data_16500 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID 16500 _Entry.Title ; (1-119)Apomyoglobin ; _Entry.Type macromolecule _Entry.Version_type original _Entry.Submission_date 2009-09-15 _Entry.Accession_date 2009-09-15 _Entry.Last_release_date 2010-11-01 _Entry.Original_release_date 2010-11-01 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.61 _Entry.Original_NMR_STAR_version 3.0.9.13 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.Details 'Assignment of 1H, 13C, and 15N Resonances in Unfolded (1-119)Apomyoglobin at pH 2.40. Chemical shift reference - DSS' _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 Daria Fedyukina . . . 16500 2 Silvia Cavagnero . . . 16500 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 16500 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '13C chemical shifts' 341 16500 '15N chemical shifts' 112 16500 '1H chemical shifts' 112 16500 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 . . 2010-11-01 2009-09-15 original author . 16500 stop_ loop_ _Related_entries.Database_name _Related_entries.Database_accession_code _Related_entries.Relationship _Related_entries.Entry_ID BMRB 16499 (1-77)Apomyoglobin 16500 BMRB 16501 (1-153)Apomyoglobin 16500 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID 16500 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID 20816043 _Citation.Full_citation . _Citation.Title 'Contribution of long-range interactions to the secondary structure of an unfolded globin.' _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev 'Biophys. J.' _Citation.Journal_name_full 'Biophysical journal' _Citation.Journal_volume 99 _Citation.Journal_issue 5 _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 L37 _Citation.Page_last L39 _Citation.Year 2010 _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 Daria Fedyukina . V. . 16500 1 2 Senapathy Rajagopalan . . . 16500 1 3 Ashok Sekhar . . . 16500 1 4 Eric Fulmer . C. . 16500 1 5 Ye-Jin Eun . . . 16500 1 6 Silvia Cavagnero . . . 16500 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID 16500 _Assembly.ID 1 _Assembly.Name '(1-119)Apomyoglobin pH 2.40' _Assembly.BMRB_code . _Assembly.Number_of_components 1 _Assembly.Organic_ligands . _Assembly.Metal_ions . _Assembly.Non_standard_bonds no _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 (1-119)Apomyoglobin 1 $1-119_Apomyoglobin A . yes unfolded no no . . . 16500 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_1-119_Apomyoglobin _Entity.Sf_category entity _Entity.Sf_framecode 1-119_Apomyoglobin _Entity.Entry_ID 16500 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name (1-119)Apomyoglobin _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 ; MVLSEGEWQLVLHVWAKVEA DVAGHGQDILIRLFKSHPET LEKFDRFKHLKTEAEMKASE DLKKHGVTVLTALGAILKKK GHHEAELKPLAQSHATKHKI PIKYLEFISEAIIHVLHSRH ; _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 120 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic no _Entity.Thiol_state 'not present' _Entity.Src_method . _Entity.Parent_entity_ID . _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 2015-11-25 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 BMRB 1027 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 2 no BMRB 1029 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 3 no BMRB 1200 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 4 no BMRB 1413 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 5 no BMRB 1455 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 6 no BMRB 1457 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 7 no BMRB 1459 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 8 no BMRB 1461 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 9 no BMRB 1463 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 10 no BMRB 1465 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 11 no BMRB 1467 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 12 no BMRB 1469 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 13 no BMRB 1471 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 14 no BMRB 15589 . Apomyoglobin_(1-77) . . . . . 64.17 77 100.00 100.00 3.04e-45 . . . . 16500 1 15 no BMRB 16217 . apomyoglobin . . . . . 99.17 119 100.00 100.00 2.74e-76 . . . . 16500 1 16 no BMRB 16218 . apoMb_1-119_fragment . . . . . 99.17 119 100.00 100.00 2.74e-76 . . . . 16500 1 17 no BMRB 16499 . 1-77_Apomyoglobin . . . . . 65.00 78 100.00 100.00 3.37e-46 . . . . 16500 1 18 no BMRB 16501 . (1-153)Apomyoglobin . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 19 no BMRB 1752 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 20 no BMRB 2345 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 21 no BMRB 2346 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 22 no BMRB 2347 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 23 no BMRB 2348 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 24 no BMRB 2431 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 25 no BMRB 2432 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 26 no BMRB 2433 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 27 no BMRB 2434 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 28 no BMRB 291 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 29 no BMRB 292 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 30 no BMRB 293 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 31 no BMRB 40 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 32 no BMRB 4061 . apomyoglobin . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 33 no BMRB 4062 . apomyoglobin . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 34 no BMRB 426 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 35 no BMRB 4568 . myoglobin . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 36 no BMRB 4676 . "unfolded myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 37 no BMRB 4695 . myoglobin . . . . . 99.17 153 99.16 99.16 2.87e-75 . . . . 16500 1 38 no PDB 101M . "Sperm Whale Myoglobin F46v N-Butyl Isocyanide At Ph 9.0" . . . . . 100.00 154 99.17 99.17 2.76e-76 . . . . 16500 1 39 no PDB 102M . "Sperm Whale Myoglobin H64a Aquomet At Ph 9.0" . . . . . 100.00 154 99.17 99.17 2.55e-76 . . . . 16500 1 40 no PDB 103M . "Sperm Whale Myoglobin H64a N-Butyl Isocyanide At Ph 9.0" . . . . . 100.00 154 99.17 99.17 2.55e-76 . . . . 16500 1 41 no PDB 104M . "Sperm Whale Myoglobin N-Butyl Isocyanide At Ph 7.0" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 42 no PDB 105M . "Sperm Whale Myoglobin N-Butyl Isocyanide At Ph 9.0" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 43 no PDB 106M . "Sperm Whale Myoglobin V68f Ethyl Isocyanide At Ph 9.0" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 44 no PDB 107M . "Sperm Whale Myoglobin V68f N-Butyl Isocyanide At Ph 9.0" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 45 no PDB 108M . "Sperm Whale Myoglobin V68f N-Butyl Isocyanide At Ph 7.0" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 46 no PDB 109M . "Sperm Whale Myoglobin D122n Ethyl Isocyanide At Ph 9.0" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 47 no PDB 110M . "Sperm Whale Myoglobin D122n Methyl Isocyanide At Ph 9.0" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 48 no PDB 111M . "Sperm Whale Myoglobin D122n N-Butyl Isocyanide At Ph 9.0" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 49 no PDB 112M . "Sperm Whale Myoglobin D122n N-Propyl Isocyanide At Ph 9.0" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 50 no PDB 1A6G . "Carbonmonoxy-Myoglobin, Atomic Resolution" . . . . . 99.17 151 100.00 100.00 1.73e-76 . . . . 16500 1 51 no PDB 1A6K . "Aquomet-Myoglobin, Atomic Resolution" . . . . . 99.17 151 100.00 100.00 2.12e-76 . . . . 16500 1 52 no PDB 1A6M . "Oxy-Myoglobin, Atomic Resolution" . . . . . 99.17 151 100.00 100.00 2.12e-76 . . . . 16500 1 53 no PDB 1A6N . "Deoxy-Myoglobin, Atomic Resolution" . . . . . 99.17 151 100.00 100.00 2.12e-76 . . . . 16500 1 54 no PDB 1ABS . "Photolysed Carbonmonoxy-Myoglobin At 20 K" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 55 no PDB 1AJG . "Carbonmonoxy Myoglobin At 40 K" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 56 no PDB 1AJH . "Photoproduct Of Carbonmonoxy Myoglobin At 40 K" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 57 no PDB 1BVC . "Structure Of A Biliverdin Apomyoglobin Complex (Form D) At 118 K" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 58 no PDB 1BVD . "Structure Of A Biliverdin Apomyoglobin Complex (Form B) At 98 K" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 59 no PDB 1BZ6 . "Atomic Resolution Crystal Structure Aquomet-Myoglobin From Sperm Whale At Room Temperature" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 60 no PDB 1BZP . "Atomic Resolution Crystal Structure Analysis Of Native Deoxy And Co Myoglobin From Sperm Whale At Room Temperature" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 61 no PDB 1BZR . "Atomic Resolution Crystal Structure Analysis Of Native Deoxy And Co Myoglobin From Sperm Whale At Room Temperature" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 62 no PDB 1CH1 . "Recombinant Sperm Whale Myoglobin L89g Mutatnt (Met)" . . . . . 100.00 154 99.17 99.17 2.85e-76 . . . . 16500 1 63 no PDB 1CH2 . "Recombinant Sperm Whale Myoglobin L89f Mutant (Met)" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 64 no PDB 1CH3 . "Recombinant Sperm Whale Myoglobin L89w Mutant (Met)" . . . . . 100.00 154 99.17 99.17 2.44e-76 . . . . 16500 1 65 no PDB 1CH5 . "Recombinant Sperm Whale Myoglobin H97v Mutant (Met)" . . . . . 100.00 154 99.17 99.17 4.26e-76 . . . . 16500 1 66 no PDB 1CH7 . "Recombinant Sperm Whale Myoglobin H97f Mutant (Met)" . . . . . 100.00 154 99.17 99.17 2.39e-76 . . . . 16500 1 67 no PDB 1CH9 . "Recombinant Sperm Whale Myoglobin H97q Mutant (Met)" . . . . . 100.00 154 99.17 99.17 1.30e-76 . . . . 16500 1 68 no PDB 1CIK . "Recombinant Sperm Whale Myoglobin I99a Mutant (Met)" . . . . . 100.00 154 99.17 99.17 1.39e-76 . . . . 16500 1 69 no PDB 1CIO . "Recombinant Sperm Whale Myoglobin I99v Mutant (Met)" . . . . . 100.00 154 99.17 100.00 4.36e-77 . . . . 16500 1 70 no PDB 1CO8 . "Recombinant Sperm Whale Myoglobin L104a Mutant (Met)" . . . . . 100.00 154 99.17 99.17 1.42e-76 . . . . 16500 1 71 no PDB 1CO9 . "Recombinant Sperm Whale Myoglobin L104v Mutant (Met)" . . . . . 100.00 154 99.17 100.00 7.05e-77 . . . . 16500 1 72 no PDB 1CP0 . "Recombinant Sperm Whale Myoglobin L104n Mutant (Met)" . . . . . 100.00 154 99.17 99.17 1.90e-76 . . . . 16500 1 73 no PDB 1CP5 . "Recombinant Sperm Whale Myoglobin L104f Mutant (Met)" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 74 no PDB 1CPW . "Recombinant Sperm Whale Myoglobin L104w Mutant (Met)" . . . . . 