data_bmse000646 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse000646 _Entry.Title indole_3_pyruvic_acid _Entry.Version_type update _Entry.Submission_date 2009-10-23 _Entry.Accession_date 2009-10-23 _Entry.Last_release_date 2012-10-17 _Entry.Original_release_date 2009-10-23 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.7 _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.DOI 10.13018/BMSE000646 _Entry.BMRB_internal_directory_name indole_3_pyruvic_acid loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.Middle_initials _Entry_author.Entry_ID 1 Francisca Jofre ? bmse000646 2 Mark Anderson E. bmse000646 3 John Markley L. bmse000646 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 metabolomics 'Madison Metabolomics Consortium' MMC bmse000646 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 bmse000646 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '13C chemical shifts' 11 bmse000646 '1H chemical shifts' 7 bmse000646 stop_ loop_ _Release.Release_number _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 2009-10-23 2009-10-23 original BMRB 'Original spectra from MMC' bmse000646 2 2009-11-30 2009-10-23 update Author 'Assignments, 13C transition lists, 1H transition lists by Francisca Jofre' bmse000646 3 2010-01-15 2009-10-23 update Author 'updated peak lists with new referencing' bmse000646 4 2010-11-12 2009-10-23 update BMRB 'Reset sweep widths to those found in parameter files' bmse000646 5 2010-11-12 2009-10-23 update BMRB 'Updated chem comp Paramagnetic and Aromatic' bmse000646 6 2010-11-30 2009-10-23 update BMRB 'Added 1 PDB ID to Chem_comp_db_link' bmse000646 7 2011-01-31 2009-10-23 update BMRB 'Reset Formula_mono_iso_wt_nat, Formula_mono_iso_wt_13C' bmse000646 8 2011-03-04 2009-10-23 update BMRB 'Fixed peak list ID issue' bmse000646 9 2011-04-04 2009-10-23 update BMRB 'Added Provenance tag to chem_comp' bmse000646 10 2011-04-11 2009-10-23 update BMRB 'Moved Dept 135 phase val info from _Peak_general_char to _Peak_char' bmse000646 11 2011-09-09 2009-10-23 update BMRB 'Brought up to date with latest Dictionary' bmse000646 12 2011-12-14 2009-10-23 update BMRB 'Set Assembly.Name to match Chem_comp.name' bmse000646 13 2011-12-16 2009-10-23 update BMRB 'Standardized solvent' bmse000646 14 2012-09-13 2009-10-23 update BMRB 'Added PubChem SID 111677785 to database loop' bmse000646 15 2012-10-17 2009-10-23 update BMRB 'Set all _Chem_comp_SMILES Types to lower case' bmse000646 16 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse000646 17 2017-12-19 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse000646 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse000646 _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. bmse000646 1 2 T. Barrett T. ? bmse000646 1 3 D. Benson D. A. bmse000646 1 4 S. Bryant S. H. bmse000646 1 5 K. Canese K. ? bmse000646 1 6 V. Chetvenin V. ? bmse000646 1 7 D. Church D. M. bmse000646 1 8 M. DiCuccio M. ? bmse000646 1 9 R. Edgar R. ? bmse000646 1 10 S. Federhen S. ? bmse000646 1 11 L. Geer L. Y. bmse000646 1 12 W. Helmberg W. ? bmse000646 1 13 Y. Kapustin Y. ? bmse000646 1 14 D. Kenton D. L. bmse000646 1 15 O. Khovayko O. ? bmse000646 1 16 D. Lipman D. J. bmse000646 1 17 T. Madden T. L. bmse000646 1 18 D. Maglott D. R. bmse000646 1 19 J. Ostell J. ? bmse000646 1 20 K. Pruitt K. D. bmse000646 1 21 G. Schuler G. D. bmse000646 1 22 L. Schriml L. M. bmse000646 1 23 E. Sequeira E. ? bmse000646 1 24 S. Sherry S. T. bmse000646 1 25 K. Sirotkin K. ? bmse000646 1 26 A. Souvorov A. ? bmse000646 1 27 G. Starchenko G. ? bmse000646 1 28 T. Suzek T. O. bmse000646 1 29 R. Tatusov R. ? bmse000646 1 30 T. Tatusova T. A. bmse000646 1 31 L. Bagner L. ? bmse000646 1 32 E. Yaschenko E. ? bmse000646 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse000646 _Assembly.ID 1 _Assembly.Name 'indole-3-pyruvic acid' _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 'indole-3-pyruvic