data_bmse010049 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse010049 _Entry.Title Pinoresinol_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.DOI 10.13018/BMSE010049 _Entry.Details ? _Entry.BMRB_internal_directory_name Pinoresinol_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 Pew J. ? ? bmse010049 2 John Ralph ? ? ? bmse010049 3 Sally Ralph ? ? ? bmse010049 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 bmse010049 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 3 bmse010049 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '13C chemical shifts' 72 bmse010049 '1H chemical shifts' 26 bmse010049 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' bmse010049 2 . . 2009-11-11 2009-05-26 update BMRB 'added author and source information' bmse010049 3 . . 2010-10-08 2009-05-26 update BMRB 'Removed empty loops for database compliance' bmse010049 4 . . 2010-12-01 2009-05-26 update BMRB 'Set correct NMR STAR version' bmse010049 5 . . 2011-04-04 2009-05-26 update BMRB 'Added Provenance tag to chem_comp' bmse010049 6 . . 2011-09-07 2009-05-26 update BMRB 'Ensured correct reference IDs' bmse010049 7 . . 2011-09-09 2009-05-26 update BMRB 'Brought up to date with latest Dictionary' bmse010049 8 . . 2011-12-14 2009-05-26 update BMRB 'Set Assembly.Name to match Chem_comp.name' bmse010049 9 . . 2011-12-16 2009-05-26 update BMRB 'Standardized solvent' bmse010049 10 . . 2012-02-24 2009-05-26 update BMRB 'Set Raw_data_flag to no, since there are no raw data' bmse010049 11 . . 2012-09-13 2009-05-26 update BMRB 'Added PubChem SID 111677943 to database loop' bmse010049 12 . . 2013-04-05 2009-05-26 update BMRB 'Adding molecule category to chem_comp Details' bmse010049 13 . . 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse010049 14 . . 2018-07-10 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse010049 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse010049 _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. ? bmse010049 1 2 John Ralph ? ? ? bmse010049 1 3 Larry Landucci ? L. ? bmse010049 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse010049 _Assembly.ID 1 _Assembly.Name 'Pinoresinol 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 Pinoresinol-diacetate 1 $Pinoresinol-diacetate yes native no no ? ? ? bmse010049 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_Pinoresinol-diacetate _Entity.Sf_category entity _Entity.Sf_framecode Pinoresinol-diacetate _Entity.Entry_ID bmse010049 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name 'Pinoresinol 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 bmse010049 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 bmse010049 _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 $Pinoresinol-diacetate . n/a 'multiple natural sources' yes 'not applicable' n/a . . Eukaryota Viridiplantae n/a n/a . . . . . . . . . . . . . . . . . . . . . bmse010049 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 bmse010049 _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 $Pinoresinol-diacetate . 