2JY9

NMR structure of putative tRNA hydrolase domain from Salmonella typhimurium. NorthEast Structural Genomics Consortium target StR220


SOLUTION NMR
NMR Experiment
ExperimentTypeSample ContentsSolventIonic StrengthpHPressureTemperature (K)Spectrometer
12D 1H-15N HSQC1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
22D 1H-13C HSQC1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
34,3D GFT CABCACONHN1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
44,3D GFT HNNCABCA1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
54,3D GFT HCCH COSY1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
63D HCCH-COSY1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
73D SimNOESY1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
84,3D HABCABCONHN1.4 mM [U-100% 13C; U-100% 15N] protein95% H2O/5% D2O1006.5ambient298
NMR Spectrometer Information
SpectrometerManufacturerModelField Strength
1VarianINOVA750
2VarianINOVA600
NMR Refinement
MethodDetailsSoftware
simulated annealingAutoAssign
NMR Ensemble Information
Conformer Selection Criteriatarget function
Conformers Calculated Total Number100
Conformers Submitted Total Number20
Representative Model1 (lowest energy)
Computation: NMR Software
#ClassificationVersionSoftware NameAuthor
1chemical shift assignmentAutoAssignZimmerman, Moseley, Kulikowski and Montelione
2chemical shift assignmentAutoStructureHuang, Tejero, Powers and Montelione
3refinementCNSBrunger, Adams, Clore, Gros, Nilges and Read
4refinementCYANAGuntert, Mumenthaler and Wuthrich
5structure solutionMOLMOLKoradi, Billeter and Wuthrich
6processingNMRPipeDelaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax
7validationPSVSBhattacharya and Montelione
8data analysisTALOSCornilescu, Delaglio and Bax
9collectionVnmrJVarian
10data analysisXEASYBartels et al.