data_4652 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID 4652 _Entry.Title ; Solution Structure of Amino Terminus of Bovine Rhodopsin (residues 1-40) ; _Entry.Type macromolecule _Entry.Version_type original _Entry.Submission_date 2000-01-28 _Entry.Accession_date 2001-03-16 _Entry.Last_release_date 2001-05-09 _Entry.Original_release_date 2001-05-09 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.61 _Entry.Original_NMR_STAR_version 2.1 _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 P. Yeagle . L. . 4652 2 A. Salloum . . . 4652 3 A. Chopra . . . 4652 4 N. Bhawsar . . . 4652 5 L. Ali . . . 4652 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 4652 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 253 4652 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 . . 2001-05-09 2000-01-28 original author . 4652 stop_ loop_ _Related_entries.Database_name _Related_entries.Database_accession_code _Related_entries.Relationship _Related_entries.Entry_ID PDB 1EDX 'BMRB Entry Tracking System' 4652 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID 4652 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID 10888202 _Citation.Full_citation . _Citation.Title ; Structures of the intradiskal loops and amino terminus of the G-protein receptor, rhodopsin ; _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev 'J. Pept. Res.' _Citation.Journal_name_full . _Citation.Journal_volume 55 _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 455 _Citation.Page_last 465 _Citation.Year 2000 _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 P. Yeagle . L. . 4652 1 2 A. Salloum . . . 4652 1 3 A. Chopra . . . 4652 1 4 N. Bhawsar . . . 4652 1 5 L. Ali . . . 4652 1 6 G. Kuzmanovski . . . 4652 1 7 J. Alderfer . L. . 4652 1 8 A. Albert . D. . 4652 1 stop_ loop_ _Citation_keyword.Keyword _Citation_keyword.Entry_ID _Citation_keyword.Citation_ID helix 4652 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_system_Rhodopsin _Assembly.Sf_category assembly _Assembly.Sf_framecode system_Rhodopsin _Assembly.Entry_ID 4652 _Assembly.ID 1 _Assembly.Name 'amino terminus of Rhodopsin (residues 1-40)' _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 'not present' _Assembly.Molecular_mass . _Assembly.Enzyme_commission_number . _Assembly.Details . _Assembly.DB_query_date . _Assembly.DB_query_revised_last_date . loop_ _Assembly_type.Type _Assembly_type.Entry_ID _Assembly_type.Assembly_ID monomer 4652 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 Rhodopsin 1 $Rhodopsin . . . native . . . . . 4652 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 . PDB 1EDX . . . . . . 4652 1 stop_ loop_ _Assembly_common_name.Name _Assembly_common_name.Type _Assembly_common_name.Entry_ID _Assembly_common_name.Assembly_ID 'amino terminus of Rhodopsin (residues 1-40)' system 4652 1 Rhodopsin abbreviation 4652 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_Rhodopsin _Entity.Sf_category entity _Entity.Sf_framecode Rhodopsin _Entity.Entry_ID 4652 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name Rhodopsin _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 ; MNGTEGPNFYVPFSNKTGVV RSPFEAPQYYLAEPWEFSML ; _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 40 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic . _Entity.Thiol_state 'not present' _Entity.Src_method . _Entity.Parent_entity_ID 1 _Entity.Fragment . _Entity.Mutation . _Entity.EC_number . _Entity.Calc_isoelectric_point . _Entity.Formula_weight . _Entity.Formula_weight_exptl . _Entity.Formula_weight_exptl_meth . _Entity.Details . _Entity.DB_query_date . _Entity.DB_query_revised_last_date 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 1EDX . "Solution Structure Of Amino Terminus Of Bovine Rhodopsin (Residues 1-40)" . . . . . 