Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our top-notch dedicated system is used to design specialised 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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8WWY3
UPID:
PRP31_HUMAN
Alternative names:
Pre-mRNA-processing factor 31; Serologically defined breast cancer antigen NY-BR-99; U4/U6 snRNP 61 kDa protein
Alternative UPACC:
Q8WWY3; E7ESA8; F1T0A4; F1T0A5; Q17RB4; Q8N7F9; Q9H271; Q9Y439
Background:
U4/U6 small nuclear ribonucleoprotein Prp31, also known as Pre-mRNA-processing factor 31 and Serologically defined breast cancer antigen NY-BR-99, plays a crucial role in pre-mRNA splicing as part of the spliceosome. It is essential for the assembly of the U4/U5/U6 tri-snRNP complex, a key component of the spliceosome machinery.
Therapeutic significance:
The protein's involvement in Retinitis pigmentosa 11, a retinal dystrophy characterized by loss of vision, highlights its potential as a target for therapeutic intervention. Understanding the role of U4/U6 small nuclear ribonucleoprotein Prp31 could open doors to potential therapeutic strategies.