data_51742 ####################### # Entry information # ####################### save_entry_information_1 _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information_1 _Entry.ID 51742 _Entry.Title ; [D-Cys5,D-Lys16]-STp(5-17), native form ; _Entry.Type macromolecule _Entry.Version_type original _Entry.Submission_date 2022-12-15 _Entry.Accession_date 2022-12-15 _Entry.Last_release_date 2022-12-15 _Entry.Original_release_date 2022-12-15 _Entry.Origination author _Entry.Format_name . _Entry.NMR_STAR_version 3.2.14.0 _Entry.NMR_STAR_dict_location . _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.Source_data_format . _Entry.Source_data_format_version . _Entry.Generated_software_name . _Entry.Generated_software_version . _Entry.Generated_software_ID 1 _Entry.Generated_software_label $software_1 _Entry.Generated_date . _Entry.DOI . _Entry.UUID . _Entry.Related_coordinate_file_name . _Entry.Details . _Entry.BMRB_internal_directory_name . 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.ORCID _Entry_author.Entry_ID 1 Shigeru Shimamoto . . . . 51742 2 Yuji Hidaka . . . . 51742 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 51742 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 63 51742 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 . . 2023-03-07 . original BMRB . 51742 stop_ loop_ _Related_entries.Database_name _Related_entries.Database_accession_code _Related_entries.Relationship _Related_entries.Entry_ID BMRB 51743 '[D-Cys5,Asp7,Val8,D-Lys16]-STp(5-17), native form' 51742 stop_ save_ ############### # Citations # ############### save_citations_1 _Citation.Sf_category citations _Citation.Sf_framecode citations_1 _Citation.Entry_ID 51742 _Citation.ID 1 _Citation.Name . _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.PubMed_ID 36770798 _Citation.DOI . _Citation.Full_citation . _Citation.Title ; The Molecular Basis of Heat-Stable Enterotoxin for Vaccine Development and Cancer Cell Detection ; _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev Molecules _Citation.Journal_name_full 'Molecules (Basel, Switzerland)' _Citation.Journal_volume 28 _Citation.Journal_issue 3 _Citation.Journal_ASTM . _Citation.Journal_ISSN 1420-3049 _Citation.Journal_CSD . _Citation.Book_title . _Citation.Book_chapter_title . _Citation.Book_volume . _Citation.Book_series . _Citation.Book_publisher . _Citation.Book_publisher_city . _Citation.Book_ISBN . _Citation.Conference_title . _Citation.Conference_site . _Citation.Conference_state_province . _Citation.Conference_country . _Citation.Conference_start_date . _Citation.Conference_end_date . _Citation.Conference_abstract_number . _Citation.Thesis_institution . _Citation.Thesis_institution_city . _Citation.Thesis_institution_country . _Citation.WWW_URL . _Citation.Page_first 1128 _Citation.Page_last 1128 _Citation.Year 2023 _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.ORCID _Citation_author.Entry_ID _Citation_author.Citation_ID 1 Masaya Goto M. . . . 51742 1 2 Shinya Yoshino S. . . . 51742 1 3 Kyona Hiroshima K. . . . 51742 1 4 Toru Kawakami T. . . . 51742 1 5 Kaeko Murota K. . . . 51742 1 6 Shigeru Shimamoto S. . . . 51742 1 7 Yuji Hidaka Y. . . . 51742 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID 51742 _Assembly.ID 1 _Assembly.Name '[D-Cys5,D-Lys16]-STp(5-17), native form' _Assembly.BMRB_code . _Assembly.Number_of_components 1 _Assembly.Organic_ligands 0 _Assembly.Metal_ions 0 _Assembly.Non_standard_bonds no _Assembly.Ambiguous_conformational_states no _Assembly.Ambiguous_chem_comp_sites . _Assembly.Molecules_in_chemical_exchange no _Assembly.Paramagnetic no _Assembly.Thiol_state . _Assembly.Molecular_mass . _Assembly.Enzyme_commission_number . _Assembly.Details . _Assembly.DB_query_date . _Assembly.DB_query_revised_last_date . loop_ _Entity_assembly.ID _Entity_assembly.Entity_assembly_name _Entity_assembly.Entity_ID _Entity_assembly.Entity_label _Entity_assembly.Asym_ID _Entity_assembly.PDB_chain_ID _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 '[D-Cys5,D-Lys16]-STp(5-17), native form' 1 $entity_1 . . yes native no no . . . 