Capsid protein
Turnip crinkle 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 | 蛋白同源多聚体 同源多聚体 蛋白 × 180 PDB 声明:180-meric(180) 与蛋白拷贝数一致 | 链 A; UniProt 1–351 链 B; UniProt 1–351 链 C; UniProt 1–351 | 未记录 | 无其他共同聚合物 | ELECTRON MICROSCOPY cryo-EM缓冲液:pH 7.4;1 mM MgSO4 1mM NaPO4 and pH7.4 cryo-EM玻璃化条件:冷冻剂 ETHANE | 分辨率 3.13 Å |
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 9QVF | 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 |
|---|---|---|---|---|---|---|---|
| 3ZX8 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 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 × 180 PDB 声明:180-MERIC |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE;pH 7.4;10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 11.50 Å |
| 3ZX8 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 3 PDB 声明:trimeric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE;pH 7.4;10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 11.50 Å |
| 3ZX8 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 15 PDB 声明:pentadecameric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE;pH 7.4;10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 11.50 Å |
| 3ZX8 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 18 PDB 声明:octadecameric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE;pH 7.4;10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 11.50 Å |
| 3ZX8 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 3 PDB 声明:trimeric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE;pH 7.4;10 MM SODIUM PHOSPHATE PH 7.4, 10 MM MAGNESIUM SULPHATE
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 11.50 Å |
| 3ZX9 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 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 × 180 PDB 声明:180-MERIC |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
100 MM TRIS PH 8.5, 5 MM EDTA;pH 8.5;100 MM TRIS PH 8.5, 5 MM EDTA
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 17.00 Å |
| 3ZX9 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 3 PDB 声明:trimeric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
100 MM TRIS PH 8.5, 5 MM EDTA;pH 8.5;100 MM TRIS PH 8.5, 5 MM EDTA
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 17.00 Å |
| 3ZX9 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 15 PDB 声明:pentadecameric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
100 MM TRIS PH 8.5, 5 MM EDTA;pH 8.5;100 MM TRIS PH 8.5, 5 MM EDTA
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 17.00 Å |
| 3ZX9 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 18 PDB 声明:octadecameric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
100 MM TRIS PH 8.5, 5 MM EDTA;pH 8.5;100 MM TRIS PH 8.5, 5 MM EDTA
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 17.00 Å |
| 3ZX9 Cryo-EM reconstruction of native and expanded Turnip Crinkle virus 提交 2011-08-08 | 构建体不同 突变/修饰不同 聚集状态不同 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 × 3 PDB 声明:trimeric |
链 A
1–221(221 aa)
链 A
225–246(22 aa)
链 A
248–351(104 aa)
链 B
1–221(221 aa)
链 B
225–246(22 aa)
链 B
248–351(104 aa)
链 C
1–221(221 aa)
链 C
225–246(22 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
100 MM TRIS PH 8.5, 5 MM EDTA;pH 8.5;100 MM TRIS PH 8.5, 5 MM EDTA
cryo-EM玻璃化条件
冷冻剂 ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, TEMPERATURE- 77, INSTRUMENT- DOUBLE SIDED AUTOMATED BLOTTER AND PLUNGER, METHOD- BLOT 1.6 SECONDS BEFORE PLUNGING,
|
分辨率 17.00 Å |
| 3ZXA Structure and Assembly of Turnip Crinkle Virus I. X-ray Crystallographic Structure Analysis at 3.2 A Resolution 提交 2011-08-08 | 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 蛋白同源多聚体 同源多聚体;蛋白 × 60 PDB 声明:60-MERIC |
链 C
1–220(220 aa)
链 C
224–246(23 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;THE METHYL MERCURY ADDUCT WAS OBTAINED BY BRINGING STOCK SOLUTION OF VIRUS (3.5% TCV (W/V) IN 0.01% SODIUM AZIDE,) TO 6 EQUIVALENT METHYL MERCURY/PROTEIN SUBUNIT BY ADDITION OF 15 MILLIMOLAR-METHYL MERCURY NITRATE AND INCUBATING FOR 1 H. CRYSTALLIZATION WAS THEN INITIATED BY ADDITION OF AN APPROXIMATELY EQUAL VOLUME OF SATURATED SODIUM CITRATE (PH 7.0) AND ALLOWED TO PROCEED UNDISTURBED FOR 2 TO 4 MONTHS. THE OPTIMUM CONCENTRATION OF SODIUM CITRATE REQUIRED TO PRODUCE LARGE CRYSTALS VARIED FROM EXPERIMENT TO EXPERIMENT BUT WAS GENERALLY IN THE RANGE 42 TO 46% SATURATED.