acid' 1 $indole-3-pyruvic-acid yes native no no bmse000646 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_indole-3-pyruvic-acid _Entity.Sf_category entity _Entity.Sf_framecode indole-3-pyruvic-acid _Entity.Entry_ID bmse000646 _Entity.ID 1 _Entity.Name 'indole-3-pyruvic acid' _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 bmse000646 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 bmse000646 _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 $indole-3-pyruvic-acid n/a 'multiple natural sources' yes 'not applicable' n/a n/a n/a n/a n/a bmse000646 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 bmse000646 _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 $indole-3-pyruvic-acid 'chemical synthesis' bmse000646 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 bmse000646 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name 'indole-3-pyruvic acid' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code bmse000646 _Chem_comp.InChI_code InChI=1S/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15) _Chem_comp.Paramagnetic no _Chem_comp.Aromatic yes _Chem_comp.Formula 'C11 H9 N O3' _Chem_comp.Formula_weight 203.19406 _Chem_comp.Formula_mono_iso_wt_nat 203.0582431604 _Chem_comp.Formula_mono_iso_wt_13C 214.0951463762 _Chem_comp.Formula_mono_iso_wt_15N 204.0552780536 _Chem_comp.Formula_mono_iso_wt_13C_15N 215.0921812694 _Chem_comp.Image_file_name bmse000646.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse000646.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 (Indol-3-yl)pyruvate synonym bmse000646 1 Indole-3-pyruvate synonym bmse000646 1 '3-(1H-indol-3-yl)-2-oxopropanoic acid' synonym bmse000646 1 '3-Indolepyruvic acid' synonym bmse000646 1 'indole-3-pyruvic acid' synonym bmse000646 1 Indolepyruvate synonym bmse000646 1 '(indol-3-yl)pyruvic acid' synonym bmse000646 1 '3-Indolylpyruvic acid' synonym bmse000646 1 3-(Indol-3-yl)pyruvate synonym bmse000646 1 3IO synonym bmse000646 1 'Indolepyruvic acid' synonym bmse000646 1 '3-(3-Indolyl)-2-oxopropanoic acid' synonym bmse000646 1 'Indole-3-pyruvic acid' synonym bmse000646 1 '3-(indol-3-yl)pyruvic acid' synonym bmse000646 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/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15) ; INCHI na na bmse000646 1 InChI=1S/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15) INCHI ALATIS 3.003 bmse000646 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 '3-(1H-indol-3-yl)-2-oxopropanoic acid' PUBCHEM_IUPAC_NAME bmse000646 1 '3-(1H-indol-3-yl)-2-keto-propionic acid' PUBCHEM_IUPAC_TRADITIONAL_NAME bmse000646 1 '3-(1H-indol-3-yl)-2-oxo-propanoic acid' PUBCHEM_IUPAC_OPENEYE_NAME bmse000646 1 '3-(1H-indol-3-yl)-2-oxopropanoic acid' PUBCHEM_IUPAC_CAS_NAME bmse000646 1 '3-(1H-indol-3-yl)-2-oxo-propanoic acid' PUBCHEM_IUPAC_SYSTEMATIC_NAME bmse000646 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID canonical C1=CC=C2C(=C1)C(=CN2)CC(=O)C(=O)O bmse000646 1 isomeric C1=CC=C2C(=C1)C(=CN2)CC(=O)C(=O)O bmse000646 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 O13 O 6.6353 0.0604 1 bmse000646 1 O14 O 7.2566 1.9615 2 bmse000646 1 O15 O 5.6103 2.4996 3 bmse000646 1 N12 N 4.6783 -1.9615 4 bmse000646 1 C7 C 4.6783 -0.3520 5 bmse000646 1 C8 C 3.7321 -0.6567 6 bmse000646 1 C9 C 3.7321 -1.6567 7 bmse000646 1 C5 C 4.9889 0.5985 8 bmse000646 1 C6 C 5.2619 -1.1567 9 bmse000646 1 C3 C 2.8660 -0.1567 10 bmse000646 1 C4 C 2.8660 -2.1567 11 bmse000646 1 C1 C 2.0000 -0.6567 12 bmse000646 1 C2 C 2.0000 -1.6567 13 bmse000646 1 C10 C 5.9674 0.8047 14 bmse000646 1 C11 C 6.2781 1.7553 15 bmse000646 1 H20 H 4.9684 1.2182 16 bmse000646 1 H21 H 4.3751 0.6859 17 bmse000646 1 H22 H 5.8819 -1.1567 18 bmse000646 1 H23 H 4.8709 -2.5508 19 bmse000646 1 H18 H 2.8660 0.4633 20 bmse000646 1 H19 H 2.8660 -2.7767 21 bmse000646 1 H16 H 1.4631 -0.3467 22 bmse000646 1 H17 H 1.4631 -1.9667 23 bmse000646 1 H24 H 7.4492 2.5508 24 