'chemical synthesis' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . bmse010049 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 bmse010049 _Chem_comp.ID 1 _Chem_comp.Provenance BMRB _Chem_comp.Name 'Pinoresinol diacetate' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InChI_code InChI=1S/C24H26O8/c1-13(25)31-19-7-5-15(9-21(19)27-3)23-17-11-30-24(18(17)12-29-23)16-6-8-20(32-14(2)26)22(10-16)28-4/h5-10,17-18,23-24H,11-12H2,1-4H3/t17-,18-,23-,24-/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 'C24 H26 O8' _Chem_comp.Formula_weight 442.45844 _Chem_comp.Formula_mono_iso_wt_nat 442.1627678114 _Chem_comp.Formula_mono_iso_wt_13C 466.2432839186 _Chem_comp.Formula_mono_iso_wt_15N 442.1627678114 _Chem_comp.Formula_mono_iso_wt_13C_15N 466.2432839186 _Chem_comp.Image_file_name bmse010049.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name bmse010049.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 'Pinoresinol diacetate' synonym bmse010049 1 'Acetic acid 4-[4-(4-acetoxy-3-methoxyphenyl) tetrahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl ester' synonym bmse010049 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/C24H26O8/c1-13(25)31-19-7-5-15(9-21(19)27-3)23-17-11-30-24(18(17)12-29-23)16-6-8-20(32-14(2)26)22(10-16)28-4/h5-10,17-18,23-24H,11-12H2,1-4H3 ; INCHI na na bmse010049 1 InChI=1S/C24H26O8/c1-13(25)31-19-7-5-15(9-21(19)27-3)23-17-11-30-24(18(17)12-29-23)16-6-8-20(32-14(2)26)22(10-16)28-4/h5-10,17-18,23-24H,11-12H2,1-4H3/t17-,18-,23-,24-/m1/s1 INCHI ALATIS 3.003 bmse010049 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 'Pinoresinol diacetate' Beilstein bmse010049 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=C1)C4C3COC(C2=CC(=C(C=C2)OC(C)=O)OC)C3CO4)OC bmse010049 1 Isomeric CC(=O)OC1=C(C=C(C=C1)C4C3COC(C2=CC(=C(C=C2)OC(C)=O)OC)C3CO4)OC bmse010049 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 ? ? ? ? 165.4010 8.8930 ? ? ? 1 bmse010049 1 C2 AcMe C ? ? ? ? 324.5810 371.1070 ? ? ? 2 bmse010049 1 C3 OMe C ? ? ? ? 253.4360 27.6040 ? ? ? 3 bmse010049 1 C4 OMe C ? ? ? ? 395.4020 253.2760 ? ? ? 4 bmse010049 1 C5 6 C ? ? ? ? 202.4840 123.0190 ? ? ? 5 bmse010049 1 C6 6 C ? ? ? ? 287.3000 257.0440 ? ? ? 6 bmse010049 1 C7 5 C ? ? ? ? 193.2140 94.4860 ? ? ? 7 bmse010049 1 C8 5 C ? ? ? ? 296.6210 285.5620 ? ? ? 8 bmse010049 1 C9 2 C ? ? ? ? 251.9030 106.9630 ? ? ? 9 bmse010049 1 C10 2 C ? ? ? ? 336.6920 240.9040 ? ? ? 10 bmse010049 1 C11 G C ? ? ? ? 298.0160 157.9180 ? ? ? 11 bmse010049 1 C12 G C ? ? ? ? 241.0970 206.3290 ? ? ? 12 bmse010049 1 C13 AcC=O C ? ? ? ? 174.6710 37.4230 ? ? ? 13 bmse010049 1 C14 AcC=O C ? ? ? ? 315.2600 342.5920 ? ? ? 14 bmse010049 1 C15 1 C ? ? ? ? 