Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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 employ our advanced, specialised process to create targeted 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
Q15438
UPID:
CYH1_HUMAN
Alternative names:
PH, SEC7 and coiled-coil domain-containing protein 1; SEC7 homolog B2-1
Alternative UPACC:
Q15438; A6NFW7; B7Z1T4; Q9P123; Q9P124
Background:
Cytohesin-1, also known as PH, SEC7 and coiled-coil domain-containing protein 1 or SEC7 homolog B2-1, plays a pivotal role in cellular processes by promoting guanine-nucleotide exchange on ARF1, ARF5, and ARF6. This action facilitates the activation of ARF factors, crucial for membrane trafficking, junctional remodeling, and epithelial polarization through the regulation of ARF6 activity.
Therapeutic significance:
Understanding the role of Cytohesin-1 could open doors to potential therapeutic strategies.