bmse000646 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID O13 O1 BMRB bmse000646 1 O14 O2 BMRB bmse000646 1 O15 O3 BMRB bmse000646 1 N12 N4 BMRB bmse000646 1 C7 C5 BMRB bmse000646 1 C8 C6 BMRB bmse000646 1 C9 C7 BMRB bmse000646 1 C5 C8 BMRB bmse000646 1 C6 C9 BMRB bmse000646 1 C3 C10 BMRB bmse000646 1 C4 C11 BMRB bmse000646 1 C1 C12 BMRB bmse000646 1 C2 C13 BMRB bmse000646 1 C10 C14 BMRB bmse000646 1 C11 C15 BMRB bmse000646 1 H20 H16 BMRB bmse000646 1 H21 H17 BMRB bmse000646 1 H22 H18 BMRB bmse000646 1 H23 H19 BMRB bmse000646 1 H18 H20 BMRB bmse000646 1 H19 H21 BMRB bmse000646 1 H16 H22 BMRB bmse000646 1 H17 H23 BMRB bmse000646 1 H24 H24 BMRB bmse000646 1 O13 O13 ALATIS bmse000646 1 O14 O14 ALATIS bmse000646 1 O15 O15 ALATIS bmse000646 1 N12 N12 ALATIS bmse000646 1 C7 C7 ALATIS bmse000646 1 C8 C8 ALATIS bmse000646 1 C9 C9 ALATIS bmse000646 1 C5 C5 ALATIS bmse000646 1 C6 C6 ALATIS bmse000646 1 C3 C3 ALATIS bmse000646 1 C4 C4 ALATIS bmse000646 1 C1 C1 ALATIS bmse000646 1 C2 C2 ALATIS bmse000646 1 C10 C10 ALATIS bmse000646 1 C11 C11 ALATIS bmse000646 1 H20 H20 ALATIS bmse000646 1 H21 H21 ALATIS bmse000646 1 H22 H22 ALATIS bmse000646 1 H23 H23 ALATIS bmse000646 1 H18 H18 ALATIS bmse000646 1 H19 H19 ALATIS bmse000646 1 H16 H16 ALATIS bmse000646 1 H17 H17 ALATIS bmse000646 1 H24 H24 ALATIS bmse000646 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 O13 C10 bmse000646 1 2 covalent SING O14 C11 bmse000646 1 3 covalent SING O14 H24 bmse000646 1 4 covalent DOUB O15 C11 bmse000646 1 5 covalent SING N12 C9 bmse000646 1 6 covalent SING N12 C6 bmse000646 1 7 covalent SING N12 H23 bmse000646 1 8 covalent SING C7 C8 bmse000646 1 9 covalent SING C7 C5 bmse000646 1 10 covalent DOUB C7 C6 bmse000646 1 11 covalent SING C8 C9 bmse000646 1 12 covalent DOUB C8 C3 bmse000646 1 13 covalent DOUB C9 C4 bmse000646 1 14 covalent SING C5 C10 bmse000646 1 15 covalent SING C5 H20 bmse000646 1 16 covalent SING C5 H21 bmse000646 1 17 covalent SING C6 H22 bmse000646 1 18 covalent SING C3 C1 bmse000646 1 19 covalent SING C3 H18 bmse000646 1 20 covalent SING C4 C2 bmse000646 1 21 covalent SING C4 H19 bmse000646 1 22 covalent DOUB C1 C2 bmse000646 1 23 covalent SING C1 H16 bmse000646 1 24 covalent SING C2 H17 bmse000646 1 25 covalent SING C10 C11 bmse000646 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 111677785 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 803 cid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 24896073 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 3625 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 8145408 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 10404787 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PubChem 11109879 sid 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no 'CAS Registry' 35656-49-6 'registry number' 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no Sigma-Aldrich I5567_ALDRICH ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no ChEBI CHEBI:29750 ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no MMDB 38473.5 ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no KEGG C00331 'compound ID' 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no NIST 238832541 ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 yes MMCD cq_00243 ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 yes MDL MFCD00005640 ? 'indole-3-pyruvic acid' 'matching entry' bmse000646 1 no PDB 3IO 'Chemical Component' 'indole-3-pyruvic acid' 'matching entry' bmse000646 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 bmse000646 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse000646 _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.Vendor_product_code _Sample_component.Entry_ID _Sample_component.Sample_ID 1 'indole-3-pyruvic acid' 'natural abundance' 1 $indole-3-pyruvic-acid Solute Saturated 1 Sigma 'indole-3-pyruvic acid' n/a bmse000646 1 2 methanol '100% deuterated' 1 ? Solvent 100 % ? ? ? bmse000646 1 3 TMS ? 