data_18409 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID 18409 _Entry.Title ; 1H Chemical Shift Assignments for the second transmembrane domain from human copper transport 1 ; _Entry.Type macromolecule _Entry.Version_type original _Entry.Submission_date 2012-04-20 _Entry.Accession_date 2012-04-20 _Entry.Last_release_date . _Entry.Original_release_date . _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.61 _Entry.Original_NMR_STAR_version 3.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype 'SOLUTION NMR' _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 Lei Yang . . . 18409 2 Zhaowei Huang . . . 18409 3 Fei Li . . . 18409 stop_ loop_ _SG_project.SG_project_ID _SG_project.Project_name _SG_project.Full_name_of_center _SG_project.Initial_of_center _SG_project.Entry_ID 1 'NPPSFA, National Project on Protein Structural and Functional Analyses' 'not applicable' . 18409 stop_ loop_ _Struct_keywords.Keywords _Struct_keywords.Text _Struct_keywords.Entry_ID 'hCtr1 TMDs' . 18409 NMR . 18409 oligomerization . 18409 structure . 18409 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 18409 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 220 18409 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 2 . . 2013-02-11 2012-04-20 update BMRB 'update entry citation' 18409 1 . . 2012-05-22 2012-04-20 original author 'original release' 18409 stop_ loop_ _Related_entries.Database_name _Related_entries.Database_accession_code _Related_entries.Relationship _Related_entries.Entry_ID BMRB 18408 'first transmembrane domain from human copper transport 1' 18409 BMRB 18410 'third transmembrane domain from the human copper transport 1' 18409 PDB 2LS3 'BMRB Entry Tracking System' 18409 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID 18409 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID 22615137 _Citation.Full_citation . _Citation.Title 'Structural insights into the transmembrane domains of human copper transporter 1.' _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev 'J. Pept. Sci.' _Citation.Journal_name_full 'Journal of peptide science : an official publication of the European Peptide Society' _Citation.Journal_volume 18 _Citation.Journal_issue 7 _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 449 _Citation.Page_last 455 _Citation.Year 2012 _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 Lei Yang . . . 18409 1 2 Zhaowei Huang . . . 18409 1 3 Fei Li . . . 18409 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID 18409 _Assembly.ID 1 _Assembly.Name 'second transmembrane domain from human copper transport 1' _Assembly.BMRB_code . _Assembly.Number_of_components 1 _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 . _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 'second transmembrane domain from human copper transport 1' 1 $hCtr1-TMD2 A . yes native no no . . . 