data_bmst000056 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmst000056 _Entry.Title chorismic_acid _Entry.Version_type update _Entry.Submission_date 2007-01-05 _Entry.Accession_date 2007-01-05 _Entry.Last_release_date 2011-09-14 _Entry.Original_release_date 2007-01-05 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.7 _Entry.Original_NMR_STAR_version 'NMR STAR v3.1' _Entry.Experimental_method NMR _Entry.Experimental_method_subtype theoretical _Entry.Details ? _Entry.BMRB_internal_directory_name chorismic_acid loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.Middle_initials _Entry_author.Family_title _Entry_author.Entry_ID 1 William Westler M. ? bmst000056 2 John Markley L. ? bmst000056 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 metabolics 'Madison Metabolomics Consortium' MMC bmst000056 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID other_data_list 1 bmst000056 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID 'theoretical chemical shifts' 1 bmst000056 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 . . 2007-01-05 2007-01-05 original BMRB 'Original theoretical calculations from NMRFAM' bmst000056 2 . . 2008-11-18 2008-11-18 update BMRB 'updated the file to match latest NMR STAR dictionary' bmst000056 3 . . 2008-11-25 2008-11-25 update BMRB 'fixed enumerations: N should be no' bmst000056 4 . . 2010-09-16 2010-09-16 update BMRB 'Removed Shielding_tensor_list_ID and Shielding_tensor_list_label from theoretical_chem_shifts' bmst000056 5 . . 2011-09-14 2011-09-14 update BMRB 'Partially brought up to date with latest Dictionary' bmst000056 6 . . 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmst000056 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.URI _Auxiliary_files.DOI _Auxiliary_files.Path _Auxiliary_files.Format _Auxiliary_files.Details _Auxiliary_files.Entry_ID 1 . . chorismic_acid_3550_opt.pdb x-chemical/x-pdb 'Name of the file containing the atomic coordinates' bmst000056 2 . . chorismic_acid_3550.g03.shifts text/plain 'Name of the file containing theoretical chemical shift data' bmst000056 stop_ save_ ############### # Citations # ############### save_citations _Citation.Sf_category citations _Citation.Sf_framecode citations _Citation.Entry_ID bmst000056 _Citation.ID 1 _Citation.Class 'reference citation' _Citation.PubMed_ID 18940862 _Citation.Title 'Database resources of the National Center for Biotechnology Information.' _Citation.Status published _Citation.Type internet _Citation.WWW_URL http://pubchem.ncbi.nlm.nih.gov/ _Citation.Year 2006 _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 D. Wheeler D. L. ? bmst000056 1 2 T. Barrett T. ? ? bmst000056 1 3 D. Benson D. A. ? bmst000056 1 4 S. Bryant S. H. ? bmst000056 1 5 K. Canese K. ? ? bmst000056 1 6 V. Chetvenin V. ? ? bmst000056 1 7 D. Church D. M. ? bmst000056 1 8 M. DiCuccio M. ? ? bmst000056 1 9 R. Edgar R. ? ? bmst000056 1 10 S. Federhen