A: Methyl-CpG-binding domain protein 3 B: Methyl-CpG-binding domain protein 3 C: DNA (5'-D(*GP*CP*CP*AP*GP*(5CM)P*GP*TP*TP*GP*GP*C)-3') D: DNA (5'-D(*GP*CP*CP*AP*AP*(5CM)P*GP*CP*TP*GP*GP*C)-3') E: DNA (5'-D(*GP*CP*CP*AP*GP*(5CM)P*GP*TP*TP*GP*GP*C)-3') F: DNA (5'-D(*GP*CP*CP*AP*AP*(5CM)P*GP*CP*TP*GP*GP*C)-3')
A: Methyl-CpG-binding domain protein 3 C: DNA (5'-D(*GP*CP*CP*AP*GP*(5CM)P*GP*TP*TP*GP*GP*C)-3') D: DNA (5'-D(*GP*CP*CP*AP*AP*(5CM)P*GP*CP*TP*GP*GP*C)-3')
B: Methyl-CpG-binding domain protein 3 E: DNA (5'-D(*GP*CP*CP*AP*GP*(5CM)P*GP*TP*TP*GP*GP*C)-3') F: DNA (5'-D(*GP*CP*CP*AP*AP*(5CM)P*GP*CP*TP*GP*GP*C)-3')
解像度: 2.005→35.202 Å / SU ML: 0.29 / 交差検証法: FREE R-VALUE / σ(F): 1.34 / 位相誤差: 27.09 / 立体化学のターゲット値: ML 詳細: Electron density did not permit unambiguous distinction between strands of non-palindromic DNA. refmac was used for intermediate refinement steps. coot was used for interactive model building. ...詳細: Electron density did not permit unambiguous distinction between strands of non-palindromic DNA. refmac was used for intermediate refinement steps. coot was used for interactive model building. Model geometry was validated with molprobity.
Rfactor
反射数
%反射
Selection details
Rfree
0.2566
1312
5.72 %
thinshells (sftools)
Rwork
0.2148
21616
-
-
obs
0.2173
22928
99.18 %
-
溶媒の処理
減衰半径: 0.9 Å / VDWプローブ半径: 1.11 Å / 溶媒モデル: FLAT BULK SOLVENT MODEL