data_bmse000806 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse000806 _Entry.Title L_glutathione_oxidized _Entry.Version_type update _Entry.Submission_date 2011-07-27 _Entry.Accession_date 2011-07-27 _Entry.Last_release_date 2012-10-17 _Entry.Original_release_date 2011-07-27 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.7 _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.DOI 10.13018/BMSE000806 _Entry.BMRB_internal_directory_name L_glutathione_oxidized loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Entry_ID 1 Dan Bearden D. bmse000806 stop_ loop_ _Entry_src.ID _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 'National Institute of Standards and Technology, Hollings Marine Laboratory' NIST bmse000806 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 . . 2011-08-16 2011-07-27 original BMRB 'Original spectra from Birmingham' bmse000806 2 . . 2011-09-09 2011-07-27 update BMRB 'Brought up to date with latest Dictionary' bmse000806 3 . . 2011-12-14 2011-07-27 update BMRB 'Set Assembly.Name to match Chem_comp.name' bmse000806 4 . . 2012-01-06 2011-07-27 update BMRB 'added spectrometer model and probe info' bmse000806 5 . . 2012-09-13 2011-07-27 update BMRB 'Added PubChem SID 126596846 to database loop' bmse000806 6 . . 2012-10-17 2011-07-27 update BMRB 'Set all _Chem_comp_SMILES Types to lower case' bmse000806 7 . . 2017-10-12 2017-10-12 update BMRB 'Remediated Experiment_file loop if present and standardized mol and png file tags.' bmse000806 8 . . 2017-12-19 2017-10-12 update BMRB 'InChI numbering updated according to ALATIS' bmse000806 stop_ save_ ############### # Citations # ############### save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID bmse000806 _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 loop_ _Citation_author.Ordinal _Citation_author.Given_name _Citation_author.Family_name _Citation_author.First_initial _Citation_author.Middle_initials _Citation_author.Entry_ID _Citation_author.Citation_ID 1 D. Wheeler D. L. bmse000806 1 2 T. Barrett T. ? bmse000806 1 3 D. Benson D. A. bmse000806 1 4 S. Bryant S. H. bmse000806 1 5 K. Canese K. ? bmse000806 1 6 V. Chetvenin V. ? bmse000806 1 7 D. Church D. M. bmse000806 1 8 M. DiCuccio M. ? bmse000806 1 9 R. Edgar R. ? bmse000806 1 10 S. Federhen S. ? bmse000806 1 11 L. Geer L. Y. bmse000806 1 12 W. Helmberg W. ? bmse000806 1 13 Y. Kapustin Y. ? bmse000806 1 14 D. Kenton D. L. bmse000806 1 15 O. Khovayko O. ? bmse000806 1 16 D. Lipman D. J. bmse000806 1 17 T. Madden T. L. bmse000806 1 18 D. Maglott D. R. bmse000806 1 19 J. Ostell J. ? bmse000806 1 20 K. Pruitt K. D. bmse000806 1 21 G. Schuler G. D. bmse000806 1 22 L. Schriml L. M. bmse000806 1 23 E. Sequeira E. ? bmse000806 1 24 S. Sherry S. T. bmse000806 1 25 K. Sirotkin K. ? bmse000806 1 26 A. Souvorov A. ? bmse000806 1 27 G. Starchenko G. ? bmse000806 1 28 T. Suzek T. O. bmse000806 1 29 R. Tatusov R. ? bmse000806 1 30 T. Tatusova T. A. bmse000806 1 31 L. Bagner L. ? bmse000806 1 32 E. Yaschenko E. ? bmse000806 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmse000806 _Assembly.ID 1 _Assembly.Name 'L(-)-Glutathione, oxidized' _Assembly.Number_of_components 