data_bmse001015 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse001015 _Entry.Title L_histidine _Entry.Version_type update _Entry.Submission_date 2011-12-23 _Entry.Accession_date 2011-12-23 _Entry.Last_release_date 2013-03-06 _Entry.Original_release_date 2011-12-23 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.31 _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.DOI 10.13018/BMSE001015 _Entry.BMRB_internal_directory_name L_histidine loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Entry_ID 1 Dan Bearden D. bmse001015 stop_ loop_ _Entry_src.ID _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 'National Institute of Standards and Technology, Hollings Marine Laboratory' NIST bmse001015 stop_ loop_ _Release.Release_number _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 2012-12-21 2011-12-23 original BMRB 'Original spectra from Birmingham' bmse001015 2 2013-03-06 2011-12-23 update BMRB 'Added PubChem SID 160963334 to database loop' bmse001015 3 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse001015 4 2017-12-19 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse001015 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse001015 _Citation.ID 1 _Citation.Class 'reference citation' _Citation.PubMed_ID 17170002 _Citation.Title 'Database resources of the National Center for Biotechnology Information.' _Citation.Status published _Citation.Type internet _Citation.WWW_URL http://pubchem.ncbi.nlm.nih.gov/ _Citation.Year 2006 loop_ _Citation_author.Ordinal _Citation_author.Given_name _Citation_author.Family_name _Citation_author.First_initial _Citation_author.Middle_initials _Citation_author.Entry_ID _Citation_author.Citation_ID 1 D. Wheeler D. L. bmse001015 1 2 T. Barrett T. ? bmse001015 1 3 D. Benson D. A. bmse001015 1 4 S. Bryant S. H. bmse001015 1 5 K. Canese K. ? bmse001015 1 6 V. Chetvenin V. ? bmse001015 1 7 D. Church D. M. bmse001015 1 8 M. DiCuccio M. ? bmse001015 1 9 R. Edgar R. ? bmse001015 1 10 S. Federhen S. ? bmse001015 1 11 L. Geer L. Y. bmse001015 1 12 W. Helmberg W. ? bmse001015 1 13 Y. Kapustin Y. ? bmse001015 1 14 D. Kenton D. L. bmse001015 1 15 O. Khovayko O. ? bmse001015 1 16 D. Lipman D. J. bmse001015 1 17 T. Madden T. L. bmse001015 1 18 D. Maglott D. R. bmse001015 1 19 J. Ostell J. ? bmse001015 1 20 K. Pruitt K. D. bmse001015 1 21 G. Schuler G. D. bmse001015 1 22 L. Schriml L. M. bmse001015 1 23 E. Sequeira E. ? bmse001015 1 24 S. Sherry S. T. bmse001015 1 25 K. Sirotkin K. ? bmse001015 1 26 A. Souvorov A. ? bmse001015 1 27 G. Starchenko G. ? bmse001015 1 28 T. Suzek T. O. bmse001015 1 29 R. Tatusov R. ? bmse001015 1 30 T. Tatusova T. A. bmse001015 1 31 L. Bagner L. ? bmse001015 1 32 E. Yaschenko E. ? bmse001015 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse001015 _Assembly.ID 1 _Assembly.Name L-Histidine _Assembly.Number_of_components 1 _Assembly.Organic_ligands 0 _Assembly.Non_standard_bonds no _Assembly.Paramagnetic no _Assembly.Thiol_state 'not reported' loop_ _Entity_assembly.ID _Entity_assembly.Entity_assembly_name _Entity_assembly.Entity_ID _Entity_assembly.Entity_label _Entity_assembly.Experimental_data_reported _Entity_assembly.Physical_state _Entity_assembly.Conformational_isomer _Entity_assembly.Chemical_exchange_state _Entity_assembly.Entry_ID _Entity_assembly.Assembly_ID 1 L_histidine 1 $L_histidine yes native no no bmse001015 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_L_histidine _Entity.Sf_category entity _Entity.Sf_framecode L_histidine _Entity.Entry_ID bmse001015 _Entity.ID 1 _Entity.Name L-histidine _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_monomer no _Entity.Nstd_chirality no _Entity.Nstd_linkage no _Entity.Paramagnetic no _Entity.Thiol_state 'not reported' loop_ _Entity_comp_index.ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 1 $chem_comp_1 bmse001015 1 stop_ save_ #################### # Natural source # #################### save_natural_source _Entity_natural_src_list.Sf_category natural_source _Entity_natural_src_list.Sf_framecode natural_source _Entity_natural_src_list.Entry_ID bmse001015 _Entity_natural_src_list.ID 1 loop_ _Entity_natural_src.ID _Entity_natural_src.Entity_ID _Entity_natural_src.Entity_label _Entity_natural_src.NCBI_taxonomy_ID _Entity_natural_src.Type _Entity_natural_src.Common _Entity_natural_src.Organism_name_scientific _Entity_natural_src.Organism_name_common _Entity_natural_src.Superkingdom _Entity_natural_src.Kingdom _Entity_natural_src.Genus _Entity_natural_src.Species _Entity_natural_src.Entry_ID _Entity_natural_src.Entity_natural_src_list_ID 1 1 $L_histidine n/a 'multiple natural sources' yes 'not applicable' n/a n/a n/a n/a n/a bmse001015 1 stop_ save_ ######################### # Experimental source # ######################### save_experimental_source _Entity_experimental_src_list.Sf_category experimental_source _Entity_experimental_src_list.Sf_framecode experimental_source _Entity_experimental_src_list.Entry_ID bmse001015 _Entity_experimental_src_list.ID 1 loop_ _Entity_experimental_src.ID _Entity_experimental_src.Entity_ID _Entity_experimental_src.Entity_label _Entity_experimental_src.Production_method _Entity_experimental_src.Entry_ID _Entity_experimental_src.Entity_experimental_src_list_ID 1 1 $L_histidine 'chemical synthesis' bmse001015 1 stop_ save_ ################################# # Polymer residues and ligands # ################################# save_chem_comp_1 _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_1 _Chem_comp.Entry_ID bmse001015 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name L-Histidine _Chem_comp.Type non-polymer _Chem_comp.InChI_code InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1 _Chem_comp.Paramagnetic no _Chem_comp.Aromatic yes _Chem_comp.Formula 'C6 H9 N3 O2' _Chem_comp.Formula_weight 155.1545600000 _Chem_comp.Formula_mono_iso_wt_nat 155.069476549 _Chem_comp.Formula_mono_iso_wt_13C 161.089605576 _Chem_comp.Formula_mono_iso_wt_15N 158.060581228 _Chem_comp.Formula_mono_iso_wt_13C_15N 164.0807102551 _Chem_comp.Image_file_name bmse001015.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse001015.mol _Chem_comp.Struct_file_format mol loop_ _Chem_comp_common_name.Name _Chem_comp_common_name.Type _Chem_comp_common_name.Entry_ID _Chem_comp_common_name.Comp_ID (S)-4-(2-Amino-2-carboxyethyl)imidazole synonym bmse001015 1 '1H-Imidazole-4-alanine, (S)-' synonym bmse001015 1 L-beta-(4-Imidazolyl)alanin synonym bmse001015 1 Histidine synonym bmse001015 1 Glyoxaline-5-alanine synonym bmse001015 1 S-Histidine synonym bmse001015 1 'HISTIDINE, L-' synonym bmse001015 1 'alpha-Amino-1H-imidazole-4-propionic acid, (S)-' synonym bmse001015 1 (L)-Histidine synonym bmse001015 1 'L-Alanine, 3-(1H-imidazol-4-yl)-' synonym bmse001015 1 '(S)-alpha-Amino-1H-imidazole-4-propionic acid' synonym bmse001015 1 L-beta-(4-Imidazolyl)-alpha-alanin synonym bmse001015 1 Istidina synonym bmse001015 1 '1H-Imidazole-4-propanoic acid, alpha-amino-, (S)-' synonym bmse001015 1 4-(2-Amino-2-carboxyethyl)imidazole synonym bmse001015 1 L-Histidine synonym bmse001015 1 'alpha-Amino-4(or 5)-imidazolepropionic acid' synonym bmse001015 1 HIS synonym