data_bmse010060 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse010060 _Entry.Title Syringylresinol_diacetate _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.Details ? _Entry.BMRB_internal_directory_name Syringylresinol_diacetate 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 John Ralph ? ? ? bmse010060 2 Sally Ralph ? ? ? bmse010060 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 bmse010060 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 3 bmse010060 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '13C chemical shifts' 78 bmse010060 '1H chemical shifts' 30 bmse010060 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' bmse010060 2 . . 2009-11-11 2009-05-26 update BMRB 'added author and source information' bmse010060 3 . . 2010-10-08 2009-05-26 update BMRB 'Removed empty loops for database compliance' bmse010060 4 . . 2010-12-01 2009-05-26 update BMRB 'Set correct NMR STAR version' bmse010060 5 . . 2011-04-04 2009-05-26 update BMRB 'Added Provenance tag to chem_comp' bmse010060 6 . . 2011-09-07 2009-05-26 update BMRB 'Ensured correct reference IDs' bmse010060 7 . . 2011-09-09 2009-05-26 update BMRB 'Brought up to date with latest Dictionary' bmse010060 8 . . 2011-12-14 2009-05-26 update BMRB 'Set Assembly.Name to match Chem_comp.name' bmse010060 9 . . 2011-12-16 2009-05-26 update BMRB 'Standardized solvent' bmse010060 10 . . 2012-02-24 2009-05-26 update BMRB 'Set Raw_data_flag to no, since there are no raw data' bmse010060 11 . . 2012-09-13 2009-05-26 update BMRB 'Added PubChem SID 111677953 to database loop' bmse010060 12 . . 2013-04-05 2009-05-26 update BMRB 'Adding molecule category to chem_comp Details' bmse010060 13 . . 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse010060 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse010060 _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. ? bmse010060 1 2 John Ralph ? ? ? bmse010060 1 3 Larry Landucci ? L. ? bmse010060 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse010060 _Assembly.ID 1 _Assembly.Name 'Syringylresinol diacetate' _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-diacetate 1 $Syringylresinol-diacetate yes native no no ? ? ? bmse010060 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_Syringylresinol-diacetate _Entity.Sf_category entity _Entity.Sf_framecode Syringylresinol-diacetate _Entity.Entry_ID bmse010060 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name 'Syringylresinol diacetate' _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 bmse010060 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 bmse010060 _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-diacetate . n/a 'multiple natural sources' yes 'not applicable' n/a . . Eukaryota Viridiplantae n/a n/a . . . . . . . . . . . . . . . . . . . . . bmse010060 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 bmse010060 _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-diacetate . 