231.8270 129.2560 ? ? ? 15 bmse010049 1 C16 1 C ? ? ? ? 307.3370 234.7150 ? ? ? 16 bmse010049 1 C17 B C ? ? ? ? 269.6300 167.0590 ? ? ? 17 bmse010049 1 C18 B C ? ? ? ? 269.6300 197.0590 ? ? ? 18 bmse010049 1 C19 4 C ? ? ? ? 213.2870 72.1930 ? ? ? 19 bmse010049 1 C20 4 C ? ? ? ? 325.9760 291.7480 ? ? ? 20 bmse010049 1 C21 3 C ? ? ? ? 242.6300 78.4300 ? ? ? 21 bmse010049 1 C22 3 C ? ? ? ? 346.0130 269.4190 ? ? ? 22 bmse010049 1 C23 A C ? ? ? ? 241.0970 157.7890 ? ? ? 23 bmse010049 1 C24 A C ? ? ? ? 298.0160 206.2000 ? ? ? 24 bmse010049 1 O25 ? O ? ? ? ? 154.5980 59.7190 ? ? ? 25 bmse010049 1 O26 ? O ? ? ? ? 285.9050 336.4060 ? ? ? 26 bmse010049 1 O27 ? O ? ? ? ? 262.7060 56.1370 ? ? ? 27 bmse010049 1 O28 ? O ? ? ? ? 375.3680 275.6050 ? ? ? 28 bmse010049 1 O29 ? O ? ? ? ? 223.4660 182.0590 ? ? ? 29 bmse010049 1 O30 ? O ? ? ? ? 315.5240 182.0590 ? ? ? 30 bmse010049 1 O31 ? O ? ? ? ? 204.0170 43.6600 ? ? ? 31 bmse010049 1 O32 ? O ? ? ? ? 335.2970 320.2630 ? ? ? 32 bmse010049 1 H35 AcMe H ? ? ? ? 147.7114 14.6407 ? ? ? 33 bmse010049 1 H33 AcMe H ? ? ? ? 159.6533 -8.7966 ? ? ? 34 bmse010049 1 H34 AcMe H ? ? ? ? 183.0906 3.1453 ? ? ? 35 bmse010049 1 H36 AcMe H ? ? ? ? 342.2604 365.3279 ? ? ? 36 bmse010049 1 H38 AcMe H ? ? ? ? 330.3600 388.7864 ? ? ? 37 bmse010049 1 H37 AcMe H ? ? ? ? 306.9016 376.8860 ? ? ? 38 bmse010049 1 H39 OMe H ? ? ? ? 235.7462 33.3512 ? ? ? 39 bmse010049 1 H40 OMe H ? ? ? ? 247.6888 9.9142 ? ? ? 40 bmse010049 1 H41 OMe H ? ? ? ? 271.1258 21.8568 ? ? ? 41 bmse010049 1 H44 OMe H ? ? ? ? 381.5576 240.8546 ? ? ? 42 bmse010049 1 H43 OMe H ? ? ? ? 407.8235 239.4316 ? ? ? 43 bmse010049 1 H42 OMe H ? ? ? ? 409.2464 265.6974 ? ? ? 44 bmse010049 1 H45 6 H ? ? ? ? 190.0380 136.8413 ? ? ? 45 bmse010049 1 H46 6 H ? ? ? ? 269.0999 253.2081 ? ? ? 46 bmse010049 1 H47 5 H ? ? ? ? 175.0205 90.6185 ? ? ? 47 bmse010049 1 H48 5 H ? ? ? ? 284.1993 299.4062 ? ? ? 48 bmse010049 1 H49 2 H ? ? ? ? 270.0965 110.8303 ? ? ? 49 bmse010049 1 H50 2 H ? ? ? ? 349.1141 227.0602 ? ? ? 50 bmse010049 1 H51 G1 H ? ? ? ? 290.4852 140.9107 ? ? ? 51 bmse010049 1 H52 G2 H ? ? ? ? 314.1375 148.6413 ? ? ? 52 bmse010049 1 H53 G1 H ? ? ? ? 248.6616 223.3212 ? ? ? 53 bmse010049 1 H54 G2 H ? ? ? ? 224.9885 215.6282 ? ? ? 54 bmse010049 1 H55 B H ? ? ? ? 269.6541 148.4590 ? ? ? 55 bmse010049 1 H56 B H ? ? ? ? 269.6541 215.6590 ? ? ? 56 bmse010049 1 H57 A H ? ? ? ? 222.7260 154.8796 ? ? ? 57 bmse010049 1 H58 A H ? ? ? ? 316.3908 209.0856 ? ? ? 