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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q9BSH4
UPID:
TACO1_HUMAN
Alternative names:
Coiled-coil domain-containing protein 44; Translational activator of mitochondrially-encoded cytochrome c oxidase I
Alternative UPACC:
Q9BSH4; B2RD21; Q8N3N6; Q9UI60
Background:
The Translational activator of cytochrome c oxidase 1, also known as Coiled-coil domain-containing protein 44, plays a pivotal role in mitochondrial function. It specifically activates the translation of mitochondrially-encoded cytochrome c oxidase 1, essential for cellular energy production.
Therapeutic significance:
Linked to Mitochondrial complex IV deficiency, nuclear type 8, this protein's dysfunction manifests in cognitive decline, dystonia, and visual impairment. Understanding its role could lead to novel treatments for mitochondrial disorders.