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 carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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 utilise our cutting-edge, exclusive workflow to develop focused 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q9UPY8
UPID:
MARE3_HUMAN
Alternative names:
EB1 protein family member 3; End-binding protein 3; RP3
Alternative UPACC:
Q9UPY8; B7WPK5; O00265; Q6FHB0; Q6FI15; Q9BZP7; Q9BZP8
Background:
Microtubule-associated protein RP/EB family member 3, also known as EB1 protein family member 3, End-binding protein 3, and RP3, plays a pivotal role in microtubule dynamics. It binds to microtubule plus-ends, promoting their growth and regulating cytoskeleton dynamics. This protein is crucial for spindle function, microtubule stabilization, and anchoring at centrosomes. It also orchestrates minus-end microtubule organization by interacting with AKAP9 and PDE4DIP, facilitating CAMSAP2 recruitment to the Golgi apparatus, essential for polarized cell movement.
Therapeutic significance:
Understanding the role of Microtubule-associated protein RP/EB family member 3 could open doors to potential therapeutic strategies.