|
3C6D
The pseudo-atomic structure of dengue immature virus
Deposited 2008-02-04
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 360
PDB declaration: 360-meric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 12.50 Å
|
|
3C6D
The pseudo-atomic structure of dengue immature virus
Deposited 2008-02-04
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 6
PDB declaration: hexameric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 12.50 Å
|
|
3C6D
The pseudo-atomic structure of dengue immature virus
Deposited 2008-02-04
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 30
PDB declaration: 30-meric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 12.50 Å
|
|
3C6D
The pseudo-atomic structure of dengue immature virus
Deposited 2008-02-04
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 36
PDB declaration: 36-meric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 12.50 Å
|
|
3C6D
The pseudo-atomic structure of dengue immature virus
Deposited 2008-02-04
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein heterocomplex
Heteromer;Protein × 6
PDB declaration: hexameric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 12.50 Å
|
|
3IXY
The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53
Deposited 2009-02-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 600
PDB declaration: 600-MERIC
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
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.;Cryogen ETHANE
|
Resolution 23.00 Å
|
|
3IXY
The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53
Deposited 2009-02-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 10
PDB declaration: decameric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
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.;Cryogen ETHANE
|
Resolution 23.00 Å
|
|
3IXY
The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53
Deposited 2009-02-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 50
PDB declaration: 50-meric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
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.;Cryogen ETHANE
|
Resolution 23.00 Å
|
|
3IXY
The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53
Deposited 2009-02-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 60
PDB declaration: 60-meric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
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.;Cryogen ETHANE
|
Resolution 23.00 Å
|
|
3IXY
The pseudo-atomic structure of dengue immature virus in complex with Fab fragments of the anti-fusion loop antibody E53
Deposited 2009-02-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein heterocomplex
Heteromer;Protein × 10
PDB declaration: decameric
|
Chain A
281–675(395 aa)
Chain B
281–675(395 aa)
Chain C
281–675(395 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.6;12 mM Tris-HCl, 120 mM NaCl, 1 mM EDTA
cryo-EM vitrification conditions
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.;Cryogen ETHANE
|
Resolution 23.00 Å
|
|
3J42
Obstruction of Dengue Virus Maturation by Fab Fragments of the 2H2 Antibody
Deposited 2013-06-13
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Insufficient information
Heteromer;Protein × 720
PDB declaration: 720-meric
|
Chain A
281–675(395 aa)
Fragment:UNP residues 281-675
Chain B
281–675(395 aa)
Fragment:UNP residues 281-675
Chain C
281–675(395 aa)
Fragment:UNP residues 281-675
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
100 mM phosphate buffer;pH 7;100 mM phosphate buffer
cryo-EM vitrification conditions
100 K;Cryogen ETHANE;Plunged into liquid ethane (homemade plunger)
|
Resolution 21.00 Å
|
|
3J42
Obstruction of Dengue Virus Maturation by Fab Fragments of the 2H2 Antibody
Deposited 2013-06-13
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Insufficient information
Heteromer;Protein × 12
PDB declaration: dodecameric
|
Chain A
281–675(395 aa)
Fragment:UNP residues 281-675
Chain B
281–675(395 aa)
Fragment:UNP residues 281-675
Chain C
281–675(395 aa)
Fragment:UNP residues 281-675
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
100 mM phosphate buffer;pH 7;100 mM phosphate buffer
cryo-EM vitrification conditions
100 K;Cryogen ETHANE;Plunged into liquid ethane (homemade plunger)
|
Resolution 21.00 Å
|
|
3J42
Obstruction of Dengue Virus Maturation by Fab Fragments of the 2H2 Antibody
Deposited 2013-06-13
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Insufficient information
Heteromer;Protein × 60
PDB declaration: 60-meric
|
Chain A
281–675(395 aa)
Fragment:UNP residues 281-675
Chain B
281–675(395 aa)
Fragment:UNP residues 281-675
Chain C
281–675(395 aa)
Fragment:UNP residues 281-675
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
100 mM phosphate buffer;pH 7;100 mM phosphate buffer
cryo-EM vitrification conditions
100 K;Cryogen ETHANE;Plunged into liquid ethane (homemade plunger)
|
Resolution 21.00 Å
|
|
3J42
Obstruction of Dengue Virus Maturation by Fab Fragments of the 2H2 Antibody
Deposited 2013-06-13
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Insufficient information
Heteromer;Protein × 72
PDB declaration: 72-meric
|
Chain A
281–675(395 aa)
Fragment:UNP residues 281-675
Chain B
281–675(395 aa)
Fragment:UNP residues 281-675
Chain C
281–675(395 aa)
Fragment:UNP residues 281-675
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
100 mM phosphate buffer;pH 7;100 mM phosphate buffer
cryo-EM vitrification conditions
100 K;Cryogen ETHANE;Plunged into liquid ethane (homemade plunger)
|
Resolution 21.00 Å
|
|
3J42
Obstruction of Dengue Virus Maturation by Fab Fragments of the 2H2 Antibody
Deposited 2013-06-13
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Insufficient information
Heteromer;Protein × 12
PDB declaration: dodecameric
|
Chain A
281–675(395 aa)
Fragment:UNP residues 281-675
Chain B
281–675(395 aa)
Fragment:UNP residues 281-675
Chain C
281–675(395 aa)
Fragment:UNP residues 281-675
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
100 mM phosphate buffer;pH 7;100 mM phosphate buffer
cryo-EM vitrification conditions
100 K;Cryogen ETHANE;Plunged into liquid ethane (homemade plunger)
|
Resolution 21.00 Å
|