Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q9UIL4
UPID:
KIF25_HUMAN
Alternative names:
Kinesin-like protein 3
Alternative UPACC:
Q9UIL4; A8K0C3; O94775; Q5SZU9
Background:
Kinesin-like protein KIF25, also known as Kinesin-like protein 3, plays a crucial role in cellular mechanics and division. It functions as a minus-end microtubule-dependent motor protein, essential for preventing premature centrosome separation during interphase and ensuring proper nucleus positioning for mitosis onset. Additionally, KIF25 may negatively regulate autophagy in response to amino acid starvation.
Therapeutic significance:
Understanding the role of Kinesin-like protein KIF25 could open doors to potential therapeutic strategies. Its involvement in critical cellular processes such as centrosome separation, nucleus positioning, and autophagy regulation highlights its potential as a target in cancer therapy and diseases related to autophagy dysfunction.