18409 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_hCtr1-TMD2 _Entity.Sf_category entity _Entity.Sf_framecode hCtr1-TMD2 _Entity.Entry_ID 18409 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name entity _Entity.Type polymer _Entity.Polymer_common_type . _Entity.Polymer_type polypeptide(L) _Entity.Polymer_type_details . _Entity.Polymer_strand_ID A _Entity.Polymer_seq_one_letter_code_can . _Entity.Polymer_seq_one_letter_code ; KHLLQTVLHIIQVVISYFLM LIFMTYNKK ; _Entity.Target_identifier . _Entity.Polymer_author_defined_seq . _Entity.Polymer_author_seq_details . _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_monomer no _Entity.Nstd_chirality no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID . _Entity.Nonpolymer_comp_label . _Entity.Number_of_monomers 29 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic no _Entity.Thiol_state 'not present' _Entity.Src_method man _Entity.Parent_entity_ID . _Entity.Fragment . _Entity.Mutation . _Entity.EC_number . _Entity.Calc_isoelectric_point . _Entity.Formula_weight 3540.426 _Entity.Formula_weight_exptl . _Entity.Formula_weight_exptl_meth . _Entity.Details . _Entity.DB_query_date . _Entity.DB_query_revised_last_date 2015-11-25 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 2LS3 . "1h Chemical Shift Assignments For The Secondary Transmembrane Domain From Human Copper Transport 1" . . . . . 100.00 29 100.00 100.00 2.37e-09 . . . . 18409 1 2 no REF XP_012317279 . "PREDICTED: LOW QUALITY PROTEIN: high affinity copper uptake protein 1 [Aotus nancymaae]" . . . . . 89.66 489 100.00 100.00 9.20e-07 . . . . 18409 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 . LYS . 18409 1 2 . HIS . 18409 1 3 . LEU . 18409 1 4 . LEU . 18409 1 5 . GLN . 18409 1 6 . THR . 18409 1 7 . VAL . 18409 1 8 . LEU . 18409 1 9 . HIS . 18409 1 10 . ILE . 18409 1 11 . ILE . 18409 1 12 . GLN . 18409 1 13 . VAL . 18409 1 14 . VAL . 18409 1 15 . ILE . 18409 1 16 . SER . 18409 1 17 . TYR . 18409 1 18 . PHE . 18409 1 19 . LEU . 18409 1 20 . MET . 18409 1 21 . LEU . 18409 1 22 . ILE . 18409 1 23 . PHE . 18409 1 24 . MET . 18409 1 25 . THR . 18409 1 26 . TYR . 18409 1 27 . ASN . 18409 1 28 . LYS . 18409 1 29 . LYS . 18409 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 . LYS 1 1 18409 1 . HIS 2 2 18409 1 . LEU 3 3 18409 1 . LEU 4 4 18409 1 . GLN 5 5 18409 1 . THR 6 6 18409 1 . VAL 7 7 18409 1 . LEU 8 8 18409 1 . HIS 9 9 18409 1 . ILE 10 10 18409 1 . ILE 11 11 18409 1 . GLN 12 12 18409 1 . VAL 13 13 18409 1 . VAL 14 14 18409 1 . ILE 15 15 18409 1 . SER 16 16 18409 1 . TYR 17 17 18409 1 . PHE 18 18 18409 1 . LEU 19 19 18409 1 . MET 20 20 18409 1 . LEU 21 21 18409 1 . ILE 22 22 18409 1 . PHE 23 23 18409 1 . MET 24 24 18409 1 . THR 25 25 18409 1 . TYR 26 26 18409 1 . ASN 27 27 18409 1 . LYS 28 28 18409 1 . LYS 29 29 18409 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 18409 _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 $hCtr1-TMD2 . 9606 organism . 'Homo sapiens' Human . . Eukaryota Metazoa Homo sapiens . . . . . . . . . . . . . . . . . . . . . 18409 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 18409 _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 $hCtr1-TMD2 . 