← Back to search

Protein Structures and Oligomeric States

Enter a protein name, UniProt accession or PDB ID. Name searches ask you to confirm the protein identity before related structures are queried.

Current Protein Identity：Q66282 New Search
3PDB entries
16Biological assembly
64chain/assembly records
Main Difference Dimensions in This Set
Different mutation/modification Different assembly state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics

Difference tags compare only the current result set; every original PDB and assembly record remains separate.

Related-Structure Differences

Each row represents one biological assembly in one PDB entry; multiple monomers of the same protein are listed separately.

PDB Entry Assembly / Oligomeric State Construct Mutations and Modifications Ligands, Ions and Non-polymers Experimental Method Experimental Conditions Structure Quality
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 1 Protein homooligomer Homooligomer；Protein × 240 PDB declaration: 240-MERIC（240） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 60 MYR MYRISTIC ACID × 60 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 2 Protein homooligomer Homooligomer；Protein × 4 PDB declaration: tetrameric（4） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 1 MYR MYRISTIC ACID × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 3 Protein homooligomer Homooligomer；Protein × 20 PDB declaration: eicosameric（20） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 5 MYR MYRISTIC ACID × 5 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 4 Protein homooligomer Homooligomer；Protein × 24 PDB declaration: 24-meric（24） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 6 MYR MYRISTIC ACID × 6 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 5 Protein homooligomer Homooligomer；Protein × 4 PDB declaration: tetrameric（4） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 1 MYR MYRISTIC ACID × 1 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1COV COXSACKIEVIRUS B3 COAT PROTEIN Deposited 1994-10-19 Assembly 6 Protein homooligomer Homooligomer；Protein × 480 PDB declaration: 480-meric（480） Consistent with protein count
Chain 1 571–851（281 aa）
Chain 2 70–332（263 aa）
Chain 3 333–570（238 aa）
Chain 4 2–69（68 aa）
Not recorded PLM PALMITIC ACID × 120 MYR MYRISTIC ACID × 120 X-RAY DIFFRACTION mmCIF provides none of the parsed conditions Resolution 3.50 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). Deposited 2001-06-19 Assembly 1 Protein heterocomplex Heteromer；Protein × 300 PDB declaration: 300-MERIC（300） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：Residues 571-851
Chain 2 70–332（263 aa） Fragment：Residues 70-332
Chain 3 333–570（238 aa） Fragment：Residues 333-570
Chain 4 2–69（68 aa） Fragment：Residues 2-69
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions 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 crystallization conditions 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
Resolution 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). Deposited 2001-06-19 Assembly 2 Protein heterocomplex Heteromer；Protein × 5 PDB declaration: pentameric（5） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：Residues 571-851
Chain 2 70–332（263 aa） Fragment：Residues 70-332
Chain 3 333–570（238 aa） Fragment：Residues 333-570
Chain 4 2–69（68 aa） Fragment：Residues 2-69
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions 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 crystallization conditions 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
Resolution 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). Deposited 2001-06-19 Assembly 3 Protein heterocomplex Heteromer；Protein × 25 PDB declaration: 25-meric（25） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：Residues 571-851
Chain 2 70–332（263 aa） Fragment：Residues 70-332
Chain 3 333–570（238 aa） Fragment：Residues 333-570
Chain 4 2–69（68 aa） Fragment：Residues 2-69
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions 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 crystallization conditions 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
Resolution 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). Deposited 2001-06-19 Assembly 4 Protein heterocomplex Heteromer；Protein × 30 PDB declaration: 30-meric（30） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：Residues 571-851
