Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner 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 use our state-of-the-art dedicated workflow for designing 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 distinguishes itself through several key aspects:
partner
Reaxense
upacc
P59998
UPID:
ARPC4_HUMAN
Alternative names:
Arp2/3 complex 20 kDa subunit
Alternative UPACC:
P59998; C9JWM7; E7ETI0; F6TTL5; O15509; Q6P0W5; Q96QJ3
Background:
The Actin-related protein 2/3 complex subunit 4, also known as the Arp2/3 complex 20 kDa subunit, plays a pivotal role in cellular dynamics. It is an actin-binding component of the Arp2/3 complex, crucial for actin polymerization in response to nucleation-promoting factors. This process underpins the formation of branched actin networks in the cytoplasm, essential for cell motility, and also facilitates actin polymerization in the nucleus, impacting gene transcription and DNA repair.
Therapeutic significance:
Linked to Developmental delay, language impairment, and ocular abnormalities, the protein's involvement in this autosomal dominant disorder highlights its potential as a therapeutic target. Understanding the role of Actin-related protein 2/3 complex subunit 4 could open doors to potential therapeutic strategies.