data_4347 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID 4347 _Entry.Title ; 1H Chemical Shift Assignments and Interproton 3JHNHA Coupling Constants of Alpha2-D, a Nativelike de Novo Designed Four Helix Bundle ; _Entry.Type macromolecule _Entry.Version_type original _Entry.Submission_date 1999-05-12 _Entry.Accession_date 1999-05-12 _Entry.Last_release_date . _Entry.Original_release_date . _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.61 _Entry.Original_NMR_STAR_version . _Entry.Experimental_method NMR _Entry.Experimental_method_subtype . _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.Entry_ID 1 R. Hill . Blake . 4347 2 William DeGrado . F. . 4347 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 4347 coupling_constants 1 4347 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 270 4347 'coupling constants' 27 4347 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 . . 2008-07-17 . update BMRB 'Updating non-standard residue' 4347 stop_ loop_ _Related_entries.Database_name _Related_entries.Database_accession_code _Related_entries.Relationship _Related_entries.Entry_ID PDB 1QP6 'BMRB Entry Tracking System' 4347 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID 4347 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID . _Citation.Full_citation ; Hill, R. Blake and Degrado, William, F., "Solution Structure of Alpha2D, a Nativelike de Novo Designed Protein," J. Am. Chem. Soc. 120, 1138-1145 (1998). ; _Citation.Title 'Solution Structure of Alpha2D, a Nativelike de Novo Designed Protein' _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev 'J. Am. Chem. Soc.' _Citation.Journal_name_full . _Citation.Journal_volume 120 _Citation.Journal_issue 6 _Citation.Journal_ASTM . _Citation.Journal_ISSN . _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 1138 _Citation.Page_last 1145 _Citation.Year 1998 _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 R. Hill . Blake . 4347 1 2 William DeGrado . F. . 4347 1 stop_ loop_ _Citation_keyword.Keyword _Citation_keyword.Entry_ID _Citation_keyword.Citation_ID 'bisecting U' 4347 1 'de novo protein design' 4347 1 'four helix bundle' 4347 1 NMR 4347 1 'nuclear magnetic resonance' 4347 1 'protein folding' 4347 1 'protein structure' 4347 1 stop_ save_ save_citation_1 _Citation.Sf_category citations _Citation.Sf_framecode citation_1 _Citation.Entry_ID 4347 _Citation.ID 2 _Citation.Class 'reference citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID . _Citation.Full_citation 'Kraulis, P.J. J. Magn. Res. 84:627-633(1989)' _Citation.Title . _Citation.Status . _Citation.Type . _Citation.Journal_abbrev . _Citation.Journal_name_full . _Citation.Journal_volume . _Citation.Journal_issue . _Citation.Journal_ASTM . _Citation.Journal_ISSN . _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 . _Citation.Page_last . _Citation.Year . _Citation.Details . save_ ############################################# # Molecular system (assembly) description # ############################################# save_alpha-2D _Assembly.Sf_category assembly _Assembly.Sf_framecode alpha-2D _Assembly.Entry_ID 4347 _Assembly.ID 1 _Assembly.Name Alpha2D _Assembly.BMRB_code . _Assembly.Number_of_components . _Assembly.Organic_ligands . _Assembly.Metal_ions . _Assembly.Non_standard_bonds . _Assembly.Ambiguous_conformational_states . _Assembly.Ambiguous_chem_comp_sites . _Assembly.Molecules_in_chemical_exchange . _Assembly.Paramagnetic no _Assembly.Thiol_state . _Assembly.Molecular_mass 8578 _Assembly.Enzyme_commission_number . _Assembly.Details ; Helix-loop-helix that dimerizes to form a 4-helix bundle. Symmetric homodimer. ; _Assembly.DB_query_date . _Assembly.DB_query_revised_last_date . loop_ _Assembly_type.Type _Assembly_type.Entry_ID _Assembly_type.Assembly_ID dimer 4347 1 stop_ 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 'A2D subunit A' 1 $A2D_monomer . . . native . . 1 . . 4347 1 2 'A2D subunit B' 1 $A2D_monomer . . . native . . 1 . . 4347 1 stop_ loop_ _Assembly_db_link.Author_supplied _Assembly_db_link.Database_code _Assembly_db_link.Accession_code _Assembly_db_link.Entry_mol_code _Assembly_db_link.Entry_mol_name _Assembly_db_link.Entry_experimental_method _Assembly_db_link.Entry_structure_resolution _Assembly_db_link.Entry_relation_type _Assembly_db_link.Entry_details _Assembly_db_link.Entry_ID _Assembly_db_link.Assembly_ID yes PDB 1QP6 . 'A Chain A, Solution Structure Of Alpha2d' . . . . 4347 1 stop_ loop_ _Assembly_common_name.Name _Assembly_common_name.Type _Assembly_common_name.Entry_ID _Assembly_common_name.Assembly_ID A2D abbreviation 4347 1 Alpha2D system 4347 1 stop_ loop_ _Assembly_bio_function.Biological_function _Assembly_bio_function.Entry_ID _Assembly_bio_function.Assembly_ID 'de novo designed protein with nativelike behavior' 4347 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_A2D_monomer _Entity.Sf_category entity _Entity.Sf_framecode A2D_monomer _Entity.Entry_ID 4347 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name Alpha2D _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 ; XGEVEELEKKFKELWKGPRR GEIEELHKKFHELIKGX ; _Entity.Target_identifier . _Entity.Polymer_author_defined_seq . _Entity.Polymer_author_seq_details . _Entity.Ambiguous_conformational_states . _Entity.Ambiguous_chem_comp_sites . _Entity.Nstd_monomer . _Entity.Nstd_chirality . _Entity.Nstd_linkage . _Entity.Nonpolymer_comp_ID . _Entity.Nonpolymer_comp_label . _Entity.Number_of_monomers 37 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic . _Entity.Thiol_state . _Entity.Src_method . _Entity.Parent_entity_ID 1 _Entity.Fragment . _Entity.Mutation . _Entity.EC_number . _Entity.Calc_isoelectric_point . _Entity.Formula_weight 4289.1 _Entity.Formula_weight_exptl . _Entity.Formula_weight_exptl_meth . _Entity.Details ; The monomer molecular weight is 4289. Molecule has been shown to be dimeric by equilibrium sedimentation analysis at 50 uM - 2 mM. A helix-loop-helix with each helix comprising 2 heptads of the helical repeat. High sequence redundancy between helix 1 and helix 2. N-terminal is acetylated and C-terminal is amidated." ; _Entity.DB_query_date . _Entity.DB_query_revised_last_date 2015-11-24 loop_ _Entity_db_link.Ordinal _Entity_db_link.Author_supplied _Entity_db_link.Database_code _Entity_db_link.Accession_code _Entity_db_link.Entry_mol_code _Entity_db_link.Entry_mol_name _Entity_db_link.Entry_experimental_method _Entity_db_link.Entry_structure_resolution _Entity_db_link.Entry_relation_type _Entity_db_link.Entry_details _Entity_db_link.Chimera_segment_ID _Entity_db_link.Seq_query_to_submitted_percent _Entity_db_link.Seq_subject_length _Entity_db_link.Seq_identity _Entity_db_link.Seq_positive _Entity_db_link.Seq_homology_expectation_val _Entity_db_link.Seq_align_begin _Entity_db_link.Seq_align_end _Entity_db_link.Seq_difference_details _Entity_db_link.Seq_alignment_details _Entity_db_link.Entry_ID _Entity_db_link.Entity_ID 1 no PDB 1QP6 . "Solution Structure Of Alpha2d" . . . . . 94.59 35 100.00 100.00 1.05e-12 . . . . 4347 1 stop_ loop_ _Entity_common_name.Name _Entity_common_name.Type _Entity_common_name.Entry_ID _Entity_common_name.Entity_ID A2D abbreviation 4347 1 Alpha2D common 4347 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 . ACE . 4347 1 2 . GLY . 4347 1 3 . GLU . 4347 1 4 . VAL . 4347 1 5 . GLU . 4347 1 6 . GLU . 4347 1 7 . LEU . 4347 1 8 . GLU . 4347 1 9 . LYS . 4347 1 10 . LYS . 4347 1 11 . PHE . 4347 1 12 . LYS . 4347 1 13 . GLU . 4347 1 14 . LEU . 4347 1 15 . TRP . 4347 1 16 . LYS . 4347 1 17 . GLY . 4347 1 18 . PRO . 4347 1 19 . ARG . 4347 1 20 . ARG . 4347 1 21 . GLY . 4347 1 22 . GLU . 4347 1 23 . ILE . 4347 1 24 . GLU . 4347 1 25 . GLU . 4347 1 26 . LEU . 4347 1 27 . HIS . 4347 1 28 . LYS . 4347 1 29 . LYS . 4347 1 30 . PHE . 4347 1 31 . HIS . 4347 1 32 . GLU . 4347 1 33 . LEU . 4347 1 34 . ILE . 4347 1 35 . LYS . 4347 1 36 . GLY . 4347 1 37 . NH2 . 4347 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 . ACE 1 1 4347 1 . GLY 2 2 4347 1 . GLU 3 3 4347 1 . VAL 4 4 4347 1 . GLU 5 5 4347 1 . GLU 6 6 4347 1 . LEU 7 7 4347 1 . GLU 8 8 4347 1 . LYS 9 9 4347 1 . LYS 10 10 4347 1 . PHE 11 11 4347 1 . LYS 12 12 4347 1 . GLU 13 13 4347 1 . LEU 14 14 4347 1 . TRP 15 15 4347 1 . LYS 16 16 4347 1 . GLY 17 17 4347 1 . PRO 18 18 4347 1 . ARG 19 19 4347 1 . ARG 20 20 4347 1 . GLY 21 21 4347 1 . GLU 22 22 4347 1 . ILE 23 23 4347 1 . GLU 24 24 4347 1 . GLU 25 25 4347 1 . LEU 26 26 4347 1 . HIS 27 27 4347 1 . LYS 28 28 4347 1 . LYS 29 29 4347 1 . PHE 30 30 4347 1 . HIS 31 31 4347 1 . GLU 32 32 4347 1 . LEU 33 33 4347 1 . ILE 34 34 4347 1 . LYS 35 35 4347 1 . GLY 36 36 4347 1 . NH2 37 37 4347 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 4347 _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 $A2D_monomer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4347 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 4347 _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 $A2D_monomer . 'chemically synthesized' . . . . . . . . . . . . . . . . . . . . . . . . . . 'Synthesized using standard FMOC chemistry, C-terminal is amidated and the N-terminus is acetylated' . . 4347 1 stop_ save_ ################################# # Polymer residues and ligands # ################################# save_chem_comp_ACE _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_ACE _Chem_comp.Entry_ID 4347 _Chem_comp.ID ACE _Chem_comp.Provenance . _Chem_comp.Name 'ACETYL GROUP' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code . _Chem_comp.PDB_code ACE _Chem_comp.Ambiguous_flag no _Chem_comp.Initial_date 1999-07-08 _Chem_comp.Modified_date 2011-06-04 _Chem_comp.Release_status REL _Chem_comp.Replaced_by . _Chem_comp.Replaces ACU _Chem_comp.One_letter_code . _Chem_comp.Three_letter_code ACE _Chem_comp.Number_atoms_all . _Chem_comp.Number_atoms_nh . _Chem_comp.PubChem_code . _Chem_comp.Subcomponent_list . _Chem_comp.InChI_code . _Chem_comp.Mon_nstd_flag . _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 'C2 H4 O' _Chem_comp.Formula_weight 44.053 _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 . _Chem_comp.Processing_site PDBE _Chem_comp.Vendor . _Chem_comp.Vendor_product_code . _Chem_comp.Details ; Information obtained from PDB's Chemical Component Dictionary at http://wwpdb-remediation.rutgers.edu/downloads.html Downloaded on Thu Jul 14 16:15:33 2011 ; _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 CC=O SMILES CACTVS 3.341 4347 ACE CC=O SMILES 'OpenEye OEToolkits' 1.5.0 4347 ACE CC=O SMILES_CANONICAL CACTVS 3.341 4347 ACE CC=O SMILES_CANONICAL 'OpenEye OEToolkits' 1.5.0 4347 ACE IKHGUXGNUITLKF-UHFFFAOYSA-N InChIKey InChI 1.03 4347 ACE InChI=1S/C2H4O/c1-2-3/h2H,1H3 InChI InChI 1.03 4347 ACE O=CC SMILES ACDLabs 10.04 4347 ACE 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 acetaldehyde 'SYSTEMATIC NAME' ACDLabs 10.04 4347 ACE ethanal 'SYSTEMATIC NAME' 'OpenEye OEToolkits' 1.5.0 4347 ACE 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 C . C . . C . . N 0 . . . . no no . . . . 