'chemical synthesis' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . bmse010060 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 bmse010060 _Chem_comp.ID 1 _Chem_comp.Provenance BMRB _Chem_comp.Name 'Syringylresinol diacetate' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InChI_code ; InChI=1/C26H30O10/c1-13(27)35-25-19(29-3)7-15(8-20(25)30-4)23-17-11-34-24(18(17)12-33-23)16-9-21(31-5)26(36-14(2)28)22(10-16)32-6/h7-10,17-18,23-24H,11-12H2,1-6H3 ; _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 'C26 H30 O10' _Chem_comp.Formula_weight 502.5104 _Chem_comp.Formula_mono_iso_wt_nat 502.183897184 _Chem_comp.Formula_mono_iso_wt_13C 528.2711229668 _Chem_comp.Formula_mono_iso_wt_15N 502.183897184 _Chem_comp.Formula_mono_iso_wt_13C_15N 528.2711229668 _Chem_comp.Image_file_name bmse010060.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name bmse010060.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 diacetate' synonym bmse010060 1 ; Acetic acid 4-[4-(4-acetoxy-3,5-dimethoxyphenyl) tetrahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenyl ester ; synonym bmse010060 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 diacetate' Beilstein bmse010060 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID Canonical CC(=O)OC1=C(C=C(C=C1OC)C4C3COC(C2=CC(=C(C(=C2)OC)OC(C)=O)OC)C3CO4)OC bmse010060 1 Isomeric CC(=O)OC1=C(C=C(C=C1OC)C4C3COC(C2=CC(=C(C(=C2)OC)OC(C)=O)OC)C3CO4)OC bmse010060 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 AcMe C ? ? ? ? 163.8560 5.4272 ? ? ? 1 bmse010060 1 C2 AcMe C ? ? ? ? 386.3328 374.5728 ? ? ? 2 bmse010060 1 C3 OMe C ? ? ? ? 257.7600 25.3888 ? ? ? 3 bmse010060 1 C4 OMe C ? ? ? ? 140.8096 113.8560 ? ? ? 4 bmse010060 1 C5 OMe C ? ? ? ? 292.3936 354.7744 ? ? ? 5 bmse010060 1 C6 OMe C ? ? ? ? 409.1904 266.1024 ? ? ? 6 bmse010060 1 C7 ? C ? ? ? ? 256.1248 110.0352 ? ? ? 7 bmse010060 1 C8 ? C ? ? ? ? 203.4112 127.1616 ? ? ? 8 bmse010060 1 C9 ? C ? ? ? ? 293.8848 270.1248 ? ? ? 9 bmse010060 1 C10 ? C ? ? ? ? 346.5664 252.9056 ? ? ? 10 bmse010060 1 C11 G C ? ? ? ? 305.3120 164.3872 ? ? ? 11 bmse010060 1 C12 G C ? ? ? ? 244.6016 216.0256 ? ? ? 12 bmse010060 1 C13 AcC=O C ? ? ? ? 173.7440 35.8624 ? ? ? 13 bmse010060 1 C14 AcC=O C ? ? ? ? 376.3904 344.1568 ? ? ? 14 bmse010060 1 C15 1 C ? ? ? ? 234.7104 133.8176 ? ? ? 15 bmse010060 1 C16 1 C ? ? ? ? 315.2544 246.3072 ? ? ? 16 bmse010060 1 C17 B C ? ? ? ? 275.0336 174.1376 ? ? ? 17 bmse010060 1 C18 B C ? ? ? ? 275.0336 206.1376 ? ? ? 18 bmse010060 1 C19 3 C ? ? ? ? 246.2368 79.6032 ? ? ? 19 bmse010060 1 C20 5 C ? ? ? ? 193.5232 96.7296 ? ? ? 20 bmse010060 1 C21 3 C ? ? ? ? 303.8240 300.5408 ? ? ? 21 bmse010060 1 C22 5 C ? ? ? ? 