100.00 40 100.00 100.00 9.29e-20 . . . . 4652 1 2 no PDB 1F88 . "Crystal Structure Of Bovine Rhodopsin" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 3 no PDB 1GZM . "Structure Of Bovine Rhodopsin In A Trigonal Crystal Form" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 4 no PDB 1HZX . "Crystal Structure Of Bovine Rhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 5 no PDB 1JFP . "Structure Of Bovine Rhodopsin (Dark Adapted)" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 6 no PDB 1L9H . "Crystal Structure Of Bovine Rhodopsin At 2.6 Angstroms Resolution" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 7 no PDB 1LN6 . "Structure Of Bovine Rhodopsin (Metarhodopsin Ii)" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 8 no PDB 1U19 . "Crystal Structure Of Bovine Rhodopsin At 2.2 Angstroms Resolution" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 9 no PDB 2G87 . "Crystallographic Model Of Bathorhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 10 no PDB 2HPY . "Crystallographic Model Of Lumirhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 11 no PDB 2I35 . "Crystal Structure Of Rhombohedral Crystal Form Of Ground-State Rhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 12 no PDB 2I36 . "Crystal Structure Of Trigonal Crystal Form Of Ground-State Rhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 13 no PDB 2I37 . "Crystal Structure Of A Photoactivated Rhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 14 no PDB 2PED . "Crystallographic Model Of 9-Cis-Rhodopsin" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 15 no PDB 3C9L . "Structure Of Ground-State Bovine Rhodospin In A Hexagonal Crystal Form" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 16 no PDB 3CAP . "Crystal Structure Of Native Opsin: The G Protein-Coupled Receptor Rhodopsin In Its Ligand-Free State" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 17 no PDB 3DQB . "Crystal Structure Of The Active G-protein-coupled Receptor Opsin In Complex With A C-terminal Peptide Derived From The Galpha S" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 18 no PDB 3OAX . "Crystal Structure Of Bovine Rhodopsin With Beta-Ionone" . . . . . 100.00 349 97.50 100.00 1.19e-18 . . . . 4652 1 19 no PDB 3PQR . "Crystal Structure Of Metarhodopsin Ii In Complex With A C-Terminal Peptide Derived From The Galpha Subunit Of Transducin" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 20 no PDB 3PXO . "Crystal Structure Of Metarhodopsin Ii" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 21 no PDB 4J4Q . "Crystal Structure Of Active Conformation Of Gpcr Opsin Stabilized By Octylglucoside" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 22 no PDB 4PXF . "Crystal Structure Of The Active G-protein-coupled Receptor Opsin In Complex With The Finger-loop Peptide Derived From The Full-" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 23 no PDB 4X1H . "Opsin/g(alpha) Peptide Complex Stabilized By Nonyl-glucoside" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 24 no DBJ BAB83621 . "rhodopsin [synthetic construct]" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 25 no GB AAA30674 . "rhodopsin [Bos taurus]" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 26 no GB AAA30675 . "rhodopsin, partial [Bos taurus]" . . . . . 87.50 343 97.14 100.00 8.21e-15 . . . . 4652 1 27 no GB ELR51227 . "Rhodopsin, partial [Bos mutus]" . . . . . 100.00 351 97.50 100.00 1.10e-18 . . . . 4652 1 28 no PRF 0811197A . rhodopsin . . . . . 