domain III of ENVELOPE PROTEIN E
Dengue virus
当前结构中的状态
| Assembly | 聚集状态 | 构建体 | 突变与修饰 | 配体、离子与共同组分 | 实验方法与环境 | 结构质量 |
|---|---|---|---|---|---|---|
| 1 | 蛋白单体 单体 蛋白 × 1 PDB 声明:monomeric(1) 与蛋白拷贝数一致 | 链 A; UniProt 469–577 | 片段:Residues 469-577 | 无其他共同聚合物 | SOLUTION NMR NMR测量条件:pH 7.4;298 K;离子强度(mmCIF原始值)0.31;压力 ambient NMR样品组成:1-5 mM EDTA, 1-5 mM DTT, 1 mM sodium azide, 90% H2O/10% D2O | 90% H2O/10% D2O | 分辨率未提供 |
数据库中的同蛋白其他状态
以下每一行都是同一 UniProt 蛋白在另一个 PDB 条目中的 biological assembly, “相对当前条目”直接指出证据层面的不同;没有差异标签表示当前已读取字段一致。
| 其他 PDB | 相对当前条目 2JSF | Assembly / 聚集状态 | 构建体 | 突变与修饰 | 配体、离子与非聚合物 | 实验方法与环境 | 结构质量 |
|---|---|---|---|---|---|---|---|
| 2R69 Crystal structure of Fab 1A1D-2 complexed with E-DIII of Dengue virus at 3.8 angstrom resolution 提交 2007-09-05 | 构建体不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 3 PDB 声明:trimeric |
链 A
478–574(97 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 5.8;298 K;12% PEG 3350, pH 5.8, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 3.80 Å R-free 0.363 |
| 2R6P Fit of E protein and Fab 1A1D-2 into 24 angstrom resolution cryoEM map of Fab complexed with dengue 2 virus. 提交 2007-09-06 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 420 PDB 声明:420-MERIC |
链 A
181–570(390 aa)
片段:E protein
链 B
181–570(390 aa)
片段:E protein
链 C
181–570(390 aa)
片段:E protein
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6
cryo-EM玻璃化条件
冷冻剂 ETHANE;SAMPLES WERE PREPARED AS
THIN LAYERS OF VITREOUS ICE
AND MAINTAINED AT LIQUID
NITROGEN TEMPERATURE IN THE
ELECTRON MICROSCOPE
|
分辨率 24.00 Å |
| 2R6P Fit of E protein and Fab 1A1D-2 into 24 angstrom resolution cryoEM map of Fab complexed with dengue 2 virus. 提交 2007-09-06 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 7 PDB 声明:heptameric |
链 A
181–570(390 aa)
片段:E protein
链 B
181–570(390 aa)
片段:E protein
链 C
181–570(390 aa)
片段:E protein
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6
cryo-EM玻璃化条件
冷冻剂 ETHANE;SAMPLES WERE PREPARED AS
THIN LAYERS OF VITREOUS ICE
AND MAINTAINED AT LIQUID
NITROGEN TEMPERATURE IN THE
ELECTRON MICROSCOPE
|
分辨率 24.00 Å |
| 2R6P Fit of E protein and Fab 1A1D-2 into 24 angstrom resolution cryoEM map of Fab complexed with dengue 2 virus. 提交 2007-09-06 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 35 PDB 声明:35-meric |
链 A
181–570(390 aa)
片段:E protein
链 B
181–570(390 aa)
片段:E protein
链 C
181–570(390 aa)
片段:E protein
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6
cryo-EM玻璃化条件
冷冻剂 ETHANE;SAMPLES WERE PREPARED AS
THIN LAYERS OF VITREOUS ICE
AND MAINTAINED AT LIQUID
NITROGEN TEMPERATURE IN THE
ELECTRON MICROSCOPE
|
分辨率 24.00 Å |
| 2R6P Fit of E protein and Fab 1A1D-2 into 24 angstrom resolution cryoEM map of Fab complexed with dengue 2 virus. 提交 2007-09-06 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 4 蛋白异源复合物 异源复合物;蛋白 × 42 PDB 声明:42-meric |
链 A
181–570(390 aa)
片段:E protein
链 B
181–570(390 aa)
片段:E protein
链 C
181–570(390 aa)
片段:E protein
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6
cryo-EM玻璃化条件
冷冻剂 ETHANE;SAMPLES WERE PREPARED AS
THIN LAYERS OF VITREOUS ICE
AND MAINTAINED AT LIQUID
NITROGEN TEMPERATURE IN THE
ELECTRON MICROSCOPE
|
分辨率 24.00 Å |
| 2R6P Fit of E protein and Fab 1A1D-2 into 24 angstrom resolution cryoEM map of Fab complexed with dengue 2 virus. 提交 2007-09-06 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 5 蛋白异源复合物 异源复合物;蛋白 × 7 PDB 声明:heptameric |
链 A
181–570(390 aa)
片段:E protein
链 B
181–570(390 aa)
片段:E protein
链 C
181–570(390 aa)
片段:E protein
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6
cryo-EM玻璃化条件
冷冻剂 ETHANE;SAMPLES WERE PREPARED AS
THIN LAYERS OF VITREOUS ICE
AND MAINTAINED AT LIQUID
NITROGEN TEMPERATURE IN THE
ELECTRON MICROSCOPE
|
分辨率 24.00 Å |
| 3C6R Low pH Immature Dengue Virus 提交 2008-02-05 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 360 PDB 声明:360-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;The virus was mixed in NTE buffer (10 mM Tris, 120 mM NaCl, and 1 mM EDTA at pH 8) with 50 mM MES, 120 mM NaCl at pH 5.6 to yield a final pH of 6
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 25.00 Å |
| 3C6R Low pH Immature Dengue Virus 提交 2008-02-05 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 6 PDB 声明:hexameric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;The virus was mixed in NTE buffer (10 mM Tris, 120 mM NaCl, and 1 mM EDTA at pH 8) with 50 mM MES, 120 mM NaCl at pH 5.6 to yield a final pH of 6
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 25.00 Å |
| 3C6R Low pH Immature Dengue Virus 提交 2008-02-05 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 30 PDB 声明:30-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;The virus was mixed in NTE buffer (10 mM Tris, 120 mM NaCl, and 1 mM EDTA at pH 8) with 50 mM MES, 120 mM NaCl at pH 5.6 to yield a final pH of 6