|
分辨率 3.20 Å |
| 3ZXA Structure and Assembly of Turnip Crinkle Virus I. X-ray Crystallographic Structure Analysis at 3.2 A Resolution 提交 2011-08-08 | 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 2 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric |
链 C
1–220(220 aa)
链 C
224–246(23 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;THE METHYL MERCURY ADDUCT WAS OBTAINED BY BRINGING STOCK SOLUTION OF VIRUS (3.5% TCV (W/V) IN 0.01% SODIUM AZIDE,) TO 6 EQUIVALENT METHYL MERCURY/PROTEIN SUBUNIT BY ADDITION OF 15 MILLIMOLAR-METHYL MERCURY NITRATE AND INCUBATING FOR 1 H. CRYSTALLIZATION WAS THEN INITIATED BY ADDITION OF AN APPROXIMATELY EQUAL VOLUME OF SATURATED SODIUM CITRATE (PH 7.0) AND ALLOWED TO PROCEED UNDISTURBED FOR 2 TO 4 MONTHS. THE OPTIMUM CONCENTRATION OF SODIUM CITRATE REQUIRED TO PRODUCE LARGE CRYSTALS VARIED FROM EXPERIMENT TO EXPERIMENT BUT WAS GENERALLY IN THE RANGE 42 TO 46% SATURATED.
|
分辨率 3.20 Å |
| 3ZXA Structure and Assembly of Turnip Crinkle Virus I. X-ray Crystallographic Structure Analysis at 3.2 A Resolution 提交 2011-08-08 | 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 3 蛋白同源多聚体 同源多聚体;蛋白 × 5 PDB 声明:pentameric |
链 C
1–220(220 aa)
链 C
224–246(23 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;THE METHYL MERCURY ADDUCT WAS OBTAINED BY BRINGING STOCK SOLUTION OF VIRUS (3.5% TCV (W/V) IN 0.01% SODIUM AZIDE,) TO 6 EQUIVALENT METHYL MERCURY/PROTEIN SUBUNIT BY ADDITION OF 15 MILLIMOLAR-METHYL MERCURY NITRATE AND INCUBATING FOR 1 H. CRYSTALLIZATION WAS THEN INITIATED BY ADDITION OF AN APPROXIMATELY EQUAL VOLUME OF SATURATED SODIUM CITRATE (PH 7.0) AND ALLOWED TO PROCEED UNDISTURBED FOR 2 TO 4 MONTHS. THE OPTIMUM CONCENTRATION OF SODIUM CITRATE REQUIRED TO PRODUCE LARGE CRYSTALS VARIED FROM EXPERIMENT TO EXPERIMENT BUT WAS GENERALLY IN THE RANGE 42 TO 46% SATURATED.
|
分辨率 3.20 Å |
| 3ZXA Structure and Assembly of Turnip Crinkle Virus I. X-ray Crystallographic Structure Analysis at 3.2 A Resolution 提交 2011-08-08 | 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 4 蛋白同源多聚体 同源多聚体;蛋白 × 6 PDB 声明:hexameric |
链 C
1–220(220 aa)
链 C
224–246(23 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;THE METHYL MERCURY ADDUCT WAS OBTAINED BY BRINGING STOCK SOLUTION OF VIRUS (3.5% TCV (W/V) IN 0.01% SODIUM AZIDE,) TO 6 EQUIVALENT METHYL MERCURY/PROTEIN SUBUNIT BY ADDITION OF 15 MILLIMOLAR-METHYL MERCURY NITRATE AND INCUBATING FOR 1 H. CRYSTALLIZATION WAS THEN INITIATED BY ADDITION OF AN APPROXIMATELY EQUAL VOLUME OF SATURATED SODIUM CITRATE (PH 7.0) AND ALLOWED TO PROCEED UNDISTURBED FOR 2 TO 4 MONTHS. THE OPTIMUM CONCENTRATION OF SODIUM CITRATE REQUIRED TO PRODUCE LARGE CRYSTALS VARIED FROM EXPERIMENT TO EXPERIMENT BUT WAS GENERALLY IN THE RANGE 42 TO 46% SATURATED.