100.00 347 97.50 100.00 1.14e-18 . . . . 4652 1 29 no PRF 0901188A . rhodopsin . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 30 no PRF 0901212A . rhodopsin . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 31 no PRF 0906201A . rhodopsin . . . . . 100.00 299 97.50 100.00 4.19e-19 . . . . 4652 1 32 no PRF 1001148A . rhodopsin . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 33 no REF NP_001014890 . "rhodopsin [Bos taurus]" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 34 no REF XP_004018583 . "PREDICTED: rhodopsin isoform X4 [Ovis aries]" . . . . . 100.00 348 97.50 100.00 1.13e-18 . . . . 4652 1 35 no REF XP_005902896 . "PREDICTED: rhodopsin [Bos mutus]" . . . . . 100.00 348 97.50 100.00 1.10e-18 . . . . 4652 1 36 no REF XP_005955807 . "PREDICTED: LOW QUALITY PROTEIN: rhodopsin [Pantholops hodgsonii]" . . . . . 100.00 375 97.50 100.00 2.04e-18 . . . . 4652 1 37 no REF XP_010860750 . "PREDICTED: rhodopsin [Bison bison bison]" . . . . . 100.00 348 97.50 100.00 1.16e-18 . . . . 4652 1 38 no SP P02699 . "RecName: Full=Rhodopsin" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 39 no SP P02700 . "RecName: Full=Rhodopsin" . . . . . 100.00 348 97.50 100.00 1.06e-18 . . . . 4652 1 40 no TPG DAA16827 . "TPA: rhodopsin [Bos taurus]" . . . . . 100.00 348 97.50 100.00 1.18e-18 . . . . 4652 1 stop_ loop_ _Entity_common_name.Name _Entity_common_name.Type _Entity_common_name.Entry_ID _Entity_common_name.Entity_ID Rhodopsin abbreviation 4652 1 Rhodopsin common 4652 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 . MET . 4652 1 2 . ASN . 4652 1 3 . GLY . 4652 1 4 . THR . 4652 1 5 . GLU . 4652 1 6 . GLY . 4652 1 7 . PRO . 4652 1 8 . ASN . 4652 1 9 . PHE . 4652 1 10 . TYR . 4652 1 11 . VAL . 4652 1 12 . PRO . 4652 1 13 . PHE . 4652 1 14 . SER . 4652 1 15 . ASN . 4652 1 16 . LYS . 4652 1 17 . THR . 4652 1 18 . GLY . 4652 1 19 . VAL . 4652 1 20 . VAL . 4652 1 21 . ARG . 4652 1 22 . SER . 4652 1 23 . PRO . 4652 1 24 . PHE . 4652 1 25 . GLU . 4652 1 26 . ALA . 4652 1 27 . PRO . 4652 1 28 . GLN . 4652 1 29 . TYR . 4652 1 30 . TYR . 4652 1 31 . LEU . 4652 1 32 . ALA . 4652 1 33 . GLU . 4652 1 34 . PRO . 4652 1 35 . TRP . 4652 1 36 . GLU . 4652 1 37 . PHE . 4652 1 38 . SER . 4652 1 39 . MET . 4652 1 40 . LEU . 4652 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 . MET 1 1 4652 1 . ASN 2 2 4652 1 . GLY 3 3 4652 1 . THR 4 4 4652 1 . GLU 5 5 4652 1 . GLY 6 6 4652 1 . PRO 7 7 4652 1 . ASN 8 8 4652 1 . PHE 9 9 4652 1 . TYR 10 10 4652 1 . VAL 11 11 4652 1 . PRO 12 12 4652 1 . PHE 13 13 4652 1 . SER 14 14 4652 1 . ASN 15 15 4652 1 . LYS 16 16 4652 1 . THR 17 17 4652 1 . GLY 18 18 4652 1 . VAL 19 19 4652 1 . VAL 20 20 4652 1 . ARG 21 21 4652 1 . SER 22 22 4652 1 . PRO 23 23 4652 1 . PHE 24 24 4652 1 . GLU 25 25 4652 1 . ALA 26 26 4652 1 . PRO 27 27 4652 1 . GLN 28 28 4652 1 . TYR 29 29 4652 1 . TYR 30 30 4652 1 . LEU 31 31 4652 1 . ALA 32 32 4652 1 . GLU 33 33 4652 1 . PRO 34 34 4652 1 . TRP 35 35 4652 1 . GLU 36 36 4652 1 . PHE 37 37 4652 1 . SER 38 38 4652 1 . MET 39 39 4652 1 . LEU 40 40 4652 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 4652 _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 $Rhodopsin . 9913 organism . 'Bos taurus' cow . . Eukaryota Metazoa Bos taurus . . . . . . . . . . . . . . . . . . . . . 4652 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 4652 _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 $Rhodopsin . 'chemical synthesis' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4652 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID 4652 _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 Rhodopsin . . . 