data_bmse001016 save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse001016 _Entry.Title L_phenylalanine _Entry.Version_type update _Entry.Submission_date 2011-12-23 _Entry.Accession_date 2011-12-23 _Entry.Last_release_date 2011-12-23 _Entry.Original_release_date 2011-12-23 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.21 _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.Details ? _Entry.BMRB_internal_directory_name L_phenylalanine 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 Dan Bearden D. ? ? bmse001016 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 ? "National Institute of Standards and Technology, Hollings Marine Laboratory" NIST bmse001016 stop_ loop_ _Release.Release_number _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 2012-12-21 2011-12-23 original BMRB "Original spectra from Birmingham" bmse001016 stop_ save_ save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse001016 _Citation.ID 1 _Citation.Class 'reference citation' _Citation.PubMed_ID 17170002 _Citation.Title 'Database resources of the National Center for Biotechnology Information.' _Citation.Status published _Citation.Type internet _Citation.WWW_URL http://pubchem.ncbi.nlm.nih.gov/ _Citation.Year 2006 _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. ? bmse001016 1 2 T. Barrett T. ? ? bmse001016 1 3 D. Benson D. A. ? bmse001016 1 4 S. Bryant S. H. ? bmse001016 1 5 K. Canese K. ? ? bmse001016 1 6 V. Chetvenin V. ? ? bmse001016 1 7 D. Church D. M. ? bmse001016 1 8 M. DiCuccio M. ? ? bmse001016 1 9 R. Edgar R. ? ? bmse001016 1 10 S. Federhen S. ? ? bmse001016 1 11 L. Geer L. Y. ? bmse001016 1 12 W. Helmberg W. ? ? bmse001016 1 13 Y. Kapustin Y. ? ? bmse001016 1 14 D. Kenton D. L. ? bmse001016 1 15 O. Khovayko O. ? ? bmse001016 1 16 D. Lipman D. J. ? bmse001016 1 17 T. Madden T. L. ? bmse001016 1 18 D. Maglott D. R. ? bmse001016 1 19 J. Ostell J. ? ? bmse001016 1 20 K. Pruitt K. D. ? bmse001016 1 21 G. Schuler G. D. ? bmse001016 1 22 L. Schriml L. M. ? bmse001016 1 23 E. Sequeira E. ? ? bmse001016 1 24 S. Sherry S. T. ? bmse001016 1 25 K. Sirotkin K. ? ? bmse001016 1 26 A. Souvorov A. ? ? bmse001016 1 27 G. Starchenko G. ? ? bmse001016 1 28 T. Suzek T. O. ? bmse001016 1 29 R. Tatusov R. ? ? bmse001016 1 30 T. Tatusova T. A. ? bmse001016 1 31 L. Bagner L. ? ? bmse001016 1 32 E. Yaschenko E. ? ? bmse001016 1 stop_ save_ save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse001016 _Assembly.ID 1 _Assembly.Name L-Phenylalanine _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 L_phenylalanine 1 $L_phenylalanine yes native no no . . . bmse001016 1 stop_ save_ save_L_phenylalanine _Entity.Sf_category entity _Entity.Sf_framecode L_phenylalanine _Entity.Entry_ID bmse001016 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name L-phenylalanine _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 bmse001016 1 stop_ save_ 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 bmse001016 _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 $L_phenylalanine . n/a "multiple natural sources" yes "not applicable" n/a . . n/a n/a n/a n/a . . . . . . . . . . . . . . . . . . . . . bmse001016 1 stop_ save_ 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 bmse001016 _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 $L_phenylalanine . "chemical synthesis" . . . . . . . . . . . . . . . . . . . . . . . . . . . . . bmse001016 1 stop_ save_ save_chem_comp_1 _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_1 _Chem_comp.Entry_ID bmse001016 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name L-Phenylalanine _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InCHi_code ; InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/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 'C9 H11 N O2' _Chem_comp.Formula_weight 165.1891400000 _Chem_comp.Formula_mono_iso_wt_nat 165.078978603 _Chem_comp.Formula_mono_iso_wt_13C 174.109172143 _Chem_comp.Formula_mono_iso_wt_15N 166.076013496 _Chem_comp.Formula_mono_iso_wt_13C_15N 175.1062070359 _Chem_comp.Image_file_name standards/L_phenylalanine/lit/3379.