data_bmse001018 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse001018 _Entry.Title guanosine _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/BMSE001018 _Entry.BMRB_internal_directory_name guanosine loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Entry_ID 1 Dan Bearden D. bmse001018 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 bmse001018 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' bmse001018 2 2013-03-06 2011-12-23 update BMRB 'Added PubChem SID 160963337 to database loop' bmse001018 3 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse001018 4 2017-12-19 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse001018 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse001018 _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. bmse001018 1 2 T. Barrett T. ? bmse001018 1 3 D. Benson D. A. bmse001018 1 4 S. Bryant S. H. bmse001018 1 5 K. Canese K. ? bmse001018 1 6 V. Chetvenin V. ? bmse001018 1 7 D. Church D. M. bmse001018 1 8 M. DiCuccio M. ? bmse001018 1 9 R. Edgar R. ? bmse001018 1 10 S. Federhen S. ? bmse001018 1 11 L. Geer L. Y. bmse001018 1 12 W. Helmberg W. ? bmse001018 1 13 Y. Kapustin Y. ? bmse001018 1 14 D. Kenton D. L. bmse001018 1 15 O. Khovayko O. ? bmse001018 1 16 D. Lipman D. J. bmse001018 1 17 T. Madden T. L. bmse001018 1 18 D. Maglott D. R. bmse001018 1 19 J. Ostell J. ? bmse001018 1 20 K. Pruitt K. D. bmse001018 1 21 G. Schuler G. D. bmse001018 1 22 L. Schriml L. M. bmse001018 1 23 E. Sequeira E. ? bmse001018 1 24 S. Sherry S. T. bmse001018 1 25 K. Sirotkin K. ? bmse001018 1 26 A. Souvorov A. ? bmse001018 1 27 G. Starchenko G. ? bmse001018 1 28 T. Suzek T. O. bmse001018 1 29 R. Tatusov R. ? bmse001018 1 30 T. Tatusova T. A. bmse001018 1 31 L. Bagner L. ? bmse001018 1 32 E. Yaschenko E. ? bmse001018 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse001018 _Assembly.ID 1 _Assembly.Name Guanosine _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 guanosine 1 $guanosine yes native no no bmse001018 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_guanosine _Entity.Sf_category entity _Entity.Sf_framecode guanosine _Entity.Entry_ID bmse001018 _Entity.ID 1 _Entity.Name guanosine _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 bmse001018 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 bmse001018 _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 $guanosine n/a 'multiple natural sources' yes 'not applicable' n/a n/a n/a n/a n/a bmse001018 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 bmse001018 _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 $guanosine 'chemical synthesis' bmse001018 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 bmse001018 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name Guanosine _Chem_comp.Type non-polymer _Chem_comp.InChI_code InChI=1S/C10H13N5O5/c11-10-13-7-4(8(19)14-10)12-2-15(7)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m1/s1 _Chem_comp.Paramagnetic no _Chem_comp.Aromatic yes _Chem_comp.Formula 'C10 H13 N5 O5' _Chem_comp.Formula_weight 283.2407200000 _Chem_comp.Formula_mono_iso_wt_nat 283.091668554 _Chem_comp.Formula_mono_iso_wt_13C 293.125216932 _Chem_comp.Formula_mono_iso_wt_15N 288.07684302 _Chem_comp.Formula_mono_iso_wt_13C_15N 298.1103913978 _Chem_comp.Image_file_name bmse001018.