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 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
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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q6ZMI3
UPID:
GLDN_HUMAN
Alternative names:
-
Alternative UPACC:
Q6ZMI3; Q6UXZ7; Q7Z359
Background:
Gliomedin, a pivotal protein, facilitates the formation and maintenance of nodes of Ranvier, essential for rapid signal transmission in myelinated axons. It acts as a ligand for NRCAM and NFASC, mediating Schwann cell and axon interactions, crucial for the saltatory conduction of action potentials. Its role extends to the clustering of sodium channels, vital for neural communication.
Therapeutic significance:
Gliomedin's association with Lethal congenital contracture syndrome 11, due to gene variants, underscores its clinical importance. Understanding Gliomedin's functions could pave the way for innovative treatments for neuromuscular disorders, highlighting its therapeutic potential.