当前蛋白身份:Q66282 重新检索
本组结构的主要差异维度
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
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 240 PDB 声明:240-MERIC(240) 与蛋白数一致
链 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 60 MYR MYRISTIC ACID × 60 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 2 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 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 1 MYR MYRISTIC ACID × 1 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 20 PDB 声明:eicosameric(20) 与蛋白数一致
链 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 5 MYR MYRISTIC ACID × 5 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 4 蛋白同源多聚体 同源多聚体;蛋白 × 24 PDB 声明:24-meric(24) 与蛋白数一致
链 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 6 MYR MYRISTIC ACID × 6 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 5 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 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 1 MYR MYRISTIC ACID × 1 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN 提交 1994-10-19 Assembly 6 蛋白同源多聚体 同源多聚体;蛋白 × 480 PDB 声明:480-meric(480) 与蛋白数一致
链 1 571–851(281 aa)
链 2 70–332(263 aa)
链 3 333–570(238 aa)
链 4 2–69(68 aa)
未记录 PLM PALMITIC ACID × 120 MYR MYRISTIC ACID × 120 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 3.50 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). 提交 2001-06-19 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 300 PDB 声明:300-MERIC(300) 与蛋白数一致
链 1 571–851(281 aa) 片段:Residues 571-851
链 2 70–332(263 aa) 片段:Residues 70-332
链 3 333–570(238 aa) 片段:Residues 333-570
链 4 2–69(68 aa) 片段:Residues 2-69
未记录 未记录非水小分子 ELECTRON MICROSCOPY
cryo-EM缓冲液 pH 7.5
cryo-EM玻璃化条件 CVB3 WAS INCUBATED WITH CAR SAMPLE FOR 1 HOURS AT 25 DEGREES CELSIUS (298 KELVIN) USING A FOUR-FOLD EXCESS OF CAR FOR EACH OF THE SIXTY POSSIBLE BINDING SITES PER VIRION. AFTER INCUBATION, SAMPLES WERE PREPARED AS THIN LAYERS OF VITREOUS ICE AND MAINTAINED AT NEAR LIQUID NITROGEN TEMPERATURE IN THE ELECTRON MICROSCOPE WITH A GATAN 626 CRYOTRANSFER HOLDER.
X-ray结晶条件 ELECTRON MICROSCOPY RECONSTRUCTION;pH 7.5;298 K;WARNING: THIS IS AN CRYO-ELECTRON MICROSCOPY MODEL DEPOSITION. CRYO-EM INFORMATION HAS BEEN INCLUDED IN THE PDB FILE., pH 7.5, ELECTRON MICROSCOPY RECONSTRUCTION, temperature 298K
分辨率 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). 提交 2001-06-19 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 5 PDB 声明:pentameric(5) 与蛋白数一致
链 1 571–851(281 aa) 片段:Residues 571-851
链 2 70–332(263 aa) 片段:Residues 70-332
链 3 333–570(238 aa) 片段:Residues 333-570
链 4 2–69(68 aa) 片段:Residues 2-69
未记录 未记录非水小分子 ELECTRON MICROSCOPY
cryo-EM缓冲液 pH 7.5
cryo-EM玻璃化条件 CVB3 WAS INCUBATED WITH CAR SAMPLE FOR 1 HOURS AT 25 DEGREES CELSIUS (298 KELVIN) USING A FOUR-FOLD EXCESS OF CAR FOR EACH OF THE SIXTY POSSIBLE BINDING SITES PER VIRION. AFTER INCUBATION, SAMPLES WERE PREPARED AS THIN LAYERS OF VITREOUS ICE AND MAINTAINED AT NEAR LIQUID NITROGEN TEMPERATURE IN THE ELECTRON MICROSCOPE WITH A GATAN 626 CRYOTRANSFER HOLDER.
