Focused On-demand Library for ADP-ribosylation factor-like protein 6

Focused On-demand Libraries - Reaxense Collaboration

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.

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 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 stands out due to several important features:

The Receptor.AI platform compiles comprehensive data on the target protein, encompassing previous experiments, literature, known ligands, structural details, and more, leading to a higher chance of selecting the most relevant compounds.
Advanced molecular simulations on the platform help pinpoint potential binding sites, making the compounds in our focused library ideal for finding allosteric inhibitors and targeting cryptic pockets.
Receptor.AI boasts over 50 tailor-made AI models, rigorously tested and proven in various drug discovery projects and research initiatives. They are crafted for efficacy, dependability, and precision, all of which are key in creating our focused libraries.
Beyond creating focused libraries, Receptor.AI offers comprehensive services and complete solutions throughout the preclinical drug discovery phase. Our success-based pricing model minimises risk and maximises the mutual benefits of the project's success.

partner

Reaxense

upacc

Q9H0F7

UPID:

ARL6_HUMAN

Alternative names:

Bardet-Biedl syndrome 3 protein

Alternative UPACC:

Q9H0F7; A8KA93; D3DN31

Background:

ADP-ribosylation factor-like protein 6 plays a pivotal role in membrane protein trafficking, particularly at the ciliary organelle base. It is crucial for the BBSome complex recruitment, influencing the sorting of specific membrane proteins to primary cilia. This protein's involvement extends to the regulation of the sonic hedgehog (SHH) pathway and possibly the Wnt signaling cascade, highlighting its significance in cellular signaling and structural integrity.

Therapeutic significance:

Given its association with Bardet-Biedl syndrome 3 and Retinitis pigmentosa 55, understanding the role of ADP-ribosylation factor-like protein 6 could open doors to potential therapeutic strategies. Its critical function in ciliary signaling and assembly suggests that targeting this protein could offer novel approaches for treating these complex genetic disorders.