Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q96RP9
UPID:
EFGM_HUMAN
Alternative names:
Elongation factor G 1, mitochondrial; Elongation factor G1
Alternative UPACC:
Q96RP9; A6NCI9; B2RCB9; B3KRW1; Q6GTN2; Q96T39
Background:
Elongation factor G, mitochondrial, also known as Elongation factor G1, plays a pivotal role in mitochondrial protein biosynthesis. It is a mitochondrial GTPase that facilitates the GTP-dependent ribosomal translocation step during translation elongation, ensuring the proper movement of tRNA molecules, mRNA, and conformational changes in the ribosome.
Therapeutic significance:
The protein is linked to Combined oxidative phosphorylation deficiency 1, a mitochondrial disease characterized by early, rapidly progressive hepatoencephalopathy. Understanding the role of Elongation factor G, mitochondrial could open doors to potential therapeutic strategies for this condition.