0.772 . -10.072 . 6.578 . -0.133 0.453 0.000 1 . 4347 ACE O . O . . O . . N 0 . . . . no no . . . . 1.973 . -10.223 . 6.862 . -1.113 -0.252 0.000 2 . 4347 ACE CH3 . CH3 . . C . . N 0 . . . . no no . . . . -0.322 . -10.677 . 7.405 . 1.241 -0.167 0.000 3 . 4347 ACE H . H . . H . . N 0 . . . . no no . . . . 0.685 . -9.453 . 5.669 . -0.240 1.528 0.000 4 . 4347 ACE H1 . H1 . . H . . N 0 . . . . no no . . . . -1.191 . -10.444 . 7.018 . 1.360 -0.785 0.890 5 . 4347 ACE H2 . H2 . . H . . N 0 . . . . no no . . . . -0.269 . -10.331 . 8.320 . 1.360 -0.785 -0.890 6 . 4347 ACE H3 . H3 . . H . . N 0 . . . . no no . . . . -0.221 . -11.652 . 7.418 . 1.995 0.620 0.000 7 . 4347 ACE 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 . DOUB C O no N 1 . 4347 ACE 2 . SING C CH3 no N 2 . 4347 ACE 3 . SING C H no N 3 . 4347 ACE 4 . SING CH3 H1 no N 4 . 4347 ACE 5 . SING CH3 H2 no N 5 . 4347 ACE 6 . SING CH3 H3 no N 6 . 4347 ACE stop_ save_ save_chem_comp_NH2 _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_NH2 _Chem_comp.Entry_ID 4347 _Chem_comp.ID NH2 _Chem_comp.Provenance . _Chem_comp.Name 'AMINO GROUP' _Chem_comp.Type non-polymer _Chem_comp.BMRB_code . _Chem_comp.PDB_code NH2 _Chem_comp.Ambiguous_flag yes _Chem_comp.Initial_date 1999-07-08 _Chem_comp.Modified_date 2008-10-14 _Chem_comp.Release_status REL _Chem_comp.Replaced_by . _Chem_comp.Replaces . _Chem_comp.One_letter_code . _Chem_comp.Three_letter_code NH2 _Chem_comp.Number_atoms_all . _Chem_comp.Number_atoms_nh . _Chem_comp.PubChem_code . _Chem_comp.Subcomponent_list . _Chem_comp.InChI_code . _Chem_comp.Mon_nstd_flag . _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 'H2 N' _Chem_comp.Formula_weight 16.023 _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 2FLY _Chem_comp.Processing_site RCSB _Chem_comp.Vendor . _Chem_comp.Vendor_product_code . _Chem_comp.Details ; Information obtained from PDB's Chemical Component Dictionary at http://wwpdb-remediation.rutgers.edu/downloads.html Downloaded on Thu Jul 14 16:09:34 2011 ; _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 InChI=1/H3N/h1H3 InChI InChI 1.02b 4347 NH2 N SMILES ACDLabs 10.04 4347 NH2 [NH2] SMILES CACTVS 3.341 4347 NH2 [NH2] SMILES 'OpenEye OEToolkits' 1.5.0 4347 NH2 [NH2] SMILES_CANONICAL CACTVS 3.341 4347 NH2 [NH2] SMILES_CANONICAL 'OpenEye OEToolkits' 1.5.0 4347 NH2 QGZKDVFQNNGYKY-UHFFFAOYAF InChIKey InChI 1.02b 4347 NH2 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 ammonia 'SYSTEMATIC NAME' ACDLabs 10.04 4347 NH2 l^{2}-azane 'SYSTEMATIC NAME' 'OpenEye OEToolkits' 1.5.0 4347 NH2 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 0 . . . . no no . . . . 10.091 . 8.978 . -7.810 . 0.000 0.000 0.000 1 . 4347 NH2 HN1 . HN1 . . H . . N 0 . . . . no no . . . . 9.517 . 8.769 . -7.044 . -0.385 -0.545 -0.771 2 . 4347 NH2 HN2 . HN2 . . H . . N 0 . . . . no no . . . . 10.323 . 9.890 . -8.082 . 1.020 0.000 0.000 3 . 4347 NH2 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 HN1 no N 1 . 4347 NH2 2 . SING N HN2 no N 2 . 4347 NH2 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_one _Sample.Sf_category sample _Sample.Sf_framecode sample_one _Sample.Entry_ID 4347 _Sample.ID 1 _Sample.Type solution _Sample.Sub_type . _Sample.Details . _Sample.Aggregate_sample_number . _Sample.Solvent_system . _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 Alpha2D . . . 1 $A2D_monomer . . 2.0 . . mM . . . . 4347 1 2 Tris [U-2H] . . . . . . 50 . . mM . . . . 4347 1 3 H2O . . . . . . . 90 . . % . . . . 4347 1 4 D2O . . . . . . . 10 . . % . . . . 4347 1 stop_ save_ ####################### # Sample conditions # ####################### save_sample_conditions_one _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_conditions_one _Sample_condition_list.Entry_ID 4347 _Sample_condition_list.ID 1 _Sample_condition_list.Details . 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' .052 .002 M 4347 1 pH 7.3 0.1 na 4347 1 temperature 298 1 K 4347 1 stop_ save_ ############################ # Computer software used # ############################ save_AZARA _Software.Sf_category software _Software.Sf_framecode AZARA _Software.Entry_ID 4347 _Software.ID 1 _Software.Name AZARA _Software.Version . _Software.Details . loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'process data' 4347 1 stop_ save_ save_ANSIG _Software.Sf_category software _Software.Sf_framecode ANSIG _Software.Entry_ID 4347 _Software.ID 2 _Software.Name ANSIG _Software.Version 3.3 _Software.Details . loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID 'Per Kraulis' . http://www.scs.uiuc.edu/documentation/ansig/ansig.html#references 4347 2 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'assignments and integration' 4347 2 stop_ loop_ _Software_citation.Citation_ID _Software_citation.Citation_label _Software_citation.Entry_ID _Software_citation.Software_ID 2 $citation_1 4347 2 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_spectrometer_1 _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode spectrometer_1 _NMR_spectrometer.Entry_ID 4347 _NMR_spectrometer.ID 1 _NMR_spectrometer.Details . _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model AMX _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 600.13 save_ save_spectrometer_list _NMR_spectrometer_list.Sf_category NMR_spectrometer_list _NMR_spectrometer_list.Sf_framecode spectrometer_list _NMR_spectrometer_list.Entry_ID 4347 _NMR_spectrometer_list.ID 1 loop_ _NMR_spectrometer_view.ID _NMR_spectrometer_view.Name _NMR_spectrometer_view.Manufacturer _NMR_spectrometer_view.Model _NMR_spectrometer_view.Serial_number _NMR_spectrometer_view.Field_strength _NMR_spectrometer_view.Details _NMR_spectrometer_view.Citation_ID _NMR_spectrometer_view.Citation_label _NMR_spectrometer_view.Entry_ID _NMR_spectrometer_view.NMR_spectrometer_list_ID 1 spectrometer_1 Bruker AMX . 600.13 . . . 4347 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 4347 _Experiment_list.ID 1 _Experiment_list.Details 'The HMQC expt. was collected observing the natural abundant 13C signal in an unlabeled sample.' loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_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.Entry_ID _Experiment.Experiment_list_ID 1 '1H-1H TOCSY' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 2 '1H-1H DQF-COSY' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 3 '1H-1H E-COSY' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 4 '1H-1H 100ms NOESY' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 5 '1H-1H 200ms NOESY' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 6 '1H-13C HMQC' . . . . . . . . . . . 1 $sample_one . . . 1 $sample_conditions_one . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4347 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chemical_shift_reference_one _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chemical_shift_reference_one _Chem_shift_reference.Entry_ID 4347 _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.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.Indirect_shift_ratio_cit_ID _Chem_shift_ref.Indirect_shift_ratio_cit_label _Chem_shift_ref.Ref_correction_type _Chem_shift_ref.Correction_val _Chem_shift_ref.Correction_val_cit_ID _Chem_shift_ref.Correction_val_cit_label _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 TSP 'methyl protons' . . . . ppm 0.0 internal direct . . . . . . . . . . 4347 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 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chemical_shifts _Assigned_chem_shift_list.Entry_ID 4347 _Assigned_chem_shift_list.ID 1 _Assigned_chem_shift_list.Sample_condition_list_ID 1 _Assigned_chem_shift_list.Sample_condition_list_label $sample_conditions_one _Assigned_chem_shift_list.Chem_shift_reference_ID 1 _Assigned_chem_shift_list.Chem_shift_reference_label $chemical_shift_reference_one _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 $sample_one . 4347 1 stop_ loop_ _Atom_chem_shift.ID _Atom_chem_shift.Assembly_atom_ID _Atom_chem_shift.Entity_assembly_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.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 2 2 GLY H H 1 8.47 0.02 . 1 . . . . . . . . 4347 1 2 . 1 1 2 2 GLY HA2 H 1 4.00 0.02 . 1 . . . . . . . . 4347 1 3 . 1 1 2 2 GLY HA3 H 1 4.00 0.02 . 1 . . . . . . . . 4347 1 4 . 1 1 3 3 GLU H H 1 8.24 0.02 . 1 . . . . . . . . 4347 1 5 . 1 1 3 3 GLU HA H 1 4.03 0.02 . 1 . . . . . . . . 4347 1 6 . 1 1 4 4 VAL H H 1 8.12 0.02 . 1 . . . . . . . . 4347 1 7 . 1 1 4 4 VAL HA H 1 3.45 0.02 . 1 . . . . . . . . 4347 1 8 . 1 1 4 4 VAL HB H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 9 . 1 1 4 4 VAL HG11 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 10 . 1 1 4 4 VAL HG12 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 11 . 1 1 4 4 VAL HG13 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 12 . 1 1 4 4 VAL HG21 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 13 . 1 1 4 4 VAL HG22 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 14 . 1 1 4 4 VAL HG23 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 15 . 1 1 5 5 GLU H H 1 8.05 0.02 . 1 . . . . . . . . 4347 1 16 . 1 1 5 5 GLU HA H 1 4.10 0.02 . 1 . . . . . . . . 4347 1 17 . 1 1 5 5 GLU HB2 H 1 1.98 0.02 . 1 . . . . . . . . 4347 1 18 . 1 1 5 5 GLU HB3 H 1 2.01 0.02 . 1 . . . . . . . . 4347 1 19 . 1 1 5 5 GLU HG2 H 1 2.29 0.02 . 1 . . . . . . . . 4347 1 20 . 1 1 5 5 GLU HG3 H 1 2.29 0.02 . 1 . . . . . . . . 4347 1 21 . 1 1 6 6 GLU H H 1 8.04 0.02 . 1 . . . . . . . . 4347 1 22 . 1 1 6 6 GLU HA H 1 4.03 0.02 . 1 . . . . . . . . 4347 1 23 . 1 1 6 6 GLU HB2 H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 24 . 1 1 6 6 GLU HB3 H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 25 . 1 1 6 6 GLU HG2 H 1 2.24 0.02 . 1 . . . . . . . . 4347 1 26 . 1 1 6 6 GLU HG3 H 1 2.24 0.02 . 1 . . . . . . . . 4347 1 27 . 1 1 7 7 LEU H H 1 7.65 0.02 . 1 . . . . . . . . 4347 1 28 . 1 1 7 7 LEU HA H 1 4.07 0.02 . 1 . . . . . . . . 4347 1 29 . 1 1 7 7 LEU HB2 H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 30 . 