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.
THE BIOLOGICAL UNITS ARE DIMERS FORMED BY DISULFIDE BONDS BETWEEN CYSTEINES 206 AND 227. THE DIMERS ARE 2-FOLD SYMMETRIC AND CONSIST OF TWO CHAINS A OR TWO CHAINS B.
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要素
#1: タンパク質
INTERNALINB / INLB
分子量: 32030.586 Da / 分子数: 2 / 断片: INTERNALIN DOMAIN, RESIDUES 36-321 / 変異: YES / 由来タイプ: 組換発現 詳細: RESIDUES 36-321 OF LISTERIA MONOCYTOGENES INLB CROSS-LINKED INTO DIMERS BY TWO INTERMOLECULAR DISULFIDE BONDS BETWEEN C206 AND C227 由来: (組換発現) LISTERIA MONOCYTOGENES (バクテリア) 株: EGD-E / プラスミド: PETM30 / 発現宿主: ESCHERICHIA COLI (大腸菌) / 株 (発現宿主): BL21 CODON PLUS (DE3) / 参照: UniProt: P25147, UniProt: P0DQD2*PLUS
ENGINEERED RESIDUE IN CHAIN A, GLY 206 TO CYS ENGINEERED RESIDUE IN CHAIN A, ALA 227 TO CYS ...ENGINEERED RESIDUE IN CHAIN A, GLY 206 TO CYS ENGINEERED RESIDUE IN CHAIN A, ALA 227 TO CYS ENGINEERED RESIDUE IN CHAIN A, CYS 242 TO ALA ENGINEERED RESIDUE IN CHAIN B, GLY 206 TO CYS ENGINEERED RESIDUE IN CHAIN B, ALA 227 TO CYS ENGINEERED RESIDUE IN CHAIN B, CYS 242 TO ALA
Has protein modification
Y
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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: 2.93 Å3/Da / 溶媒含有率: 57.71 % / 解説: NONE
結晶化
温度: 293 K / pH: 9.5 詳細: 293 K. PROTEIN (6.7 MG/ML) PLUS RESERVOIR = 2 PLUS 1. RESERVOIR SOLUTION IS 44-52% PEG2000, 0.1 M CHES PH=9,5, 0.2M NACL., PH 9.5
解像度: 2.24→46.88 Å / Cor.coef. Fo:Fc: 0.947 / Cor.coef. Fo:Fc free: 0.927 / SU B: 12.37 / SU ML: 0.14 / 交差検証法: THROUGHOUT / ESU R: 0.244 / ESU R Free: 0.199 / 立体化学のターゲット値: MAXIMUM LIKELIHOOD / 詳細: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
Rfactor
反射数
%反射
Selection details
Rfree
0.239
1849
5 %
RANDOM
Rwork
0.199
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obs
0.201
35166
99.9 %
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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: 1.4 Å / 溶媒モデル: MASK