|
1J7N
Anthrax Toxin Lethal factor
Deposited 2001-05-17
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
34–809(776 aa)
Chain B
34–809(776 aa)
|
Not recorded
|
SO4 SULFATE ION × 2
ZN ZINC ION × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;298 K;ammonium sulfate, TRIS, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.30 Å
R-free 0.261
|
|
1JKY
Crystal Structure of the Anthrax Lethal Factor (LF): Wild-type LF Complexed with the N-terminal Sequence of MAPKK2
Deposited 2001-07-13
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
34–809(776 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
pH 8;1.9M Ammonium sulfate, 0.2M Tris pH 8.0, 2mM EDTA
|
Resolution 3.90 Å
R-free 0.316
|
|
1PWP
Crystal Structure of the Anthrax Lethal Factor complexed with Small Molecule Inhibitor NSC 12155
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
34–809(776 aa)
|
Not recorded
|
ZN ZINC ION × 1
NSC N,N'-BIS(4-AMINO-2-METHYLQUINOLIN-6-YL)UREA × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.90 Å
R-free 0.274
|
|
1PWP
Crystal Structure of the Anthrax Lethal Factor complexed with Small Molecule Inhibitor NSC 12155
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
34–809(776 aa)
|
Not recorded
|
ZN ZINC ION × 1
NSC N,N'-BIS(4-AMINO-2-METHYLQUINOLIN-6-YL)UREA × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.90 Å
R-free 0.274
|
|
1PWQ
Crystal structure of Anthrax Lethal Factor complexed with Thioacetyl-Tyr-Pro-Met-Amide, a metal-chelating peptidyl small molecule inhibitor
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
34–809(776 aa)
|
Not recorded
|
ZN ZINC ION × 1
SD2 N-(SULFANYLACETYL)TYROSYLPROLYLMETHIONINAMIDE × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 3.52 Å
R-free 0.311
|
|
1PWQ
Crystal structure of Anthrax Lethal Factor complexed with Thioacetyl-Tyr-Pro-Met-Amide, a metal-chelating peptidyl small molecule inhibitor
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
34–809(776 aa)
|
Not recorded
|
ZN ZINC ION × 1
SD2 N-(SULFANYLACETYL)TYROSYLPROLYLMETHIONINAMIDE × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 3.52 Å
R-free 0.311
|
|
1PWU
Crystal Structure of Anthrax Lethal Factor complexed with (3-(N-hydroxycarboxamido)-2-isobutylpropanoyl-Trp-methylamide), a known small molecule inhibitor of matrix metalloproteases.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
34–809(776 aa)
|
Mutation:E720C
|
ZN ZINC ION × 1
GM6 3-(N-HYDROXYCARBOXAMIDO)-2-ISOBUTYLPROPANOYL-TRP-METHYLAMIDE × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA., pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.70 Å
R-free 0.270
|
|
1PWU
Crystal Structure of Anthrax Lethal Factor complexed with (3-(N-hydroxycarboxamido)-2-isobutylpropanoyl-Trp-methylamide), a known small molecule inhibitor of matrix metalloproteases.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
34–809(776 aa)
|
Mutation:E720C
|
ZN ZINC ION × 1
GM6 3-(N-HYDROXYCARBOXAMIDO)-2-ISOBUTYLPROPANOYL-TRP-METHYLAMIDE × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulfate, Tris-HCl, EDTA., pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.70 Å
R-free 0.270
|
|
1PWV
Crystal structure of Anthrax Lethal Factor wild-type protein complexed with an optimised peptide substrate.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
34–809(776 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA., pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.85 Å
R-free 0.279
|
|
1PWV
Crystal structure of Anthrax Lethal Factor wild-type protein complexed with an optimised peptide substrate.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
34–809(776 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA., pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.85 Å
R-free 0.279
|
|
1PWV
Crystal structure of Anthrax Lethal Factor wild-type protein complexed with an optimised peptide substrate.
Deposited 2003-07-02
|
Different construct
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 4
PDB declaration: tetrameric
|
Chain A
34–809(776 aa)
Chain B
34–809(776 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA., pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.85 Å
R-free 0.279
|
|
1PWW
Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
34–809(776 aa)
|
Mutation:E687C
|
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA. , pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.80 Å
R-free 0.288
|
|
1PWW
Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
34–809(776 aa)
|
Mutation:E687C
|
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA. , pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.80 Å
R-free 0.288
|
|
1PWW
Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc.
