| NMR software | | 名称 | バージョン | 開発者 | 分類 |
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| ARIA | 2.2 | Linge, O'Donoghue and Nilges| 構造決定 | | ARIA | 2.2 | Linge, O'Donoghue and Nilgesnoe assignment| CNS | 1.1 | Brunger, Adams, Clore, Gros, Nilges and Read| 構造決定 | | CNS | 1.1 | Brunger, Adams, Clore, Gros, Nilges and Read| 精密化 | | VnmrJ | 2.1BVariancollection NMRPipe | | Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax| 解析 | | NMRView | 5.2.2Johnson, One Moon Scientific| データ解析 | | NMRView | 5.2.2Johnson, One Moon Scientificchemical shift assignment| NMRView | 5.2.2Johnson, One Moon Scientificpeak picking| ProcheckNMR | 3.4 | Laskowski and MacArthur| データ解析 | | WHAT IF | | Vriend| データ解析 | | | | | | | | | | | | | | | | | | | |
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| 精密化 | 手法: simulated annealing / ソフトェア番号: 1 詳細: Residues 1-12 are disordered. Only coordinates for residues 11-56 are included. Structures were calculated with restraints for residues 11-56. |
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| NMR constraints | NOE constraints total: 4072 / NOE intraresidue total count: 1075 / NOE long range total count: 453 / NOE medium range total count: 740 / NOE sequential total count: 808 / Hydrogen bond constraints total count: 54 / Protein chi angle constraints total count: 0 / Protein other angle constraints total count: 0 / Protein phi angle constraints total count: 60 / Protein psi angle constraints total count: 0 |
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| 代表構造 | 選択基準: lowest energy |
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| 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 / Maximum lower distance constraint violation: 0.1 Å / Maximum torsion angle constraint violation: 5 ° / Maximum upper distance constraint violation: 0.1 Å / Torsion angle constraint violation method: CNS |
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| NMR ensemble rms | Distance rms dev: 0.0205 Å / Distance rms dev error: 0.0001 Å |
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