Focused On-demand Library for Serine/threonine-protein kinase 10

Focused On-demand Libraries - Receptor.AI 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. Reaxense aids in their synthesis and provision.


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 for enzymes.


 

Fig. 1. The screening workflow of Receptor.AI

The method includes detailed molecular simulations of the catalytic and allosteric binding pockets, along with ensemble virtual screening that considers their conformational flexibility. In the design of modulators, structural changes induced by reaction intermediates are taken into account to enhance activity and selectivity.


Our library is unique due to several crucial aspects:


  • Receptor.AI compiles all relevant data on the target protein, such as past experimental results, literature findings, known ligands, and structural data, thereby enhancing the likelihood of focusing on the most significant compounds.

  • By utilizing advanced molecular simulations, the platform is adept at locating potential binding sites, rendering the compounds in the focused library well-suited for unearthing allosteric inhibitors and binders for hidden pockets.

  • The platform is supported by more than 50 highly specialized AI models, all of which have been rigorously tested and validated in diverse drug discovery and research programs. Its design emphasizes efficiency, reliability, and accuracy, crucial for producing focused libraries.

  • Receptor.AI extends beyond just creating focused libraries; it offers a complete spectrum of services and solutions during the preclinical drug discovery phase, with a success-dependent pricing strategy that reduces risk and fosters shared success in the project.


PARTNER
Receptor.AI
 
UPACC
O94804

UPID:
STK10_HUMAN

ALTERNATIVE NAMES:
Lymphocyte-oriented kinase

ALTERNATIVE UPACC:
O94804; A6ND35; B2R8F5; B3KMY1; Q6NSK0; Q9UIW4

BACKGROUND:
The Serine/threonine-protein kinase 10, known alternatively as Lymphocyte-oriented kinase, is integral to lymphocyte migration regulation through phosphorylation of MSN and ERM proteins. It serves as a negative regulator of MAP3K1/MEKK1 and is implicated in cell cycle regulation by potentially phosphorylating PLK1, highlighting its multifaceted biological roles.

THERAPEUTIC SIGNIFICANCE:
The association of Serine/threonine-protein kinase 10 with Testicular germ cell tumor, a significant male malignancy, underscores its therapeutic potential. Exploring its functions could lead to groundbreaking therapeutic approaches for TGCT, leveraging its regulatory capabilities in cell migration and cycle control.

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