58 bmse010049 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 bmse010049 1 C2 C2 BMRB bmse010049 1 C3 C3 BMRB bmse010049 1 C4 C4 BMRB bmse010049 1 C5 C5 BMRB bmse010049 1 C6 C6 BMRB bmse010049 1 C7 C7 BMRB bmse010049 1 C8 C8 BMRB bmse010049 1 C9 C9 BMRB bmse010049 1 C10 C10 BMRB bmse010049 1 C11 C11 BMRB bmse010049 1 C12 C12 BMRB bmse010049 1 C13 C13 BMRB bmse010049 1 C14 C14 BMRB bmse010049 1 C15 C15 BMRB bmse010049 1 C16 C16 BMRB bmse010049 1 C17 C17 BMRB bmse010049 1 C18 C18 BMRB bmse010049 1 C19 C19 BMRB bmse010049 1 C20 C20 BMRB bmse010049 1 C21 C21 BMRB bmse010049 1 C22 C22 BMRB bmse010049 1 C23 C23 BMRB bmse010049 1 C24 C24 BMRB bmse010049 1 O25 O25 BMRB bmse010049 1 O26 O26 BMRB bmse010049 1 O27 O27 BMRB bmse010049 1 O28 O28 BMRB bmse010049 1 O29 O29 BMRB bmse010049 1 O30 O30 BMRB bmse010049 1 O31 O31 BMRB bmse010049 1 O32 O32 BMRB bmse010049 1 H35 H33 BMRB bmse010049 1 H33 H34 BMRB bmse010049 1 H34 H35 BMRB bmse010049 1 H36 H36 BMRB bmse010049 1 H38 H37 BMRB bmse010049 1 H37 H38 BMRB bmse010049 1 H39 H39 BMRB bmse010049 1 H40 H40 BMRB bmse010049 1 H41 H41 BMRB bmse010049 1 H44 H42 BMRB bmse010049 1 H43 H43 BMRB bmse010049 1 H42 H44 BMRB bmse010049 1 H45 H45 BMRB bmse010049 1 H46 H46 BMRB bmse010049 1 H47 H47 BMRB bmse010049 1 H48 H48 BMRB bmse010049 1 H49 H49 BMRB bmse010049 1 H50 H50 BMRB bmse010049 1 H51 H51 BMRB bmse010049 1 H52 H52 BMRB bmse010049 1 H53 H53 BMRB bmse010049 1 H54 H54 BMRB bmse010049 1 H55 H55 BMRB bmse010049 1 H56 H56 BMRB bmse010049 1 H57 H57 BMRB bmse010049 1 H58 H58 BMRB bmse010049 1 C1 C1 ALATIS bmse010049 1 C2 C2 ALATIS bmse010049 1 C3 C3 ALATIS bmse010049 1 C4 C4 ALATIS bmse010049 1 C5 C5 ALATIS bmse010049 1 C6 C6 ALATIS bmse010049 1 C7 C7 ALATIS bmse010049 1 C8 C8 ALATIS bmse010049 1 C9 C9 ALATIS bmse010049 1 C10 C10 ALATIS bmse010049 1 C11 C11 ALATIS bmse010049 1 C12 C12 ALATIS bmse010049 1 C13 C13 ALATIS bmse010049 1 C14 C14 ALATIS bmse010049 1 C15 C15 ALATIS bmse010049 1 C16 C16 ALATIS bmse010049 1 C17 C17 ALATIS bmse010049 1 C18 C18 ALATIS bmse010049 1 C19 C19 ALATIS bmse010049 1 C20 C20 ALATIS bmse010049 1 C21 C21 ALATIS bmse010049 1 C22 C22 ALATIS bmse010049 1 C23 C23 ALATIS bmse010049 1 C24 C24 ALATIS bmse010049 1 O25 O25 ALATIS bmse010049 1 O26 O26 ALATIS bmse010049 1 O27 O27 ALATIS bmse010049 1 O28 O28 ALATIS bmse010049 1 O29 O29 ALATIS bmse010049 1 O30 O30 ALATIS bmse010049 1 O31 O31 ALATIS bmse010049 1 O32 O32 ALATIS bmse010049 1 H35 H35 ALATIS bmse010049 1 H33 H33 ALATIS bmse010049 1 H34 H34 ALATIS bmse010049 1 H36 H36 ALATIS bmse010049 1 H38 H38 ALATIS bmse010049 1 H37 H37 ALATIS bmse010049 1 H39 H39 ALATIS bmse010049 1 H40 H40 ALATIS bmse010049 1 H41 H41 ALATIS bmse010049 1 H44 H44 ALATIS bmse010049 1 H43 H43 ALATIS bmse010049 1 H42 H42 ALATIS bmse010049 1 H45 H45 ALATIS bmse010049 1 H46 H46 ALATIS bmse010049 1 H47 H47 ALATIS bmse010049 1 H48 H48 ALATIS bmse010049 1 H49 H49 ALATIS bmse010049 1 H50 H50 ALATIS bmse010049 1 H51 H51 ALATIS bmse010049 1 H52 H52 ALATIS bmse010049 1 H53 H53 ALATIS bmse010049 1 H54 H54 ALATIS bmse010049 1 H55 H55 ALATIS bmse010049 1 H56 H56 ALATIS bmse010049 1 H57 H57 ALATIS bmse010049 1 H58 H58 ALATIS bmse010049 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 ? bmse010049 1 2 covalent SING C2 C14 ? bmse010049 