'obtained from a vendor' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18409 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID 18409 _Sample.ID 1 _Sample.Type solution _Sample.Sub_type . _Sample.Details . _Sample.Aggregate_sample_number . _Sample.Solvent_system '40% hexafluoroisopropanol (HFIP) aqueous solution' _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 hCtr1-TMD2 'natural abundance' . . 1 $hCtr1-TMD2 . . 2 . . mM . . . . 18409 1 2 '40% hexafluoroisopropanol (HFIP) aqueous solution' 'natural abundance' . . . . . . 40 . . % . . . . 18409 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 18409 _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 pressure 1 . atm 18409 1 temperature 298 . K 18409 1 stop_ save_ ############################ # Computer software used # ############################ save_CYANA _Software.Sf_category software _Software.Sf_framecode CYANA _Software.Entry_ID 18409 _Software.ID 1 _Software.Name CYANA _Software.Version . _Software.Details . loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID 'Guntert P.' . . 18409 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID refinement 18409 1 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 18409 _NMR_spectrometer.ID 1 _NMR_spectrometer.Details . _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model Avance _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 500 save_ save_NMR_spectrometer_list _NMR_spectrometer_list.Sf_category NMR_spectrometer_list _NMR_spectrometer_list.Sf_framecode NMR_spectrometer_list _NMR_spectrometer_list.Entry_ID 18409 _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 Avance . 500 . . . 18409 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 18409 _Experiment_list.ID 1 _Experiment_list.Details . loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _Experiment.NMR_spec_expt_ID _Experiment.NMR_spec_expt_label _Experiment.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 '2D 1H-1H NOESY' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 18409 1 2 '2D 1H-1H TOCSY' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 18409 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chemical_shift_reference_1 _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chemical_shift_reference_1 _Chem_shift_reference.Entry_ID 18409 _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 internal direct 1 . . . . . . . . . 18409 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_chem_shift_list_1 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode assigned_chem_shift_list_1 _Assigned_chem_shift_list.Entry_ID 18409 _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_1 _Assigned_chem_shift_list.Chem_shift_reference_ID 1 _Assigned_chem_shift_list.Chem_shift_reference_label $chemical_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 1H-1H NOESY' . . . 18409 1 2 '2D 1H-1H TOCSY' . . . 18409 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 1 1 LYS HA H 1 4.084 0.000 . 1 . . . A 1 LYS HA . 18409 1 2 . 1 1 2 2 HIS H H 1 8.967 0.002 . 1 . . . A 2 HIS HN . 18409 1 3 . 1 1 2 2 HIS HA H 1 5.073 0.001 . 1 . . . A 2 HIS HA . 18409 1 4 . 1 1 2 2 HIS HB2 H 1 3.414 0.000 . 2 . . . A 2 HIS HB2 . 18409 1 5 . 1 1 2 2 HIS HB3 H 1 3.316 0.001 . 