AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Importin subunit alpha-7

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

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.

Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner 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.

We employ our advanced, specialised process to create targeted libraries.

 Fig. 1. The sreening workflow of Receptor.AI

Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.

Our library distinguishes itself through several key aspects:

  • The Receptor.AI platform integrates all available data about the target protein, including past experiments, literature data, known ligands, structural information and more. This consolidated approach maximises the probability of prioritising highly relevant compounds.
  • The platform uses sophisticated molecular simulations to identify possible binding sites so that the compounds in the focused library are suitable for discovering allosteric inhibitors and the binders for cryptic pockets.
  • The platform integrates over 50 highly customisable AI models, which are thoroughly tested and validated on a multitude of commercial drug discovery programs and research projects. It is designed to be efficient, reliable and accurate. All this power is utilised when producing the focused libraries.
  • In addition to producing the focused libraries, Receptor.AI provides services and end-to-end solutions at every stage of preclinical drug discovery. The pricing model is success-based, which reduces your risks and leverages the mutual benefits of the project's success.

partner

Reaxense

upacc

O60684

UPID:

IMA7_HUMAN

Alternative names:

Karyopherin subunit alpha-6

Alternative UPACC:

O60684; B2RDC7; D3DPP5; Q5VVU3

Background:

Importin subunit alpha-7, also known as Karyopherin subunit alpha-6, plays a crucial role in nuclear protein import. It functions as an adapter for nuclear receptor KPNB1, binding directly to substrates with NLS motifs. This protein is essential for the docking of the importin/substrate complex to the nuclear pore complex, facilitated by KPNB1's interaction with nucleoporin FxFG repeats. The complex's translocation through the pore is powered by a Ran-dependent mechanism, highlighting the protein's significance in cellular function.

Therapeutic significance:

Understanding the role of Importin subunit alpha-7 could open doors to potential therapeutic strategies. Its pivotal function in nuclear import underscores its potential as a target in diseases where this process is dysregulated.

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