Ontology highlight
ABSTRACT:
SUBMITTER: Wagner SA
PROVIDER: S-EPMC3518112 | biostudies-other | 2012 Dec
REPOSITORIES: biostudies-other
Wagner Sebastian A SA Beli Petra P Weinert Brian T BT Schölz Christian C Kelstrup Christian D CD Young Clifford C Nielsen Michael L ML Olsen Jesper V JV Brakebusch Cord C Choudhary Chunaram C
Molecular & cellular proteomics : MCP 20120711 12
Posttranslational modifications of proteins increase the complexity of the cellular proteome and enable rapid regulation of protein functions in response to environmental changes. Protein ubiquitylation is a central regulatory posttranslational modification that controls numerous biological processes including proteasomal degradation of proteins, DNA damage repair and innate immune responses. Here we combine high-resolution mass spectrometry with single-step immunoenrichment of di-glycine modifi ...[more]