1 _Assembly.Organic_ligands 0 _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.Entry_ID _Entity_assembly.Assembly_ID 1 L_glutathione_oxidized 1 $L_glutathione_oxidized yes native no no bmse000806 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_L_glutathione_oxidized _Entity.Sf_category entity _Entity.Sf_framecode L_glutathione_oxidized _Entity.Entry_ID bmse000806 _Entity.ID 1 _Entity.Name 'L(-)-Glutathione, oxidized' _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 bmse000806 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 bmse000806 _Entity_natural_src_list.ID 1 loop_ _Entity_natural_src.ID _Entity_natural_src.Entity_ID _Entity_natural_src.Entity_label _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.Superkingdom _Entity_natural_src.Kingdom _Entity_natural_src.Genus _Entity_natural_src.Species _Entity_natural_src.Entry_ID _Entity_natural_src.Entity_natural_src_list_ID 1 1 $L_glutathione_oxidized n/a 'multiple natural sources' yes 'not applicable' n/a n/a n/a n/a n/a bmse000806 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 bmse000806 _Entity_experimental_src_list.ID 1 loop_ _Entity_experimental_src.ID _Entity_experimental_src.Entity_ID _Entity_experimental_src.Entity_label _Entity_experimental_src.Production_method _Entity_experimental_src.Entry_ID _Entity_experimental_src.Entity_experimental_src_list_ID 1 1 $L_glutathione_oxidized 'chemical synthesis' bmse000806 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 bmse000806 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name 'L(-)-Glutathione, oxidized' _Chem_comp.Type non-polymer _Chem_comp.InChI_code InChI=1S/C20H32N6O12S2/c21-9(19(35)36)1-3-13(27)25-11(17(33)23-5-15(29)30)7-39-40-8-12(18(34)24-6-16(31)32)26-14(28)4-2-10(22)20(37)38/h9-12H,1-8,21-22H2,(H,23,33)(H,24,34)(H,25,27)(H,26,28)(H,29,30)(H,31,32)(H,35,36)(H,37,38)/t9-,10-,11-,12-/m0/s1 _Chem_comp.Paramagnetic no _Chem_comp.Aromatic no _Chem_comp.Formula 'C20 H32 N6 O12 S2' _Chem_comp.Formula_weight 612.6310800000 _Chem_comp.Formula_mono_iso_wt_nat 612.151961904 _Chem_comp.Formula_mono_iso_wt_13C 632.21905866 _Chem_comp.Formula_mono_iso_wt_15N 618.134171263 _Chem_comp.Formula_mono_iso_wt_13C_15N 638.2012680188 _Chem_comp.Image_file_name bmse000806.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse000806.mol _Chem_comp.Struct_file_format mol loop_ _Chem_comp_common_name.Name _Chem_comp_common_name.Type _Chem_comp_common_name.Entry_ID _Chem_comp_common_name.Comp_ID 'L-Oxidized glutathione' synonym bmse000806 1 Bi(glutathion-S-yl) synonym bmse000806 1 'Oxidized glutathione' synonym bmse000806 1 S,S'-Ethylenebis(glutathione) synonym bmse000806 1 'Oxiglutationa [INN-Spanish]' synonym bmse000806 1 N-(N-gamma-Glutamyl-cysteinyl)glycine-(2,2)-disulfide synonym bmse000806 1 GSSG synonym bmse000806 1 'Glutathione disulfide' synonym bmse000806 1 'Glutathione disulphide' synonym bmse000806 1 Glutathione-ssg synonym bmse000806 1 'Glutathone disulfide' synonym bmse000806 1 'Oxiglutatione [INN]' synonym bmse000806 1 'Oxiglutationum [INN-Latin]' synonym bmse000806 1 'Bis(gamma-glutamyl-L-cysteinylglycine) disulfide' synonym bmse000806 1 