1 $Rhodopsin . . 2 . . mM . . . . 4652 1 2 DMSO . . . . . . . . . . % . . . . 4652 1 stop_ save_ ####################### # Sample conditions # ####################### save_sample_cond_1 _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_cond_1 _Sample_condition_list.Entry_ID 4652 _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 4652 1 temperature 303 . K 4652 1 stop_ save_ ############################ # Computer software used # ############################ save_FELIX _Software.Sf_category software _Software.Sf_framecode FELIX _Software.Entry_ID 4652 _Software.ID 1 _Software.Name FELIX _Software.Version . _Software.Details . loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' 4652 1 stop_ save_ save_DIANA _Software.Sf_category software _Software.Sf_framecode DIANA _Software.Entry_ID 4652 _Software.ID 2 _Software.Name DIANA _Software.Version . _Software.Details . loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'structure solution' 4652 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 4652 _NMR_spectrometer.ID 1 _NMR_spectrometer.Details . _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model AMX _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 600 save_ save_spectrometer_list _NMR_spectrometer_list.Sf_category NMR_spectrometer_list _NMR_spectrometer_list.Sf_framecode spectrometer_list _NMR_spectrometer_list.Entry_ID 4652 _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 . . . 4652 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 4652 _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 NOESY' . . . . . . . . . . . 1 $sample_1 . . . 1 $sample_cond_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4652 1 2 DQF-COSY . . . . . . . . . . . 1 $sample_1 . . . 1 $sample_cond_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 4652 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chemical_shift_ref_1 _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chemical_shift_ref_1 _Chem_shift_reference.Entry_ID 4652 _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 . . . . . . ppm . . . . . . . 1 $entry_citation . . 1 $entry_citation 4652 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_chemical_shift_set_1 _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode chemical_shift_set_1 _Assigned_chem_shift_list.Entry_ID 4652 _Assigned_chem_shift_list.ID 1 _Assigned_chem_shift_list.Sample_condition_list_ID 1 _Assigned_chem_shift_list.Sample_condition_list_label $sample_cond_1 _Assigned_chem_shift_list.Chem_shift_reference_ID 1 _Assigned_chem_shift_list.Chem_shift_reference_label $chemical_shift_ref_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 $sample_1 . 4652 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 MET HA H 1 3.92 . . . . . . . . . . . 4652 1 2 . 1 1 1 1 MET HB2 H 1 1.99 . . . . . . . . . . . 4652 1 3 . 1 1 1 1 MET HB3 H 1 1.99 . . . . . . . . . . . 4652 1 4 . 1 1 2 2 ASN H H 1 8.67 . . . . . . . . . . . 4652 1 5 . 1 1 2 2 ASN HA H 1 4.67 . . . . . . . . . . . 4652 1 6 . 1 1 2 2 ASN HB2 H 1 2.69 . . . . . . . . . . . 4652 1 7 . 1 1 2 2 ASN HB3 H 1 2.57 . . . . . . . . . . . 4652 1 8 . 1 1 2 2 ASN HD21 H 1 7.56 . . . . . . . . . . . 4652 1 9 . 1 1 2 2 ASN HD22 H 1 6.92 . . . . . . . . . . . 4652 1 10 . 1 1 3 3 GLY H H 1 8.21 . . . . . . . . . . . 4652 1 11 . 1 1 3 3 GLY HA2 H 1 3.84 . . . . . . . . . . . 4652 1 12 . 1 1 3 3 GLY HA3 H 1 3.84 . . . . . . . . . . . 4652 1 13 . 1 1 4 4 THR H H 1 7.82 . . . . . . . . . . . 4652 1 14 . 1 1 4 4 THR HA H 1 4.24 . . . . . . . . . . . 4652 1 15 . 1 1 4 4 THR HB H 1 4.02 . . . . . . . . . . . 4652 1 16 . 1 1 4 4 THR HG21 H 1 1.05 . . . . . . . . . . . 4652 1 17 . 