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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
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
Q9BRT3
UPID:
MIEN1_HUMAN
Alternative names:
HBV X-transactivated gene 4 protein; HBV XAg-transactivated protein 4; Protein C35
Alternative UPACC:
Q9BRT3
Background:
Migration and invasion enhancer 1, also known as HBV X-transactivated gene 4 protein, HBV XAg-transactivated protein 4, and Protein C35, plays a pivotal role in cellular processes. It enhances cell migration by promoting filopodia formation at the leading edge of migrating cells, regulates apoptosis potentially through CASP3 control, and may participate in redox-related processes.
Therapeutic significance:
Understanding the role of Migration and invasion enhancer 1 could open doors to potential therapeutic strategies.