bmse001015 1 (S)-2-Amino-3-(4-imidazolyl)propionsaeure synonym bmse001015 1 Anti-rheuma synonym bmse001015 1 'Histidinum [INN-Latin]' synonym bmse001015 1 'Histidina [INN-Spanish]' synonym bmse001015 1 '(S)-alpha-Amino-1H-imidazole-4-propanoic acid' synonym bmse001015 1 stop_ loop_ _Chem_comp_descriptor.Descriptor _Chem_comp_descriptor.Type _Chem_comp_descriptor.Program _Chem_comp_descriptor.Program_version _Chem_comp_descriptor.Entry_ID _Chem_comp_descriptor.Comp_ID ; InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1 ; INCHI na na bmse001015 1 InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1 INCHI ALATIS 3.003 bmse001015 1 stop_ loop_ _Chem_comp_systematic_name.Name _Chem_comp_systematic_name.Naming_system _Chem_comp_systematic_name.Entry_ID _Chem_comp_systematic_name.Comp_ID '(2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid' IUPAC bmse001015 1 '(2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid' IUPAC_TRADITIONAL bmse001015 1 '(2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid' IUPAC_CAS bmse001015 1 '(2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid' IUPAC_OPENEYE bmse001015 1 '(2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid' IUPAC_SYSTEMATIC bmse001015 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID isomeric C1=C(NC=N1)C[C@@H](C(=O)O)N bmse001015 1 canonical C1=C(NC=N1)CC(C(=O)O)N bmse001015 1 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Drawing_2D_coord_x _Chem_comp_atom.Drawing_2D_coord_y _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID C2 C 3.3090 0.6784 1 bmse001015 1 C3 C 2.0000 -0.2727 2 bmse001015 1 C1 C 4.5691 -0.5817 3 bmse001015 1 C4 C 3.6180 -0.2727 4 bmse001015 1 C5 C 5.3122 0.0874 5 bmse001015 1 C6 C 6.2633 -0.2216 6 bmse001015 1 N7 N 5.1043 1.0656 7 bmse001015 1 N9 N 2.8090 -0.8605 8 bmse001015 1 N8 N 2.3090 0.6784 9 bmse001015 1 O10 O 7.0064 0.4476 10 bmse001015 1 O11 O 6.4712 -1.1997 11 bmse001015 1 H14 H 3.6734 1.1800 12 bmse001015 1 H15 H 1.4103 -0.4643 13 bmse001015 1 H12 H 4.2780 -1.1291 14 bmse001015 1 H13 H 5.0577 -0.9634 15 bmse001015 1 H16 H 4.7226 0.2790 16 bmse001015 1 H17 H 5.5651 1.4805 17 bmse001015 1 H18 H 4.5147 1.2572 18 bmse001015 1 H19 H 2.8090 -1.4805 19 bmse001015 1 H20 H 7.5961 0.2560 20 bmse001015 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID C2 C1 BMRB bmse001015 1 C3 C2 BMRB bmse001015 1 C1 C3 BMRB bmse001015 1 C4 C4 BMRB bmse001015 1 C5 C5 BMRB bmse001015 1 C6 C6 BMRB bmse001015 1 N7 N7 BMRB bmse001015 1 N9 N8 BMRB bmse001015 1 N8 N9 BMRB bmse001015 1 O10 O10 BMRB bmse001015 1 O11 O11 BMRB bmse001015 1 H14 H12 BMRB bmse001015 1 H15 H13 BMRB bmse001015 1 H12 H14 BMRB bmse001015 1 H13 H15 BMRB bmse001015 1 H16 H16 BMRB bmse001015 1 H17 H17 BMRB bmse001015 1 H18 H18 BMRB bmse001015 1 H19 H19 BMRB bmse001015 1 H20 H20 BMRB bmse001015 1 C2 C2 ALATIS bmse001015 1 C3 C3 ALATIS bmse001015 1 C1 C1 ALATIS bmse001015 1 C4 C4 ALATIS bmse001015 1 C5 C5 ALATIS bmse001015 1 C6 C6 ALATIS bmse001015 1 N7 N7 ALATIS bmse001015 1 N9 N9 ALATIS bmse001015 1 N8 N8 ALATIS bmse001015 1 O10 O10 ALATIS bmse001015 1 O11 O11 ALATIS bmse001015 1 H14 H14 ALATIS bmse001015 1 H15 H15 ALATIS bmse001015 1 H12 H12 ALATIS bmse001015 1 H13 H13 ALATIS bmse001015 1 H16 H16 ALATIS bmse001015 1 H17 H17 ALATIS bmse001015 1 H18 H18 ALATIS bmse001015 1 H19 H19 ALATIS bmse001015 1 H20 H20 ALATIS bmse001015 1 stop_ loop_ _Chem_comp_bond.ID _Chem_comp_bond.Type _Chem_comp_bond.Value_order _Chem_comp_bond.Atom_ID_1 _Chem_comp_bond.Atom_ID_2 _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent DOUB C2 C4 bmse001015 1 