Search

NMR solution structure of YfiD
Authors
Bowman, S.E.J., Drennan, C.L.
Assembly
Autonomous glycyl radical cofactor
Entity
1. Autonomous glycyl radical cofactor (polymer), 127 monomers, 14268.00 Da Detail

MITGIQITKA ANDDLLNSFW LLDSEKGEAR CIVAKAGFAE DEVVAVSKLG DIEYREVPVE VKPEVRVEGG QHLNVNVLRR ETLEDAVKHP EKYPQLTIRV SGYAVRFNSL TPEQQRDVIA RTFTESL


Formula weight
14268.0 Da
Source organism
Escherichia coli
Exptl. method
solution NMR
Refine. method
molecular dynamics
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 52.0 %, Completeness: 31.8 %, Completeness (bb): 36.4 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All31.8 % (469 of 1474)40.3 % (308 of 765)17.5 % (101 of 576)45.1 % (60 of 133)
Backbone36.4 % (274 of 752)47.7 % (122 of 256)24.6 % (92 of 374)49.2 % (60 of 122)
Sidechain25.7 % (216 of 842)36.0 % (183 of 509)10.2 % (33 of 322) 0.0 % (0 of 11)
Aromatic 0.0 % (0 of 84) 0.0 % (0 of 42) 0.0 % (0 of 41) 0.0 % (0 of 1)
Methyl21.1 % (35 of 166)34.9 % (29 of 83) 7.2 % (6 of 83)

1. entity 1

MITGIQITKA ANDDLLNSFW LLDSEKGEAR CIVAKAGFAE DEVVAVSKLG DIEYREVPVE VKPEVRVEGG QHLNVNVLRR ETLEDAVKHP EKYPQLTIRV SGYAVRFNSL TPEQQRDVIA RTFTESL

Sample #1

Solvent system 90% H2O/10% D2O, Pressure 760 mmHg, Temperature 293 K, pH 7.2, Details 0.7 mM [U-15N] YfiD, 18 mM HEPES, 2.7 mM ammonium sulfate, 10 % v/v D2O, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
1YfiD[U-15N]0.7 mM
2HEPESnatural abundance18 mM
3ammonium sulfatenatural abundance2.7 mM
4D2Onatural abundance10 % v/v
Sample #2

Solvent system 90% H2O/10% D2O, Pressure 760 mmHg, Temperature 293 K, pH 7.2, Details 1.3 mM [U-100% 13C; U-100% 15N] YfiD, 18 mM HEPES, 2.7 mM ammonium sulfate, 10 % v/v D2O, 90% H2O/10% D2O


#NameIsotope labelingTypeConcentration
5YfiD[U-100% 13C; U-100% 15N]1.3 mM
6HEPESnatural abundance18 mM
7ammonium sulfatenatural abundance2.7 mM
8D2Onatural abundance10 % v/v

Protein Blocks Logo
Calculated from 10 models in PDB: 6OWR, Strand ID: A Detail


Release date
2019-07-02
Citation
Solution structure and biochemical characterization of a spare part protein that restores activity to an oxygen-damaged glycyl radical enzyme
Bowman, S.E.J., Backman, L.R.F., Bjork, R.E., Andorfer, M.C., Yori, S., Caruso, A., Stultz, C.M., Drennan, C.L.
J. Biol. Inorg. Chem. (2019), 24, 817-829, PubMed 31250200 , DOI 10.1007/s00775-019-01681-2 ,
Related entities 1. Autonomous glycyl radical cofactor, : 1 : 4 : 1 : 35 entities Detail
Interaction partners 1. Autonomous glycyl radical cofactor, : 21 interactors Detail
Experiments performed 8 experiments Detail
Chemical shift validation 3 contents Detail
Keywords Cofactor repair, Glycyl radical enzyme, PROTEIN BINDING