1 1 7 7 LEU HB3 H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 31 . 1 1 7 7 LEU HG H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 32 . 1 1 7 7 LEU HD11 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 33 . 1 1 7 7 LEU HD12 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 34 . 1 1 7 7 LEU HD13 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 35 . 1 1 7 7 LEU HD21 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 36 . 1 1 7 7 LEU HD22 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 37 . 1 1 7 7 LEU HD23 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 38 . 1 1 8 8 GLU H H 1 8.34 0.02 . 1 . . . . . . . . 4347 1 39 . 1 1 8 8 GLU HA H 1 3.97 0.02 . 1 . . . . . . . . 4347 1 40 . 1 1 8 8 GLU HB2 H 1 2.33 0.02 . 1 . . . . . . . . 4347 1 41 . 1 1 8 8 GLU HB3 H 1 2.12 0.02 . 1 . . . . . . . . 4347 1 42 . 1 1 8 8 GLU HG2 H 1 2.23 0.02 . 1 . . . . . . . . 4347 1 43 . 1 1 8 8 GLU HG3 H 1 2.23 0.02 . 1 . . . . . . . . 4347 1 44 . 1 1 9 9 LYS H H 1 8.02 0.02 . 1 . . . . . . . . 4347 1 45 . 1 1 9 9 LYS HA H 1 3.98 0.02 . 1 . . . . . . . . 4347 1 46 . 1 1 9 9 LYS HB2 H 1 1.93 0.02 . 1 . . . . . . . . 4347 1 47 . 1 1 9 9 LYS HB3 H 1 1.93 0.02 . 1 . . . . . . . . 4347 1 48 . 1 1 9 9 LYS HG2 H 1 1.40 0.02 . 1 . . . . . . . . 4347 1 49 . 1 1 9 9 LYS HG3 H 1 1.63 0.02 . 1 . . . . . . . . 4347 1 50 . 1 1 9 9 LYS HD2 H 1 1.67 0.02 . 1 . . . . . . . . 4347 1 51 . 1 1 9 9 LYS HD3 H 1 1.67 0.02 . 1 . . . . . . . . 4347 1 52 . 1 1 9 9 LYS HE2 H 1 2.92 0.02 . 1 . . . . . . . . 4347 1 53 . 1 1 9 9 LYS HE3 H 1 2.92 0.02 . 1 . . . . . . . . 4347 1 54 . 1 1 10 10 LYS H H 1 8.11 0.02 . 1 . . . . . . . . 4347 1 55 . 1 1 10 10 LYS HA H 1 4.16 0.02 . 1 . . . . . . . . 4347 1 56 . 1 1 10 10 LYS HB2 H 1 1.89 0.02 . 1 . . . . . . . . 4347 1 57 . 1 1 10 10 LYS HB3 H 1 1.96 0.02 . 1 . . . . . . . . 4347 1 58 . 1 1 10 10 LYS HG2 H 1 1.54 0.02 . 1 . . . . . . . . 4347 1 59 . 1 1 10 10 LYS HG3 H 1 1.54 0.02 . 1 . . . . . . . . 4347 1 60 . 1 1 10 10 LYS HD2 H 1 1.68 0.02 . 1 . . . . . . . . 4347 1 61 . 1 1 10 10 LYS HD3 H 1 1.68 0.02 . 1 . . . . . . . . 4347 1 62 . 1 1 10 10 LYS HE2 H 1 2.86 0.02 . 1 . . . . . . . . 4347 1 63 . 1 1 10 10 LYS HE3 H 1 2.95 0.02 . 1 . . . . . . . . 4347 1 64 . 1 1 11 11 PHE H H 1 8.72 0.02 . 1 . . . . . . . . 4347 1 65 . 1 1 11 11 PHE HA H 1 3.80 0.02 . 1 . . . . . . . . 4347 1 66 . 1 1 11 11 PHE HB2 H 1 2.93 0.02 . 1 . . . . . . . . 4347 1 67 . 1 1 11 11 PHE HB3 H 1 2.93 0.02 . 1 . . . . . . . . 4347 1 68 . 1 1 11 11 PHE HD1 H 1 6.52 0.02 . 1 . . . . . . . . 4347 1 69 . 1 1 11 11 PHE HD2 H 1 6.52 0.02 . 1 . . . . . . . . 4347 1 70 . 1 1 11 11 PHE HE1 H 1 6.59 0.02 . 1 . . . . . . . . 4347 1 71 . 1 1 11 11 PHE HE2 H 1 6.59 0.02 . 1 . . . . . . . . 4347 1 72 . 1 1 11 11 PHE HZ H 1 6.64 0.02 . 1 . . . . . . . . 4347 1 73 . 1 1 12 12 LYS H H 1 8.13 0.02 . 1 . . . . . . . . 4347 1 74 . 1 1 12 12 LYS HA H 1 3.98 0.02 . 1 . . . . . . . . 4347 1 75 . 1 1 12 12 LYS HB2 H 1 1.89 0.02 . 1 . . . . . . . . 4347 1 76 . 1 1 12 12 LYS HB3 H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 77 . 1 1 12 12 LYS HG2 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 78 . 1 1 12 12 LYS HG3 H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 79 . 1 1 12 12 LYS HD2 H 1 1.49 0.02 . 1 . . . . . . . . 4347 1 80 . 1 1 12 12 LYS HD3 H 1 1.49 0.02 . 1 . . . . . . . . 4347 1 81 . 1 1 12 12 LYS HE2 H 1 2.28 0.02 . 1 . . . . . . . . 4347 1 82 . 1 1 12 12 LYS HE3 H 1 2.28 0.02 . 1 . . . . . . . . 4347 1 83 . 1 1 13 13 GLU H H 1 8.18 0.02 . 1 . . . . . . . . 4347 1 84 . 1 1 13 13 GLU HA H 1 4.01 0.02 . 1 . . . . . . . . 4347 1 85 . 1 1 13 13 GLU HB2 H 1 2.20 0.02 . 1 . . . . . . . . 4347 1 86 . 1 1 13 13 GLU HB3 H 1 2.11 0.02 . 1 . . . . . . . . 4347 1 87 . 1 1 13 13 GLU HG2 H 1 2.36 0.02 . 1 . . . . . . . . 4347 1 88 . 1 1 13 13 GLU HG3 H 1 2.36 0.02 . 1 . . . . . . . . 4347 1 89 . 1 1 14 14 LEU H H 1 7.65 0.02 . 1 . . . . . . . . 4347 1 90 . 1 1 14 14 LEU HA H 1 4.07 0.02 . 1 . . . . . . . . 4347 1 91 . 1 1 14 14 LEU HB2 H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 92 . 1 1 14 14 LEU HB3 H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 93 . 1 1 14 14 LEU HG H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 94 . 1 1 14 14 LEU HD11 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 95 . 1 1 14 14 LEU HD12 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 96 . 1 1 14 14 LEU HD13 H 1 0.76 0.02 . 1 . . . . . . . . 4347 1 97 . 1 1 14 14 LEU HD21 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 98 . 1 1 14 14 LEU HD22 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 99 . 1 1 14 14 LEU HD23 H 1 0.86 0.02 . 1 . . . . . . . . 4347 1 100 . 1 1 15 15 TRP H H 1 8.48 0.02 . 1 . . . . . . . . 4347 1 101 . 1 1 15 15 TRP HA H 1 3.82 0.02 . 1 . . . . . . . . 4347 1 102 . 1 1 15 15 TRP HB2 H 1 3.37 0.02 . 1 . . . . . . . . 4347 1 103 . 1 1 15 15 TRP HB3 H 1 3.07 0.02 . 1 . . . . . . . . 4347 1 104 . 1 1 15 15 TRP HD1 H 1 6.95 0.02 . 1 . . . . . . . . 4347 1 105 . 1 1 15 15 TRP HE1 H 1 11.18 0.02 . 1 . . . . . . . . 4347 1 106 . 1 1 15 15 TRP HE3 H 1 7.34 0.02 . 1 . . . . . . . . 4347 1 107 . 1 1 15 15 TRP HZ2 H 1 7.34 0.02 . 1 . . . . . . . . 4347 1 108 . 1 1 15 15 TRP HZ3 H 1 6.95 0.02 . 1 . . . . . . . . 