data_bmse010057 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse010057 _Entry.Title Syringylresinol _Entry.Version_type update _Entry.Submission_date 2009-05-26 _Entry.Accession_date 2009-09-01 _Entry.Last_release_date 2013-04-05 _Entry.Original_release_date 2009-09-25 _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/BMSE010057 _Entry.Details ? _Entry.BMRB_internal_directory_name Syringylresinol loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Middle_initials _Entry_author.Family_title _Entry_author.Entry_ID 1 Irwin Pearl I. A. ? bmse010057 2 John Ralph ? ? ? bmse010057 3 Sally Ralph ? ? ? bmse010057 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 'NMR Database of Lignin and Cell Wall Model Compounds' 'United States Department of Agriculture' USDA bmse010057 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 3 bmse010057 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '13C chemical shifts' 66 bmse010057 '1H chemical shifts' 16 bmse010057 stop_ loop_ _Release.Release_number _Release.Format_type _Release.Format_version _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 . . 2009-09-25 2009-05-26 original Author 'Original spectra from USDA' bmse010057 2 . . 2009-11-11 2009-05-26 update BMRB 'added author and source information' bmse010057 3 . . 2010-10-08 2009-05-26 update BMRB 'Removed empty loops for database compliance' bmse010057 4 . . 2010-12-01 2009-05-26 update BMRB 'Set correct NMR STAR version' bmse010057 5 . . 2011-04-04 2009-05-26 update BMRB 'Added Provenance tag to chem_comp' bmse010057 6 . . 2011-09-07 2009-05-26 update BMRB 'Ensured correct reference IDs' bmse010057 7 . . 2011-09-09 2009-05-26 update BMRB 'Brought up to date with latest Dictionary' bmse010057 8 . . 2011-12-14 2009-05-26 update BMRB 'Set Assembly.Name to match Chem_comp.name' bmse010057 9 . . 2011-12-16 2009-05-26 update BMRB 'Standardized solvent' bmse010057 10 . . 2012-02-24 2009-05-26 update BMRB 'Set Raw_data_flag to no, since there are no raw data' bmse010057 11 . . 2012-09-13 2009-05-26 update BMRB 'Added PubChem SID 111677950 to database loop' bmse010057 12 . . 2013-04-05 2009-05-26 update BMRB 'Adding molecule category to chem_comp Details' bmse010057 13 . . 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse010057 14 . . 2018-07-10 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse010057 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse010057 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.PubMed_ID ? _Citation.Title 'NMR Database of Lignin and Cell Wall Model Compounds.' _Citation.Status published _Citation.Type internet _Citation.WWW_URL http://ars.usda.gov/Services/docs.htm?docid=10491 _Citation.Year 2004 _Citation.Details ? loop_ _Citation_author.Ordinal _Citation_author.Given_name _Citation_author.Family_name _Citation_author.First_initial _Citation_author.Middle_initials _Citation_author.Family_title _Citation_author.Entry_ID _Citation_author.Citation_ID 1 Sally Ralph ? A. ? bmse010057 1 2 John Ralph ? ? ? bmse010057 1 3 Larry Landucci ? L. ? bmse010057 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse010057 _Assembly.ID 1 _Assembly.Name Syringylresinol _Assembly.Number_of_components 1 _Assembly.Organic_ligands 0 _Assembly.Metal_ions ? _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.Magnetic_equivalence_group_code _Entity_assembly.Role _Entity_assembly.Details _Entity_assembly.Entry_ID _Entity_assembly.Assembly_ID 1 Syringylresinol 1 $Syringylresinol yes native no no ? ? ? bmse010057 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_Syringylresinol _Entity.Sf_category entity _Entity.Sf_framecode Syringylresinol _Entity.Entry_ID bmse010057 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name Syringylresinol _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 bmse010057 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 bmse010057 _Entity_natural_src_list.ID 1 loop_ _Entity_natural_src.ID _Entity_natural_src.Entity_ID _Entity_natural_src.Entity_label _Entity_natural_src.Entity_chimera_segment_ID _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.Organism_acronym _Entity_natural_src.ICTVdb_decimal_code _Entity_natural_src.Superkingdom _Entity_natural_src.Kingdom _Entity_natural_src.Genus _Entity_natural_src.Species _Entity_natural_src.Strain _Entity_natural_src.Variant _Entity_natural_src.Subvariant _Entity_natural_src.Organ _Entity_natural_src.Tissue _Entity_natural_src.Tissue_fraction _Entity_natural_src.Cell_line _Entity_natural_src.Cell_type _Entity_natural_src.ATCC_number _Entity_natural_src.Organelle _Entity_natural_src.Cellular_location _Entity_natural_src.Fragment _Entity_natural_src.Fraction _Entity_natural_src.Secretion _Entity_natural_src.Plasmid _Entity_natural_src.Plasmid_details _Entity_natural_src.Gene_mnemonic _Entity_natural_src.Dev_stage _Entity_natural_src.Details _Entity_natural_src.Citation_ID _Entity_natural_src.Citation_label _Entity_natural_src.Entry_ID _Entity_natural_src.Entity_natural_src_list_ID 1 1 $Syringylresinol . n/a 'multiple natural sources' yes 'not applicable' n/a . . Eukaryota Viridiplantae n/a n/a . . . . . . . . . . . . . . . . . . . . . bmse010057 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 bmse010057 _Entity_experimental_src_list.ID 1 loop_ _Entity_experimental_src.ID _Entity_experimental_src.Entity_ID _Entity_experimental_src.Entity_label _Entity_experimental_src.Entity_chimera_segment_ID _Entity_experimental_src.Production_method _Entity_experimental_src.Host_org_scientific_name _Entity_experimental_src.Host_org_name_common _Entity_experimental_src.Host_org_details _Entity_experimental_src.Host_org_NCBI_taxonomy_ID _Entity_experimental_src.Host_org_genus _Entity_experimental_src.Host_org_species _Entity_experimental_src.Host_org_strain _Entity_experimental_src.Host_org_variant _Entity_experimental_src.Host_org_subvariant _Entity_experimental_src.Host_org_organ _Entity_experimental_src.Host_org_tissue _Entity_experimental_src.Host_org_tissue_fraction _Entity_experimental_src.Host_org_cell_line _Entity_experimental_src.Host_org_cell_type _Entity_experimental_src.Host_org_cellular_location _Entity_experimental_src.Host_org_organelle _Entity_experimental_src.Host_org_gene _Entity_experimental_src.Host_org_culture_collection _Entity_experimental_src.Host_org_ATCC_number _Entity_experimental_src.Vector_type _Entity_experimental_src.PDBview_host_org_vector_name _Entity_experimental_src.PDBview_plasmid_name _Entity_experimental_src.Vector_name _Entity_experimental_src.Vector_details _Entity_experimental_src.Vendor_name _Entity_experimental_src.Host_org_dev_stage _Entity_experimental_src.Details _Entity_experimental_src.Citation_ID _Entity_experimental_src.Citation_label _Entity_experimental_src.Entry_ID _Entity_experimental_src.Entity_experimental_src_list_ID 1 1 $Syringylresinol . 'chemical synthesis' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . bmse010057 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 bmse010057 _Chem_comp.ID 1 _Chem_comp.Provenance BMRB _Chem_comp.Name Syringylresinol _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InChI_code InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3/t13-,14-,21-,22-/m1/s1 _Chem_comp.Mon_nstd_flag ? _Chem_comp.Std_deriv_one_letter_code ? _Chem_comp.Std_deriv_three_letter_code ? _Chem_comp.Std_deriv_BMRB_code ? _Chem_comp.Std_deriv_PDB_code ? _Chem_comp.Formal_charge ? _Chem_comp.Paramagnetic no _Chem_comp.Aromatic yes _Chem_comp.Formula 'C22 H26 O8' _Chem_comp.Formula_weight 418.43704 _Chem_comp.Formula_mono_iso_wt_nat 418.1627678114 _Chem_comp.Formula_mono_iso_wt_13C 440.236574243 _Chem_comp.Formula_mono_iso_wt_15N 418.1627678114 _Chem_comp.Formula_mono_iso_wt_13C_15N 440.236574243 _Chem_comp.Image_file_name bmse010057.