1 1 4 4 THR HG22 H 1 1.05 . . . . . . . . . . . 4652 1 18 . 1 1 4 4 THR HG23 H 1 1.05 . . . . . . . . . . . 4652 1 19 . 1 1 5 5 GLU H H 1 7.88 . . . . . . . . . . . 4652 1 20 . 1 1 5 5 GLU HA H 1 4.50 . . . . . . . . . . . 4652 1 21 . 1 1 5 5 GLU HB2 H 1 1.85 . . . . . . . . . . . 4652 1 22 . 1 1 5 5 GLU HB3 H 1 1.63 . . . . . . . . . . . 4652 1 23 . 1 1 5 5 GLU HG2 H 1 2.30 . . . . . . . . . . . 4652 1 24 . 1 1 5 5 GLU HG3 H 1 2.10 . . . . . . . . . . . 4652 1 25 . 1 1 6 6 GLY H H 1 8.13 . . . . . . . . . . . 4652 1 26 . 1 1 6 6 GLY HA2 H 1 3.91 . . . . . . . . . . . 4652 1 27 . 1 1 6 6 GLY HA3 H 1 3.91 . . . . . . . . . . . 4652 1 28 . 1 1 7 7 PRO HB2 H 1 1.83 . . . . . . . . . . . 4652 1 29 . 1 1 7 7 PRO HB3 H 1 1.83 . . . . . . . . . . . 4652 1 30 . 1 1 7 7 PRO HG2 H 1 3.83 . . . . . . . . . . . 4652 1 31 . 1 1 7 7 PRO HG3 H 1 3.83 . . . . . . . . . . . 4652 1 32 . 1 1 7 7 PRO HD2 H 1 3.44 . . . . . . . . . . . 4652 1 33 . 1 1 7 7 PRO HD3 H 1 3.44 . . . . . . . . . . . 4652 1 34 . 1 1 8 8 ASN H H 1 8.685 . . . . . . . . . . . 4652 1 35 . 1 1 8 8 ASN HA H 1 4.65 . . . . . . . . . . . 4652 1 36 . 1 1 8 8 ASN HB2 H 1 2.64 . . . . . . . . . . . 4652 1 37 . 1 1 8 8 ASN HB3 H 1 2.56 . . . . . . . . . . . 4652 1 38 . 1 1 8 8 ASN HD21 H 1 7.44 . . . . . . . . . . . 4652 1 39 . 1 1 8 8 ASN HD22 H 1 6.96 . . . . . . . . . . . 4652 1 40 . 1 1 9 9 PHE H H 1 8.30 . . . . . . . . . . . 4652 1 41 . 1 1 9 9 PHE HA H 1 4.48 . . . . . . . . . . . 4652 1 42 . 1 1 9 9 PHE HB2 H 1 3.08 . . . . . . . . . . . 4652 1 43 . 1 1 9 9 PHE HB3 H 1 2.84 . . . . . . . . . . . 4652 1 44 . 1 1 9 9 PHE HD1 H 1 7.34 . . . . . . . . . . . 4652 1 45 . 1 1 9 9 PHE HD2 H 1 7.34 . . . . . . . . . . . 4652 1 46 . 1 1 10 10 TYR H H 1 8.04 . . . . . . . . . . . 4652 1 47 . 1 1 10 10 TYR HA H 1 4.47 . . . . . . . . . . . 4652 1 48 . 1 1 10 10 TYR HB2 H 1 2.90 . . . . . . . . . . . 4652 1 49 . 1 1 10 10 TYR HB3 H 1 2.78 . . . . . . . . . . . 4652 1 50 . 1 1 10 10 TYR HD1 H 1 7.18 . . . . . . . . . . . 4652 1 51 . 1 1 10 10 TYR HD2 H 1 7.18 . . . . . . . . . . . 4652 1 52 . 1 1 10 10 TYR HE1 H 1 6.86 . . . . . . . . . . . 4652 1 53 . 1 1 10 10 TYR HE2 H 1 6.86 . . . . . . . . . . . 4652 1 54 . 1 1 11 11 VAL H H 1 7.86 . . . . . . . . . . . 4652 1 55 . 1 1 11 11 VAL HA H 1 4.13 . . . . . . . . . . . 4652 1 56 . 1 1 11 11 VAL HB H 1 1.97 . . . . . . . . . . . 4652 1 57 . 1 1 11 11 VAL HG11 H 1 0.85 . . . . . . . . . . . 4652 1 58 . 1 1 11 11 VAL HG12 H 1 0.85 . . . . . . . . . . . 4652 1 59 . 1 1 11 11 VAL HG13 H 1 0.85 . . . . . . . . . . . 4652 1 60 . 1 1 11 11 VAL HG21 H 1 0.85 . . . . . . . . . . . 4652 1 61 . 1 1 11 11 VAL HG22 H 1 0.85 . . . . . . . . . . . 4652 1 62 . 1 1 11 11 VAL HG23 H 1 0.85 . . . . . . . . . . . 4652 1 63 . 1 1 12 12 PRO HA H 1 4.32 . . . . . . . . . . . 4652 1 64 . 1 1 12 12 PRO HB2 H 1 3.60 . . . . . . . . . . . 4652 1 65 . 1 1 12 12 PRO HB3 H 1 3.50 . . . . . . . . . . . 4652 1 66 . 1 1 13 13 PHE H H 1 7.86 . . . . . . . . . . . 4652 1 67 . 1 1 13 13 PHE HA H 1 4.59 . . . . . . . . . . . 4652 1 68 . 1 1 13 13 PHE HB2 H 1 3.05 . . . . . . . . . . . 4652 1 69 . 1 1 13 13 PHE HB3 H 1 2.78 . . . . . . . . . . . 4652 1 70 . 1 1 14 14 SER H H 1 8.165 . . . . . . . . . . . 4652 1 71 . 1 1 14 14 SER HA H 1 4.33 . . . . . . . . . . . 4652 1 72 . 1 1 14 14 SER HB2 H 1 3.64 . . . . . . . . . . . 4652 1 73 . 1 1 14 14 SER HB3 H 1 3.56 . . . . . . . . . . . 4652 1 74 . 1 1 15 15 ASN H H 1 8.762 . . . . . . . . . . . 4652 1 75 . 1 1 15 15 ASN HA H 1 4.63 . . . . . . . . . . . 4652 1 76 . 1 1 15 15 ASN HB2 H 1 2.60 . . . . . . . . . . . 4652 1 77 . 1 1 15 15 ASN HB3 H 1 2.52 . . . . . . . . . . . 