4347 1 109 . 1 1 15 15 TRP HH2 H 1 7.03 0.02 . 1 . . . . . . . . 4347 1 110 . 1 1 16 16 LYS H H 1 7.28 0.02 . 1 . . . . . . . . 4347 1 111 . 1 1 16 16 LYS HA H 1 3.78 0.02 . 1 . . . . . . . . 4347 1 112 . 1 1 16 16 LYS HB2 H 1 1.88 0.02 . 1 . . . . . . . . 4347 1 113 . 1 1 16 16 LYS HB3 H 1 1.84 0.02 . 1 . . . . . . . . 4347 1 114 . 1 1 16 16 LYS HG2 H 1 1.50 0.02 . 1 . . . . . . . . 4347 1 115 . 1 1 16 16 LYS HG3 H 1 1.50 0.02 . 1 . . . . . . . . 4347 1 116 . 1 1 16 16 LYS HD2 H 1 1.68 0.02 . 1 . . . . . . . . 4347 1 117 . 1 1 16 16 LYS HD3 H 1 1.72 0.02 . 1 . . . . . . . . 4347 1 118 . 1 1 16 16 LYS HE2 H 1 2.96 0.02 . 1 . . . . . . . . 4347 1 119 . 1 1 16 16 LYS HE3 H 1 2.96 0.02 . 1 . . . . . . . . 4347 1 120 . 1 1 17 17 GLY H H 1 6.99 0.02 . 1 . . . . . . . . 4347 1 121 . 1 1 17 17 GLY HA2 H 1 4.04 0.02 . 1 . . . . . . . . 4347 1 122 . 1 1 17 17 GLY HA3 H 1 4.36 0.02 . 1 . . . . . . . . 4347 1 123 . 1 1 18 18 PRO HA H 1 4.37 0.02 . 1 . . . . . . . . 4347 1 124 . 1 1 18 18 PRO HB2 H 1 1.93 0.02 . 1 . . . . . . . . 4347 1 125 . 1 1 18 18 PRO HB3 H 1 2.34 0.02 . 1 . . . . . . . . 4347 1 126 . 1 1 18 18 PRO HG2 H 1 1.92 0.02 . 1 . . . . . . . . 4347 1 127 . 1 1 18 18 PRO HG3 H 1 2.01 0.02 . 1 . . . . . . . . 4347 1 128 . 1 1 18 18 PRO HD2 H 1 3.57 0.02 . 1 . . . . . . . . 4347 1 129 . 1 1 18 18 PRO HD3 H 1 3.68 0.02 . 1 . . . . . . . . 4347 1 130 . 1 1 19 19 ARG H H 1 9.01 0.02 . 1 . . . . . . . . 4347 1 131 . 1 1 19 19 ARG HA H 1 4.65 0.02 . 1 . . . . . . . . 4347 1 132 . 1 1 19 19 ARG HB2 H 1 1.65 0.02 . 1 . . . . . . . . 4347 1 133 . 1 1 19 19 ARG HB3 H 1 1.65 0.02 . 1 . . . . . . . . 4347 1 134 . 1 1 19 19 ARG HG2 H 1 1.57 0.02 . 1 . . . . . . . . 4347 1 135 . 1 1 19 19 ARG HG3 H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 136 . 1 1 19 19 ARG HD2 H 1 1.49 0.02 . 1 . . . . . . . . 4347 1 137 . 1 1 19 19 ARG HD3 H 1 3.07 0.02 . 1 . . . . . . . . 4347 1 138 . 1 1 20 20 ARG H H 1 7.44 0.02 . 1 . . . . . . . . 4347 1 139 . 1 1 20 20 ARG HA H 1 3.65 0.02 . 1 . . . . . . . . 4347 1 140 . 1 1 20 20 ARG HB2 H 1 2.05 0.02 . 1 . . . . . . . . 4347 1 141 . 1 1 20 20 ARG HB3 H 1 1.40 0.02 . 1 . . . . . . . . 4347 1 142 . 1 1 20 20 ARG HG2 H 1 1.01 0.02 . 1 . . . . . . . . 4347 1 143 . 1 1 20 20 ARG HG3 H 1 1.10 0.02 . 1 . . . . . . . . 4347 1 144 . 1 1 20 20 ARG HD2 H 1 2.66 0.02 . 1 . . . . . . . . 4347 1 145 . 1 1 20 20 ARG HD3 H 1 2.69 0.02 . 1 . . . . . . . . 4347 1 146 . 1 1 21 21 GLY H H 1 8.83 0.02 . 1 . . . . . . . . 4347 1 147 . 1 1 21 21 GLY HA2 H 1 3.79 0.02 . 1 . . . . . . . . 4347 1 148 . 1 1 21 21 GLY HA3 H 1 3.87 0.02 . 1 . . . . . . . . 4347 1 149 . 1 1 22 22 GLU H H 1 7.82 0.02 . 1 . . . . . . . . 4347 1 150 . 1 1 22 22 GLU HA H 1 4.09 0.02 . 1 . . . . . . . . 4347 1 151 . 1 1 22 22 GLU HB2 H 1 2.09 0.02 . 1 . . . . . . . . 4347 1 152 . 1 1 22 22 GLU HB3 H 1 2.19 0.02 . 1 . . . . . . . . 4347 1 153 . 1 1 22 22 GLU HG2 H 1 2.28 0.02 . 1 . . . . . . . . 4347 1 154 . 1 1 22 22 GLU HG3 H 1 2.28 0.02 . 1 . . . . . . . . 4347 1 155 . 1 1 23 23 ILE H H 1 8.06 0.02 . 1 . . . . . . . . 4347 1 156 . 1 1 23 23 ILE HA H 1 3.79 0.02 . 1 . . . . . . . . 4347 1 157 . 1 1 23 23 ILE HB H 1 2.29 0.02 . 1 . . . . . . . . 4347 1 158 . 1 1 23 23 ILE HG12 H 1 0.91 0.02 . 1 . . . . . . . . 4347 1 159 . 1 1 23 23 ILE HG13 H 1 1.45 0.02 . 1 . . . . . . . . 4347 1 160 . 1 1 23 23 ILE HG21 H 1 0.47 0.02 . 1 . . . . . . . . 4347 1 161 . 1 1 23 23 ILE HG22 H 1 0.47 0.02 . 1 . . . . . . . . 4347 1 162 . 1 1 23 23 ILE HG23 H 1 0.47 0.02 . 1 . . . . . . . . 4347 1 163 . 1 1 23 23 ILE HD11 H 1 0.44 0.02 . 1 . . . . . . . . 4347 1 164 . 1 1 23 23 ILE HD12 H 1 0.44 0.02 . 1 . . . . . . . . 4347 1 165 . 1 1 23 23 ILE HD13 H 1 0.44 0.02 . 1 . . . . . . . . 4347 1 166 . 1 1 24 24 GLU H H 1 8.69 0.02 . 1 . . . . . . . . 4347 1 167 . 1 1 24 24 GLU HA H 1 3.97 0.02 . 1 . . . . . . . . 4347 1 168 . 1 1 24 24 GLU HB2 H 1 2.14 0.02 . 1 . . . . . . . . 4347 1 169 . 1 1 24 24 GLU HB3 H 1 2.25 0.02 . 1 . . . . . . . . 4347 1 170 . 1 1 24 24 GLU HG2 H 1 2.87 0.02 . 1 . . . . . . . . 4347 1 171 . 1 1 24 24 GLU HG3 H 1 2.24 0.02 . 1 . . . . . . . . 4347 1 172 . 1 1 25 25 GLU H H 1 7.87 0.02 . 1 . . . . . . . . 4347 1 173 . 1 1 25 25 GLU HA H 1 4.10 0.02 . 1 . . . . . . . . 4347 1 174 . 1 1 25 25 GLU HB2 H 1 2.04 0.02 . 1 . . . . . . . . 4347 1 175 . 1 1 25 25 GLU HB3 H 1 2.08 0.02 . 1 . . . . . . . . 4347 1 176 . 1 1 25 25 GLU HG2 H 1 2.30 0.02 . 1 . . . . . . . . 4347 1 177 . 1 1 25 25 GLU HG3 H 1 2.30 0.02 . 1 . . . . . . . . 4347 1 178 . 1 1 26 26 LEU H H 1 7.85 0.02 . 1 . . . . . . . . 4347 1 179 . 1 1 26 26 LEU HA H 1 3.86 0.02 . 1 . . . . . . . . 4347 1 180 . 1 1 26 26 LEU HB2 H 1 1.74 0.02 . 1 . . . . . . . . 4347 1 181 . 1 1 26 26 LEU HB3 H 1 1.60 0.02 . 1 . . . . . . . . 4347 1 182 . 1 1 26 26 LEU HG H 1 1.16 0.02 . 1 . . . . . . . . 4347 1 183 . 1 1 26 26 LEU HD11 H 1 0.68 0.02 . 1 . . . . . . . . 4347 1 184 . 1 1 26 26 LEU HD12 H 1 0.68 0.02 . 1 . . . . . . . . 4347 1 185 . 1 1 26 26 LEU HD13 H 1 0.68 0.02 . 1 . . . . . . . . 4347 1 186 . 1 1 26 26 LEU HD21 H 1 0.70 0.02 . 1 . . . . . . . . 4347 1 187 . 1 1 26 26 LEU HD22 H 1 0.70 0.02 . 1 . . . . . . . . 4347 1 188 . 1 1 26 26 LEU HD23 H 1 0.70 0.02 . 1 . . . . . . . . 4347 1 189 . 1 1 27 27 HIS H H 1 8.58 0.02 . 