100.00 154 99.17 99.17 2.44e-76 . . . . 16500 1 75 no PDB 1CQ2 . "Neutron Struture Of Fully Deuterated Sperm Whale Myoglobin At 2.0 Angstrom" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 76 no PDB 1DO1 . "Carbonmonoxy-Myoglobin Mutant L29w At 105k" . . . . . 99.17 154 99.16 99.16 2.09e-75 . . . . 16500 1 77 no PDB 1DO3 . "Carbonmonoxy-Myoglobin (Mutant L29w) After Photolysis At T>180k" . . . . . 99.17 154 99.16 99.16 2.09e-75 . . . . 16500 1 78 no PDB 1DO4 . "Carbonmonoxy-Myoglobin (Mutant L29w) After Photolysis At T<180k" . . . . . 99.17 154 99.16 99.16 2.09e-75 . . . . 16500 1 79 no PDB 1DO7 . "Carbonmonoxy-Myoglobin (Mutant L29w) Rebinding Structure After Photolysis At T< 180k" . . . . . 99.17 154 99.16 99.16 2.09e-75 . . . . 16500 1 80 no PDB 1DTI . "Recombinant Sperm Whale Myoglobin H97d, D122n Mutant (Met)" . . . . . 100.00 154 99.17 99.17 2.61e-76 . . . . 16500 1 81 no PDB 1DTM . "Crystal Structure Of The Sperm-Whale Myoglobin Mutant H93g Complexed With 4-Methylimidazole, Metaquo Form" . . . . . 99.17 153 99.16 99.16 3.50e-75 . . . . 16500 1 82 no PDB 1DUK . "Wild-Type Recombinant Sperm Whale Metaquomyoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 83 no PDB 1DUO . "Sperm Whale Metaquomyoglobin Proximal Histidine Mutant H93g With 1-Methylimidazole As Proximal Ligand." . . . . . 99.17 153 99.16 99.16 3.50e-75 . . . . 16500 1 84 no PDB 1DXC . "Co Complex Of Myoglobin Mb-Yqr At 100k" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 85 no PDB 1DXD . "Photolyzed Co Complex Of Myoglobin Mb-Yqr At 20k" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 86 no PDB 1EBC . "Sperm Whale Met-Myoglobin:cyanide Complex" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 87 no PDB 1F63 . "Crystal Structure Of Deoxy Sperm Whale Myoglobin Mutant Y(B10)q(E7)r(E10)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 88 no PDB 1F65 . "Crystal Structure Of Oxy Sperm Whale Myoglobin Mutant Y(B10)q(E7)r(E10)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 89 no PDB 1F6H . "Combined Rietveld And Stereochemical Restraint Refinement Of A Protein" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 90 no PDB 1FCS . "Crystal Structure Of A Distal Site Double Mutant Of Sperm Whale Myoglobin At 1.6 Angstroms Resolution" . . . . . 100.00 154 98.33 98.33 3.86e-75 . . . . 16500 1 91 no PDB 1H1X . "Sperm Whale Myoglobin Mutant T67r S92d" . . . . . 100.00 154 98.33 98.33 8.75e-76 . . . . 16500 1 92 no PDB 1HJT . "Sperm Whale Myoglobin (Ferrous, Nitric Oxide Bound)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 93 no PDB 1IOP . "Incorporation Of A Hemin With The Shortest Acid Side-Chains Into Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 94 no PDB 1IRC . "Cysteine Rich Intestinal Protein" . . . . . 100.00 154 99.17 99.17 3.86e-76 . . . . 16500 1 95 no PDB 1J3F . "Crystal Structure Of An Artificial Metalloprotein:cr(iii)(3, 3'-me2-salophen)/apo-a71g Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 96 no PDB 1J52 . "Recombinant Sperm Whale Myoglobin In The Presence Of 7atm Xenon" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 97 no PDB 1JDO . "Sperm Whale Myoglobin (Ferrous, Nitric Oxide Bound)" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 98 no PDB 1JP6 . "Sperm Whale Met-Myoglobin (Room Temperature; Room Pressure)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 99 no PDB 1JP8 . "Sperm Whale Met-Myoglobin (Room Temperature; High Pressure)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 100 no PDB 1JP9 . "Sperm Whale Met-Myoglobin (Low Temperature; High Pressure)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 101 no PDB 1JPB . "Sperm Whale Met-Myoglobin (Low Temperature; High Pressure)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 102 no PDB 1JW8 . "1.3 Angstrom Resolution Crystal Structure Of P6 Form Of Myoglobin" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 103 no PDB 1L2K . "Neutron Structure Determination Of Sperm Whale Met-Myoglobin At 1.5a Resolution." . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 104 no PDB 1LTW . "Recombinant Sperm Whale Myoglobin 29w Mutant (oxy)" . . . . . 100.00 154 99.17 99.17 2.44e-76 . . . . 16500 1 105 no PDB 1LUE . "Recombinant Sperm Whale Myoglobin H64d/v68a/d122n Mutant (met)" . . . . . 100.00 154 98.33 98.33 8.20e-76 . . . . 16500 1 106 no PDB 1MBC . "X-Ray Structure And Refinement Of Carbon-Monoxy (Fe Ii)- Myoglobin At 1.5 Angstroms Resolution" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 107 no PDB 1MBD . "Neutron Diffraction Reveals Oxygen-Histidine Hydrogen Bond In Oxymyoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 108 no PDB 1MBI . "X-Ray Crystal Structure Of The Ferric Sperm Whale Myoglobin: Imidazole Complex At 2.0 Angstroms Resolution" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 109 no PDB 1MBN . "The Stereochemistry Of The Protein Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 110 no PDB 1MBO . "Structure And Refinement Of Oxymyoglobin At 1.6 Angstroms Resolution" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 111 no PDB 1MCY . "Sperm Whale Myoglobin (Mutant With Initiator Met And With His 64 Replaced By Gln, Leu 29 Replaced By Phe" . . . . . 100.00 154 98.33 98.33 5.24e-76 . . . . 16500 1 112 no PDB 1MGN . "His64(E7)-> Tyr Apomyoglobin As A Reagent For Measuring Rates Of Hemin Dissociation" . . . . . 100.00 154 99.17 100.00 6.82e-77 . . . . 16500 1 113 no PDB 1MLF . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 114 no PDB 1MLG . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 115 no PDB 1MLH . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 116 no PDB 1MLJ . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 117 no PDB 1MLK . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 118 no PDB 1MLL . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 99.17 1.27e-76 . . . . 16500 1 119 no PDB 1MLM . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 4.13e-77 . . . . 16500 1 120 no PDB 1MLN . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 4.13e-77 . . . . 16500 1 121 no PDB 1MLO . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 4.13e-77 . . . . 16500 1 122 no PDB 1MLQ . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 8.77e-77 . . . . 16500 1 123 no PDB 1MLR . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 8.77e-77 . . . . 16500 1 124 no PDB 1MLS . "Structural And Functional Effects Of Apolar Mutations Of Val68(E11) In Myoglobin" . . . . . 100.00 154 99.17 100.00 8.77e-77 . . . . 16500 1 125 no PDB 1MLU . "Nitric Oxide Recombination To Double Mutants Of Myoglobin: The Role Of Ligand Diffusion In A Fluctuating Heme Pocket" . . . . . 100.00 154 98.33 98.33 9.55e-76 . . . . 16500 1 126 no PDB 1MOA . "A Novel Site-Directed Mutant Of Myoglobin With An Unusually High O2 Affinity And Low Autooxidation Rate" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 127 no PDB 1MOB . "High-Resolution Crystal Structures Of Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.79e-76 . . . . 16500 1 128 no PDB 1MOC . "High-Resolution Crystal Structures Of Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.58e-76 . . . . 16500 1 129 no PDB 1MOD . "High-Resolution Crystal Structures Of Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.58e-76 . . . . 16500 1 130 no PDB 1MTI . "Phe46(Cd4) Orients The Distal Histidine For Hydrogen Bonding To Bound Ligands In Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 1.97e-76 . . . . 16500 1 131 no PDB 1MTJ . "Phe46(Cd4) Orients The Distal Histidine For Hydrogen Bonding To Bound Ligands In Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.76e-76 . . . . 16500 1 132 no PDB 1MTK . "Phe46(cd4) Orients The Distal Histidine For Hydrogen Bonding To Bound Ligands In Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.76e-76 . . . . 16500 1 133 no PDB 1MYF . "Solution Structure Of Carbonmonoxy Myoglobin Determined From Nmr Distance And Chemical Shift Constraints" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 134 no PDB 1MYM . "Structural Determinants Of Co Stretching Vibration Frequencies In Myoglobin" . . . . . 100.00 154 99.17 99.17 2.76e-76 . . . . 16500 1 135 no PDB 1MYZ . "Co Complex Of Myoglobin Mb-yqr At Rt Solved From Laue Data." . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 136 no PDB 1MZ0 . "Structure Of Myoglobin Mb-yqr 316 Ns After Photolysis Of Carbon Monoxide Solved From Laue Data At Rt" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 137 no PDB 1N9F . "Structure Of Earth-Grown Oxidized Myoglobin Mutant Yqr (Iss6a)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 138 no PDB 1N9H . "Structure Of Microgravity-Grown Oxidized Myoglobin Mutant Yqr (Iss6a)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 139 no PDB 1N9I . "Structure Of Earth-Grown Oxidized Myoglobin Mutant Yqr (Iss8a)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 140 no PDB 1N9X . "Structure Of Microgravity-Grown Oxidized Myoglobin Mutant Yqr (Iss8a)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 141 no PDB 1NAZ . "Structure Of Microgravity-Grown Oxidized Myoglobin Mutant Yqr (Iss8a)" . . . . . 100.00 154 97.50 97.50 3.50e-75 . . . . 16500 1 142 no PDB 1O16 . "Recombinant Sperm Whale Myoglobin H64dV68SD122N MUTANT (Met)" . . . . . 100.00 154 98.33 98.33 1.32e-75 . . . . 16500 1 143 no PDB 1OBM . "Recombinant Sperm Whale Myoglobin 29f64Q68F122N MUTANT (Met)" . . . . . 100.00 154 97.50 97.50 2.09e-75 . . . . 16500 1 144 no PDB 1OFJ . "Recombinant Sperm Whale Myoglobin L29hH64LD122N MUTANT (With Initiator Met)" . . . . . 100.00 154 98.33 98.33 1.37e-74 . . . . 16500 1 145 no PDB 1OFK . "Recombinant Sperm Whale Myoglobin F43h, H64l Mutant (Met)" . . . . . 100.00 154 98.33 98.33 1.64e-74 . . . . 16500 1 146 no PDB 1SPE . "Sperm Whale Native Co Myoglobin At Ph 4.0, Temp 4c" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 147 no PDB 1SWM . "X-Ray Crystal Structure Of The Ferric Sperm Whale Myoglobin: Imidazole Complex At 2.0 Angstroms Resolution" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 148 no PDB 1TES . "Oxygen Binding Muscle Protein" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 149 no PDB 1U7R . "Crystal Structure Of Native Sperm Whale Myoglobin From Low Ionic Strength Enviroment (form2 )" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 150 no PDB 1U7S . "Crystal Structure Of Native Sperm Whale Myoglobin From Low Ionic Strength Enviroment (form 1)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 151 no PDB 1UFJ . "Crystal Structure Of An Artificial Metalloprotein:fe(Iii)(3, 3'-Me2-Salophen)APO-A71g Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 152 no PDB 1UFP . "Crystal Structure Of An Artificial Metalloprotein:fe(Iii)(3, 3'-Me2-Salophen)APO-Wild Type Myoglobin" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 153 no PDB 1V9Q . "Crystal Structure Of An Artificial Metalloprotein:mn(iii)(3, 3'-me2-salophen)/apo-a71g Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 154 no PDB 1VXA . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 155 no PDB 1VXB . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 156 no PDB 1VXC . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 157 no PDB 1VXD . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 158 no PDB 1VXE . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 159 no PDB 1VXF . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 160 no PDB 1VXG . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 161 no PDB 1VXH . "Native Sperm Whale Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 162 no PDB 1WVP . "Structure Of Chemically Modified Myoglobin With Distal N- Tetrazolyl-Histidine E7(64)" . . . . . 99.17 153 99.16 99.16 2.44e-75 . . . . 16500 1 163 no PDB 1YOG . "Cobalt Myoglobin (Deoxy)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 164 no PDB 1YOH . "Cobalt Myoglobin (Met)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 165 no PDB 1YOI . "Cobalt Myoglobin (Oxy)" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 166 no PDB 2BLH . "Ligand Migration And Protein Fluctuations In Myoglobin Mutant L29w" . . . . . 99.17 153 99.16 99.16 2.03e-75 . . . . 16500 1 167 no PDB 2BLI . "L29w Mb Deoxy" . . . . . 99.17 153 99.16 99.16 2.03e-75 . . . . 16500 1 168 no PDB 2BLJ . "Structure Of L29w Mbco" . . . . . 99.17 153 99.16 99.16 2.03e-75 . . . . 16500 1 169 no PDB 2BW9 . "Laue Structure Of L29w Mbco" . . . . . 99.17 153 99.16 99.16 2.03e-75 . . . . 16500 1 170 no PDB 2BWH . "Laue Structure Of A Short Lived State Of L29w Myoglobin" . . . . . 99.17 153 99.16 99.16 2.03e-75 . . . . 16500 1 171 no PDB 2CMM . "Structural Analysis Of The Myoglobin Reconstituted With Iron Porphine" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 172 no PDB 2D6C . "Crystal Structure Of Myoglobin Reconstituted With Iron Porphycene" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 173 no PDB 2E2Y . "Crystal Structure Of F43wH64DV68I MYOGLOBIN" . . . . . 100.00 154 97.50 99.17 4.49e-75 . . . . 16500 1 174 no PDB 2EB8 . "Crystal Structure Of Cu(Ii)(Sal-Phe)APO-Myoglobin" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 175 no PDB 2EB9 . "Crystal Structure Of Cu(ii)(sal-leu)/apo-myoglobin" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 176 no PDB 2EF2 . "Crystal Structure Of An Artificial Metalloprotein:rh(Phebox- Ph)APO-A71g Myoglobin" . . . . . 100.00 154 99.17 99.17 1.04e-76 . . . . 16500 1 177 no PDB 2EKT . "Crystal Structure Of Myoglobin Reconstituted With 6-Methyl-6- Depropionatehemin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 178 no PDB 2EKU . "Crystal Structure Of Myoglobin Reconstituted With 7-Methyl-7- Depropionatehemin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 179 no PDB 2EVK . "The Structures Of Thiolate- And Carboxylate-Ligated Ferric H93g Myoglobin: Models For Cytochrome P450 And For Oxyanion-Bound He" . . . . . 99.17 153 99.16 99.16 3.50e-75 . . . . 16500 1 180 no PDB 2EVP . "The Structures Of Thiolate- And Carboxylate-Ligated Ferric H93g Myoglobin: Models For Cytochrome P450 And For Oxyanion-Bound He" . . . . . 99.17 153 99.16 99.16 3.50e-75 . . . . 16500 1 181 no PDB 2G0R . "Unphotolyzed Co-bound L29f Myoglobin" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 182 no PDB 2G0S . "Unphotolyzed Co-bound L29f Myoglobin, Crystal 2" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 183 no PDB 2G0V . "Photolyzed Co L29f Myoglobin: 100ps" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 184 no PDB 2G0X . "Photolyzed Co L29f Myoglobin: 316ps" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 185 no PDB 2G0Z . "Photolyzed Co L29f Myoglobin: 1ns" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 186 no PDB 2G10 . "Photolyzed Co L29f Myoglobin: 3.16ns" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 187 no PDB 2G11 . "Photolyzed Co L29f Myoglobin: 31.6ns" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 188 no PDB 2G12 . "Photolyzed Co L29f Myoglobin: 316ns" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 189 no PDB 2G14 . "Photolyzed Co L29f Myoglobin: 3.16us" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 190 no PDB 2JHO . "Cyanomet Sperm Whale Myoglobin At 1.4a Resolution" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 191 no PDB 2MB5 . "Hydration In Protein Crystals. A Neutron Diffraction Analysis Of Carbonmonoxymyoglobin" . . . . . 98.33 153 100.00 100.00 9.45e-76 . . . . 16500 1 192 no PDB 2MBW . "Recombinant Sperm Whale Myoglobin (Met)" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 193 no PDB 2MGA . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.79e-76 . . . . 16500 1 194 no PDB 2MGB . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.79e-76 . . . . 16500 1 195 no PDB 2MGC . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 4.60e-76 . . . . 16500 1 196 no PDB 2MGD . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 4.60e-76 . . . . 16500 1 197 no PDB 2MGE . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 4.60e-76 . . . . 16500 1 198 no PDB 2MGF . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 1.30e-76 . . . . 16500 1 199 no PDB 2MGG . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 1.30e-76 . . . . 16500 1 200 no PDB 2MGH . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 1.30e-76 . . . . 16500 1 201 no PDB 2MGI . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.58e-76 . . . . 16500 1 202 no PDB 2MGJ . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 4.26e-76 . . . . 16500 1 203 no PDB 2MGK . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 204 no PDB 2MGL . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 205 no PDB 2MGM . "High Resolution Crystal Structures Of Five Distal Histidine Mutants Of Sperm Whale Myoglobin" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 206 no PDB 2MYA . "High Resolution X-Ray Structures Of Myoglobin-And Hemoglobin-Alkyl Isocyanide Complexes" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 207 no PDB 2MYB . "High Resolution X-Ray Structures Of Myoglobin-And Hemoglobin-Alkyl Isocyanide Complexes" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 208 no PDB 2MYC . "High Resolution X-Ray Structures Of Myoglobin-And Hemoglobin-Alkyl Isocyanide Complexes" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 209 no PDB 2MYD . "High Resolution X-ray Structures Of Myoglobin-and Hemoglobin-alkyl Isocyanide Complexes" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 210 no PDB 2MYE . "High Resolution X-Ray Structures Of Myoglobin-And Hemoglobin-Alkyl Isocyanide Complexes" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 211 no PDB 2OH8 . "Myoglobin Cavity Mutant I28w" . . . . . 100.00 154 99.17 99.17 4.08e-76 . . . . 16500 1 212 no PDB 2OH9 . "Myoglobin Cavity Mutant V68w" . . . . . 100.00 154 99.17 99.17 4.26e-76 . . . . 16500 1 213 no PDB 2OHA . "Myoglobin Cavity Mutant F138w" . . . . . 100.00 154 100.00 100.00 3.40e-77 . . . . 16500 1 214 no PDB 2OHB . "Myoglobin Cavity Mutant I107w" . . . . . 100.00 154 99.17 99.17 4.08e-76 . . . . 16500 1 215 no PDB 2SPL . "A Novel Site-Directed Mutant Of Myoglobin With An Unusually High O2 Affinity And Low Autooxidation Rate" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 216 no PDB 2SPM . "A Novel Site-Directed Mutant Of Myoglobin With An Unusually High O2 Affinity And Low Autooxidation Rate" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 217 no PDB 2SPN . "A Novel Site-Directed Mutant Of Myoglobin With An Unusually High O2 Affinity And Low Autooxidation Rate" . . . . . 100.00 154 99.17 99.17 7.61e-77 . . . . 16500 1 218 no PDB 2SPO . "A Novel Site-directed Mutant Of Myoglobin With An Unusually High O2 Affinity And Low Autooxidation Rate" . . . . . 100.00 154 99.17 100.00 7.05e-77 . . . . 16500 1 219 no PDB 2W6W . "Crystal Structure Of Recombinant Sperm Whale Myoglobin Under 1atm Of Xenon" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 220 no PDB 2W6Y . "Crystal Structure Of Sperm Whale Myoglobin Mutant Yqr In Complex With Xenon" . . . . . 100.00 154 97.50 97.50 5.47e-75 . . . . 16500 1 221 no PDB 2Z6S . "Crystal Structure Of The Oxy Myoglobin Free From X-ray- Induced Photoreduction" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 222 no PDB 2Z6T . "Crystal Structure Of The Ferric Peroxo Myoglobin" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 223 no PDB 2ZSN . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [300 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 224 no PDB 2ZSO . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [450 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 225 no PDB 2ZSP . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [300 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 226 no PDB 2ZSQ . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [150 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 227 no PDB 2ZSR . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [450 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 228 no PDB 2ZSS . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [300 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 229 no PDB 2ZST . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [450 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 230 no PDB 2ZSX . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [600 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 231 no PDB 2ZSY . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [750 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 232 no PDB 2ZSZ . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [600 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 233 no PDB 2ZT0 . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [750 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 234 no PDB 2ZT1 . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [810 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 235 no PDB 2ZT2 . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [600 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 236 no PDB 2ZT3 . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [750 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 237 no PDB 2ZT4 . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [810 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 238 no PDB 3A2G . "Crystal Structure Of K102c-Myoglobin Conjugated With Fluorescein" . . . . . 100.00 154 99.17 99.17 2.31e-76 . . . . 