N,N'-(Dithiobis((R)-1-((carboxymethyl)carbamoyl)ethylene))di-L-glutamine synonym bmse000806 1 Oxigluthione synonym bmse000806 1 "Glutamine, N,N'-(dithiobis(1-((carboxymethyl)carbamoyl)ethylene))di-, L-" synonym bmse000806 1 'Glutathione, oxidized' synonym bmse000806 1 "Glycine, L-gamma-glutamyl-L-cysteinyl-, (2,2')-disulfide" synonym bmse000806 1 Oxiglutatione synonym bmse000806 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=1S/C20H32N6O12S2/c21-9(19(35)36)1-3-13(27)25-11(17(33)23-5-15(29)30)7-39-40-8-12(18(34)24-6-16(31)32)26-14(28)4-2-10(22)20(37)38/h9-12H,1-8,21-22H2,(H,23,33)(H,24,34)(H,25,27)(H,26,28)(H,29,30)(H,31,32)(H,35,36)(H,37,38)/t9-,10-,11-,12-/m0/s1 ; INCHI na na bmse000806 1 InChI=1S/C20H32N6O12S2/c21-9(19(35)36)1-3-13(27)25-11(17(33)23-5-15(29)30)7-39-40-8-12(18(34)24-6-16(31)32)26-14(28)4-2-10(22)20(37)38/h9-12H,1-8,21-22H2,(H,23,33)(H,24,34)(H,25,27)(H,26,28)(H,29,30)(H,31,32)(H,35,36)(H,37,38)/t9-,10-,11-,12-/m0/s1 INCHI ALATIS 3.003 bmse000806 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-4-[[(1R)-2-[(2R)-2-[[(4S)-4-amino-4-carboxy-butanoyl]amino]-2-(carboxymethylcarbamoyl)ethyl]disulfanyl-1-(carboxymethylcarbamoyl)ethyl]carbamoyl]butanoic acid ; IUPAC bmse000806 1 ; (2S)-2-amino-4-[[[(1R)-2-[(2R)-2-[[(4S)-4-amino-4-carboxy-1-oxo-butyl]amino]-2-[(carboxymethylamino)-oxo-methyl]ethyl]disulfanyl-1-[(carboxymethylamino)-oxo-methyl]ethyl]amino]-oxo-methyl]butanoic acid ; IUPAC_CAS bmse000806 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID isomeric C(CC(=O)N[C@@H](CSSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)C(=O)NCC(=O)O)[C@@H](C(=O)O)N bmse000806 1 canonical C(CC(=O)NC(CSSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)C(=O)NCC(=O)O)C(C(=O)O)N bmse000806 1 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Drawing_2D_coord_x _Chem_comp_atom.Drawing_2D_coord_y _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID N21 N 4.2690 5.4050 1 bmse000806 1 C9 C 4.2690 4.4050 2 bmse000806 1 C19 C 3.4030 3.9050 3 bmse000806 1 O35 O 3.4030 2.9050 4 bmse000806 1 O36 O 2.5369 4.4050 5 bmse000806 1 C1 C 5.1350 3.9050 6 bmse000806 1 C3 C 6.0010 4.4050 7 bmse000806 1 C13 C 6.8671 3.9050 8 bmse000806 1 O27 O 6.8671 2.9050 9 bmse000806 1 N25 N 7.7331 4.4050 10 bmse000806 1 C11 C 8.5991 3.9050 11 bmse000806 1 C17 C 9.4651 4.4050 12 bmse000806 1 O33 O 9.4651 5.4050 13 bmse000806 1 C7 C 8.5991 2.9050 14 bmse000806 1 S39 S 7.7331 2.4050 15 bmse000806 1 N23 N 10.3312 3.9050 16 bmse000806 1 C5 C 11.1972 4.4050 17 bmse000806 1 C15 C 12.0632 3.9050 18 bmse000806 1 O29 O 12.0632 2.9050 19 bmse000806 1 O30 O 12.9292 4.4050 20 bmse000806 1 N24 N 5.1350 -0.0950 21 bmse000806 1 C6 C 4.2690 -0.5950 22 bmse000806 1 C16 C 3.4030 -0.0950 23 bmse000806 1 O31 O 3.4030 0.9050 24 bmse000806 1 O32 O 2.5369 -0.5950 25 bmse000806 1 C18 C 6.0010 -0.5950 26 bmse000806 1 O34 O 6.0010 -1.5950 27 bmse000806 1 C12 C 6.8671 -0.0950 28 bmse000806 1 N26 N 7.7331 -0.5950 29 bmse000806 1 C8 C 6.8671 0.9050 30 bmse000806 1 S40 S 7.7331 1.4050 31 bmse000806 1 C10 C 9.4651 -3.5950 32 bmse000806 1 C20 C 9.4651 -4.5950 33 bmse000806 1 O37 O 8.5991 -5.0950 34 bmse000806 1 O38 O 10.3312 -5.0950 35 bmse000806 1 N22 N 