The SIGnaling Network Open Resource (SIGNOR 4.0, https://signor.uniroma2.it) is a database of manually curated causal interactions between biological entities. These signaling events are annotated along with their effect—denoting the activation or inactivation of a target entity—and mechanism through which it is mediated, such as phosphorylation, binding, or transcriptional regulation. The data is freely accessible and can be explored as customizable signaling networks, allowing users to adapt them for different modeling purposes. In our latest update (version 4.0), we improved our curation interface to include additional data-validation tools, integrated text-mining-assisted curation, increased our curation content, and expanded the scope of our curation efforts, with a particular emphasis on phosphorylation data. Furthermore, we developed a subdomain of SIGNOR, PhosphoSIGNOR, a dedicated user interface designed to enable targeted access to phosphorylation-specific information and network visualization. This expanded dataset allows for a more comprehensive mapping of signaling alterations and their associations with dysregulated cellular processes. The platform enables users to dynamically query phosphosite-specific data, examine context-dependent modifications, and integrate findings with known regulatory mechanisms. The PhosphoSIGNOR section of SIGNOR serves as an essential resource for cancer systems biology, offering an intuitive interface for hypothesis generation and mechanistic insights.

Lo Surdo, P., Iannuccelli, M., Karis, K., Meo, E., Omidi, P., Tosoni, M., et al. (2026). SIGNOR 4.0: the 2025 update with focus on phosphorylation data. NUCLEIC ACIDS RESEARCH, 54(D1), D682-D690 [10.1093/nar/gkaf1237].

SIGNOR 4.0: the 2025 update with focus on phosphorylation data

Lo Surdo, Prisca;Iannuccelli, Marta;Meo, Eleonora;Graziosi, Simone;Panni, Simona;Licata, Luana;Sacco, Francesca;Perfetto, Livia
2026-01-06

Abstract

The SIGnaling Network Open Resource (SIGNOR 4.0, https://signor.uniroma2.it) is a database of manually curated causal interactions between biological entities. These signaling events are annotated along with their effect—denoting the activation or inactivation of a target entity—and mechanism through which it is mediated, such as phosphorylation, binding, or transcriptional regulation. The data is freely accessible and can be explored as customizable signaling networks, allowing users to adapt them for different modeling purposes. In our latest update (version 4.0), we improved our curation interface to include additional data-validation tools, integrated text-mining-assisted curation, increased our curation content, and expanded the scope of our curation efforts, with a particular emphasis on phosphorylation data. Furthermore, we developed a subdomain of SIGNOR, PhosphoSIGNOR, a dedicated user interface designed to enable targeted access to phosphorylation-specific information and network visualization. This expanded dataset allows for a more comprehensive mapping of signaling alterations and their associations with dysregulated cellular processes. The platform enables users to dynamically query phosphosite-specific data, examine context-dependent modifications, and integrate findings with known regulatory mechanisms. The PhosphoSIGNOR section of SIGNOR serves as an essential resource for cancer systems biology, offering an intuitive interface for hypothesis generation and mechanistic insights.
6-gen-2026
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIOS-14/A - Genetica
English
Con Impact Factor ISI
Lo Surdo, P., Iannuccelli, M., Karis, K., Meo, E., Omidi, P., Tosoni, M., et al. (2026). SIGNOR 4.0: the 2025 update with focus on phosphorylation data. NUCLEIC ACIDS RESEARCH, 54(D1), D682-D690 [10.1093/nar/gkaf1237].
Lo Surdo, P; Iannuccelli, M; Karis, K; Meo, E; Omidi, P; Tosoni, M; Graziosi, S; Panni, S; Fiorillo, Mt; Licata, L; Sacco, F; Gyori, Bm; Perfetto, L...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/454288
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