SHEET DETERMINATION METHOD: DSSP THE SHEETS PRESENTED AS "AA" IN EACH CHAIN ON SHEET RECORDS BELOW ... SHEET DETERMINATION METHOD: DSSP THE SHEETS PRESENTED AS "AA" IN EACH CHAIN ON SHEET RECORDS BELOW IS ACTUALLY AN 8-STRANDED BARREL THIS IS REPRESENTED BY A 9-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL.
解像度: 1.9→82.5 Å / Num. obs: 10376 / % possible obs: 100 % / Observed criterion σ(I): 0 / 冗長度: 11.9 % / Rmerge(I) obs: 0.09 / Net I/σ(I): 21
反射 シェル
解像度: 1.9→1.94 Å / 冗長度: 12 % / Rmerge(I) obs: 0.83 / Mean I/σ(I) obs: 3.7 / % possible all: 100
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解析
ソフトウェア
名称
バージョン
分類
REFMAC
5.8.0033
精密化
MOSFLM
データ削減
SCALA
データスケーリング
SHELX
位相決定
精密化
構造決定の手法: 単波長異常分散 開始モデル: NONE 解像度: 1.9→82.47 Å / Cor.coef. Fo:Fc: 0.966 / Cor.coef. Fo:Fc free: 0.96 / SU B: 2.731 / SU ML: 0.079 / 交差検証法: THROUGHOUT / ESU R: 0.122 / ESU R Free: 0.115 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. THE PROTEIN STRUCTURE IS VAPD-CORE IN WHICH THE DISORDERED N-TERMINUS (RESIDUE 1-19) IS ABSENT FROM THE PROTEIN CONSTRUCT.
Rfactor
反射数
%反射
Selection details
Rfree
0.19078
497
4.8 %
RANDOM
Rwork
0.15923
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-
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obs
0.16077
9823
99.54 %
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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: 1.2 Å / 溶媒モデル: MASK