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 carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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.
We employ our advanced, specialised process to create targeted 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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8IWE4
UPID:
DCNL3_HUMAN
Alternative names:
DCUN1 domain-containing protein 3; Defective in cullin neddylation protein 1-like protein 3; Squamous cell carcinoma-related oncogene 3
Alternative UPACC:
Q8IWE4; B3KVY4
Background:
DCN1-like protein 3, known alternatively as DCUN1 domain-containing protein 3, plays a crucial role in protein neddylation, impacting cullin-RBX complexes and cell cycle progression. Its involvement in both promoting and inhibiting cullins neddylation at the cell membrane underscores its complex regulatory functions.
Therapeutic significance:
Understanding the role of DCN1-like protein 3 could open doors to potential therapeutic strategies, especially considering its pivotal role in cell cycle regulation and response to UV damage.