10.3312 -3.0950 36 bmse000806 1 C2 C 8.5991 -3.0950 37 bmse000806 1 C4 C 8.5991 -2.0950 38 bmse000806 1 C14 C 7.7331 -1.5950 39 bmse000806 1 O28 O 6.8671 -2.0950 40 bmse000806 1 H61 H 3.7321 5.7150 41 bmse000806 1 H62 H 4.8059 5.7150 42 bmse000806 1 H57 H 4.8059 4.7150 43 bmse000806 1 H71 H 2.0000 4.0950 44 bmse000806 1 H41 H 4.7365 3.4301 45 bmse000806 1 H42 H 5.5335 3.4301 46 bmse000806 1 H45 H 6.3996 4.8799 47 bmse000806 1 H46 H 5.6025 4.8799 48 bmse000806 1 H67 H 7.7331 5.0250 49 bmse000806 1 H59 H 8.0622 3.5950 50 bmse000806 1 H53 H 8.8112 2.3224 51 bmse000806 1 H54 H 9.2097 3.0127 52 bmse000806 1 H65 H 10.3312 3.2850 53 bmse000806 1 H49 H 11.5957 4.8799 54 bmse000806 1 H50 H 10.7987 4.8799 55 bmse000806 1 H69 H 13.4662 4.0950 56 bmse000806 1 H66 H 5.1350 0.5250 57 bmse000806 1 H51 H 3.8705 -1.0699 58 bmse000806 1 H52 H 4.6675 -1.0699 59 bmse000806 1 H70 H 2.0000 -0.2850 60 bmse000806 1 H60 H 7.4040 0.2150 61 bmse000806 1 H68 H 8.2700 -0.2850 62 bmse000806 1 H55 H 6.6550 1.4876 63 bmse000806 1 H56 H 6.2565 0.7973 64 bmse000806 1 H58 H 10.0021 -3.9050 65 bmse000806 1 H72 H 10.3312 -5.7150 66 bmse000806 1 H63 H 10.8681 -3.4050 67 bmse000806 1 H64 H 10.3312 -2.4750 68 bmse000806 1 H43 H 7.9885 -2.9873 69 bmse000806 1 H44 H 8.3871 -3.6776 70 bmse000806 1 H47 H 9.2097 -2.2027 71 bmse000806 1 H48 H 8.8112 -1.5124 72 bmse000806 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID N21 N1 BMRB bmse000806 1 C9 C2 BMRB bmse000806 1 C19 C3 BMRB bmse000806 1 O35 O4 BMRB bmse000806 1 O36 O5 BMRB bmse000806 1 C1 C6 BMRB bmse000806 1 C3 C7 BMRB bmse000806 1 C13 C8 BMRB bmse000806 1 O27 O9 BMRB bmse000806 1 N25 N10 BMRB bmse000806 1 C11 C11 BMRB bmse000806 1 C17 C12 BMRB bmse000806 1 O33 O13 BMRB bmse000806 1 C7 C14 BMRB bmse000806 1 S39 S15 BMRB bmse000806 1 N23 N16 BMRB bmse000806 1 C5 C17 BMRB bmse000806 1 C15 C18 BMRB bmse000806 1 O29 O19 BMRB bmse000806 1 O30 O20 BMRB bmse000806 1 N24 N21 BMRB bmse000806 1 C6 C22 BMRB bmse000806 1 C16 C23 BMRB bmse000806 1 O31 O24 BMRB bmse000806 1 O32 O25 BMRB bmse000806 1 C18 C26 BMRB bmse000806 1 O34 O27 BMRB bmse000806 1 C12 C28 BMRB bmse000806 1 N26 N29 BMRB bmse000806 1 C8 C30 BMRB bmse000806 1 S40 S31 BMRB bmse000806 1 C10 C32 BMRB bmse000806 1 C20 C33 BMRB bmse000806 1 O37 O34 BMRB bmse000806 1 O38 O35 BMRB bmse000806 1 N22 N36 BMRB bmse000806 1 C2 C37 BMRB bmse000806 1 C4 C38 BMRB bmse000806 1 C14 C39 BMRB bmse000806 1 O28 O40 BMRB bmse000806 1 H61 H41 BMRB bmse000806 1 H62 H42 BMRB bmse000806 1 H57 H43 BMRB bmse000806 1 H71 H44 BMRB bmse000806 1 H41 H45 BMRB bmse000806 1 H42 H46 BMRB bmse000806 1 H45 H47 BMRB bmse000806 1 H46 H48 BMRB bmse000806 1 H67 H49 BMRB bmse000806 1 H59 H50 BMRB bmse000806 1 H53 H51 BMRB bmse000806 1 H54 H52 BMRB bmse000806 1 H65 H53 BMRB bmse000806 1 H49 H54 BMRB bmse000806 1 H50 H55 BMRB bmse000806 1 H69 H56 BMRB bmse000806 1 H66 H57 BMRB bmse000806 1 H51 H58 BMRB bmse000806 1 H52 H59 BMRB bmse000806 1 H70 H60 BMRB bmse000806 1 H60 H61 BMRB bmse000806 1 H68 H62 BMRB bmse000806 1 H55 H63 BMRB bmse000806 1 H56 H64 BMRB bmse000806 1 H58 H65 BMRB bmse000806 1 H72 H66 BMRB bmse000806 1 H63 H67 BMRB bmse000806 1 H64 H68 BMRB bmse000806 1 H43 H69 