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.
The library 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.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q68DC2
UPID:
ANKS6_HUMAN
Alternative names:
Ankyrin repeat domain-containing protein 14; SamCystin; Sterile alpha motif domain-containing protein 6
Alternative UPACC:
Q68DC2; A0SE62; Q5VSL0; Q5VSL2; Q5VSL3; Q5VSL4; Q68DB8; Q6P2R2; Q8N9L6; Q96D62
Background:
Ankyrin repeat and SAM domain-containing protein 6, also known as Ankyrin repeat domain-containing protein 14, SamCystin, and Sterile alpha motif domain-containing protein 6, plays a crucial role in renal function. Its unique structure, characterized by ankyrin repeats and a sterile alpha motif (SAM) domain, suggests a significant role in cellular processes.
Therapeutic significance:
Nephronophthisis 16, a chronic tubulo-interstitial nephritis leading to end-stage renal failure, is directly associated with mutations in this protein. Understanding the role of Ankyrin repeat and SAM domain-containing protein 6 could open doors to potential therapeutic strategies for this debilitating disease.