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 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.
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 employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
P61218
UPID:
RPAB2_HUMAN
Alternative names:
DNA-directed RNA polymerase II subunit F; DNA-directed RNA polymerases I, II, and III 14.4 kDa polypeptide; RPABC14.4; RPB6 homolog; RPC15
Alternative UPACC:
P61218; P41584; Q6IAY3
Background:
DNA-directed RNA polymerases I, II, and III subunit RPABC2, also known as DNA-directed RNA polymerase II subunit F, plays a pivotal role in the transcription of DNA into RNA, utilizing ribonucleoside triphosphates. It is a crucial component of RNA polymerases I, II, and III, which are responsible for synthesizing ribosomal RNA precursors, mRNA precursors, functional non-coding RNAs, and small RNAs such as 5S rRNA and tRNAs. The protein is part of the clamp element in Pol II, contributing to the formation of a pocket essential for binding the RPB4-RPB7 subcomplex.
Therapeutic significance:
Understanding the role of DNA-directed RNA polymerases I, II, and III subunit RPABC2 could open doors to potential therapeutic strategies.