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name bmse010057.mol _Chem_comp.Struct_file_format mol _Chem_comp.Stereochem_param_file_name ? _Chem_comp.Details 'b-b Dimers' _Chem_comp.DB_query_date ? _Chem_comp.DB_last_query_revised_last_date ? loop_ _Chem_comp_common_name.Name _Chem_comp_common_name.Type _Chem_comp_common_name.Entry_ID _Chem_comp_common_name.Comp_ID Syringylresinol synonym bmse010057 1 3,3,5,5-tetramethoxy-7,9,7,9-diepoxylignan-4,4-diol synonym bmse010057 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=1/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3 ; INCHI na na bmse010057 1 InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3/t13-,14-,21-,22-/m1/s1 INCHI ALATIS 3.003 bmse010057 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 Syringylresinol Beilstein bmse010057 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID Canonical SMILES_STRING bmse010057 1 Isomeric SMILES_STRING bmse010057 1 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Auth_atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Oxidation_number _Chem_comp_atom.Unpaired_electron_number _Chem_comp_atom.Drawing_2D_coord_x _Chem_comp_atom.Drawing_2D_coord_y _Chem_comp_atom.Model_Cartn_x _Chem_comp_atom.Model_Cartn_y _Chem_comp_atom.Model_Cartn_z _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID C1 OMe C ? ? ? ? 257.7600 25.3056 ? ? ? 1 bmse010057 1 C2 OMe C ? ? ? ? 140.8096 113.7760 ? ? ? 2 bmse010057 1 C3 OMe C ? ? ? ? 292.3936 354.6944 ? ? ? 3 bmse010057 1 C4 OMe C ? ? ? ? 409.1904 266.0224 ? ? ? 4 bmse010057 1 C5 2 C ? ? ? ? 256.1248 109.9552 ? ? ? 5 bmse010057 1 C6 6 C ? ? ? ? 203.4112 127.0816 ? ? ? 6 bmse010057 1 C7 2 C ? ? ? ? 293.8848 270.0416 ? ? ? 7 bmse010057 1 C8 6 C ? ? ? ? 346.5664 252.8256 ? ? ? 8 bmse010057 1 C9 G C ? ? ? ? 305.3120 164.3072 ? ? ? 9 bmse010057 1 C10 G C ? ? ? ? 244.6016 215.9456 ? ? ? 10 bmse010057 1 C11 1 C ? ? ? ? 234.7104 133.7344 ? ? ? 11 bmse010057 1 C12 1 C ? ? ? ? 315.2544 246.2240 ? ? ? 12 bmse010057 1 C13 B C ? ? ? ? 275.0336 174.0576 ? ? ? 13 bmse010057 1 C14 B C ? ? ? ? 275.0336 206.0576 ? ? ? 14 bmse010057 1 C15 3 C ? ? ? ? 246.2368 79.5200 ? ? ? 15 bmse010057 1 C16 5 C ? ? ? ? 193.5232 96.6464 ? ? ? 16 bmse010057 1 C17 3 C ? ? ? ? 303.8240 300.4608 ? ? ? 17 bmse010057 1 C18 5 C ? ? ? ? 356.5088 283.2416 ? ? ? 18 bmse010057 1 C19 4 C ? ? ? ? 214.9344 72.8672 ? ? ? 19 bmse010057 1 C20 4 C ? ? ? ? 335.1360 307.0592 ? ? ? 20 bmse010057 1 C21 A C ? ? ? ? 244.6016 164.1696 ? ? ? 21 bmse010057 1 C22 A C ? ? ? ? 305.3120 215.8080 ? ? ? 22 bmse010057 1 O23 ? O ? ? ? ? 205.0464 42.4320 ? ? ? 23 bmse010057 1 O24 ? O ? ? ? ? 345.0784 337.4752 ? ? ? 24 bmse010057 1 O25 ? O ? ? ? ? 267.6480 55.7408 ? ? ? 25 bmse010057 1 O26 ? O ? ? ? ? 162.2208 89.9936 ? ? ? 26 bmse010057 1 O27 ? O ? ? ? ? 282.4544 324.2784 ? ? ? 27 bmse010057 1 O28 ? O ? ? ? ? 387.8208 289.8400 ? ? ? 28 bmse010057 1 O29 ? O ? ? ? ? 225.7920 190.0576 ? ? ? 29 bmse010057 1 O30 ? O ? ? ? ? 323.9872 190.0576 ? ? ? 30 bmse010057 1 H31 ? H ? ? ? ? 238.8909 31.4359 ? ? ? 31 bmse010057 1 H33 OMe H ? ? ? ? 251.6297 6.4365 ? ? ? 32 bmse010057 1 H32 OMe H ? ? ? ? 276.6292 19.1753 ? ? ? 33 bmse010057 1 H34 OMe H ? ? ? ? 155.5544 127.0507 ? ? ? 34 bmse010057 1 H35 OMe H ? ? ? ? 127.5349 128.5208 ? ? ? 35 bmse010057 1 H36 OMe H ? ? ? ? 126.0648 100.5013 ? ? ? 36 bmse010057 1 H39 OMe H ? ? ? ? 311.2522 348.5319 ? ? ? 37 bmse010057 1 H37 ? H ? ? ? ? 298.5561 373.5530 ? ? ? 38 bmse010057 1 H38 ? H ? ? ? ? 273.5349 360.8569 ? ? ? 39 bmse010057 1 H42 ? H ? ? ? ? 394.4230 252.7728 ? ? ? 40 bmse010057 1 H41 ? H ? ? ? ? 422.4399 251.2550 ? ? ? 41 bmse010057 1 H40 ? H ? ? ? ? 423.9578 279.2719 ? ? ? 42 bmse010057 1 H43 2 H ? ? ? ? 275.5310 114.0812 ? ? ? 43 bmse010057 1 H44 6 H ? ? ? ? 190.1354 141.8254 ? ? ? 44 bmse010057 1 H45 2 H ? ? ? ? 274.4713 265.9497 ? ? ? 45 bmse010057 1 H46 6 H ? ? ? ? 359.8167 238.0589 ? ? ? 46 bmse010057 1 H47 ? H ? ? ? ? 297.2792 146.1661 ? ? ? 47 bmse010057 1 H48 G2 H ? ? ? ? 322.5082 154.4120 ? ? ? 48 bmse010057 1 H49 ? H ? ? ? ? 252.6714 234.0703 ? ? ? 49 bmse010057 1 H50 G2 H ? ? ? ? 