1 . . . . . . . . 4347 1 190 . 1 1 27 27 HIS HA H 1 4.09 0.02 . 1 . . . . . . . . 4347 1 191 . 1 1 27 27 HIS HB2 H 1 3.36 0.02 . 1 . . . . . . . . 4347 1 192 . 1 1 27 27 HIS HB3 H 1 3.04 0.02 . 1 . . . . . . . . 4347 1 193 . 1 1 27 27 HIS HD2 H 1 6.76 0.02 . 1 . . . . . . . . 4347 1 194 . 1 1 27 27 HIS HE1 H 1 7.00 0.02 . 1 . . . . . . . . 4347 1 195 . 1 1 28 28 LYS H H 1 7.82 0.02 . 1 . . . . . . . . 4347 1 196 . 1 1 28 28 LYS HA H 1 4.01 0.02 . 1 . . . . . . . . 4347 1 197 . 1 1 28 28 LYS HB2 H 1 2.00 0.02 . 1 . . . . . . . . 4347 1 198 . 1 1 28 28 LYS HB3 H 1 2.00 0.02 . 1 . . . . . . . . 4347 1 199 . 1 1 28 28 LYS HG2 H 1 1.46 0.02 . 1 . . . . . . . . 4347 1 200 . 1 1 28 28 LYS HG3 H 1 1.46 0.02 . 1 . . . . . . . . 4347 1 201 . 1 1 28 28 LYS HD2 H 1 1.71 0.02 . 1 . . . . . . . . 4347 1 202 . 1 1 28 28 LYS HD3 H 1 1.71 0.02 . 1 . . . . . . . . 4347 1 203 . 1 1 28 28 LYS HE2 H 1 2.93 0.02 . 1 . . . . . . . . 4347 1 204 . 1 1 28 28 LYS HE3 H 1 2.93 0.02 . 1 . . . . . . . . 4347 1 205 . 1 1 29 29 LYS H H 1 7.91 0.02 . 1 . . . . . . . . 4347 1 206 . 1 1 29 29 LYS HA H 1 3.99 0.02 . 1 . . . . . . . . 4347 1 207 . 1 1 29 29 LYS HB2 H 1 1.74 0.02 . 1 . . . . . . . . 4347 1 208 . 1 1 29 29 LYS HB3 H 1 1.85 0.02 . 1 . . . . . . . . 4347 1 209 . 1 1 29 29 LYS HG2 H 1 1.26 0.02 . 1 . . . . . . . . 4347 1 210 . 1 1 29 29 LYS HG3 H 1 1.26 0.02 . 1 . . . . . . . . 4347 1 211 . 1 1 29 29 LYS HD2 H 1 1.52 0.02 . 1 . . . . . . . . 4347 1 212 . 1 1 29 29 LYS HD3 H 1 1.52 0.02 . 1 . . . . . . . . 4347 1 213 . 1 1 29 29 LYS HE2 H 1 2.81 0.02 . 1 . . . . . . . . 4347 1 214 . 1 1 29 29 LYS HE3 H 1 2.81 0.02 . 1 . . . . . . . . 4347 1 215 . 1 1 30 30 PHE H H 1 8.42 0.02 . 1 . . . . . . . . 4347 1 216 . 1 1 30 30 PHE HA H 1 4.07 0.02 . 1 . . . . . . . . 4347 1 217 . 1 1 30 30 PHE HB2 H 1 2.52 0.02 . 1 . . . . . . . . 4347 1 218 . 1 1 30 30 PHE HB3 H 1 2.88 0.02 . 1 . . . . . . . . 4347 1 219 . 1 1 30 30 PHE HD1 H 1 6.59 0.02 . 1 . . . . . . . . 4347 1 220 . 1 1 30 30 PHE HD2 H 1 6.59 0.02 . 1 . . . . . . . . 4347 1 221 . 1 1 30 30 PHE HE1 H 1 6.74 0.02 . 1 . . . . . . . . 4347 1 222 . 1 1 30 30 PHE HE2 H 1 6.74 0.02 . 1 . . . . . . . . 4347 1 223 . 1 1 30 30 PHE HZ H 1 6.93 0.02 . 1 . . . . . . . . 4347 1 224 . 1 1 31 31 HIS H H 1 8.27 0.02 . 1 . . . . . . . . 4347 1 225 . 1 1 31 31 HIS HA H 1 3.75 0.02 . 1 . . . . . . . . 4347 1 226 . 1 1 31 31 HIS HB2 H 1 3.33 0.02 . 1 . . . . . . . . 4347 1 227 . 1 1 31 31 HIS HB3 H 1 2.98 0.02 . 1 . . . . . . . . 4347 1 228 . 1 1 31 31 HIS HD2 H 1 6.87 0.02 . 1 . . . . . . . . 4347 1 229 . 1 1 31 31 HIS HE1 H 1 7.51 0.02 . 1 . . . . . . . . 4347 1 230 . 1 1 32 32 GLU H H 1 7.40 0.02 . 1 . . . . . . . . 4347 1 231 . 1 1 32 32 GLU HA H 1 3.78 0.02 . 1 . . . . . . . . 4347 1 232 . 1 1 32 32 GLU HB2 H 1 2.00 0.02 . 1 . . . . . . . . 4347 1 233 . 1 1 32 32 GLU HB3 H 1 2.00 0.02 . 1 . . . . . . . . 4347 1 234 . 1 1 32 32 GLU HG2 H 1 2.26 0.02 . 1 . . . . . . . . 4347 1 235 . 1 1 32 32 GLU HG3 H 1 2.33 0.02 . 1 . . . . . . . . 4347 1 236 . 1 1 33 33 LEU H H 1 7.29 0.02 . 1 . . . . . . . . 4347 1 237 . 1 1 33 33 LEU HA H 1 3.85 0.02 . 1 . . . . . . . . 4347 1 238 . 1 1 33 33 LEU HB2 H 1 1.40 0.02 . 1 . . . . . . . . 4347 1 239 . 1 1 33 33 LEU HB3 H 1 1.35 0.02 . 1 . . . . . . . . 4347 1 240 . 1 1 33 33 LEU HG H 1 0.87 0.02 . 1 . . . . . . . . 4347 1 241 . 1 1 33 33 LEU HD11 H 1 0.54 0.02 . 1 . . . . . . . . 4347 1 242 . 1 1 33 33 LEU HD12 H 1 0.54 0.02 . 1 . . . . . . . . 4347 1 243 . 1 1 33 33 LEU HD13 H 1 0.54 0.02 . 1 . . . . . . . . 4347 1 244 . 1 1 33 33 LEU HD21 H 1 0.61 0.02 . 1 . . . . . . . . 4347 1 245 . 1 1 33 33 LEU HD22 H 1 0.61 0.02 . 1 . . . . . . . . 4347 1 246 . 1 1 33 33 LEU HD23 H 1 0.61 0.02 . 1 . . . . . . . . 4347 1 247 . 1 1 34 34 ILE H H 1 7.48 0.02 . 1 . . . . . . . . 4347 1 248 . 1 1 34 34 ILE HA H 1 3.51 0.02 . 1 . . . . . . . . 4347 1 249 . 1 1 34 34 ILE HB H 1 1.40 0.02 . 1 . . . . . . . . 4347 1 250 . 1 1 34 34 ILE HG12 H 1 0.60 0.02 . 1 . . . . . . . . 4347 1 251 . 1 1 34 34 ILE HG13 H 1 0.89 0.02 . 1 . . . . . . . . 4347 1 252 . 1 1 34 34 ILE HG21 H 1 0.37 0.02 . 1 . . . . . . . . 4347 1 253 . 1 1 34 34 ILE HG22 H 1 0.37 0.02 . 1 . . . . . . . . 4347 1 254 . 1 1 34 34 ILE HG23 H 1 0.37 0.02 . 1 . . . . . . . . 4347 1 255 . 1 1 34 34 ILE HD11 H 1 0.24 0.02 . 1 . . . . . . . . 4347 1 256 . 1 1 34 34 ILE HD12 H 1 0.24 0.02 . 1 . . . . . . . . 4347 1 257 . 1 1 34 34 ILE HD13 H 1 0.24 0.02 . 1 . . . . . . . . 4347 1 258 . 1 1 35 35 LYS H H 1 7.71 0.02 . 1 . . . . . . . . 4347 1 259 . 1 1 35 35 LYS HA H 1 3.99 0.02 . 1 . . . . . . . . 4347 1 260 . 1 1 35 35 LYS HB2 H 1 1.59 0.02 . 1 . . . . . . . . 4347 1 261 . 1 1 35 35 LYS HB3 H 1 1.59 0.02 . 1 . . . . . . . . 4347 1 262 . 1 1 35 35 LYS HG2 H 1 1.20 0.02 . 1 . . . . . . . . 4347 1 263 . 1 1 35 35 LYS HG3 H 1 1.20 0.02 . 1 . . . . . . . . 4347 1 264 . 1 1 35 35 LYS HD2 H 1 1.45 0.02 . 1 . . . . . . . . 4347 1 265 . 1 1 35 35 LYS HD3 H 1 1.45 0.02 . 1 . . . . . . . . 4347 1 266 . 1 1 35 35 LYS HE2 H 1 2.76 0.02 . 1 . . . . . . . . 4347 1 267 . 1 1 35 35 LYS HE3 H 1 2.76 0.02 . 1 . . . . . . . . 4347 1 268 . 1 1 36 36 GLY H H 1 7.68 0.02 . 1 . . . . . . . . 4347 1 269 . 1 1 36 36 GLY HA2 H 1 3.85 0.02 . 1 . . . . . . . . 4347 1 270 . 1 1 36 36 GLY HA3 H 1 3.85 0.02 . 