eye morphogenesis and retinal ganglion cell projection development.
Therapeutic significance:
Linked to Myopia 27, autosomal dominant, this protein's mutation affects early-onset high myopia, characterized by increased axial lengths and specific fundus changes. Understanding the role of Cleavage and polyadenylation specificity factor subunit 1 could open doors to potential therapeutic strategies for myopia and related visual impairments.