Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced 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 use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
O14966
UPID:
RAB7L_HUMAN
Alternative names:
Rab-7-like protein 1; Ras-related protein Rab-29
Alternative UPACC:
O14966; B4E1K3; C9JE77
Background:
Ras-related protein Rab-7L1, also known as Rab-7-like protein 1 or Ras-related protein Rab-29, plays a pivotal role in vesicle trafficking, ensuring the integrity of the endosome-trans-Golgi network. It is involved in the retrograde trafficking pathway, crucial for recycling proteins between lysosomes and the Golgi apparatus. Rab-7L1's interaction with LRRK2 enhances kinase activity, contributing to neuronal process morphology and potentially influencing typhoid toxin transport during Salmonella enterica infections.
Therapeutic significance:
Understanding the role of Ras-related protein Rab-7L1 could open doors to potential therapeutic strategies.