1 3 covalent SING C3 O27 ? bmse010049 1 4 covalent SING C4 O28 ? bmse010049 1 5 covalent DOUB C5 C7 ? bmse010049 1 6 covalent SING C5 C15 ? bmse010049 1 7 covalent DOUB C6 C8 ? bmse010049 1 8 covalent SING C6 C16 ? bmse010049 1 9 covalent SING C7 C19 ? bmse010049 1 10 covalent SING C8 C20 ? bmse010049 1 11 covalent DOUB C9 C15 ? bmse010049 1 12 covalent SING C9 C21 ? bmse010049 1 13 covalent DOUB C10 C16 ? bmse010049 1 14 covalent SING C10 C22 ? bmse010049 1 15 covalent SING C11 C17 ? bmse010049 1 16 covalent SING C11 O30 ? bmse010049 1 17 covalent SING C12 C18 ? bmse010049 1 18 covalent SING C12 O29 ? bmse010049 1 19 covalent DOUB C13 O25 ? bmse010049 1 20 covalent SING C13 O31 ? bmse010049 1 21 covalent DOUB C14 O26 ? bmse010049 1 22 covalent SING C14 O32 ? bmse010049 1 23 covalent SING C15 C23 ? bmse010049 1 24 covalent SING C16 C24 ? bmse010049 1 25 covalent SING C17 C18 ? bmse010049 1 26 covalent SING C17 C23 ? bmse010049 1 27 covalent SING C18 C24 ? bmse010049 1 28 covalent DOUB C19 C21 ? bmse010049 1 29 covalent SING C19 O31 ? bmse010049 1 30 covalent DOUB C20 C22 ? bmse010049 1 31 covalent SING C20 O32 ? bmse010049 1 32 covalent SING C21 O27 ? bmse010049 1 33 covalent SING C22 O28 ? bmse010049 1 34 covalent SING C23 O29 ? bmse010049 1 35 covalent SING C24 O30 ? bmse010049 1 36 covalent SING C1 H35 ? bmse010049 1 37 covalent SING C1 H33 ? bmse010049 1 38 covalent SING C1 H34 ? bmse010049 1 39 covalent SING C2 H36 ? bmse010049 1 40 covalent SING C2 H38 ? bmse010049 1 41 covalent SING C2 H37 ? bmse010049 1 42 covalent SING C3 H39 ? bmse010049 1 43 covalent SING C3 H40 ? bmse010049 1 44 covalent SING C3 H41 ? bmse010049 1 45 covalent SING C4 H44 ? bmse010049 1 46 covalent SING C4 H43 ? bmse010049 1 47 covalent SING C4 H42 ? bmse010049 1 48 covalent SING C5 H45 ? bmse010049 1 49 covalent SING C6 H46 ? bmse010049 1 50 covalent SING C7 H47 ? bmse010049 1 51 covalent SING C8 H48 ? bmse010049 1 52 covalent SING C9 H49 ? bmse010049 1 53 covalent SING C10 H50 ? bmse010049 1 54 covalent SING C11 H51 ? bmse010049 1 55 covalent SING C11 H52 ? bmse010049 1 56 covalent SING C12 H53 ? bmse010049 1 57 covalent SING C12 H54 ? bmse010049 1 58 covalent SING C17 H55 ? bmse010049 1 59 covalent SING C18 H56 ? bmse010049 1 60 covalent SING C23 H57 ? bmse010049 1 61 covalent SING C24 H58 ? bmse010049 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 111677943 sid ? 'Pinoresinol diacetate' ? 'matching entry' ? bmse010049 1 yes USDA_NMR_database 109 'Compound Number' ? 'Pinoresinol diacetate' ? 'matching entry' ? bmse010049 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 bmse010049 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse010049 _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 'Pinoresinol diacetate' 'natural abundance' 1 $Pinoresinol-diacetate ? Solute Saturated ? ? mg/ml ? 