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name standards/L_phenylalanine/lit/3379.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 "Phenylalanine, L-" synonym bmse001016 1 "(S)-alpha-Aminohydrocinnamic acid" synonym bmse001016 1 (S)-Phenylalanine synonym bmse001016 1 "L-Alanine, 3-phenyl-" synonym bmse001016 1 Phenylalanine synonym bmse001016 1 3-Phenyl-L-alanine synonym bmse001016 1 "Phenylalanine (VAN)" synonym bmse001016 1 "(S)-alpha-Amino-beta-phenylpropionic acid" synonym bmse001016 1 "Phenylalaninum [Latin]" synonym bmse001016 1 "alpha-Aminohydrocinnamic acid, L-" synonym bmse001016 1 (L)-Phenylalanine synonym bmse001016 1 "alpha-Amino-beta-phenylpropionic acid, L-" synonym bmse001016 1 L-Phenylalanine synonym bmse001016 1 "Hydrocinnamic acid, alpha-amino-" synonym bmse001016 1 "2-Amino-3-phenylpropionic acid, L-" synonym bmse001016 1 "(S)-2-Amino-3-phenylpropanoic acid" synonym bmse001016 1 beta-Phenyl-L-alanine synonym bmse001016 1 "Alanine, 3-phenyl-" synonym bmse001016 1 "(S)-alpha-Amino-benzenepropanoic acid" synonym bmse001016 1 "Fenilalanina [Spanish]" synonym bmse001016 1 "(S)-2-Amino-3-phenylpropionic acid" synonym bmse001016 1 L-PHENYLALININE synonym bmse001016 1 "L-Alanine, phenyl-" synonym bmse001016 1 "Phenylalanine [USAN:INN:JAN]" synonym bmse001016 1 "L-Antibiotic FN 1636" synonym bmse001016 1 "beta-Phenylalnine, (-)-" synonym bmse001016 1 "Alanine, phenyl-, L-" synonym bmse001016 1 3-Phenylalanine synonym bmse001016 1 "Benzenepropanoic acid, alpha-amino-, (S)-" synonym bmse001016 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 "(2S)-2-amino-3-phenyl-propanoic acid" IUPAC bmse001016 1 "(2S)-2-amino-3-phenyl-propanoic acid" IUPAC_TRADITIONAL bmse001016 1 "(2S)-2-amino-3-phenyl-propanoic acid" IUPAC_CAS bmse001016 1 "(2S)-2-amino-3-phenyl-propanoic acid" IUPAC_OPENEYE bmse001016 1 "(2S)-2-amino-3-phenyl-propanoic acid" IUPAC_SYSTEMATIC bmse001016 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID isomeric C1=CC=C(C=C1)C[C@@H](C(=O)O)N bmse001016 1 canonical C1=CC=C(C=C1)CC(C(=O)O)N bmse001016 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.Entry_ID _Chem_comp_atom.Comp_ID C1 C ? ? ? ? 2.8660 -2.8100 bmse001016 1 C2 C ? ? ? ? 3.7321 -2.3100 bmse001016 1 C3 C ? ? ? ? 2.0000 -2.3100 bmse001016 1 C4 C ? ? ? ? 3.7321 -1.3100 bmse001016 1 C5 C ? ? ? ? 2.0000 -1.3100 bmse001016 1 C6 C ? ? ? ? 2.8660 0.1900 bmse001016 1 C7 C ? ? ? ? 2.8660 -0.8100 bmse001016 1 C8 C ? ? ? ? 3.7321 0.6900 bmse001016 1 C9 C ? ? ? ? 3.7321 1.6900 bmse001016 1 N10 N ? ? ? ? 4.5981 0.1900 bmse001016 1 O11 O ? ? ? ? 4.5981 2.1900 bmse001016 1 O12 O ? ? ? ? 2.8660 2.1900 bmse001016 1 H13 H ? ? ? ? 2.8660 -3.4300 bmse001016 1 H14 H ? ? ? ? 4.2690 -2.6200 bmse001016 1 H15 H ? ? ? ? 1.4631 -2.6200 bmse001016 1 H16 H ? ? ? ? 4.2690 -1.0000 bmse001016 1 H17 H ? ? ? ? 1.4631 -1.0000 bmse001016 1 H18 H ? ? ? ? 2.6540 0.7726 bmse001016 1 H19 H ? ? ? ? 2.2554 0.0823 bmse001016 1 H20 H ? ? ? ? 3.7321 0.0700 bmse001016 1 H21 H ? ? ? ? 5.1350 0.5000 bmse001016 1 H22 H ? ? ? ? 4.5981 -0.4300 bmse001016 1 H23 H ? ? ? ? 