deoxyribonucleoside triphosphate biosynthetic process / meiotic recombination checkpoint signaling / dual-specificity kinase / telomere maintenance in response to DNA damage / negative regulation of DNA damage checkpoint / DNA replication origin binding / DNA replication initiation / regulation of DNA repair / protein serine/threonine/tyrosine kinase activity / DNA damage checkpoint signaling ...deoxyribonucleoside triphosphate biosynthetic process / meiotic recombination checkpoint signaling / dual-specificity kinase / telomere maintenance in response to DNA damage / negative regulation of DNA damage checkpoint / DNA replication origin binding / DNA replication initiation / regulation of DNA repair / protein serine/threonine/tyrosine kinase activity / DNA damage checkpoint signaling / intracellular protein localization / protein tyrosine kinase activity / protein kinase activity / protein serine kinase activity / DNA repair / protein serine/threonine kinase activity / ATP binding / nucleus / cytosol / cytoplasm 類似検索 - 分子機能
Serine/threonine-protein kinase Rad53 / Tumour Suppressor Smad4 - #20 / Tumour Suppressor Smad4 / Aurora kinase / Forkhead associated domain / Forkhead-associated (FHA) domain profile. / FHA domain / Forkhead-associated (FHA) domain / SMAD/FHA domain superfamily / Serine/threonine-protein kinase, active site ...Serine/threonine-protein kinase Rad53 / Tumour Suppressor Smad4 - #20 / Tumour Suppressor Smad4 / Aurora kinase / Forkhead associated domain / Forkhead-associated (FHA) domain profile. / FHA domain / Forkhead-associated (FHA) domain / SMAD/FHA domain superfamily / Serine/threonine-protein kinase, active site / Serine/Threonine protein kinases active-site signature. / Protein kinase domain / Serine/Threonine protein kinases, catalytic domain / Protein kinase, ATP binding site / Protein kinases ATP-binding region signature. / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily / Sandwich / Mainly Beta 類似検索 - ドメイン・相同性
溶液NMR / The structures are based on a total of 2377 restraints. Among them, 2107 are NOE-derived distance constraints, 192 TALOS-derived dihedral angle restraints, and 78 restraints from hydrogen bonds.
Text: The structure was refined by adding 221 NOE-derived distance constraints and by revising a few previous NOE assignments.
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試料調製
詳細
内容: 0.5 mM protein U-15N,13C; 10 mM sodium phosphate buffer (pH 6.5), 1 mM DTT, and 1 mM EDTA; 90% H2O, 10% D2O 溶媒系: 90% H2O/10% D2O
試料状態
イオン強度: 10 mM sodium phosphate, 1mM DTT, and 1 mM EDTA pH: 6.5 / 圧: ambient / 温度: 293 K
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NMR測定
放射
プロトコル: SINGLE WAVELENGTH / 単色(M)・ラウエ(L): M
放射波長
相対比: 1
NMRスペクトロメーター
タイプ
製造業者
モデル
磁場強度 (MHz)
Spectrometer-ID
Bruker DRX
Bruker
DRX
800
1
Bruker DMX
Bruker
DMX
600
2
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解析
NMR software
名称
バージョン
開発者
分類
XwinNMR
2.6
Bruker
collection
XwinNMR
2.6
Bruker
解析
CNS
1
Brungeretal.
構造決定
CNS
1
Brungeretal.
精密化
精密化
手法: The structures are based on a total of 2377 restraints. Among them, 2107 are NOE-derived distance constraints, 192 TALOS-derived dihedral angle restraints, and 78 restraints from hydrogen bonds. ソフトェア番号: 1
NMRアンサンブル
コンフォーマー選択の基準: structures with the least restraint violations, structures with the lowest energy 計算したコンフォーマーの数: 50 / 登録したコンフォーマーの数: 20