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SIGNOR:一个生物实体之间因果关系的数据库。

SIGNOR: a database of causal relationships between biological entities.

作者信息

Perfetto Livia, Briganti Leonardo, Calderone Alberto, Cerquone Perpetuini Andrea, Iannuccelli Marta, Langone Francesca, Licata Luana, Marinkovic Milica, Mattioni Anna, Pavlidou Theodora, Peluso Daniele, Petrilli Lucia Lisa, Pirrò Stefano, Posca Daniela, Santonico Elena, Silvestri Alessandra, Spada Filomena, Castagnoli Luisa, Cesareni Gianni

机构信息

Department of Biology, University of Rome Tor Vergata, Rome, Italy.

Department of Biology, University of Rome Tor Vergata, Rome, Italy

出版信息

Nucleic Acids Res. 2016 Jan 4;44(D1):D548-54. doi: 10.1093/nar/gkv1048. Epub 2015 Oct 13.

Abstract

Assembly of large biochemical networks can be achieved by confronting new cell-specific experimental data with an interaction subspace constrained by prior literature evidence. The SIGnaling Network Open Resource, SIGNOR (available on line at http://signor.uniroma2.it), was developed to support such a strategy by providing a scaffold of prior experimental evidence of causal relationships between biological entities. The core of SIGNOR is a collection of approximately 12,000 manually-annotated causal relationships between over 2800 human proteins participating in signal transduction. Other entities annotated in SIGNOR are complexes, chemicals, phenotypes and stimuli. The information captured in SIGNOR can be represented as a signed directed graph illustrating the activation/inactivation relationships between signalling entities. Each entry is associated to the post-translational modifications that cause the activation/inactivation of the target proteins. More than 4900 modified residues causing a change in protein concentration or activity have been curated and linked to the modifying enzymes (about 351 human kinases and 94 phosphatases). Additional modifications such as ubiquitinations, sumoylations, acetylations and their effect on the modified target proteins are also annotated. This wealth of structured information can support experimental approaches based on multi-parametric analysis of cell systems after physiological or pathological perturbations and to assemble large logic models.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cf3/4702784/583072810061/gkv1048fig1.jpg

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