S. ? ? bmst000056 1 11 L. Geer L. Y. ? bmst000056 1 12 W. Helmberg W. ? ? bmst000056 1 13 Y. Kapustin Y. ? ? bmst000056 1 14 D. Kenton D. L. ? bmst000056 1 15 O. Khovayko O. ? ? bmst000056 1 16 D. Lipman D. J. ? bmst000056 1 17 T. Madden T. L. ? bmst000056 1 18 D. Maglott D. R. ? bmst000056 1 19 J. Ostell J. ? ? bmst000056 1 20 K. Pruitt K. D. ? bmst000056 1 21 G. Schuler G. D. ? bmst000056 1 22 L. Schriml L. M. ? bmst000056 1 23 E. Sequeira E. ? ? bmst000056 1 24 S. Sherry S. T. ? bmst000056 1 25 K. Sirotkin K. ? ? bmst000056 1 26 A. Souvorov A. ? ? bmst000056 1 27 G. Starchenko G. ? ? bmst000056 1 28 T. Suzek T. O. ? bmst000056 1 29 R. Tatusov R. ? ? bmst000056 1 30 T. Tatusova T. A. ? bmst000056 1 31 L. Bagner L. ? ? bmst000056 1 32 E. Yaschenko E. ? ? bmst000056 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmst000056 _Assembly.ID 1 _Assembly.Name ASSEMBLY_NAME _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 ENT_NAME 1 $chorismic_acid yes native no no ? ? ? bmst000056 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_chorismic_acid _Entity.Sf_category entity _Entity.Sf_framecode chorismic_acid _Entity.Entry_ID bmst000056 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name 'chorismic acid' _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_monomer no _Entity.Nstd_chirality no _Entity.Nstd_linkage no _Entity.Paramagnetic no _Entity.Thiol_state 'not reported' loop_ _Entity_comp_index.ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 1 $chem_comp_1 bmst000056 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 bmst000056 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name 'chorismic acid' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InChI_code ; InChI=1/C10H10O6/c1-5(9(12)13)16-8-4-6(10(14)15)2-3-7(8)11/h2-4,7-8,11H,1H2,(H,12,13)(H,14,15)/t7-,8-/m1/s1/f/h12,14H ; _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 no _Chem_comp.Formula 'C10 H10 O6' _Chem_comp.Formula_weight 226.1828000000 _Chem_comp.Formula_mono_iso_wt_nat 226.047738054 _Chem_comp.Formula_mono_iso_wt_13C 236.081286432 _Chem_comp.Formula_mono_iso_wt_15N 226.047738054 _Chem_comp.Formula_mono_iso_wt_13C_15N 236.081286432 _Chem_comp.Image_file_name bmst000056.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name bmst000056.mol _Chem_comp.Struct_file_format mol _Chem_comp.Stereochem_param_file_name ? _Chem_comp.Details ? _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 '1,5-Cyclohexadiene-1-carboxylic acid, 3-((1-carboxyethenyl)oxy)-4-hydroxy-, (3R-trans)-' synonym bmst000056 1 'CHORISMIC ACID' synonym bmst000056 1 55508-12-8 synonym bmst000056 1 Chorismate synonym bmst000056 1 'Chorismic acid' synonym bmst000056 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 '(3R,4R)-3-(1-carboxyethenoxy)-4-hydroxy-cyclohexa-1,5-diene-1-carboxylic acid' IUPAC bmst000056 1 '(3R,4R)-3-(1-carboxyethenoxy)-4-hydroxy-cyclohexa-1,5-diene-1-carboxylic acid' IUPAC_TRADITIONAL