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 25.00 Å |
| 3C6R Low pH Immature Dengue Virus 提交 2008-02-05 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 4 蛋白同源多聚体 同源多聚体;蛋白 × 36 PDB 声明:36-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;The virus was mixed in NTE buffer (10 mM Tris, 120 mM NaCl, and 1 mM EDTA at pH 8) with 50 mM MES, 120 mM NaCl at pH 5.6 to yield a final pH of 6
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 25.00 Å |
| 3C6R Low pH Immature Dengue Virus 提交 2008-02-05 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 5 蛋白同源多聚体 同源多聚体;蛋白 × 6 PDB 声明:hexameric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;The virus was mixed in NTE buffer (10 mM Tris, 120 mM NaCl, and 1 mM EDTA at pH 8) with 50 mM MES, 120 mM NaCl at pH 5.6 to yield a final pH of 6
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 25.00 Å |
| 3IXY The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53 提交 2009-02-26 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 600 PDB 声明:600-MERIC |
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 23.00 Å |
| 3IXY The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53 提交 2009-02-26 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 10 PDB 声明:decameric |
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 23.00 Å |
| 3IXY The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53 提交 2009-02-26 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 50 PDB 声明:50-meric |
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 23.00 Å |
| 3IXY The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53 提交 2009-02-26 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 4 蛋白异源复合物 异源复合物;蛋白 × 60 PDB 声明:60-meric |
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 23.00 Å |
| 3IXY The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53 提交 2009-02-26 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 5 蛋白异源复合物 异源复合物;蛋白 × 10 PDB 声明:decameric |
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 23.00 Å |
| 3IYA Association of the pr peptides with dengue virus blocks membrane fusion at acidic pH 提交 2009-06-01 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 360 PDB 声明:360-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;6 mM Tris-HCL 25 mM MES 120 mM NaCl 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 22.00 Å |
| 3IYA Association of the pr peptides with dengue virus blocks membrane fusion at acidic pH 提交 2009-06-01 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 6 PDB 声明:hexameric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;6 mM Tris-HCL 25 mM MES 120 mM NaCl 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 22.00 Å |
| 3IYA Association of the pr peptides with dengue virus blocks membrane fusion at acidic pH 提交 2009-06-01 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 30 PDB 声明:30-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;6 mM Tris-HCL 25 mM MES 120 mM NaCl 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 22.00 Å |
| 3IYA Association of the pr peptides with dengue virus blocks membrane fusion at acidic pH 提交 2009-06-01 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 4 蛋白同源多聚体 同源多聚体;蛋白 × 36 PDB 声明:36-meric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;6 mM Tris-HCL 25 mM MES 120 mM NaCl 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 22.00 Å |
| 3IYA Association of the pr peptides with dengue virus blocks membrane fusion at acidic pH 提交 2009-06-01 | 构建体不同 突变/修饰不同 聚集状态不同 实验方法不同 实验环境不同 结构质量不同 | Assembly 5 蛋白同源多聚体 同源多聚体;蛋白 × 6 PDB 声明:hexameric |
链 A
181–575(395 aa)
链 B
181–575(395 aa)
链 C
181–575(395 aa)
链 D
15–95(81 aa)
链 E
15–95(81 aa)
链 F
15–95(81 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 6;6 mM Tris-HCL 25 mM MES 120 mM NaCl 1 mM EDTA
cryo-EM玻璃化条件
A small vial of ethane is placed inside a larger liquid nitrogen reservoir. The grid holding a few microliters of the sample is held in place at the bottom of a plunger by the means of fine tweezers. Once the ethane in the vial is completely frozen, it needs to be slightly melted. When the liquid ethane is ready, a piece of filter paper is then pressed against the sample to blot of excess buffer, sufficient to leave a thin layer on the grid. After a predetermined time, the filter paper is removed, and the plunger is allowed to drop into the liquid ethane. Once the grid enters the liquid ethane, the sample is rapidly frozen, and the grid is transferred under liquid nitrogen to a storage box immersed liquid nitrogen for later use in the microscope.;冷冻剂 ETHANE
|
分辨率 22.00 Å |
共 5 个其他 PDB 条目、21 个 assembly。 打开独立比较页并筛选聚集状态
查看构建体与数据证据
| UniProt名称 | POLG_DEN2U |
| Isoform | — |
| PDB实体 | 1 |
| 链与序列区间 | 作者链 A; PDB构建体 1–109; UniProt 469–577 |