2 . . . A 2 HIS HB3 . 18409 1 6 . 1 1 2 2 HIS HD1 H 1 7.346 0.000 . 1 . . . A 2 HIS HD1 . 18409 1 7 . 1 1 3 3 LEU H H 1 8.324 0.001 . 1 . . . A 3 LEU HN . 18409 1 8 . 1 1 3 3 LEU HA H 1 4.348 0.000 . 1 . . . A 3 LEU HA . 18409 1 9 . 1 1 3 3 LEU HB2 H 1 1.804 0.000 . 2 . . . A 3 LEU QB . 18409 1 10 . 1 1 3 3 LEU HB3 H 1 1.804 0.000 . 2 . . . A 3 LEU QB . 18409 1 11 . 1 1 3 3 LEU HG H 1 1.713 0.001 . 1 . . . A 3 LEU HG . 18409 1 12 . 1 1 3 3 LEU HD11 H 1 1.008 0.001 . 2 . . . A 3 LEU QD1 . 18409 1 13 . 1 1 3 3 LEU HD12 H 1 1.008 0.001 . 2 . . . A 3 LEU QD1 . 18409 1 14 . 1 1 3 3 LEU HD13 H 1 1.008 0.001 . 2 . . . A 3 LEU QD1 . 18409 1 15 . 1 1 3 3 LEU HD21 H 1 0.976 0.000 . 2 . . . A 3 LEU QD2 . 18409 1 16 . 1 1 3 3 LEU HD22 H 1 0.976 0.000 . 2 . . . A 3 LEU QD2 . 18409 1 17 . 1 1 3 3 LEU HD23 H 1 0.976 0.000 . 2 . . . A 3 LEU QD2 . 18409 1 18 . 1 1 4 4 LEU H H 1 8.113 0.001 . 1 . . . A 4 LEU HN . 18409 1 19 . 1 1 4 4 LEU HA H 1 4.178 0.001 . 1 . . . A 4 LEU HA . 18409 1 20 . 1 1 4 4 LEU HB2 H 1 1.694 0.001 . 2 . . . A 4 LEU QB . 18409 1 21 . 1 1 4 4 LEU HB3 H 1 1.694 0.001 . 2 . . . A 4 LEU QB . 18409 1 22 . 1 1 4 4 LEU HD11 H 1 1.009 0.000 . 2 . . . A 4 LEU QD1 . 18409 1 23 . 1 1 4 4 LEU HD12 H 1 1.009 0.000 . 2 . . . A 4 LEU QD1 . 18409 1 24 . 1 1 4 4 LEU HD13 H 1 1.009 0.000 . 2 . . . A 4 LEU QD1 . 18409 1 25 . 1 1 4 4 LEU HD21 H 1 0.966 0.000 . 2 . . . A 4 LEU QD2 . 18409 1 26 . 1 1 4 4 LEU HD22 H 1 0.966 0.000 . 2 . . . A 4 LEU QD2 . 18409 1 27 . 1 1 4 4 LEU HD23 H 1 0.966 0.000 . 2 . . . A 4 LEU QD2 . 18409 1 28 . 1 1 5 5 GLN H H 1 8.413 0.001 . 1 . . . A 5 GLN HN . 18409 1 29 . 1 1 5 5 GLN HA H 1 4.007 0.001 . 1 . . . A 5 GLN HA . 18409 1 30 . 1 1 5 5 GLN HB2 H 1 2.188 0.001 . 2 . . . A 5 GLN QB . 18409 1 31 . 1 1 5 5 GLN HB3 H 1 2.188 0.001 . 2 . . . A 5 GLN QB . 18409 1 32 . 1 1 5 5 GLN HG2 H 1 2.636 0.001 . 2 . . . A 5 GLN HG2 . 18409 1 33 . 1 1 5 5 GLN HG3 H 1 2.435 0.001 . 2 . . . A 5 GLN HG3 . 18409 1 34 . 1 1 5 5 GLN HE21 H 1 6.985 0.001 . 2 . . . A 5 GLN HE21 . 18409 1 35 . 1 1 5 5 GLN HE22 H 1 6.720 0.000 . 2 . . . A 5 GLN HE22 . 18409 1 36 . 1 1 6 6 THR H H 1 7.843 0.001 . 1 . . . A 6 THR HN . 18409 1 37 . 1 1 6 6 THR HA H 1 4.087 0.001 . 1 . . . A 6 THR HA . 18409 1 38 . 1 1 6 6 THR HB H 1 4.555 0.001 . 1 . . . A 6 THR HB . 18409 1 39 . 1 1 6 6 THR HG21 H 1 1.371 0.001 . 1 . . . A 6 THR QG2 . 18409 1 40 . 1 1 6 6 THR HG22 H 1 1.371 0.001 . 1 . . . A 6 THR QG2 . 18409 1 41 . 1 1 6 6 THR HG23 H 1 1.371 0.001 . 1 . . . A 6 THR QG2 . 18409 1 42 . 1 1 7 7 VAL H H 1 8.073 0.001 . 1 . . . A 7 VAL HN . 18409 1 43 . 1 1 7 7 VAL HA H 1 3.737 0.001 . 1 . . . A 7 VAL HA . 18409 1 44 . 1 1 7 7 VAL HB H 1 2.297 0.002 . 1 . . . A 7 VAL HB . 18409 1 45 . 1 1 7 7 VAL HG11 H 1 1.126 0.002 . 2 . . . A 7 VAL QG1 . 18409 1 46 . 1 1 7 7 VAL HG12 H 1 1.126 0.002 . 2 . . . A 7 VAL QG1 . 18409 1 47 . 1 1 7 7 VAL HG13 H 1 1.126 0.002 . 2 . . . A 7 VAL QG1 . 18409 1 48 . 1 1 7 7 VAL HG21 H 1 1.045 0.001 . 2 . . . A 7 VAL QG2 . 18409 1 49 . 1 1 7 7 VAL HG22 H 1 1.045 0.001 . 2 . . . A 7 VAL QG2 . 18409 1 50 . 1 1 7 7 VAL HG23 H 1 1.045 0.001 . 