51742 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID 51742 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name entity_1 _Entity.Type polymer _Entity.Polymer_common_type . _Entity.Polymer_type polypeptide(L) _Entity.Polymer_type_details . _Entity.Polymer_strand_ID . _Entity.Polymer_seq_one_letter_code_can . _Entity.Polymer_seq_one_letter_code ; XCELCCNPACAXC ; _Entity.Target_identifier . _Entity.Polymer_author_defined_seq 5-17 _Entity.Polymer_author_seq_details . _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_monomer no _Entity.Nstd_chirality yes _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID . _Entity.Nonpolymer_comp_label . _Entity.Number_of_monomers 13 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic no _Entity.Thiol_state 'all disulfide bound' _Entity.Src_method . _Entity.Parent_entity_ID 1 _Entity.Fragment . _Entity.Mutation D-Cys5,D-Lys16 _Entity.EC_number . _Entity.Calc_isoelectric_point . _Entity.Formula_weight . _Entity.Formula_weight_exptl . _Entity.Formula_weight_exptl_meth . _Entity.Details . _Entity.DB_query_date . _Entity.DB_query_revised_last_date . loop_ _Entity_biological_function.Biological_function _Entity_biological_function.Entry_ID _Entity_biological_function.Entity_ID 'heat-stable enterotoxin' 51742 1 stop_ loop_ _Entity_comp_index.ID _Entity_comp_index.Auth_seq_ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 5 DCY . 51742 1 2 6 CYS . 51742 1 3 7 GLU . 51742 1 4 8 LEU . 51742 1 5 9 CYS . 51742 1 6 10 CYS . 51742 1 7 11 ASN . 51742 1 8 12 PRO . 51742 1 9 13 ALA . 51742 1 10 14 CYS . 51742 1 11 15 ALA . 51742 1 12 16 DLY . 51742 1 13 17 CYS . 51742 1 stop_ loop_ _Entity_poly_seq.Hetero _Entity_poly_seq.Mon_ID _Entity_poly_seq.Num _Entity_poly_seq.Comp_index_ID _Entity_poly_seq.Entry_ID _Entity_poly_seq.Entity_ID . DCY 1 1 51742 1 . CYS 2 2 51742 1 . GLU 3 3 51742 1 . LEU 4 4 51742 1 . CYS 5 5 51742 1 . CYS 6 6 51742 1 . ASN 7 7 51742 1 . PRO 8 8 51742 1 . ALA 9 9 51742 1 . CYS 10 10 51742 1 . ALA 11 11 51742 1 . DLY 12 12 51742 1 . CYS 13 13 51742 1 stop_ save_ #################### # Natural source # #################### save_natural_source_1 _Entity_natural_src_list.Sf_category natural_source _Entity_natural_src_list.Sf_framecode natural_source_1 _Entity_natural_src_list.Entry_ID 51742 _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.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.Secretion _Entity_natural_src.Plasmid _Entity_natural_src.Gene_mnemonic _Entity_natural_src.Details _Entity_natural_src.Entry_ID _Entity_natural_src.Entity_natural_src_list_ID 1 1 $entity_1 . 562 organism . 'Escherichia coli' 'E. coli' . . Bacteria . Escherichia coli . . . . . . . . . . . . . 51742 1 stop_ save_ ######################### # Experimental source # ######################### save_experimental_source_1 _Entity_experimental_src_list.Sf_category experimental_source _Entity_experimental_src_list.Sf_framecode experimental_source_1 _Entity_experimental_src_list.Entry_ID 51742 _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_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.Details _Entity_experimental_src.Entry_ID _Entity_experimental_src.Entity_experimental_src_list_ID 1 1 $entity_1 . 'chemical synthesis' . . . . . . . . . . . . . . . . 51742 1 stop_ save_ ################################# # Polymer residues and ligands # ################################# save_chem_comp_DCY _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_DCY _Chem_comp.Entry_ID 51742 _Chem_comp.ID DCY _Chem_comp.Provenance PDB _Chem_comp.Name D-CYSTEINE _Chem_comp.Type 'D-PEPTIDE LINKING' _Chem_comp.BMRB_code DCY _Chem_comp.PDB_code DCY _Chem_comp.Ambiguous_flag no _Chem_comp.Initial_date 2020-07-10 _Chem_comp.Modified_date 2020-07-10 _Chem_comp.Release_status REL _Chem_comp.Replaced_by . _Chem_comp.Replaces . _Chem_comp.One_letter_code C _Chem_comp.Three_letter_code DCY _Chem_comp.Number_atoms_all 14 _Chem_comp.Number_atoms_nh 7 _Chem_comp.Atom_nomenclature_source . _Chem_comp.PubChem_code . _Chem_comp.Subcomponent_list . _Chem_comp.InChI_code InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1 _Chem_comp.Mon_nstd_flag no _Chem_comp.Mon_nstd_class . _Chem_comp.Mon_nstd_details . _Chem_comp.Mon_nstd_parent . _Chem_comp.Mon_nstd_parent_comp_ID . _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.Std_deriv_chem_comp_name . _Chem_comp.Synonyms . _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic . _Chem_comp.Aromatic no _Chem_comp.Formula 'C3 H7 N O2 S' _Chem_comp.Formula_weight 121.158 _Chem_comp.Formula_mono_iso_wt_nat . _Chem_comp.Formula_mono_iso_wt_13C . _Chem_comp.Formula_mono_iso_wt_15N . _Chem_comp.Formula_mono_iso_wt_13C_15N . _Chem_comp.Image_file_name . _Chem_comp.Image_file_format . _Chem_comp.Topo_file_name . _Chem_comp.Topo_file_format . _Chem_comp.Struct_file_name . _Chem_comp.Struct_file_format . _Chem_comp.Stereochem_param_file_name . _Chem_comp.Stereochem_param_file_format . _Chem_comp.Model_details . _Chem_comp.Model_erf . _Chem_comp.Model_source . _Chem_comp.Model_coordinates_details . _Chem_comp.Model_coordinates_missing_flag no _Chem_comp.Ideal_coordinates_details . _Chem_comp.Ideal_coordinates_missing_flag no _Chem_comp.Model_coordinates_db_code 1F57 _Chem_comp.Processing_site RCSB _Chem_comp.Vendor . _Chem_comp.Vendor_product_code . _Chem_comp.Details . _Chem_comp.DB_query_date . _Chem_comp.DB_last_query_revised_last_date . 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 C(C(C(=O)O)N)S SMILES 'OpenEye OEToolkits' 1.5.0 51742 DCY C([C@H](C(=O)O)N)S SMILES_CANONICAL 'OpenEye OEToolkits' 1.5.0 51742 DCY InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1 InChI InChI 1.03 51742 DCY N[C@H](CS)C(O)=O SMILES_CANONICAL CACTVS 3.341 51742 DCY N[CH](CS)C(O)=O SMILES CACTVS 3.341 51742 DCY O=C(O)C(N)CS SMILES ACDLabs 10.04 51742 DCY XUJNEKJLAYXESH-UWTATZPHSA-N InChIKey InChI 1.03 51742 DCY stop_ loop_ _Chem_comp_identifier.Identifier _Chem_comp_identifier.Type _Chem_comp_identifier.Program _Chem_comp_identifier.Program_version _Chem_comp_identifier.Entry_ID _Chem_comp_identifier.Comp_ID '(2S)-2-amino-3-sulfanyl-propanoic acid' 'SYSTEMATIC NAME' 'OpenEye OEToolkits' 1.5.0 51742 DCY D-cysteine 'SYSTEMATIC NAME' ACDLabs 10.04 51742 DCY stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.BMRB_code _Chem_comp_atom.PDB_atom_ID _Chem_comp_atom.Alt_atom_ID _Chem_comp_atom.Auth_atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Isotope_number _Chem_comp_atom.Chirality _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Partial_charge _Chem_comp_atom.Oxidation_number _Chem_comp_atom.Unpaired_electron_number _Chem_comp_atom.Align _Chem_comp_atom.Aromatic_flag _Chem_comp_atom.Leaving_atom_flag _Chem_comp_atom.Substruct_code _Chem_comp_atom.Ionizable _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_x_esd _Chem_comp_atom.Model_Cartn_y _Chem_comp_atom.Model_Cartn_y_esd _Chem_comp_atom.Model_Cartn_z _Chem_comp_atom.Model_Cartn_z_esd _Chem_comp_atom.Model_Cartn_x_ideal _Chem_comp_atom.Model_Cartn_y_ideal _Chem_comp_atom.Model_Cartn_z_ideal _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Details _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID N N N N . N . . N 0 . . . 1 N N . . . . 10.380 . -11.139 . 23.139 . 1.592 0.453 0.079 1 . 51742 DCY CA CA CA CA . C . . S 0 . . . 1 N N . . . . 9.835 . -9.750 . 23.203 . 0.145 0.444 -0.175 2 . 51742 DCY C C C C . C . . N 0 . . . 1 N N . . . . 9.754 . -9.262 . 24.656 . -0.113 -0.000 -1.591 3 . 51742 DCY O O O O . O . . N 0 . . . 1 N N . . . . 9.179 . -8.183 . 24.900 . 0.649 -0.765 -2.133 4 . 51742 DCY CB CB CB CB . C . . N 0 . . . 1 N N . . . . 10.742 . -8.821 . 22.398 . -0.537 -0.521 0.795 5 . 51742 DCY SG SG SG SG . S . . N 0 . . . 1 N N . . . . 12.422 . -8.587 . 23.046 . -0.226 0.014 2.500 6 . 51742 DCY OXT OXT OXT OXT . O . . N 0 . . . 1 N Y . . . . 10.282 . -9.969 . 