1 ? Reference 10 mM ? ? ? bmse000646 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 bmse000646 _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 n/a pH bmse000646 1 temperature 298 K bmse000646 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse000646 _Software.ID 1 _Software.Name NMRPipe loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'F Delaglio, S Grzesiek, GW Vuister, G Zhu, J Pfeifer and A Bax' bmse000646 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Processing bmse000646 1 stop_ save_ save_software_2 _Software.Sf_category software _Software.Sf_framecode software_2 _Software.Entry_ID bmse000646 _Software.ID 2 _Software.Name XWIN-NMR _Software.Version 3.5 loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'Bruker Biospin' bmse000646 2 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Collection bmse000646 2 Processing bmse000646 2 'Data analysis' bmse000646 2 'Peak picking' bmse000646 2 stop_ save_ save_software_3 _Software.Sf_category software _Software.Sf_framecode software_3 _Software.Entry_ID bmse000646 _Software.ID 3 _Software.Name NMRDraw _Software.Version 2.3 loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'F Delaglio, S Grzesiek, GW Vuister, G Zhu, J Pfeifer and A Bax' bmse000646 3 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'Data analysis' bmse000646 3 'Peak picking' bmse000646 3 stop_ save_ save_software_4 _Software.Sf_category software _Software.Sf_framecode software_4 _Software.Entry_ID bmse000646 _Software.ID 4 _Software.Name NUTS _Software.Version '1D Version - 20060331' loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'Acorn NMR Inc.' bmse000646 4 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'Data analysis' bmse000646 4 'Peak picking' bmse000646 4 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_Bruker_DMX_400 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode Bruker_DMX_400 _NMR_spectrometer.Entry_ID bmse000646 _NMR_spectrometer.ID 1 _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model DMX _NMR_spectrometer.Field_strength 400 save_ ############################# # NMR applied experiments # ############################# save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse000646 _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 '1D 1H' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 2 '2D [1H,1H]-TOCSY' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 3 '1D 13C' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 4 '1D DEPT90' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 5 '1D DEPT135' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 6 '2D [1H,13C]-HSQC' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 7 '2D [1H,13C]-HMBC' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 1 8 '2D [1H,1H]-COSY' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_DMX_400 bmse000646 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 text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 1 1H.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 2 HH_TOCSY text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 2 HH_TOCSY.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 3 13C text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 3 13C.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 4 DEPT_90 text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 4 DEPT_90.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 5 DEPT_135 text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 5 DEPT_135.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 6 1H_13C_HSQC text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 6 1H_13C_HSQC.