eprintid: 1462917 rev_number: 57 eprint_status: archive userid: 608 dir: disk0/01/46/29/17 datestamp: 2015-04-29 12:36:59 lastmod: 2021-12-13 02:44:16 status_changed: 2015-04-29 12:36:59 type: article metadata_visibility: show item_issues_count: 0 creators_name: Morgan, RE creators_name: Chudasama, V creators_name: Moody, P creators_name: Smith, ME creators_name: Caddick, S title: A novel synthetic chemistry approach to linkage-specific ubiquitin conjugation. ispublished: pub divisions: UCL divisions: B04 divisions: C06 divisions: F56 note: Copyright © Royal Society of Chemistry 2015. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. abstract: Ubiquitination is of great importance as the post-translational modification of proteins with ubiquitin, or ubiquitin chains, facilitates a number of vital cellular processes. Herein we present a facile method of preparing various ubiquitin conjugates under mild conditions using michael acceptors based on dibromo-maleimides and dibromo-pyridazinediones. date: 2015-04-14 official_url: http://dx.doi.org/10.1039/c5ob00130g vfaculties: VMPS oa_status: green full_text_type: pub language: eng primo: open primo_central: open_green article_type_text: Journal Article verified: verified_manual elements_source: PubMed elements_id: 1018453 doi: 10.1039/c5ob00130g lyricists_name: Caddick, Stephen lyricists_name: Chudasama, Vijay lyricists_name: Morgan, Rachel Elizabeth lyricists_id: SCADD46 lyricists_id: VCHUD30 lyricists_id: RMORG12 full_text_status: public publication: Org Biomol Chem volume: 13 number: 14 pagerange: 4165 - 4168 event_location: England issn: 1477-0520 citation: Morgan, RE; Chudasama, V; Moody, P; Smith, ME; Caddick, S; (2015) A novel synthetic chemistry approach to linkage-specific ubiquitin conjugation. Org Biomol Chem , 13 (14) 4165 - 4168. 10.1039/c5ob00130g <https://doi.org/10.1039/c5ob00130g>. Green open access document_url: https://discovery.ucl.ac.uk/id/eprint/1462917/1/c5ob00130g.pdf