Deposited 2003-07-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 4
PDB declaration: tetrameric
|
Chain A
34–809(776 aa)
Chain B
34–809(776 aa)
|
Mutation:E687C
Mutation:E687C
|
ZN ZINC ION × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Ammonium sulphate, Tris-HCl, EDTA. , pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
Resolution 2.80 Å
R-free 0.288
|
|
1YQY
Structure of B. Anthrax Lethal factor in complex with a hydroxamate inhibitor
Deposited 2005-02-02
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
297–809(513 aa)
Fragment:domains II-IV (residues 297-809)
|
Not recorded
|
ZN ZINC ION × 1
915 (2R)-2-{[(4-FLUORO-3-METHYLPHENYL)SULFONYL]AMINO}-N-HYDROXY-2-TETRAHYDRO-2H-PYRAN-4-YLACETAMIDE × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;293 K;Peg 8K, magnesium acetate, Sodium cacodylate, pH 6.8, VAPOR DIFFUSION, HANGING DROP, temperature 293K
|
Resolution 2.30 Å
R-free 0.269
|
|
2L0R
Conformational Dynamics of the Anthrax Lethal Factor Catalytic Center
Deposited 2010-07-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
705–809(105 aa)
Fragment:C-terminal 106 residues catalytic core domain (Domain IV), UNP residues 705-809
|
Not recorded
|
No recorded non-water small molecule
|
SOLUTION NMR
NMR measurement conditions
pH 7.2;298 K;Ionic strength (raw mmCIF value) Pi 50;Pressure ambient
NMR sample composition
0.6 mM [U-99% 13C; U-99% 15N] Anthrax LF C-term-1, 10 % % [U-99% 2H] D2O-2, 90 % % H2O-3, 90% H2O/10% D2O | 90% H2O/10% D2O
|
Resolution not provided
|
|
3KWV
Structural basis for the unfolding of anthrax lethal factor by protective antigen oligomers
Deposited 2009-12-01
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 12
PDB declaration: dodecameric
|
Chain C
34–296(263 aa)
Fragment:protective antigen binding domain (UNP residues 34-296)
|
Not recorded
|
CA CALCIUM ION × 16
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 7.2;291 K;16% PEG 3000, 0.1M cacodylic acid, 0.2M magnesium chloride, 10 mM Tris-Cl, 75 mM sodium chloride, 10 mM adenosine-5'-triphosphate, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 291K
|
Resolution 3.10 Å
R-free 0.281
|
|
3KWV
Structural basis for the unfolding of anthrax lethal factor by protective antigen oligomers
Deposited 2009-12-01
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 12
PDB declaration: dodecameric
|
Chain F
34–296(263 aa)
Fragment:protective antigen binding domain (UNP residues 34-296)
|
Not recorded
|
CA CALCIUM ION × 16
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 7.2;291 K;16% PEG 3000, 0.1M cacodylic acid, 0.2M magnesium chloride, 10 mM Tris-Cl, 75 mM sodium chloride, 10 mM adenosine-5'-triphosphate, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 291K
|
Resolution 3.10 Å
R-free 0.281
|
|
4DV8
Anthrax Lethal Factor metalloproteinase in complex with the Hydroxamic acid based small molecule PT8421
Deposited 2012-02-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
296–809(514 aa)
|
Not recorded
|
ZN ZINC ION × 1
0LX (2S)-6-[(4-fluorobenzyl)amino]-2-[(2R)-2-(4-fluorophenyl)-2-methoxyethyl]-N-hydroxyhexanamide × 1
MLI MALONATE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 7.6;291 K;0.03M citric acid, 0.01M BIS-Tris, Propane, pH7.6, 20% PEG3350, 14 mg/mL protein, VAPOR DIFFUSION, HANGING DROP, temperature 291K
|
Resolution 1.63 Å
R-free 0.204
|
|
4PKQ
Anthrax toxin lethal factor with bound zinc
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
ZN ZINC ION × 1
PGE TRIETHYLENE GLYCOL × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.20 Å
R-free 0.217
|
|
4PKR
Anthrax toxin lethal factor with bound small molecule inhibitor 10
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
2ZL N~2~-benzyl-N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
ZN ZINC ION × 1
CL CHLORIDE ION × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.20 Å
R-free 0.253
|
|
4PKS
Anthrax toxin lethal factor with bound small molecule inhibitor 11
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
ZN ZINC ION × 1
30H N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-N~2~-(pyridin-3-ylmethyl)-D-alaninamide × 1
GOL GLYCEROL × 1
EDO 1,2-ETHANEDIOL × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.30 Å
R-free 0.260
|
|
4PKT
Anthrax toxin lethal factor with bound small molecule inhibitor 13
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
30O N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-N~2~-(4-nitrobenzyl)-D-alaninamide × 1
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.40 Å
R-free 0.240
|
|
4PKU
Anthrax toxin lethal factor with bound small molecule inhibitor 15
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
30P N~2~-(3-aminobenzyl)-N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.40 Å
R-free 0.249
|
|
4PKV
Anthrax toxin lethal factor with bound small molecule inhibitor 16
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
30R N~2~-[4-(aminomethyl)benzyl]-N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.50 Å
R-free 0.253
|
|
4PKW
Anthrax toxin lethal factor with bound small molecule inhibitor GM6001
Deposited 2014-05-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
ZN ZINC ION × 1
