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.
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 includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
We utilise our cutting-edge, exclusive workflow to develop focused 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.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
P25787
UPID:
PSA2_HUMAN
Alternative names:
Macropain subunit C3; Multicatalytic endopeptidase complex subunit C3; Proteasome component C3
Alternative UPACC:
P25787; Q6ICS6; Q9BU45
Background:
Proteasome subunit alpha type-2, known as Macropain subunit C3, plays a crucial role in the proteolytic degradation of intracellular proteins. It forms part of the 20S core proteasome complex, essential for cellular function by maintaining protein homeostasis. This complex is pivotal in removing misfolded or damaged proteins and those no longer needed, through ATP-dependent and independent pathways.
Therapeutic significance:
Understanding the role of Proteasome subunit alpha type-2 could open doors to potential therapeutic strategies. Its involvement in protein homeostasis and degradation pathways highlights its importance in cellular health and disease prevention.