Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
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 distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9H6K4
UPID:
OPA3_HUMAN
Alternative names:
-
Alternative UPACC:
Q9H6K4; Q6P384; Q8N784
Background:
The Optic atrophy 3 protein, encoded by the gene with accession number Q9H6K4, is implicated in mitochondrial processes. This protein's involvement in the mitochondrial function suggests a critical role in cellular energy management and apoptosis. The protein is associated with diseases such as 3-methylglutaconic aciduria 3 and Optic atrophy 3, both of which affect the nervous system and vision.
Therapeutic significance:
Given its association with neuro-ophthalmologic disorders, targeting the Optic atrophy 3 protein could lead to innovative treatments for 3-methylglutaconic aciduria 3 and Optic atrophy 3. These conditions, characterized by optic atrophy, spasticity, and cognitive deficits, highlight the protein's potential as a therapeutic target.