Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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.
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 top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q68DK2
UPID:
ZFY26_HUMAN
Alternative names:
FYVE domain-containing centrosomal protein; Spastizin
Alternative UPACC:
Q68DK2; B1B5Y3; B4E2U3; O15035; Q68DT9; Q6AW90; Q6ZR50; Q7Z3A4; Q7Z3I1; Q8N4W7; Q96H43
Background:
Zinc finger FYVE domain-containing protein 26, also known as Spastizin or FYVE domain-containing centrosomal protein, plays a crucial role in cytokinesis, specifically in the abcission step. It is recruited to the midbody during cytokinesis, acting as a regulator of abcission. Additionally, it is implicated in the efficient repair of DNA double-strand breaks through homologous recombination.
Therapeutic significance:
Spastizin is linked to Spastic paraplegia 15, a neurodegenerative disorder characterized by progressive weakness and spasticity of the lower limbs, among other neurological symptoms. Understanding the role of Spastizin could lead to novel therapeutic strategies for this condition, potentially addressing symptoms and progression.