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.
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.
We employ our advanced, specialised process to create targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The procedure entails thorough molecular simulations of the catalytic and allosteric binding pockets, accompanied by ensemble virtual screening that factors in their conformational flexibility. When developing modulators, the structural modifications brought about by reaction intermediates are factored in to optimize activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q01814
UPID:
AT2B2_HUMAN
Alternative names:
Plasma membrane calcium ATPase isoform 2; Plasma membrane calcium pump isoform 2
Alternative UPACC:
Q01814; O00766; Q12994; Q16818
Background:
Plasma membrane calcium-transporting ATPase 2, also known as Plasma membrane calcium ATPase isoform 2, plays a pivotal role in maintaining basal intracellular Ca(2+) levels in specialized cells. It is crucial for the functioning of cerebellar circuits, vestibular and cochlear systems, facilitating fast neuronal Ca(2+) dynamics, and is essential in hearing and balance. This protein mediates presynaptic Ca(2+) efflux and contributes to motor learning by controlling Ca(2+) clearance rates.
Therapeutic significance:
The protein's involvement in Deafness, autosomal dominant, 82, a form of sensorineural hearing loss, underscores its therapeutic significance. Understanding the role of Plasma membrane calcium-transporting ATPase 2 could open doors to potential therapeutic strategies for hearing loss and balance disorders.