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6KGI

RLGS-yUbr1 Ubr box

6KGI の概要
エントリーDOI10.2210/pdb6kgi/pdb
分子名称E3 ubiquitin-protein ligase UBR1, ZINC ION (3 entities in total)
機能のキーワードubr1, ubr box, ligase
由来する生物種Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast)
タンパク質・核酸の鎖数1
化学式量合計9875.11
構造登録者
Heo, J.,Kwon, D.H.,Kim, L.,Song, H.K. (登録日: 2019-07-11, 公開日: 2020-01-22, 最終更新日: 2023-11-22)
主引用文献Kim, L.,Kwon, D.H.,Heo, J.,Park, M.R.,Song, H.K.
Use of the LC3B-fusion technique for biochemical and structural studies of proteins involved in the N-degron pathway.
J.Biol.Chem., 295:2590-2600, 2020
Cited by
PubMed Abstract: The N-degron pathway, formerly the N-end rule pathway, is a protein degradation process that determines the half-life of proteins based on their N-terminal residues. In contrast to the well-established studies over decades, studies of this pathway, including biochemical characterization and high-resolution structures, are relatively limited. In this study, we have developed a unique fusion technique using microtubule-associated protein 1A/1B light chain 3B, a key marker protein of autophagy, to tag the N terminus of the proteins involved in the N-degron pathway, which enables high yield of homogeneous target proteins with variable N-terminal residues for diverse biochemical studies including enzymatic and binding assays and substrate identification. Intriguingly, crystallization showed a markedly enhanced probability, even for the N-degron complexes. To validate our results, we determined the structures of select proteins in the N-degron pathway and compared them with the Protein Data Bank-deposited proteins. Furthermore, several biochemical applications of this technique were introduced. Therefore, this technique can be used as a general tool for the study of the N-degron pathway.
PubMed: 31919097
DOI: 10.1074/jbc.RA119.010912
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.04 Å)
構造検証レポート
Validation report summary of 6kgi
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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