Focused On-demand Library for Kinesin-like protein KIF25

Focused On-demand Libraries - Reaxense Collaboration

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.

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 features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.

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:

Receptor.AI compiles an all-encompassing dataset on the target protein, including historical experiments, literature data, known ligands, and structural insights, maximising the chances of prioritising the most pertinent compounds.
The platform employs state-of-the-art molecular simulations to identify potential binding sites, ensuring the focused library is primed for discovering allosteric inhibitors and binders of concealed pockets.
Over 50 customisable AI models, thoroughly evaluated in various drug discovery endeavours and research projects, make Receptor.AI both efficient and accurate. This technology is integral to the development of our focused libraries.
In addition to generating focused libraries, Receptor.AI offers a full range of services and solutions for every step of preclinical drug discovery, with a pricing model based on success, thereby reducing risk and promoting joint project success.

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.