4652 1 78 . 1 1 15 15 ASN HD21 H 1 7.44 . . . . . . . . . . . 4652 1 79 . 1 1 15 15 ASN HD22 H 1 6.96 . . . . . . . . . . . 4652 1 80 . 1 1 16 16 LYS H H 1 7.95 . . . . . . . . . . . 4652 1 81 . 1 1 16 16 LYS HA H 1 4.30 . . . . . . . . . . . 4652 1 82 . 1 1 16 16 LYS HB2 H 1 1.74 . . . . . . . . . . . 4652 1 83 . 1 1 16 16 LYS HB3 H 1 1.55 . . . . . . . . . . . 4652 1 84 . 1 1 16 16 LYS HG2 H 1 1.53 . . . . . . . . . . . 4652 1 85 . 1 1 16 16 LYS HG3 H 1 1.53 . . . . . . . . . . . 4652 1 86 . 1 1 16 16 LYS HD2 H 1 1.33 . . . . . . . . . . . 4652 1 87 . 1 1 16 16 LYS HD3 H 1 1.33 . . . . . . . . . . . 4652 1 88 . 1 1 16 16 LYS HE2 H 1 2.76 . . . . . . . . . . . 4652 1 89 . 1 1 16 16 LYS HE3 H 1 2.76 . . . . . . . . . . . 4652 1 90 . 1 1 16 16 LYS HZ1 H 1 7.64 . . . . . . . . . . . 4652 1 91 . 1 1 16 16 LYS HZ2 H 1 7.64 . . . . . . . . . . . 4652 1 92 . 1 1 16 16 LYS HZ3 H 1 7.64 . . . . . . . . . . . 4652 1 93 . 1 1 17 17 THR H H 1 7.69 . . . . . . . . . . . 4652 1 94 . 1 1 17 17 THR HA H 1 4.17 . . . . . . . . . . . 4652 1 95 . 1 1 17 17 THR HB H 1 4.00 . . . . . . . . . . . 4652 1 96 . 1 1 17 17 THR HG21 H 1 1.07 . . . . . . . . . . . 4652 1 97 . 1 1 17 17 THR HG22 H 1 1.07 . . . . . . . . . . . 4652 1 98 . 1 1 17 17 THR HG23 H 1 1.07 . . . . . . . . . . . 4652 1 99 . 1 1 18 18 GLY H H 1 7.98 . . . . . . . . . . . 4652 1 100 . 1 1 18 18 GLY HA2 H 1 3.77 . . . . . . . . . . . 4652 1 101 . 1 1 18 18 GLY HA3 H 1 3.77 . . . . . . . . . . . 4652 1 102 . 1 1 19 19 VAL H H 1 7.76 . . . . . . . . . . . 4652 1 103 . 1 1 19 19 VAL HA H 1 4.26 . . . . . . . . . . . 4652 1 104 . 1 1 19 19 VAL HB H 1 1.95 . . . . . . . . . . . 4652 1 105 . 1 1 19 19 VAL HG11 H 1 0.83 . . . . . . . . . . . 4652 1 106 . 1 1 19 19 VAL HG12 H 1 0.83 . . . . . . . . . . . 4652 1 107 . 1 1 19 19 VAL HG13 H 1 0.83 . . . . . . . . . . . 4652 1 108 . 1 1 19 19 VAL HG21 H 1 0.83 . . . . . . . . . . . 4652 1 109 . 1 1 19 19 VAL HG22 H 1 0.83 . . . . . . . . . . . 4652 1 110 . 1 1 19 19 VAL HG23 H 1 0.83 . . . . . . . . . . . 4652 1 111 . 1 1 20 20 VAL H H 1 8.30 . . . . . . . . . . . 4652 1 112 . 1 1 20 20 VAL HB H 1 1.91 . . . . . . . . . . . 4652 1 113 . 1 1 20 20 VAL HG11 H 1 0.79 . . . . . . . . . . . 4652 1 114 . 1 1 20 20 VAL HG12 H 1 0.79 . . . . . . . . . . . 4652 1 115 . 1 1 20 20 VAL HG13 H 1 0.79 . . . . . . . . . . . 4652 1 116 . 1 1 20 20 VAL HG21 H 1 0.79 . . . . . . . . . . . 4652 1 117 . 1 1 20 20 VAL HG22 H 1 0.79 . . . . . . . . . . . 4652 1 118 . 1 1 20 20 VAL HG23 H 1 0.79 . . . . . . . . . . . 4652 1 119 . 1 1 21 21 ARG H H 1 7.66 . . . . . . . . . . . 4652 1 120 . 1 1 21 21 ARG HA H 1 4.51 . . . . . . . . . . . 4652 1 121 . 1 1 21 21 ARG HB2 H 1 1.73 . . . . . . . . . . . 4652 1 122 . 1 1 21 21 ARG HB3 H 1 1.64 . . . . . . . . . . . 4652 1 123 . 1 1 21 21 ARG HG2 H 1 1.46 . . . . . . . . . . . 4652 1 124 . 1 1 21 21 ARG HG3 H 1 1.46 . . . . . . . . . . . 4652 1 125 . 1 1 21 21 ARG HD2 H 1 3.08 . . . . . . . . . . . 4652 1 126 . 1 1 21 21 ARG HD3 H 1 3.08 . . . . . . . . . . . 4652 1 127 . 1 1 21 21 ARG HH11 H 1 7.46 . . . . . . . . . . . 4652 1 128 . 1 1 21 21 ARG HH12 H 1 7.46 . . . . . . . . . . . 4652 1 129 . 1 1 21 21 ARG HH21 H 1 6.96 . . . . . . . . . . . 4652 1 130 . 1 1 21 21 ARG HH22 H 1 6.96 . . . . . . . . . . . 4652 1 131 . 1 1 22 22 SER H H 1 8.02 . . . . . . . . . . . 4652 1 132 . 1 1 22 22 SER HA H 1 4.57 . . . . . . . . . . . 4652 1 133 . 1 1 22 22 SER HB2 H 1 3.61 . . . . . . . . . . . 4652 1 134 . 1 1 22 22 SER HB3 H 1 3.61 . . . . . . . . . . . 4652 1 135 . 1 1 23 23 PRO HA H 1 4.50 . . . . . . . . . . . 4652 1 136 . 1 1 23 23 PRO HB2 H 1 1.91 . . . . . . . . . . . 4652 1 137 . 