16500 1 239 no PDB 3ASE . "Crystal Structure Of Zinc Myoglobin Soaked With Ru3o Cluster" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 240 no PDB 3E4N . "Carbonmonoxy Sperm Whale Myoglobin At 40 K: Laser Off" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 241 no PDB 3E55 . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser Off" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 242 no PDB 3E5I . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser Off" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 243 no PDB 3E5O . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser Off" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 244 no PDB 3ECL . "Carbonmonoxy Sperm Whale Myoglobin At 40 K: Laser On" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 245 no PDB 3ECX . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [30 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 246 no PDB 3ECZ . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [30 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 247 no PDB 3ED9 . "Carbonmonoxy Sperm Whale Myoglobin At 140 K: Laser On [30 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 248 no PDB 3EDA . "Carbonmonoxy Sperm Whale Myoglobin At 100 K: Laser On [150 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 249 no PDB 3EDB . "Carbonmonoxy Sperm Whale Myoglobin At 120 K: Laser On [150 Min]" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 250 no PDB 3H57 . "Myoglobin Cavity Mutant H64lv68n Deoxy Form" . . . . . 100.00 154 98.33 98.33 3.50e-75 . . . . 16500 1 251 no PDB 3H58 . "Myoglobin Cavity Mutant H64lv68n Met Form" . . . . . 100.00 154 98.33 98.33 3.50e-75 . . . . 16500 1 252 no PDB 3K9Z . "Rational Design Of A Structural And Functional Nitric Oxide Reductase" . . . . . 99.17 153 97.48 97.48 1.48e-72 . . . . 16500 1 253 no PDB 3MN0 . "Introducing A 2-His-1-Glu Non-Heme Iron Center Into Myoglobin Confers Nitric Oxide Reductase Activity: Cu(Ii)-Cn-Febmb(-His) Fo" . . . . . 99.17 153 98.32 98.32 6.93e-74 . . . . 16500 1 254 no PDB 3NML . "Sperm Whale Myoglobin Mutant H64w Carbonmonoxy-Form" . . . . . 100.00 154 99.17 99.17 5.98e-76 . . . . 16500 1 255 no PDB 3O89 . "Crystal Structure Of Sperm Whale Myoglobin G65t" . . . . . 99.17 153 99.16 99.16 3.35e-75 . . . . 16500 1 256 no PDB 3OGB . "Sperm Whale Myoglobin Mutant H64w Deoxy-Form" . . . . . 100.00 154 99.17 99.17 5.98e-76 . . . . 16500 1 257 no PDB 3SDN . "Structure Of G65i Sperm Whale Myoglobin Mutant" . . . . . 100.00 154 99.17 99.17 1.08e-75 . . . . 16500 1 258 no PDB 3U3E . "Complex Of Wild Type Myoglobin With Phenol In Its Proximal Cavity" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 259 no PDB 4FWX . "Aquoferric F33y Cub Myoglobin (F33y L29h F43h Sperm Whale Myoglobin)" . . . . . 99.17 153 97.48 98.32 2.77e-73 . . . . 16500 1 260 no PDB 4FWY . "F33y Cub Myoglobin (F33y L29h F43h Sperm Whale Myoglobin) With Copper Bound" . . . . . 99.17 153 97.48 98.32 2.77e-73 . . . . 16500 1 261 no PDB 4FWZ . "Aquoferric Cub Myoglobin (L29h F43h Sperm Whale Myoglobin)" . . . . . 99.17 153 98.32 98.32 1.29e-73 . . . . 16500 1 262 no PDB 4H07 . "Complex Of G65t Myoglobin With Phenol In Its Proximal Cavity" . . . . . 100.00 154 99.17 99.17 4.17e-76 . . . . 16500 1 263 no PDB 4H0B . "Complex Of G65t Myoglobin With Dmso In Its Distal Cavity" . . . . . 100.00 154 99.17 99.17 4.17e-76 . . . . 16500 1 264 no PDB 4IT8 . "A Sperm Whale Myoglobin Mutant L29h Mb With Two Distal Histidines" . . . . . 100.00 154 99.17 99.17 5.60e-76 . . . . 16500 1 265 no PDB 4LPI . "A Sperm Whale Myoglobin Double Mutant L29h/f43y Mb With A Distal Hydrogen-bonding Network" . . . . . 100.00 154 98.33 99.17 1.45e-75 . . . . 16500 1 266 no PDB 4MBN . "Refinement Of Myoglobin And Cytochrome C" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 267 no PDB 4MXK . "X-ray Structure Of Fe(ii)-znpixfebmb1" . . . . . 99.17 153 97.48 97.48 1.48e-72 . . . . 16500 1 268 no PDB 4MXL . "X-ray Structure Of Znpfebmb1" . . . . . 99.17 153 97.48 97.48 1.48e-72 . . . . 16500 1 269 no PDB 4NXA . "Sperm Whale Myoglobin Under Xenon Pressure 30 Bar" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 270 no PDB 4NXC . "Sperm Whale Myoglobin Under 30 Bar Nitrous Oxide" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 271 no PDB 4OF9 . "Structure Of K42n Variant Of Sperm Whale Myoglobin" . . . . . 99.17 153 99.16 99.16 7.35e-76 . . . . 16500 1 272 no PDB 4OOD . "Structure Of K42y Mutant Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 99.17 2.08e-76 . . . . 16500 1 273 no PDB 4PNJ . "Recombinant Sperm Whale P6 Myoglobin Solved With Single Pulse Free Electron Laser Data" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 274 no PDB 4PQ6 . "A Sperm Whale Myoglobin Single Mutant L29e Mb With Native His93 Coordination" . . . . . 100.00 154 99.17 99.17 3.74e-76 . . . . 16500 1 275 no PDB 4PQB . "A Sperm Whale Myoglobin Double Mutant L29e/f43h Mb With A Non-native Bis-his (his64/his93) Coordination" . . . . . 100.00 154 98.33 98.33 1.03e-74 . . . . 16500 1 276 no PDB 4PQC . "A Sperm Whale Myoglobin Single Mutant F43h Mb With Native His93 Coordination" . . . . . 100.00 154 99.17 99.17 8.29e-76 . . . . 16500 1 277 no PDB 4QAU . "Crystal Structure Of F43y Mutant Of Sperm Whale Myoglobin" . . . . . 100.00 154 99.17 100.00 7.78e-77 . . . . 16500 1 278 no PDB 5C6Y . "A Sperm Whale Myoglobin Double Mutant L29h/f43y Mb With A Tyr-heme Cross-link" . . . . . 100.00 154 98.33 99.17 1.45e-75 . . . . 16500 1 279 no PDB 5MBN . "Refinement Of Myoglobin And Cytochrome C" . . . . . 99.17 153 100.00 100.00 2.24e-76 . . . . 16500 1 280 no DBJ BAF03579 . "myoglobin [Physeter catodon]" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 281 no DBJ BAF03582 . "myoglobin [Kogia breviceps]" . . . . . 100.00 154 97.50 99.17 1.82e-75 . . . . 16500 1 282 no GB AAA72199 . "synthetic myoglobin [synthetic construct]" . . . . . 100.00 154 100.00 100.00 2.59e-77 . . . . 16500 1 283 no PRF 742482A . myoglobin . . . . . 99.17 153 100.00 100.00 1.94e-76 . . . . 16500 1 284 no REF NP_001277651 . "myoglobin [Physeter catodon]" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 285 no SP P02184 . "RecName: Full=Myoglobin" . . . . . 100.00 154 97.50 99.17 1.82e-75 . . . . 16500 1 286 no SP P02185 . "RecName: Full=Myoglobin" . . . . . 100.00 154 100.00 100.00 3.01e-77 . . . . 16500 1 287 no SP Q0KIY5 . "RecName: Full=Myoglobin" . . . . . 100.00 154 97.50 99.17 1.82e-75 . . . . 16500 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 0 MET . 16500 1 2 1 VAL . 16500 1 3 2 LEU . 16500 1 4 3 SER . 16500 1 5 4 GLU . 16500 1 6 5 GLY . 16500 1 7 6 GLU . 16500 1 8 7 TRP . 16500 1 9 8 GLN . 16500 1 10 9 LEU . 16500 1 11 10 VAL . 16500 1 12 11 LEU . 16500 1 13 12 HIS . 16500 1 14 13 VAL . 16500 1 15 14 TRP . 16500 1 16 15 ALA . 16500 1 17 16 LYS . 16500 1 18 17 VAL . 16500 1 19 18 GLU . 16500 1 20 19 ALA . 16500 1 21 20 ASP . 16500 1 22 21 VAL . 16500 1 23 22 ALA . 16500 1 24 23 GLY . 16500 1 25 24 HIS . 16500 1 26 25 GLY . 16500 1 27 26 GLN . 16500 1 28 27 ASP . 16500 1 29 28 ILE . 16500 1 30 29 LEU . 16500 1 31 30 ILE . 16500 1 32 31 ARG . 16500 1 33 32 LEU . 16500 1 34 33 PHE . 16500 1 35 34 LYS . 16500 1 36 35 SER . 16500 1 37 36 HIS . 16500 1 38 37 PRO . 16500 1 39 38 GLU . 16500 1 40 39 THR . 16500 1 41 40 LEU . 16500 1 42 41 GLU . 16500 1 43 42 LYS . 16500 1 44 43 PHE . 16500 1 45 44 ASP . 16500 1 46 45 ARG . 16500 1 47 46 PHE . 16500 1 48 47 LYS . 16500 1 49 48 HIS . 16500 1 50 49 LEU . 16500 1 51 50 LYS . 16500 1 52 51 THR . 16500 1 53 52 GLU . 16500 1 54 53 ALA . 16500 1 55 54 GLU . 16500 1 56 55 MET . 16500 1 57 56 LYS . 16500 1 58 57 ALA . 16500 1 59 58 SER . 16500 1 60 59 GLU . 16500 1 61 60 ASP . 16500 1 62 61 LEU . 16500 1 63 62 LYS . 16500 1 64 63 LYS . 16500 1 65 64 HIS . 16500 1 66 65 GLY . 16500 1 67 66 VAL . 16500 1 68 67 THR . 16500 1 69 68 VAL . 16500 1 70 69 LEU . 16500 1 71 70 THR . 16500 1 72 71 ALA . 16500 1 73 72 LEU . 16500 1 74 73 GLY . 16500 1 75 74 ALA . 16500 1 76 75 ILE . 16500 1 77 76 LEU . 16500 1 78 77 LYS . 16500 1 79 78 LYS . 16500 1 80 79 LYS . 16500 1 81 80 GLY . 16500 1 82 81 HIS . 16500 1 83 82 HIS . 16500 1 84 83 GLU . 16500 1 85 84 ALA . 16500 1 86 85 GLU . 16500 1 87 86 LEU . 16500 1 88 87 LYS . 16500 1 89 88 PRO . 16500 1 90 89 LEU . 16500 1 91 90 ALA . 16500 1 92 91 GLN . 16500 1 93 92 SER . 16500 1 94 93 HIS . 16500 1 95 94 ALA . 16500 1 96 95 THR . 16500 1 97 96 LYS . 16500 1 98 97 HIS . 16500 1 99 98 LYS . 16500 1 100 99 ILE . 16500 1 101 100 PRO . 16500 1 102 101 ILE . 16500 1 103 102 LYS . 16500 1 104 103 TYR . 16500 1 105 104 LEU . 16500 1 106 105 GLU . 16500 1 107 106 PHE . 16500 1 108 107 ILE . 16500 1 109 108 SER . 16500 1 110 109 GLU . 16500 1 111 110 ALA . 16500 1 112 111 ILE . 16500 1 113 112 ILE . 16500 1 114 113 HIS . 16500 1 115 114 VAL . 16500 1 116 115 LEU . 16500 1 117 116 HIS . 16500 1 118 117 SER . 16500 1 119 118 ARG . 16500 1 120 119 HIS . 16500 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 16500 1 . VAL 2 2 16500 1 . LEU 3 3 16500 1 . SER 4 4 16500 1 . GLU 5 5 16500 1 . GLY 6 6 16500 1 . GLU 7 7 16500 1 . TRP 8 8 16500 1 . GLN 9 9 16500 1 . LEU 10 10 16500 1 . VAL 11 11 16500 1 . LEU 12 12 16500 1 . HIS 13 13 16500 1 . VAL 14 14 16500 1 . TRP 15 15 16500 1 . ALA 16 16 16500 1 . LYS 17 17 16500 1 . VAL 18 18 16500 1 . GLU 19 19 16500 1 . ALA 20 20 16500 1 . ASP 21 21 16500 1 . VAL 22 22 16500 1 . ALA 23 23 16500 1 . GLY 24 24 16500 1 . HIS 25 25 16500 1 . GLY 26 26 16500 1 . GLN 27 27 16500 1 . ASP 28 28 16500 1 . ILE 29 29 16500 1 . LEU 30 30 16500 1 . ILE 31 31 16500 1 . ARG 32 32 16500 1 . LEU 33 33 16500 1 . PHE 34 34 16500 1 . LYS 35 35 16500 1 . SER 36 36 16500 1 . HIS 37 37 16500 1 . PRO 38 38 16500 1 . GLU 39 39 16500 1 . THR 40 40 16500 1 . LEU 41 41 16500 1 . GLU 42 42 16500 1 . LYS 43 43 16500 1 . PHE 44 44 16500 1 . ASP 45 45 16500 1 . ARG 46 46 16500 1 . PHE 47 47 16500 1 . LYS 48 48 16500 1 . HIS 49 49 16500 1 . LEU 50 50 16500 1 . LYS 51 51 16500 1 . THR 52 52 16500 1 . GLU 53 53 16500 1 . ALA 54 54 16500 1 . GLU 55 55 16500 1 . MET 56 56 16500 1 . LYS 57 57 16500 1 . ALA 58 58 16500 1 . SER 59 59 16500 1 . GLU 60 60 16500 1 . ASP 61 61 16500 1 . LEU 62 62 16500 1 . LYS 63 63 16500 1 . LYS 64 64 16500 1 . HIS 65 65 16500 1 . GLY 66 66 16500 1 . VAL 67 67 16500 1 . THR 68 68 16500 1 . VAL 69 69 16500 1 . LEU 70 70 16500 1 . THR 71 71 16500 1 . ALA 72 72 16500 1 . LEU 73 73 16500 1 . GLY 74 74 16500 1 . ALA 75 75 16500 1 . ILE 76 76 16500 1 . LEU 77 77 16500 1 . LYS 78 78 16500 1 . LYS 79 79 16500 1 . LYS 80 80 16500 1 . GLY 81 81 16500 1 . HIS 82 82 16500 1 . HIS 83 83 16500 1 . GLU 84 84 16500 1 . ALA 85 85 16500 1 . GLU 86 86 16500 1 . LEU 87 87 16500 1 . LYS 88 88 16500 1 . PRO 89 89 16500 1 . LEU 90 90 16500 1 . ALA 91 91 16500 1 . GLN 92 92 16500 1 . SER 93 93 16500 1 . HIS 94 94 16500 1 . ALA 95 95 16500 1 . THR 96 96 16500 1 . LYS 97 97 16500 1 . HIS 98 98 16500 1 . LYS 99 99 16500 1 . ILE 100 100 16500 1 . PRO 101 101 16500 1 . ILE 102 102 16500 1 . LYS 103 103 16500 1 . TYR 104 104 16500 1 . LEU 105 105 16500 1 . GLU 106 106 16500 1 . PHE 107 107 16500 1 . ILE 108 108 16500 1 . SER 109 109 16500 1 . GLU 110 110 16500 1 . ALA 111 111 16500 1 . ILE 112 112 16500 1 . ILE 113 113 16500 1 . HIS 114 114 16500 1 . VAL 115 115 16500 1 . LEU 116 116 16500 1 . HIS 117 117 16500 1 . SER 118 118 16500 1 . ARG 119 119 16500 1 . HIS 120 120 16500 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 16500 _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 $1-119_Apomyoglobin . 