Current Protein Identity:P03070 New Search
Main Difference Dimensions in This Set
Different construct 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
1EJL MOUSE IMPORTIN ALPHA-SV40 LARGE T ANTIGEN NLS PEPTIDE COMPLEX Deposited 2000-03-03 Assembly 1 Protein heterocomplex Heteromer;Protein × 3 PDB declaration: trimeric(3) Consistent with protein count
Chain A 126–132(7 aa) Fragment:NLS (NUCLEAR LOCALIZATION SIGNAL) MONOPARTITE PEPTIDE, RESIDUES 126-132
Chain B 126–132(7 aa) Fragment:NLS (NUCLEAR LOCALIZATION SIGNAL) MONOPARTITE PEPTIDE, RESIDUES 126-132
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.5;293 K;sodium citrate, Hepes, DTT, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Resolution 2.80 Å R-free 0.254
1GH6 RETINOBLASTOMA POCKET COMPLEXED WITH SV40 LARGE T ANTIGEN Deposited 2000-11-15 Assembly 1 Protein heterocomplex Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 7–117(111 aa)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions pH 7.2;pH 7.2
Resolution 3.20 Å R-free 0.314
1N25 Crystal structure of the SV40 Large T antigen helicase domain Deposited 2002-10-21 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 260–627(368 aa) Fragment:helicase domain
Chain B 260–627(368 aa) Fragment:helicase domain
Not recorded ZN ZINC ION × 6 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 7.6;291 K;glycerol, DTT, Hepes, NaCl, EtOH, EDTA, pH 7.6, VAPOR DIFFUSION, HANGING DROP, temperature 291K
Resolution 2.80 Å R-free 0.276
1Q1S Mouse Importin alpha- phosphorylated SV40 CN peptide complex Deposited 2003-07-22 Assembly 1 Protein homooligomer Homooligomer;Protein × 3 PDB declaration: trimeric(3) Consistent with protein count
Chain A 110–133(24 aa) Fragment:CN peptide - Ser112 chemically phosphorylated
Chain B 110–133(24 aa) Fragment:CN peptide - Ser112 chemically phosphorylated
Chain C 70–529(460 aa) Fragment:NLS binding domain (70-529)
Mutation:S120A, S123A, T124A Non-standard monomer:Yes (specific site not provided by mmCIF) Mutation:S120A, S123A, T124A Non-standard monomer:Yes (specific site not provided by mmCIF) No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.5;293 K;Sodium Citrate, DTT, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Resolution 2.30 Å R-free 0.221
1Q1T Mouse Importin alpha: non-phosphorylated SV40 CN peptide complex Deposited 2003-07-22 Assembly 1 Protein homooligomer Homooligomer;Protein × 3 PDB declaration: trimeric(3) Consistent with protein count
Chain A 110–133(24 aa) Fragment:CN peptide
Chain B 110–133(24 aa) Fragment:CN peptide
Chain C 70–529(460 aa) Fragment:NLS binding domain (70-529)
Mutation:S120A, S123A, T124A Mutation:S120A, S123A, T124A No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.25;293 K;Sodium Citrate, DTT, pH 6.25, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Resolution 2.50 Å R-free 0.233
1SVL Co-crystal structure of SV40 large T antigen helicase domain and ADP Deposited 2004-03-29 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain B 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain C 251–627(377 aa) Fragment:HELICASE DOMAIN
Not recorded ZN ZINC ION × 6 MG MAGNESIUM ION × 6 ADP ADENOSINE-5'-DIPHOSPHATE × 6 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 7.25;277 K;Tris, magnesium chloride, PEG 8000, DTT, pH 7.25, VAPOR DIFFUSION, HANGING DROP, temperature 277K
Resolution 1.95 Å R-free 0.264
1SVM Co-crystal structure of SV40 large T antigen helicase domain and ATP Deposited 2004-03-29 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain B 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain C 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain D 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain E 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain F 251–627(377 aa) Fragment:HELICASE DOMAIN
Not recorded ZN ZINC ION × 6 MG MAGNESIUM ION × 6 ATP ADENOSINE-5'-TRIPHOSPHATE × 6 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 7.25;277 K;Tris, magnesium chloride, PEG 8000, DTT, pH 7.25, VAPOR DIFFUSION, HANGING DROP, temperature 277K
Resolution 1.94 Å R-free 0.241
1SVO Structure of SV40 large T antigen helicase domain Deposited 2004-03-29 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 251–627(377 aa) Fragment:HELICASE DOMAIN
Chain B 251–627(377 aa) Fragment:HELICASE DOMAIN