227.4198 225.8659 ? ? ? 50 bmse010057 1 H51 B H ? ? ? ? 275.0596 154.2176 ? ? ? 51 bmse010057 1 H52 B H ? ? ? ? 275.0596 225.8976 ? ? ? 52 bmse010057 1 H53 A H ? ? ? ? 225.0058 161.0664 ? ? ? 53 bmse010057 1 H54 A H ? ? ? ? 324.9118 218.8859 ? ? ? 54 bmse010057 1 H55 ? H ? ? ? ? 185.6401 38.3065 ? ? ? 55 bmse010057 1 H56 ? H ? ? ? ? 364.4921 341.5657 ? ? ? 56 bmse010057 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID C1 C1 BMRB bmse010057 1 C2 C2 BMRB bmse010057 1 C3 C3 BMRB bmse010057 1 C4 C4 BMRB bmse010057 1 C5 C5 BMRB bmse010057 1 C6 C6 BMRB bmse010057 1 C7 C7 BMRB bmse010057 1 C8 C8 BMRB bmse010057 1 C9 C9 BMRB bmse010057 1 C10 C10 BMRB bmse010057 1 C11 C11 BMRB bmse010057 1 C12 C12 BMRB bmse010057 1 C13 C13 BMRB bmse010057 1 C14 C14 BMRB bmse010057 1 C15 C15 BMRB bmse010057 1 C16 C16 BMRB bmse010057 1 C17 C17 BMRB bmse010057 1 C18 C18 BMRB bmse010057 1 C19 C19 BMRB bmse010057 1 C20 C20 BMRB bmse010057 1 C21 C21 BMRB bmse010057 1 C22 C22 BMRB bmse010057 1 O23 O23 BMRB bmse010057 1 O24 O24 BMRB bmse010057 1 O25 O25 BMRB bmse010057 1 O26 O26 BMRB bmse010057 1 O27 O27 BMRB bmse010057 1 O28 O28 BMRB bmse010057 1 O29 O29 BMRB bmse010057 1 O30 O30 BMRB bmse010057 1 H31 H31 BMRB bmse010057 1 H33 H32 BMRB bmse010057 1 H32 H33 BMRB bmse010057 1 H34 H34 BMRB bmse010057 1 H35 H35 BMRB bmse010057 1 H36 H36 BMRB bmse010057 1 H39 H37 BMRB bmse010057 1 H37 H38 BMRB bmse010057 1 H38 H39 BMRB bmse010057 1 H42 H40 BMRB bmse010057 1 H41 H41 BMRB bmse010057 1 H40 H42 BMRB bmse010057 1 H43 H43 BMRB bmse010057 1 H44 H44 BMRB bmse010057 1 H45 H45 BMRB bmse010057 1 H46 H46 BMRB bmse010057 1 H47 H47 BMRB bmse010057 1 H48 H48 BMRB bmse010057 1 H49 H49 BMRB bmse010057 1 H50 H50 BMRB bmse010057 1 H51 H51 BMRB bmse010057 1 H52 H52 BMRB bmse010057 1 H53 H53 BMRB bmse010057 1 H54 H54 BMRB bmse010057 1 H55 H55 BMRB bmse010057 1 H56 H56 BMRB bmse010057 1 C1 C1 ALATIS bmse010057 1 C2 C2 ALATIS bmse010057 1 C3 C3 ALATIS bmse010057 1 C4 C4 ALATIS bmse010057 1 C5 C5 ALATIS bmse010057 1 C6 C6 ALATIS bmse010057 1 C7 C7 ALATIS bmse010057 1 C8 C8 ALATIS bmse010057 1 C9 C9 ALATIS bmse010057 1 C10 C10 ALATIS bmse010057 1 C11 C11 ALATIS bmse010057 1 C12 C12 ALATIS bmse010057 1 C13 C13 ALATIS bmse010057 1 C14 C14 ALATIS bmse010057 1 C15 C15 ALATIS bmse010057 1 C16 C16 ALATIS bmse010057 1 C17 C17 ALATIS bmse010057 1 C18 C18 ALATIS bmse010057 1 C19 C19 ALATIS bmse010057 1 C20 C20 ALATIS bmse010057 1 C21 C21 ALATIS bmse010057 1 C22 C22 ALATIS bmse010057 1 O23 O23 ALATIS bmse010057 1 O24 O24 ALATIS bmse010057 1 O25 O25 ALATIS bmse010057 1 O26 O26 ALATIS bmse010057 1 O27 O27 ALATIS bmse010057 1 O28 O28 ALATIS bmse010057 1 O29 O29 ALATIS bmse010057 1 O30 O30 ALATIS bmse010057 1 H31 H31 ALATIS bmse010057 1 H33 H33 ALATIS bmse010057 1 H32 H32 ALATIS bmse010057 1 H34 H34 ALATIS bmse010057 1 H35 H35 ALATIS bmse010057 1 H36 H36 ALATIS bmse010057 1 H39 H39 ALATIS bmse010057 1 H37 H37 ALATIS bmse010057 1 H38 H38 ALATIS bmse010057 1 H42 H42 ALATIS bmse010057 1 H41 H41 ALATIS bmse010057 1 H40 H40 ALATIS bmse010057 1 H43 H43 ALATIS bmse010057 1 H44 H44 ALATIS bmse010057 1 H45 H45 ALATIS bmse010057 1 H46 H46 ALATIS bmse010057 1 H47 H47 ALATIS bmse010057 1 H48 H48 ALATIS bmse010057 1 H49 H49 ALATIS bmse010057 1 H50 H50 ALATIS bmse010057 1 H51 H51 ALATIS bmse010057 1 H52 H52 ALATIS bmse010057 1 H53 H53 ALATIS bmse010057 1 H54 H54 ALATIS bmse010057 1 H55 H55 ALATIS bmse010057 1 H56 H56 ALATIS bmse010057 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.Details _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent SING C1 O25 ? bmse010057 1 2 covalent SING C2 O26 ? bmse010057 1 3 covalent SING C3 O27 ? bmse010057 1 4 covalent SING C4 O28 ? bmse010057 1 5 covalent DOUB C5 C11 ? bmse010057 1 6 covalent SING C5 C15 ? bmse010057 1 7 covalent SING C6 C11 ? bmse010057 1 8 covalent DOUB C6 C16 ? bmse010057 1 9 covalent DOUB C7 C12 ? bmse010057 1 10 covalent SING C7 C17 ? bmse010057 1 11 covalent SING C8 C12 ? bmse010057 