6BK5
Inactive choanoflagellate E3 ubiquitin ligase Cbl TKB
6BK5 の概要
エントリーDOI | 10.2210/pdb6bk5/pdb |
分子名称 | Ubiquitin Ligase Cbl, CALCIUM ION (3 entities in total) |
機能のキーワード | ubiquitin ligase, cbl, signaling protein |
由来する生物種 | Salpingoeca rosetta (strain ATCC 50818 / BSB-021) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 41062.02 |
構造登録者 | |
主引用文献 | Amacher, J.F.,Hobbs, H.T.,Cantor, A.C.,Shah, L.,Rivero, M.J.,Mulchand, S.A.,Kuriyan, J. Phosphorylation control of the ubiquitin ligase Cbl is conserved in choanoflagellates. Protein Sci., 27:923-932, 2018 Cited by PubMed Abstract: Cbl proteins are E3 ubiquitin ligases specialized for the regulation of tyrosine kinases by ubiquitylation. Human Cbl proteins are activated by tyrosine phosphorylation, thus setting up a feedback loop whereby the activation of tyrosine kinases triggers their own degradation. Cbl proteins are targeted to their substrates by a phosphotyrosine-binding SH2 domain. Choanoflagellates, unicellular eukaryotes that are closely related to metazoans, also contain Cbl. The tyrosine kinase complement of choanoflagellates is distinct from that of metazoans, and it is unclear if choanoflagellate Cbl is regulated similarly to metazoan Cbl. Here, we performed structure-function studies on Cbl from the choanoflagellate species Salpingoeca rosetta and found that it undergoes phosphorylation-dependent activation. We show that S. rosetta Cbl can be phosphorylated by S. rosetta Src kinase, and that it can ubiquitylate S. rosetta Src. We also compared the substrate selectivity of human and S. rosetta Cbl by measuring ubiquitylation of Src constructs in which Cbl-recruitment sites are placed in different contexts with respect to the kinase domain. Our results indicate that for both human and S. rosetta Cbl, ubiquitylation depends on proximity and accessibility, rather than being targeted toward specific lysine residues. Our results point to an ancient interplay between phosphotyrosine and ubiquitin signaling in the metazoan lineage. PubMed: 29498112DOI: 10.1002/pro.3397 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.401 Å) |
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