AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Kinesin-like protein KIF24

Available from Reaxense
Predicted by Alphafold

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.

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.

Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.

Our high-tech, dedicated method is applied to construct targeted 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.

Our library stands out due to several important features:

  • The Receptor.AI platform compiles comprehensive data on the target protein, encompassing previous experiments, literature, known ligands, structural details, and more, leading to a higher chance of selecting the most relevant compounds.
  • Advanced molecular simulations on the platform help pinpoint potential binding sites, making the compounds in our focused library ideal for finding allosteric inhibitors and targeting cryptic pockets.
  • Receptor.AI boasts over 50 tailor-made AI models, rigorously tested and proven in various drug discovery projects and research initiatives. They are crafted for efficacy, dependability, and precision, all of which are key in creating our focused libraries.
  • Beyond creating focused libraries, Receptor.AI offers comprehensive services and complete solutions throughout the preclinical drug discovery phase. Our success-based pricing model minimises risk and maximises the mutual benefits of the project's success.

partner

Reaxense

upacc

Q5T7B8

UPID:

KIF24_HUMAN

Alternative names:

-

Alternative UPACC:

Q5T7B8; Q2TB93; Q5T7B5; Q5T7B7; Q6ZU97; Q6ZUZ2; Q86XZ0; Q9NV43

Background:

Kinesin-like protein KIF24 is a microtubule-dependent motor protein, crucial for regulating ciliogenesis. It acts by recruiting CCP110 to the mother centriole, restricting cilia nucleation. KIF24 mediates microtubule depolymerization at centrioles, aiming to prevent aberrant cilia formation. It plays a pivotal role in cilium disassembly during the cell cycle's G2/M phase, without fully disassembling ciliary axonemes. The dynamic equilibrium between cilium assembly and disassembly highlights KIF24's role in suppressing nascent cilium assembly and potentially ciliary re-assembly, ensuring cilium removal completion.

Therapeutic significance:

Understanding the role of Kinesin-like protein KIF24 could open doors to potential therapeutic strategies.

Looking for more information on this library or underlying technology? Fill out the form below and we'll be in touch with all the details you need.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.