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse001018.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 'Guanine, 9-beta-D-ribofuranosyl-' synonym bmse001018 1 'beta-D-Ribofuranoside, guanine-9' synonym bmse001018 1 'Vernine (VAN)' synonym bmse001018 1 GUANOSINE synonym bmse001018 1 Guo synonym bmse001018 1 Guanozin synonym bmse001018 1 Vernine synonym bmse001018 1 'Inosine, 2-amino- (VAN)' synonym bmse001018 1 '6H-Purin-6-one, 2-amino-1,9-dihydro-9-beta-D-ribofuranosyl-' synonym bmse001018 1 'Guanine riboside' synonym bmse001018 1 GUANINE-9:BETA-D-RIBOFURANOSIDE synonym bmse001018 1 'Guanine, 9-beta-D-ribofuranosyl- (VAN)' synonym bmse001018 1 2(3H)-Imino-9-beta-D-ribofuranosyl-9H-purin-6(1H)-one synonym bmse001018 1 GR synonym bmse001018 1 'Ribofuranoside, guanine-9, beta-D-' synonym bmse001018 1 'Inosine, 2-amino-' synonym bmse001018 1 2-Amino-1,9-dihydro-9-beta-D-ribofuranosyl-6H-purin-6-one synonym bmse001018 1 Guanosine synonym bmse001018 1 9-beta-D-Ribofuranosylguanine synonym bmse001018 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/C10H13N5O5/c11-10-13-7-4(8(19)14-10)12-2-15(7)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m1/s1 ; INCHI na na bmse001018 1 InChI=1S/C10H13N5O5/c11-10-13-7-4(8(19)14-10)12-2-15(7)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m1/s1 INCHI ALATIS 3.003 bmse001018 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 2-amino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one IUPAC bmse001018 1 2-amino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-methylol-tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_TRADITIONAL bmse001018 1 2-amino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_CAS bmse001018 1 2-amino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_OPENEYE bmse001018 1 2-amino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one IUPAC_SYSTEMATIC bmse001018 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID isomeric C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)NC(=NC2=O)N bmse001018 1 canonical C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N bmse001018 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 O20 O 7.3435 0.6702 1 bmse001018 1 O18 O 4.8055 1.1746 2 bmse001018 1 O17 O 6.0873 2.9324 3 bmse001018 1 O16 O 9.0681 1.8482 4 bmse001018 1 O19 O 4.2690 -3.3924 5 bmse001018 1 N15 N 6.0812 -0.5877 6 bmse001018 1 N13 N 4.2690 -0.3925 7 bmse001018 1 N12 N 6.0812 -2.1972 8 bmse001018 1 N14 N 3.4030 -1.8924 9 bmse001018 1 N11 N 2.5369 -0.3925 10 bmse001018 1 C9 C 6.3919 0.3628 11 bmse001018 1 C6 C 5.8055 1.1728 12 bmse001018 1 C5 C 6.3947 1.9808 13 bmse001018 1 C3 C 7.3452 1.6702 14 bmse001018 1 C1 C 8.1552 2.2566 15 bmse001018 1 C7 C 5.1350 -0.8925 16 bmse001018 1 C2 C 6.6648 -1.3924 17 bmse001018 1 C4 C 5.1350 -1.8924 18 bmse001018 1 C8 C 4.2690 -2.3925 19 bmse001018 1 C10 C 3.4030 -0.8925 20 bmse001018 1 H27 H 5.7794 0.2669 21 bmse001018 1 H26 H 5.5250 1.7257 22 bmse001018 1 H25 H 5.7825 2.0789 23 bmse001018 1 H24 H 7.8972 1.3877 24 bmse001018 1 H21 H 8.5028 2.7700 25 bmse001018 1 H22 H 7.7100 2.6880 26 bmse001018 1 H33 H 4.4964 1.7120 27 bmse001018 1 H23 H 7.2848 -1.3924 28 bmse001018 1 H32 H 6.5030 3.3924 29 bmse001018 1 H30 H 4.2690 0.2275 30 bmse001018 1 H31 H 9.5703 2.2118 31 bmse001018 