構造決定の手法: 単波長異常分散 / 解像度: 2.49→48.68 Å / Cor.coef. Fo:Fc: 0.905 / Cor.coef. Fo:Fc free: 0.845 / SU B: 17.206 / SU ML: 0.214 / TLS residual ADP flag: LIKELY RESIDUAL / Isotropic thermal model: Isotropic / 交差検証法: THROUGHOUT / σ(F): 0 / ESU R: 0.629 / ESU R Free: 0.335 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD 詳細: The N-terminal His-tag (-19 to -1) is not visible in the electron density except for His (0). The inactive apo protein (no substrate) is cluster-free. The N-terminal domain, which normally ...詳細: The N-terminal His-tag (-19 to -1) is not visible in the electron density except for His (0). The inactive apo protein (no substrate) is cluster-free. The N-terminal domain, which normally contains the active site with a [4Fe-4S] cluster and a site for substrate-binding is largely disordered. Residues 34-89, 93-95, 106, 110-11, 181-199 and 226-230 are not visible in the electron density in chain a. in chain b residues 34-92, 106-107, 110-111, 155 and 181-230 are disordered and not visible in the electron density. In addition, side chains of residues 95, 97 and 98 in chain b are truncated because of missing electron density.
Rfactor
反射数
%反射
Selection details
Rfree
0.2908
2086
5 %
RANDOM
Rwork
0.2295
-
-
-
all
0.2325
39386
-
-
obs
0.2325
39386
100 %
-
溶媒の処理
イオンプローブ半径: 0.8 Å / 減衰半径: 0.8 Å / VDWプローブ半径: 1.4 Å / 溶媒モデル: MASK