356.5088 283.3216 ? ? ? 22 bmse010060 1 C23 A C ? ? ? ? 244.6016 164.2496 ? ? ? 23 bmse010060 1 C24 A C ? ? ? ? 305.3120 215.8912 ? ? ? 24 bmse010060 1 C25 4 C ? ? ? ? 214.9344 72.9472 ? ? ? 25 bmse010060 1 C26 4 C ? ? ? ? 335.1360 307.1392 ? ? ? 26 bmse010060 1 O27 ? O ? ? ? ? 152.3328 59.6416 ? ? ? 27 bmse010060 1 O28 ? O ? ? ? ? 397.7600 320.3392 ? ? ? 28 bmse010060 1 O29 ? O ? ? ? ? 267.6480 55.8208 ? ? ? 29 bmse010060 1 O30 ? O ? ? ? ? 162.2208 90.0768 ? ? ? 30 bmse010060 1 O31 ? O ? ? ? ? 282.4544 324.3584 ? ? ? 31 bmse010060 1 O32 ? O ? ? ? ? 387.8208 289.9200 ? ? ? 32 bmse010060 1 O33 ? O ? ? ? ? 225.7920 190.1376 ? ? ? 33 bmse010060 1 O34 ? O ? ? ? ? 323.9872 190.1376 ? ? ? 34 bmse010060 1 O35 ? O ? ? ? ? 205.0464 42.5152 ? ? ? 35 bmse010060 1 O36 ? O ? ? ? ? 345.0784 337.5552 ? ? ? 36 bmse010060 1 H37 AcMe H ? ? ? ? 144.9869 11.5575 ? ? ? 37 bmse010060 1 H38 AcMe H ? ? ? ? 157.7257 -13.4419 ? ? ? 38 bmse010060 1 H39 AcMe H ? ? ? ? 182.7251 -0.7031 ? ? ? 39 bmse010060 1 H40 AcMe H ? ? ? ? 405.1909 368.4085 ? ? ? 40 bmse010060 1 H41 AcMe H ? ? ? ? 392.4971 393.4309 ? ? ? 41 bmse010060 1 H42 AcMe H ? ? ? ? 367.4747 380.7372 ? ? ? 42 bmse010060 1 H43 OMe H ? ? ? ? 238.8911 31.5197 ? ? ? 43 bmse010060 1 H44 OMe H ? ? ? ? 251.6291 6.5198 ? ? ? 44 bmse010060 1 H45 OMe H ? ? ? ? 276.6290 19.2579 ? ? ? 45 bmse010060 1 H46 OMe H ? ? ? ? 155.5535 127.1317 ? ? ? 46 bmse010060 1 H47 OMe H ? ? ? ? 127.5339 128.5999 ? ? ? 47 bmse010060 1 H48 OMe H ? ? ? ? 126.0657 100.5803 ? ? ? 48 bmse010060 1 H49 OMe H ? ? ? ? 311.2522 348.6119 ? ? ? 49 bmse010060 1 H50 OMe H ? ? ? ? 298.5561 373.6331 ? ? ? 50 bmse010060 1 H51 OMe H ? ? ? ? 273.5349 360.9370 ? ? ? 51 bmse010060 1 H52 OMe H ? ? ? ? 394.4230 252.8528 ? ? ? 52 bmse010060 1 H53 OMe H ? ? ? ? 422.4399 251.3350 ? ? ? 53 bmse010060 1 H54 OMe H ? ? ? ? 423.9578 279.3519 ? ? ? 54 bmse010060 1 H55 A2 H ? ? ? ? 275.5312 114.1603 ? ? ? 55 bmse010060 1 H56 A6 H ? ? ? ? 190.1349 141.9050 ? ? ? 56 bmse010060 1 H57 A2 H ? ? ? ? 274.4713 266.0332 ? ? ? 57 bmse010060 1 H58 A6 H ? ? ? ? 359.8160 238.1383 ? ? ? 58 bmse010060 1 H59 G1 H ? ? ? ? 297.2792 146.2461 ? ? ? 59 bmse010060 1 H60 G2 H ? ? ? ? 322.5082 154.4920 ? ? ? 60 bmse010060 1 H61 G1 H ? ? ? ? 252.6714 234.1503 ? ? ? 61 bmse010060 1 H62 G2 H ? ? ? ? 227.4198 225.9459 ? ? ? 62 bmse010060 1 H63 B H ? ? ? ? 275.0596 154.2976 ? ? ? 63 bmse010060 1 H64 B H ? ? ? ? 275.0587 225.9776 ? ? ? 64 bmse010060 1 H65 A H ? ? ? ? 225.0057 161.1467 ? ? ? 65 bmse010060 1 H66 A H ? ? ? ? 324.9119 218.9686 ? ? ? 