X-ray结晶条件 ELECTRON MICROSCOPY RECONSTRUCTION;pH 7.5;298 K;WARNING: THIS IS AN CRYO-ELECTRON MICROSCOPY MODEL DEPOSITION. CRYO-EM INFORMATION HAS BEEN INCLUDED IN THE PDB FILE., pH 7.5, ELECTRON MICROSCOPY RECONSTRUCTION, temperature 298K
分辨率 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). 提交 2001-06-19 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 25 PDB 声明:25-meric(25) 与蛋白数一致
链 1 571–851(281 aa) 片段:Residues 571-851
链 2 70–332(263 aa) 片段:Residues 70-332
链 3 333–570(238 aa) 片段:Residues 333-570
链 4 2–69(68 aa) 片段:Residues 2-69
未记录 未记录非水小分子 ELECTRON MICROSCOPY
cryo-EM缓冲液 pH 7.5
cryo-EM玻璃化条件 CVB3 WAS INCUBATED WITH CAR SAMPLE FOR 1 HOURS AT 25 DEGREES CELSIUS (298 KELVIN) USING A FOUR-FOLD EXCESS OF CAR FOR EACH OF THE SIXTY POSSIBLE BINDING SITES PER VIRION. AFTER INCUBATION, SAMPLES WERE PREPARED AS THIN LAYERS OF VITREOUS ICE AND MAINTAINED AT NEAR LIQUID NITROGEN TEMPERATURE IN THE ELECTRON MICROSCOPE WITH A GATAN 626 CRYOTRANSFER HOLDER.
X-ray结晶条件 ELECTRON MICROSCOPY RECONSTRUCTION;pH 7.5;298 K;WARNING: THIS IS AN CRYO-ELECTRON MICROSCOPY MODEL DEPOSITION. CRYO-EM INFORMATION HAS BEEN INCLUDED IN THE PDB FILE., pH 7.5, ELECTRON MICROSCOPY RECONSTRUCTION, temperature 298K
分辨率 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). 提交 2001-06-19 Assembly 4 蛋白异源复合物 异源复合物;蛋白 × 30 PDB 声明:30-meric(30) 与蛋白数一致
链 1 571–851(281 aa) 片段:Residues 571-851
链 2 70–332(263 aa) 片段:Residues 70-332
链 3 333–570(238 aa) 片段:Residues 333-570
链 4 2–69(68 aa) 片段:Residues 2-69
未记录 未记录非水小分子 ELECTRON MICROSCOPY
cryo-EM缓冲液 pH 7.5
cryo-EM玻璃化条件 CVB3 WAS INCUBATED WITH CAR SAMPLE FOR 1 HOURS AT 25 DEGREES CELSIUS (298 KELVIN) USING A FOUR-FOLD EXCESS OF CAR FOR EACH OF THE SIXTY POSSIBLE BINDING SITES PER VIRION. AFTER INCUBATION, SAMPLES WERE PREPARED AS THIN LAYERS OF VITREOUS ICE AND MAINTAINED AT NEAR LIQUID NITROGEN TEMPERATURE IN THE ELECTRON MICROSCOPE WITH A GATAN 626 CRYOTRANSFER HOLDER.
X-ray结晶条件 ELECTRON MICROSCOPY RECONSTRUCTION;pH 7.5;298 K;WARNING: THIS IS AN CRYO-ELECTRON MICROSCOPY MODEL DEPOSITION. CRYO-EM INFORMATION HAS BEEN INCLUDED IN THE PDB FILE., pH 7.5, ELECTRON MICROSCOPY RECONSTRUCTION, temperature 298K
分辨率 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). 提交 2001-06-19 Assembly 5 蛋白异源复合物 异源复合物;蛋白 × 5 PDB 声明:pentameric(5) 与蛋白数一致
链 1 571–851(281 aa) 片段:Residues 571-851
链 2 70–332(263 aa) 片段:Residues 70-332
链 3 333–570(238 aa) 片段:Residues 333-570
链 4 2–69(68 aa) 片段:Residues 2-69
未记录 未记录非水小分子 ELECTRON MICROSCOPY
cryo-EM缓冲液 pH 7.5
cryo-EM玻璃化条件 CVB3 WAS INCUBATED WITH CAR SAMPLE FOR 1 HOURS AT 25 DEGREES CELSIUS (298 KELVIN) USING A FOUR-FOLD EXCESS OF CAR FOR EACH OF THE SIXTY POSSIBLE BINDING SITES PER VIRION. AFTER INCUBATION, SAMPLES WERE PREPARED AS THIN LAYERS OF VITREOUS ICE AND MAINTAINED AT NEAR LIQUID NITROGEN TEMPERATURE IN THE ELECTRON MICROSCOPE WITH A GATAN 626 CRYOTRANSFER HOLDER.
