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.
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.
We employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q6XZF7
UPID:
DNMBP_HUMAN
Alternative names:
Scaffold protein Tuba
Alternative UPACC:
Q6XZF7; Q8IVY3; Q9Y2L3
Background:
The Dynamin-binding protein, also known as Scaffold protein Tuba, is pivotal in cellular processes related to the actin and microtubule cytoskeleton. It functions as a guanine nucleotide exchange factor for CDC42, influencing F-actin organization in epithelial cells, spindle orientation during lumenogenesis, and potentially playing roles in ciliogenesis and membrane trafficking.
Therapeutic significance:
Linked to Cataract 48, a condition characterized by lens opacification leading to visual impairment, the Dynamin-binding protein's genetic variants highlight its clinical relevance. Understanding the role of Dynamin-binding protein could open doors to potential therapeutic strategies for cataract and related visual disorders.