|
分辨率 3.20 Å |
| 3ZXA Structure and Assembly of Turnip Crinkle Virus I. X-ray Crystallographic Structure Analysis at 3.2 A Resolution 提交 2011-08-08 | 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 5 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric |
链 C
1–220(220 aa)
链 C
224–246(23 aa)
链 C
248–351(104 aa)
|
未记录 | 未记录非水小分子 |
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;THE METHYL MERCURY ADDUCT WAS OBTAINED BY BRINGING STOCK SOLUTION OF VIRUS (3.5% TCV (W/V) IN 0.01% SODIUM AZIDE,) TO 6 EQUIVALENT METHYL MERCURY/PROTEIN SUBUNIT BY ADDITION OF 15 MILLIMOLAR-METHYL MERCURY NITRATE AND INCUBATING FOR 1 H. CRYSTALLIZATION WAS THEN INITIATED BY ADDITION OF AN APPROXIMATELY EQUAL VOLUME OF SATURATED SODIUM CITRATE (PH 7.0) AND ALLOWED TO PROCEED UNDISTURBED FOR 2 TO 4 MONTHS. THE OPTIMUM CONCENTRATION OF SODIUM CITRATE REQUIRED TO PRODUCE LARGE CRYSTALS VARIED FROM EXPERIMENT TO EXPERIMENT BUT WAS GENERALLY IN THE RANGE 42 TO 46% SATURATED.
|
分辨率 3.20 Å |
| 9GDW RNA binding domain of Turnip crinkle virus p38, p38R 提交 2024-08-06 | 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 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric |
链 A
1–45(45 aa)
|
未记录 | 未记录非水小分子 |
SOLUTION NMR
NMR测量条件
pH 7;283 K;离子强度(mmCIF原始值)50;压力 1
NMR样品组成
1.0 mM [U-100% 13C; U-100% 15N] protein, 90% H2O/10% D2O | 90% H2O/10% D2O
|
分辨率未提供 |
| 9QVG Turnip Crinkle Virus: virions (TCV-M) 提交 2025-04-11 | 结构质量不同 | Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 180 PDB 声明:180-meric |
链 A
1–351(351 aa)
链 B
1–351(351 aa)
链 C
1–351(351 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.4;1 mM MgSO4 1mM NaPO4 and pH7.4
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 3.43 Å |
| 9QVH Turnip Crinkle Virus: virus-like particles (TCV-P38) 提交 2025-04-11 | 结构质量不同 | Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 180 PDB 声明:180-meric |
链 A
1–351(351 aa)
链 B
1–351(351 aa)
链 C
1–351(351 aa)
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.4;1 mM MgSO4 1mM NaPO4 and pH7.4
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 3.47 Å |
| 9Y2Z Icosahedral symmetric structure of an expansion intermediate of Turnip Crinkle Virus (Asymmetric Trimer Unit) 提交 2025-09-01 | 构建体不同 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 × 180 PDB 声明:180-meric |
链 A
1–351(351 aa)
片段:R domain
链 B
1–351(351 aa)
片段:R domain
链 C
1–351(351 aa)
片段:R domain
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 5.4
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 2.87 Å |
| 9Y31 Symmetry relaxed asymmetric structure of an expansion intermediate of Turnip crinkle virus 提交 2025-09-01 | 构建体不同 聚集状态不同 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 × 3 PDB 声明:trimeric |
链 C
1–351(351 aa)
片段:R domain
链 E
1–351(351 aa)
片段:R domain
链 H
1–351(351 aa)
片段:R domain
|
未记录 | 未记录非水小分子 |
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 5.4
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 3.62 Å |
共 8 个其他 PDB 条目、20 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 | CAPSD_TCV |
| Isoform | — |
| PDB实体 | 1 |
| 链与序列区间 | 作者链 A; PDB构建体 1–351; UniProt 1–351 作者链 B; PDB构建体 1–351; UniProt 1–351 作者链 C; PDB构建体 1–351; UniProt 1–351 |