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 7 1H_13C_HMBC text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 7 1H_13C_HMBC.png image/png nmr/set01/spectra 'Spectral image' bmse000646 1 8 HH_COSY text/directory nmr/set01/ 'NMR experiment directory' bmse000646 1 8 HH_COSY.png image/png nmr/set01/spectra 'Spectral image' bmse000646 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 bmse000646 _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 TMS 'methyl protons' ppm 0.00 internal direct 1.000000000 bmse000646 1 C 13 TMS 'methyl protons' ppm 0.00 ? indirect 1.000000000 bmse000646 1 stop_ save_ ################################### # Assigned chemical shift lists # ################################### ################################################################### # Chemical Shift Ambiguity Index Value Definitions # # # # The values other than 1 are used for those atoms with different # # chemical shifts that cannot be assigned to stereospecific atoms # # or to specific residues or chains. # # # # Index Value Definition # # # # 1 Unique (including isolated methyl protons, # # geminal atoms, and geminal methyl # # groups with identical chemical shifts) # # (e.g. ILE HD11, HD12, HD13 protons) # # 2 Ambiguity of geminal atoms or geminal methyl # # proton groups (e.g. ASP HB2 and HB3 # # protons, LEU CD1 and CD2 carbons, or # # LEU HD11, HD12, HD13 and HD21, HD22, # # HD23 methyl protons) # # 3 Aromatic atoms on opposite sides of # # symmetrical rings (e.g. TYR HE1 and HE2 # # protons) # # 4 Intraresidue ambiguities (e.g. LYS HG and # # HD protons or TRP HZ2 and HZ3 protons) # # 5 Interresidue ambiguities (LYS 12 vs. LYS 27) # # 6 Intermolecular ambiguities (e.g. ASP 31 CA # # in monomer 1 and ASP 31 CA in monomer 2 # # of an asymmetrical homodimer, duplex # # DNA assignments, or other assignments # # that may apply to atoms in one or more # # molecule in the molecular assembly) # # 9 Ambiguous, specific ambiguity not defined # # # ################################################################### save_assigned_chemical_shifts _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chemical_shifts _Assigned_chem_shift_list.Entry_ID bmse000646 _Assigned_chem_shift_list.ID 1 _Assigned_chem_shift_list.Sample_condition_list_ID 1 _Assigned_chem_shift_list.Sample_condition_list_label $sample_conditions_1 _Assigned_chem_shift_list.Chem_shift_reference_ID 1 _Assigned_chem_shift_list.Chem_shift_reference_label $chem_shift_reference loop_ _Chem_shift_experiment.Experiment_ID _Chem_shift_experiment.Experiment_name _Chem_shift_experiment.Sample_ID _Chem_shift_experiment.Sample_label _Chem_shift_experiment.Entry_ID _Chem_shift_experiment.Assigned_chem_shift_list_ID 1 '1D 1H' 1 $sample_1 bmse000646 1 2 '2D [1H,1H]-TOCSY' 1 $sample_1 bmse000646 1 3 '1D 13C' 1 $sample_1 bmse000646 1 4 '1D DEPT90' 1 $sample_1 bmse000646 1 5 '1D DEPT135' 1 $sample_1 bmse000646 1 6 '2D [1H,13C]-HSQC' 1 $sample_1 bmse000646 1 7 '2D [1H,13C]-HMBC' 1 $sample_1 bmse000646 1 8 '2D [1H,1H]-COSY' 1 $sample_1 bmse000646 1 stop_ loop_ _Chem_shift_software.Software_ID _Chem_shift_software.Software_label _Chem_shift_software.Entry_ID _Chem_shift_software.Assigned_chem_shift_list_ID 1 $software_2 bmse000646 1 stop_ loop_ _Atom_chem_shift.ID _Atom_chem_shift.Entity_ID _Atom_chem_shift.Comp_index_ID _Atom_chem_shift.Comp_ID _Atom_chem_shift.Atom_ID _Atom_chem_shift.Atom_type _Atom_chem_shift.Atom_isotope_number _Atom_chem_shift.Val _Atom_chem_shift.Ambiguity_code _Atom_chem_shift.Auth_atom_ID _Atom_chem_shift.Entry_ID _Atom_chem_shift.Assigned_chem_shift_list_ID 1 1 1 1 C7 C 13 111.694 1 C5 bmse000646 1 2 1 1 1 C8 C 13 128.570 1 C6 bmse000646 1 3 1 1 1 C9 C 13 137.687 1 C7 bmse000646 1 4 1 1 1 C5 C 13 106.010 1 C8 bmse000646 1 5 1 1 1 C6 C 13 128.959 1 C9 bmse000646 1 6 1 1 1 C3 C 13 119.306 1 C10 bmse000646 1 7 1 1 1 C4 C 13 112.660 1 C11 bmse000646 1 8 1 1 1 C1 C 13 120.974 1 C12 bmse000646 1 9 1 1 1 C2 C 13 123.229 1 C13 bmse000646 1 10 1 1 1 C10 C 13 168.878 1 C14 bmse000646 1 11 1 1 1 C11 C 13 138.932 1 C15 bmse000646 1 12 1 1 1 H20 H 1 6.947 1 H16 bmse000646 1 13 1 1 1 H21 H 1 6.947 1 H17 