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.
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
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q96PF1
UPID:
TGM7_HUMAN
Alternative names:
Transglutaminase Z; Transglutaminase-7
Alternative UPACC:
Q96PF1
Background:
Protein-glutamine gamma-glutamyltransferase Z, also known as Transglutaminase Z or Transglutaminase-7, plays a crucial role in cellular processes by catalyzing the cross-linking of proteins and the conjugation of polyamines to proteins. This enzymatic activity is vital for the post-translational modification of proteins, influencing their structure and function.
Therapeutic significance:
Understanding the role of Protein-glutamine gamma-glutamyltransferase Z could open doors to potential therapeutic strategies. Its unique ability to modify proteins post-translationally positions it as a key player in cellular homeostasis and disease modulation.