Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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 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 employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q96EY7
UPID:
PTCD3_HUMAN
Alternative names:
28S ribosomal protein S39, mitochondrial; Pentatricopeptide repeat domain-containing protein 3, mitochondrial; Transformation-related gene 15 protein
Alternative UPACC:
Q96EY7; A6NHD2; D6W5M1; Q597H0; Q658Y9; Q9BUZ8; Q9NWL0
Background:
Small ribosomal subunit protein mS39, also known as 28S ribosomal protein S39, mitochondrial, Pentatricopeptide repeat domain-containing protein 3, mitochondrial, and Transformation-related gene 15 protein, plays a crucial role in mitochondrial translation. Its function as a mitochondrial RNA-binding protein underscores its importance in the synthesis of proteins within mitochondria, essential for cellular energy production.
Therapeutic significance:
Given its involvement in Combined oxidative phosphorylation deficiency 51, a disorder marked by mitochondrial dysfunction, the study of Small ribosomal subunit protein mS39 offers a promising avenue for therapeutic intervention. Understanding its role could pave the way for novel treatments targeting mitochondrial diseases, enhancing patient outcomes.