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.
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 includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal 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
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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q92901
UPID:
RL3L_HUMAN
Alternative names:
60S ribosomal protein L3-like; Large ribosomal subunit protein uL3-like
Alternative UPACC:
Q92901
Background:
The Ribosomal protein uL3-like, known alternatively as 60S ribosomal protein L3-like or Large ribosomal subunit protein uL3-like, plays a pivotal role in the synthesis of proteins within the cell. Specifically, it is a heart- and skeletal muscle-specific component of the ribosome, crucial for regulating muscle function. This protein uniquely replaces the RPL3 paralog in the ribosome of striated muscle cells, highlighting its specialized function in muscle tissue.
Therapeutic significance:
Given its involvement in Cardiomyopathy, dilated, 2D, a severe disorder marked by ventricular dilation, impaired systolic function, and an elevated risk of premature death, the Ribosomal protein uL3-like represents a significant target for therapeutic intervention. Understanding the role of Ribosomal protein uL3-like could open doors to potential therapeutic strategies, particularly for treating severe forms of cardiomyopathy with neonatal onset.