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Dehydroascorbate reductase 3A from Populus trichocarpa complexed with GSH.
Authors
Roret, T., Tsan, P.
Assembly
Dehydroascorbate reductase family protein
Entity
1. Dehydroascorbate reductase family protein, entity 1 (polymer, Thiol state: free and other bound), 218 monomers, 24325.85 Da Detail

MALEICVKAA VGAPNILGDC PFCQRVLLSL EEKKIPYKSH LINLGDKPQW FLEISPEGKV PVVKIDDKWV ADSDVIVGIL EEKNPEPPLA TPPEFASVGS KIFPSFVKFL KSKDPNDGTE QALLEELKAL DGHLKVHGPF IAGEKITAVD LSLAPKLYHL EVALGHFKNW PIPDNLTHVL NYIKLLFSRE SFKKTRAAEE HVIAGWEPKV NAHHHHHH


2. Dehydroascorbate reductase family protein, entity GSH (non-polymer), 307.323 Da
Total weight
24633.172 Da
Max. entity weight
24325.85 Da
Entity Connection
disulfide 1 Detail

IDTypeValue orderAtom ID 1Atom ID 2
1disulfidesing1:CYS20:SG2:GSH1:SG2

Source organism
Populus trichocarpa
Exptl. method
solution NMR
Refine. method
molecular dynamics
Data set
assigned_chemical_shifts
Chem. Shift Complete1
Sequence coverage: 87.2 %, Completeness: 31.2 %, Completeness (bb): 64.1 % Detail

Polymer type: polypeptide(L)

Total1H15N
All31.2 % (491 of 1572)22.2 % (301 of 1357)88.4 % (190 of 215)
Backbone64.1 % (404 of 630)50.0 % (215 of 430)94.5 % (189 of 200)
Sidechain 9.2 % (87 of 942) 9.3 % (86 of 927) 6.7 % (1 of 15)
Aromatic 0.0 % (0 of 116) 0.0 % (0 of 112) 0.0 % (0 of 4)
Methyl11.9 % (16 of 134)11.9 % (16 of 134)

1. entity 1

MALEICVKAA VGAPNILGDC PFCQRVLLSL EEKKIPYKSH LINLGDKPQW FLEISPEGKV PVVKIDDKWV ADSDVIVGIL EEKNPEPPLA TPPEFASVGS KIFPSFVKFL KSKDPNDGTE QALLEELKAL DGHLKVHGPF IAGEKITAVD LSLAPKLYHL EVALGHFKNW PIPDNLTHVL NYIKLLFSRE SFKKTRAAEE HVIAGWEPKV NAHHHHHH

Sample #1

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 8.0, Details 0.37 mM [U-100% 15N] Dehydroascorbate reductase, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
1Dehydroascorbate reductase[U-100% 15N]0.37 mM
Sample #2

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 8.0, Details 0.37 mM [U-100% 15N] Dehydroascorbate reductase, 74.0 mM GLUTATHIONE, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
2Dehydroascorbate reductase[U-100% 15N]0.37 mM
3GLUTATHIONEnatural abundance74.0 mM

Chem. Shift Complete2
Sequence coverage: 88.5 %, Completeness: 31.6 %, Completeness (bb): 64.6 % Detail

Polymer type: polypeptide(L)

Total1H15N
All31.6 % (994 of 3144)22.6 % (613 of 2714)88.6 % (381 of 430)
Backbone64.6 % (814 of 1260)50.5 % (434 of 860)95.0 % (380 of 400)
Sidechain 9.6 % (180 of 1884) 9.7 % (179 of 1854) 3.3 % (1 of 30)
Aromatic 0.0 % (0 of 232) 0.0 % (0 of 224) 0.0 % (0 of 8)
Methyl14.9 % (40 of 268)14.9 % (40 of 268)

1. entity 1

MALEICVKAA VGAPNILGDC PFCQRVLLSL EEKKIPYKSH LINLGDKPQW FLEISPEGKV PVVKIDDKWV ADSDVIVGIL EEKNPEPPLA TPPEFASVGS KIFPSFVKFL KSKDPNDGTE QALLEELKAL DGHLKVHGPF IAGEKITAVD LSLAPKLYHL EVALGHFKNW PIPDNLTHVL NYIKLLFSRE SFKKTRAAEE HVIAGWEPKV NAHHHHHH

Sample #1

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 8.0, Details 0.37 mM [U-100% 15N] Dehydroascorbate reductase, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
1Dehydroascorbate reductase[U-100% 15N]0.37 mM
Sample #2

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 8.0, Details 0.37 mM [U-100% 15N] Dehydroascorbate reductase, 74.0 mM GLUTATHIONE, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
2Dehydroascorbate reductase[U-100% 15N]0.37 mM
3GLUTATHIONEnatural abundance74.0 mM

Protein Blocks Logo
Calculated from 10 models in PDB: 5N9U, Strand ID: A Detail


Release date
2017-03-06
Citation
Insights into ascorbate regeneration in plants: investigating the redox and structural properties of dehydroascorbate reductases from Populus trichocarpa
Lallement, P.A., Roret, T., Tsan, P., Gualberto, J.M., Girardet, J.M., Didierjean, C., Rouhier, N., Hecker, A.
Biochem. J. (2016), 473, 717-731, PubMed 26699905 , DOI 10.1042/BJ20151147 ,
Entries sharing articles BMRB: 2 entries Detail
  BMRB: 34093 released on 2017-03-14
    Title Solution structure of C20S variant of Dehydroascorbate reductase 3A from Populus trichocarpa in complex with dehydroascorbic acid.
  BMRB: 25712 released on 2016-03-13
    Title Solution structure of the dehydroascorbate reductase 3A from Populus trichocarpa
Related entities 1. Dehydroascorbate reductase family protein, entity 1, : 1 : 1 : 1 : 154 entities Detail
Experiments performed 1 experiments Detail
nullKeywords Dehydroascorbate reductase, Glutathione transferase, Oxidoreductase, Plant