4.5981 2.8100 bmse001016 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 bmse001016 1 C2 C2 BMRB bmse001016 1 C3 C3 BMRB bmse001016 1 C4 C4 BMRB bmse001016 1 C5 C5 BMRB bmse001016 1 C6 C6 BMRB bmse001016 1 C7 C7 BMRB bmse001016 1 C8 C8 BMRB bmse001016 1 C9 C9 BMRB bmse001016 1 N10 N10 BMRB bmse001016 1 O11 O11 BMRB bmse001016 1 O12 O12 BMRB bmse001016 1 H13 H13 BMRB bmse001016 1 H14 H14 BMRB bmse001016 1 H15 H15 BMRB bmse001016 1 H16 H16 BMRB bmse001016 1 H17 H17 BMRB bmse001016 1 H18 H18 BMRB bmse001016 1 H19 H19 BMRB bmse001016 1 H20 H20 BMRB bmse001016 1 H21 H21 BMRB bmse001016 1 H22 H22 BMRB bmse001016 1 H23 H23 BMRB bmse001016 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 DOUB C1 C2 ? bmse001016 1 2 covalent SING C1 C3 ? bmse001016 1 3 covalent SING C1 H13 ? bmse001016 1 4 covalent SING C2 C4 ? bmse001016 1 5 covalent SING C2 H14 ? bmse001016 1 6 covalent DOUB C3 C5 ? bmse001016 1 7 covalent SING C3 H15 ? bmse001016 1 8 covalent DOUB C4 C7 ? bmse001016 1 9 covalent SING C4 H16 ? bmse001016 1 10 covalent SING C5 C7 ? bmse001016 1 11 covalent SING C5 H17 ? bmse001016 1 12 covalent SING C6 C7 ? bmse001016 1 13 covalent SING C6 C8 ? bmse001016 1 14 covalent SING C6 H18 ? bmse001016 1 15 covalent SING C6 H19 ? bmse001016 1 16 covalent SING C8 C9 ? bmse001016 1 17 covalent SING C8 N10 ? bmse001016 1 18 covalent SING C8 H20 ? bmse001016 1 19 covalent SING C9 O11 ? bmse001016 1 20 covalent DOUB C9 O12 ? bmse001016 1 21 covalent SING N10 H21 ? bmse001016 1 22 covalent SING N10 H22 ? bmse001016 1 23 covalent SING O11 H23 ? bmse001016 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 85164893 sid ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PubChem 149037 sid ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PubChem 6140 cid ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PubChem 3379 sid ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no KEGG C00079 "compound ID" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 10549-09-4 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 3617-44-5 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 5297-02-9 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 63-91-2 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 673-06-3 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "CAS Registry" 67675-33-6 "registry number" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no CHEBI 17295 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no CCRIS 6767 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no "FEMA No." 3585 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no EINECS 200-568-1 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no NSC 79477 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no HSDB 1825 ? ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PDB PHE "Chemical Component" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PDB PHE_LFOH "Chemical Component" ? L-Phenylalanine ? "matching entry" ? bmse001016 1 no PDB PHE_LFZW "Chemical Component" ? L-Phenylalanine ? "matching entry" ? bmse001016 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 bmse001016 1 stop_ save_ save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse001016 _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 L-Phenylalanine "natural abundance" 1 $L_phenylalanine ? Solute 20 ? ? mM ? sigma/aldrich L-Phenylalanine ? bmse001016 1 2 D2O ? ? ? ? Solvent 100 ? ? % ? ? ? ? bmse001016 1 3 "sodium phosphate" ? ? ? ? Buffer 200 ? ? mM ? ? ? ? bmse001016 1 4 "sodium azide" ? ? ? ? Cytocide 500 ? ? uM ? ? ? ? bmse001016 1 5 DSS ? ? ? ? Reference 500 ? ? uM ? ? ? ? bmse001016 1 stop_ save_ save_sample_conditions_1 _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_conditions_1 _Sample_condition_list.Entry_ID bmse001016 _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 7.4 ? pH bmse001016 1 temperature 298 ? K bmse001016 1 stop_ save_ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse001016 _Software.ID 1 _Software.Name TopSpin _Software.Version 2.1 _Software.Details ? loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID "Bruker Biospin" ? ? bmse001016 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Collection bmse001016 1 Processing bmse001016 1 "Data analysis" bmse001016 1 "Peak picking" bmse001016 1 stop_ save_ save_Bruker_700 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode Bruker_700 _NMR_spectrometer.Entry_ID bmse001016 _NMR_spectrometer.ID 1 _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model 'Avance II' _NMR_spectrometer.Field_strength 700 save_ save_TCI_cryoprobe _NMR_spectrometer_probe.Sf_category NMR_spectrometer_probe _NMR_spectrometer_probe.Sf_framecode TCI_cryoprobe _NMR_spectrometer_probe.Entry_ID bmse001016 _NMR_spectrometer_probe.ID 1 _NMR_spectrometer_probe.Details 'single z-axis gradient' _NMR_spectrometer_probe.Manufacturer Bruker _NMR_spectrometer_probe.Model 'TCI CryoProbe' _NMR_spectrometer_probe.Serial_number ? _NMR_spectrometer_probe.Diameter 5 _NMR_spectrometer_probe.Rotor_length ? _NMR_spectrometer_probe.Rotor_composition ? _NMR_spectrometer_probe.Internal_volume ? loop_ _NMR_probe.Type _NMR_probe.Entry_ID _NMR_probe.NMR_spectrometer_probe_ID Cryoprobe bmse001016 1 stop_ save_ save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse001016 _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 "2D J-resolved 1H" yes ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 ? ? bmse001016 1 2 "2D [1H,13C]-HSQC" yes ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 ? ? bmse001016 1 3 "1D 1H, NOESY" yes ? ? 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 ? ? bmse001016 1 stop_ loop_ _Experiment_file.Experiment_ID _Experiment_file.Name _Experiment_file.Type _Experiment_file.Details _Experiment_file.Entry_ID _Experiment_file.Experiment_list_ID 1 standards/L_phenylalanine/nmr/bmse001016/1H_1H_JRES/ "Time-domain (raw spectral data)" ? bmse001016 1 1 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_1H_JRES/00.png "Spectral image" ? bmse001016 1 1 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_1H_JRES/01.png "Spectral image" ? bmse001016 1 2 standards/L_phenylalanine/nmr/bmse001016/1H_13C_HSQC/ "Time-domain (raw spectral data)" ? bmse001016 1 2 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_13C_HSQC/00.png "Spectral image" ? bmse001016 1 2 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_13C_HSQC/02.png "Spectral image" ? bmse001016 1 2 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_13C_HSQC/03.png "Spectral image" ? bmse001016 1 3 standards/L_phenylalanine/nmr/bmse001016/1H_NOESY/ "Time-domain (raw spectral data)" ? bmse001016 1 3 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_NOESY/00.png "Spectral image" ? bmse001016 1 3 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_NOESY/01.png "Spectral image" ? bmse001016 1 3 standards/L_phenylalanine/nmr/bmse001016/spectra_png/1H_NOESY/02.png "Spectral image" ? bmse001016 1 stop_ save_ 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 bmse001016 _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 DSS "methyl protons" ppm 0.00 internal direct 1.000000000 ? ? ? bmse001016 1 C 13 DSS "methyl carbons" ppm 0.00 internal direct 1.000000000 ? ? ? bmse001016 1 stop_ save_