66 bmse010060 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 bmse010060 1 C2 C2 BMRB bmse010060 1 C3 C3 BMRB bmse010060 1 C4 C4 BMRB bmse010060 1 C5 C5 BMRB bmse010060 1 C6 C6 BMRB bmse010060 1 C7 C7 BMRB bmse010060 1 C8 C8 BMRB bmse010060 1 C9 C9 BMRB bmse010060 1 C10 C10 BMRB bmse010060 1 C11 C11 BMRB bmse010060 1 C12 C12 BMRB bmse010060 1 C13 C13 BMRB bmse010060 1 C14 C14 BMRB bmse010060 1 C15 C15 BMRB bmse010060 1 C16 C16 BMRB bmse010060 1 C17 C17 BMRB bmse010060 1 C18 C18 BMRB bmse010060 1 C19 C19 BMRB bmse010060 1 C20 C20 BMRB bmse010060 1 C21 C21 BMRB bmse010060 1 C22 C22 BMRB bmse010060 1 C23 C23 BMRB bmse010060 1 C24 C24 BMRB bmse010060 1 C25 C25 BMRB bmse010060 1 C26 C26 BMRB bmse010060 1 O27 O27 BMRB bmse010060 1 O28 O28 BMRB bmse010060 1 O29 O29 BMRB bmse010060 1 O30 O30 BMRB bmse010060 1 O31 O31 BMRB bmse010060 1 O32 O32 BMRB bmse010060 1 O33 O33 BMRB bmse010060 1 O34 O34 BMRB bmse010060 1 O35 O35 BMRB bmse010060 1 O36 O36 BMRB bmse010060 1 H37 H37 BMRB bmse010060 1 H38 H38 BMRB bmse010060 1 H39 H39 BMRB bmse010060 1 H40 H40 BMRB bmse010060 1 H41 H41 BMRB bmse010060 1 H42 H42 BMRB bmse010060 1 H43 H43 BMRB bmse010060 1 H44 H44 BMRB bmse010060 1 H45 H45 BMRB bmse010060 1 H46 H46 BMRB bmse010060 1 H47 H47 BMRB bmse010060 1 H48 H48 BMRB bmse010060 1 H49 H49 BMRB bmse010060 1 H50 H50 BMRB bmse010060 1 H51 H51 BMRB bmse010060 1 H52 H52 BMRB bmse010060 1 H53 H53 BMRB bmse010060 1 H54 H54 BMRB bmse010060 1 H55 H55 BMRB bmse010060 1 H56 H56 BMRB bmse010060 1 H57 H57 BMRB bmse010060 1 H58 H58 BMRB bmse010060 1 H59 H59 BMRB bmse010060 1 H60 H60 BMRB bmse010060 1 H61 H61 BMRB bmse010060 1 H62 H62 BMRB bmse010060 1 H63 H63 BMRB bmse010060 1 H64 H64 BMRB bmse010060 1 H65 H65 BMRB bmse010060 1 H66 H66 BMRB bmse010060 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 C13 ? bmse010060 1 2 covalent SING C2 C14 ? bmse010060 1 3 covalent SING C3 O29 ? bmse010060 1 4 covalent SING C4 O30 ? bmse010060 1 5 covalent SING C5 O31 ? bmse010060 1 6 covalent SING C6 O32 ? bmse010060 1 7 covalent DOUB C7 C15 ? bmse010060 1 8 covalent SING C7 C19 ? bmse010060 1 9 covalent SING C8 C15 ? bmse010060 1 10 covalent DOUB C8 C20 ? bmse010060 1 11 covalent DOUB C9 C16 ? bmse010060 1 12 covalent SING C9 C21 ? bmse010060 1 13 covalent SING C10 C16 ? bmse010060 1 14 covalent DOUB C10 C22 ? bmse010060 1 15 covalent SING C11 C17 ? bmse010060 1 16 covalent SING C11 O34 ? bmse010060 1 17 covalent SING C12 C18 ? bmse010060 1 18 covalent SING C12 O33 ? bmse010060 1 19 covalent DOUB C13 O27 ? bmse010060 1 20 covalent SING C13 O35 ? bmse010060 1 21 covalent DOUB C14 O28 ? bmse010060 1 22 covalent SING C14 O36 ? bmse010060 1 23 covalent SING C15 C23 ? bmse010060 1 24 covalent SING C16 C24 ? bmse010060 1 25 covalent SING C17 C18 ? bmse010060 1 26 covalent SING C17 C23 ? bmse010060 1 27 covalent SING C18 C24 ? bmse010060 1 28 covalent DOUB C19 C25 ? bmse010060 1 29 covalent SING C19 O29 ? bmse010060 1 30 covalent SING C20 C25 ? bmse010060 1 31 covalent SING C20 O30 ? bmse010060 1 32 covalent DOUB C21 C26 ? bmse010060 1 33 covalent SING C21 O31 ? bmse010060 1 