25.533 . -1.190 0.452 -2.251 7 . 51742 DCY H H H H . H . . N 0 . . . 1 N N . . . . 10.433 . -11.463 . 22.173 . 2.010 1.018 -0.644 8 . 51742 DCY H2 H2 H2 HN2 . H . . N 0 . . . 1 N Y . . . . 9.845 . -11.781 . 23.723 . 1.917 -0.491 -0.065 9 . 51742 DCY HA HA HA HA . H . . N 0 . . . 1 N N . . . . 8.805 . -9.745 . 22.774 . -0.255 1.447 -0.030 10 . 51742 DCY HB2 HB2 HB2 1HB . H . . N 0 . . . 1 N N . . . . 10.790 . -9.164 . 21.338 . -1.610 -0.527 0.606 11 . 51742 DCY HB3 HB3 HB3 2HB . H . . N 0 . . . 1 N N . . . . 10.246 . -7.830 . 22.265 . -0.137 -1.525 0.651 12 . 51742 DCY HG HG HG HG . H . . N 0 . . . 1 N N . . . . 12.986 . -8.009 . 22.545 . -0.893 -0.942 3.171 13 . 51742 DCY HXT HXT HXT HXT . H . . N 0 . . . 1 N Y . . . . 10.231 . -9.667 . 26.432 . -1.356 0.166 -3.160 14 . 51742 DCY 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.Aromatic_flag _Chem_comp_bond.Stereo_config _Chem_comp_bond.Ordinal _Chem_comp_bond.Details _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 . SING N CA N N 1 . 51742 DCY 2 . SING N H N N 2 . 51742 DCY 3 . SING N H2 N N 3 . 51742 DCY 4 . SING CA C N N 4 . 51742 DCY 5 . SING CA CB N N 5 . 51742 DCY 6 . SING CA HA N N 6 . 51742 DCY 7 . DOUB C O N N 7 . 51742 DCY 8 . SING C OXT N N 8 . 51742 DCY 9 . SING CB SG N N 9 . 51742 DCY 10 . SING CB HB2 N N 10 . 51742 DCY 11 . SING CB HB3 N N 11 . 51742 DCY 12 . SING SG HG N N 12 . 51742 DCY 13 . SING OXT HXT N N 13 . 51742 DCY stop_ save_ save_chem_comp_DLY _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_DLY _Chem_comp.Entry_ID 51742 _Chem_comp.ID DLY _Chem_comp.Provenance PDB _Chem_comp.Name D-LYSINE _Chem_comp.Type 'D-PEPTIDE LINKING' _Chem_comp.BMRB_code DLY _Chem_comp.PDB_code DLY _Chem_comp.Ambiguous_flag no _Chem_comp.Initial_date 2020-07-10 _Chem_comp.Modified_date 2020-07-10 _Chem_comp.Release_status REL _Chem_comp.Replaced_by . _Chem_comp.Replaces . _Chem_comp.One_letter_code K _Chem_comp.Three_letter_code DLY _Chem_comp.Number_atoms_all 24 _Chem_comp.Number_atoms_nh 10 _Chem_comp.Atom_nomenclature_source . _Chem_comp.PubChem_code . _Chem_comp.Subcomponent_list . _Chem_comp.InChI_code InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m1/s1 _Chem_comp.Mon_nstd_flag no _Chem_comp.Mon_nstd_class . _Chem_comp.Mon_nstd_details . _Chem_comp.Mon_nstd_parent . _Chem_comp.Mon_nstd_parent_comp_ID . _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.Std_deriv_chem_comp_name . _Chem_comp.Synonyms . _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic . _Chem_comp.Aromatic no _Chem_comp.Formula 'C6 H14 N2 O2' _Chem_comp.Formula_weight 146.188 _Chem_comp.Formula_mono_iso_wt_nat . _Chem_comp.Formula_mono_iso_wt_13C . _Chem_comp.Formula_mono_iso_wt_15N . _Chem_comp.Formula_mono_iso_wt_13C_15N . _Chem_comp.Image_file_name . _Chem_comp.Image_file_format . _Chem_comp.Topo_file_name . _Chem_comp.Topo_file_format . _Chem_comp.Struct_file_name . _Chem_comp.Struct_file_format . _Chem_comp.Stereochem_param_file_name . _Chem_comp.Stereochem_param_file_format . _Chem_comp.Model_details . _Chem_comp.Model_erf . _Chem_comp.Model_source . _Chem_comp.Model_coordinates_details . _Chem_comp.Model_coordinates_missing_flag no _Chem_comp.Ideal_coordinates_details . _Chem_comp.Ideal_coordinates_missing_flag no _Chem_comp.Model_coordinates_db_code 1C4B _Chem_comp.Processing_site RCSB _Chem_comp.Vendor . _Chem_comp.Vendor_product_code . _Chem_comp.Details . _Chem_comp.DB_query_date . _Chem_comp.DB_last_query_revised_last_date . 