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.
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.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
P63121
UPID:
VP113_HUMAN
Alternative names:
HERV-K113 envelope protein; HERV-K_19p13.11 provirus ancestral Pro protein; Protease; Proteinase
Alternative UPACC:
P63121
Background:
The Endogenous retrovirus group K member 113 Pro protein, known by alternative names such as HERV-K113 envelope protein and HERV-K_19p13.11 provirus ancestral Pro protein, plays a crucial role in the life cycle of retroviruses. It is involved in the processing of primary translation products and the maturation of the viral particle, indicating its pivotal role in viral replication and assembly.
Therapeutic significance:
Understanding the role of Endogenous retrovirus group K member 113 Pro protein could open doors to potential therapeutic strategies. Its involvement in viral maturation processes makes it a target for antiviral drug development, offering a promising avenue for therapeutic intervention in diseases caused by retroviruses.