BMRB bmse000806 1 H44 H70 BMRB bmse000806 1 H47 H71 BMRB bmse000806 1 H48 H72 BMRB bmse000806 1 N21 N21 ALATIS bmse000806 1 C9 C9 ALATIS bmse000806 1 C19 C19 ALATIS bmse000806 1 O35 O35 ALATIS bmse000806 1 O36 O36 ALATIS bmse000806 1 C1 C1 ALATIS bmse000806 1 C3 C3 ALATIS bmse000806 1 C13 C13 ALATIS bmse000806 1 O27 O27 ALATIS bmse000806 1 N25 N25 ALATIS bmse000806 1 C11 C11 ALATIS bmse000806 1 C17 C17 ALATIS bmse000806 1 O33 O33 ALATIS bmse000806 1 C7 C7 ALATIS bmse000806 1 S39 S39 ALATIS bmse000806 1 N23 N23 ALATIS bmse000806 1 C5 C5 ALATIS bmse000806 1 C15 C15 ALATIS bmse000806 1 O29 O29 ALATIS bmse000806 1 O30 O30 ALATIS bmse000806 1 N24 N24 ALATIS bmse000806 1 C6 C6 ALATIS bmse000806 1 C16 C16 ALATIS bmse000806 1 O31 O31 ALATIS bmse000806 1 O32 O32 ALATIS bmse000806 1 C18 C18 ALATIS bmse000806 1 O34 O34 ALATIS bmse000806 1 C12 C12 ALATIS bmse000806 1 N26 N26 ALATIS bmse000806 1 C8 C8 ALATIS bmse000806 1 S40 S40 ALATIS bmse000806 1 C10 C10 ALATIS bmse000806 1 C20 C20 ALATIS bmse000806 1 O37 O37 ALATIS bmse000806 1 O38 O38 ALATIS bmse000806 1 N22 N22 ALATIS bmse000806 1 C2 C2 ALATIS bmse000806 1 C4 C4 ALATIS bmse000806 1 C14 C14 ALATIS bmse000806 1 O28 O28 ALATIS bmse000806 1 H61 H61 ALATIS bmse000806 1 H62 H62 ALATIS bmse000806 1 H57 H57 ALATIS bmse000806 1 H71 H71 ALATIS bmse000806 1 H41 H41 ALATIS bmse000806 1 H42 H42 ALATIS bmse000806 1 H45 H45 ALATIS bmse000806 1 H46 H46 ALATIS bmse000806 1 H67 H67 ALATIS bmse000806 1 H59 H59 ALATIS bmse000806 1 H53 H53 ALATIS bmse000806 1 H54 H54 ALATIS bmse000806 1 H65 H65 ALATIS bmse000806 1 H49 H49 ALATIS bmse000806 1 H50 H50 ALATIS bmse000806 1 H69 H69 ALATIS bmse000806 1 H66 H66 ALATIS bmse000806 1 H51 H51 ALATIS bmse000806 1 H52 H52 ALATIS bmse000806 1 H70 H70 ALATIS bmse000806 1 H60 H60 ALATIS bmse000806 1 H68 H68 ALATIS bmse000806 1 H55 H55 ALATIS bmse000806 1 H56 H56 ALATIS bmse000806 1 H58 H58 ALATIS bmse000806 1 H72 H72 ALATIS bmse000806 1 H63 H63 ALATIS bmse000806 1 H64 H64 ALATIS bmse000806 1 H43 H43 ALATIS bmse000806 1 H44 H44 ALATIS bmse000806 1 H47 H47 ALATIS bmse000806 1 H48 H48 ALATIS bmse000806 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.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent SING C9 N21 bmse000806 1 2 covalent SING N21 H61 bmse000806 1 3 covalent SING N21 H62 bmse000806 1 4 covalent SING C9 C19 bmse000806 1 5 covalent SING C9 C1 bmse000806 1 6 covalent SING C9 H57 bmse000806 1 7 covalent DOUB C19 O35 bmse000806 1 8 covalent SING C19 O36 bmse000806 1 9 covalent SING O36 H71 bmse000806 1 10 covalent SING C1 C3 bmse000806 1 11 covalent SING C1 H41 bmse000806 1 12 covalent SING C1 H42 bmse000806 1 13 covalent SING C3 C13 bmse000806 1 14 covalent SING C3 H45 bmse000806 1 15 covalent SING C3 H46 bmse000806 1 16 covalent DOUB C13 O27 bmse000806 1 17 covalent SING C13 N25 bmse000806 1 18 covalent SING C11 N25 bmse000806 1 19 covalent SING N25 H67 bmse000806 1 20 covalent SING C11 C17 bmse000806 1 21 covalent SING C11 C7 bmse000806 1 22 covalent SING C11 H59 bmse000806 1 23 covalent DOUB C17 O33 bmse000806 1 24 covalent SING C17 N23 bmse000806 1 25 covalent SING C7 S39 bmse000806 1 26 covalent SING C7 H53 bmse000806 1 27 