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 carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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.
We utilise our cutting-edge, exclusive workflow to develop focused 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q96BR5
UPID:
COA7_HUMAN
Alternative names:
Beta-lactamase hcp-like protein; Respiratory chain assembly factor 1; Sel1 repeat-containing protein 1
Alternative UPACC:
Q96BR5; Q0P6I7; Q9H9Z9
Background:
Cytochrome c oxidase assembly factor 7, also known as Beta-lactamase hcp-like protein, Respiratory chain assembly factor 1, and Sel1 repeat-containing protein 1, plays a crucial role in the assembly of mitochondrial respiratory chain complex I and IV. This protein is pivotal for cellular energy production, influencing both the efficiency and integrity of mitochondrial function.
Therapeutic significance:
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3, a disorder characterized by progressive muscle weakness, sensory impairment, and cerebellar ataxia, is linked to mutations affecting Cytochrome c oxidase assembly factor 7. Understanding the role of this protein could open doors to potential therapeutic strategies for treating such neurodegenerative diseases.