当前蛋白身份:P27958 重新检索
本组结构的主要差异维度
构建体不同 突变/修饰不同 组装状态不同 配体/离子不同 实验方法不同 实验环境不同 结构质量指标不同

差异标签只比较当前检索结果;所有PDB和assembly原始记录仍分别保留。

相关结构差异明细

一行代表一个 PDB 条目中的一个 biological assembly;同一蛋白的多个单体会分别列出。

PDB 条目 Assembly / 聚集状态 构建体 突变与修饰 配体、离子与非聚合物 实验方法 实验环境 结构质量
1A1R HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX 提交 1997-12-15 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 1026–1205(180 aa) 片段:PROTEASE DOMAIN
链 C 1677–1695(19 aa) 片段:ACTIVATION DOMAIN
突变:INS(ASMTGGQQMG) AT N-TERMINUS, INS(GSHHHHHH) AT C-TERMINUS 突变:INS(KK) AT N-TERMINUS, C22S, INS(KK) AT C-TERMINUS ZN ZINC ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;PROTEIN WAS CRYSTALLIZED FROM 1.8 M NACL, 100 MM NA/K PHOSPHATE, 10 MM B-MERCAPTOETHANOL, 100 MM MES, PH 6.5.
分辨率 2.50 Å R-free 0.261
1A1R HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX 提交 1997-12-15 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 1026–1205(180 aa) 片段:PROTEASE DOMAIN
链 D 1677–1695(19 aa) 片段:ACTIVATION DOMAIN
突变:INS(ASMTGGQQMG) AT N-TERMINUS, INS(GSHHHHHH) AT C-TERMINUS 突变:INS(KK) AT N-TERMINUS, C22S, INS(KK) AT C-TERMINUS ZN ZINC ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;PROTEIN WAS CRYSTALLIZED FROM 1.8 M NACL, 100 MM NA/K PHOSPHATE, 10 MM B-MERCAPTOETHANOL, 100 MM MES, PH 6.5.
分辨率 2.50 Å R-free 0.261
1A1R HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX 提交 1997-12-15 Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 1026–1205(180 aa) 片段:PROTEASE DOMAIN
链 B 1026–1205(180 aa) 片段:PROTEASE DOMAIN
链 C 1677–1695(19 aa) 片段:ACTIVATION DOMAIN
链 D 1677–1695(19 aa) 片段:ACTIVATION DOMAIN
突变:INS(ASMTGGQQMG) AT N-TERMINUS, INS(GSHHHHHH) AT C-TERMINUS 突变:INS(ASMTGGQQMG) AT N-TERMINUS, INS(GSHHHHHH) AT C-TERMINUS 突变:INS(KK) AT N-TERMINUS, C22S, INS(KK) AT C-TERMINUS 突变:INS(KK) AT N-TERMINUS, C22S, INS(KK) AT C-TERMINUS ZN ZINC ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;PROTEIN WAS CRYSTALLIZED FROM 1.8 M NACL, 100 MM NA/K PHOSPHATE, 10 MM B-MERCAPTOETHANOL, 100 MM MES, PH 6.5.