GM6 3-(N-HYDROXYCARBOXAMIDO)-2-ISOBUTYLPROPANOYL-TRP-METHYLAMIDE × 1
GOL GLYCEROL × 2
EDO 1,2-ETHANEDIOL × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 1.75 Å
R-free 0.207
|
|
4WF6
Anthrax toxin lethal factor with bound small molecule inhibitor MK-31
Deposited 2014-09-12
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
ZN ZINC ION × 1
407 N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.65 Å
R-free 0.240
|
|
4XM6
Anthrax toxin lethal factor with ligand-induced binding pocket
Deposited 2015-01-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
41R N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-N~2~-(2-methylpropyl)-D-valinamide × 1
ZN ZINC ION × 1
EDO 1,2-ETHANEDIOL × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.35 Å
R-free 0.246
|
|
4XM7
Anthrax toxin lethal factor with ligand-induced binding pocket
Deposited 2015-01-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
|
Mutation:A266S
|
41S N~2~-[(4-fluoro-3-methoxyphenyl)sulfonyl]-N-hydroxy-N~2~-(2-methylpropyl)-D-valinamide × 1
ZN ZINC ION × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.70 Å
R-free 0.269
|
|
4XM8
Anthrax toxin lethal factor with ligand-induced binding pocket
Deposited 2015-01-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:UNP residues 298-809
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Mutation:A266S
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41T N-hydroxy-N~2~-{[3-(methoxymethyl)phenyl]sulfonyl}-N~2~-(2-methylpropyl)-D-valinamide × 1
ZN ZINC ION × 1
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X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.70 Å
R-free 0.276
|
|
5D1S
Anthrax toxin lethal factor with hydroxamic acid inhibitor
Deposited 2015-08-04
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:residues 298-809
|
Mutation:A299S
|
56Q N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-N~2~-methyl-D-alaninamide × 1
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.10 Å
R-free 0.247
|
|
5D1T
Anthrax toxin lethal factor with hydroxamic acid inhibitor
Deposited 2015-08-04
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:residues 298-809
|
Mutation:A299S
|
ZN ZINC ION × 1
56R N~2~-[3-(aminomethyl)benzyl]-N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.20 Å
R-free 0.255
|
|
5D1U
Anthrax toxin lethal factor with hydroxamic acid inhibitor
Deposited 2015-08-04
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
298–809(512 aa)
Fragment:residues 298-809
|
Mutation:A299S
|
56P N~2~-(6-aminohexyl)-N~2~-[(4-fluoro-3-methylphenyl)sulfonyl]-N-hydroxy-D-alaninamide × 1
ZN ZINC ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 6.8;286 K;11-16% PEG 8K, 50 mM Bis-Tris, 100 mM magnesium acetate
|
Resolution 2.85 Å
R-free 0.252
|
|
6PSN
Anthrax toxin protective antigen channels bound to lethal factor
Deposited 2019-07-12
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 8
PDB declaration: octameric
|
Chain L
1–809(809 aa)
|
Not recorded
|
CA CALCIUM ION × 14
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 8
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 4.60 Å
|
|
6ZXK
Fully-loaded anthrax lethal toxin in its heptameric pre-pore state and PA7LF(2+1B) arrangement
Deposited 2020-07-29
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Different construct
Different mutation/modification
Different oligomeric state
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 10
PDB declaration: decameric
|
Chain H
1–809(809 aa)
Chain I
1–809(809 aa)
Chain J
1–809(809 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 8.5
cryo-EM vitrification conditions
Cryogen ETHANE;4 uL sample was applied to grid (with 2 nm additional carbon layer) and incubated for 45 s prior blotting.
|
Resolution 3.80 Å
|
|
6ZXL
Fully-loaded anthrax lethal toxin in its heptameric pre-pore state and PA7LF(2+1A) arrangement
Deposited 2020-07-29
|
Different construct
Different mutation/modification
Different oligomeric state
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 10
PDB declaration: decameric
|
Chain H
1–809(809 aa)
Chain I
1–809(809 aa)
Chain J
1–809(809 aa)
|
Not recorded
|
No recorded non-water small molecule
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 8.5
cryo-EM vitrification conditions
Cryogen ETHANE;4 uL sample was applied to grid (with 2 nm additional carbon layer) and incubated for 45 s prior blotting.
|
Resolution 4.20 Å
|
|
7KXR
Protective antigen pore translocating lethal factor N-terminal domain
Deposited 2020-12-04
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 8
PDB declaration: octameric
|
Chain L
34–296(263 aa)
Fragment:UNP Residues 34-296
|
Mutation:E126C
|
CA CALCIUM ION × 14
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 5.5
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 3.30 Å
|
|
8FVU
Cryo-EM structure of human Needle/NAIP/NLRC4 (R288A)
Deposited 2023-01-19
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Insufficient information
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain U
34–296(263 aa)
|
Not recorded
|
ATP ADENOSINE-5'-TRIPHOSPHATE × 1
ZN ZINC ION × 3
|
ELECTRON MICROSCOPY
cryo-EM buffer
pH 7.5
cryo-EM vitrification conditions
Cryogen ETHANE
|
Resolution 3.60 Å
|