9755 organism . 'Physeter catodon' 'Sperm Whale' . . Eukaryota Metazoa Physeter catodon . . . . . . . . . . . . . . . . . . . . . 16500 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 16500 _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 $1-119_Apomyoglobin . 'recombinant technology' 'Escherichia coli' 'E. coli' . 562 Escherichia coli BL21-DE3 . . . . . . . . . . . . . . . pET-17b . . . . . . 16500 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID 16500 _Sample.ID 1 _Sample.Type solution _Sample.Sub_type . _Sample.Details '5 mM CD3COOH in H2O, pH 2.40, 5% D2O' _Sample.Aggregate_sample_number . _Sample.Solvent_system '95% H2O/5% D2O' _Sample.Preparation_date . _Sample.Preparation_expiration_date . _Sample.Polycrystallization_protocol . _Sample.Single_crystal_protocol . _Sample.Crystal_grow_apparatus . _Sample.Crystal_grow_atmosphere . _Sample.Crystal_grow_details . _Sample.Crystal_grow_method . _Sample.Crystal_grow_method_cit_ID . _Sample.Crystal_grow_pH . _Sample.Crystal_grow_pH_range . _Sample.Crystal_grow_pressure . _Sample.Crystal_grow_pressure_esd . _Sample.Crystal_grow_seeding . _Sample.Crystal_grow_seeding_cit_ID . _Sample.Crystal_grow_temp . _Sample.Crystal_grow_temp_details . _Sample.Crystal_grow_temp_esd . _Sample.Crystal_grow_time . _Sample.Oriented_sample_prep_protocol . _Sample.Lyophilization_cryo_protectant . _Sample.Storage_protocol . loop_ _Sample_component.ID _Sample_component.Mol_common_name _Sample_component.Isotopic_labeling _Sample_component.Assembly_ID _Sample_component.Assembly_label _Sample_component.Entity_ID _Sample_component.Entity_label _Sample_component.Product_ID _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_min _Sample_component.Concentration_val_max _Sample_component.Concentration_val_units _Sample_component.Concentration_val_err _Sample_component.Vendor _Sample_component.Vendor_product_name _Sample_component.Vendor_product_code _Sample_component.Entry_ID _Sample_component.Sample_ID 1 (1-119)Apomyoglobin '[U-99% 13C; U-99% 15N]' . . 1 $1-119_Apomyoglobin . . 280 . . uM . . . . 16500 1 2 CD3COOH 'natural abundance' . . . . . . 5 . . mM . . . . 16500 1 3 H2O 'natural abundance' . . . . . . 95 . . % . . . . 16500 1 4 D2O 'natural abundance' . . . . . . 5 . . % . . . . 16500 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 16500 _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 pH 2.40 . pH 16500 1 pressure 1 . atm 16500 1 temperature 298.15 . K 16500 1 stop_ save_ ############################ # Computer software used # ############################ save_SPARKY _Software.Sf_category software _Software.Sf_framecode SPARKY _Software.Entry_ID 16500 _Software.ID 1 _Software.Name SPARKY _Software.Version . _Software.Details . loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID Goddard . . 16500 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'chemical shift assignment' 16500 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 16500 _NMR_spectrometer.ID 1 _NMR_spectrometer.Details . _NMR_spectrometer.Manufacturer Varian _NMR_spectrometer.Model INOVA _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 600 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 16500 _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 Varian INOVA . 600 . . . 16500 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 16500 _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-15N HSQC' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 16500 1 2 '3D HNCA' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 16500 1 3 '3D HNCO' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 16500 1 4 '3D HNCACB' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 16500 1 5 '3D HN(CO)CA' no . . . . . . . . . . 1 $sample_1 isotropic . . 1 $sample_conditions_1 . . . 1 $spectrometer_1 . . . . . . . . . . . . . . . . 16500 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 16500 _Chem_shift_reference.ID 1 _Chem_shift_reference.Details 'external referencing to DSS' 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 C 13 DSS 'methyl carbon' . . . . ppm 0.0 external indirect 1 . . . . . . . . . 16500 1 H 1 DSS 'methyl protons' . . . . ppm 0.0 external direct 1 . . . . . . . . . 16500 1 N 15 DSS nitrogen . . . . ppm 0.0 external indirect 1 . . . . . . . . . 16500 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 16500 _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-15N HSQC' . . . 16500 1 2 '3D HNCA' . . . 16500 1 3 '3D HNCO' . . . 16500 1 4 '3D HNCACB' . . . 16500 1 5 '3D HN(CO)CA' . . . 16500 1 stop_ loop_ _Chem_shift_software.Software_ID _Chem_shift_software.Software_label _Chem_shift_software.Method_ID _Chem_shift_software.Method_label _Chem_shift_software.Entry_ID _Chem_shift_software.Assigned_chem_shift_list_ID 1 $SPARKY . . 16500 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 C C 13 178.527 . . 1 . . . . 0 M C . 16500 1 2 . 1 1 1 1 MET CA C 13 55.119 . . 1 . . . . 0 M C . 16500 1 3 . 1 1 2 2 VAL H H 1 8.608 . . 1 . . . . 1 V H . 16500 1 4 . 1 1 2 2 VAL C C 13 175.478 . . 1 . . . . 1 V C . 16500 1 5 . 1 1 2 2 VAL CA C 13 62.314 . . 1 . . . . 1 V CA . 16500 1 6 . 1 1 2 2 VAL CB C 13 32.984 . . 1 . . . . 1 V CB . 16500 1 7 . 1 1 2 2 VAL N N 15 123.76 . . 1 . . . . 1 V N . 16500 1 8 . 1 1 3 3 LEU H H 1 8.469 . . 1 . . . . 2 L H . 16500 1 9 . 1 1 3 3 LEU C C 13 177.072 . . 1 . . . . 2 L C . 16500 1 10 . 1 1 3 3 LEU CA C 13 54.969 . . 1 . . . . 2 L CA . 16500 1 11 . 1 1 3 3 LEU CB C 13 42.638 . . 1 . . . . 2 L CB . 16500 1 12 . 1 1 3 3 LEU N N 15 127.166 . . 1 . . . . 2 L N . 16500 1 13 . 1 1 4 4 SER H H 1 8.283 . . 1 . . . . 3 S H . 16500 1 14 . 1 1 4 4 SER C C 13 174.574 . . 1 . . . . 3 S C . 16500 1 15 . 1 1 4 4 SER CA C 13 58.032 . . 1 . . . . 3 S CA . 16500 1 16 . 1 1 4 4 SER CB C 13 63.923 . . 1 . . . . 3 S CB . 16500 1 17 . 1 1 4 4 SER N N 15 117.094 . . 1 . . . . 3 S N . 16500 1 18 . 1 1 5 5 GLU H H 1 8.512 . . 1 . . . . 4 E H . 16500 1 19 . 1 1 5 5 GLU C C 13 176.801 . . 1 . . . . 4 E C . 16500 1 20 . 1 1 5 5 GLU CA C 13 56.67 . . 1 . . . . 4 E CA . 16500 1 21 . 1 1 5 5 GLU CB C 13 28.631 . . 1 . . . . 4 E CB . 16500 1 22 . 1 1 5 5 GLU N N 15 122.172 . . 1 . . . . 4 E N . 16500 1 23 . 1 1 6 6 GLY H H 1 8.435 . . 1 . . . . 5 G H . 16500 1 24 . 1 1 6 6 GLY C C 13 174.659 . . 1 . . . . 5 G C . 16500 1 25 . 1 1 6 6 GLY CA C 13 45.789 . . 1 . . . . 5 G CA . 16500 1 26 . 1 1 6 6 GLY N N 15 108.837 . . 1 . . . . 5 G N . 16500 1 27 . 1 1 7 7 GLU H H 1 8.115 . . 1 . . . . 6 E H . 16500 1 28 . 1 1 7 7 GLU C C 13 176.527 . . 1 . . . . 6 E C . 16500 1 29 . 1 1 7 7 GLU CA C 13 56.644 . . 1 . . . . 6 E CA . 16500 1 30 . 1 1 7 7 GLU CB C 13 28.698 . . 1 . . . . 6 E CB . 16500 1 31 . 1 1 7 7 GLU N N 15 120.223 . . 1 . . . . 6 E N . 16500 1 32 . 1 1 8 8 TRP H H 1 8.185 . . 1 . . . . 7 W H . 16500 1 33 . 1 1 8 8 TRP C C 13 176.57 . . 1 . . . . 7 W C . 16500 1 34 . 1 1 8 8 TRP CA C 13 58.043 . . 1 . . . . 7 W CA . 16500 1 35 . 1 1 8 8 TRP CB C 13 29.464 . . 1 . . . . 7 W CB . 16500 1 36 . 1 1 8 8 TRP N N 15 121.087 . . 1 . . . . 7 W N . 16500 1 37 . 1 1 9 9 GLN H H 1 8.101 . . 1 . . . . 8 Q H . 16500 1 38 . 1 1 9 9 GLN C C 13 176.138 . . 1 . . . . 8 Q C . 16500 1 39 . 1 1 9 9 GLN CA C 13 56.71 . . 1 . . . . 8 Q CA . 16500 1 40 . 1 1 9 9 GLN CB C 13 29.276 . . 1 . . . . 8 Q CB . 16500 1 41 . 1 1 9 9 GLN N N 15 119.752 . . 1 . . . . 8 Q N . 16500 1 42 . 1 1 10 10 LEU H H 1 7.879 . . 1 . . . . 9 L H . 16500 1 43 . 1 1 10 10 LEU C C 13 177.596 . . 1 . . . . 9 L C . 16500 1 44 . 1 1 10 10 LEU CA C 13 56.098 . . 1 . . . . 9 L CA . 16500 1 45 . 1 1 10 10 LEU CB C 13 42.306 . . 1 . . . . 9 L CB . 16500 1 46 . 1 1 10 10 LEU N N 15 121.838 . . 1 . . . . 9 L N . 16500 1 47 . 1 1 11 11 VAL H H 1 7.947 . . 1 . . . . 10 V H . 16500 1 48 . 1 1 11 11 VAL C C 13 176.184 . . 1 . . . . 10 V C . 16500 1 49 . 1 1 11 11 VAL CA C 13 63.006 . . 1 . . . . 10 V CA . 16500 1 50 . 1 1 11 11 VAL N N 15 120.742 . . 1 . . . . 10 V N . 16500 1 51 . 1 1 12 12 LEU H H 1 8.118 . . 1 . . . . 11 L H . 16500 1 52 . 1 1 12 12 LEU C C 13 177.261 . . 1 . . . . 11 L C . 16500 1 53 . 1 1 12 12 LEU CA C 13 55.584 . . 1 . . . . 11 L CA . 16500 1 54 . 1 1 12 12 LEU CB C 13 42.233 . . 1 . . . . 11 L CB . 16500 1 55 . 1 1 12 12 LEU N N 15 123.811 . . 1 . . . . 11 L N . 16500 1 56 . 1 1 13 13 HIS H H 1 8.265 . . 1 . . . . 12 H H . 16500 1 57 . 1 1 13 13 HIS C C 13 174.393 . . 1 . . . . 12 H C . 16500 1 58 . 1 1 13 13 HIS CA C 13 55.657 . . 1 . . . . 12 H CA . 16500 1 59 . 1 1 13 13 HIS CB C 13 28.647 . . 1 . . . . 12 H CB . 16500 1 60 . 1 1 13 13 HIS N N 15 117.859 . . 1 . . . . 12 H N . 16500 1 61 . 1 1 14 14 VAL H H 1 7.996 . . 1 . . . . 13 V H . 16500 1 62 . 1 1 14 14 VAL C C 13 175.856 . . 1 . . . . 13 V C . 16500 1 63 . 1 1 14 14 VAL CA C 13 62.769 . . 1 . . . . 13 V CA . 16500 1 64 . 1 1 14 14 VAL CB C 13 33.007 . . 1 . . . . 13 V CB . 16500 1 65 . 1 1 14 14 VAL N N 15 120.798 . . 1 . . . . 13 V N . 16500 1 66 . 1 1 15 15 TRP H H 1 8.259 . . 1 . . . . 14 W H . 16500 1 67 . 1 1 15 15 TRP CA C 13 57.445 . . 1 . . . . 14 W CA . 16500 1 68 . 1 1 15 15 TRP CB C 13 29.749 . . 1 . . . . 14 W CB . 16500 1 69 . 1 1 15 15 TRP N N 15 124.37 . . 1 . . . . 14 W N . 16500 1 70 . 1 1 16 16 ALA C C 13 177.366 . . 1 . . . . 15 A C . 16500 1 71 . 1 1 16 16 ALA CA C 13 52.628 . . 1 . . . . 15 A CA . 16500 1 72 . 1 1 16 16 ALA CB C 13 19.878 . . 1 . . . . 15 A CB . 16500 1 73 . 1 1 17 17 LYS H H 1 8.051 . . 1 . . . . 16 K H . 16500 1 74 . 1 1 17 17 LYS C C 13 176.77 . . 1 . . . . 16 K C . 16500 1 75 . 1 1 17 17 LYS CA C 13 56.726 . . 1 . . . . 16 K CA . 16500 1 76 . 1 1 17 17 LYS CB C 13 32.92 . . 1 . . . . 16 K CB . 16500 1 77 . 1 1 17 17 LYS N N 15 120.318 . . 1 . . . . 16 K N . 16500 1 78 . 1 1 18 18 VAL H H 1 8.069 . . 1 . . . . 17 V H . 16500 1 79 . 1 1 18 18 VAL C C 13 176.357 . . 1 . . . . 17 V C . 