S1P4FirstExtracellularLoopPeptidomimetic / Arfaptin-2 / ADP-ribosylation factor-interacting protein 2 / Partner of RAC1 / Protein ...Arfaptin-2 / ADP-ribosylation factor-interacting protein 2 / Partner of RAC1 / Protein POR1phingosine 1-phosphate receptor Edg-6 / S1P receptor Edg-6 / Endothelial differentiation G-protein coupled receptor 6 / Sphingosine 1-phosphate receptor 4 / S1P4
分子量: 3891.223 Da / 分子数: 1 / 断片: Extracellular Loop 1 / 変異: L10C/A28C / 由来タイプ: 組換発現 詳細: This protein is a fusion protein. Residues 13-26 and 29-30 are from the first extracellular loop of S1P4 receptor. The rest, residues 3-12, 27-28, and 31-34 are from Arfatin (PDB entry 1I49) ...詳細: This protein is a fusion protein. Residues 13-26 and 29-30 are from the first extracellular loop of S1P4 receptor. The rest, residues 3-12, 27-28, and 31-34 are from Arfatin (PDB entry 1I49) segments 139-148, 164-164, 168-171 of 1I49 that we designed to be in the sequence. 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: S1P4 / プラスミド: pET-32a, CCE1a / 生物種 (発現宿主): Escherichia coli / 発現宿主: Escherichia coli BL21(DE3) (大腸菌) / 株 (発現宿主): BL21(DE3) / 参照: UniProt: P53365, UniProt: O95977
Has protein modification
Y
-
実験情報
-
実験
実験
手法: 溶液NMR
NMR実験
Conditions-ID
Experiment-ID
Solution-ID
タイプ
2
1
2
3D 15N-separated NOESY
2
2
2
3D 13C-separated NOESY
NMR実験の詳細
Text: The structure was determined using triple-resonance NMR spectroscopy.
手法: simulated annealing, matrix relaxation, torsion angle dynamics, energy minimization ソフトェア番号: 1 詳細: the structures are based on a total of 748 NOE-derived distance constraints
代表構造
選択基準: extended first helix
NMRアンサンブル
コンフォーマー選択の基準: structures with the lowest energy 計算したコンフォーマーの数: 200 / 登録したコンフォーマーの数: 10