34 covalent SING C22 C26 ? bmse010060 1 35 covalent SING C22 O32 ? bmse010060 1 36 covalent SING C23 O33 ? bmse010060 1 37 covalent SING C24 O34 ? bmse010060 1 38 covalent SING C25 O35 ? bmse010060 1 39 covalent SING C26 O36 ? bmse010060 1 40 covalent SING C1 H37 ? bmse010060 1 41 covalent SING C1 H38 ? bmse010060 1 42 covalent SING C1 H39 ? bmse010060 1 43 covalent SING C2 H40 ? bmse010060 1 44 covalent SING C2 H41 ? bmse010060 1 45 covalent SING C2 H42 ? bmse010060 1 46 covalent SING C3 H43 ? bmse010060 1 47 covalent SING C3 H44 ? bmse010060 1 48 covalent SING C3 H45 ? bmse010060 1 49 covalent SING C4 H46 ? bmse010060 1 50 covalent SING C4 H47 ? bmse010060 1 51 covalent SING C4 H48 ? bmse010060 1 52 covalent SING C5 H49 ? bmse010060 1 53 covalent SING C5 H50 ? bmse010060 1 54 covalent SING C5 H51 ? bmse010060 1 55 covalent SING C6 H52 ? bmse010060 1 56 covalent SING C6 H53 ? bmse010060 1 57 covalent SING C6 H54 ? bmse010060 1 58 covalent SING C7 H55 ? bmse010060 1 59 covalent SING C8 H56 ? bmse010060 1 60 covalent SING C9 H57 ? bmse010060 1 61 covalent SING C10 H58 ? bmse010060 1 62 covalent SING C11 H59 ? bmse010060 1 63 covalent SING C11 H60 ? bmse010060 1 64 covalent SING C12 H61 ? bmse010060 1 65 covalent SING C12 H62 ? bmse010060 1 66 covalent SING C17 H63 ? bmse010060 1 67 covalent SING C18 H64 ? bmse010060 1 68 covalent SING C23 H65 ? bmse010060 1 69 covalent SING C24 H66 ? bmse010060 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 111677953 sid ? 'Syringylresinol diacetate' ? 'matching entry' ? bmse010060 1 yes USDA_NMR_database 123 'Compound Number' ? 'Syringylresinol diacetate' ? 'matching entry' ? bmse010060 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 bmse010060 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse010060 _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 diacetate' 'natural abundance' 1 $Syringylresinol-diacetate ? Solute 40 ? ? mg/ml ? 'Sally Ralph' 'Syringylresinol diacetate' n/a bmse010060 1 2 CDCl3 ? 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010060 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_2 _Sample.Sf_category sample _Sample.Sf_framecode sample_2 _Sample.Entry_ID bmse010060 _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 diacetate' 'natural abundance' 1 $Syringylresinol-diacetate ? Solute 40 ? ? mg/ml ? 'Sally Ralph' 'Syringylresinol diacetate' n/a bmse010060 2 2 acetone '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010060 2 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_3 _Sample.Sf_category sample _Sample.Sf_framecode sample_3 _Sample.Entry_ID bmse010060 _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 diacetate' 'natural abundance' 1 $Syringylresinol-diacetate ? Solute 40 ? ? mg/ml ? 