AI-ACCELERATED DRUG DISCOVERY
Available from Reaxense
This protein is integrated into the Receptor.AI ecosystem as a prospective target with high therapeutic potential. We performed a comprehensive characterization of Cytochrome c oxidase assembly factor 3 homolog, mitochondrial including:
1. LLM-powered literature research
Our custom-tailored LLM extracted and formalized all relevant information about the protein from a large set of structured and unstructured data sources and stored it in the form of a Knowledge Graph. This comprehensive analysis allowed us to gain insight into Cytochrome c oxidase assembly factor 3 homolog, mitochondrial therapeutic significance, existing small molecule ligands, relevant off-targets, and protein-protein interactions.
Fig. 1. Preliminary target research workflow
2. AI-Driven Conformational Ensemble Generation
Starting from the initial protein structure, we employed advanced AI algorithms to predict alternative functional states of Cytochrome c oxidase assembly factor 3 homolog, mitochondrial, including large-scale conformational changes along "soft" collective coordinates. Through molecular simulations with AI-enhanced sampling and trajectory clustering, we explored the broad conformational space of the protein and identified its representative structures. Utilizing diffusion-based AI models and active learning AutoML, we generated a statistically robust ensemble of equilibrium protein conformations that capture the receptor's full dynamic behavior, providing a robust foundation for accurate structure-based drug design.
Fig. 2. AI-powered molecular dynamics simulations workflow
3. Binding pockets identification and characterization
We employed the AI-based pocket prediction module to discover orthosteric, allosteric, hidden, and cryptic binding pockets on the protein’s surface. Our technique integrates the LLM-driven literature search and structure-aware ensemble-based pocket detection algorithm that utilizes previously established protein dynamics. Tentative pockets are then subject to AI scoring and ranking with simultaneous detection of false positives. In the final step, the AI model assesses the druggability of each pocket enabling a comprehensive selection of the most promising pockets for further targeting.
Fig. 3. AI-based binding pocket detection workflow
4. AI-Powered Virtual Screening
Our ecosystem is equipped to perform AI-driven virtual screening on Cytochrome c oxidase assembly factor 3 homolog, mitochondrial. With access to a vast chemical space and cutting-edge AI docking algorithms, we can rapidly and reliably predict the most promising, novel, diverse, potent, and safe small molecule ligands of Cytochrome c oxidase assembly factor 3 homolog, mitochondrial. This approach allows us to achieve an excellent hit rate and to identify compounds ready for advanced lead discovery and optimization.
Fig. 4. The screening workflow of Receptor.AI
Receptor.AI, in partnership with Reaxense, developed a next-generation technology for on-demand focused library design to enable extensive target exploration.
The focused library for Cytochrome c oxidase assembly factor 3 homolog, mitochondrial includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
Cytochrome c oxidase assembly factor 3 homolog, mitochondrial
partner:
Reaxense
upacc:
Q9Y2R0
UPID:
COA3_HUMAN
Alternative names:
Coiled-coil domain-containing protein 56; Mitochondrial translation regulation assembly intermediate of cytochrome c oxidase protein of 12 kDa
Alternative UPACC:
Q9Y2R0; A8K498
Background:
Cytochrome c oxidase assembly factor 3 homolog, mitochondrial, also known as Coiled-coil domain-containing protein 56, plays a pivotal role in the mitochondrial respiratory chain. It is a core component of the MITRAC complex, crucial for the regulation of cytochrome c oxidase assembly. This protein ensures the efficient translation of MT-CO1 and the assembly of mitochondrial respiratory chain complex IV, highlighting its essential function in cellular energy production.
Therapeutic significance:
The protein is linked to Mitochondrial complex IV deficiency, nuclear type 14, a disorder marked by developmental delay, cognitive impairment, and motor issues. Understanding the role of Cytochrome c oxidase assembly factor 3 homolog, mitochondrial could open doors to potential therapeutic strategies for this mitochondrial disorder, offering hope for targeted treatments.