Not recorded ZN ZINC ION × 6 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 7.6;277 K;HEPES, NACL, ETHANOL, EDTA, DTT, pH 7.6, VAPOR DIFFUSION, HANGING DROP, temperature 277K
Resolution 2.60 Å R-free 0.271
1TBD SOLUTION STRUCTURE OF THE ORIGIN DNA BINDING DOMAIN OF SV40 T-ANTIGEN, NMR, MINIMIZED AVERAGE STRUCTURE Deposited 1996-11-04 Assembly 1 Protein monomer Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 131–260(130 aa) Fragment:DNA BINDING DOMAIN
Not recorded No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 5.5;303 K
Resolution not provided
1Z1D Structural Model for the interaction between RPA32 C-terminal domain and SV40 T antigen origin binding domain. Deposited 2005-03-03 Assembly 1 Protein heterocomplex Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain B 131–259(129 aa) Fragment:SV40 T antigen Origin binding domain
Not recorded No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 7;298 K;Ionic strength (raw mmCIF value) 0.03 M;Pressure ambient
NMR sample composition 0.2mM RPA32C U-15N, 0.6mM Tag-OBD, 20mM Tris buffer pH 7.0, 2 mM DTT, 5mM MgCl2, 90% H2O, 10% D2O | 90% H2O/10% D2O
NMR sample composition 0.2mM Tag-OBD U-15N, 0.6mM RPA32C, 20mM Tris buffer pH 7.0, 2mM DTT, 5mM MgCl2, 90% H2O, 10% D2O | 90% H2O/10% D2O
Resolution not provided
2FUF Crystal structure of the SV40 large T antigen origin-binding domain Deposited 2006-01-26 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 131–260(130 aa) Fragment:DNA binding domain (residues 131-259)
Non-standard monomer:Yes (specific site not provided by mmCIF) FLC CITRATE ANION × 6 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.7;298 K;1.6 M Sodium citrate, pH 6.7, VAPOR DIFFUSION, HANGING DROP, temperature 298K
Resolution 1.45 Å R-free 0.189
2IF9 Crystal Structure of SV40 T-antigen origin binding domain disulfide-linked dimer Deposited 2006-09-20 Assembly 1 Protein homooligomer Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 131–260(130 aa) Fragment:origin binding domain
Chain B 131–260(130 aa) Fragment:origin binding domain
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 5.6;293 K;30 % peg 4000, 0.1M sodium citrate (pH 5.6), 0.2 M ammonium acetate, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Resolution 2.59 Å R-free 0.296
2IPR Origin binding domain of the SV40 large T antigen (residues 131-259). P21 crystal form Deposited 2006-10-12 Assembly 1 Protein homooligomer Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Chain B 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 8.1;300 K;20 mM NaSCN, 10% P4K, 0.1 Tris, pH 8.1, VAPOR DIFFUSION, HANGING DROP, temperature 300K
Resolution 1.50 Å R-free 0.204
2ITJ Origin binding domain of the SV40 large T antigen (residues 131-259). P212121 crystal form Deposited 2006-10-19 Assembly 1 Protein homooligomer Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Chain B 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, SITTING DROP;pH 7.5;297 K;20 mM NaAc, 20% PEG4K, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 297K
Resolution 2.50 Å R-free 0.289
2ITL The origin binding domain of the SV40 large T antigen bound to the functional pen palindrome DNA (23 bp) Deposited 2006-10-19 Assembly 1 Protein–DNA Homooligomer;Protein × 4 PDB declaration: octameric(8) Consistent with all polymers
Chain A 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Chain B 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, SITTING DROP;pH 7.5;297 K;20 mM di-ammonium hydrogen citrate, 20% PEG 3000, and 10 mM MgCl2, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 297K
Resolution 1.65 Å R-free 0.251
2NL8 The origin binding domain of the SV40 large T antigen bound non specifically to a 17 bp palindrome DNA (sites 1 and 3) Deposited 2006-10-19 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 131–259(129 aa) Fragment:Origin binding domain (residues 131-259)
Mutation:CYS216SER No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 7.5;297 K;20 mM NaAcetate, 20% PEG 3000 + 4% PEG 600, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 297K
Resolution 2.30 Å R-free 0.299
2NTC Crystal Structure of sv40 large T antigen origin binding domain with DNA Deposited 2006-11-07 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 131–260(130 aa) Fragment:Origin binding domain (residues 131-259)