分辨率 2.50 Å R-free 0.261
1A1V HEPATITIS C VIRUS NS3 HELICASE DOMAIN COMPLEXED WITH SINGLE STRANDED SDNA 提交 1997-12-17 Assembly 1 蛋白–DNA 单体;蛋白 × 1 PDB 声明:dimeric(2) 与全部聚合物一致
链 A 1193–1657(465 aa) 片段:HELICASE DOMAIN
突变:;N-TERMINAL MET, K221Q, A277G, S301L, S332P, S410A, G530E, R582W, AND A 10 RESIDUE (GSGSHHHHHH) HISTIDINE TAG ATTACHED TO THE C-TERMINUS ; 非标准单体:是(mmCIF未提供具体位点) SO4 SULFATE ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 pH 8;pH 8.0
分辨率 2.20 Å R-free 0.287
1CWX SOLUTION STRUCTURE OF THE HEPATITIS C VIRUS N-TERMINAL CAPSID PROTEIN 2-45 [C-HCV(2-45)] 提交 1999-08-27 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 2–45(44 aa) 片段:N-TERMINAL FRAGMENT
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 5.9;293 K;离子强度(mmCIF原始值)0.1M NACL;压力 AMBIENT
NMR样品组成 40% D2-TRIFLUOROETHANOL;0.01M SODIUM PHOSPHATE;0.1M NACL
分辨率未提供
1HEI STRUCTURE OF THE HEPATITIS C VIRUS RNA HELICASE DOMAIN 提交 1997-03-31 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 1206–1656(451 aa)
链 B 1206–1656(451 aa)
未记录 CA CALCIUM ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;50MM CA ACETATE, 20MM NACACODYLATE PH 6.5, 8% PEG5000
分辨率 2.10 Å R-free 0.320
1JR6 Solution Structure of an Engineered Arginine-rich Subdomain 2 of the Hepatitis C Virus NS3 RNA Helicase 提交 2001-08-10 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1353–1507(155 aa) 片段:arginine-rich subdomain 2
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6.5;298 K;离子强度(mmCIF原始值)75 mM KiPO4;压力 ambient
NMR样品组成 0.6 mM, U-15N,13C; | 75 mM PHOSPHATE BUFFER; 5 mM DTT, 90%H2O, 10%D2O, 0.015% NaN3
NMR样品组成 0.6 mM, U-15N,13C; | 75 mM PHOSPHATE BUFFER; 5 mM DTT, 99%D2O, 0.015% NaN3
NMR样品组成 0.3 mM, U-15N | 75 mM PHOSPHATE BUFFER; 5 mM DTT, 90%H2O, 10%D2O, 0.015% NaN3
分辨率未提供
1N1L CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND INHIBITOR (GW472467X) 提交 2002-10-18 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 1026–1205(180 aa) 片段:Protease domain
突变:A164T ZN ZINC ION × 1 TRL {1-[2-(1-FORMYL-PROPYL)-3-METHANESULFONYLAMINO-PYRROLIDINE-1-CARBONYL]-2-METHYL-PROPYL}-CARBAMIC ACID TERT-BUTYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;pH 6.5;277 K;Inhibitor soaked into crystal generated according to Kim et al. (1996) Cell, 87, 343-355, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 277.0K
分辨率 2.60 Å R-free 0.220
1N1L CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND INHIBITOR (GW472467X) 提交 2002-10-18 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 1026–1205(180 aa) 片段:Protease domain
突变:A164T ZN ZINC ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;pH 6.5;277 K;Inhibitor soaked into crystal generated according to Kim et al. (1996) Cell, 87, 343-355, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 277.0K
分辨率 2.60 Å R-free 0.220
1N1L CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND INHIBITOR (GW472467X) 提交 2002-10-18 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 1026–1205(180 aa) 片段:Protease domain
链 B 1026–1205(180 aa) 片段:Protease domain
突变:A164T 突变:A164T ZN ZINC ION × 2 TRL {1-[2-(1-FORMYL-PROPYL)-3-METHANESULFONYLAMINO-PYRROLIDINE-1-CARBONYL]-2-METHYL-PROPYL}-CARBAMIC ACID TERT-BUTYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;pH 6.5;277 K;Inhibitor soaked into crystal generated according to Kim et al. (1996) Cell, 87, 343-355, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 277.0K
分辨率 2.60 Å R-free 0.220
1ONB Solution structure of an engineered arginine-rich subdomain 2 of the hepatitis C virus NS3 RNA helicase 提交 2003-02-27 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1353–1507(155 aa) 片段:Arginine-rich subdomain 2
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6.5;298 K;离子强度(mmCIF原始值)75 mM KIPO4;压力 ambient
NMR样品组成 0.6 mM, U-15N,13C | 90% H2O/10% D2O
NMR样品组成 0.6 mM, U-15N,13C | 99.9%D2O
分辨率未提供
1R7C NMR structure of the membrane anchor domain (1-31) of the nonstructural protein 5A (NS5A) of hepatitis C virus (Minimized average structure, Sample in 50% tfe) 提交 2003-10-21 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1973–2003(31 aa) 片段:Nonstructural protein NS5A (P56)(residues 1973-2003 OF SWISS-PROT SEQUENCE P27958)