2 . . . A 7 VAL QG2 . 18409 1 51 . 1 1 8 8 LEU H H 1 8.398 0.001 . 1 . . . A 8 LEU HN . 18409 1 52 . 1 1 8 8 LEU HA H 1 4.203 0.001 . 1 . . . A 8 LEU HA . 18409 1 53 . 1 1 8 8 LEU HB2 H 1 1.904 0.000 . 2 . . . A 8 LEU QB . 18409 1 54 . 1 1 8 8 LEU HB3 H 1 1.904 0.000 . 2 . . . A 8 LEU QB . 18409 1 55 . 1 1 8 8 LEU HG H 1 1.502 0.001 . 1 . . . A 8 LEU HG . 18409 1 56 . 1 1 8 8 LEU HD11 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 57 . 1 1 8 8 LEU HD12 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 58 . 1 1 8 8 LEU HD13 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 59 . 1 1 8 8 LEU HD21 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 60 . 1 1 8 8 LEU HD22 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 61 . 1 1 8 8 LEU HD23 H 1 0.915 0.000 . 2 . . . A 8 LEU QQD . 18409 1 62 . 1 1 9 9 HIS H H 1 7.857 0.001 . 1 . . . A 9 HIS HN . 18409 1 63 . 1 1 9 9 HIS HA H 1 4.503 0.001 . 1 . . . A 9 HIS HA . 18409 1 64 . 1 1 9 9 HIS HB2 H 1 3.558 0.001 . 2 . . . A 9 HIS HB2 . 18409 1 65 . 1 1 9 9 HIS HB3 H 1 3.489 0.000 . 2 . . . A 9 HIS HB3 . 18409 1 66 . 1 1 9 9 HIS HD1 H 1 7.258 0.001 . 1 . . . A 9 HIS HD1 . 18409 1 67 . 1 1 10 10 ILE H H 1 8.114 0.001 . 1 . . . A 10 ILE HN . 18409 1 68 . 1 1 10 10 ILE HA H 1 3.682 0.001 . 1 . . . A 10 ILE HA . 18409 1 69 . 1 1 10 10 ILE HB H 1 2.184 0.001 . 1 . . . A 10 ILE HB . 18409 1 70 . 1 1 10 10 ILE HG12 H 1 1.921 0.001 . 2 . . . A 10 ILE HG12 . 18409 1 71 . 1 1 10 10 ILE HG13 H 1 1.194 0.001 . 2 . . . A 10 ILE HG13 . 18409 1 72 . 1 1 11 11 ILE H H 1 8.451 0.001 . 1 . . . A 11 ILE HN . 18409 1 73 . 1 1 11 11 ILE HA H 1 3.724 0.001 . 1 . . . A 11 ILE HA . 18409 1 74 . 1 1 11 11 ILE HB H 1 2.012 0.001 . 1 . . . A 11 ILE HB . 18409 1 75 . 1 1 11 11 ILE HG12 H 1 1.861 0.001 . 2 . . . A 11 ILE HG12 . 18409 1 76 . 1 1 11 11 ILE HG13 H 1 1.230 0.001 . 2 . . . A 11 ILE HG13 . 18409 1 77 . 1 1 11 11 ILE HG21 H 1 0.993 0.000 . 1 . . . A 11 ILE QG2 . 18409 1 78 . 1 1 11 11 ILE HG22 H 1 0.993 0.000 . 1 . . . A 11 ILE QG2 . 18409 1 79 . 1 1 11 11 ILE HG23 H 1 0.993 0.000 . 1 . . . A 11 ILE QG2 . 18409 1 80 . 1 1 11 11 ILE HD11 H 1 0.908 0.000 . 1 . . . A 11 ILE QD1 . 18409 1 81 . 1 1 11 11 ILE HD12 H 1 0.908 0.000 . 1 . . . A 11 ILE QD1 . 18409 1 82 . 1 1 11 11 ILE HD13 H 1 0.908 0.000 . 1 . . . A 11 ILE QD1 . 18409 1 83 . 1 1 12 12 GLN H H 1 7.794 0.001 . 1 . . . A 12 GLN HN . 18409 1 84 . 1 1 12 12 GLN HA H 1 4.021 0.001 . 1 . . . A 12 GLN HA . 18409 1 85 . 1 1 12 12 GLN HB2 H 1 2.360 0.001 . 2 . . . A 12 GLN HB2 . 18409 1 86 . 1 1 12 12 GLN HB3 H 1 2.225 0.001 . 2 . . . A 12 GLN HB3 . 18409 1 87 . 1 1 12 12 GLN HG2 H 1 2.745 0.001 . 2 . . . A 12 GLN QG . 18409 1 88 . 1 1 12 12 GLN HG3 H 1 2.745 0.001 . 2 . . . A 12 GLN QG . 18409 1 89 . 1 1 12 12 GLN HE21 H 1 6.718 0.001 . 2 . . . A 12 GLN HE21 . 18409 1 90 . 1 1 12 12 GLN HE22 H 1 6.276 0.000 . 2 . . . A 12 GLN HE22 . 18409 1 91 . 1 1 13 13 VAL H H 1 8.041 0.001 . 1 . . . A 13 VAL HN . 18409 1 92 . 1 1 13 13 VAL HA H 1 3.625 0.001 . 1 . . . A 13 VAL HA . 18409 1 93 . 1 1 13 13 VAL HB H 1 2.454 0.001 . 1 . . . A 13 VAL HB . 18409 1 94 . 