2 covalent SING C2 N8 bmse001015 1 3 covalent SING C2 H14 bmse001015 1 4 covalent SING C3 N9 bmse001015 1 5 covalent DOUB C3 N8 bmse001015 1 6 covalent SING C3 H15 bmse001015 1 7 covalent SING C1 C4 bmse001015 1 8 covalent SING C1 C5 bmse001015 1 9 covalent SING C1 H12 bmse001015 1 10 covalent SING C1 H13 bmse001015 1 11 covalent SING C4 N9 bmse001015 1 12 covalent SING C5 C6 bmse001015 1 13 covalent SING C5 N7 bmse001015 1 14 covalent SING C5 H16 bmse001015 1 15 covalent SING C6 O10 bmse001015 1 16 covalent DOUB C6 O11 bmse001015 1 17 covalent SING N7 H17 bmse001015 1 18 covalent SING N7 H18 bmse001015 1 19 covalent SING N9 H19 bmse001015 1 20 covalent SING O10 H20 bmse001015 1 stop_ loop_ _Chem_comp_db_link.Author_supplied _Chem_comp_db_link.Database_code _Chem_comp_db_link.Accession_code _Chem_comp_db_link.Accession_code_type _Chem_comp_db_link.Entry_mol_name _Chem_comp_db_link.Entry_relation_type _Chem_comp_db_link.Entry_ID _Chem_comp_db_link.Comp_ID no PubChem 160963334 sid L-Histidine 'matching entry' bmse001015 1 no PubChem 85164887 sid L-Histidine 'matching entry' bmse001015 1 no PubChem 149204 sid L-Histidine 'matching entry' bmse001015 1 no PubChem 6274 cid L-Histidine 'matching entry' bmse001015 1 no PubChem 3435 sid L-Histidine 'matching entry' bmse001015 1 no KEGG C00135 'compound ID' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 150-35-6 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 155304-24-8 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 35479-49-3 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 35558-59-9 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 45955-20-2 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 54166-13-1 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 7006-35-1 'registry number' L-Histidine 'matching entry' bmse001015 1 no 'CAS Registry' 71-00-1 'registry number' L-Histidine 'matching entry' bmse001015 1 no CHEBI 15971 ? L-Histidine 'matching entry' bmse001015 1 no 'FEMA No.' 3694 ? L-Histidine 'matching entry' bmse001015 1 no EINECS 200-745-3 ? L-Histidine 'matching entry' bmse001015 1 no NSC 137773 ? L-Histidine 'matching entry' bmse001015 1 no HSDB 1810 ? L-Histidine 'matching entry' bmse001015 1 no PDB HIS 'Chemical Component' L-Histidine 'matching entry' bmse001015 1 no PDB HIS_LFOH 'Chemical Component' L-Histidine 'matching entry' bmse001015 1 stop_ loop_ _Chem_comp_citation.Citation_ID _Chem_comp_citation.Citation_label _Chem_comp_citation.Entry_ID _Chem_comp_citation.Comp_ID 1 $citation_1 bmse001015 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse001015 _Sample.ID 1 _Sample.Type solution loop_ _Sample_component.ID _Sample_component.Mol_common_name _Sample_component.Isotopic_labeling _Sample_component.Entity_ID _Sample_component.Entity_label _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_units _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Entry_ID _Sample_component.Sample_ID 1 L-Histidine 'natural abundance' 1 $L_histidine Solute 20 mM sigma/aldrich L-Histidine bmse001015 1 2 D2O ? ? ? Solvent 100 % ? ? bmse001015 1 3 'sodium phosphate' ? ? ? Buffer 200 mM ? ? bmse001015 1 4 'sodium azide' ? ? ? Cytocide 500 uM ? ? bmse001015 1 5 DSS ? ? ? Reference 1 % ? ? bmse001015 1 stop_ save_ ####################### # Sample conditions # ####################### save_sample_conditions_1 _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_conditions_1 _Sample_condition_list.Entry_ID bmse001015 _Sample_condition_list.ID 1 loop_ _Sample_condition_variable.Type _Sample_condition_variable.Val _Sample_condition_variable.Val_units _Sample_condition_variable.Entry_ID _Sample_condition_variable.Sample_condition_list_ID pH 7.4 pH bmse001015 1 temperature 298 K bmse001015 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse001015 _Software.ID 1 _Software.Name TopSpin _Software.Version 2.1 loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'Bruker Biospin' bmse001015 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Collection bmse001015 1 Processing bmse001015 1 'Data analysis' bmse001015 1 'Peak picking' bmse001015 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_Bruker_700 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode Bruker_700 _NMR_spectrometer.Entry_ID bmse001015 _NMR_spectrometer.ID 1 _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model 'Avance II' _NMR_spectrometer.Field_strength 700 save_ save_TCI_cryoprobe _NMR_spectrometer_probe.Sf_category NMR_spectrometer_probe _NMR_spectrometer_probe.Sf_framecode TCI_cryoprobe _NMR_spectrometer_probe.Entry_ID bmse001015 _NMR_spectrometer_probe.ID 1 _NMR_spectrometer_probe.Details 'single z-axis gradient' _NMR_spectrometer_probe.Manufacturer Bruker _NMR_spectrometer_probe.Model 'TCI CryoProbe' _NMR_spectrometer_probe.Diameter 5 loop_ _NMR_probe.Type _NMR_probe.Entry_ID _NMR_probe.NMR_spectrometer_probe_ID Cryoprobe bmse001015 1 stop_ save_ ############################# # NMR applied experiments # ############################# save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse001015 _Experiment_list.ID 1 loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _Experiment.Sample_ID _Experiment.Sample_label _Experiment.Sample_state _Experiment.Sample_condition_list_ID _Experiment.Sample_condition_list_label _Experiment.NMR_spectrometer_ID _Experiment.NMR_spectrometer_label _Experiment.Entry_ID _Experiment.Experiment_list_ID 1 '2D J-resolved 1H' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse001015 1 2 '2D [1H,13C]-HSQC' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse001015 1 3 '1D 1H, NOESY' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse001015 1 stop_ loop_ _Experiment_file.Experiment_ID _Experiment_file.Name _Experiment_file.Type _Experiment_file.Directory_path _Experiment_file.Details _Experiment_file.Entry_ID _Experiment_file.Experiment_list_ID 1 1H_1H_JRES text/directory nmr/set01/ 'NMR experiment directory' bmse001015 1 1 00.png image/png nmr/set01/spectra/1H_1H_JRES 'Spectral image' bmse001015 1 1 01.png image/png nmr/set01/spectra/1H_1H_JRES 'Spectral image' bmse001015 1 2 1H_13C_HSQC text/directory nmr/set01/ 'NMR experiment directory' bmse001015 1 2 00.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse001015 1 2 01.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse001015 1 3 1H_NOESY text/directory nmr/set01/ 'NMR experiment directory' bmse001015 1 3 00.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse001015 1 3 01.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse001015 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference _Chem_shift_reference.Entry_ID bmse001015 _Chem_shift_reference.ID 1 loop_ _Chem_shift_ref.Atom_type _Chem_shift_ref.Atom_isotope_number _Chem_shift_ref.Mol_common_name _Chem_shift_ref.Atom_group _Chem_shift_ref.Chem_shift_units _Chem_shift_ref.Chem_shift_val _Chem_shift_ref.Ref_method _Chem_shift_ref.Ref_type _Chem_shift_ref.Indirect_shift_ratio _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 DSS 'methyl protons' ppm 0.00 internal direct 1.000000000 bmse001015 1 C 13 DSS 'methyl carbons' ppm 0.00 internal direct 1.000000000 bmse001015 1 stop_ save_