covalent SING C7 H54 bmse000806 1 28 covalent SING S39 S40 bmse000806 1 29 covalent SING N23 C5 bmse000806 1 30 covalent SING N23 H65 bmse000806 1 31 covalent SING C5 C15 bmse000806 1 32 covalent SING C5 H49 bmse000806 1 33 covalent SING C5 H50 bmse000806 1 34 covalent DOUB C15 O29 bmse000806 1 35 covalent SING C15 O30 bmse000806 1 36 covalent SING O30 H69 bmse000806 1 37 covalent SING N24 C6 bmse000806 1 38 covalent SING N24 C18 bmse000806 1 39 covalent SING N24 H66 bmse000806 1 40 covalent SING C6 C16 bmse000806 1 41 covalent SING C6 H51 bmse000806 1 42 covalent SING C6 H52 bmse000806 1 43 covalent DOUB C16 O31 bmse000806 1 44 covalent SING C16 O32 bmse000806 1 45 covalent SING O32 H70 bmse000806 1 46 covalent DOUB C18 O34 bmse000806 1 47 covalent SING C18 C12 bmse000806 1 48 covalent SING C12 N26 bmse000806 1 49 covalent SING C12 C8 bmse000806 1 50 covalent SING C12 H60 bmse000806 1 51 covalent SING N26 C14 bmse000806 1 52 covalent SING N26 H68 bmse000806 1 53 covalent SING C8 S40 bmse000806 1 54 covalent SING C8 H55 bmse000806 1 55 covalent SING C8 H56 bmse000806 1 56 covalent SING C10 C20 bmse000806 1 57 covalent SING C10 N22 bmse000806 1 58 covalent SING C10 C2 bmse000806 1 59 covalent SING C10 H58 bmse000806 1 60 covalent DOUB C20 O37 bmse000806 1 61 covalent SING C20 O38 bmse000806 1 62 covalent SING O38 H72 bmse000806 1 63 covalent SING N22 H63 bmse000806 1 64 covalent SING N22 H64 bmse000806 1 65 covalent SING C2 C4 bmse000806 1 66 covalent SING C2 H43 bmse000806 1 67 covalent SING C2 H44 bmse000806 1 68 covalent SING C4 C14 bmse000806 1 69 covalent SING C4 H47 bmse000806 1 70 covalent SING C4 H48 bmse000806 1 71 covalent DOUB C14 O28 bmse000806 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_name _Chem_comp_db_link.Entry_relation_type _Chem_comp_db_link.Entry_ID _Chem_comp_db_link.Comp_ID no PubChem 126596846 sid 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no PubChem 207340 sid 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no PubChem 65359 cid 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no PubChem 3427 sid 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no KEGG C00127 'compound ID' 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no 'CAS Registry' 10421-65-5 'registry number' 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no 'CAS Registry' 121-24-4 'registry number' 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no 'CAS Registry' 27025-41-8 'registry number' 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no CHEBI 17858 ? 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no EINECS 248-170-7 ? 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no CCRIS 780 ? 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 1 no PDB GDS 'Chemical Component' 'L(-)-Glutathione, oxidized' 'matching entry' bmse000806 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 bmse000806 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse000806 _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.