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 4.5;293 K;压力 ambient
NMR样品组成 1.2mM NS5A[1-31], 10mM DTTd10 | H2O/TFEd2 50/50 (v/v)
分辨率未提供
1R7D NMR structure of the membrane anchor domain (1-31) of the nonstructural protein 5A (NS5A) of hepatitis C virus (Ensemble of 51 structures, sample in 50% tfe) 提交 2003-10-21 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1973–2003(31 aa) 片段:Nonstructural protein NS5A (P56)(residues 1973-2003 of Swiss-Prot sequence P27958)
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 4.5;293 K;压力 ambient
NMR样品组成 1.2mM NS5A[1-31], 10mM DTTd10 | H2O/TFEd2 50/50 (v/v)
分辨率未提供
1R7E NMR structure of the membrane anchor domain (1-31) of the nonstructural protein 5A (NS5A) of hepatitis C virus (Minimized average structure. Sample in 100mM SDS). 提交 2003-10-21 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1973–2003(31 aa) 片段:Nonstructural protein NS5A (P56)(residues 1973-2003 OF SWISS-PROT SEQUENCE P27958)
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6;313 K;压力 ambient
NMR样品组成 1.2mM NS5A[1-31], 10mM DTTd10 | 100mM SDS in H2O/D2O 95/5 (v/v)
分辨率未提供
1R7F NMR structure of the membrane anchor domain (1-31) of the nonstructural protein 5A (NS5A) of hepatitis C virus (Ensemble of 43 structures. Sample in 100mM SDS) 提交 2003-10-21 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1973–2003(31 aa) 片段:Nonstructural protein NS5A (P56)(residues 1973-2003 of Swiss-Prot sequence P27958)
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6;313 K;压力 ambient
NMR样品组成 1.2mM NS5A[1-31], 10mM DTTd10 | 100mM SDS in H2O/D2O 95/5 (v/v)
分辨率未提供
1R7G NMR structure of the membrane anchor domain (1-31) of the nonstructural protein 5A (NS5A) of hepatitis C virus (Minimized average structure, Sample in 100mM DPC) 提交 2003-10-21 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1973–2003(31 aa) 片段:Nonstructural protein NS5A (P56)(residues 1973-2003 OF SWISS-PROT SEQUENCE P27958)
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6;313 K;压力 ambient
NMR样品组成 1.2mM NS5A[1-31], 10mM DTTd10 | 100mM DPC in H2O/D2O 95/5 (v/v)
分辨率未提供
1RGQ M9A HCV Protease complex with pentapeptide keto-amide inhibitor 提交 2003-11-12 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 1026–1206(181 aa) 片段:RESIDUES 1027-1207
链 B 1026–1206(181 aa) 片段:RESIDUES 1027-1207
未记录 ZN ZINC ION × 2 AKP N-(PYRAZIN-2-YLCARBONYL)LEUCYLISOLEUCYL-N~1~-{1-[2-({1-CARBOXY-2-[4-(PHOSPHONOOXY)PHENYL]ETHYL}AMINO)-1,1-DIHYDROXY-2-OXOETHYL]BUT-3-ENYL}-3-CYCLOHEXYLALANINAMIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;0.2M N/KPO4, 2.0M NaCl, 10mM MES, 15% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K
分辨率 2.90 Å R-free 0.312
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 902–1025(124 aa) 片段:protease domain of NS2
链 B 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 C 902–1025(124 aa) 片段:protease domain of NS2
链 D 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 E 902–1025(124 aa) 片段:protease domain of NS2
链 F 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 4 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 G 902–1025(124 aa) 片段:protease domain of NS2
链 H 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 5 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 I 902–1025(124 aa) 片段:protease domain of NS2
链 J 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 2 DMU DECYL-BETA-D-MALTOPYRANOSIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2HD0 Structure of the catalytic domain of hepatitis C virus NS2 提交 2006-06-19 Assembly 6 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 K 902–1025(124 aa) 片段:protease domain of NS2
链 L 902–1025(124 aa) 片段:protease domain of NS2
未记录 BOG octyl beta-D-glucopyranoside × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;0.1 M Tris pH 8.5 0.8 M Ammonium Acetate 0.25 M Lithium Chloride 12% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277.0K
分辨率 2.28 Å R-free 0.268
2JXF The solution structure of HCV NS4B(40-69) 提交 2007-11-19 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 1751–1780(30 aa) 片段:Non-structural protein 4B, UNP residues 1751-1780