'John Pew' 'Pinoresinol diacetate' n/a bmse010049 1 2 CDCl3 ? 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010049 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_2 _Sample.Sf_category sample _Sample.Sf_framecode sample_2 _Sample.Entry_ID bmse010049 _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 'Pinoresinol diacetate' 'natural abundance' 1 $Pinoresinol-diacetate ? Solute Saturated ? ? mg/ml ? 'John Pew' 'Pinoresinol diacetate' n/a bmse010049 2 2 acetone '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010049 2 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_3 _Sample.Sf_category sample _Sample.Sf_framecode sample_3 _Sample.Entry_ID bmse010049 _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 'Pinoresinol diacetate' 'natural abundance' 1 $Pinoresinol-diacetate ? Solute Saturated ? ? mg/ml ? 'John Pew' 'Pinoresinol diacetate' n/a bmse010049 3 2 DMSO '100% deuterated' 1 ? ? Solvent 100 ? ? % ? ? ? ? bmse010049 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 bmse010049 _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 bmse010049 1 temperature 297 ? K bmse010049 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse010049 _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 ? ? bmse010049 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Processing bmse010049 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 bmse010049 _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 bmse010049 _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 ? ? bmse010049 1 2 '1D 13C' no ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010049 1 3 '1D 13C' no ? ? 2 $sample_2 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010049 1 4 '1D 13C' no ? ? 3 $sample_3 isotropic 1 $sample_conditions_1 1 $Bruker_250 ? ? bmse010049 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 bmse010049 _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 ? ? ? bmse010049 1 C 13 CDCl3 'solvent carbon' ppm 77.00 internal direct ? ? ? ? bmse010049 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 bmse010049 _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 ? ? ? bmse010049 2 C 13 Acetone-d6 'solvent methyl carbon' ppm 29.83 internal direct ? ? ? ? bmse010049 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 bmse010049 _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 ? ? ? bmse010049 3 C 13 DMSO-d6 'solvent methyl carbon' ppm 39.50 internal direct ? ? ? ? bmse010049 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 bmse010049 _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 bmse010049 1 2 '1D 13C' 1 $sample_1 bmse010049 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 ? ? bmse010049 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 20.62 ? ? 1 ? ? ? AcMe ? bmse010049 1 2 1 1 1 C2 C 13 20.62 ? ? 1 ? ? ? AcMe ? bmse010049 1 3 1 1 1 C17 C 13 54.36 ? ? 