bmst000056 1 '(3R,4R)-3-(1-carboxyethenoxy)-4-hydroxy-cyclohexa-1,5-diene-1-carboxylic acid' IUPAC_CAS bmst000056 1 '(3R,4R)-3-(1-carboxyethenoxy)-4-hydroxy-cyclohexa-1,5-diene-1-carboxylic acid' IUPAC_OPENEYE bmst000056 1 '(3R,4R)-3-(1-carboxyethenoxy)-4-hydroxy-cyclohexa-1,5-diene-1-carboxylic acid' IUPAC_SYSTEMATIC bmst000056 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID Isomeric C=C(C(=O)O)O[C@@H]1C=C(C=C[C@H]1O)C(=O)O bmst000056 1 Canonical C=C(C(=O)O)OC1C=C(C=CC1O)C(=O)O bmst000056 1 stop_ loop_ _Chem_comp_atom.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 C ? ? ? ? 4.2690 -0.1550 0.095 0.309 0.545 1 bmst000056 1 C2 C ? ? ? ? 5.1350 -0.6550 -0.762 -0.729 -0.133 2 bmst000056 1 C3 C ? ? ? ? 3.4030 -0.6550 -0.720 1.547 0.919 3 bmst000056 1 O4 O ? ? ? ? 4.2690 0.8450 1.170 0.786 -0.274 4 bmst000056 1 C5 C ? ? ? ? 5.1350 -1.6550 -2.042 -0.885 0.259 5 bmst000056 1 C6 C ? ? ? ? 3.4030 -1.6550 -1.987 1.134 1.625 6 bmst000056 1 O7 O ? ? ? ? 2.5369 -0.1550 0.026 2.420 1.748 7 bmst000056 1 C8 C ? ? ? ? 5.1350 1.3450 2.295 0.026 -0.395 8 bmst000056 1 C9 C ? ? ? ? 4.2690 -2.1550 -2.617 -0.001 1.290 9 bmst000056 1 C10 C ? ? ? ? 6.0010 -2.1550 -2.840 -1.972 -0.376 10 bmst000056 1 C11 C ? ? ? ? 5.1350 2.3450 3.392 0.731 -1.136 11 bmst000056 1 C12 C ? ? ? ? 6.0010 0.8450 2.507 -1.213 0.069 12 bmst000056 1 O13 O ? ? ? ? 6.0010 -3.1550 -4.108 -2.030 0.106 13 bmst000056 1 O14 O ? ? ? ? 6.8671 -1.6550 -2.435 -2.736 -1.227 14 bmst000056 1 O15 O ? ? ? ? 6.0010 2.8450 3.076 2.008 -1.447 15 bmst000056 1 O16 O ? ? ? ? 4.2690 2.8450 4.457 0.225 -1.419 16 bmst000056 1 H17 H ? ? ? ? 4.8059 0.1550 0.517 -0.107 1.476 17 bmst000056 1 H18 H ? ? ? ? 5.6719 -0.3450 -0.334 -1.379 -0.890 18 bmst000056 1 H19 H ? ? ? ? 3.4030 -0.0350 -0.995 2.058 -0.024 19 bmst000056 1 H20 H ? ? ? ? 2.8660 -1.9650 -2.394 1.831 2.352 20 bmst000056 1 H21 H ? ? ? ? 2.0000 -0.4650 0.812 2.675 1.235 21 bmst000056 1 H22 H ? ? ? ? 4.2690 -2.7750 -3.563 -0.279 1.741 22 bmst000056 1 H23 H ? ? ? ? 6.0010 0.2250 1.761 -1.784 0.606 23 bmst000056 1 H24 H ? ? ? ? 6.5380 1.1550 3.472 -1.668 -0.109 24 bmst000056 1 H25 H ? ? ? ? 6.5380 -3.4650 -4.538 -2.767 -0.367 25 bmst000056 1 H26 H ? ? ? ? 6.0010 3.4650 3.854 2.359 -1.920 26 bmst000056 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 ? bmst000056 1 C2 C2 ? bmst000056 1 C3 C3 ? bmst000056 1 O4 O4 ? bmst000056 1 C5 C5 ? bmst000056 1 C6 C6 ? bmst000056 1 O7 O7 ? bmst000056 1 C8 C8 ? bmst000056 1 C9 C9 ? bmst000056 1 C10 C10 ? bmst000056 1 C11 C11 ? bmst000056 1 C12 C12 ? bmst000056 1 O13 O13 ? bmst000056 1 O14 O14 ? bmst000056 1 O15 O15 ? bmst000056 1 O16 O16 ? bmst000056 1 H17 H17 ? bmst000056 1 H18 H18 ? bmst000056 1 H19 H19 ? bmst000056 1 H20 H20 ? bmst000056 1 H21 H21 ? bmst000056 1 H22 H22 ? bmst000056 1 H23 H23 ? bmst000056 1 H24 H24 ? bmst000056 1 H25 H25 ? bmst000056 1 H26 H26 ? bmst000056 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 C2 ? bmst000056 1 2 covalent SING C1 C3 ? bmst000056 1 3 covalent SING C1 O4 ? bmst000056 1 4 covalent SING C1 H17 ? bmst000056 1 5 covalent DOUB C2 C5 ? bmst000056 1 6 covalent SING C2 H18 ? bmst000056 1 7 covalent SING C3 C6 ? bmst000056 1 8 covalent SING C3 O7 ? bmst000056 1 9 covalent SING C3 H19 ? bmst000056 1 10 covalent SING O4 C8 ? bmst000056 1 11 covalent SING C5 C9 ? bmst000056 1 12 covalent SING C5 C10 ? bmst000056 1 13 covalent DOUB C6 C9 ? bmst000056 1 14 covalent SING C6 H20 ? bmst000056 1 15 covalent SING O7 H21 ? bmst000056 1 16 covalent SING C8 C11 ? bmst000056 1 17 covalent DOUB C8 C12 ? bmst000056 1 18 covalent SING C9 H22 ? bmst000056 1 19 covalent SING C10 O13 ? bmst000056 1 20 covalent DOUB C10 O14 ? bmst000056 1 21 covalent SING C11 O15 ? bmst000056 1 22 covalent DOUB C11 O16 ? bmst000056 1 23 covalent SING C12 H23 ? bmst000056 1 24 covalent SING C12 H24 ? bmst000056 1 25 covalent SING O13 H25 ? bmst000056 1 26 covalent SING O15 H26 ? bmst000056 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 155352 sid ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 no PubChem 12039 cid ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 no PubChem 3550 sid ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 no KEGG C00251 'compound ID' ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 no 'CAS Registry' 617-12-9 'registry number' ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 no CHEBI 17333 ? ? 'chorismic acid' ? 'matching entry' ? bmst000056 1 stop_ loop_ _Chem_comp_citation.Citation_ID _Chem_comp_citation.Citation_label _Chem_comp_citation.Entry_ID _Chem_comp_citation.Comp_ID 1 $citations bmst000056 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmst000056 _Software.ID 1 _Software.Name Gaussian _Software.Version ? _Software.Details ? loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID 'Gaussian, Inc.' ? http://www.gaussian.com/home.htm bmst000056 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'geometry optimization' bmst000056 1 'chemical shift calculation' bmst000056 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference _Chem_shift_reference.Entry_ID bmst000056 _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.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 TMS 'methyl protons' ppm 0.00 na direct ? bmst000056 1 C 13 TMS 'methyl carbons' ppm 0.00 na direct ? bmst000056 1 N 15 'ammonia pentamer' nitrogen ppm 0.00 na direct ? bmst000056 1 P 31 'phosphoric acid' phosphorus ppm 0.00 na direct ? bmst000056 1 stop_ save_ save_chem_shifts_calc_type _Chem_shifts_calc_type.Sf_category chem_shifts_calc_type _Chem_shifts_calc_type.Sf_framecode chem_shifts_calc_type _Chem_shifts_calc_type.Entry_ID bmst000056 _Chem_shifts_calc_type.ID 1 _Chem_shifts_calc_type.Calculation_level 'Density Functional Theory' _Chem_shifts_calc_type.Quantum_mechanical_method GIAO _Chem_shifts_calc_type.Quantum_mechanical_theory_level B3LYP _Chem_shifts_calc_type.Quantum_mechanical_basis_set 3-21g** _Chem_shifts_calc_type.Chem_shift_nucleus ? _Chem_shifts_calc_type.Chem_shift_reference_ID 1 _Chem_shifts_calc_type.Chem_shift_reference_label $chem_shift_reference loop_ _Chem_shifts_calc_software.Software_ID _Chem_shifts_calc_software.Software_label _Chem_shifts_calc_software.Entry_ID _Chem_shifts_calc_software.Chem_shifts_calc_type_ID 1 $software_1 bmst000056 1 stop_ save_ ################################# # Theoretical chemical shifts # ################################# save_theoretical_chem_shifts _Theoretical_chem_shift_list.Sf_category theoretical_chem_shifts _Theoretical_chem_shift_list.Sf_framecode theoretical_chem_shifts _Theoretical_chem_shift_list.Entry_ID bmst000056 _Theoretical_chem_shift_list.ID 1 _Theoretical_chem_shift_list.Chem_shifts_calc_type_ID 1 _Theoretical_chem_shift_list.Chem_shifts_calc_type_label $chem_shifts_calc_type _Theoretical_chem_shift_list.Model_atomic_coordinates_ID 1 _Theoretical_chem_shift_list.Model_atomic_coordinates_label $conformer_family_coord_set_1 _Theoretical_chem_shift_list.Fermi_contact_spin_density_units ? _Theoretical_chem_shift_list.Chem_shift_1H_err ? _Theoretical_chem_shift_list.Chem_shift_2H_err ? _Theoretical_chem_shift_list.Chem_shift_13C_err ? _Theoretical_chem_shift_list.Chem_shift_15N_err ? _Theoretical_chem_shift_list.Chem_shift_19F_err ? _Theoretical_chem_shift_list.Chem_shift_31P_err ? _Theoretical_chem_shift_list.Details ? _Theoretical_chem_shift_list.Text_data_format ? _Theoretical_chem_shift_list.Text_data ? loop_ _Theoretical_chem_shift.ID _Theoretical_chem_shift.Entity_assembly_ID _Theoretical_chem_shift.Entity_ID _Theoretical_chem_shift.Comp_index_ID _Theoretical_chem_shift.Comp_ID _Theoretical_chem_shift.Atom_ID _Theoretical_chem_shift.Atom_type _Theoretical_chem_shift.Fermi_contact_spin_density _Theoretical_chem_shift.Val _Theoretical_chem_shift.Val_err _Theoretical_chem_shift.Auth_seq_ID _Theoretical_chem_shift.Auth_comp_ID _Theoretical_chem_shift.Auth_atom_ID _Theoretical_chem_shift.Entry_ID _Theoretical_chem_shift.Theoretical_chem_shift_list_ID 1 1 1 1 1 C1 C ? 84.981 ? chorismic_acid ? ? bmst000056 1 2 1 1 1 1 C2 C ? 141.806 ? chorismic_acid ? ? bmst000056 1 3 1 1 1 1 C3 C ? 72.700 ? chorismic_acid ? ? bmst000056 1 4 1 1 1 1 C5 C ? 132.362 ? chorismic_acid ? ? bmst000056 1 5 1 1 1 1 C6 C ? 137.884 ? chorismic_acid ? ? bmst000056 1 6 1 1 1 1 C8 C ? 155.092 ? chorismic_acid ? ? bmst000056 1 7 1 1 1 1 C9 C ? 125.609 ? chorismic_acid ? ? bmst000056 1 8 1 1 1 1 C10 C ? 168.013 ? chorismic_acid ? ? bmst000056 1 9 1 1 1 1 C11 C ? 168.378 ? chorismic_acid ? ? bmst000056 1 10 1 1 1 1 C12 C ? 101.246 ? chorismic_acid ? ? bmst000056 1 11 1 1 1 1 H17 H ? 6.082 ? chorismic_acid ? ? bmst000056 1 12 1 1 1 1 H18 H ? 8.960 ? chorismic_acid ? ? bmst000056 1 13 1 1 1 1 H19 H ? 6.384 ? chorismic_acid ? ? bmst000056 1 14 1 1 1 1 H20 H ? 