1 1 13 13 VAL HG11 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 95 . 1 1 13 13 VAL HG12 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 96 . 1 1 13 13 VAL HG13 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 97 . 1 1 13 13 VAL HG21 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 98 . 1 1 13 13 VAL HG22 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 99 . 1 1 13 13 VAL HG23 H 1 0.975 0.000 . 2 . . . A 13 VAL QQG . 18409 1 100 . 1 1 14 14 VAL H H 1 8.501 0.001 . 1 . . . A 14 VAL HN . 18409 1 101 . 1 1 14 14 VAL HA H 1 3.679 0.001 . 1 . . . A 14 VAL HA . 18409 1 102 . 1 1 14 14 VAL HB H 1 2.321 0.001 . 1 . . . A 14 VAL HB . 18409 1 103 . 1 1 14 14 VAL HG11 H 1 1.115 0.002 . 2 . . . A 14 VAL QG1 . 18409 1 104 . 1 1 14 14 VAL HG12 H 1 1.115 0.002 . 2 . . . A 14 VAL QG1 . 18409 1 105 . 1 1 14 14 VAL HG13 H 1 1.115 0.002 . 2 . . . A 14 VAL QG1 . 18409 1 106 . 1 1 14 14 VAL HG21 H 1 1.047 0.001 . 2 . . . A 14 VAL QG2 . 18409 1 107 . 1 1 14 14 VAL HG22 H 1 1.047 0.001 . 2 . . . A 14 VAL QG2 . 18409 1 108 . 1 1 14 14 VAL HG23 H 1 1.047 0.001 . 2 . . . A 14 VAL QG2 . 18409 1 109 . 1 1 15 15 ILE H H 1 8.912 0.001 . 1 . . . A 15 ILE HN . 18409 1 110 . 1 1 15 15 ILE HA H 1 3.963 0.001 . 1 . . . A 15 ILE HA . 18409 1 111 . 1 1 15 15 ILE HB H 1 2.005 0.001 . 1 . . . A 15 ILE HB . 18409 1 112 . 1 1 15 15 ILE HG12 H 1 1.893 0.001 . 2 . . . A 15 ILE HG12 . 18409 1 113 . 1 1 15 15 ILE HG13 H 1 1.316 0.001 . 2 . . . A 15 ILE HG13 . 18409 1 114 . 1 1 15 15 ILE HG21 H 1 1.048 0.001 . 1 . . . A 15 ILE QG2 . 18409 1 115 . 1 1 15 15 ILE HG22 H 1 1.048 0.001 . 1 . . . A 15 ILE QG2 . 18409 1 116 . 1 1 15 15 ILE HG23 H 1 1.048 0.001 . 1 . . . A 15 ILE QG2 . 18409 1 117 . 1 1 15 15 ILE HD11 H 1 0.903 0.000 . 1 . . . A 15 ILE QD1 . 18409 1 118 . 1 1 15 15 ILE HD12 H 1 0.903 0.000 . 1 . . . A 15 ILE QD1 . 18409 1 119 . 1 1 15 15 ILE HD13 H 1 0.903 0.000 . 1 . . . A 15 ILE QD1 . 18409 1 120 . 1 1 16 16 SER H H 1 8.045 0.001 . 1 . . . A 16 SER HN . 18409 1 121 . 1 1 16 16 SER HA H 1 4.217 0.001 . 1 . . . A 16 SER HA . 18409 1 122 . 1 1 16 16 SER HB2 H 1 4.066 0.001 . 2 . . . A 16 SER QB . 18409 1 123 . 1 1 16 16 SER HB3 H 1 4.066 0.001 . 2 . . . A 16 SER QB . 18409 1 124 . 1 1 17 17 TYR H H 1 8.272 0.001 . 1 . . . A 17 TYR HN . 18409 1 125 . 1 1 17 17 TYR HA H 1 4.360 0.000 . 1 . . . A 17 TYR HA . 18409 1 126 . 1 1 17 17 TYR HB2 H 1 3.319 0.001 . 2 . . . A 17 TYR HB2 . 18409 1 127 . 1 1 17 17 TYR HB3 H 1 3.235 0.001 . 2 . . . A 17 TYR HB3 . 18409 1 128 . 1 1 17 17 TYR HD1 H 1 6.993 0.001 . 3 . . . A 17 TYR HD1 . 18409 1 129 . 1 1 18 18 PHE H H 1 8.411 0.001 . 1 . . . A 18 PHE HN . 18409 1 130 . 1 1 18 18 PHE HA H 1 4.344 0.001 . 1 . . . A 18 PHE HA . 18409 1 131 . 1 1 18 18 PHE HB2 H 1 3.331 0.001 . 2 . . . A 18 PHE QB . 18409 1 132 . 1 1 18 18 PHE HB3 H 1 3.331 0.001 . 2 . . . A 18 PHE QB . 18409 1 133 . 1 1 18 18 PHE HD2 H 1 7.258 0.001 . 3 . . . A 18 PHE HD2 . 18409 1 134 . 1 1 19 19 LEU H H 1 8.868 0.001 . 1 . . . A 19 LEU HN . 18409 1 135 . 1 1 19 19 LEU HA H 1 4.080 0.001 . 1 . . . A 19 LEU HA . 18409 1 136 . 1 1 19 19 LEU HB2 H 1 1.466 0.001 . 