16500 1 80 . 1 1 18 18 VAL CA C 13 62.583 . . 1 . . . . 17 V CA . 16500 1 81 . 1 1 18 18 VAL CB C 13 32.895 . . 1 . . . . 17 V CB . 16500 1 82 . 1 1 18 18 VAL N N 15 121.219 . . 1 . . . . 17 V N . 16500 1 83 . 1 1 19 19 GLU H H 1 8.359 . . 1 . . . . 18 E H . 16500 1 84 . 1 1 19 19 GLU CA C 13 55.9 . . 1 . . . . 18 E CA . 16500 1 85 . 1 1 19 19 GLU CB C 13 28.846 . . 1 . . . . 18 E CB . 16500 1 86 . 1 1 19 19 GLU N N 15 123.665 . . 1 . . . . 18 E N . 16500 1 87 . 1 1 20 20 ALA C C 13 177.511 . . 1 . . . . 19 A C . 16500 1 88 . 1 1 20 20 ALA CA C 13 52.817 . . 1 . . . . 19 A CA . 16500 1 89 . 1 1 20 20 ALA CB C 13 19.411 . . 1 . . . . 19 A CB . 16500 1 90 . 1 1 21 21 ASP H H 1 8.351 . . 1 . . . . 20 D H . 16500 1 91 . 1 1 21 21 ASP C C 13 175.328 . . 1 . . . . 20 D C . 16500 1 92 . 1 1 21 21 ASP CA C 13 53.124 . . 1 . . . . 20 D CA . 16500 1 93 . 1 1 21 21 ASP CB C 13 38.153 . . 1 . . . . 20 D CB . 16500 1 94 . 1 1 21 21 ASP N N 15 117.807 . . 1 . . . . 20 D N . 16500 1 95 . 1 1 22 22 VAL H H 1 8.007 . . 1 . . . . 21 V H . 16500 1 96 . 1 1 22 22 VAL C C 13 176.033 . . 1 . . . . 21 V C . 16500 1 97 . 1 1 22 22 VAL CA C 13 62.456 . . 1 . . . . 21 V CA . 16500 1 98 . 1 1 22 22 VAL CB C 13 32.754 . . 1 . . . . 21 V CB . 16500 1 99 . 1 1 22 22 VAL N N 15 120.267 . . 1 . . . . 21 V N . 16500 1 100 . 1 1 23 23 ALA H H 1 8.32 . . 1 . . . . 22 A H . 16500 1 101 . 1 1 23 23 ALA C C 13 178.249 . . 1 . . . . 22 A C . 16500 1 102 . 1 1 23 23 ALA CA C 13 52.882 . . 1 . . . . 22 A CA . 16500 1 103 . 1 1 23 23 ALA CB C 13 19.127 . . 1 . . . . 22 A CB . 16500 1 104 . 1 1 23 23 ALA N N 15 126.909 . . 1 . . . . 22 A N . 16500 1 105 . 1 1 24 24 GLY H H 1 8.283 . . 1 . . . . 23 G H . 16500 1 106 . 1 1 24 24 GLY C C 13 174.243 . . 1 . . . . 23 G C . 16500 1 107 . 1 1 24 24 GLY CA C 13 45.527 . . 1 . . . . 23 G CA . 16500 1 108 . 1 1 24 24 GLY N N 15 107.736 . . 1 . . . . 23 G N . 16500 1 109 . 1 1 25 25 HIS H H 1 8.374 . . 1 . . . . 24 H H . 16500 1 110 . 1 1 25 25 HIS C C 13 175.016 . . 1 . . . . 24 H C . 16500 1 111 . 1 1 25 25 HIS CA C 13 55.414 . . 1 . . . . 24 H CA . 16500 1 112 . 1 1 25 25 HIS CB C 13 28.992 . . 1 . . . . 24 H CB . 16500 1 113 . 1 1 25 25 HIS N N 15 117.696 . . 1 . . . . 24 H N . 16500 1 114 . 1 1 26 26 GLY H H 1 8.543 . . 1 . . . . 25 G H . 16500 1 115 . 1 1 26 26 GLY C C 13 174.177 . . 1 . . . . 25 G C . 16500 1 116 . 1 1 26 26 GLY CA C 13 45.689 . . 1 . . . . 25 G CA . 16500 1 117 . 1 1 26 26 GLY N N 15 109.752 . . 1 . . . . 25 G N . 16500 1 118 . 1 1 27 27 GLN H H 1 8.338 . . 1 . . . . 26 Q H . 16500 1 119 . 1 1 27 27 GLN C C 13 175.893 . . 1 . . . . 26 Q C . 16500 1 120 . 1 1 27 27 GLN CA C 13 56.171 . . 1 . . . . 26 Q CA . 16500 1 121 . 1 1 27 27 GLN CB C 13 29.613 . . 1 . . . . 26 Q CB . 16500 1 122 . 1 1 27 27 GLN N N 15 119.752 . . 1 . . . . 26 Q N . 16500 1 123 . 1 1 28 28 ASP H H 1 8.55 . . 1 . . . . 27 D H . 16500 1 124 . 1 1 28 28 ASP C C 13 175.247 . . 1 . . . . 27 D C . 16500 1 125 . 1 1 28 28 ASP CA C 13 53.449 . . 1 . . . . 27 D CA . 16500 1 126 . 1 1 28 28 ASP CB C 13 38.198 . . 1 . . . . 27 D CB . 16500 1 127 . 1 1 28 28 ASP N N 15 120.211 . . 1 . . . . 27 D N . 16500 1 128 . 1 1 29 29 ILE H H 1 8.065 . . 1 . . . . 28 I H . 16500 1 129 . 1 1 29 29 ILE C C 13 176.017 . . 1 . . . . 28 I C . 16500 1 130 . 1 1 29 29 ILE CA C 13 61.585 . . 1 . . . . 28 I CA . 16500 1 131 . 1 1 29 29 ILE CB C 13 38.481 . . 1 . . . . 28 I CB . 16500 1 132 . 1 1 29 29 ILE N N 15 121.146 . . 1 . . . . 28 I N . 16500 1 133 . 1 1 30 30 LEU H H 1 8.134 . . 1 . . . . 29 L H . 16500 1 134 . 1 1 30 30 LEU C C 13 177.201 . . 1 . . . . 29 L C . 16500 1 135 . 1 1 30 30 LEU CA C 13 55.571 . . 1 . . . . 29 L CA . 16500 1 136 . 1 1 30 30 LEU CB C 13 42.167 . . 1 . . . . 29 L CB . 16500 1 137 . 1 1 30 30 LEU N N 15 125.229 . . 1 . . . . 29 L N . 16500 1 138 . 1 1 31 31 ILE H H 1 8.019 . . 1 . . . . 30 I H . 16500 1 139 . 1 1 31 31 ILE C C 13 176.232 . . 1 . . . . 30 I C . 16500 1 140 . 1 1 31 31 ILE CA C 13 61.47 . . 1 . . . . 30 I CA . 16500 1 141 . 1 1 31 31 ILE CB C 13 38.587 . . 1 . . . . 30 I CB . 16500 1 142 . 1 1 31 31 ILE N N 15 121.788 . . 1 . . . . 30 I N . 16500 1 143 . 1 1 32 32 ARG H H 1 8.198 . . 1 . . . . 31 R H . 16500 1 144 . 1 1 32 32 ARG C C 13 176.045 . . 1 . . . . 31 R C . 16500 1 145 . 1 1 32 32 ARG CA C 13 56.356 . . 1 . . . . 31 R CA . 16500 1 146 . 1 1 32 32 ARG N N 15 124.271 . . 1 . . . . 31 R N . 16500 1 147 . 1 1 33 33 LEU H H 1 8.103 . . 1 . . . . 32 L H . 16500 1 148 . 1 1 33 33 LEU C C 13 177.033 . . 1 . . . . 32 L C . 16500 1 149 . 1 1 33 33 LEU CA C 13 55.243 . . 1 . . . . 32 L CA . 16500 1 150 . 1 1 33 33 LEU CB C 13 42.528 . . 1 . . . . 32 L CB . 16500 1 151 . 1 1 33 33 LEU N N 15 122.972 . . 1 . . . . 32 L N . 16500 1 152 . 1 1 34 34 PHE H H 1 8.219 . . 1 . . . . 33 F H . 16500 1 153 . 1 1 34 34 PHE C C 13 175.667 . . 1 . . . . 33 F C . 16500 1 154 . 1 1 34 34 PHE CA C 13 57.751 . . 1 . . . . 33 F CA . 16500 1 155 . 1 1 34 34 PHE CB C 13 39.625 . . 1 . . . . 33 F CB . 16500 1 156 . 1 1 34 34 PHE N N 15 121.003 . . 1 . . . . 33 F N . 16500 1 157 . 1 1 35 35 LYS H H 1 8.187 . . 1 . . . . 34 K H . 16500 1 158 . 1 1 35 35 LYS C C 13 176.169 . . 1 . . . . 34 K C . 16500 1 159 . 1 1 35 35 LYS CA C 13 56.285 . . 1 . . . . 34 K CA . 16500 1 160 . 1 1 35 35 LYS CB C 13 33.154 . . 1 . . . . 34 K CB . 16500 1 161 . 1 1 35 35 LYS N N 15 122.75 . . 1 . . . . 34 K N . 16500 1 162 . 1 1 36 36 SER H H 1 8.168 . . 1 . . . . 35 S H . 16500 1 163 . 1 1 36 36 SER C C 13 173.861 . . 1 . . . . 35 S C . 16500 1 164 . 1 1 36 36 SER CA C 13 58.304 . . 1 . . . . 35 S CA . 16500 1 165 . 1 1 36 36 SER CB C 13 63.91 . . 1 . . . . 35 S CB . 16500 1 166 . 1 1 36 36 SER N N 15 116.485 . . 1 . . . . 35 S N . 16500 1 167 . 1 1 37 37 HIS H H 1 8.484 . . 1 . . . . 36 H H . 16500 1 168 . 1 1 37 37 HIS CA C 13 53.48 . . 1 . . . . 36 H CA . 16500 1 169 . 1 1 37 37 HIS CB C 13 28.78 . . 1 . . . . 36 H CB . 16500 1 170 . 1 1 37 37 HIS N N 15 120.219 . . 1 . . . . 36 H N . 16500 1 171 . 1 1 38 38 PRO C C 13 177.06 . . 1 . . . . 37 P C . 16500 1 172 . 1 1 38 38 PRO CA C 13 63.408 . . 1 . . . . 37 P CA . 16500 1 173 . 1 1 38 38 PRO CB C 13 32.118 . . 1 . . . . 37 P CB . 16500 1 174 . 1 1 39 39 GLU H H 1 8.626 . . 1 . . . . 38 E H . 16500 1 175 . 1 1 39 39 GLU C C 13 176.352 . . 1 . . . . 38 E C . 16500 1 176 . 1 1 39 39 GLU CA C 13 56.065 . . 1 . . . . 38 E CA . 16500 1 177 . 1 1 39 39 GLU CB C 13 28.981 . . 1 . . . . 38 E CB . 16500 1 178 . 1 1 39 39 GLU N N 15 121.158 . . 1 . . . . 38 E N . 16500 1 179 . 1 1 40 40 THR H H 1 8.247 . . 1 . . . . 39 T H . 16500 1 180 . 1 1 40 40 THR C C 13 174.401 . . 1 . . . . 39 T C . 16500 1 181 . 1 1 40 40 THR CA C 13 62.209 . . 1 . . . . 39 T CA . 16500 1 182 . 1 1 40 40 THR CB C 13 69.745 . . 1 . . . . 39 T CB . 16500 1 183 . 1 1 40 40 THR N N 15 116.417 . . 1 . . . . 39 T N . 16500 1 184 . 1 1 41 41 LEU H H 1 8.269 . . 1 . . . . 40 L H . 16500 1 185 . 1 1 41 41 LEU C C 13 177.28 . . 1 . . . . 40 L C . 16500 1 186 . 1 1 41 41 LEU CA C 13 55.438 . . 1 . . . . 40 L CA . 16500 1 187 . 1 1 41 41 LEU CB C 13 42.369 . . 1 . . . . 40 L CB . 16500 1 188 . 1 1 41 41 LEU N N 15 124.871 . . 1 . . . . 40 L N . 16500 1 189 . 1 1 42 42 GLU H H 1 8.297 . . 1 . . . . 41 E H . 16500 1 190 . 1 1 42 42 GLU C C 13 176.134 . . 1 . . . . 41 E C . 16500 1 191 . 1 1 42 42 GLU CA C 13 56.16 . . 1 . . . . 41 E CA . 16500 1 192 . 1 1 42 42 GLU CB C 13 28.84 . . 1 . . . . 41 E CB . 16500 1 193 . 1 1 42 42 GLU N N 15 121.411 . . 1 . . . . 41 E N . 16500 1 194 . 1 1 43 43 LYS H H 1 8.221 . . 1 . . . . 42 K H . 16500 1 195 . 1 1 43 43 LYS C C 13 176.378 . . 1 . . . . 42 K C . 16500 1 196 . 1 1 43 43 LYS CA C 13 56.733 . . 1 . . . . 42 K CA . 16500 1 197 . 1 1 43 43 LYS CB C 13 32.983 . . 1 . . . . 42 K CB . 16500 1 198 . 1 1 43 43 LYS N N 15 122.069 . . 1 . . . . 42 K N . 16500 1 199 . 1 1 44 44 PHE H H 1 8.172 . . 1 . . . . 43 F H . 16500 1 200 . 1 1 44 44 PHE C C 13 175.532 . . 1 . . . . 43 F C . 16500 1 201 . 1 1 44 44 PHE CA C 13 57.893 . . 1 . . . . 43 F CA . 16500 1 202 . 1 1 44 44 PHE CB C 13 39.654 . . 1 . . . . 43 F CB . 16500 1 203 . 1 1 44 44 PHE N N 15 120.75 . . 1 . . . . 43 F N . 16500 1 204 . 1 1 45 45 ASP H H 1 8.37 . . 1 . . . . 44 D H . 16500 1 205 . 1 1 45 45 ASP C C 13 175.483 . . 1 . . . . 44 D C . 16500 1 206 . 1 1 45 45 ASP CA C 13 53.202 . . 1 . . . . 44 D CA . 16500 1 207 . 1 1 45 45 ASP CB C 13 38.75 . . 1 . . . . 44 D CB . 16500 1 208 . 1 1 45 45 ASP N N 15 121.261 . . 1 . . . . 44 D N . 16500 1 209 . 1 1 46 46 ARG H H 1 8.149 . . 1 . . . . 45 R H . 16500 1 210 . 1 1 46 46 ARG C C 13 176.225 . . 1 . . . . 45 R C . 16500 1 211 . 1 1 46 46 ARG CA C 13 57.009 . . 1 . . . . 45 R CA . 16500 1 212 . 1 1 46 46 ARG CB C 13 30.423 . . 1 . . . . 45 R CB . 16500 1 213 . 1 1 46 46 ARG N N 15 121.93 . . 1 . . . . 45 R N . 16500 1 214 . 1 1 47 47 PHE H H 1 7.994 . . 1 . . . . 46 F H . 16500 1 215 . 1 1 47 47 PHE C C 13 175.797 . . 1 . . . . 46 F C . 16500 1 216 . 1 1 47 47 PHE CA C 13 57.813 . . 1 . . . . 46 F CA . 16500 1 217 . 1 1 47 47 PHE CB C 13 39.178 . . 1 . . . . 46 F CB . 16500 1 218 . 1 1 47 47 PHE N N 15 119.384 . . 1 . . . . 46 F N . 16500 1 219 . 1 1 48 48 LYS H H 1 7.98 . . 1 . . . . 47 K H . 16500 1 220 . 1 1 48 48 LYS C C 13 176.216 . . 1 . . . . 47 K C . 16500 1 221 . 1 1 48 48 LYS CA C 13 56.642 . . 1 . . . . 47 K CA . 16500 1 222 . 1 1 48 48 LYS CB C 13 33.101 . . 1 . . . . 47 K CB . 16500 1 223 . 1 1 48 48 LYS N N 15 121.53 . . 1 . . . . 47 K N . 16500 1 224 . 1 1 49 49 HIS H H 1 8.444 . . 1 . . . . 48 H H . 16500 1 225 . 1 1 49 49 HIS C C 13 174.326 . . 1 . . . . 48 H C . 16500 1 226 . 1 1 49 49 HIS CA C 13 55.309 . . 1 . . . . 48 H CA . 16500 1 227 . 1 1 49 49 HIS CB C 13 28.851 . . 1 . . . . 48 H CB . 16500 1 228 . 1 1 49 49 HIS N N 15 119.459 . . 1 . . . . 48 H N . 16500 1 229 . 1 1 50 50 LEU H H 1 8.275 . . 1 . . . . 49 L H . 16500 1 230 . 1 1 50 50 LEU C C 13 177.414 . . 1 . . . . 49 L C . 16500 1 231 . 1 1 50 50 LEU CA C 13 55.381 . . 1 . . . . 49 L CA . 16500 1 232 . 1 1 50 50 LEU CB C 13 42.597 . . 1 . . . . 49 L CB . 16500 1 233 . 1 1 50 50 LEU N N 15 123.792 . . 1 . . . . 49 L N . 16500 1 234 . 1 1 51 51 LYS H H 1 8.402 . . 1 . . . . 50 K H . 16500 1 235 . 1 1 51 51 LYS C C 13 176.861 . . 1 . . . . 50 K C . 16500 1 236 . 1 1 51 51 LYS CA C 13 56.67 . . 1 . . . . 50 K CA . 16500 1 237 . 1 1 51 51 LYS CB C 13 33.214 . . 1 . . . . 50 K CB . 16500 1 238 . 1 1 51 51 LYS N N 15 122.611 . . 1 . . . . 50 K N . 16500 1 239 . 1 1 52 52 THR H H 1 8.076 . . 1 . . . . 51 T H . 16500 1 240 . 1 1 52 52 THR C C 13 174.887 . . 1 . . . . 51 T C . 16500 1 241 . 1 1 52 52 THR CA C 13 61.851 . . 1 . . . . 51 T CA . 16500 1 242 . 1 1 52 52 THR CB C 13 70.027 . . 