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.
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.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our high-tech, dedicated method is applied to construct targeted 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q7L9L4
UPID:
MOB1B_HUMAN
Alternative names:
Mob1 homolog 1A; Mob1B; Mps one binder kinase activator-like 1A
Alternative UPACC:
Q7L9L4; B2R8U6; B4DRY3; Q8IY23
Background:
MOB kinase activator 1B, also known as Mob1 homolog 1A, Mob1B, and Mps one binder kinase activator-like 1A, is a crucial activator in the Hippo signaling pathway. This pathway is essential for organ size control and tumor suppression, functioning through a kinase cascade that restricts proliferation and promotes apoptosis. MOB kinase activator 1B enhances the kinase activity of STK38L and plays a significant role in phosphorylating and activating LATS1/2, which in turn phosphorylates and inactivates the YAP1 oncoprotein and WWTR1/TAZ, inhibiting their nuclear translocation.
Therapeutic significance:
Understanding the role of MOB kinase activator 1B could open doors to potential therapeutic strategies.