Chain B 131–260(130 aa) Fragment:Origin binding domain (residues 131-259)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION;pH 6.5;273 K;0.1 M sodium cacodylate pH 6.5, 0.1 M calcium acetate, 30 % v/v peg 8000, 20 % glycerol, VAPOR DIFFUSION, temperature 273K
Resolution 2.40 Å R-free 0.287
2TBD SV40 T ANTIGEN DNA-BINDING DOMAIN, NMR, 30 STRUCTURES Deposited 1997-01-09 Assembly 1 Protein monomer Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 131–260(130 aa) Fragment:DNA BINDING DOMAIN, RESIDUES 131 - 260
Not recorded No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 5.5;303 K
Resolution not provided
3QK2 Structure-Based Analysis of the Interaction between the Simian Virus 40 T-Antigen Origin Binding Domain and Single-Stranded DNA Deposited 2011-01-31 Assembly 1 Protein monomer Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 131–260(130 aa) Fragment:origin binding domain
Non-standard monomer:Yes (specific site not provided by mmCIF) SCN THIOCYANATE ION × 1 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION;278 K;0.2 M thiocyanate [SCN], 17.5% PEG 3350, 5% glycerol, VAPOR DIFFUSION, temperature 278K
Resolution 1.64 Å R-free 0.187
3QN2 Structure-based design of a disulfide-linked oligomeric form of the Simian Virus 40 (SV40) large T antigen DNA binding domain Deposited 2011-02-07 Assembly 1 Protein monomer Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 131–260(130 aa) Fragment:origin binding domain
Mutation:F151C, C216A, D256C FLC CITRATE ANION × 1 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;1.6 M sodium citrate, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K
Resolution 1.66 Å R-free 0.191
4FGN Crystal structure of the SV40 large T-antigen origin bining domain bound to Site I DNA Deposited 2012-06-04 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 131–260(130 aa) Fragment:origin binding domain, UNP residues 131-260
Chain B 131–260(130 aa) Fragment:origin binding domain, UNP residues 131-260
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 4.6;291 K;0.1M sodium acetate pH 4.6, .2M ammonium sulfate, 30 % Peg 4000, 10 mM CaCl2, VAPOR DIFFUSION, HANGING DROP, temperature 291K
Resolution 3.20 Å R-free 0.267
4RXH Crystal Structure of Importin-alpha from Neurospora crassa complexed with SV40NLS Deposited 2014-12-11 Assembly 1 Protein heterocomplex Heteromer;Protein × 3 PDB declaration: trimeric(3) Consistent with protein count
Chain A 125–132(8 aa)
Chain C 125–132(8 aa)
Not recorded No recorded non-water small molecule X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, SITTING DROP;pH 8.5;297 K;20 Mm Bicine pH 8.5, 20%(w/v) PEG 6000, VAPOR DIFFUSION, SITTING DROP, temperature 297K
Resolution 1.76 Å R-free 0.211
5D9I SV40 Large T antigen origin binding domain bound to artificial DNA fork Deposited 2015-08-18 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 131–260(130 aa) Fragment:unp residues 131-260
Chain B 131–260(130 aa) Fragment:unp residues 131-260
Non-standard monomer:Yes (specific site not provided by mmCIF) Non-standard monomer:Yes (specific site not provided by mmCIF) EDO 1,2-ETHANEDIOL × 2 CA CALCIUM ION × 2 ACT ACETATE ION × 1 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 8.5;277 K;100 mM Tris, 300 mM NH4Cl, 28% polyethylene glycol [PEG] 4000, 20 mM CaCl2
Resolution 1.70 Å R-free 0.223
9EVH SV40 large T antigen assembly with DNA in presence of ADP Deposited 2024-03-29 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 1–708(708 aa)
Chain B 1–708(708 aa)
Chain C 1–708(708 aa)
Chain D 1–708(708 aa)
Chain E 1–708(708 aa)
Chain F 1–708(708 aa)
Not recorded ADP ADENOSINE-5'-DIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8;200 mM NaCl, 50 mM Tris-HCl (pH 8.0), 1 mM ADP.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.38 Å
9EVP SV40 LTAg assembly with DNA in presence of AMPPNP and Mg2+. Deposited 2024-04-01 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ANP PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER × 6 MG MAGNESIUM ION × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM TrisHCl (pH 7.5), 1 mM DTT, 100 mM NaCl, 5 mM MgCl, 3 mM AMP-PMP.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.12 Å
9EXD SV40 LTAg assembly in presence of ATP. Deposited 2024-04-07 Assembly 1 Protein homooligomer Homooligomer;Protein × 6 PDB declaration: hexameric(6) Consistent with protein count
Chain A 1–708(708 aa)
Chain B 1–708(708 aa)
Chain C 1–708(708 aa)
Chain D 1–708(708 aa)
Chain E 1–708(708 aa)
