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.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
P61289
UPID:
PSME3_HUMAN
Alternative names:
11S regulator complex subunit gamma; Activator of multicatalytic protease subunit 3; Ki nuclear autoantigen; Proteasome activator 28 subunit gamma
Alternative UPACC:
P61289; A8K9A3; O35563; P97373; Q12920; Q13172; Q9BQD9
Background:
Proteasome activator complex subunit 3, also known as 11S regulator complex subunit gamma, plays a pivotal role in proteasome regulation. It forms a homoheptamer, activating the proteasome's trypsin-like subunit while inhibiting others, crucial for protein degradation. This protein is instrumental in the MDM2-p53/TP53 interaction, facilitating p53/TP53 degradation, impacting apoptosis post-DNA damage, and is implicated in cell cycle regulation and SIRT1 inhibition.
Therapeutic significance:
Understanding the role of Proteasome activator complex subunit 3 could open doors to potential therapeutic strategies.