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 pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
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 for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
This approach involves comprehensive molecular simulations of the catalytic and allosteric binding pockets and ensemble virtual screening that accounts for their conformational flexibility. In the case of designing modulators, the structural adjustments caused by reaction intermediates are considered to improve activity and selectivity.
Our library stands out due to several important features:
partner
Reaxense
upacc
P50579
UPID:
MAP2_HUMAN
Alternative names:
Initiation factor 2-associated 67 kDa glycoprotein; Peptidase M
Alternative UPACC:
P50579; B2RDI8; B4DUX5; G3XA91; Q8NB11
Background:
Methionine aminopeptidase 2 (METAP2), also known as Peptidase M and Initiation factor 2-associated 67 kDa glycoprotein, plays a pivotal role in protein synthesis. It cotranslationally removes the N-terminal methionine from nascent proteins, a process critical for protein maturation and function. METAP2 exhibits a preference for Met-Val and Met-Thr sequences, significantly influencing the processing of proteins with these N-terminal sequences in vivo. Additionally, METAP2 protects the eukaryotic initiation factor EIF2S1 from inhibitory phosphorylation, thereby playing a crucial role in the regulation of protein synthesis.
Therapeutic significance:
Understanding the role of Methionine aminopeptidase 2 could open doors to potential therapeutic strategies.