'Sally Ralph' 'Syringylresinol diacetate' n/a bmse010060 3 2 DMSO '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010060 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 bmse010060 _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 bmse010060 1 temperature 297 ? K bmse010060 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse010060 _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 ? ? bmse010060 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Processing bmse010060 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 bmse010060 _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 bmse010060 _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 ? ? bmse010060 1 2 '1D 13C' no ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010060 1 3 '1D 13C' no ? ? 2 $sample_2 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010060 1 4 '1D 13C' no ? ? 3 $sample_3 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010060 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 bmse010060 _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 ? ? ? bmse010060 1 C 13 CDCl3 'solvent carbon' ppm 77.00 internal direct ? ? ? ? bmse010060 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 bmse010060 _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 ? ? ? bmse010060 2 C 13 Acetone-d6 'solvent methyl carbon' ppm 29.83 internal direct ? ? ? ? bmse010060 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 bmse010060 _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 ? ? ? bmse010060 3 C 13 DMSO-d6 'solvent methyl carbon' ppm 39.50 internal direct ? ? ? ? bmse010060 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 bmse010060 _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 bmse010060 1 2 '1D 13C' 1 $sample_1 bmse010060 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 ? ? bmse010060 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 C1 C 13 20.46 ? ? 1 ? ? ? AcMe ? bmse010060 1 2 1 1 1 C2 C 13 20.46 ? ? 1 ? ? ? AcMe ? bmse010060 1 3 1 1 1 C17 C 13 54.42 ? ? 1 ? ? ? B ? bmse010060 1 4 1 1 1 C18 C 13 54.42 ? ? 1 ? ? ? B ? bmse010060 1 5 1 1 1 C3 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010060 1 6 1 1 1 C4 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010060 1 7 1 1 1 C5 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010060 1 8 1 1 1 C6 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010060 1 9 1 1 1 C11 C 13 72.11 ? ? 1 ? ? ? G ? bmse010060 1 10 1 1 1 C12 C 13 72.11 ? ? 1 ? ? ? G ? bmse010060 1 11 1 1 1 C23 C 13 85.85 ? ? 1 ? ? ? A ? bmse010060 1 12 1 1 1 C24 C 13 85.85 ? ? 1 ? ? ? A ? bmse010060 1 13 1 1 1 C55 C 13 102.29 ? ? 1 ? ? ? 2 ? bmse010060 1 14 1 1 1 C57 C 13 102.29 ? ? 1 ? ? ? 2 ? bmse010060 1 15 1 1 1 C56 C 13 102.29 ? ? 1 ? ? ? 6 ? bmse010060 1 16 1 1 1 C58 C 13 102.29 ? ? 1 ? ? ? 6 ? bmse010060 1 17 1 1 1 C15 C 13 128.06 ? ? 1 ? ? ? 