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_units _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Entry_ID _Sample_component.Sample_ID 1 'L(-)-Glutathione, oxidized' 'natural abundance' 1 $L_glutathione_oxidized Solute 20 mM sigma 'L(-)-Glutathione, oxidized' bmse000806 1 2 D2O ? ? ? Solvent 100 % ? ? bmse000806 1 3 'sodium phosphate' ? ? ? Buffer 200 mM ? ? bmse000806 1 4 'sodium azide' ? ? ? Cytocide 500 uM ? ? bmse000806 1 5 DSS ? ? ? Reference 0.1 % ? ? bmse000806 1 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 bmse000806 _Sample_condition_list.ID 1 loop_ _Sample_condition_variable.Type _Sample_condition_variable.Val _Sample_condition_variable.Val_units _Sample_condition_variable.Entry_ID _Sample_condition_variable.Sample_condition_list_ID pH 7.4 pH bmse000806 1 temperature 298 K bmse000806 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmse000806 _Software.ID 1 _Software.Name TopSpin _Software.Version 2.1 loop_ _Vendor.Name _Vendor.Entry_ID _Vendor.Software_ID 'Bruker Biospin' bmse000806 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID Collection bmse000806 1 Processing bmse000806 1 'Data analysis' bmse000806 1 'Peak picking' bmse000806 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_Bruker_700 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode Bruker_700 _NMR_spectrometer.Entry_ID bmse000806 _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 bmse000806 _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.Diameter 5 loop_ _NMR_probe.Type _NMR_probe.Entry_ID _NMR_probe.NMR_spectrometer_probe_ID Cryoprobe bmse000806 1 stop_ save_ ############################# # NMR applied experiments # ############################# save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse000806 _Experiment_list.ID 1 loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _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.Entry_ID _Experiment.Experiment_list_ID 1 '2D J-resolved 1H' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse000806 1 2 '2D [1H,13C]-HSQC' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse000806 1 3 '1D 1H, NOESY' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $Bruker_700 bmse000806 1 stop_ loop_ _Experiment_file.Experiment_ID _Experiment_file.Name _Experiment_file.Type _Experiment_file.Directory_path _Experiment_file.Details _Experiment_file.Entry_ID _Experiment_file.Experiment_list_ID 1 1H_1H_JRES text/directory nmr/set01/ 'NMR experiment directory' bmse000806 1 1 00.png image/png nmr/set01/spectra/1H_1H_JRES 'Spectral image' bmse000806 1 2 1H_13C_HSQC text/directory nmr/set01/ 'NMR experiment directory' bmse000806 1 2 00.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse000806 1 2 01.png image/png nmr/set01/spectra/1H_13C_HSQC 'Spectral image' bmse000806 1 3 1H_NOESY text/directory nmr/set01/ 'NMR experiment directory' bmse000806 1 3 00.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse000806 1 3 01.png image/png nmr/set01/spectra/1H_NOESY 'Spectral image' bmse000806 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 bmse000806 _Chem_shift_reference.ID 1 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 DSS 'methyl protons' ppm 0.00 internal direct 1.000000000 bmse000806 1 C 13 DSS 'methyl carbons' ppm 0.00 internal direct 1.000000000 bmse000806 1 stop_ save_