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.
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
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.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9NVN8
UPID:
GNL3L_HUMAN
Alternative names:
-
Alternative UPACC:
Q9NVN8
Background:
The Guanine nucleotide-binding protein-like 3-like protein, identified by the accession number Q9NVN8, plays a crucial role in cellular processes. It stabilizes TERF1 telomeric association, preventing TERF1's ubiquitination and proteasomal degradation by interfering with its binding to FBXO4 E3 ubiquitin-protein ligase. This protein is essential for cell proliferation, facilitating the metaphase-to-anaphase transition during mitosis. Additionally, it stabilizes MDM2 protein, indirectly influencing TP53 activity, and is involved in the processing of ribosomal pre-rRNA.
Therapeutic significance:
Understanding the role of Guanine nucleotide-binding protein-like 3-like protein could open doors to potential therapeutic strategies.