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6.5;298 K;离子强度(mmCIF原始值)0;压力 ambient
NMR样品组成 1mM NS4B(40-69); 50% v/v Trifluoro Ethanol D2OH; 50% v/v H2O | 50% v/v Trifluoro Ethanol D2OH; 50% v/v H2O
分辨率未提供
2KDR Solution structure of HCV NS4B(227-254) 提交 2009-01-15 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 X 1938–1965(28 aa) 片段:UNP residues 1938-1965
未记录 未记录非水小分子 SOLUTION NMR
NMR测量条件 pH 6;298 K;离子强度(mmCIF原始值)none;压力 ambient
NMR样品组成 2mM protein-1, 50% v/v Trifluoro Ethanol D2OH; 50% v/v H2O | 50% v/v Trifluoro Ethanol D2OH; 50% v/v H2O
分辨率未提供
2N1P Structure of the C-terminal membrane domain of HCV NS5B protein 提交 2015-04-15 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 2982–3011(30 aa) 片段:C-terminal domain (UNP residues 2982-3011)
突变:C14S 未记录非水小分子 SOLUTION NMR
NMR测量条件 298 K;压力 ambient
NMR样品组成 1.4 mM protein, 1 M [U-2H] SDS, 95% H2O/5% D2O | 95% H2O/5% D2O
分辨率未提供
2O8M Crystal structure of the S139A mutant of Hepatitis C Virus NS3/4A protease 提交 2006-12-12 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 C 1677–1695(19 aa)
链 D 1677–1695(19 aa)
未记录 ZN ZINC ION × 2 NA SODIUM ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;277 K;1.25 to 1.5M NaCl, 0.1 M MES, .1M Na/K PO4, 5mM beta-mercaptoethanol, pH 5.6-6.2, VAPOR DIFFUSION, HANGING DROP, temperature 277K
分辨率 2.00 Å R-free 0.228
2OBQ Discovery of the HCV NS3/4A Protease Inhibitor SCH503034. Key Steps in Structure-Based Optimization 提交 2006-12-19 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 B 1677–1695(19 aa)
链 D 1677–1695(19 aa)
突变:C22S 突变:C22S ZN ZINC ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;277 K;The protein (NS3 complexed with KK-NS4a(21-39)-KK peptide) was at 12-15 mg/ml in 15 mM MES, pH 6.5 1 M NaCl 20 mM b-mercaptoethanol. Hanging Drops were formed by mixing 4:l protein solution with 4:l {0.75-1.0 M NaCl, 0.1M Na/K phosphate 0.1 M Mes, pH 5.8-6.1 20 mM b-mercaptoethanol} The drop was equilibrated the drops over 1 ml {(1.25-1.50 M) NaCl - 0.1M Na/K phosphate 0.1 M Mes, pH 5.6-5.8, 20 mM b-mercaptoethanol} , VAPOR DIFFUSION, HANGING DROP, temperature 277K
分辨率 2.50 Å R-free 0.264
2XI2 HCV-H77 NS5B Apo Polymerase 提交 2010-06-25 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 2421–2990(570 aa) 片段:CATALYTIC DOMAIN, RESIDUES 2421-2990
突变:YES SO4 SULFATE ION × 7 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;MES 0.1M PH 6.5, AMMONIUM SULFATE 0.2M, PEG 5000 MONOMETHYL ETHER
分辨率 1.80 Å R-free 0.207
2XI2 HCV-H77 NS5B Apo Polymerase 提交 2010-06-25 Assembly 2 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 2421–2990(570 aa) 片段:CATALYTIC DOMAIN, RESIDUES 2421-2990
突变:YES SO4 SULFATE ION × 7 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;MES 0.1M PH 6.5, AMMONIUM SULFATE 0.2M, PEG 5000 MONOMETHYL ETHER
分辨率 1.80 Å R-free 0.207
2XI2 HCV-H77 NS5B Apo Polymerase 提交 2010-06-25 Assembly 3 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 C 2421–2990(570 aa) 片段:CATALYTIC DOMAIN, RESIDUES 2421-2990
突变:YES SO4 SULFATE ION × 6 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;MES 0.1M PH 6.5, AMMONIUM SULFATE 0.2M, PEG 5000 MONOMETHYL ETHER
分辨率 1.80 Å R-free 0.207
2XI3 HCV-H77 NS5B Polymerase Complexed With GTP 提交 2010-06-25 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 2421–2990(570 aa) 片段:CATALYTIC DOMAIN, RESIDUES 2421-2990
突变:YES GTP GUANOSINE-5'-TRIPHOSPHATE × 3 MG MAGNESIUM ION × 3 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;MES 50MM PH 6.5, AMMONIUM SULFATE 0.2M, AMMONIUM ACETATE 0.25M, PEG 1000 25%-30%
分辨率 1.70 Å R-free 0.198
2XI3 HCV-H77 NS5B Polymerase Complexed With GTP 提交 2010-06-25 Assembly 2 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 2421–2990(570 aa) 片段:CATALYTIC DOMAIN, RESIDUES 2421-2990
突变:YES GTP GUANOSINE-5'-TRIPHOSPHATE × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 pH 6.5;MES 50MM PH 6.5, AMMONIUM SULFATE 0.2M, AMMONIUM ACETATE 0.25M, PEG 1000 25%-30%
分辨率 1.70 Å R-free 0.198
4JZN Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC84-1 提交 2013-04-03 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 K 434–446(13 aa) 片段:Residues 434-446 of HCV strain H77 polyprotein