1 ? bmse010060 1 18 1 1 1 C16 C 13 128.06 ? ? 1 ? ? ? 1 ? bmse010060 1 19 1 1 1 C25 C 13 139.63 ? ? 1 ? ? ? 4 ? bmse010060 1 20 1 1 1 C26 C 13 139.63 ? ? 1 ? ? ? 4 ? bmse010060 1 21 1 1 1 C19 C 13 152.30 ? ? 1 ? ? ? 3 ? bmse010060 1 22 1 1 1 C21 C 13 152.30 ? ? 1 ? ? ? 3 ? bmse010060 1 23 1 1 1 C20 C 13 152.30 ? ? 1 ? ? ? 5 ? bmse010060 1 24 1 1 1 C22 C 13 152.30 ? ? 1 ? ? ? 5 ? bmse010060 1 25 1 1 1 C13 C 13 168.76 ? ? 1 ? ? ? AcC=O ? bmse010060 1 26 1 1 1 C14 C 13 168.76 ? ? 1 ? ? ? AcC=O ? bmse010060 1 27 1 1 1 H37 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 28 1 1 1 H38 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 29 1 1 1 H39 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 30 1 1 1 H40 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 31 1 1 1 H41 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 32 1 1 1 H42 H 1 2.33 ? ? 1 ? ? ? AcMe ? bmse010060 1 33 1 1 1 H63 H 1 3.09 ? ? 1 ? ? ? B ? bmse010060 1 34 1 1 1 H64 H 1 3.09 ? ? 1 ? ? ? B ? bmse010060 1 35 1 1 1 H43 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 36 1 1 1 H44 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 37 1 1 1 H45 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 38 1 1 1 H46 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 39 1 1 1 H47 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 40 1 1 1 H48 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 41 1 1 1 H49 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 42 1 1 1 H50 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 43 1 1 1 H51 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 44 1 1 1 H52 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 45 1 1 1 H53 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 46 1 1 1 H54 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010060 1 47 1 1 1 H59 H 1 3.95 ? ? 1 ? ? ? G1 ? bmse010060 1 48 1 1 1 H60 H 1 4.31 ? ? 1 ? ? ? G2 ? bmse010060 1 49 1 1 1 H61 H 1 3.95 ? ? 1 ? ? ? G1 ? bmse010060 1 50 1 1 1 H62 H 1 4.31 ? ? 1 ? ? ? G2 ? bmse010060 1 51 1 1 1 H65 H 1 4.77 ? ? 1 ? ? ? A ? bmse010060 1 52 1 1 1 H66 H 1 4.77 ? ? 1 ? ? ? A ? bmse010060 1 53 1 1 1 H55 H 1 6.59 ? ? 1 ? ? ? A2 ? bmse010060 1 54 1 1 1 H57 H 1 6.59 ? ? 1 ? ? ? A2 ? bmse010060 1 55 1 1 1 H56 H 1 6.59 ? ? 1 ? ? ? A6 ? bmse010060 1 56 1 1 1 H58 H 1 6.59 ? ? 1 ? ? ? A6 ? bmse010060 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 bmse010060 _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 bmse010060 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 ? ? bmse010060 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 C1 C 13 20.26 ? ? 1 ? ? ? AcMe ? bmse010060 2 2 1 1 1 C2 C 13 20.26 ? ? 1 ? ? ? AcMe ? bmse010060 2 3 1 1 1 C17 C 13 55.41 ? ? 1 ? ? ? B ? bmse010060 2 4 1 1 1 C18 C 13 55.41 ? ? 1 ? ? ? B ? bmse010060 2 5 1 1 1 C3 C 13 56.46 ? ? 