bmse000646 1 14 1 1 1 H22 H 1 7.944 1 H18 bmse000646 1 15 1 1 1 H18 H 1 7.695 1 H20 bmse000646 1 16 1 1 1 H19 H 1 7.382 1 H21 bmse000646 1 17 1 1 1 H16 H 1 7.123 4 H22 bmse000646 1 18 1 1 1 H17 H 1 7.123 4 H23 bmse000646 1 stop_ save_ ######################### # Spectral peak lists # ######################### save_spectral_peak_1H _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peak_1H _Spectral_peak_list.Entry_ID bmse000646 _Spectral_peak_list.ID 1 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 1 _Spectral_peak_list.Experiment_name '1D 1H' _Spectral_peak_list.Number_of_spectral_dimensions 1 loop_ _Spectral_dim.ID _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 H 1 'Full H' 4807.69230769231 bmse000646 1 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 2 $software_2 bmse000646 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse000646 1 2 bmse000646 1 3 bmse000646 1 4 bmse000646 1 5 bmse000646 1 stop_ loop_ _Peak_general_char.Peak_ID _Peak_general_char.Intensity_val _Peak_general_char.Measurement_method _Peak_general_char.Entry_ID _Peak_general_char.Spectral_peak_list_ID 1 1 integration bmse000646 1 2 1 integration bmse000646 1 3 1 integration bmse000646 1 4 2 integration bmse000646 1 5 1 integration bmse000646 1 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Coupling_pattern _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 7.937 s bmse000646 1 2 1 7.688 d bmse000646 1 3 1 7.375 d bmse000646 1 4 1 7.116 m bmse000646 1 5 1 6.940 s bmse000646 1 stop_ loop_ _Assigned_peak_chem_shift.Peak_ID _Assigned_peak_chem_shift.Spectral_dim_ID _Assigned_peak_chem_shift.Val _Assigned_peak_chem_shift.Entity_ID _Assigned_peak_chem_shift.Comp_index_ID _Assigned_peak_chem_shift.Comp_ID _Assigned_peak_chem_shift.Atom_ID _Assigned_peak_chem_shift.Entry_ID _Assigned_peak_chem_shift.Spectral_peak_list_ID 1 1 7.937 1 1 1 H22 bmse000646 1 2 1 7.688 1 1 1 H18 bmse000646 1 3 1 7.375 1 1 1 H19 bmse000646 1 4 1 7.116 1 1 1 H16 bmse000646 1 4 1 7.116 1 1 1 H17 bmse000646 1 5 1 6.940 1 1 1 H20 bmse000646 1 5 1 6.940 1 1 1 H21 bmse000646 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse000646 1 2 bmse000646 1 3 bmse000646 1 4 bmse000646 1 5 bmse000646 1 6 bmse000646 1 7 bmse000646 1 8 bmse000646 1 9 bmse000646 1 10 bmse000646 1 11 bmse000646 1 12 bmse000646 1 stop_ loop_ _Spectral_transition_general_char.Spectral_transition_ID _Spectral_transition_general_char.Intensity_val _Spectral_transition_general_char.Measurement_method _Spectral_transition_general_char.Entry_ID _Spectral_transition_general_char.Spectral_peak_list_ID 1 76.168 Height bmse000646 1 2 43.008 Height bmse000646 1 3 47.059 Height bmse000646 1 4 36.087 Height bmse000646 1 5 44.448 Height bmse000646 1 6 19.221 Height bmse000646 1 7 42.492 Height bmse000646 1 8 31.079 Height bmse000646 1 9 36.589 Height bmse000646 1 10 45.723 Height bmse000646 1 11 19.945 Height bmse000646 1 12 101.220 Height bmse000646 1 stop_ loop_ _Spectral_transition_char.Spectral_transition_ID _Spectral_transition_char.Spectral_dim_ID _Spectral_transition_char.Chem_shift_val _Spectral_transition_char.Entry_ID _Spectral_transition_char.Spectral_peak_list_ID 1 1 7.937 bmse000646 1 2 1 7.699 bmse000646 1 3 1 7.679 bmse000646 1 4 1 7.385 bmse000646 1 5 1 7.366 bmse000646 1 6 1 7.160 bmse000646 1 7 1 7.143 bmse000646 1 8 1 7.125 bmse000646 1 9 1 7.106 bmse000646 1 10 1 7.088 bmse000646 1 11 1 7.071 bmse000646 1 12 1 6.941 bmse000646 1 stop_ save_ save_spectral_peak_13C _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peak_13C _Spectral_peak_list.Entry_ID bmse000646 _Spectral_peak_list.ID 2 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 3 _Spectral_peak_list.Experiment_name '1D 13C' _Spectral_peak_list.Number_of_spectral_dimensions 1 loop_ _Spectral_dim.ID _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 C 13 'Full C' 24038.4615384615 bmse000646 2 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 