2 . . . A 19 LEU QB . 18409 1 137 . 1 1 19 19 LEU HB3 H 1 1.466 0.001 . 2 . . . A 19 LEU QB . 18409 1 138 . 1 1 19 19 LEU HD11 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 139 . 1 1 19 19 LEU HD12 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 140 . 1 1 19 19 LEU HD13 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 141 . 1 1 19 19 LEU HD21 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 142 . 1 1 19 19 LEU HD22 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 143 . 1 1 19 19 LEU HD23 H 1 0.916 0.000 . 2 . . . A 19 LEU QQD . 18409 1 144 . 1 1 20 20 MET H H 1 7.910 0.001 . 1 . . . A 20 MET HN . 18409 1 145 . 1 1 20 20 MET HA H 1 4.305 0.001 . 1 . . . A 20 MET HA . 18409 1 146 . 1 1 20 20 MET HB2 H 1 2.328 0.001 . 2 . . . A 20 MET QB . 18409 1 147 . 1 1 20 20 MET HB3 H 1 2.328 0.001 . 2 . . . A 20 MET QB . 18409 1 148 . 1 1 20 20 MET HG2 H 1 2.743 0.001 . 2 . . . A 20 MET HG2 . 18409 1 149 . 1 1 20 20 MET HG3 H 1 2.637 0.001 . 2 . . . A 20 MET HG3 . 18409 1 150 . 1 1 21 21 LEU H H 1 8.081 0.001 . 1 . . . A 21 LEU HN . 18409 1 151 . 1 1 21 21 LEU HA H 1 4.096 0.002 . 1 . . . A 21 LEU HA . 18409 1 152 . 1 1 21 21 LEU HB2 H 1 1.896 0.001 . 2 . . . A 21 LEU QB . 18409 1 153 . 1 1 21 21 LEU HB3 H 1 1.896 0.001 . 2 . . . A 21 LEU QB . 18409 1 154 . 1 1 21 21 LEU HG H 1 1.674 0.001 . 1 . . . A 21 LEU HG . 18409 1 155 . 1 1 21 21 LEU HD11 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 156 . 1 1 21 21 LEU HD12 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 157 . 1 1 21 21 LEU HD13 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 158 . 1 1 21 21 LEU HD21 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 159 . 1 1 21 21 LEU HD22 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 160 . 1 1 21 21 LEU HD23 H 1 0.856 0.000 . 2 . . . A 21 LEU QQD . 18409 1 161 . 1 1 22 22 ILE H H 1 8.503 0.001 . 1 . . . A 22 ILE HN . 18409 1 162 . 1 1 22 22 ILE HA H 1 3.665 0.001 . 1 . . . A 22 ILE HA . 18409 1 163 . 1 1 22 22 ILE HB H 1 2.058 0.001 . 1 . . . A 22 ILE HB . 18409 1 164 . 1 1 22 22 ILE HG12 H 1 1.635 0.001 . 2 . . . A 22 ILE HG12 . 18409 1 165 . 1 1 22 22 ILE HG13 H 1 1.063 0.002 . 2 . . . A 22 ILE HG13 . 18409 1 166 . 1 1 22 22 ILE HG21 H 1 0.912 0.000 . 1 . . . A 22 ILE QG2 . 18409 1 167 . 1 1 22 22 ILE HG22 H 1 0.912 0.000 . 1 . . . A 22 ILE QG2 . 18409 1 168 . 1 1 22 22 ILE HG23 H 1 0.912 0.000 . 1 . . . A 22 ILE QG2 . 18409 1 169 . 1 1 22 22 ILE HD11 H 1 0.779 0.000 . 1 . . . A 22 ILE QD1 . 18409 1 170 . 1 1 22 22 ILE HD12 H 1 0.779 0.000 . 1 . . . A 22 ILE QD1 . 18409 1 171 . 1 1 22 22 ILE HD13 H 1 0.779 0.000 . 1 . . . A 22 ILE QD1 . 18409 1 172 . 1 1 23 23 PHE H H 1 8.695 0.001 . 1 . . . A 23 PHE HN . 18409 1 173 . 1 1 23 23 PHE HA H 1 4.294 0.001 . 1 . . . A 23 PHE HA . 18409 1 174 . 1 1 23 23 PHE HB2 H 1 3.378 0.001 . 2 . . . A 23 PHE QB . 18409 1 175 . 1 1 23 23 PHE HB3 H 1 3.378 0.001 . 2 . . . A 23 PHE QB . 18409 1 176 . 1 1 23 23 PHE HD1 H 1 7.254 0.001 . 3 . . . A 23 PHE HD1 . 18409 1 177 . 1 1 24 24 MET H H 1 9.154 0.001 . 1 . . . A 24 MET HN . 18409 1 178 . 