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1IR2
Crystal Structure of Activated Ribulose-1,5-bisphosphate Carboxylase/oxygenase (Rubisco) from Green alga, Chlamydomonas reinhardtii Complexed with 2-Carboxyarabinitol-1,5-bisphosphate (2-CABP)
Deposited 2001-09-03
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Different construct
Different mutation/modification
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
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Assembly 1
Protein heterocomplex
Heteromer;Protein × 16
PDB declaration: hexadecameric
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Chain I
46–185(140 aa)
Chain J
46–185(140 aa)
Chain K
46–185(140 aa)
Chain L
46–185(140 aa)
Chain M
46–185(140 aa)
Chain N
46–185(140 aa)
Chain O
46–185(140 aa)
Chain P
46–185(140 aa)
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Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
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MG MAGNESIUM ION × 8
CAP 2-CARBOXYARABINITOL-1,5-DIPHOSPHATE × 8
GOL GLYCEROL × 20
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X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;PEG4000, HEPES-KOH, glycerol, NaHCO3, MgCl2, DTT, 2-carboxyarabinitol-1,5-bisphosphate (2-CABP), EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
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Resolution 1.84 Å
R-free 0.181
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1IR2
Crystal Structure of Activated Ribulose-1,5-bisphosphate Carboxylase/oxygenase (Rubisco) from Green alga, Chlamydomonas reinhardtii Complexed with 2-Carboxyarabinitol-1,5-bisphosphate (2-CABP)
Deposited 2001-09-03
|
Different construct
Different mutation/modification
Different ligand/ion
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 16
PDB declaration: hexadecameric
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Chain 1
46–185(140 aa)
Chain 2
46–185(140 aa)
Chain 3
46–185(140 aa)
Chain 4
46–185(140 aa)
Chain 5
46–185(140 aa)
Chain 6
46–185(140 aa)
Chain 7
46–185(140 aa)
Chain 8
46–185(140 aa)
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Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
Non-standard monomer:Yes (specific site not provided by mmCIF)
|
MG MAGNESIUM ION × 8
CAP 2-CARBOXYARABINITOL-1,5-DIPHOSPHATE × 8
GOL GLYCEROL × 20
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;PEG4000, HEPES-KOH, glycerol, NaHCO3, MgCl2, DTT, 2-carboxyarabinitol-1,5-bisphosphate (2-CABP), EDTA, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
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Resolution 1.84 Å
R-free 0.181
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7JFO
EPYC1(49-72)-bound Rubisco
Deposited 2020-07-17
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Different oligomeric state
Different structure-quality metrics
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Assembly 1
Protein heterocomplex
Heteromer;Protein × 24
PDB declaration: 24-meric
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Chain B
1–185(185 aa)
Chain D
1–185(185 aa)
Chain F
1–185(185 aa)
Chain H
1–185(185 aa)
Chain J
1–185(185 aa)
Chain L
1–185(185 aa)
Chain N
1–185(185 aa)
Chain P
1–185(185 aa)
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Not recorded
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No recorded non-water small molecule
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ELECTRON MICROSCOPY
cryo-EM buffer
pH 6.8;200 mM sorbitol, 50 mM HEPES, 50 mM KOAc, 2 mM Mg(OAc)2.4H2O and 1 mM CaCl2
cryo-EM vitrification conditions
Cryogen ETHANE
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Resolution 2.13 Å
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7JSX
EPYC1(106-135) peptide-bound Rubisco
Deposited 2020-08-16
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Different oligomeric state
Different structure-quality metrics
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Assembly 1
Protein heterocomplex
Heteromer;Protein × 24
PDB declaration: 24-meric
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Chain B
1–185(185 aa)
Chain D
1–185(185 aa)
Chain F
1–185(185 aa)
Chain H
1–185(185 aa)
Chain J
1–185(185 aa)
Chain L
1–185(185 aa)
Chain N
1–185(185 aa)
Chain P
1–185(185 aa)
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Not recorded
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No recorded non-water small molecule
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ELECTRON MICROSCOPY
cryo-EM buffer
pH 6.8;200 mM sorbitol, 50 mM HEPES, 50 mM KOAc, 2 mM Mg(OAc)2.4H2O and 1 mM CaCl2
cryo-EM vitrification conditions
Cryogen ETHANE
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Resolution 2.06 Å
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