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 C(CCN)CC(C(=O)O)N SMILES 'OpenEye OEToolkits' 1.5.0 51742 DLY C(CCN)C[C@H](C(=O)O)N SMILES_CANONICAL 'OpenEye OEToolkits' 1.5.0 51742 DLY InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m1/s1 InChI InChI 1.03 51742 DLY KDXKERNSBIXSRK-RXMQYKEDSA-N InChIKey InChI 1.03 51742 DLY NCCCC[C@@H](N)C(O)=O SMILES_CANONICAL CACTVS 3.341 51742 DLY NCCCC[CH](N)C(O)=O SMILES CACTVS 3.341 51742 DLY O=C(O)C(N)CCCCN SMILES ACDLabs 10.04 51742 DLY stop_ loop_ _Chem_comp_identifier.Identifier _Chem_comp_identifier.Type _Chem_comp_identifier.Program _Chem_comp_identifier.Program_version _Chem_comp_identifier.Entry_ID _Chem_comp_identifier.Comp_ID '(2R)-2,6-diaminohexanoic acid' 'SYSTEMATIC NAME' 'OpenEye OEToolkits' 1.5.0 51742 DLY D-lysine 'SYSTEMATIC NAME' ACDLabs 10.04 51742 DLY stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.BMRB_code _Chem_comp_atom.PDB_atom_ID _Chem_comp_atom.Alt_atom_ID _Chem_comp_atom.Auth_atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Isotope_number _Chem_comp_atom.Chirality _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Partial_charge _Chem_comp_atom.Oxidation_number _Chem_comp_atom.Unpaired_electron_number _Chem_comp_atom.Align _Chem_comp_atom.Aromatic_flag _Chem_comp_atom.Leaving_atom_flag _Chem_comp_atom.Substruct_code _Chem_comp_atom.Ionizable _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_x_esd _Chem_comp_atom.Model_Cartn_y _Chem_comp_atom.Model_Cartn_y_esd _Chem_comp_atom.Model_Cartn_z _Chem_comp_atom.Model_Cartn_z_esd _Chem_comp_atom.Model_Cartn_x_ideal _Chem_comp_atom.Model_Cartn_y_ideal _Chem_comp_atom.Model_Cartn_z_ideal _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Details _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID N N N N . N . . N 0 . . . 1 N N . . . . 1.958 . -1.185 . 0.419 . 1.770 0.232 -1.331 1 . 51742 DLY CA CA CA CA . C . . R 0 . . . 1 N N . . . . 2.544 . 0.113 . 0.712 . 0.326 0.498 -1.348 2 . 51742 DLY C C C C . C . . N 0 . . . 1 N N . . . . 1.902 . 1.172 . -0.185 . -0.271 -0.054 -2.616 3 . 51742 DLY O O O O . O . . N 0 . . . 1 N N . . . . 0.678 . 1.242 . -0.292 . 0.220 -1.024 -3.143 4 . 51742 DLY CB CB CB CB . C . . N 0 . . . 1 N N . . . . 2.435 . 0.424 . 2.206 . -0.329 -0.173 -0.140 5 . 51742 DLY CG CG CG CG . C . . N 0 . . . 1 N N . . . . 2.618 . -0.842 . 3.046 . 0.277 0.387 1.147 6 . 51742 DLY CD CD CD CD . C . . N 0 . . . 1 N N . . . . 1.297 . -1.601 . 3.190 . -0.378 -0.283 2.355 7 . 51742 DLY CE CE CE CE . C . . N 0 . . . 1 N N . . . . 1.544 . -3.098 . 3.389 . 0.228 0.277 3.642 8 . 51742 DLY NZ NZ NZ NZ . N . . N 0 . . . 1 N N . . . . 1.361 . -3.467 . 4.810 . -0.401 -0.367 4.802 9 . 51742 DLY OXT OXT OXT OXT . O . . N 0 . . . 1 N Y . . . . 2.756 . 1.971 . -0.809 . -1.350 0.530 -3.160 10 . 51742 DLY H H H H . H . . N 0 . . . 1 N N . . . . 0.978 . -1.170 . 0.222 . 2.143 0.602 -2.193 11 . 51742 DLY H2 H2 H2 HN2 . H . . N 0 . . . 1 N Y . . . . 2.024 . -1.424 . -0.570 . 1.882 -0.769 -1.373 12 . 51742 DLY HA HA HA HA . H . . N 0 . . . 1 N N . . . . 3.606 . 0.053 . 0.471 . 0.153 1.573 -1.304 13 . 51742 DLY HB2 HB2 HB2 1HB . H . . N 0 . . . 1 N N . . . . 1.462 . 0.868 . 2.419 . -0.157 -1.248 -0.184 14 . 51742 DLY HB3 HB3 HB3 2HB . H . . N 0 . . . 1 N N . . . . 3.189 . 1.161 . 2.484 . -1.401 0.023 -0.152 15 . 51742 DLY HG2 HG2 HG2 1HG . H . . N 0 . . . 1 N N . . . . 2.999 . -0.577 . 4.031 . 0.104 1.463 1.191 16 . 51742 DLY HG3 HG3 HG3 2HG . H . . N 0 . . . 1 N N . . . . 3.363 . -1.486 . 2.579 . 1.349 0.191 1.159 17 . 51742 DLY HD2 HD2 HD2 1HD . H . . N 0 . . . 1 N N . . . . 0.685 . -1.444 . 2.301 . -0.206 -1.359 2.311 18 . 51742 DLY HD3 HD3 HD3 2HD . H . . N 0 . . . 1 N N . . . . 0.737 . -1.204 . 4.036 . -1.450 -0.087 2.343 19 . 51742 DLY HE2 HE2 HE2 1HE . H . . N 0 . . . 1 N N . . . . 2.554 . -3.352 . 3.067 . 0.055 1.352 3.686 20 . 51742 DLY HE3 HE3 HE3 2HE . H . . N 0 . . . 1 N N . . . . 0.857 . -3.671 . 2.766 . 1.300 0.080 3.655 21 . 51742 DLY HZ1 HZ1 HZ1 1HZ . H . . N 0 . . . 1 N N . . . . 0.413 . -3.297 . 5.129 . 0.027 0.031 5.624 22 . 51742 DLY HZ2 HZ2 HZ2 2HZ . H . . N 0 . . . 1 N N . . . . 1.976 . -2.941 . 5.422 . -1.367 -0.074 4.808 23 . 51742 DLY HXT HXT HXT HXT . H . . N 0 . . . 1 N Y . . . . 2.357 . 2.628 . -1.366 . -1.734 0.175 -3.974 24 . 51742 DLY 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.Aromatic_flag _Chem_comp_bond.Stereo_config _Chem_comp_bond.Ordinal _Chem_comp_bond.Details _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 . SING N CA N N 1 . 