1 1 24 24 MET HA H 1 4.237 0.001 . 1 . . . A 24 MET HA . 18409 1 179 . 1 1 24 24 MET HB2 H 1 2.415 0.000 . 2 . . . A 24 MET HB2 . 18409 1 180 . 1 1 24 24 MET HB3 H 1 2.167 0.000 . 2 . . . A 24 MET HB3 . 18409 1 181 . 1 1 24 24 MET HG2 H 1 2.917 0.001 . 2 . . . A 24 MET HG2 . 18409 1 182 . 1 1 24 24 MET HG3 H 1 2.827 0.001 . 2 . . . A 24 MET HG3 . 18409 1 183 . 1 1 25 25 THR H H 1 8.255 0.001 . 1 . . . A 25 THR HN . 18409 1 184 . 1 1 25 25 THR HA H 1 4.030 0.002 . 1 . . . A 25 THR HA . 18409 1 185 . 1 1 25 25 THR HB H 1 4.389 0.001 . 1 . . . A 25 THR HB . 18409 1 186 . 1 1 25 25 THR HG21 H 1 1.215 0.000 . 1 . . . A 25 THR QG2 . 18409 1 187 . 1 1 25 25 THR HG22 H 1 1.215 0.000 . 1 . . . A 25 THR QG2 . 18409 1 188 . 1 1 25 25 THR HG23 H 1 1.215 0.000 . 1 . . . A 25 THR QG2 . 18409 1 189 . 1 1 26 26 TYR H H 1 8.672 0.001 . 1 . . . A 26 TYR HN . 18409 1 190 . 1 1 26 26 TYR HA H 1 4.280 0.001 . 1 . . . A 26 TYR HA . 18409 1 191 . 1 1 26 26 TYR HB2 H 1 3.174 0.000 . 2 . . . A 26 TYR HB2 . 18409 1 192 . 1 1 26 26 TYR HB3 H 1 3.083 0.000 . 2 . . . A 26 TYR HB3 . 18409 1 193 . 1 1 26 26 TYR HD1 H 1 7.135 0.001 . 3 . . . A 26 TYR HD1 . 18409 1 194 . 1 1 26 26 TYR HE1 H 1 6.841 0.001 . 3 . . . A 26 TYR HE1 . 18409 1 195 . 1 1 27 27 ASN H H 1 7.822 0.001 . 1 . . . A 27 ASN HN . 18409 1 196 . 1 1 27 27 ASN HA H 1 4.543 0.001 . 1 . . . A 27 ASN HA . 18409 1 197 . 1 1 27 27 ASN HB2 H 1 2.682 0.000 . 2 . . . A 27 ASN HB2 . 18409 1 198 . 1 1 27 27 ASN HB3 H 1 2.603 0.001 . 2 . . . A 27 ASN HB3 . 18409 1 199 . 1 1 27 27 ASN HD21 H 1 6.894 0.001 . 2 . . . A 27 ASN HD21 . 18409 1 200 . 1 1 27 27 ASN HD22 H 1 5.888 0.001 . 2 . . . A 27 ASN HD22 . 18409 1 201 . 1 1 28 28 LYS H H 1 7.928 0.001 . 1 . . . A 28 LYS HN . 18409 1 202 . 1 1 28 28 LYS HA H 1 4.409 0.000 . 1 . . . A 28 LYS HA . 18409 1 203 . 1 1 28 28 LYS HB2 H 1 1.989 0.001 . 2 . . . A 28 LYS HB2 . 18409 1 204 . 1 1 28 28 LYS HB3 H 1 1.898 0.001 . 2 . . . A 28 LYS HB3 . 18409 1 205 . 1 1 28 28 LYS HG2 H 1 1.498 0.001 . 2 . . . A 28 LYS QG . 18409 1 206 . 1 1 28 28 LYS HG3 H 1 1.498 0.001 . 2 . . . A 28 LYS QG . 18409 1 207 . 1 1 28 28 LYS HD2 H 1 1.718 0.001 . 2 . . . A 28 LYS QD . 18409 1 208 . 1 1 28 28 LYS HD3 H 1 1.718 0.001 . 2 . . . A 28 LYS QD . 18409 1 209 . 1 1 28 28 LYS HE2 H 1 3.024 0.000 . 2 . . . A 28 LYS QE . 18409 1 210 . 1 1 28 28 LYS HE3 H 1 3.024 0.000 . 2 . . . A 28 LYS QE . 18409 1 211 . 1 1 29 29 LYS H H 1 7.837 0.001 . 1 . . . A 29 LYS HN . 18409 1 212 . 1 1 29 29 LYS HA H 1 4.304 0.000 . 1 . . . A 29 LYS HA . 18409 1 213 . 1 1 29 29 LYS HB2 H 1 1.989 0.001 . 2 . . . A 29 LYS QB . 18409 1 214 . 1 1 29 29 LYS HB3 H 1 1.989 0.001 . 2 . . . A 29 LYS QB . 18409 1 215 . 1 1 29 29 LYS HG2 H 1 1.550 0.001 . 2 . . . A 29 LYS QG . 18409 1 216 . 1 1 29 29 LYS HG3 H 1 1.550 0.001 . 2 . . . A 29 LYS QG . 18409 1 217 . 1 1 29 29 LYS HD2 H 1 1.765 0.000 . 2 . . . A 29 LYS QD . 18409 1 218 . 1 1 29 29 LYS HD3 H 1 1.765 0.000 . 2 . . . A 29 LYS QD . 18409 1 219 . 1 1 29 29 LYS HE2 H 1 3.083 0.000 . 2 . . . A 29 LYS QE . 18409 1 220 . 1 1 29 29 LYS HE3 H 1 3.083 0.000 . 2 . . . A 29 LYS QE . 18409 1 stop_ save_