1 1 23 23 PRO HB3 H 1 1.91 . . . . . . . . . . . 4652 1 138 . 1 1 23 23 PRO HG2 H 1 3.54 . . . . . . . . . . . 4652 1 139 . 1 1 23 23 PRO HG3 H 1 3.54 . . . . . . . . . . . 4652 1 140 . 1 1 23 23 PRO HD2 H 1 3.62 . . . . . . . . . . . 4652 1 141 . 1 1 23 23 PRO HD3 H 1 3.62 . . . . . . . . . . . 4652 1 142 . 1 1 24 24 PHE H H 1 7.66 . . . . . . . . . . . 4652 1 143 . 1 1 24 24 PHE HA H 1 4.51 . . . . . . . . . . . 4652 1 144 . 1 1 24 24 PHE HB2 H 1 3.07 . . . . . . . . . . . 4652 1 145 . 1 1 24 24 PHE HB3 H 1 2.72 . . . . . . . . . . . 4652 1 146 . 1 1 24 24 PHE HD1 H 1 7.22 . . . . . . . . . . . 4652 1 147 . 1 1 24 24 PHE HD2 H 1 7.22 . . . . . . . . . . . 4652 1 148 . 1 1 25 25 GLU H H 1 7.86 . . . . . . . . . . . 4652 1 149 . 1 1 25 25 GLU HA H 1 4.28 . . . . . . . . . . . 4652 1 150 . 1 1 25 25 GLU HB2 H 1 1.93 . . . . . . . . . . . 4652 1 151 . 1 1 25 25 GLU HB3 H 1 1.75 . . . . . . . . . . . 4652 1 152 . 1 1 25 25 GLU HG2 H 1 2.28 . . . . . . . . . . . 4652 1 153 . 1 1 25 25 GLU HG3 H 1 2.28 . . . . . . . . . . . 4652 1 154 . 1 1 26 26 ALA H H 1 8.056 . . . . . . . . . . . 4652 1 155 . 1 1 26 26 ALA HA H 1 4.28 . . . . . . . . . . . 4652 1 156 . 1 1 26 26 ALA HB1 H 1 1.22 . . . . . . . . . . . 4652 1 157 . 1 1 26 26 ALA HB2 H 1 1.22 . . . . . . . . . . . 4652 1 158 . 1 1 26 26 ALA HB3 H 1 1.22 . . . . . . . . . . . 4652 1 159 . 1 1 27 27 PRO HA H 1 4.27 . . . . . . . . . . . 4652 1 160 . 1 1 27 27 PRO HB2 H 1 1.97 . . . . . . . . . . . 4652 1 161 . 1 1 27 27 PRO HB3 H 1 1.81 . . . . . . . . . . . 4652 1 162 . 1 1 27 27 PRO HG2 H 1 1.77 . . . . . . . . . . . 4652 1 163 . 1 1 27 27 PRO HG3 H 1 1.77 . . . . . . . . . . . 4652 1 164 . 1 1 27 27 PRO HD2 H 1 3.58 . . . . . . . . . . . 4652 1 165 . 1 1 27 27 PRO HD3 H 1 3.525 . . . . . . . . . . . 4652 1 166 . 1 1 28 28 GLN H H 1 8.05 . . . . . . . . . . . 4652 1 167 . 1 1 28 28 GLN HA H 1 4.105 . . . . . . . . . . . 4652 1 168 . 1 1 28 28 GLN HB2 H 1 1.85 . . . . . . . . . . . 4652 1 169 . 1 1 28 28 GLN HB3 H 1 1.70 . . . . . . . . . . . 4652 1 170 . 1 1 28 28 GLN HG2 H 1 2.09 . . . . . . . . . . . 4652 1 171 . 1 1 28 28 GLN HG3 H 1 2.09 . . . . . . . . . . . 4652 1 172 . 1 1 28 28 GLN HE21 H 1 6.92 . . . . . . . . . . . 4652 1 173 . 1 1 28 28 GLN HE22 H 1 7.63 . . . . . . . . . . . 4652 1 174 . 1 1 29 29 TYR H H 1 7.62 . . . . . . . . . . . 4652 1 175 . 1 1 29 29 TYR HA H 1 4.36 . . . . . . . . . . . 4652 1 176 . 1 1 29 29 TYR HB2 H 1 2.92 . . . . . . . . . . . 4652 1 177 . 1 1 29 29 TYR HB3 H 1 2.66 . . . . . . . . . . . 4652 1 178 . 1 1 29 29 TYR HD1 H 1 7.14 . . . . . . . . . . . 4652 1 179 . 1 1 29 29 TYR HD2 H 1 7.14 . . . . . . . . . . . 4652 1 180 . 1 1 29 29 TYR HE1 H 1 6.91 . . . . . . . . . . . 4652 1 181 . 1 1 29 29 TYR HE2 H 1 6.91 . . . . . . . . . . . 4652 1 182 . 1 1 30 30 TYR H H 1 7.98 . . . . . . . . . . . 4652 1 183 . 1 1 30 30 TYR HA H 1 4.58 . . . . . . . . . . . 4652 1 184 . 1 1 30 30 TYR HB2 H 1 2.93 . . . . . . . . . . . 4652 1 185 . 1 1 30 30 TYR HB3 H 1 2.73 . . . . . . . . . . . 4652 1 186 . 1 1 30 30 TYR HD1 H 1 7.14 . . . . . . . . . . . 4652 1 187 . 1 1 30 30 TYR HD2 H 1 7.14 . . . . . . . . . . . 4652 1 188 . 1 1 30 30 TYR HE1 H 1 7.00 . . . . . . . . . . . 4652 1 189 . 1 1 30 30 TYR HE2 H 1 7.00 . . . . . . . . . . . 4652 1 190 . 1 1 31 31 LEU H H 1 7.89 . . . . . . . . . . . 4652 1 191 . 1 1 31 31 LEU HA H 1 4.30 . . . . . . . . . . . 4652 1 192 . 1 1 31 31 LEU HB2 H 1 1.48 . . . . . . . . . . . 4652 1 193 . 1 1 31 31 LEU HB3 H 1 1.48 . . . . . . . . . . . 4652 1 194 . 1 1 31 31 LEU HG H 1 1.47 . . . . . . . . . . . 4652 1 195 . 1 1 31 31 LEU HD11 H 1 0.86 . . . . . . . . . . . 4652 1 196 . 