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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
The library includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
O95398
UPID:
RPGF3_HUMAN
Alternative names:
Exchange factor directly activated by cAMP 1; Exchange protein directly activated by cAMP 1; Rap1 guanine-nucleotide-exchange factor directly activated by cAMP; cAMP-regulated guanine nucleotide exchange factor I
Alternative UPACC:
O95398; A8K2G5; E7EQC8; O95634; Q8WVN0
Background:
Rap guanine nucleotide exchange factor 3, also known as Exchange factor directly activated by cAMP 1, plays a pivotal role in cellular processes by acting as a Guanine nucleotide exchange factor (GEF) for RAP1A and RAP2A small GTPases. Its activation by cAMP leads to the assembly of a signaling complex that activates the PI3K gamma complex, crucial for angiogenesis. This protein is instrumental in modulating cAMP-induced endothelial barrier function and is essential for actin rearrangement at cell-cell junctions.
Therapeutic significance:
Understanding the role of Rap guanine nucleotide exchange factor 3 could open doors to potential therapeutic strategies.