1 ? ? ? B ? bmse010049 1 4 1 1 1 C18 C 13 54.36 ? ? 1 ? ? ? B ? bmse010049 1 5 1 1 1 C3 C 13 55.92 ? ? 1 ? ? ? OMe ? bmse010049 1 6 1 1 1 C4 C 13 55.92 ? ? 1 ? ? ? OMe ? bmse010049 1 7 1 1 1 C11 C 13 71.95 ? ? 1 ? ? ? G ? bmse010049 1 8 1 1 1 C12 C 13 71.95 ? ? 1 ? ? ? G ? bmse010049 1 9 1 1 1 C23 C 13 85.50 ? ? 1 ? ? ? A ? bmse010049 1 10 1 1 1 C24 C 13 85.50 ? ? 1 ? ? ? A ? bmse010049 1 11 1 1 1 C9 C 13 109.91 ? ? 1 ? ? ? 2 ? bmse010049 1 12 1 1 1 C10 C 13 109.91 ? ? 1 ? ? ? 2 ? bmse010049 1 13 1 1 1 C5 C 13 117.92 ? ? 1 ? ? ? 6 ? bmse010049 1 14 1 1 1 C6 C 13 117.92 ? ? 1 ? ? ? 6 ? bmse010049 1 15 1 1 1 C7 C 13 122.74 ? ? 1 ? ? ? 5 ? bmse010049 1 16 1 1 1 C8 C 13 122.74 ? ? 1 ? ? ? 5 ? bmse010049 1 17 1 1 1 C19 C 13 139.13 ? ? 1 ? ? ? 4 ? bmse010049 1 18 1 1 1 C20 C 13 139.13 ? ? 1 ? ? ? 4 ? bmse010049 1 19 1 1 1 C15 C 13 140.11 ? ? 1 ? ? ? 1 ? bmse010049 1 20 1 1 1 C16 C 13 140.11 ? ? 1 ? ? ? 1 ? bmse010049 1 21 1 1 1 C21 C 13 151.23 ? ? 1 ? ? ? 3 ? bmse010049 1 22 1 1 1 C22 C 13 151.23 ? ? 1 ? ? ? 3 ? bmse010049 1 23 1 1 1 C13 C 13 168.99 ? ? 1 ? ? ? AcC=O ? bmse010049 1 24 1 1 1 C14 C 13 168.99 ? ? 1 ? ? ? AcC=O ? bmse010049 1 25 1 1 1 H35 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 26 1 1 1 H33 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 27 1 1 1 H34 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 28 1 1 1 H36 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 29 1 1 1 H38 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 30 1 1 1 H37 H 1 2.30 ? ? 1 ? ? ? AcMe ? bmse010049 1 31 1 1 1 H39 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 32 1 1 1 H40 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 33 1 1 1 H41 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 34 1 1 1 H44 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 35 1 1 1 H43 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 36 1 1 1 H42 H 1 3.83 ? ? 1 ? ? ? OMe ? bmse010049 1 37 1 1 1 H55 H 1 3.08 ? ? 1 ? ? ? B ? bmse010049 1 38 1 1 1 H56 H 1 3.08 ? ? 1 ? ? ? B ? bmse010049 1 39 1 1 1 H51 H 1 3.92 ? ? 1 ? ? ? G1 ? bmse010049 1 40 1 1 1 H53 H 1 3.92 ? ? 1 ? ? ? G1 ? bmse010049 1 41 1 1 1 H52 H 1 4.27 ? ? 1 ? ? ? G2 ? bmse010049 1 42 1 1 1 H54 H 1 4.27 ? ? 1 ? ? ? G2 ? bmse010049 1 43 1 1 1 H57 H 1 4.78 ? ? 1 ? ? ? A ? bmse010049 1 44 1 1 1 H58 H 1 4.78 ? ? 1 ? ? ? A ? bmse010049 1 45 1 1 1 H45 H 1 6.88 ? ? 1 ? ? ? 6 ? bmse010049 1 46 1 1 1 H46 H 1 6.88 ? ? 1 ? ? ? 6 ? bmse010049 1 47 1 1 1 H49 H 1 6.99 ? ? 1 ? ? ? 2 ? bmse010049 1 48 1 1 1 H50 H 1 6.99 ? ? 1 ? ? ? 2 ? bmse010049 1 49 1 1 1 H47 H 1 7.00 ? ? 1 ? ? ? 5 ? bmse010049 1 50 1 1 1 H48 H 1 7.00 ? ? 1 ? ? ? 5 ? bmse010049 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 bmse010049 _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 bmse010049 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 ? ? bmse010049 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 20.48 ? ? 