1 H28 H 2.0000 -0.7025 32 bmse001018 1 H29 H 2.5369 0.2275 33 bmse001018 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID O20 O1 BMRB bmse001018 1 O18 O2 BMRB bmse001018 1 O17 O3 BMRB bmse001018 1 O16 O4 BMRB bmse001018 1 O19 O5 BMRB bmse001018 1 N15 N6 BMRB bmse001018 1 N13 N7 BMRB bmse001018 1 N12 N8 BMRB bmse001018 1 N14 N9 BMRB bmse001018 1 N11 N10 BMRB bmse001018 1 C9 C11 BMRB bmse001018 1 C6 C12 BMRB bmse001018 1 C5 C13 BMRB bmse001018 1 C3 C14 BMRB bmse001018 1 C1 C15 BMRB bmse001018 1 C7 C16 BMRB bmse001018 1 C2 C17 BMRB bmse001018 1 C4 C18 BMRB bmse001018 1 C8 C19 BMRB bmse001018 1 C10 C20 BMRB bmse001018 1 H27 H21 BMRB bmse001018 1 H26 H22 BMRB bmse001018 1 H25 H23 BMRB bmse001018 1 H24 H24 BMRB bmse001018 1 H21 H25 BMRB bmse001018 1 H22 H26 BMRB bmse001018 1 H33 H27 BMRB bmse001018 1 H23 H28 BMRB bmse001018 1 H32 H29 BMRB bmse001018 1 H30 H30 BMRB bmse001018 1 H31 H31 BMRB bmse001018 1 H28 H32 BMRB bmse001018 1 H29 H33 BMRB bmse001018 1 O20 O20 ALATIS bmse001018 1 O18 O18 ALATIS bmse001018 1 O17 O17 ALATIS bmse001018 1 O16 O16 ALATIS bmse001018 1 O19 O19 ALATIS bmse001018 1 N15 N15 ALATIS bmse001018 1 N13 N13 ALATIS bmse001018 1 N12 N12 ALATIS bmse001018 1 N14 N14 ALATIS bmse001018 1 N11 N11 ALATIS bmse001018 1 C9 C9 ALATIS bmse001018 1 C6 C6 ALATIS bmse001018 1 C5 C5 ALATIS bmse001018 1 C3 C3 ALATIS bmse001018 1 C1 C1 ALATIS bmse001018 1 C7 C7 ALATIS bmse001018 1 C2 C2 ALATIS bmse001018 1 C4 C4 ALATIS bmse001018 1 C8 C8 ALATIS bmse001018 1 C10 C10 ALATIS bmse001018 1 H27 H27 ALATIS bmse001018 1 H26 H26 ALATIS bmse001018 1 H25 H25 ALATIS bmse001018 1 H24 H24 ALATIS bmse001018 1 H21 H21 ALATIS bmse001018 1 H22 H22 ALATIS bmse001018 1 H33 H33 ALATIS bmse001018 1 H23 H23 ALATIS bmse001018 1 H32 H32 ALATIS bmse001018 1 H30 H30 ALATIS bmse001018 1 H31 H31 ALATIS bmse001018 1 H28 H28 ALATIS bmse001018 1 H29 H29 ALATIS bmse001018 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 SING O20 C9 bmse001018 1 2 covalent SING O20 C3 bmse001018 1 3 covalent SING C6 O18 bmse001018 1 4 covalent SING O18 H33 bmse001018 1 5 covalent SING C5 O17 bmse001018 1 6 covalent SING O17 H32 bmse001018 1 7 covalent SING O16 C1 bmse001018 1 8 covalent SING O16 H31 bmse001018 1 9 covalent DOUB O19 C8 bmse001018 1 10 covalent SING C9 N15 bmse001018 1 11 covalent SING N15 C7 bmse001018 1 12 covalent SING N15 C2 bmse001018 1 13 covalent SING N13 C7 bmse001018 1 14 covalent SING N13 C10 bmse001018 1 15 covalent SING N13 H30 bmse001018 1 16 covalent DOUB N12 C2 bmse001018 1 17 covalent SING N12 C4 bmse001018 1 18 covalent SING N14 C8 bmse001018 1 19 covalent DOUB N14 C10 bmse001018 1 20 covalent SING N11 C10 bmse001018 1 21 covalent SING N11 H28 bmse001018 1 22 covalent SING N11 H29 bmse001018 1 23 covalent SING C9 C6 bmse001018 1 24 covalent SING C9 H27 bmse001018 1 25 covalent SING C6 C5 bmse001018 1 26 covalent SING C6 H26 bmse001018 1 27 covalent SING C5 C3 bmse001018 1 28 covalent SING C5 H25 bmse001018 1 29 covalent SING C3 C1 bmse001018 1 30 covalent SING C3 H24 bmse001018 1 31 covalent SING C1 H21 bmse001018 1 32 covalent SING C1 H22 bmse001018 1 33 covalent DOUB C7 C4 bmse001018 1 34 covalent SING C2 H23 bmse001018 1 35 covalent SING C4 C8 bmse001018 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 160963337 sid Guanosine 