2 $software_2 bmse000646 2 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse000646 2 2 bmse000646 2 3 bmse000646 2 4 bmse000646 2 5 bmse000646 2 6 bmse000646 2 7 bmse000646 2 8 bmse000646 2 9 bmse000646 2 10 bmse000646 2 11 bmse000646 2 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Coupling_pattern _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 168.728 s bmse000646 2 2 1 138.782 s bmse000646 2 3 1 137.537 s bmse000646 2 4 1 128.809 s bmse000646 2 5 1 128.420 s bmse000646 2 6 1 214.079 s bmse000646 2 7 1 120.824 s bmse000646 2 8 1 119.156 s bmse000646 2 9 1 112.510 s bmse000646 2 10 1 111.544 s bmse000646 2 11 1 105.860 s bmse000646 2 stop_ loop_ _Assigned_peak_chem_shift.Peak_ID _Assigned_peak_chem_shift.Spectral_dim_ID _Assigned_peak_chem_shift.Val _Assigned_peak_chem_shift.Entity_ID _Assigned_peak_chem_shift.Comp_index_ID _Assigned_peak_chem_shift.Comp_ID _Assigned_peak_chem_shift.Atom_ID _Assigned_peak_chem_shift.Entry_ID _Assigned_peak_chem_shift.Spectral_peak_list_ID 1 1 168.728 1 1 1 C10 bmse000646 2 2 1 138.782 1 1 1 C11 bmse000646 2 3 1 137.537 1 1 1 C9 bmse000646 2 4 1 128.809 1 1 1 C6 bmse000646 2 5 1 128.420 1 1 1 C8 bmse000646 2 6 1 214.079 1 1 1 C2 bmse000646 2 7 1 120.824 1 1 1 C1 bmse000646 2 8 1 119.156 1 1 1 C3 bmse000646 2 9 1 112.510 1 1 1 C4 bmse000646 2 10 1 111.544 1 1 1 C7 bmse000646 2 11 1 105.860 1 1 1 C5 bmse000646 2 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse000646 2 2 bmse000646 2 3 bmse000646 2 4 bmse000646 2 5 bmse000646 2 6 bmse000646 2 7 bmse000646 2 8 bmse000646 2 9 bmse000646 2 10 bmse000646 2 11 bmse000646 2 stop_ loop_ _Spectral_transition_general_char.Spectral_transition_ID _Spectral_transition_general_char.Intensity_val _Spectral_transition_general_char.Measurement_method _Spectral_transition_general_char.Entry_ID _Spectral_transition_general_char.Spectral_peak_list_ID 1 5.015 Height bmse000646 2 2 6.156 Height bmse000646 2 3 5.241 Height bmse000646 2 4 20.306 Height bmse000646 2 5 6.408 Height bmse000646 2 6 24.285 Height bmse000646 2 7 27.374 Height bmse000646 2 8 23.095 Height bmse000646 2 9 27.188 Height bmse000646 2 10 5.829 Height bmse000646 2 11 24.780 Height bmse000646 2 stop_ loop_ _Spectral_transition_char.Spectral_transition_ID _Spectral_transition_char.Spectral_dim_ID _Spectral_transition_char.Chem_shift_val _Spectral_transition_char.Entry_ID _Spectral_transition_char.Spectral_peak_list_ID 1 1 168.739 bmse000646 2 2 1 138.796 bmse000646 2 3 1 137.545 bmse000646 2 4 1 128.820 bmse000646 2 5 1 128.438 bmse000646 2 6 1 123.095 bmse000646 2 7 1 120.838 bmse000646 2 8 1 119.166 bmse000646 2 9 1 112.529 bmse000646 2 10 1 111.561 bmse000646 2 11 1 105.879 bmse000646 2 stop_ save_ save_spectral_peak_DEPT_90 _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peak_DEPT_90 _Spectral_peak_list.Entry_ID bmse000646 _Spectral_peak_list.ID 3 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 4 _Spectral_peak_list.Experiment_name '1D DEPT90' _Spectral_peak_list.Number_of_spectral_dimensions 1 loop_ _Spectral_dim.ID _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 C 13 'Full C' 24038.4615384615 bmse000646 3 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 2 $software_2 bmse000646 3 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse000646 3 2 bmse000646 3 3 bmse000646 3 4 bmse000646 3 5 bmse000646 3 6 bmse000646 3 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Coupling_pattern _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 128.808 s bmse000646 3 2 1 123.078 s bmse000646 3 3 1 120.838 s bmse000646 3 4 1 119.155 s bmse000646 3 5 1 112.509 s bmse000646 3 6 1 105.859 s bmse000646 3 stop_ loop_ _Assigned_peak_chem_shift.Peak_ID _Assigned_peak_chem_shift.Spectral_dim_ID _Assigned_peak_chem_shift.Val _Assigned_peak_chem_shift.Entity_ID _Assigned_peak_chem_shift.Comp_index_ID _Assigned_peak_chem_shift.Comp_ID _Assigned_peak_chem_shift.Atom_ID _Assigned_peak_chem_shift.Entry_ID _Assigned_peak_chem_shift.Spectral_peak_list_ID 1 1 128.808 1 1 1 C6 bmse000646 3 2 1 123.078 1 1 1 C2 bmse000646 3 3 1 120.838 1 1 1 C1 bmse000646 3 4 1 119.155 1 1 1 C3 bmse000646 3 5 1 112.509 1 1 1 C4 bmse000646 3 6 1 105.859 1 1 1 C5 bmse000646 3 stop_ save_ save_spectral_peak_DEPT_135 _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peak_DEPT_135 _Spectral_peak_list.Entry_ID bmse000646 _Spectral_peak_list.ID 4 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 5 _Spectral_peak_list.Experiment_name '1D DEPT135' _Spectral_peak_list.Number_of_spectral_dimensions 1 loop_ _Spectral_dim.ID _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 C 13 'Full C' 24038.4615384615 bmse000646 4 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 2 $software_2 bmse000646 4 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse000646 4 2 bmse000646 4 3 bmse000646 4 4 bmse000646 4 5 bmse000646 4 6 bmse000646 4 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Phase_val _Peak_char.Coupling_pattern _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 128.810 positive s bmse000646 4 2 1 123.080 positive s bmse000646 4 3 1 120.840 positive s bmse000646 4 4 1 119.157 positive s bmse000646 4 5 1 112.511 positive s bmse000646 4 6 1 105.861 positive s bmse000646 4 stop_ loop_ _Assigned_peak_chem_shift.Peak_ID _Assigned_peak_chem_shift.Spectral_dim_ID _Assigned_peak_chem_shift.Val _Assigned_peak_chem_shift.Entity_ID _Assigned_peak_chem_shift.Comp_index_ID _Assigned_peak_chem_shift.Comp_ID _Assigned_peak_chem_shift.Atom_ID _Assigned_peak_chem_shift.Entry_ID _Assigned_peak_chem_shift.Spectral_peak_list_ID 1 1 128.810 1 1 1 C6 bmse000646 4 2 1 123.080 1 1 1 C2 bmse000646 4 3 1 120.840 1 1 1 C1 bmse000646 4 4 1 119.157 1 1 1 C3 bmse000646 4 5 1 112.511 1 1 1 C4 bmse000646 4 6 1 105.861 1 1 1 C5 bmse000646 4 stop_ save_ save_spectral_peak_1H_13C_HSQC _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peak_1H_13C_HSQC _Spectral_peak_list.Entry_ID bmse000646 _Spectral_peak_list.ID 5 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 6 _Spectral_peak_list.Experiment_name '2D [1H,13C]-HSQC' _Spectral_peak_list.Number_of_spectral_dimensions 2 loop_ _Spectral_dim.ID _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 H 1 'Full H' 4807.69230769231 bmse000646 5 2 C 13 'Full C' 17961.383026493 bmse000646 5 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 1 $software_1 bmse000646 5 3 $software_3 bmse000646 5 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse000646 5 2 bmse000646 5 3 bmse000646 5 4 bmse000646 5 5 bmse000646 5 6 bmse000646 5 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 7.936 bmse000646 5 1 2 128.701 bmse000646 5 2 1 7.142 bmse000646 5 2 2 123.104 bmse000646 5 3 1 7.098 bmse000646 5 3 2 120.829 bmse000646 5 4 1 7.695 bmse000646 5 4 2 119.175 bmse000646 5 5 1 7.381 bmse000646 5 5 2 112.654 bmse000646 5 6 1 6.946 bmse000646 5 6 2 105.882 bmse000646 5 stop_ loop_ _Assigned_peak_chem_shift.Peak_ID _Assigned_peak_chem_shift.Spectral_dim_ID _Assigned_peak_chem_shift.Val _Assigned_peak_chem_shift.Entity_ID _Assigned_peak_chem_shift.Comp_index_ID _Assigned_peak_chem_shift.Comp_ID _Assigned_peak_chem_shift.Atom_ID _Assigned_peak_chem_shift.Details _Assigned_peak_chem_shift.Entry_ID _Assigned_peak_chem_shift.Spectral_peak_list_ID 1 1 7.936 1 1 1 H22 ? bmse000646 5 1 2 128.701 1 1 1 C6 ? bmse000646 5 2 1 7.142 1 1 1 H17 ? bmse000646 5 2 2 123.104 1 1 1 C2 'Long range coupling with peak(s) to c 11' bmse000646 5 3 1 7.098 1 1 1 H16 ? bmse000646 5 3 2 120.829 1 1 1 C1 'Long range coupling with peak(s) to c 10' bmse000646 5 4 1 7.695 1 1 1 H18 ? bmse000646 5 4 2 119.175 1 1 1 C3 ? bmse000646 5 5 1 7.381 1 1 1 H19 ? bmse000646 5 5 2 112.654 1 1 1 C4 ? bmse000646 5 6 1 6.946 1 1 1 H20 ? bmse000646 5 6 1 6.946 1 1 1 H21 ? bmse000646 5 6 2 105.882 1 1 1 C5 ? bmse000646 5 stop_ save_