Chain 2 70–332（263 aa） Fragment：Residues 70-332
Chain 3 333–570（238 aa） Fragment：Residues 333-570
Chain 4 2–69（68 aa） Fragment：Residues 2-69
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions 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 crystallization conditions 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
Resolution 22.00 Å
1JEW CRYO-EM STRUCTURE OF COXSACKIEVIRUS B3(M STRAIN) WITH ITS CELLULAR RECEPTOR, COXSACKIEVIRUS AND ADENOVIRUS RECEPTOR (CAR). Deposited 2001-06-19 Assembly 5 Protein heterocomplex Heteromer；Protein × 5 PDB declaration: pentameric（5） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：Residues 571-851
Chain 2 70–332（263 aa） Fragment：Residues 70-332
Chain 3 333–570（238 aa） Fragment：Residues 333-570
Chain 4 2–69（68 aa） Fragment：Residues 2-69
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions 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 crystallization conditions 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
Resolution 22.00 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs Deposited 2016-04-29 Assembly 1 Protein homooligomer Homooligomer；Protein × 240 PDB declaration: 240-meric（240） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：UNP residues 571-851
Chain 2 70–332（263 aa） Fragment：UNP residues 70-332
Chain 3 333–570（238 aa） Fragment：UNP residues 333-570
Chain 4 2–69（68 aa） Fragment：UNP residues 2-69
Not recorded PLM PALMITIC ACID × 60 ELECTRON MICROSCOPY
cryo-EM vitrification conditions 102 K；Cryogen ETHANE；Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
Resolution 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs Deposited 2016-04-29 Assembly 2 Protein homooligomer Homooligomer；Protein × 4 PDB declaration: tetrameric（4） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：UNP residues 571-851
Chain 2 70–332（263 aa） Fragment：UNP residues 70-332
Chain 3 333–570（238 aa） Fragment：UNP residues 333-570
Chain 4 2–69（68 aa） Fragment：UNP residues 2-69
Not recorded PLM PALMITIC ACID × 1 ELECTRON MICROSCOPY
cryo-EM vitrification conditions 102 K；Cryogen ETHANE；Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
Resolution 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs Deposited 2016-04-29 Assembly 3 Protein homooligomer Homooligomer；Protein × 20 PDB declaration: eicosameric（20） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：UNP residues 571-851
Chain 2 70–332（263 aa） Fragment：UNP residues 70-332
Chain 3 333–570（238 aa） Fragment：UNP residues 333-570
Chain 4 2–69（68 aa） Fragment：UNP residues 2-69
Not recorded PLM PALMITIC ACID × 5 ELECTRON MICROSCOPY
cryo-EM vitrification conditions 102 K；Cryogen ETHANE；Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
Resolution 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs Deposited 2016-04-29 Assembly 4 Protein homooligomer Homooligomer；Protein × 24 PDB declaration: 24-meric（24） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：UNP residues 571-851
Chain 2 70–332（263 aa） Fragment：UNP residues 70-332
Chain 3 333–570（238 aa） Fragment：UNP residues 333-570
Chain 4 2–69（68 aa） Fragment：UNP residues 2-69
Not recorded PLM PALMITIC ACID × 6 ELECTRON MICROSCOPY
cryo-EM vitrification conditions 102 K；Cryogen ETHANE；Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
Resolution 3.90 Å
3JD7 The novel asymmetric entry intermediate of a picornavirus captured with nanodiscs Deposited 2016-04-29 Assembly 5 Protein homooligomer Homooligomer；Protein × 4 PDB declaration: tetrameric（4） Consistent with protein count
Chain 1 571–851（281 aa） Fragment：UNP residues 571-851
Chain 2 70–332（263 aa） Fragment：UNP residues 70-332
Chain 3 333–570（238 aa） Fragment：UNP residues 333-570
Chain 4 2–69（68 aa） Fragment：UNP residues 2-69
Not recorded PLM PALMITIC ACID × 1 ELECTRON MICROSCOPY
cryo-EM vitrification conditions 102 K；Cryogen ETHANE；Plunged into liquid ethane (GATAN CRYOPLUNGE 3)
Resolution 3.90 Å

This page presents structural evidence recorded in PDB/mmCIF.“No recorded non-water small molecule” does not prove that the experimental sample was ligand-free; experimental conditions belong to the PDB experiment, while ligands and copy counts are shown for each biological assembly.