未记录 SO4 SULFATE ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;100mM TRIS pH 8.0 19% PEG4000 170mM Lithium Sulfate 15% Glycerol, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.05 Å R-free 0.235
4JZO Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC84-27 提交 2013-04-03 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 J 434–446(13 aa) 片段:Residues 434-446 of HCV strain H77 polyprotein
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;23% PEG 3350 250mM Sodium Thiocyanate, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.22 Å R-free 0.236
4JZO Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC84-27 提交 2013-04-03 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 K 434–446(13 aa) 片段:Residues 434-446 of HCV strain H77 polyprotein
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;23% PEG 3350 250mM Sodium Thiocyanate, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.22 Å R-free 0.236
4JZO Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC84-27 提交 2013-04-03 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 I 434–446(13 aa) 片段:Residues 434-446 of HCV strain H77 polyprotein
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;23% PEG 3350 250mM Sodium Thiocyanate, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.22 Å R-free 0.236
4JZO Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC84-27 提交 2013-04-03 Assembly 4 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 L 434–446(13 aa) 片段:Residues 434-446 of HCV strain H77 polyprotein
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;23% PEG 3350 250mM Sodium Thiocyanate, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.22 Å R-free 0.236
4MWF Structure of Hepatitis C Virus Envelope Glycoprotein E2 core bound to broadly neutralizing antibody AR3C 提交 2013-09-24 Assembly 1 其他组合 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 D 412–459(48 aa)
链 D 486–645(160 aa)
突变:N448D, N576D 突变:N448D, N576D NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;20% (w/v) PEG 4000, 10% (v/v) isopropanol, and 0.1 M HEPES pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
分辨率 2.65 Å R-free 0.270
4MWF Structure of Hepatitis C Virus Envelope Glycoprotein E2 core bound to broadly neutralizing antibody AR3C 提交 2013-09-24 Assembly 2 其他组合 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 C 412–459(48 aa)
链 C 486–645(160 aa)
突变:N448D, N576D 突变:N448D, N576D NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;20% (w/v) PEG 4000, 10% (v/v) isopropanol, and 0.1 M HEPES pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
分辨率 2.65 Å R-free 0.270
4Q0X Crystal structure of non-neutralizing antibody in complex with Epitope II of HCV E2 提交 2014-04-02 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 E 421–446(26 aa) 片段:epitope II (UNP residues 421-446)
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;293 K;0.1 M imidazole, 14% w/v PEG550 MME, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 2.90 Å R-free 0.285
5FGB Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC33.4 提交 2015-12-20 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 F 405–425(21 aa)
未记录 GOL GLYCEROL × 2 SO4 SULFATE ION × 5 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 5.2;293 K;100 mM sodium citrate pH 5.2 300 mM ammonium sulfate 100 mM potassium phosphate 1 M lithium chloride
分辨率 1.65 Å R-free 0.190
5FGB Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC33.4 提交 2015-12-20 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 G 405–425(21 aa)
未记录 GOL GLYCEROL × 2 SO4 SULFATE ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 5.2;293 K;100 mM sodium citrate pH 5.2 300 mM ammonium sulfate 100 mM potassium phosphate 1 M lithium chloride
分辨率 1.65 Å R-free 0.190
5FGC Three dimensional structure of broadly neutralizing human anti - Hepatitis C virus (HCV) glycoprotein E2 Fab fragment HC33.8 提交 2015-12-20 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric(3) 与蛋白数一致
链 A 405–425(21 aa)
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8.5;293 K;32% PEG 4000 100 mM Tris-HCl pH 8.5 800 mM lithium chloride Crystals obtained using heterologous microseeding.
分辨率 1.90 Å R-free 0.236