Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced 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 features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We use our state-of-the-art dedicated workflow for designing focused 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 distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q96P53
UPID:
WDFY2_HUMAN
Alternative names:
Propeller-FYVE protein; WD40- and FYVE domain-containing protein 2; Zinc finger FYVE domain-containing protein 22
Alternative UPACC:
Q96P53; B1AL86; Q96CS1
Background:
WD repeat and FYVE domain-containing protein 2, also known as Propeller-FYVE protein, plays a crucial role in cellular processes. It mediates interactions between kinase PRKCZ and VAMP2, enhancing PRKCZ-dependent phosphorylation of VAMP2. This protein is instrumental in adipocyte differentiation, aiding in the phosphorylation and inactivation of FOXO1 by AKT1, and is vital for insulin-stimulated AKT2 signaling and glucose uptake.
Therapeutic significance:
Understanding the role of WD repeat and FYVE domain-containing protein 2 could open doors to potential therapeutic strategies.