Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced activity, selectivity, and safety.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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 top-notch dedicated system is used to design specialised 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q7Z3K3
UPID:
POGZ_HUMAN
Alternative names:
Suppressor of hairy wing homolog 5; Zinc finger protein 280E; Zinc finger protein 635
Alternative UPACC:
Q7Z3K3; B4DTP8; B4DYL9; B7ZBY5; E9PM80; O75049; Q3LIC4; Q5SZS1; Q5SZS2; Q5SZS3; Q5SZS4; Q8TDZ7; Q9Y4X7
Background:
The Pogo transposable element with ZNF domain, also known as Suppressor of hairy wing homolog 5, Zinc finger protein 280E, and Zinc finger protein 635, is pivotal in mitotic cell cycle progression. It plays a crucial role in kinetochore assembly, sister chromatid cohesion, and DNA double-strand break repair through homologous recombination, influencing chromosome segregation and genomic stability.
Therapeutic significance:
Linked to White-Sutton syndrome, characterized by developmental delay and intellectual disability, this protein's genetic variants highlight its clinical relevance. Understanding its role could unveil novel therapeutic strategies for managing this syndrome and related chromosomal disorders.