The submitted conformer models are the 20 structures with the lowest energy.
代表モデル
モデル #8
closest to the average
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要素
#1: タンパク質・ペプチド
PROTEINMRIB-NH2
分子量: 1397.732 Da / 分子数: 1 / 由来タイプ: 合成 詳細: This peptide was chemically syntesized. This sequence occurs in Conus marmoreus (mollusc-hunting cone snail). However, the C-terminus has been amidated whereas it exists as a free-acid in the native form. 参照: UniProt: P58810
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実験情報
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実験
実験
手法: 溶液NMR
NMR実験
Conditions-ID
Experiment-ID
Solution-ID
タイプ
1
1
1
2D NOESY
1
2
1
DQF-COSY
1
3
1
E-COSY
NMR実験の詳細
Text: The sample was a purified single peptide component but on dissolution displayed evidence of multiple conformations (manifest by peaks "brothering" in the N-terminal region). The structures ...Text: The sample was a purified single peptide component but on dissolution displayed evidence of multiple conformations (manifest by peaks "brothering" in the N-terminal region). The structures shown are for the major solution conformer.
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試料調製
詳細
内容: 2 mM MrIB-NH2 / 溶媒系: 90% H2O/10% D2O
試料状態
pH: 3.5 / 圧: ambient / 温度: 285 K
結晶化
*PLUS
手法: other / 詳細: NMR
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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 ARX
Bruker
ARX
500
1
Bruker AVANCE
Bruker
AVANCE
750
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
Felix
230
BiosymTechnologies
データ解析
X-PLOR
3.851
Brunger
構造決定
X-PLOR
3.851
Brunger
精密化
精密化
手法: torsion angle dynamics / ソフトェア番号: 1 詳細: The structures are calculated from a total of 82 distance restraints derived from 14 intra-residue, 42 sequential, 3 medium and 23 long range NOEs, and 4 dihedral restraints.
代表構造
選択基準: closest to the average
NMRアンサンブル
コンフォーマー選択の基準: The submitted conformer models are the 20 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