1 12 covalent DOUB C8 C18 ? bmse010057 1 13 covalent SING C9 C13 ? bmse010057 1 14 covalent SING C9 O30 ? bmse010057 1 15 covalent SING C10 C14 ? bmse010057 1 16 covalent SING C10 O29 ? bmse010057 1 17 covalent SING C11 C21 ? bmse010057 1 18 covalent SING C12 C22 ? bmse010057 1 19 covalent SING C13 C14 ? bmse010057 1 20 covalent SING C13 C21 ? bmse010057 1 21 covalent SING C14 C22 ? bmse010057 1 22 covalent DOUB C15 C19 ? bmse010057 1 23 covalent SING C15 O25 ? bmse010057 1 24 covalent SING C16 C19 ? bmse010057 1 25 covalent SING C16 O26 ? bmse010057 1 26 covalent DOUB C17 C20 ? bmse010057 1 27 covalent SING C17 O27 ? bmse010057 1 28 covalent SING C18 C20 ? bmse010057 1 29 covalent SING C18 O28 ? bmse010057 1 30 covalent SING C19 O23 ? bmse010057 1 31 covalent SING C20 O24 ? bmse010057 1 32 covalent SING C21 O29 ? bmse010057 1 33 covalent SING C22 O30 ? bmse010057 1 34 covalent SING C1 H31 ? bmse010057 1 35 covalent SING C1 H33 ? bmse010057 1 36 covalent SING C1 H32 ? bmse010057 1 37 covalent SING C2 H34 ? bmse010057 1 38 covalent SING C2 H35 ? bmse010057 1 39 covalent SING C2 H36 ? bmse010057 1 40 covalent SING C3 H39 ? bmse010057 1 41 covalent SING C3 H37 ? bmse010057 1 42 covalent SING C3 H38 ? bmse010057 1 43 covalent SING C4 H42 ? bmse010057 1 44 covalent SING C4 H41 ? bmse010057 1 45 covalent SING C4 H40 ? bmse010057 1 46 covalent SING C5 H43 ? bmse010057 1 47 covalent SING C6 H44 ? bmse010057 1 48 covalent SING C7 H45 ? bmse010057 1 49 covalent SING C8 H46 ? bmse010057 1 50 covalent SING C9 H47 ? bmse010057 1 51 covalent SING C9 H48 ? bmse010057 1 52 covalent SING C10 H49 ? bmse010057 1 53 covalent SING C10 H50 ? bmse010057 1 54 covalent SING C13 H51 ? bmse010057 1 55 covalent SING C14 H52 ? bmse010057 1 56 covalent SING C21 H53 ? bmse010057 1 57 covalent SING C22 H54 ? bmse010057 1 58 covalent SING O23 H55 ? bmse010057 1 59 covalent SING O24 H56 ? bmse010057 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_code _Chem_comp_db_link.Entry_mol_name _Chem_comp_db_link.Entry_experimental_method _Chem_comp_db_link.Entry_relation_type _Chem_comp_db_link.Entry_details _Chem_comp_db_link.Entry_ID _Chem_comp_db_link.Comp_ID no PubChem 111677950 sid ? Syringylresinol ? 'matching entry' ? bmse010057 1 yes USDA_NMR_database 117 'Compound Number' ? Syringylresinol ? 'matching entry' ? bmse010057 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 bmse010057 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse010057 _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.Product_ID _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_min _Sample_component.Concentration_val_max _Sample_component.Concentration_val_units _Sample_component.Concentration_val_err _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Vendor_product_code _Sample_component.Entry_ID _Sample_component.Sample_ID 1 Syringylresinol 'natural abundance' 1 $Syringylresinol ? Solute 28 ? ? mg/ml ? 'Irwin A. Pearl' Syringylresinol n/a bmse010057 1 2 CDCl3 ? 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010057 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_2 _Sample.Sf_category sample _Sample.Sf_framecode sample_2 _Sample.Entry_ID bmse010057 _Sample.ID 2 _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.Product_ID _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_min _Sample_component.Concentration_val_max _Sample_component.Concentration_val_units _Sample_component.Concentration_val_err _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Vendor_product_code _Sample_component.Entry_ID _Sample_component.Sample_ID 1 Syringylresinol 'natural abundance' 1 $Syringylresinol ? Solute 28 ? ? mg/ml ? 