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.
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.
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.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q16864
UPID:
VATF_HUMAN
Alternative names:
V-ATPase 14 kDa subunit; Vacuolar proton pump subunit F
Alternative UPACC:
Q16864; C9J2K4; Q6IBA8
Background:
V-type proton ATPase subunit F, also known as V-ATPase 14 kDa subunit or Vacuolar proton pump subunit F, plays a crucial role in the V1 complex of vacuolar(H+)-ATPase. This multisubunit enzyme is pivotal for hydrolyzing ATP and translocating protons, thereby acidifying intracellular compartments and, in certain cells, the extracellular environment.
Therapeutic significance:
Understanding the role of V-type proton ATPase subunit F could open doors to potential therapeutic strategies.