Chain F 1–708(708 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8;200 mM NaCl, 50 mM Tris-HCl (pH 8.0), 1 mM ATP.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.40 Å
9F3T Active SV40 LTAg complex with DNA (3D variability component_000, frame_010). Deposited 2024-04-25 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F3U Active SV40 LTAg complex with DNA (3D variability component_001, frame_010). Deposited 2024-04-26 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F5I Active SV40 LTAg complex with DNA (3D variability component_000, frame_005). Deposited 2024-04-28 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F73 Active SV40 LTAg complex with DNA (3D variability component_002, frame_015). Deposited 2024-05-03 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F74 Active SV40 LTAg complex with DNA (3D variability component_000, frame_015). Deposited 2024-05-03 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F75 Active SV40 LTAg complex with DNA (3D variability component_000, frame_019). Deposited 2024-05-03 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F7N Active SV40 LTAg complex with DNA (3D variability component_000, frame_000). Deposited 2024-05-04 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F9N Active SV40 LTAg complex with DNA (3D variability component_001, frame_005). Deposited 2024-05-08 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F9O Active SV40 LTAg complex with DNA (3D variability component_001, frame_015). Deposited 2024-05-08 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F9W Active SV40 LTAg complex with DNA (3D variability component_001, frame_019). Deposited 2024-05-09 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 5 ADP ADENOSINE-5'-DIPHOSPHATE × 1 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9F9X Active SV40 LTAg complex with DNA (3D variability component_001, frame_000). Deposited 2024-05-09 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9FA1 Active SV40 LTAg complex with DNA (3D variability component_002, frame_010). Deposited 2024-05-09 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9FA2 Active SV40 LTAg complex with DNA (3D variability component_002, frame_005). Deposited 2024-05-10 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9FB0 Active SV40 LTAg complex with DNA (3D variability component_002, frame_019). Deposited 2024-05-10 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9FB4 SV40 large T antigen assembly with DNA in presence of ATP. Deposited 2024-05-11 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: octameric(8) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8;200 mM NaCl, 50 mM Tris-HCl (pH 8.0), 1 mM ATP.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.13 Å
9FB5 Active SV40 LTAg complex with DNA (3D variability component_002, frame_000). Deposited 2024-05-12 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: heptameric(7) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES (pH 7.5), 1 mM ATP, 3 mM MgCl2, 1 mM DTT and 50 mM NaCl.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9FB6 SV40 large T antigen assembly with DNA in presence of ATP. Deposited 2024-05-12 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: octameric(8) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ATP ADENOSINE-5'-TRIPHOSPHATE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8;200 mM NaCl, 50 mM Tris-HCl (pH 8.0), 1 mM ATP.
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.13 Å
9KAE CryoEM structure of LTag bound to SV40 EP half origin DNA Deposited 2024-10-28 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: octameric(8) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ANP PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER × 6 MG MAGNESIUM ION × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å
9KAK CryoEM structure of LTag bound to SV40 AT half origin DNA Deposited 2024-10-29 Assembly 1 Protein–DNA Homooligomer;Protein × 6 PDB declaration: octameric(8) Consistent with all polymers
Chain A 266–627(362 aa)
Chain B 266–627(362 aa)
Chain C 266–627(362 aa)
Chain D 266–627(362 aa)
Chain E 266–627(362 aa)
Chain F 266–627(362 aa)
Not recorded ANP PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER × 6 MG MAGNESIUM ION × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 8
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å