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.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best 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 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
P43897
UPID:
EFTS_HUMAN
Alternative names:
-
Alternative UPACC:
P43897; B4E391; F5H2T7; Q561V7; Q8TBC2; Q9UQK0
Background:
Elongation factor Ts, mitochondrial (EF-Ts, mitochondrial), encoded by the gene with accession number P43897, plays a pivotal role in protein synthesis. It facilitates the exchange of GDP to GTP, remaining bound to the aminoacyl-tRNA.EF-Tu.GTP complex during the GTP hydrolysis stage on the ribosome. This process is crucial for the efficient translation of genetic information into functional proteins.
Therapeutic significance:
The protein is implicated in Combined oxidative phosphorylation deficiency 3, a mitochondrial disease characterized by severe metabolic acidosis and encephalomyopathy or hypertrophic cardiomyopathy. This association highlights the protein's potential as a target for therapeutic intervention in mitochondrial disorders.