X-ray结晶条件 ELECTRON MICROSCOPY RECONSTRUCTION;pH 7.5;298 K;WARNING: THIS IS AN CRYO-ELECTRON MICROSCOPY MODEL DEPOSITION. CRYO-EM INFORMATION HAS BEEN INCLUDED IN THE PDB FILE., pH 7.5, ELECTRON MICROSCOPY RECONSTRUCTION, temperature 298K
分辨率 22.00 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs 提交 2016-04-29 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 240 PDB 声明:240-meric(240) 与蛋白数一致
链 1 571–851(281 aa) 片段:UNP residues 571-851
链 2 70–332(263 aa) 片段:UNP residues 70-332
链 3 333–570(238 aa) 片段:UNP residues 333-570
链 4 2–69(68 aa) 片段:UNP residues 2-69
未记录 PLM PALMITIC ACID × 60 ELECTRON MICROSCOPY
cryo-EM玻璃化条件 102 K;冷冻剂 ETHANE;Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
分辨率 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs 提交 2016-04-29 Assembly 2 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 1 571–851(281 aa) 片段:UNP residues 571-851
链 2 70–332(263 aa) 片段:UNP residues 70-332
链 3 333–570(238 aa) 片段:UNP residues 333-570
链 4 2–69(68 aa) 片段:UNP residues 2-69
未记录 PLM PALMITIC ACID × 1 ELECTRON MICROSCOPY
cryo-EM玻璃化条件 102 K;冷冻剂 ETHANE;Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
分辨率 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs 提交 2016-04-29 Assembly 3 蛋白同源多聚体 同源多聚体;蛋白 × 20 PDB 声明:eicosameric(20) 与蛋白数一致
链 1 571–851(281 aa) 片段:UNP residues 571-851
链 2 70–332(263 aa) 片段:UNP residues 70-332
链 3 333–570(238 aa) 片段:UNP residues 333-570
链 4 2–69(68 aa) 片段:UNP residues 2-69
未记录 PLM PALMITIC ACID × 5 ELECTRON MICROSCOPY
cryo-EM玻璃化条件 102 K;冷冻剂 ETHANE;Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
分辨率 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs 提交 2016-04-29 Assembly 4 蛋白同源多聚体 同源多聚体;蛋白 × 24 PDB 声明:24-meric(24) 与蛋白数一致
链 1 571–851(281 aa) 片段:UNP residues 571-851
链 2 70–332(263 aa) 片段:UNP residues 70-332
链 3 333–570(238 aa) 片段:UNP residues 333-570
链 4 2–69(68 aa) 片段:UNP residues 2-69
未记录 PLM PALMITIC ACID × 6 ELECTRON MICROSCOPY
cryo-EM玻璃化条件 102 K;冷冻剂 ETHANE;Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
分辨率 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs 提交 2016-04-29 Assembly 5 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 1 571–851(281 aa) 片段:UNP residues 571-851
链 2 70–332(263 aa) 片段:UNP residues 70-332
链 3 333–570(238 aa) 片段:UNP residues 333-570
链 4 2–69(68 aa) 片段:UNP residues 2-69
未记录 PLM PALMITIC ACID × 1 ELECTRON MICROSCOPY
cryo-EM玻璃化条件 102 K;冷冻剂 ETHANE;Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
分辨率 3.90 Å