51742 DLY 2 . SING N H N N 2 . 51742 DLY 3 . SING N H2 N N 3 . 51742 DLY 4 . SING CA C N N 4 . 51742 DLY 5 . SING CA CB N N 5 . 51742 DLY 6 . SING CA HA N N 6 . 51742 DLY 7 . DOUB C O N N 7 . 51742 DLY 8 . SING C OXT N N 8 . 51742 DLY 9 . SING CB CG N N 9 . 51742 DLY 10 . SING CB HB2 N N 10 . 51742 DLY 11 . SING CB HB3 N N 11 . 51742 DLY 12 . SING CG CD N N 12 . 51742 DLY 13 . SING CG HG2 N N 13 . 51742 DLY 14 . SING CG HG3 N N 14 . 51742 DLY 15 . SING CD CE N N 15 . 51742 DLY 16 . SING CD HD2 N N 16 . 51742 DLY 17 . SING CD HD3 N N 17 . 51742 DLY 18 . SING CE NZ N N 18 . 51742 DLY 19 . SING CE HE2 N N 19 . 51742 DLY 20 . SING CE HE3 N N 20 . 51742 DLY 21 . SING NZ HZ1 N N 21 . 51742 DLY 22 . SING NZ HZ2 N N 22 . 51742 DLY 23 . SING OXT HXT N N 23 . 51742 DLY stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID 51742 _Sample.ID 1 _Sample.Name [D-Cys5,D-Lys16]-STp(5-17) _Sample.Type solution _Sample.Sub_type . _Sample.Details . _Sample.Aggregate_sample_number 1 _Sample.Solvent_system '90% H2O/10% D2O' _Sample.Preparation_date . _Sample.Preparation_expiration_date . _Sample.Polycrystallization_protocol . _Sample.Single_crystal_protocol . _Sample.Crystal_grow_apparatus . _Sample.Crystal_grow_atmosphere . _Sample.Crystal_grow_details . _Sample.Crystal_grow_method . _Sample.Crystal_grow_method_cit_ID . _Sample.Crystal_grow_pH . _Sample.Crystal_grow_pH_range . _Sample.Crystal_grow_pressure . _Sample.Crystal_grow_pressure_esd . _Sample.Crystal_grow_seeding . _Sample.Crystal_grow_seeding_cit_ID . _Sample.Crystal_grow_temp . _Sample.Crystal_grow_temp_details . _Sample.Crystal_grow_temp_esd . _Sample.Crystal_grow_time . _Sample.Oriented_sample_prep_protocol . _Sample.Lyophilization_cryo_protectant . _Sample.Storage_protocol . loop_ _Sample_component.ID _Sample_component.Mol_common_name _Sample_component.Isotopic_labeling _Sample_component.Assembly_ID _Sample_component.Assembly_label _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 [D-Cys5,D-Lys16]-STp(5-17) 'natural abundance' . . 1 $entity_1 . . 3 . . mM . . . . 51742 1 2 'sodium phosphate buffer' 'natural abundance' . . . . . . 25 . . mM . . . . 51742 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 51742 _Sample_condition_list.ID 1 _Sample_condition_list.Name condition_1 _Sample_condition_list.Details '20 mM sodium phosphate buffer prepared with a 90% H2O/10% D2O mixture at pH 6.5' 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 'ionic strength' 25 . mM 51742 1 pH 6.5 . pH 51742 1 pressure 1 . atm 51742 1 temperature 298 . K 51742 1 stop_ save_ ############################ # Computer software used # ############################ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID 51742 _Software.ID 1 _Software.Type . _Software.Name NMRPipe _Software.Version . _Software.DOI . _Software.Details . loop_ _Task.Task _Task.Software_module _Task.Entry_ID _Task.Software_ID 'chemical shift assignment' . 51742 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_NMR_spectrometer_1 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode NMR_spectrometer_1 _NMR_spectrometer.Entry_ID 51742 _NMR_spectrometer.ID 1 _NMR_spectrometer.Name JNM-ECA800 _NMR_spectrometer.Details . _NMR_spectrometer.Manufacturer JEOL _NMR_spectrometer.Model JNM-ECA800 _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 800 save_ ############################# # NMR applied experiments # ############################# save_experiment_list_1 _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list_1 _Experiment_list.Entry_ID 51742 _Experiment_list.ID 1 _Experiment_list.Details . loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _Experiment.NUS_flag _Experiment.Interleaved_flag _Experiment.NMR_spec_expt_ID _Experiment.NMR_spec_expt_label _Experiment.MS_expt_ID _Experiment.MS_expt_label _Experiment.SAXS_expt_ID _Experiment.SAXS_expt_label _Experiment.FRET_expt_ID _Experiment.FRET_expt_label _Experiment.EMR_expt_ID _Experiment.EMR_expt_label _Experiment.Sample_ID _Experiment.Sample_label _Experiment.Sample_state _Experiment.Sample_volume _Experiment.Sample_volume_units _Experiment.Sample_condition_list_ID _Experiment.Sample_condition_list_label _Experiment.Sample_spinning_rate _Experiment.Sample_angle _Experiment.NMR_tube_type _Experiment.NMR_spectrometer_ID _Experiment.NMR_spectrometer_label _Experiment.NMR_spectrometer_probe_ID _Experiment.NMR_spectrometer_probe_label _Experiment.NMR_spectral_processing_ID _Experiment.NMR_spectral_processing_label _Experiment.Mass_spectrometer_ID _Experiment.Mass_spectrometer_label _Experiment.Xray_instrument_ID _Experiment.Xray_instrument_label _Experiment.Fluorescence_instrument_ID _Experiment.Fluorescence_instrument_label _Experiment.EMR_instrument_ID _Experiment.EMR_instrument_label _Experiment.Chromatographic_system_ID _Experiment.Chromatographic_system_label _Experiment.Chromatographic_column_ID _Experiment.Chromatographic_column_label _Experiment.Details _Experiment.Entry_ID _Experiment.Experiment_list_ID 1 '2D DQF-COSY' no no no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $NMR_spectrometer_1 . . . . . . . . . . . . . . . . . 51742 1 2 '2D 1H-1H NOESY' no no no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $NMR_spectrometer_1 . . . . . . . . . . . . . . . . . 51742 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 51742 _Chem_shift_reference.ID 1 _Chem_shift_reference.Name chemical_shift_reference_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.Concentration_val _Chem_shift_ref.Concentration_units _Chem_shift_ref.Solvent _Chem_shift_ref.Rank _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.Ref_correction_type _Chem_shift_ref.Correction_val _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 DSS 'methyl protons' . . . . ppm 0.00 internal direct 1.000000000 . . . . . 51742 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_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 51742 _Assigned_chem_shift_list.ID 1 _Assigned_chem_shift_list.Name 1H _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.Chem_shift_1H_err . _Assigned_chem_shift_list.Chem_shift_13C_err . _Assigned_chem_shift_list.Chem_shift_15N_err . _Assigned_chem_shift_list.Chem_shift_31P_err . _Assigned_chem_shift_list.Chem_shift_2H_err . _Assigned_chem_shift_list.Chem_shift_19F_err . _Assigned_chem_shift_list.Error_derivation_method . _Assigned_chem_shift_list.Details . _Assigned_chem_shift_list.Text_data_format . _Assigned_chem_shift_list.Text_data . loop_ _Chem_shift_experiment.Experiment_ID _Chem_shift_experiment.Experiment_name _Chem_shift_experiment.Sample_ID _Chem_shift_experiment.Sample_label _Chem_shift_experiment.Sample_state _Chem_shift_experiment.Entry_ID _Chem_shift_experiment.Assigned_chem_shift_list_ID 1 '2D DQF-COSY' . . . 51742 1 2 '2D 1H-1H NOESY' . . . 51742 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 . . 51742 1 stop_ loop_ _Atom_chem_shift.ID _Atom_chem_shift.Assembly_atom_ID _Atom_chem_shift.Entity_assembly_ID _Atom_chem_shift.Entity_assembly_asym_ID _Atom_chem_shift.Entity_ID _Atom_chem_shift.Comp_index_ID _Atom_chem_shift.Seq_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.Ambiguity_set_ID _Atom_chem_shift.Occupancy _Atom_chem_shift.Resonance_ID _Atom_chem_shift.Auth_entity_assembly_ID _Atom_chem_shift.Auth_asym_ID _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 1 DCY HA H 1 4.505 0.010 . 1 . . . . . 5 DCY HA . 51742 1 2 . 1 . 1 1 1 DCY HB2 H 1 3.385 0.010 . 2 . . . . . 5 DCY HB2 . 51742 1 3 . 1 . 1 2 2 CYS HB2 H 1 3.049 0.010 . 1 . . . . . 6 CYS HB2 . 51742 1 4 . 1 . 1 2 2 CYS HB3 H 1 3.540 0.010 . 1 . . . . . 6 CYS HB3 . 51742 1 5 . 1 . 1 3 3 GLU HA H 1 4.389 0.010 . 1 . . . . . 7 GLU HA . 51742 1 6 . 1 . 1 3 3 GLU HB2 H 1 2.126 0.010 . 1 . . . . . 7 GLU HB2 . 51742 1 7 . 1 . 1 3 3 GLU HB3 H 1 2.199 0.010 . 1 . . . . . 7 GLU HB3 . 51742 1 8 . 1 . 1 3 3 GLU HG2 H 1 2.292 0.010 . 1 . . . . . 7 GLU HG2 . 51742 1 9 . 1 . 1 3 3 GLU HG3 H 1 2.539 0.010 . 1 . . . . . 7 GLU HG3 . 51742 1 10 . 