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DEGRONOPEDIA: a web server for proteome-wide inspection of degrons.
Szulc, Natalia A; Stefaniak, Filip; Piechota, Malgorzata; Soszynska, Anna; Piórkowska, Gabriela; Cappannini, Andrea; Bujnicki, Janusz M; Maniaci, Chiara; Pokrzywa, Wojciech.
Affiliation
  • Szulc NA; Laboratory of Protein Metabolism, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Stefaniak F; Laboratory of Bioinformatics and Protein Engineering, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Piechota M; Laboratory of Protein Metabolism, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Soszynska A; Laboratory of Protein Metabolism, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Piórkowska G; Laboratory of Protein Metabolism, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Cappannini A; Laboratory of Bioinformatics and Protein Engineering, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Bujnicki JM; Laboratory of Bioinformatics and Protein Engineering, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
  • Maniaci C; Medical Research Council (MRC) Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.
  • Pokrzywa W; Laboratory of Protein Metabolism, International Institute of Molecular and Cell Biology in Warsaw, 4 Ks. Trojdena Str., 02-109 Warsaw, Poland.
Nucleic Acids Res ; 52(W1): W221-W232, 2024 Jul 05.
Article in En | MEDLINE | ID: mdl-38567734
ABSTRACT
E3 ubiquitin ligases recognize substrates through their short linear motifs termed degrons. While degron-signaling has been a subject of extensive study, resources for its systematic screening are limited. To bridge this gap, we developed DEGRONOPEDIA, a web server that searches for degrons and maps them to nearby residues that can undergo ubiquitination and disordered regions, which may act as protein unfolding seeds. Along with an evolutionary assessment of degron conservation, the server also reports on post-translational modifications and mutations that may modulate degron availability. Acknowledging the prevalence of degrons at protein termini, DEGRONOPEDIA incorporates machine learning to assess N-/C-terminal stability, supplemented by simulations of proteolysis to identify degrons in newly formed termini. An experimental validation of a predicted C-terminal destabilizing motif, coupled with the confirmation of a post-proteolytic degron in another case, exemplifies its practical application. DEGRONOPEDIA can be freely accessed at degronopedia.com.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Software / Protein Processing, Post-Translational / Internet / Proteome / Ubiquitin-Protein Ligases / Ubiquitination / Proteolysis Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2024 Document type: Article Affiliation country: Poland Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Software / Protein Processing, Post-Translational / Internet / Proteome / Ubiquitin-Protein Ligases / Ubiquitination / Proteolysis Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2024 Document type: Article Affiliation country: Poland Country of publication: United kingdom