1 ? ? ? AcMe ? bmse010049 2 2 1 1 1 C2 C 13 20.48 ? ? 1 ? ? ? AcMe ? bmse010049 2 3 1 1 1 C17 C 13 55.42 ? ? 1 ? ? ? B ? bmse010049 2 4 1 1 1 C18 C 13 55.42 ? ? 1 ? ? ? B ? bmse010049 2 5 1 1 1 C3 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010049 2 6 1 1 1 C4 C 13 56.23 ? ? 1 ? ? ? OMe ? bmse010049 2 7 1 1 1 C11 C 13 72.58 ? ? 1 ? ? ? G ? bmse010049 2 8 1 1 1 C12 C 13 72.58 ? ? 1 ? ? ? G ? bmse010049 2 9 1 1 1 C23 C 13 86.22 ? ? 1 ? ? ? A ? bmse010049 2 10 1 1 1 C24 C 13 86.22 ? ? 1 ? ? ? A ? bmse010049 2 11 1 1 1 C9 C 13 111.12 ? ? 1 ? ? ? 2 ? bmse010049 2 12 1 1 1 C10 C 13 111.12 ? ? 1 ? ? ? 2 ? bmse010049 2 13 1 1 1 C5 C 13 118.63 ? ? 1 ? ? ? 6 ? bmse010049 2 14 1 1 1 C6 C 13 118.63 ? ? 1 ? ? ? 6 ? bmse010049 2 15 1 1 1 C7 C 13 123.46 ? ? 1 ? ? ? 5 ? bmse010049 2 16 1 1 1 C8 C 13 123.46 ? ? 1 ? ? ? 5 ? bmse010049 2 17 1 1 1 C19 C 13 140.15 ? ? 1 ? ? ? 4 ? bmse010049 2 18 1 1 1 C20 C 13 140.15 ? ? 1 ? ? ? 4 ? bmse010049 2 19 1 1 1 C15 C 13 141.80 ? ? 1 ? ? ? 1 ? bmse010049 2 20 1 1 1 C16 C 13 141.80 ? ? 1 ? ? ? 1 ? bmse010049 2 21 1 1 1 C21 C 13 152.28 ? ? 1 ? ? ? 3 ? bmse010049 2 22 1 1 1 C22 C 13 152.28 ? ? 1 ? ? ? 3 ? bmse010049 2 23 1 1 1 C13 C 13 168.98 ? ? 1 ? ? ? AcC=O ? bmse010049 2 24 1 1 1 C14 C 13 168.98 ? ? 1 ? ? ? AcC=O ? bmse010049 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 bmse010049 _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 bmse010049 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 ? ? bmse010049 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 20.28 ? ? 1 ? ? ? AcMe ? bmse010049 3 2 1 1 1 C2 C 13 20.28 ? ? 1 ? ? ? AcMe ? bmse010049 3 3 1 1 1 C17 C 13 53.75 ? ? 1 ? ? ? B ? bmse010049 3 4 1 1 1 C18 C 13 53.75 ? ? 1 ? ? ? B ? bmse010049 3 5 1 1 1 C3 C 13 55.67 ? ? 1 ? ? ? OMe ? bmse010049 3 6 1 1 1 C4 C 13 55.67 ? ? 1 ? ? ? OMe ? bmse010049 3 7 1 1 1 C11 C 13 71.24 ? ? 1 ? ? ? G ? bmse010049 3 8 1 1 1 C12 C 13 71.24 ? ? 1 ? ? ? G ? bmse010049 3 9 1 1 1 C23 C 13 84.64 ? ? 1 ? ? ? A ? bmse010049 3 10 1 1 1 C24 C 13 84.64 ? ? 1 ? ? ? A ? bmse010049 3 11 1 1 1 C9 C 13 110.33 ? ? 1 ? ? ? 2 ? bmse010049 3 12 1 1 1 C10 C 13 110.33 ? ? 1 ? ? ? 2 ? bmse010049 3 13 1 1 1 C5 C 13 117.78 ? ? 1 ? ? ? 6 ? bmse010049 3 14 1 1 1 C6 C 13 117.78 ? ? 1 ? ? ? 6 ? bmse010049 3 15 1 1 1 C7 C 13 122.50 ? ? 1 ? ? ? 5 ? bmse010049 3 16 1 1 1 C8 C 13 122.50 ? ? 1 ? ? ? 5 ? bmse010049 3 17 1 1 1 C19 C 13 138.42 ? ? 1 ? ? ? 4 ? bmse010049 3 18 1 1 1 C20 C 13 138.42 ? ? 1 ? ? ? 4 ? bmse010049 3 19 1 1 1 C15 C 13 140.41 ? ? 1 ? ? ? 1 ? bmse010049 3 20 1 1 1 C16 C 13 140.41 ? ? 1 ? ? ? 1 ? bmse010049 3 21 1 1 1 C21 C 13 150.70 ? ? 1 ? ? ? 3 ? bmse010049 3 22 1 1 1 C22 C 13 150.70 ? ? 1 ? ? ? 3 ? bmse010049 3 23 1 1 1 C13 C 13 168.44 ? ? 1 ? ? ? AcC=O ? bmse010049 3 24 1 1 1 C14 C 13 168.44 ? ? 1 ? ? ? AcC=O ? bmse010049 3 stop_ save_