1 . 1 4 4 LEU H H 1 7.481 0.010 . 1 . . . . . 8 LEU H . 51742 1 11 . 1 . 1 4 4 LEU HA H 1 4.780 0.010 . 1 . . . . . 8 LEU HA . 51742 1 12 . 1 . 1 4 4 LEU HB2 H 1 1.654 0.010 . 1 . . . . . 8 LEU HB2 . 51742 1 13 . 1 . 1 4 4 LEU HB3 H 1 1.909 0.010 . 1 . . . . . 8 LEU HB3 . 51742 1 14 . 1 . 1 4 4 LEU HG H 1 1.654 0.010 . 1 . . . . . 8 LEU HG . 51742 1 15 . 1 . 1 4 4 LEU HD11 H 1 0.930 0.010 . 1 . . . . . 8 LEU MD1 . 51742 1 16 . 1 . 1 4 4 LEU HD12 H 1 0.930 0.010 . 1 . . . . . 8 LEU MD1 . 51742 1 17 . 1 . 1 4 4 LEU HD13 H 1 0.930 0.010 . 1 . . . . . 8 LEU MD1 . 51742 1 18 . 1 . 1 4 4 LEU HD21 H 1 0.996 0.010 . 1 . . . . . 8 LEU MD2 . 51742 1 19 . 1 . 1 4 4 LEU HD22 H 1 0.996 0.010 . 1 . . . . . 8 LEU MD2 . 51742 1 20 . 1 . 1 4 4 LEU HD23 H 1 0.996 0.010 . 1 . . . . . 8 LEU MD2 . 51742 1 21 . 1 . 1 5 5 CYS H H 1 8.496 0.010 . 1 . . . . . 9 CYS H . 51742 1 22 . 1 . 1 5 5 CYS HA H 1 4.406 0.010 . 1 . . . . . 9 CYS HA . 51742 1 23 . 1 . 1 5 5 CYS HB2 H 1 2.936 0.010 . 1 . . . . . 9 CYS HB2 . 51742 1 24 . 1 . 1 5 5 CYS HB3 H 1 3.229 0.010 . 1 . . . . . 9 CYS HB3 . 51742 1 25 . 1 . 1 6 6 CYS H H 1 6.932 0.010 . 1 . . . . . 10 CYS H . 51742 1 26 . 1 . 1 6 6 CYS HA H 1 4.441 0.010 . 1 . . . . . 10 CYS HA . 51742 1 27 . 1 . 1 6 6 CYS HB2 H 1 3.340 0.010 . 1 . . . . . 10 CYS HB2 . 51742 1 28 . 1 . 1 6 6 CYS HB3 H 1 3.489 0.010 . 1 . . . . . 10 CYS HB3 . 51742 1 29 . 1 . 1 7 7 ASN H H 1 7.234 0.010 . 1 . . . . . 11 ASN H . 51742 1 30 . 1 . 1 7 7 ASN HA H 1 5.131 0.010 . 1 . . . . . 11 ASN HA . 51742 1 31 . 1 . 1 7 7 ASN HB2 H 1 2.873 0.010 . 2 . . . . . 11 ASN HB2 . 51742 1 32 . 1 . 1 7 7 ASN HD21 H 1 6.896 0.010 . 1 . . . . . 11 ASN HD21 . 51742 1 33 . 1 . 1 7 7 ASN HD22 H 1 7.683 0.010 . 1 . . . . . 11 ASN HD22 . 51742 1 34 . 1 . 1 8 8 PRO HA H 1 4.378 0.010 . 1 . . . . . 12 PRO HA . 51742 1 35 . 1 . 1 8 8 PRO HB2 H 1 2.397 0.010 . 2 . . . . . 12 PRO HB2 . 51742 1 36 . 1 . 1 8 8 PRO HG2 H 1 2.013 0.010 . 2 . . . . . 12 PRO HG2 . 51742 1 37 . 1 . 1 8 8 PRO HD2 H 1 3.734 0.010 . 1 . . . . . 12 PRO HD2 . 51742 1 38 . 1 . 1 8 8 PRO HD3 H 1 3.819 0.010 . 1 . . . . . 12 PRO HD3 . 51742 1 39 . 1 . 1 9 9 ALA H H 1 8.487 0.010 . 1 . . . . . 13 ALA H . 51742 1 40 . 1 . 1 9 9 ALA HA H 1 4.360 0.010 . 1 . . . . . 13 ALA HA . 51742 1 41 . 1 . 1 9 9 ALA HB1 H 1 1.410 0.010 . 1 . . . . . 13 ALA MB . 51742 1 42 . 1 . 1 9 9 ALA HB2 H 1 1.410 0.010 . 1 . . . . . 13 ALA MB . 51742 1 43 . 1 . 1 9 9 ALA HB3 H 1 1.410 0.010 . 1 . . . . . 13 ALA MB . 51742 1 44 . 1 . 1 10 10 CYS H H 1 7.665 0.010 . 1 . . . . . 14 CYS H . 51742 1 45 . 1 . 1 10 10 CYS HA H 1 4.418 0.010 . 1 . . . . . 14 CYS HA . 51742 1 46 . 1 . 1 10 10 CYS HB2 H 1 3.150 0.010 . 2 . . . . . 14 CYS HB2 . 51742 1 47 . 1 . 1 11 11 ALA H H 1 8.682 0.010 . 1 . . . . . 15 ALA H . 51742 1 48 . 1 . 1 11 11 ALA HA H 1 4.271 0.010 . 1 . . . . . 15 ALA HA . 51742 1 49 . 1 . 1 11 11 ALA HB1 H 1 1.437 0.010 . 1 . . . . . 15 ALA MB . 51742 1 50 . 1 . 1 11 11 ALA HB2 H 1 1.437 0.010 . 1 . . . . . 15 ALA MB . 51742 1 51 . 1 . 1 11 11 ALA HB3 H 1 1.437 0.010 . 1 . . . . . 15 ALA MB . 51742 1 52 . 1 . 1 12 12 DLY H H 1 8.738 0.010 . 1 . . . . . 16 DLY H . 51742 1 53 . 1 . 1 12 12 DLY HA H 1 4.205 0.010 . 1 . . . . . 16 DLY HA . 51742 1 54 . 1 . 1 12 12 DLY HB2 H 1 1.878 0.010 . 1 . . . . . 16 DLY HB2 . 51742 1 55 . 1 . 1 12 12 DLY HB3 H 1 2.005 0.010 . 1 . . . . . 16 DLY HB3 . 51742 1 56 . 1 . 1 12 12 DLY HG2 H 1 1.524 0.010 . 1 . . . . . 16 DLY HG2 . 51742 1 57 . 1 . 1 12 12 DLY HG3 H 1 1.555 0.010 . 1 . . . . . 16 DLY HG3 . 51742 1 58 . 1 . 1 12 12 DLY HD2 H 1 1.726 0.010 . 2 . . . . . 16 DLY HD2 . 51742 1 59 . 1 . 1 12 12 DLY HE2 H 1 3.059 0.010 . 2 . . . . . 16 DLY HE2 . 51742 1 60 . 1 . 1 13 13 CYS H H 1 7.494 0.010 . 1 . . . . . 17 CYS H . 51742 1 61 . 1 . 1 13 13 CYS HA H 1 4.600 0.010 . 1 . . . . . 17 CYS HA . 51742 1 62 . 1 . 1 13 13 CYS HB2 H 1 2.910 0.010 . 1 . . . . . 17 CYS HB2 . 51742 1 63 . 1 . 1 13 13 CYS HB3 H 1 3.070 0.010 . 1 . . . . . 17 CYS HB3 . 51742 1 stop_ save_