Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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 high-tech, dedicated method is applied to construct targeted 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
O60508
UPID:
PRP17_HUMAN
Alternative names:
Cell division cycle 40 homolog; EH-binding protein 3; PRP17 homolog
Alternative UPACC:
O60508; B2RBC5; O75471; Q5SRN0; Q9UPG1
Background:
Pre-mRNA-processing factor 17, also known as Cell division cycle 40 homolog, EH-binding protein 3, and PRP17 homolog, plays a crucial role in pre-mRNA splicing as part of the activated spliceosome. Its involvement in embryonic brain development, independent of proline isomerization, underscores its significance in cellular processes.
Therapeutic significance:
The protein's link to Pontocerebellar hypoplasia 15, characterized by severe brain structural defects and impaired intellectual development, highlights its therapeutic potential. Understanding the role of Pre-mRNA-processing factor 17 could open doors to potential therapeutic strategies for this debilitating condition.