4C0A
Arf1(Delta1-17)in complex with BRAG2 Sec7-PH domain
4C0A の概要
| エントリーDOI | 10.2210/pdb4c0a/pdb |
| 分子名称 | IQ MOTIF AND SEC7 DOMAIN-CONTAINING PROTEIN 1, ADP-RIBOSYLATION FACTOR 1, GUANOSINE-3'-MONOPHOSPHATE-5'-DIPHOSPHATE (3 entities in total) |
| 機能のキーワード | protein transport, endocytosis |
| 由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
| タンパク質・核酸の鎖数 | 8 |
| 化学式量合計 | 255020.54 |
| 構造登録者 | Aizel, K.,Biou, V.,Navaza, J.,Duarte, L.,Campanacci, V.,Cherfils, J.,Zeghouf, M. (登録日: 2013-08-01, 公開日: 2013-09-25, 最終更新日: 2023-12-20) |
| 主引用文献 | Aizel, K.,Biou, V.,Navaza, J.,Duarte, L.V.,Campanacci, V.,Cherfils, J.,Zeghouf, M. Integrated conformational and lipid-sensing regulation of endosomal ArfGEF BRAG2. PLoS Biol., 11:e1001652-e1001652, 2013 Cited by PubMed Abstract: The mechanisms whereby guanine nucleotide exchange factors (GEFs) coordinate their subcellular targeting to their activation of small GTPases remain poorly understood. Here we analyzed how membranes control the efficiency of human BRAG2, an ArfGEF involved in receptor endocytosis, Wnt signaling, and tumor invasion. The crystal structure of an Arf1-BRAG2 complex that mimics a membrane-bound intermediate revealed an atypical PH domain that is constitutively anchored to the catalytic Sec7 domain and interacts with Arf. Combined with the quantitative analysis of BRAG2 exchange activity reconstituted on membranes, we find that this PH domain potentiates nucleotide exchange by about 2,000-fold by cumulative conformational and membrane-targeting contributions. Furthermore, it restricts BRAG2 activity to negatively charged membranes without phosphoinositide specificity, using a positively charged surface peripheral to but excluding the canonical lipid-binding pocket. This suggests a model of BRAG2 regulation along the early endosomal pathway that expands the repertoire of GEF regulatory mechanisms. Notably, it departs from the auto-inhibitory and feedback loop paradigm emerging from studies of SOS and cytohesins. It also uncovers a novel mechanism of unspecific lipid-sensing by PH domains that may allow sustained binding to maturating membranes. PubMed: 24058294DOI: 10.1371/journal.pbio.1001652 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3.3 Å) |
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