SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN ... SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN THE SHEET RECORDS BELOW, TWO SHEETS ARE DEFINED.
CLPP ENDOPEPTIDASES ARE KNOWN TO BE TETRADECAMERICAND THIS IS THE MULTIMERIC STATE FOUND IN THISSTRUCTURE.HOWEVER, IN THIS PROTEIN, GEL FILTRATION AND INTER-COMPLEX REGIONS BETWEEN THE TWO HEPTAMERIC RINGS WOULDINDICATE THAT THE OLIGOMER IS LIKELY TO BE HEPTAMERICIN SOLUTION.IN ORDER TO GENERATE THE 14-MER, THE FOLLOWINGTRANSFORMATION NEEDS TO BE APPLIED TO ALL THE SEVENCHAINS IN THIS FILE.BIOMT1 2 0.500000 -0.866025 0. 000000 89.12738BIOMT2 2 -0.866025 -0. 500000 0.000000 154.37311BIOMT3 2 0. 000000 0.000000 -1.000000 220.76231
CLEAVES PEPTIDES IN VARIOUS PROTEINS IN A PROCESS THAT REQUIRES ATP HYDROLYSIS. HAS A CHYMOTRYPSIN- ...CLEAVES PEPTIDES IN VARIOUS PROTEINS IN A PROCESS THAT REQUIRES ATP HYDROLYSIS. HAS A CHYMOTRYPSIN-LIKE ACTIVITY. PLAYS A MAJOR ROLE IN THE DEGRADATION OF MISFOLDED PROTEINS.
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実験情報
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実験
実験
手法: X線回折 / 使用した結晶の数: 1
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試料調製
結晶
マシュー密度: 3.83 Å3/Da / 溶媒含有率: 67.91 %
結晶化
手法: 蒸気拡散法, ハンギングドロップ法 / pH: 8 詳細: THE PROTEIN WAS CRYSTALLISED BY THE VAPOUR DIFFUSION METHOD IN HANGING DROPS CONTAINING A 1:1 MIXTURE OF 3 MG/ML PROTEIN SOLUTION (IN 50 MM TRIS-HCL PH 8) AND RESERVOIR SOLUTION INCLUDING 1 M ...詳細: THE PROTEIN WAS CRYSTALLISED BY THE VAPOUR DIFFUSION METHOD IN HANGING DROPS CONTAINING A 1:1 MIXTURE OF 3 MG/ML PROTEIN SOLUTION (IN 50 MM TRIS-HCL PH 8) AND RESERVOIR SOLUTION INCLUDING 1 M AMMONIUM SULPHATE IN 0.1 M HEPES PH 8.
解像度: 2.6→154.3 Å / Cor.coef. Fo:Fc: 0.932 / Cor.coef. Fo:Fc free: 0.901 / SU B: 12.914 / SU ML: 0.141 / TLS residual ADP flag: LIKELY RESIDUAL / 交差検証法: THROUGHOUT / ESU R: 0.264 / ESU R Free: 0.219 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. THE N-TERMINAL REGION OF EACH MONOMER, UP TO RESIDUE LEU14 IS NOT VISIBLE IN THE ELECTRON DENSITY MAP AND HAS NOT BEEN MODELLED. THE REGION ...詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS. THE N-TERMINAL REGION OF EACH MONOMER, UP TO RESIDUE LEU14 IS NOT VISIBLE IN THE ELECTRON DENSITY MAP AND HAS NOT BEEN MODELLED. THE REGION COMPRISING RESIDUES LEU126 TO D135 OF EACH MONOMER IS NOT VISIBLE IN THE ELECTRON DENSITY MAP AND HAS NOT BEEN MODELLED. THE 13-17 C-TERMINAL RESIDUES OF THE MONOMER ARE NOT VISIBLE IN THE ELECTRON DENSITY AND HAVE NOT BEEN MODELLED.
Rfactor
反射数
%反射
Selection details
Rfree
0.229
3895
5.12 %
RANDOM
Rwork
0.192
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obs
0.194
76647
100 %
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溶媒の処理
イオンプローブ半径: 0.8 Å / VDWプローブ半径: 1.4 Å / 溶媒モデル: BABINET MODEL PLUS MASK