Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved 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.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
Our high-tech, dedicated method is applied to construct targeted 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 is unique due to several crucial aspects:
partner
Reaxense
upacc
Q9H5X1
UPID:
CIA2A_HUMAN
Alternative names:
MIP18 family protein FAM96A
Alternative UPACC:
Q9H5X1; A6NKS1; B2R5F8; B7Z8Z5
Background:
Cytosolic iron-sulfur assembly component 2A (CIA2A), also known as MIP18 family protein FAM96A, plays a crucial role in the cytosolic iron-sulfur protein assembly (CIA) complex. This complex is essential for the incorporation of iron-sulfur clusters into extramitochondrial Fe/S proteins, maturing ACO1 and stabilizing IREB2, thereby linking cytosolic iron-sulfur protein maturation with cellular iron regulation. Additionally, CIA2A may contribute to chromosome segregation and apoptosis in collaboration with APAF1.
Therapeutic significance:
Understanding the role of Cytosolic iron-sulfur assembly component 2A could open doors to potential therapeutic strategies.