2HQ3
Solution NMR structure of the apo-NosL protein from Achromobacter cycloclastes
SOLUTION NMR
NMR Experiment | ||||||||
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Experiment | Type | Sample Contents | Solvent | Ionic Strength | pH | Pressure | Temperature (K) | Spectrometer |
1 | HNCA | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
2 | HNCO | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
3 | HNCACB | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
4 | CBCA(CO)NH | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
5 | C(CO)NH | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
6 | HCC(CO)NH | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 90% H2O, 10% D2O | 90% H2O/10% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
7 | 1H-13C-CT HSQC | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; > 95% D2O | > 95% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
8 | HCCH-TOCSY | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; > 95% D2O | > 95% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
9 | 3D 15N NOESY | 1.0 mM NosL, U-15N; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 95% H2O, 5% D2O | 95% H2O/5% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
10 | 15N NOESY-HSQC | 1.0 mM NosL, U-15N; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; 95% H2O, 5% D2O | 95% H2O/5% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 | |
11 | 13C NOESY-HSQC | 1.0 mM NosL, U-15N, 13C; 100mM sodium phosphate; 1mM EDTA; 1mM DTT; > 95% D2O | > 95% D2O | 100 mM sodium phosphate | 6.5 | ambient | 303 |
NMR Spectrometer Information | |||
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Spectrometer | Manufacturer | Model | Field Strength |
1 | Bruker | DRX | 600 |
2 | Varian | INOVA | 800 |
NMR Refinement | ||
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Method | Details | Software |
Ambiguous Restraints for Iterative Assignments (ARIA 1.2), torsion angle dynamics, simulated annealing. | XwinNMR |
NMR Ensemble Information | |
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Conformer Selection Criteria | minimized average structure |
Conformers Calculated Total Number | |
Conformers Submitted Total Number | 1 |
Representative Model | 1 (minimized average structure) |
Additional NMR Experimental Information | |
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Details | Sequential and intra-residue 1H, 15N, and 13C backbone and side-chain chemical shift assignments were extracted from a series of double and triple resonance NMR experiments (HNCA, HNCO, HNCACB, CBCA(CO)NH, C(CO)NH, HCC(CO)NH, 1H-13C-CT HSQC,and HCCH-TOCSY) conducted on a DRX600. nOe data were obtained from 3D 15N NOESY experiments with mixing times (tmix) of 100, 120, and 140 msec and from 3D HCHC-NOESY (tmix=140 msec) spectra acquired at 600 MHz. Additional 15N NOESY-HSQC and 13C NOESY-HSQC experiments (nOe mixing times of 120 msec) were acquired on a Varian 800 INOVA (800 MHz) instrument. |
Computation: NMR Software | ||||
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# | Classification | Version | Software Name | Author |
1 | processing | XwinNMR | 3.1 | Bruker Inc. |
2 | processing | NMRPipe | 2.4 | Delaglio |
3 | data analysis | NMRView | 5.0 | Johnson |
4 | structure solution | ARIA | 1.2 | Nilges |
5 | refinement | CNS | 1.1 | BRUNGER,ADAMS,CLORE,DELANO,GROS,GROSSE-KUNSTLEVE,JIANG,KUSZEWSKI,NILGES,PANNU,READ,RICE,SIMONSON,WARREN |