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.
We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
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.
Our top-notch dedicated system is used to design specialised 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.
Key features that set our library apart include:
partner
Reaxense
upacc
P52298
UPID:
NCBP2_HUMAN
Alternative names:
20 kDa nuclear cap-binding protein; Cell proliferation-inducing gene 55 protein; NCBP 20 kDa subunit; NCBP-interacting protein 1
Alternative UPACC:
P52298; B2RE91; B4DMK7; E9PAR5; Q14924; Q2TS50
Background:
Nuclear cap-binding protein subunit 2, also known as NCBP 20 kDa subunit, plays a pivotal role in RNA metabolism, including pre-mRNA splicing, translation regulation, and mRNA export. It forms part of the cap-binding complex (CBC), essential for mRNA export from the nucleus and a pioneer round of mRNA translation critical for nonsense-mediated mRNA decay (NMD). Additionally, it participates in microRNA biogenesis and acts as a negative regulator of mRNA deadenylation.
Therapeutic significance:
Understanding the role of Nuclear cap-binding protein subunit 2 could open doors to potential therapeutic strategies.