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ELIOT: A platform to navigate the E3 pocketome and aid the design of new PROTACs.
Palomba, Tommaso; Baroni, Massimo; Cross, Simon; Cruciani, Gabriele; Siragusa, Lydia.
Afiliación
  • Palomba T; Laboratory for Chemometrics and Molecular Modeling, Department of Chemistry, Biology, and Biotechnology, University of Perugia, Perugia, Italy.
  • Baroni M; Molecular Discovery Ltd., The Kinetic Centre, Hertfordshire, UK.
  • Cross S; Molecular Discovery Ltd., The Kinetic Centre, Hertfordshire, UK.
  • Cruciani G; Laboratory for Chemometrics and Molecular Modeling, Department of Chemistry, Biology, and Biotechnology, University of Perugia, Perugia, Italy.
  • Siragusa L; Molecular Discovery Ltd., The Kinetic Centre, Hertfordshire, UK.
Chem Biol Drug Des ; 101(1): 69-86, 2023 01.
Article en En | MEDLINE | ID: mdl-35857806
Proteolysis-targeting chimeras (PROTACs) are novel therapeutics for the treatment of human disease. They exploit the enormous potential of the E3 ligases, a class of proteins that mark a target protein for degradation via the ubiquitin-proteasome system. Despite the existence of several E3 ligase-related databases, the choice of the functioning ligase is limited to only 1.6% of those available, probably due to the fragmentary understanding of their structures and their known ligands; in fact, none of the existing databases report detailed studies covering their 3D structure or their pockets. Here, we report ELIOT (E3 LIgase pocketOme navigaTor), an accurate and complete platform containing the E3 ligase pocketome to enable navigation and selection of new E3 ligases and new ligands for the design of new PROTACs. All E3 ligase pockets were characterized with innovative 3D descriptors including their PROTAC-ability score, and similarity analyses between E3 pockets are presented. Tissue specificity and their degree of involvement in patients with specific cancer types are also annotated for each E3 ligase, enabling appropriate selection for the design of a PROTAC with improved specificity. All data are available at https://eliot.moldiscovery.com.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ubiquitina-Proteína Ligasas / Complejo de la Endopetidasa Proteasomal Límite: Humans Idioma: En Revista: Chem Biol Drug Des Asunto de la revista: BIOQUIMICA / FARMACIA / FARMACOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ubiquitina-Proteína Ligasas / Complejo de la Endopetidasa Proteasomal Límite: Humans Idioma: En Revista: Chem Biol Drug Des Asunto de la revista: BIOQUIMICA / FARMACIA / FARMACOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia