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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We utilise our cutting-edge, exclusive workflow to develop focused 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
Q9P2W1
UPID:
HOP2_HUMAN
Alternative names:
Nuclear receptor coactivator GT198; PSMC3-interacting protein; Proteasome 26S ATPase subunit 3-interacting protein; Tat-binding protein 1-interacting protein
Alternative UPACC:
Q9P2W1; C5ILB7; Q14458; Q8WXG2; Q96HA2
Background:
Homologous-pairing protein 2 homolog, also known as Nuclear receptor coactivator GT198, plays a pivotal role in meiotic recombination. It enhances DMC1-mediated strand exchange, crucial for homologous chromosome pairing during meiosis, and modulates activities of proteasomes and HIV-1 viral protein TAT.
Therapeutic significance:
Linked to Ovarian dysgenesis 3, a disorder marked by primary amenorrhea and hypergonadotropic hypogonadism, understanding the role of Homologous-pairing protein 2 homolog could open doors to potential therapeutic strategies.