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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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 top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q9Y241
UPID:
HIG1A_HUMAN
Alternative names:
Hypoxia-inducible gene 1 protein; RCF1 homolog A
Alternative UPACC:
Q9Y241; Q9UFZ2
Background:
HIG1 domain family member 1A, mitochondrial, also known as Hypoxia-inducible gene 1 protein and RCF1 homolog A, is proposed to be a subunit of cytochrome c oxidase (COX, complex IV). This complex is the terminal component of the mitochondrial respiratory chain, crucial for the reduction of oxygen to water. It is suggested to play a pivotal role in the assembly of respiratory supercomplexes.
Therapeutic significance:
Understanding the role of HIG1 domain family member 1A could open doors to potential therapeutic strategies by elucidating its contribution to mitochondrial function and energy production.