1 1 31 31 LEU HD12 H 1 0.86 . . . . . . . . . . . 4652 1 197 . 1 1 31 31 LEU HD13 H 1 0.86 . . . . . . . . . . . 4652 1 198 . 1 1 31 31 LEU HD21 H 1 0.86 . . . . . . . . . . . 4652 1 199 . 1 1 31 31 LEU HD22 H 1 0.86 . . . . . . . . . . . 4652 1 200 . 1 1 31 31 LEU HD23 H 1 0.86 . . . . . . . . . . . 4652 1 201 . 1 1 32 32 ALA H H 1 7.888 . . . . . . . . . . . 4652 1 202 . 1 1 32 32 ALA HA H 1 4.27 . . . . . . . . . . . 4652 1 203 . 1 1 32 32 ALA HB1 H 1 1.19 . . . . . . . . . . . 4652 1 204 . 1 1 32 32 ALA HB2 H 1 1.19 . . . . . . . . . . . 4652 1 205 . 1 1 32 32 ALA HB3 H 1 1.19 . . . . . . . . . . . 4652 1 206 . 1 1 33 33 GLU H H 1 7.98 . . . . . . . . . . . 4652 1 207 . 1 1 33 33 GLU HA H 1 4.32 . . . . . . . . . . . 4652 1 208 . 1 1 33 33 GLU HB2 H 1 1.95 . . . . . . . . . . . 4652 1 209 . 1 1 33 33 GLU HB3 H 1 1.73 . . . . . . . . . . . 4652 1 210 . 1 1 33 33 GLU HG2 H 1 2.26 . . . . . . . . . . . 4652 1 211 . 1 1 33 33 GLU HG3 H 1 2.26 . . . . . . . . . . . 4652 1 212 . 1 1 34 34 PRO HA H 1 4.41 . . . . . . . . . . . 4652 1 213 . 1 1 34 34 PRO HB2 H 1 2.09 . . . . . . . . . . . 4652 1 214 . 1 1 34 34 PRO HB3 H 1 2.09 . . . . . . . . . . . 4652 1 215 . 1 1 34 34 PRO HG2 H 1 1.73 . . . . . . . . . . . 4652 1 216 . 1 1 34 34 PRO HG3 H 1 1.73 . . . . . . . . . . . 4652 1 217 . 1 1 34 34 PRO HD2 H 1 3.90 . . . . . . . . . . . 4652 1 218 . 1 1 34 34 PRO HD3 H 1 3.37 . . . . . . . . . . . 4652 1 219 . 1 1 35 35 TRP H H 1 7.91 . . . . . . . . . . . 4652 1 220 . 1 1 35 35 TRP HA H 1 4.50 . . . . . . . . . . . 4652 1 221 . 1 1 35 35 TRP HB2 H 1 3.10 . . . . . . . . . . . 4652 1 222 . 1 1 35 35 TRP HB3 H 1 2.95 . . . . . . . . . . . 4652 1 223 . 1 1 35 35 TRP HD1 H 1 6.94 . . . . . . . . . . . 4652 1 224 . 1 1 35 35 TRP HE3 H 1 7.14 . . . . . . . . . . . 4652 1 225 . 1 1 35 35 TRP HZ2 H 1 7.14 . . . . . . . . . . . 4652 1 226 . 1 1 35 35 TRP HH2 H 1 7.54 . . . . . . . . . . . 4652 1 227 . 1 1 36 36 GLU H H 1 7.83 . . . . . . . . . . . 4652 1 228 . 1 1 36 36 GLU HA H 1 4.22 . . . . . . . . . . . 4652 1 229 . 1 1 36 36 GLU HB2 H 1 1.83 . . . . . . . . . . . 4652 1 230 . 1 1 36 36 GLU HB3 H 1 1.69 . . . . . . . . . . . 4652 1 231 . 1 1 36 36 GLU HG2 H 1 2.27 . . . . . . . . . . . 4652 1 232 . 1 1 36 36 GLU HG3 H 1 2.11 . . . . . . . . . . . 4652 1 233 . 1 1 37 37 PHE H H 1 7.86 . . . . . . . . . . . 4652 1 234 . 1 1 37 37 PHE HB2 H 1 3.06 . . . . . . . . . . . 4652 1 235 . 1 1 37 37 PHE HB3 H 1 2.87 . . . . . . . . . . . 4652 1 236 . 1 1 37 37 PHE HD1 H 1 7.40 . . . . . . . . . . . 4652 1 237 . 1 1 37 37 PHE HD2 H 1 7.40 . . . . . . . . . . . 4652 1 238 . 1 1 38 38 SER H H 1 7.94 . . . . . . . . . . . 4652 1 239 . 1 1 38 38 SER HA H 1 4.33 . . . . . . . . . . . 4652 1 240 . 1 1 38 38 SER HB2 H 1 3.60 . . . . . . . . . . . 4652 1 241 . 1 1 38 38 SER HB3 H 1 3.53 . . . . . . . . . . . 4652 1 242 . 1 1 39 39 MET H H 1 8.26 . . . . . . . . . . . 4652 1 243 . 1 1 39 39 MET HA H 1 4.41 . . . . . . . . . . . 4652 1 244 . 1 1 39 39 MET HB2 H 1 1.88 . . . . . . . . . . . 4652 1 245 . 1 1 39 39 MET HB3 H 1 2.40 . . . . . . . . . . . 4652 1 246 . 1 1 40 40 LEU HB2 H 1 1.47 . . . . . . . . . . . 4652 1 247 . 1 1 40 40 LEU HB3 H 1 1.47 . . . . . . . . . . . 4652 1 248 . 1 1 40 40 LEU HD11 H 1 0.85 . . . . . . . . . . . 4652 1 249 . 1 1 40 40 LEU HD12 H 1 0.85 . . . . . . . . . . . 4652 1 250 . 1 1 40 40 LEU HD13 H 1 0.85 . . . . . . . . . . . 4652 1 251 . 1 1 40 40 LEU HD21 H 1 0.85 . . . . . . . . . . . 4652 1 252 . 1 1 40 40 LEU HD22 H 1 0.85 . . . . . . . . . . . 4652 1 253 . 1 1 40 40 LEU HD23 H 1 0.85 . . . . . . . . . . . 4652 1 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