1 ? ? ? OMe ? bmse010060 2 6 1 1 1 C4 C 13 56.46 ? ? 1 ? ? ? OMe ? bmse010060 2 7 1 1 1 C5 C 13 56.46 ? ? 1 ? ? ? OMe ? bmse010060 2 8 1 1 1 C6 C 13 56.46 ? ? 1 ? ? ? OMe ? bmse010060 2 9 1 1 1 C11 C 13 72.71 ? ? 1 ? ? ? G ? bmse010060 2 10 1 1 1 C12 C 13 72.71 ? ? 1 ? ? ? G ? bmse010060 2 11 1 1 1 C23 C 13 86.51 ? ? 1 ? ? ? A ? bmse010060 2 12 1 1 1 C24 C 13 86.51 ? ? 1 ? ? ? A ? bmse010060 2 13 1 1 1 C55 C 13 103.30 ? ? 1 ? ? ? 2 ? bmse010060 2 14 1 1 1 C57 C 13 103.30 ? ? 1 ? ? ? 2 ? bmse010060 2 15 1 1 1 C56 C 13 103.30 ? ? 1 ? ? ? 6 ? bmse010060 2 16 1 1 1 C58 C 13 103.30 ? ? 1 ? ? ? 6 ? bmse010060 2 17 1 1 1 C15 C 13 128.91 ? ? 1 ? ? ? 1 ? bmse010060 2 18 1 1 1 C16 C 13 128.91 ? ? 1 ? ? ? 1 ? bmse010060 2 19 1 1 1 C25 C 13 141.41 ? ? 1 ? ? ? 4 ? bmse010060 2 20 1 1 1 C26 C 13 141.41 ? ? 1 ? ? ? 4 ? bmse010060 2 21 1 1 1 C19 C 13 153.23 ? ? 1 ? ? ? 3 ? bmse010060 2 22 1 1 1 C21 C 13 153.23 ? ? 1 ? ? ? 3 ? bmse010060 2 23 1 1 1 C20 C 13 153.23 ? ? 1 ? ? ? 5 ? bmse010060 2 24 1 1 1 C22 C 13 153.23 ? ? 1 ? ? ? 5 ? bmse010060 2 25 1 1 1 C13 C 13 168.59 ? ? 1 ? ? ? AcC=O ? bmse010060 2 26 1 1 1 C14 C 13 168.59 ? ? 1 ? ? ? AcC=O ? bmse010060 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 bmse010060 _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 bmse010060 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 ? ? bmse010060 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 C1 C 13 20.07 ? ? 1 ? ? ? AcMe ? bmse010060 3 2 1 1 1 C2 C 13 20.07 ? ? 1 ? ? ? AcMe ? bmse010060 3 3 1 1 1 C17 C 13 53.72 ? ? 1 ? ? ? B ? bmse010060 3 4 1 1 1 C18 C 13 53.72 ? ? 1 ? ? ? B ? bmse010060 3 5 1 1 1 C3 C 13 55.90 ? ? 1 ? ? ? OMe ? bmse010060 3 6 1 1 1 C4 C 13 55.90 ? ? 1 ? ? ? OMe ? bmse010060 3 7 1 1 1 C5 C 13 55.90 ? ? 1 ? ? ? OMe ? bmse010060 3 8 1 1 1 C6 C 13 55.90 ? ? 1 ? ? ? OMe ? bmse010060 3 9 1 1 1 C11 C 13 71.38 ? ? 1 ? ? ? G ? bmse010060 3 10 1 1 1 C12 C 13 71.38 ? ? 1 ? ? ? G ? bmse010060 3 11 1 1 1 C23 C 13 84.93 ? ? 1 ? ? ? A ? bmse010060 3 12 1 1 1 C24 C 13 84.93 ? ? 1 ? ? ? A ? bmse010060 3 13 1 1 1 C55 C 13 102.44 ? ? 1 ? ? ? 2 ? bmse010060 3 14 1 1 1 C57 C 13 102.44 ? ? 1 ? ? ? 2 ? bmse010060 3 15 1 1 1 C56 C 13 102.44 ? ? 1 ? ? ? 6 ? bmse010060 3 16 1 1 1 C58 C 13 102.44 ? ? 1 ? ? ? 6 ? bmse010060 3 17 1 1 1 C15 C 13 127.04 ? ? 1 ? ? ? 1 ? bmse010060 3 18 1 1 1 C16 C 13 127.04 ? ? 1 ? ? ? 1 ? bmse010060 3 19 1 1 1 C25 C 13 140.03 ? ? 1 ? ? ? 4 ? bmse010060 3 20 1 1 1 C26 C 13 140.03 ? ? 1 ? ? ? 4 ? bmse010060 3 21 1 1 1 C19 C 13 151.60 ? ? 1 ? ? ? 3 ? bmse010060 3 22 1 1 1 C21 C 13 151.60 ? ? 1 ? ? ? 3 ? bmse010060 3 23 1 1 1 C20 C 13 151.60 ? ? 1 ? ? ? 5 ? bmse010060 3 24 1 1 1 C22 C 13 151.60 ? ? 1 ? ? ? 5 ? bmse010060 3 25 1 1 1 C13 C 13 168.01 ? ? 1 ? ? ? AcC=O ? bmse010060 3 26 1 1 1 C14 C 13 168.01 ? ? 1 ? ? ? AcC=O ? bmse010060 3 stop_ save_