1 . . . . 51 T CB . 16500 1 243 . 1 1 52 52 THR N N 15 115.158 . . 1 . . . . 51 T N . 16500 1 244 . 1 1 53 53 GLU H H 1 8.501 . . 1 . . . . 52 E H . 16500 1 245 . 1 1 53 53 GLU C C 13 176.595 . . 1 . . . . 52 E C . 16500 1 246 . 1 1 53 53 GLU CA C 13 56.9 . . 1 . . . . 52 E CA . 16500 1 247 . 1 1 53 53 GLU CB C 13 28.661 . . 1 . . . . 52 E CB . 16500 1 248 . 1 1 53 53 GLU N N 15 122.473 . . 1 . . . . 52 E N . 16500 1 249 . 1 1 54 54 ALA H H 1 8.344 . . 1 . . . . 53 A H . 16500 1 250 . 1 1 54 54 ALA C C 13 178.662 . . 1 . . . . 53 A C . 16500 1 251 . 1 1 54 54 ALA CA C 13 53.511 . . 1 . . . . 53 A CA . 16500 1 252 . 1 1 54 54 ALA CB C 13 18.939 . . 1 . . . . 53 A CB . 16500 1 253 . 1 1 54 54 ALA N N 15 124.067 . . 1 . . . . 53 A N . 16500 1 254 . 1 1 55 55 GLU H H 1 8.145 . . 1 . . . . 54 E H . 16500 1 255 . 1 1 55 55 GLU C C 13 177.023 . . 1 . . . . 54 E C . 16500 1 256 . 1 1 55 55 GLU CA C 13 56.533 . . 1 . . . . 54 E CA . 16500 1 257 . 1 1 55 55 GLU CB C 13 28.767 . . 1 . . . . 54 E CB . 16500 1 258 . 1 1 55 55 GLU N N 15 119.095 . . 1 . . . . 54 E N . 16500 1 259 . 1 1 56 56 MET H H 1 8.336 . . 1 . . . . 55 M H . 16500 1 260 . 1 1 56 56 MET C C 13 176.907 . . 1 . . . . 55 M C . 16500 1 261 . 1 1 56 56 MET CA C 13 56.441 . . 1 . . . . 55 M CA . 16500 1 262 . 1 1 56 56 MET CB C 13 32.764 . . 1 . . . . 55 M CB . 16500 1 263 . 1 1 56 56 MET N N 15 121.625 . . 1 . . . . 55 M N . 16500 1 264 . 1 1 57 57 LYS H H 1 8.265 . . 1 . . . . 56 K H . 16500 1 265 . 1 1 57 57 LYS C C 13 176.935 . . 1 . . . . 56 K C . 16500 1 266 . 1 1 57 57 LYS CA C 13 57.079 . . 1 . . . . 56 K CA . 16500 1 267 . 1 1 57 57 LYS CB C 13 32.88 . . 1 . . . . 56 K CB . 16500 1 268 . 1 1 57 57 LYS N N 15 122.239 . . 1 . . . . 56 K N . 16500 1 269 . 1 1 58 58 ALA H H 1 8.22 . . 1 . . . . 57 A H . 16500 1 270 . 1 1 58 58 ALA C C 13 178.461 . . 1 . . . . 57 A C . 16500 1 271 . 1 1 58 58 ALA CA C 13 53.22 . . 1 . . . . 57 A CA . 16500 1 272 . 1 1 58 58 ALA CB C 13 19.178 . . 1 . . . . 57 A CB . 16500 1 273 . 1 1 58 58 ALA N N 15 124.4 . . 1 . . . . 57 A N . 16500 1 274 . 1 1 59 59 SER H H 1 8.182 . . 1 . . . . 58 S H . 16500 1 275 . 1 1 59 59 SER C C 13 175.143 . . 1 . . . . 58 S C . 16500 1 276 . 1 1 59 59 SER CA C 13 59.051 . . 1 . . . . 58 S CA . 16500 1 277 . 1 1 59 59 SER CB C 13 63.676 . . 1 . . . . 58 S CB . 16500 1 278 . 1 1 59 59 SER N N 15 114.488 . . 1 . . . . 58 S N . 16500 1 279 . 1 1 60 60 GLU H H 1 8.223 . . 1 . . . . 59 E H . 16500 1 280 . 1 1 60 60 GLU C C 13 176.11 . . 1 . . . . 59 E C . 16500 1 281 . 1 1 60 60 GLU CA C 13 56.371 . . 1 . . . . 59 E CA . 16500 1 282 . 1 1 60 60 GLU CB C 13 28.772 . . 1 . . . . 59 E CB . 16500 1 283 . 1 1 60 60 GLU N N 15 121.716 . . 1 . . . . 59 E N . 16500 1 284 . 1 1 61 61 ASP H H 1 8.372 . . 1 . . . . 60 D H . 16500 1 285 . 1 1 61 61 ASP C C 13 175.375 . . 1 . . . . 60 D C . 16500 1 286 . 1 1 61 61 ASP CA C 13 53.437 . . 1 . . . . 60 D CA . 16500 1 287 . 1 1 61 61 ASP CB C 13 38.331 . . 1 . . . . 60 D CB . 16500 1 288 . 1 1 61 61 ASP N N 15 119.661 . . 1 . . . . 60 D N . 16500 1 289 . 1 1 62 62 LEU H H 1 8.101 . . 1 . . . . 61 L H . 16500 1 290 . 1 1 62 62 LEU C C 13 177.505 . . 1 . . . . 61 L C . 16500 1 291 . 1 1 62 62 LEU CA C 13 55.622 . . 1 . . . . 61 L CA . 16500 1 292 . 1 1 62 62 LEU CB C 13 42.308 . . 1 . . . . 61 L CB . 16500 1 293 . 1 1 62 62 LEU N N 15 122.659 . . 1 . . . . 61 L N . 16500 1 294 . 1 1 63 63 LYS H H 1 8.123 . . 1 . . . . 62 K H . 16500 1 295 . 1 1 63 63 LYS CA C 13 56.36 . . 1 . . . . 62 K CA . 16500 1 296 . 1 1 63 63 LYS CB C 13 32.893 . . 1 . . . . 62 K CB . 16500 1 297 . 1 1 63 63 LYS N N 15 121.34 . . 1 . . . . 62 K N . 16500 1 298 . 1 1 64 64 LYS C C 13 176.41 . . 1 . . . . 63 K C . 16500 1 299 . 1 1 64 64 LYS CA C 13 56.379 . . 1 . . . . 63 K CA . 16500 1 300 . 1 1 64 64 LYS CB C 13 38.709 . . 1 . . . . 63 K CB . 16500 1 301 . 1 1 65 65 HIS H H 1 8.529 . . 1 . . . . 64 H H . 16500 1 302 . 1 1 65 65 HIS C C 13 174.742 . . 1 . . . . 64 H C . 16500 1 303 . 1 1 65 65 HIS CA C 13 55.315 . . 1 . . . . 64 H CA . 16500 1 304 . 1 1 65 65 HIS CB C 13 29.314 . . 1 . . . . 64 H CB . 16500 1 305 . 1 1 65 65 HIS N N 15 119.712 . . 1 . . . . 64 H N . 16500 1 306 . 1 1 66 66 GLY H H 1 8.467 . . 1 . . . . 65 G H . 16500 1 307 . 1 1 66 66 GLY C C 13 173.79 . . 1 . . . . 65 G C . 16500 1 308 . 1 1 66 66 GLY CA C 13 45.34 . . 1 . . . . 65 G CA . 16500 1 309 . 1 1 66 66 GLY N N 15 110.524 . . 1 . . . . 65 G N . 16500 1 310 . 1 1 67 67 VAL H H 1 8.14 . . 1 . . . . 66 V H . 16500 1 311 . 1 1 67 67 VAL C C 13 176.373 . . 1 . . . . 66 V C . 16500 1 312 . 1 1 67 67 VAL CA C 13 62.162 . . 1 . . . . 66 V CA . 16500 1 313 . 1 1 67 67 VAL CB C 13 33.148 . . 1 . . . . 66 V CB . 16500 1 314 . 1 1 67 67 VAL N N 15 119.558 . . 1 . . . . 66 V N . 16500 1 315 . 1 1 68 68 THR H H 1 8.382 . . 1 . . . . 67 T H . 16500 1 316 . 1 1 68 68 THR C C 13 174.215 . . 1 . . . . 67 T C . 16500 1 317 . 1 1 68 68 THR CA C 13 62.209 . . 1 . . . . 67 T CA . 16500 1 318 . 1 1 68 68 THR CB C 13 69.878 . . 1 . . . . 67 T CB . 16500 1 319 . 1 1 68 68 THR N N 15 119.988 . . 1 . . . . 67 T N . 16500 1 320 . 1 1 69 69 VAL H H 1 8.314 . . 1 . . . . 68 V H . 16500 1 321 . 1 1 69 69 VAL C C 13 175.869 . . 1 . . . . 68 V C . 16500 1 322 . 1 1 69 69 VAL CA C 13 62.265 . . 1 . . . . 68 V CA . 16500 1 323 . 1 1 69 69 VAL CB C 13 32.981 . . 1 . . . . 68 V CB . 16500 1 324 . 1 1 69 69 VAL N N 15 124.398 . . 1 . . . . 68 V N . 16500 1 325 . 1 1 70 70 LEU H H 1 8.42 . . 1 . . . . 69 L H . 16500 1 326 . 1 1 70 70 LEU C C 13 177.495 . . 1 . . . . 69 L C . 16500 1 327 . 1 1 70 70 LEU CA C 13 55.218 . . 1 . . . . 69 L CA . 16500 1 328 . 1 1 70 70 LEU CB C 13 42.434 . . 1 . . . . 69 L CB . 16500 1 329 . 1 1 70 70 LEU N N 15 126.722 . . 1 . . . . 69 L N . 16500 1 330 . 1 1 71 71 THR H H 1 8.106 . . 1 . . . . 70 T H . 16500 1 331 . 1 1 71 71 THR C C 13 174.281 . . 1 . . . . 70 T C . 16500 1 332 . 1 1 71 71 THR CA C 13 61.926 . . 1 . . . . 70 T CA . 16500 1 333 . 1 1 71 71 THR CB C 13 69.85 . . 1 . . . . 70 T CB . 16500 1 334 . 1 1 71 71 THR N N 15 115.649 . . 1 . . . . 70 T N . 16500 1 335 . 1 1 72 72 ALA H H 1 8.347 . . 1 . . . . 71 A H . 16500 1 336 . 1 1 72 72 ALA C C 13 177.896 . . 1 . . . . 71 A C . 16500 1 337 . 1 1 72 72 ALA CA C 13 52.736 . . 1 . . . . 71 A CA . 16500 1 338 . 1 1 72 72 ALA CB C 13 19.14 . . 1 . . . . 71 A CB . 16500 1 339 . 1 1 72 72 ALA N N 15 126.604 . . 1 . . . . 71 A N . 16500 1 340 . 1 1 73 73 LEU H H 1 8.216 . . 1 . . . . 72 L H . 16500 1 341 . 1 1 73 73 LEU C C 13 178.227 . . 1 . . . . 72 L C . 16500 1 342 . 1 1 73 73 LEU CA C 13 55.803 . . 1 . . . . 72 L CA . 16500 1 343 . 1 1 73 73 LEU CB C 13 42.342 . . 1 . . . . 72 L CB . 16500 1 344 . 1 1 73 73 LEU N N 15 121.534 . . 1 . . . . 72 L N . 16500 1 345 . 1 1 74 74 GLY H H 1 8.344 . . 1 . . . . 73 G H . 16500 1 346 . 1 1 74 74 GLY C C 13 174.225 . . 1 . . . . 73 G C . 16500 1 347 . 1 1 74 74 GLY CA C 13 45.72 . . 1 . . . . 73 G CA . 16500 1 348 . 1 1 74 74 GLY N N 15 108.94 . . 1 . . . . 73 G N . 16500 1 349 . 1 1 75 75 ALA H H 1 8.041 . . 1 . . . . 74 A H . 16500 1 350 . 1 1 75 75 ALA C C 13 178.133 . . 1 . . . . 74 A C . 16500 1 351 . 1 1 75 75 ALA CA C 13 52.927 . . 1 . . . . 74 A CA . 16500 1 352 . 1 1 75 75 ALA CB C 13 19.238 . . 1 . . . . 74 A CB . 16500 1 353 . 1 1 75 75 ALA N N 15 123.534 . . 1 . . . . 74 A N . 16500 1 354 . 1 1 76 76 ILE H H 1 8.022 . . 1 . . . . 75 I H . 16500 1 355 . 1 1 76 76 ILE C C 13 176.62 . . 1 . . . . 75 I C . 16500 1 356 . 1 1 76 76 ILE CA C 13 61.6 . . 1 . . . . 75 I CA . 16500 1 357 . 1 1 76 76 ILE CB C 13 38.489 . . 1 . . . . 75 I CB . 16500 1 358 . 1 1 76 76 ILE N N 15 120.021 . . 1 . . . . 75 I N . 16500 1 359 . 1 1 77 77 LEU H H 1 8.214 . . 1 . . . . 76 L H . 16500 1 360 . 1 1 77 77 LEU C C 13 177.466 . . 1 . . . . 76 L C . 16500 1 361 . 1 1 77 77 LEU CA C 13 55.434 . . 1 . . . . 76 L CA . 16500 1 362 . 1 1 77 77 LEU CB C 13 42.242 . . 1 . . . . 76 L CB . 16500 1 363 . 1 1 77 77 LEU N N 15 125.641 . . 1 . . . . 76 L N . 16500 1 364 . 1 1 78 78 LYS H H 1 8.175 . . 1 . . . . 77 K H . 16500 1 365 . 1 1 78 78 LYS CA C 13 56.463 . . 1 . . . . 77 K CA . 16500 1 366 . 1 1 78 78 LYS N N 15 122.256 . . 1 . . . . 77 K N . 16500 1 367 . 1 1 79 79 LYS C C 13 176.68 . . 1 . . . . 78 K C . 16500 1 368 . 1 1 79 79 LYS CA C 13 56.459 . . 1 . . . . 78 K CA . 16500 1 369 . 1 1 80 80 LYS H H 1 8.341 . . 1 . . . . 79 K H . 16500 1 370 . 1 1 80 80 LYS C C 13 177.087 . . 1 . . . . 79 K C . 16500 1 371 . 1 1 80 80 LYS CA C 13 56.571 . . 1 . . . . 79 K CA . 16500 1 372 . 1 1 80 80 LYS CB C 13 33.266 . . 1 . . . . 79 K CB . 16500 1 373 . 1 1 80 80 LYS N N 15 122.794 . . 1 . . . . 79 K N . 16500 1 374 . 1 1 81 81 GLY H H 1 8.37 . . 1 . . . . 80 G H . 16500 1 375 . 1 1 81 81 GLY C C 13 173.568 . . 1 . . . . 80 G C . 16500 1 376 . 1 1 81 81 GLY CA C 13 45.24 . . 1 . . . . 80 G CA . 16500 1 377 . 1 1 81 81 GLY N N 15 109.736 . . 1 . . . . 80 G N . 16500 1 378 . 1 1 82 82 HIS H H 1 8.422 . . 1 . . . . 81 H H . 16500 1 379 . 1 1 82 82 HIS C C 13 174.108 . . 1 . . . . 81 H C . 16500 1 380 . 1 1 82 82 HIS CA C 13 55.171 . . 1 . . . . 81 H CA . 16500 1 381 . 1 1 82 82 HIS CB C 13 29.411 . . 1 . . . . 81 H CB . 16500 1 382 . 1 1 82 82 HIS N N 15 118.061 . . 1 . . . . 81 H N . 16500 1 383 . 1 1 83 83 HIS H H 1 8.679 . . 1 . . . . 82 H H . 16500 1 384 . 1 1 83 83 HIS C C 13 174.027 . . 1 . . . . 82 H C . 16500 1 385 . 1 1 83 83 HIS CA C 13 55.364 . . 1 . . . . 82 H CA . 16500 1 386 . 1 1 83 83 HIS CB C 13 29.277 . . 1 . . . . 82 H CB . 16500 1 387 . 1 1 83 83 HIS N N 15 121.043 . . 1 . . . . 82 H N . 16500 1 388 . 1 1 84 84 GLU H H 1 8.52 . . 1 . . . . 83 E H . 16500 1 389 . 1 1 84 84 GLU C C 13 175.362 . . 1 . . . . 83 E C . 16500 1 390 . 1 1 84 84 GLU CA C 13 55.635 . . 1 . . . . 83 E CA . 16500 1 391 . 1 1 84 84 GLU CB C 13 29.295 . . 1 . . . . 83 E CB . 16500 1 392 . 1 1 84 84 GLU N N 15 123.225 . . 1 . . . . 83 E N . 16500 1 393 . 1 1 85 85 ALA H H 1 8.458 . . 1 . . . . 84 A H . 16500 1 394 . 1 1 85 85 ALA C C 13 177.332 . . 1 . . . . 84 A C . 16500 1 395 . 1 1 85 85 ALA CA C 13 52.491 . . 1 . . . . 84 A CA . 16500 1 396 . 1 1 85 85 ALA CB C 13 19.388 . . 1 . . . . 84 A CB . 16500 1 397 . 1 1 85 85 ALA N N 15 126.085 . . 1 . . . . 84 A N . 16500 1 398 . 1 1 86 86 GLU H H 1 8.356 . . 1 . . . . 85 E H . 16500 1 399 . 1 1 86 86 GLU C C 13 175.755 . . 1 . . . . 85 E C . 16500 1 400 . 1 1 86 86 GLU CA C 13 55.523 . . 1 . . . . 85 E CA . 16500 1 401 . 1 1 86 86 GLU CB C 13 29.086 . . 1 . . . . 85 E CB . 16500 1 402 . 1 1 86 86 GLU N N 15 120.223 . . 1 . . . . 85 E N . 16500 1 403 . 1 1 87 87 LEU H H 1 8.332 . . 1 . . . . 86 L H . 16500 1 404 . 1 1 87 87 LEU C C 13 176.937 . . 1 . . . . 86 L C . 16500 1 405 . 