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 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.
We employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q14738
UPID:
2A5D_HUMAN
Alternative names:
PP2A B subunit isoform B'-delta; PP2A B subunit isoform B56-delta; PP2A B subunit isoform PR61-delta; PP2A B subunit isoform R5-delta
Alternative UPACC:
Q14738; A8K3I9; B5BUA6; O00494; O00696; Q15171; Q5TC39
Background:
Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform, known by alternative names such as PP2A B subunit isoform B'-delta, plays a crucial role in modulating substrate selectivity, catalytic activity, and subcellular compartment localization of the catalytic enzyme. This protein's multifaceted role underscores its significance in cellular processes.
Therapeutic significance:
Linked to Intellectual developmental disorder, autosomal dominant 35, this protein's involvement in disease pathways highlights its potential as a target for therapeutic intervention. Understanding the role of Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform could open doors to potential therapeutic strategies.