PH-domain like - #80 / Domain of unknown function DUF1508 / Domain of unknown function (DUF1508) / YegP-like superfamily / PH-domain like / Roll / Mainly Beta / UPF0339 protein SO_3888
Text: The protein is a monomer by gel filtration chromatography and static light scattering.
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試料調製
詳細
Solution-ID
内容
溶媒系
1
1.3 mM [U-100% 13C; U-100% 15N] SoR190, 5 mM CaCl2, 100 mM sodium chloride, 20 mM ammonium acetate, 10 mM DTT, 0.02 % NaN3, 95% H2O/5% D2O
95% H2O/5% D2O
2
1.3 mM [U-5% 13C; U-100% 15N] SoR190, 5 mM CaCl2, 100 mM sodium chloride, 20 mM ammonium acetate, 10 mM DTT, 0.02 % NaN3, 95% H2O/5% D2O
95% H2O/5% D2O
試料
濃度 (mg/ml)
構成要素
Isotopic labeling
Solution-ID
1.3mM
SoR190
[U-100% 13C; U-100% 15N]
1
5mM
CaCl2
1
100mM
sodiumchloride
1
20mM
ammoniumacetate
1
10mM
DTT
1
0.02 %
NaN3
1
1.3mM
SoR190
[U-5% 13C; U-100% 15N]
2
5mM
CaCl2
2
100mM
sodiumchloride
2
20mM
ammoniumacetate
2
10mM
DTT
2
0.02 %
NaN3
2
試料状態
イオン強度: 0.1 M / pH: 5.5 / 圧: ambient / 温度: 293 K
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NMR測定
NMRスペクトロメーター
タイプ
製造業者
モデル
磁場強度 (MHz)
Spectrometer-ID
Bruker Avance
Bruker
AVANCE
800
1
Bruker Avance
Bruker
AVANCE
600
2
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解析
NMR software
名称
バージョン
開発者
分類
TopSpin
2.1
BrukerBiospin
collection
AutoAssign
2.2.1
Zimmerman, Moseley, KulikowskiandMontelione
chemicalshiftassignment
Sparky
3.11
Goddard
peakpicking
Sparky
3.11
Goddard
データ解析
AutoStructure
2.2.1
Huang, Tejero, PowersandMontelione
構造決定
NMRPipe
2.3
Delaglio, Grzesiek, Vuister, Zhu, PfeiferandBax
解析
CYANA
2.1
Guntert, MumenthalerandWuthrich
構造決定
CNS
1.1
Brunger, Adams, Clore, Gros, NilgesandRead
精密化
PSVS
1.3
BhattacharyaandMontelione
データ解析
PdbStat
5
TejeroandMontelione
pdbanalysis
精密化
手法: simulated annealing / ソフトェア番号: 1 詳細: THE STRUCTURES ARE BASED ON A TOTAL OF 2291 COMFORMATIONALLY-RESTRICTING NOE-DERIVED DISTANCE CONSTRAINTS, 146 DIHEDRAL ANGLE CONSTRAINTS, AND 92 HYDROGEN BOND CONSTRAINTS (22.4 CONSTRAINTS ...詳細: THE STRUCTURES ARE BASED ON A TOTAL OF 2291 COMFORMATIONALLY-RESTRICTING NOE-DERIVED DISTANCE CONSTRAINTS, 146 DIHEDRAL ANGLE CONSTRAINTS, AND 92 HYDROGEN BOND CONSTRAINTS (22.4 CONSTRAINTS PER RESIDUE, 7.7 LONG RANGE CONSTRAINTS PER RESIDUE, COMPUTED FOR RESIDUES 1 TO 118 BY PSVS 1.3) STRUCTURE DETERMINATION WAS PERFORMED ITERATIVELY USING AUTOSTRUCTURE AND CYANA. THE 20 LOWEST ENERGY STRUCTURES OUT OF 100 WERE FURTHER REFINED BY RESTRAINED MOLECULAR DYNAMICS/ENERGY MINIMIZATION IN EXPLICIT WATER (CNS). THE C-TERMINAL HIS TAG RESIDUES OF THE PROTEIN (HHHHHH) WERE INCLUDED IN ALL STRUCTURE CALCULATIONS AND HAVE BEEN INCLUDED IN THIS DEPOSITION. COORDINATES FOR THE FOLLOWING RESIDUES ARE NOT WELL DETERMINED (S(PHI)+S(PSI)<1.8): 1-3, 21-22, 112-118. THE STRUCTURE WAS DETERMINED USING TRIPLE RESONANCE NMR SPECTROSCOPY. AUTOMATED BACKBONE ASSIGNMENTS WERE MADE USING AUTOASSIGN AND THE SIDE CHAIN ASSIGNMENTS WERE COMPLETED MANUALLY. AUTOMATIC NOESY ASSIGNMENTS AS WELL AS DISTANCE, DIHEDRAL ANGLE (TALOS) AND HYDROGEN BOND CONSTRAINTS WERE DETERMINED USING CYANA. COMPLETENESS OF NMR ASSIGNMENT: BACKBONE, 94.10%, SIDE CHAIN, 82.27%, AROMATICS, 76.92%, STEREOSPECIFIC METHYL, 91.67%, FINAL STRUCTURE QUALITY FACTORS (FOR RESIDUE 1-118 PSVS 1.3), WHERE ORDERED RESIDUE RANGES (S(PHI)+S(PSI)>1.8) COMPRISE: 4-20, 23-111. (A) RMSD (ORDERED RESIDUES): BB 0.6, HEAVY ATOM: 1.1 (B) RAMACHANDRAN STATISTICS FOR ORDERED RESIDUES: MOST FAVORED, 88.1%, ADDITIONALLY ALLOWED: 11.8%, GENEROUSLY ALLOWED : 0.1%, DISALLOWED, 0.0%. (C) PROCHECK SCORES FOR ORDERED RESIDUES (RAW/Z): PHI-PSI, -0.30/-0.87, ALL , -0.12/-0.71. (D) MOLPROBITY CLASH SCORE (RAW/Z): 13.32/-0.76. (E) RPF SCORES FOR GOODNESS OF FIT TO NOESY DATA (RESIDUE 1-118): RECALL, 1, PRECISION, 0.975, F-MEASURE, 0.987, DP-SCORE, 0.89.
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: 100 / 登録したコンフォーマーの数: 20 / Maximum upper distance constraint violation: 0.22 Å