1 . . . . . . . . 4347 1 stop_ save_ ######################## # Coupling constants # ######################## save_coupling_constant _Coupling_constant_list.Sf_category coupling_constants _Coupling_constant_list.Sf_framecode coupling_constant _Coupling_constant_list.Entry_ID 4347 _Coupling_constant_list.ID 1 _Coupling_constant_list.Sample_condition_list_ID 1 _Coupling_constant_list.Sample_condition_list_label $sample_conditions_one _Coupling_constant_list.Spectrometer_frequency_1H . _Coupling_constant_list.Details ; 3JHNHA coupling constants were measured at two transforms, one phased in pure absorption and the other in pure dispersion, of the DQF-COSY spectrum. From these values the real coupling constants were calculated according to Kim, Y. and Prestegard, J.H. (1989) J. Magn. Reson. 84, 9-13 ; _Coupling_constant_list.Text_data_format . _Coupling_constant_list.Text_data . loop_ _Coupling_constant_experiment.Experiment_ID _Coupling_constant_experiment.Experiment_name _Coupling_constant_experiment.Sample_ID _Coupling_constant_experiment.Sample_label _Coupling_constant_experiment.Sample_state _Coupling_constant_experiment.Entry_ID _Coupling_constant_experiment.Coupling_constant_list_ID . . 1 $sample_one . 4347 1 stop_ loop_ _Coupling_constant.ID _Coupling_constant.Code _Coupling_constant.Assembly_atom_ID_1 _Coupling_constant.Entity_assembly_ID_1 _Coupling_constant.Entity_ID_1 _Coupling_constant.Comp_index_ID_1 _Coupling_constant.Seq_ID_1 _Coupling_constant.Comp_ID_1 _Coupling_constant.Atom_ID_1 _Coupling_constant.Atom_type_1 _Coupling_constant.Atom_isotope_number_1 _Coupling_constant.Ambiguity_code_1 _Coupling_constant.Assembly_atom_ID_2 _Coupling_constant.Entity_assembly_ID_2 _Coupling_constant.Entity_ID_2 _Coupling_constant.Comp_index_ID_2 _Coupling_constant.Seq_ID_2 _Coupling_constant.Comp_ID_2 _Coupling_constant.Atom_ID_2 _Coupling_constant.Atom_type_2 _Coupling_constant.Atom_isotope_number_2 _Coupling_constant.Ambiguity_code_2 _Coupling_constant.Val _Coupling_constant.Val_min _Coupling_constant.Val_max _Coupling_constant.Val_err _Coupling_constant.Resonance_ID_1 _Coupling_constant.Resonance_ID_2 _Coupling_constant.Auth_entity_assembly_ID_1 _Coupling_constant.Auth_seq_ID_1 _Coupling_constant.Auth_comp_ID_1 _Coupling_constant.Auth_atom_ID_1 _Coupling_constant.Auth_entity_assembly_ID_2 _Coupling_constant.Auth_seq_ID_2 _Coupling_constant.Auth_comp_ID_2 _Coupling_constant.Auth_atom_ID_2 _Coupling_constant.Details _Coupling_constant.Entry_ID _Coupling_constant.Coupling_constant_list_ID 1 3JHNHA . 1 1 3 3 GLU H H 1 . . 1 1 3 3 GLU HA H 1 . 11.0 . . 1.0 . . . . . . . . . . . 4347 1 2 3JHNHA . 1 1 4 4 VAL H H 1 . . 1 1 4 4 VAL HA H 1 . 3.0 . . 1.0 . . . . . . . . . . . 4347 1 3 3JHNHA . 1 1 5 5 GLU H H 1 . . 1 1 5 5 GLU HA H 1 . 6.0 . . 1.0 . . . . . . . . . . . 4347 1 4 3JHNHA . 1 1 6 6 GLU H H 1 . . 1 1 6 6 GLU HA H 1 . 4.0 . . 1.0 . . . . . . . . . . . 4347 1 5 3JHNHA . 1 1 7 7 LEU H H 1 . . 1 1 7 7 LEU HA H 1 . 4.0 . . 1.0 . . . . . . . . . . . 4347 1 6 3JHNHA . 1 1 8 8 GLU H H 1 . . 1 1 8 8 GLU HA H 1 . 4.5 . . 1.0 . . . . . . . . . . . 4347 1 7 3JHNHA . 1 1 9 9 LYS H H 1 . . 1 1 9 9 LYS HA H 1 . 4.5 . . 1.0 . . . . . . . . . . . 4347 1 8 3JHNHA . 1 1 10 10 LYS H H 1 . . 1 1 10 10 LYS HA H 1 . 6.0 . . 1.0 . . . . . . . . . . . 4347 1 9 3JHNHA . 1 1 11 11 PHE H H 1 . . 1 1 11 11 PHE HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 10 3JHNHA . 1 1 12 12 LYS H H 1 . . 1 1 12 12 LYS HA H 1 . 6.0 . . 1.0 . . . . . . . . . . . 4347 1 11 3JHNHA . 1 1 13 13 GLU H H 1 . . 1 1 13 13 GLU HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 12 3JHNHA . 1 1 14 14 LEU H H 1 . . 1 1 14 14 LEU HA H 1 . 3.0 . . 1.0 . . . . . . . . . . . 4347 1 13 3JHNHA . 1 1 16 16 LYS H H 1 . . 1 1 16 16 LYS HA H 1 . 7.0 . . 1.0 . . . . . . . . . . . 4347 1 14 3JHNHA . 1 1 19 19 ARG H H 1 . . 1 1 19 19 ARG HA H 1 . 7.0 . . 1.0 . . . . . . . . . . . 4347 1 15 3JHNHA . 1 1 21 21 GLY H H 1 . . 1 1 21 21 GLY HA H 1 . 10.0 . . 1.0 . . . . . . . . . . . 4347 1 16 3JHNHA . 1 1 22 22 GLU H H 1 . . 1 1 22 22 GLU HA H 1 . 10.0 . . 1.0 . . . . . . . . . . . 4347 1 17 3JHNHA . 1 1 23 23 ILE H H 1 . . 1 1 23 23 ILE HA H 1 . 4.0 . . 1.0 . . . . . . . . . . . 4347 1 18 3JHNHA . 1 1 24 24 GLU H H 1 . . 1 1 24 24 GLU HA H 1 . 7.0 . . 1.0 . . . . . . . . . . . 4347 1 19 3JHNHA . 1 1 25 25 GLU H H 1 . . 1 1 25 25 GLU HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 20 3JHNHA . 1 1 26 26 LEU H H 1 . . 1 1 26 26 LEU HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 21 3JHNHA . 1 1 28 28 LYS H H 1 . . 1 1 28 28 LYS HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 22 3JHNHA . 1 1 29 29 LYS H H 1 . . 1 1 29 29 LYS HA H 1 . 7.0 . . 1.0 . . . . . . . . . . . 4347 1 23 3JHNHA . 1 1 30 30 PHE H H 1 . . 1 1 30 30 PHE HA H 1 . 12.0 . . 1.0 . . . . . . . . . . . 4347 1 24 3JHNHA . 1 1 32 32 GLU H H 1 . . 1 1 32 32 GLU HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 25 3JHNHA . 1 1 33 33 LEU H H 1 . . 1 1 33 33 LEU HA H 1 . 4.0 . . 1.0 . . . . . . . . . . . 4347 1 26 3JHNHA . 1 1 34 34 ILE H H 1 . . 1 1 34 34 ILE HA H 1 . 6.0 . . 1.0 . . . . . . . . . . . 4347 1 27 3JHNHA . 1 1 35 35 LYS H H 1 . . 1 1 35 35 LYS HA H 1 . 5.0 . . 1.0 . . . . . . . . . . . 4347 1 stop_ save_