'Irwin A. Pearl' Syringylresinol n/a bmse010057 2 2 acetone '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010057 2 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_3 _Sample.Sf_category sample _Sample.Sf_framecode sample_3 _Sample.Entry_ID bmse010057 _Sample.ID 3 _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.Product_ID _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_min _Sample_component.Concentration_val_max _Sample_component.Concentration_val_units _Sample_component.Concentration_val_err _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Vendor_product_code _Sample_component.Entry_ID _Sample_component.Sample_ID 1 Syringylresinol 'natural abundance' 1 $Syringylresinol ? Solute 28 ? ? mg/ml ? 'Irwin A. Pearl' Syringylresinol n/a bmse010057 3 2 DMSO '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010057 3 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 bmse010057 _Sample_condition_list.ID 1 loop_ _Sample_condition_variable.Type _Sample_condition_variable.Val _Sample_condition_variable.Val_err _Sample_condition_variable.Val_units _Sample_condition_variable.Entry_ID _Sample_condition_variable.Sample_condition_list_ID pH n/a ? pH bmse010057 1 temperature 297 ? K bmse010057 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse010057 _Software.ID 1 _Software.Name X-WINNMR _Software.Version ? _Software.Details ? loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID Bruker ? ? bmse010057 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Processing bmse010057 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_Bruker_250 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode Bruker_250 _NMR_spectrometer.Entry_ID bmse010057 _NMR_spectrometer.ID 1 _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model WM _NMR_spectrometer.Field_strength 250 save_ ############################# # NMR applied experiments # ############################# save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse010057 _Experiment_list.ID 1 _Experiment_list.Details ? loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _Experiment.NMR_spec_expt_ID _Experiment.NMR_spec_expt_label _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.NMR_spectral_processing_ID _Experiment.NMR_spectral_processing_label _Experiment.Entry_ID _Experiment.Experiment_list_ID 1 '1D 1H' no ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010057 1 2 '1D 13C' no ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010057 1 3 '1D 13C' no ? ? 2 $sample_2 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010057 1 4 '1D 13C' no ? ? 3 $sample_3 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010057 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference_1 _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference_1 _Chem_shift_reference.Entry_ID bmse010057 _Chem_shift_reference.ID 1 _Chem_shift_reference.Details ? 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.External_ref_loc _Chem_shift_ref.External_ref_sample_geometry _Chem_shift_ref.External_ref_axis _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 CDCl3 'residual solvent proton' ppm 7.24 internal direct 1.000000000 ? ? ? bmse010057 1 C 13 CDCl3 'solvent carbon' ppm 77.00 internal direct ? ? ? ? bmse010057 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference_2 _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference_2 _Chem_shift_reference.Entry_ID bmse010057 _Chem_shift_reference.ID 2 _Chem_shift_reference.Details ? 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.External_ref_loc _Chem_shift_ref.External_ref_sample_geometry _Chem_shift_ref.External_ref_axis _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 Acetone-d6 'residual solvent methyl proton' ppm 2.04 internal direct 1.000000000 ? ? ? bmse010057 2 C 13 Acetone-d6 'solvent methyl carbon' ppm 29.83 internal direct ? ? ? ? bmse010057 2 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference_3 _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference_3 _Chem_shift_reference.Entry_ID bmse010057 _Chem_shift_reference.ID 3 _Chem_shift_reference.Details ? 