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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner 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 high-tech, dedicated method is applied to construct targeted 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q969T9
UPID:
WBP2_HUMAN
Alternative names:
-
Alternative UPACC:
Q969T9; B4DFG2; O95638
Background:
WW domain-binding protein 2 (WWBP2) plays a pivotal role as a transcriptional coactivator of hormone receptors such as estrogen and progesterone. It activates these receptors upon hormone binding, influencing the expression of genes involved in various cellular processes. WWBP2's interaction with YAP1 and WBP2 enhances progesterone receptor activity, further modulating the expression of key post-synaptic scaffolding proteins.
Therapeutic significance:
The association of WW domain-binding protein 2 with autosomal recessive deafness, 107, underscores its clinical relevance. Understanding the role of WWBP2 could open doors to potential therapeutic strategies for sensorineural hearing loss, a condition resulting from damage to the inner ear or its neural pathways.