分子量: 846.980 Da / 分子数: 1 / 断片: C-TERMINAL DOMAIN 130-135 / 由来タイプ: 合成 詳細: The peptide was chemically synthesized. The sequence CGG was added as a linker to the dextran matrix in Biacore experiments via the Cys thiol group. NH2-CO was added at the C-terminal ...詳細: The peptide was chemically synthesized. The sequence CGG was added as a linker to the dextran matrix in Biacore experiments via the Cys thiol group. NH2-CO was added at the C-terminal extremity of the retro-inverso peptide in order to mimic the N-terminal of the parent peptide. All non glycine residues present a D-configuration except CYS. Two RI(mA) diastereisomers were obtained and couldn't be separated.
タイプ: Bruker DRX / 製造業者: Bruker / モデル: DRX / 磁場強度: 400 MHz
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解析
NMR software
名称
バージョン
開発者
分類
DYANA
1.4
Guntert, Wuthrich
構造決定
Discover
3
MolecularSimulationsInc., SanDiego, CA
構造決定
Discover
3
MolecularSimulationsInc., SanDiego, CA
精密化
XwinNMR
1.2
Bruker
collection
精密化
手法: Energy minimisation Molecular dynamics (Simulated Annealing) ソフトェア番号: 1 詳細: The structures are based on a set of 35 to 60 backbone-backbone, backbone-side chain and side chain-side chain distance restraints. The phi angle for the non glycine D-residues was ...詳細: The structures are based on a set of 35 to 60 backbone-backbone, backbone-side chain and side chain-side chain distance restraints. The phi angle for the non glycine D-residues was constrained between 0 and 175. A distance dependent dielectric constant equal to 4r was applied. The net electric charges were decreased, while those of the N and C terminal charged groups were neglected.
代表構造
選択基準: lowest energy
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: 50 / 登録したコンフォーマーの数: 6