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.External_ref_loc _Chem_shift_ref.External_ref_sample_geometry _Chem_shift_ref.External_ref_axis _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 DMSO-d6 'residual solvent methyl proton' ppm 2.49 internal direct 1.000000000 ? ? ? bmse010057 3 C 13 DMSO-d6 'solvent methyl carbon' ppm 39.50 internal direct ? ? ? ? bmse010057 3 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_1 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chemical_shifts_1 _Assigned_chem_shift_list.Entry_ID bmse010057 _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_1 _Assigned_chem_shift_list.Error_derivation_method ? _Assigned_chem_shift_list.Details ? 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 bmse010057 1 2 '1D 13C' 1 $sample_1 bmse010057 1 stop_ loop_ _Chem_shift_software.Software_ID _Chem_shift_software.Software_label _Chem_shift_software.Method_ID _Chem_shift_software.Method_label _Chem_shift_software.Entry_ID _Chem_shift_software.Assigned_chem_shift_list_ID 1 $software_1 ? ? bmse010057 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.Val_err _Atom_chem_shift.Assign_fig_of_merit _Atom_chem_shift.Ambiguity_code _Atom_chem_shift.Occupancy _Atom_chem_shift.Auth_seq_ID _Atom_chem_shift.Auth_comp_ID _Atom_chem_shift.Auth_atom_ID _Atom_chem_shift.Details _Atom_chem_shift.Entry_ID _Atom_chem_shift.Assigned_chem_shift_list_ID 1 1 1 1 C13 C 13 54.38 ? ? 1 ? ? ? B ? bmse010057 1 2 1 1 1 C14 C 13 54.38 ? ? 1 ? ? ? B ? bmse010057 1 3 1 1 1 C1 C 13 56.41 ? ? 1 ? ? ? OMe ? bmse010057 1 4 1 1 1 C2 C 13 56.41 ? ? 1 ? ? ? OMe ? bmse010057 1 5 1 1 1 C3 C 13 56.41 ? ? 1 ? ? ? OMe ? bmse010057 1 6 1 1 1 C4 C 13 56.41 ? ? 1 ? ? ? OMe ? bmse010057 1 7 1 1 1 C9 C 13 71.83 ? ? 1 ? ? ? G ? bmse010057 1 8 1 1 1 C10 C 13 71.83 ? ? 1 ? ? ? G ? bmse010057 1 9 1 1 1 C21 C 13 86.08 ? ? 1 ? ? ? A ? bmse010057 1 10 1 1 1 C22 C 13 86.08 ? ? 1 ? ? ? A ? bmse010057 1 11 1 1 1 C5 C 13 102.78 ? ? 1 ? ? ? 2 ? bmse010057 1 12 1 1 1 C7 C 13 102.78 ? ? 1 ? ? ? 2 ? bmse010057 1 13 1 1 1 C6 C 13 102.78 ? ? 1 ? ? ? 6 ? bmse010057 1 14 1 1 1 C8 C 13 102.78 ? ? 1 ? ? ? 6 ? bmse010057 1 15 1 1 1 C11 C 13 132.13 ? ? 1 ? ? ? 1 ? bmse010057 1 16 1 1 1 C12 C 13 132.13 ? ? 1 ? ? ? 1 ? bmse010057 1 17 1 1 1 C19 C 13 134.38 ? ? 1 ? ? ? 4 ? bmse010057 1 18 1 1 1 C20 C 13 134.38 ? ? 1 ? ? ? 4 ? bmse010057 1 19 1 1 1 C15 C 13 147.19 ? ? 1 ? ? ? 3 ? bmse010057 1 20 1 1 1 C17 C 13 147.19 ? ? 1 ? ? ? 3 ? bmse010057 1 21 1 1 1 C16 C 13 147.19 ? ? 1 ? ? ? 5 ? bmse010057 1 22 1 1 1 C18 C 13 147.19 ? ? 1 ? ? ? 5 ? bmse010057 1 23 1 1 1 H51 H 1 4.28 ? ? 1 ? ? ? B ? bmse010057 1 24 1 1 1 H52 H 1 4.28 ? ? 1 ? ? ? B ? bmse010057 1 25 1 1 1 H33 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 26 1 1 1 H32 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 27 1 1 1 H34 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 28 1 1 1 H35 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 29 1 1 1 H36 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 30 1 1 1 H39 H 1 3.90 ? ? 1 ? ? ? OMe ? bmse010057 1 31 1 1 1 H48 H 1 4.28 ? ? 1 ? ? ? G2 ? bmse010057 1 32 1 1 1 H50 H 1 4.28 ? ? 1 ? ? ? G2 ? bmse010057 1 33 1 1 1 H53 H 1 4.73 ? ? 1 ? ? ? A ? bmse010057 1 34 1 1 1 H54 H 1 4.73 ? ? 1 ? ? ? A ? bmse010057 1 35 1 1 1 H43 H 1 6.58 ? ? 1 ? ? ? 2 ? bmse010057 1 36 1 1 1 H45 H 1 6.58 ? ? 1 ? ? ? 2 ? bmse010057 1 37 1 1 1 H44 H 1 6.58 ? ? 1 ? ? ? 6 ? bmse010057 1 38 1 1 1 H46 H 1 6.58 ? ? 1 ? ? ? 6 ? bmse010057 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_2 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chemical_shifts_2 _Assigned_chem_shift_list.Entry_ID bmse010057 _Assigned_chem_shift_list.ID 2 _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 2 _Assigned_chem_shift_list.Chem_shift_reference_label $chem_shift_reference_2 _Assigned_chem_shift_list.Error_derivation_method ? _Assigned_chem_shift_list.Details ? 