7.763 ? chorismic_acid ? ? bmst000056 1 15 1 1 1 1 H21 H ? 1.698 ? chorismic_acid ? ? bmst000056 1 16 1 1 1 1 H22 H ? 7.877 ? chorismic_acid ? ? bmst000056 1 17 1 1 1 1 H23 H ? 6.160 ? chorismic_acid ? ? bmst000056 1 18 1 1 1 1 H24 H ? 7.514 ? chorismic_acid ? ? bmst000056 1 19 1 1 1 1 H25 H ? 6.468 ? chorismic_acid ? ? bmst000056 1 20 1 1 1 1 H26 H ? 6.562 ? chorismic_acid ? ? bmst000056 1 stop_ save_ ##################################### # Conformer family coordinate set # ##################################### save_conformer_family_coord_set_1 _Conformer_family_coord_set.Sf_category conformer_family_coord_set _Conformer_family_coord_set.Sf_framecode conformer_family_coord_set_1 _Conformer_family_coord_set.Entry_ID bmst000056 _Conformer_family_coord_set.ID 1 _Conformer_family_coord_set.Details ? loop_ _Conformer_family_software.Software_ID _Conformer_family_software.Software_label _Conformer_family_software.Entry_ID _Conformer_family_software.Conformer_family_coord_set_ID 1 $software_1 bmst000056 1 stop_ loop_ _Atom_site.Model_ID _Atom_site.ID _Atom_site.Label_entity_assembly_ID _Atom_site.Label_entity_ID _Atom_site.Label_comp_index_ID _Atom_site.Label_comp_ID _Atom_site.Label_atom_ID _Atom_site.Auth_seq_ID _Atom_site.Auth_comp_ID _Atom_site.Auth_atom_ID _Atom_site.Type_symbol _Atom_site.Cartn_x _Atom_site.Cartn_y _Atom_site.Cartn_z _Atom_site.Entry_ID _Atom_site.Conformer_family_coord_set_ID 1 1 1 1 1 1 C1 1 1 C1 C 0.095 0.309 0.545 bmst000056 1 1 2 1 1 1 1 C2 1 1 C2 C -0.762 -0.729 -0.133 bmst000056 1 1 3 1 1 1 1 C3 1 1 C3 C -0.720 1.547 0.919 bmst000056 1 1 4 1 1 1 1 O4 1 1 O4 O 1.170 0.786 -0.274 bmst000056 1 1 5 1 1 1 1 C5 1 1 C5 C -2.042 -0.885 0.259 bmst000056 1 1 6 1 1 1 1 C6 1 1 C6 C -1.987 1.134 1.625 bmst000056 1 1 7 1 1 1 1 O7 1 1 O7 O 0.026 2.420 1.748 bmst000056 1 1 8 1 1 1 1 C8 1 1 C8 C 2.295 0.026 -0.395 bmst000056 1 1 9 1 1 1 1 C9 1 1 C9 C -2.617 -0.001 1.290 bmst000056 1 1 10 1 1 1 1 C10 1 1 C10 C -2.840 -1.972 -0.376 bmst000056 1 1 11 1 1 1 1 C11 1 1 C11 C 3.392 0.731 -1.136 bmst000056 1 1 12 1 1 1 1 C12 1 1 C12 C 2.507 -1.213 0.069 bmst000056 1 1 13 1 1 1 1 O13 1 1 O13 O -4.108 -2.030 0.106 bmst000056 1 1 14 1 1 1 1 O14 1 1 O14 O -2.435 -2.736 -1.227 bmst000056 1 1 15 1 1 1 1 O15 1 1 O15 O 3.076 2.008 -1.447 bmst000056 1 1 16 1 1 1 1 O16 1 1 O16 O 4.457 0.225 -1.419 bmst000056 1 1 17 1 1 1 1 H17 1 1 H17 H 0.517 -0.107 1.476 bmst000056 1 1 18 1 1 1 1 H18 1 1 H18 H -0.334 -1.379 -0.890 bmst000056 1 1 19 1 1 1 1 H19 1 1 H19 H -0.995 2.058 -0.024 bmst000056 1 1 20 1 1 1 1 H20 1 1 H20 H -2.394 1.831 2.352 bmst000056 1 1 21 1 1 1 1 H21 1 1 H21 H 0.812 2.675 1.235 bmst000056 1 1 22 1 1 1 1 H22 1 1 H22 H -3.563 -0.279 1.741 bmst000056 1 1 23 1 1 1 1 H23 1 1 H23 H 1.761 -1.784 0.606 bmst000056 1 1 24 1 1 1 1 H24 1 1 H24 H 3.472 -1.668 -0.109 bmst000056 1 1 25 1 1 1 1 H25 1 1 H25 H -4.538 -2.767 -0.367 bmst000056 1 1 26 1 1 1 1 H26 1 1 H26 H 3.854 2.359 -1.920 bmst000056 1 stop_ save_