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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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 use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q969S9
UPID:
RRF2M_HUMAN
Alternative names:
Elongation factor G 2, mitochondrial; Elongation factor G2
Alternative UPACC:
Q969S9; A0AR28; Q8N6D8; Q8WYI0; Q9H6Z1
Background:
Ribosome-releasing factor 2, mitochondrial, also known as Elongation factor G2, plays a crucial role in mitochondrial protein biosynthesis. It mediates the disassembly of ribosomes from messenger RNA post-translation, in collaboration with MRRF, ensuring efficient mitochondrial function.
Therapeutic significance:
Linked to Combined oxidative phosphorylation deficiency 39, a disorder stemming from mitochondrial dysfunction, understanding Ribosome-releasing factor 2's role could open doors to potential therapeutic strategies.