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 3 '1D 13C' 2 $sample_2 bmse010057 2 stop_ loop_ _Chem_shift_software.Software_ID _Chem_shift_software.Software_label _Chem_shift_software.Method_ID _Chem_shift_software.Method_label _Chem_shift_software.Entry_ID _Chem_shift_software.Assigned_chem_shift_list_ID 1 $software_1 ? ? bmse010057 2 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.Val_err _Atom_chem_shift.Assign_fig_of_merit _Atom_chem_shift.Ambiguity_code _Atom_chem_shift.Occupancy _Atom_chem_shift.Auth_seq_ID _Atom_chem_shift.Auth_comp_ID _Atom_chem_shift.Auth_atom_ID _Atom_chem_shift.Details _Atom_chem_shift.Entry_ID _Atom_chem_shift.Assigned_chem_shift_list_ID 1 1 1 1 C13 C 13 55.33 ? ? 1 ? ? ? B ? bmse010057 2 2 1 1 1 C14 C 13 55.33 ? ? 1 ? ? ? B ? bmse010057 2 3 1 1 1 C1 C 13 56.69 ? ? 1 ? ? ? OMe ? bmse010057 2 4 1 1 1 C2 C 13 56.69 ? ? 1 ? ? ? OMe ? bmse010057 2 5 1 1 1 C3 C 13 56.69 ? ? 1 ? ? ? OMe ? bmse010057 2 6 1 1 1 C4 C 13 56.69 ? ? 1 ? ? ? OMe ? bmse010057 2 7 1 1 1 C9 C 13 72.37 ? ? 1 ? ? ? G ? bmse010057 2 8 1 1 1 C10 C 13 72.37 ? ? 1 ? ? ? G ? bmse010057 2 9 1 1 1 C21 C 13 86.81 ? ? 1 ? ? ? A ? bmse010057 2 10 1 1 1 C22 C 13 86.81 ? ? 1 ? ? ? A ? bmse010057 2 11 1 1 1 C5 C 13 104.52 ? ? 1 ? ? ? 2 ? bmse010057 2 12 1 1 1 C7 C 13 104.52 ? ? 1 ? ? ? 2 ? bmse010057 2 13 1 1 1 C6 C 13 104.52 ? ? 1 ? ? ? 6 ? bmse010057 2 14 1 1 1 C8 C 13 104.52 ? ? 1 ? ? ? 6 ? bmse010057 2 15 1 1 1 C11 C 13 133.24 ? ? 1 ? ? ? 1 ? bmse010057 2 16 1 1 1 C12 C 13 133.24 ? ? 1 ? ? ? 1 ? bmse010057 2 17 1 1 1 C19 C 13 136.23 ? ? 1 ? ? ? 4 ? bmse010057 2 18 1 1 1 C20 C 13 136.23 ? ? 1 ? ? ? 4 ? bmse010057 2 19 1 1 1 C15 C 13 148.69 ? ? 1 ? ? ? 3 ? bmse010057 2 20 1 1 1 C17 C 13 148.69 ? ? 1 ? ? ? 3 ? bmse010057 2 21 1 1 1 C16 C 13 148.69 ? ? 1 ? ? ? 5 ? bmse010057 2 22 1 1 1 C18 C 13 148.69 ? ? 1 ? ? ? 5 ? bmse010057 2 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_3 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chemical_shifts_3 _Assigned_chem_shift_list.Entry_ID bmse010057 _Assigned_chem_shift_list.ID 3 _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 3 _Assigned_chem_shift_list.Chem_shift_reference_label $chem_shift_reference_3 _Assigned_chem_shift_list.Error_derivation_method ? _Assigned_chem_shift_list.Details ? 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 4 '1D 13C' 3 $sample_3 bmse010057 3 stop_ loop_ _Chem_shift_software.Software_ID _Chem_shift_software.Software_label _Chem_shift_software.Method_ID _Chem_shift_software.Method_label _Chem_shift_software.Entry_ID _Chem_shift_software.Assigned_chem_shift_list_ID 1 $software_1 ? ? bmse010057 3 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.Val_err _Atom_chem_shift.Assign_fig_of_merit _Atom_chem_shift.Ambiguity_code _Atom_chem_shift.Occupancy _Atom_chem_shift.Auth_seq_ID _Atom_chem_shift.Auth_comp_ID _Atom_chem_shift.Auth_atom_ID _Atom_chem_shift.Details _Atom_chem_shift.Entry_ID _Atom_chem_shift.Assigned_chem_shift_list_ID 1 1 1 1 C13 C 13 53.59 ? ? 1 ? ? ? B ? bmse010057 3 2 1 1 1 C14 C 13 53.59 ? ? 1 ? ? ? B ? bmse010057 3 3 1 1 1 C1 C 13 55.95 ? ? 1 ? ? ? OMe ? bmse010057 3 4 1 1 1 C2 C 13 55.95 ? ? 1 ? ? ? OMe ? bmse010057 3 5 1 1 1 C3 C 13 55.95 ? ? 1 ? ? ? OMe ? bmse010057 3 6 1 1 1 C4 C 13 55.95 ? ? 1 ? ? ? OMe ? bmse010057 3 7 1 1 1 C9 C 13 70.99 ? ? 1 ? ? ? G ? bmse010057 3 8 1 1 1 C10 C 13 70.99 ? ? 1 ? ? ? G ? bmse010057 3 9 1 1 1 C21 C 13 85.26 ? ? 1 ? ? ? A ? bmse010057 3 10 1 1 1 C22 C 13 85.26 ? ? 1 ? ? ? A ? bmse010057 3 11 1 1 1 C5 C 13 103.59 ? ? 1 ? ? ? 2 ? bmse010057 3 12 1 1 1 C7 C 13 103.59 ? ? 1 ? ? ? 2 ? bmse010057 3 13 1 1 1 C6 C 13 103.59 ? ? 1 ? ? ? 6 ? bmse010057 3 14 1 1 1 C8 C 13 103.59 ? ? 1 ? ? ? 6 ? bmse010057 3 15 1 1 1 C11 C 13 131.36 ? ? 1 ? ? ? 1 ? bmse010057 3 16 1 1 1 C12 C 13 131.36 ? ? 1 ? ? ? 1 ? bmse010057 3 17 1 1 1 C19 C 13 134.81 ? ? 1 ? ? ? 4 ? bmse010057 3 18 1 1 1 C20 C 13 134.81 ? ? 1 ? ? ? 4 ? bmse010057 3 19 1 1 1 C15 C 13 147.82 ? ? 1 ? ? ? 3 ? bmse010057 3 20 1 1 1 C17 C 13 147.82 ? ? 1 ? ? ? 3 ? bmse010057 3 21 1 1 1 C16 C 13 147.82 ? ? 1 ? ? ? 5 ? bmse010057 3 22 1 1 1 C18 C 13 147.82 ? ? 1 ? ? ? 5 ? bmse010057 3 stop_ save_