'matching entry' bmse001018 1 no PubChem 85164932 sid Guanosine 'matching entry' bmse001018 1 no PubChem 151492 sid Guanosine 'matching entry' bmse001018 1 no PubChem 6802 cid Guanosine 'matching entry' bmse001018 1 no PubChem 3677 sid Guanosine 'matching entry' bmse001018 1 no KEGG C00387 'compound ID' Guanosine 'matching entry' bmse001018 1 no 'CAS Registry' 118-00-3 'registry number' Guanosine 'matching entry' bmse001018 1 no 'CAS Registry' 484-80-0 'registry number' Guanosine 'matching entry' bmse001018 1 no 'CAS Registry' 85-30-3 'registry number' Guanosine 'matching entry' bmse001018 1 no CHEBI 16750 ? Guanosine 'matching entry' bmse001018 1 no NSC 19994 ? Guanosine 'matching entry' bmse001018 1 no EINECS 204-227-8 ? Guanosine 'matching entry' bmse001018 1 no PDB GMP 'Chemical Component' Guanosine 'matching entry' bmse001018 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 bmse001018 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse001018 _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 Guanosine 'natural abundance' 1 $guanosine Solute 20 mM sigma/aldrich Guanosine bmse001018 1 2 D2O ? ? ? Solvent 100 % ? ? bmse001018 1 3 'sodium phosphate' ? ? ? Buffer 200 mM ? ? bmse001018 1 4 'sodium azide' ? ? ? Cytocide 500 uM ? ? bmse001018 1 5 DSS ? ? ? Reference 0.1 % ? ? bmse001018 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 bmse001018 _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 11.36 pH bmse001018 1 temperature 298 K bmse001018 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse001018 _Software.ID 1 _Software.Name TopSpin _Software.Version 2.1 loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'Bruker Biospin' bmse001018 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Collection bmse001018 1 Processing bmse001018 1 'Data analysis' bmse001018 1 'Peak picking' bmse001018 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 bmse001018 _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 bmse001018 _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 bmse001018 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 bmse001018 _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 bmse001018 1 2 '2D [1H,13C]-HSQC' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse001018 1 3 '1D 1H, NOESY' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse001018 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' bmse001018 1 1 00.png image/png nmr/set01/spectra/1H_1H_JRES 'Spectral image' bmse001018 1 1 01.png image/png nmr/set01/spectra/1H_1H_JRES 'Spectral image' bmse001018 1 2 1H_13C_HSQC text/directory nmr/set01/ 'NMR experiment directory' bmse001018 1 2 00.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse001018 1 2 01.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse001018 1 3 1H_NOESY text/directory nmr/set01/ 'NMR experiment directory' bmse001018 1 3 00.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse001018 1 3 01.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse001018 1 3 02.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse001018 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 bmse001018 _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 bmse001018 1 C 13 DSS 'methyl carbons' ppm 0.00 internal direct 1.000000000 bmse001018 1 stop_ save_