1 1 87 87 LEU CA C 13 55.032 . . 1 . . . . 86 L CA . 16500 1 406 . 1 1 87 87 LEU CB C 13 42.446 . . 1 . . . . 86 L CB . 16500 1 407 . 1 1 87 87 LEU N N 15 124.675 . . 1 . . . . 86 L N . 16500 1 408 . 1 1 88 88 LYS H H 1 8.334 . . 1 . . . . 87 K H . 16500 1 409 . 1 1 88 88 LYS CA C 13 54.138 . . 1 . . . . 87 K CA . 16500 1 410 . 1 1 88 88 LYS CB C 13 32.621 . . 1 . . . . 87 K CB . 16500 1 411 . 1 1 88 88 LYS N N 15 123.987 . . 1 . . . . 87 K N . 16500 1 412 . 1 1 89 89 PRO C C 13 176.877 . . 1 . . . . 88 P C . 16500 1 413 . 1 1 89 89 PRO CA C 13 62.916 . . 1 . . . . 88 P CA . 16500 1 414 . 1 1 89 89 PRO CB C 13 32.213 . . 1 . . . . 88 P CB . 16500 1 415 . 1 1 90 90 LEU H H 1 8.349 . . 1 . . . . 89 L H . 16500 1 416 . 1 1 90 90 LEU C C 13 177.373 . . 1 . . . . 89 L C . 16500 1 417 . 1 1 90 90 LEU CA C 13 55.176 . . 1 . . . . 89 L CA . 16500 1 418 . 1 1 90 90 LEU CB C 13 42.503 . . 1 . . . . 89 L CB . 16500 1 419 . 1 1 90 90 LEU N N 15 122.972 . . 1 . . . . 89 L N . 16500 1 420 . 1 1 91 91 ALA H H 1 8.333 . . 1 . . . . 90 A H . 16500 1 421 . 1 1 91 91 ALA C C 13 177.655 . . 1 . . . . 90 A C . 16500 1 422 . 1 1 91 91 ALA CA C 13 52.545 . . 1 . . . . 90 A CA . 16500 1 423 . 1 1 91 91 ALA CB C 13 19.387 . . 1 . . . . 90 A CB . 16500 1 424 . 1 1 91 91 ALA N N 15 125.415 . . 1 . . . . 90 A N . 16500 1 425 . 1 1 92 92 GLN H H 1 8.372 . . 1 . . . . 91 Q H . 16500 1 426 . 1 1 92 92 GLN C C 13 176.017 . . 1 . . . . 91 Q C . 16500 1 427 . 1 1 92 92 GLN CA C 13 55.65 . . 1 . . . . 91 Q CA . 16500 1 428 . 1 1 92 92 GLN CB C 13 29.758 . . 1 . . . . 91 Q CB . 16500 1 429 . 1 1 92 92 GLN N N 15 119.986 . . 1 . . . . 91 Q N . 16500 1 430 . 1 1 93 93 SER H H 1 8.36 . . 1 . . . . 92 S H . 16500 1 431 . 1 1 93 93 SER C C 13 174.476 . . 1 . . . . 92 S C . 16500 1 432 . 1 1 93 93 SER CA C 13 58.314 . . 1 . . . . 92 S CA . 16500 1 433 . 1 1 93 93 SER CB C 13 63.831 . . 1 . . . . 92 S CB . 16500 1 434 . 1 1 93 93 SER N N 15 117.241 . . 1 . . . . 92 S N . 16500 1 435 . 1 1 94 94 HIS H H 1 8.601 . . 1 . . . . 93 H H . 16500 1 436 . 1 1 94 94 HIS C C 13 173.958 . . 1 . . . . 93 H C . 16500 1 437 . 1 1 94 94 HIS CA C 13 55.064 . . 1 . . . . 93 H CA . 16500 1 438 . 1 1 94 94 HIS CB C 13 29.117 . . 1 . . . . 93 H CB . 16500 1 439 . 1 1 94 94 HIS N N 15 120.592 . . 1 . . . . 93 H N . 16500 1 440 . 1 1 95 95 ALA H H 1 8.344 . . 1 . . . . 94 A H . 16500 1 441 . 1 1 95 95 ALA C C 13 177.767 . . 1 . . . . 94 A C . 16500 1 442 . 1 1 95 95 ALA CA C 13 52.583 . . 1 . . . . 94 A CA . 16500 1 443 . 1 1 95 95 ALA CB C 13 19.377 . . 1 . . . . 94 A CB . 16500 1 444 . 1 1 95 95 ALA N N 15 125.328 . . 1 . . . . 94 A N . 16500 1 445 . 1 1 96 96 THR H H 1 8.275 . . 1 . . . . 95 T H . 16500 1 446 . 1 1 96 96 THR C C 13 174.356 . . 1 . . . . 95 T C . 16500 1 447 . 1 1 96 96 THR CA C 13 61.822 . . 1 . . . . 95 T CA . 16500 1 448 . 1 1 96 96 THR CB C 13 69.96 . . 1 . . . . 95 T CB . 16500 1 449 . 1 1 96 96 THR N N 15 115.106 . . 1 . . . . 95 T N . 16500 1 450 . 1 1 97 97 LYS H H 1 8.382 . . 1 . . . . 96 K H . 16500 1 451 . 1 1 97 97 LYS C C 13 176.201 . . 1 . . . . 96 K C . 16500 1 452 . 1 1 97 97 LYS CA C 13 56.214 . . 1 . . . . 96 K CA . 16500 1 453 . 1 1 97 97 LYS CB C 13 33.173 . . 1 . . . . 96 K CB . 16500 1 454 . 1 1 97 97 LYS N N 15 124.243 . . 1 . . . . 96 K N . 16500 1 455 . 1 1 98 98 HIS H H 1 8.564 . . 1 . . . . 97 H H . 16500 1 456 . 1 1 98 98 HIS C C 13 174.023 . . 1 . . . . 97 H C . 16500 1 457 . 1 1 98 98 HIS CA C 13 54.958 . . 1 . . . . 97 H CA . 16500 1 458 . 1 1 98 98 HIS CB C 13 29.428 . . 1 . . . . 97 H CB . 16500 1 459 . 1 1 98 98 HIS N N 15 120.429 . . 1 . . . . 97 H N . 16500 1 460 . 1 1 99 99 LYS H H 1 8.508 . . 1 . . . . 98 K H . 16500 1 461 . 1 1 99 99 LYS C C 13 176.09 . . 1 . . . . 98 K C . 16500 1 462 . 1 1 99 99 LYS CA C 13 56.356 . . 1 . . . . 98 K CA . 16500 1 463 . 1 1 99 99 LYS CB C 13 33.194 . . 1 . . . . 98 K CB . 16500 1 464 . 1 1 99 99 LYS N N 15 124.208 . . 1 . . . . 98 K N . 16500 1 465 . 1 1 100 100 ILE H H 1 8.319 . . 1 . . . . 99 I H . 16500 1 466 . 1 1 100 100 ILE CA C 13 58.631 . . 1 . . . . 99 I CA . 16500 1 467 . 1 1 100 100 ILE CB C 13 38.83 . . 1 . . . . 99 I CB . 16500 1 468 . 1 1 100 100 ILE N N 15 125.015 . . 1 . . . . 99 I N . 16500 1 469 . 1 1 101 101 PRO C C 13 177.464 . . 1 . . . . 100 P C . 16500 1 470 . 1 1 101 101 PRO CA C 13 62.993 . . 1 . . . . 100 P CA . 16500 1 471 . 1 1 101 101 PRO CB C 13 33.045 . . 1 . . . . 100 P CB . 16500 1 472 . 1 1 102 102 ILE H H 1 8.176 . . 1 . . . . 101 I H . 16500 1 473 . 1 1 102 102 ILE C C 13 176.234 . . 1 . . . . 101 I C . 16500 1 474 . 1 1 102 102 ILE CA C 13 61.491 . . 1 . . . . 101 I CA . 16500 1 475 . 1 1 102 102 ILE CB C 13 38.778 . . 1 . . . . 101 I CB . 16500 1 476 . 1 1 102 102 ILE N N 15 122.005 . . 1 . . . . 101 I N . 16500 1 477 . 1 1 103 103 LYS H H 1 8.265 . . 1 . . . . 102 K H . 16500 1 478 . 1 1 103 103 LYS C C 13 176.1 . . 1 . . . . 102 K C . 16500 1 479 . 1 1 103 103 LYS CA C 13 56.497 . . 1 . . . . 102 K CA . 16500 1 480 . 1 1 103 103 LYS CB C 13 33.1 . . 1 . . . . 102 K CB . 16500 1 481 . 1 1 103 103 LYS N N 15 124.871 . . 1 . . . . 102 K N . 16500 1 482 . 1 1 104 104 TYR H H 1 8.112 . . 1 . . . . 103 Y H . 16500 1 483 . 1 1 104 104 TYR C C 13 175.614 . . 1 . . . . 103 Y C . 16500 1 484 . 1 1 104 104 TYR CA C 13 58.085 . . 1 . . . . 103 Y CA . 16500 1 485 . 1 1 104 104 TYR CB C 13 38.824 . . 1 . . . . 103 Y CB . 16500 1 486 . 1 1 104 104 TYR N N 15 121.815 . . 1 . . . . 103 Y N . 16500 1 487 . 1 1 105 105 LEU H H 1 8.09 . . 1 . . . . 104 L H . 16500 1 488 . 1 1 105 105 LEU C C 13 176.941 . . 1 . . . . 104 L C . 16500 1 489 . 1 1 105 105 LEU CA C 13 55.3 . . 1 . . . . 104 L CA . 16500 1 490 . 1 1 105 105 LEU CB C 13 42.383 . . 1 . . . . 104 L CB . 16500 1 491 . 1 1 105 105 LEU N N 15 123.558 . . 1 . . . . 104 L N . 16500 1 492 . 1 1 106 106 GLU H H 1 8.094 . . 1 . . . . 105 E H . 16500 1 493 . 1 1 106 106 GLU C C 13 175.586 . . 1 . . . . 105 E C . 16500 1 494 . 1 1 106 106 GLU CA C 13 56.047 . . 1 . . . . 105 E CA . 16500 1 495 . 1 1 106 106 GLU CB C 13 28.946 . . 1 . . . . 105 E CB . 16500 1 496 . 1 1 106 106 GLU N N 15 120.564 . . 1 . . . . 105 E N . 16500 1 497 . 1 1 107 107 PHE H H 1 8.164 . . 1 . . . . 106 F H . 16500 1 498 . 1 1 107 107 PHE C C 13 175.618 . . 1 . . . . 106 F C . 16500 1 499 . 1 1 107 107 PHE CA C 13 57.911 . . 1 . . . . 106 F CA . 16500 1 500 . 1 1 107 107 PHE CB C 13 39.558 . . 1 . . . . 106 F CB . 16500 1 501 . 1 1 107 107 PHE N N 15 121.194 . . 1 . . . . 106 F N . 16500 1 502 . 1 1 108 108 ILE H H 1 8.01 . . 1 . . . . 107 I H . 16500 1 503 . 1 1 108 108 ILE C C 13 175.96 . . 1 . . . . 107 I C . 16500 1 504 . 1 1 108 108 ILE CA C 13 61.13 . . 1 . . . . 107 I CA . 16500 1 505 . 1 1 108 108 ILE CB C 13 38.952 . . 1 . . . . 107 I CB . 16500 1 506 . 1 1 108 108 ILE N N 15 122.845 . . 1 . . . . 107 I N . 16500 1 507 . 1 1 109 109 SER H H 1 8.218 . . 1 . . . . 108 S H . 16500 1 508 . 1 1 109 109 SER C C 13 174.737 . . 1 . . . . 108 S C . 16500 1 509 . 1 1 109 109 SER CA C 13 58.491 . . 1 . . . . 108 S CA . 16500 1 510 . 1 1 109 109 SER CB C 13 63.734 . . 1 . . . . 108 S CB . 16500 1 511 . 1 1 109 109 SER N N 15 119.308 . . 1 . . . . 108 S N . 16500 1 512 . 1 1 110 110 GLU H H 1 8.326 . . 1 . . . . 109 E H . 16500 1 513 . 1 1 110 110 GLU C C 13 175.793 . . 1 . . . . 109 E C . 16500 1 514 . 1 1 110 110 GLU CA C 13 56.031 . . 1 . . . . 109 E CA . 16500 1 515 . 1 1 110 110 GLU CB C 13 28.793 . . 1 . . . . 109 E CB . 16500 1 516 . 1 1 110 110 GLU N N 15 122.457 . . 1 . . . . 109 E N . 16500 1 517 . 1 1 111 111 ALA H H 1 8.176 . . 1 . . . . 110 A H . 16500 1 518 . 1 1 111 111 ALA C C 13 177.72 . . 1 . . . . 110 A C . 16500 1 519 . 1 1 111 111 ALA CA C 13 52.869 . . 1 . . . . 110 A CA . 16500 1 520 . 1 1 111 111 ALA CB C 13 19.058 . . 1 . . . . 110 A CB . 16500 1 521 . 1 1 111 111 ALA N N 15 124.501 . . 1 . . . . 110 A N . 16500 1 522 . 1 1 112 112 ILE H H 1 7.975 . . 1 . . . . 111 I H . 16500 1 523 . 1 1 112 112 ILE C C 13 176.191 . . 1 . . . . 111 I C . 16500 1 524 . 1 1 112 112 ILE CA C 13 61.215 . . 1 . . . . 111 I CA . 16500 1 525 . 1 1 112 112 ILE CB C 13 38.525 . . 1 . . . . 111 I CB . 16500 1 526 . 1 1 112 112 ILE N N 15 119.962 . . 1 . . . . 111 I N . 16500 1 527 . 1 1 113 113 ILE H H 1 8.058 . . 1 . . . . 112 I H . 16500 1 528 . 1 1 113 113 ILE C C 13 176.092 . . 1 . . . . 112 I C . 16500 1 529 . 1 1 113 113 ILE CA C 13 61.148 . . 1 . . . . 112 I CA . 16500 1 530 . 1 1 113 113 ILE CB C 13 38.6 . . 1 . . . . 112 I CB . 16500 1 531 . 1 1 113 113 ILE N N 15 124.461 . . 1 . . . . 112 I N . 16500 1 532 . 1 1 114 114 HIS H H 1 8.56 . . 1 . . . . 113 H H . 16500 1 533 . 1 1 114 114 HIS C C 13 174.156 . . 1 . . . . 113 H C . 16500 1 534 . 1 1 114 114 HIS CA C 13 55.126 . . 1 . . . . 113 H CA . 16500 1 535 . 1 1 114 114 HIS CB C 13 29.028 . . 1 . . . . 113 H CB . 16500 1 536 . 1 1 114 114 HIS N N 15 122.806 . . 1 . . . . 113 H N . 16500 1 537 . 1 1 115 115 VAL H H 1 8.184 . . 1 . . . . 114 V H . 16500 1 538 . 1 1 115 115 VAL C C 13 175.833 . . 1 . . . . 114 V C . 16500 1 539 . 1 1 115 115 VAL CA C 13 62.439 . . 1 . . . . 114 V CA . 16500 1 540 . 1 1 115 115 VAL CB C 13 33.045 . . 1 . . . . 114 V CB . 16500 1 541 . 1 1 115 115 VAL N N 15 122.301 . . 1 . . . . 114 V N . 16500 1 542 . 1 1 116 116 LEU H H 1 8.371 . . 1 . . . . 115 L H . 16500 1 543 . 1 1 116 116 LEU C C 13 177.091 . . 1 . . . . 115 L C . 16500 1 544 . 1 1 116 116 LEU CA C 13 55.215 . . 1 . . . . 115 L CA . 16500 1 545 . 1 1 116 116 LEU CB C 13 42.575 . . 1 . . . . 115 L CB . 16500 1 546 . 1 1 116 116 LEU N N 15 126.16 . . 1 . . . . 115 L N . 16500 1 547 . 1 1 117 117 HIS H H 1 8.557 . . 1 . . . . 116 H H . 16500 1 548 . 1 1 117 117 HIS C C 13 174.279 . . 1 . . . . 116 H C . 16500 1 549 . 1 1 117 117 HIS CA C 13 55.091 . . 1 . . . . 116 H CA . 16500 1 550 . 1 1 117 117 HIS CB C 13 28.981 . . 1 . . . . 116 H CB . 16500 1 551 . 1 1 117 117 HIS N N 15 119.372 . . 1 . . . . 116 H N . 16500 1 552 . 1 1 118 118 SER H H 1 8.317 . . 1 . . . . 117 S H . 16500 1 553 . 1 1 118 118 SER C C 13 174.207 . . 1 . . . . 117 S C . 16500 1 554 . 1 1 118 118 SER CA C 13 58.352 . . 1 . . . . 117 S CA . 16500 1 555 . 1 1 118 118 SER CB C 13 63.89 . . 1 . . . . 117 S CB . 16500 1 556 . 1 1 118 118 SER N N 15 117.194 . . 1 . . . . 117 S N . 16500 1 557 . 1 1 119 119 ARG H H 1 8.437 . . 1 . . . . 118 R H . 16500 1 558 . 1 1 119 119 ARG C C 13 175.697 . . 1 . . . . 118 R C . 16500 1 559 . 1 1 119 119 ARG CA C 13 56.309 . . 1 . . . . 118 R CA . 16500 1 560 . 1 1 119 119 ARG CB C 13 30.959 . . 1 . . . . 118 R CB . 16500 1 561 . 1 1 119 119 ARG N N 15 122.964 . . 1 . . . . 118 R N . 16500 1 562 . 1 1 120 120 HIS H H 1 8.41 . . 1 . . . . 119 H H . 16500 1 563 . 1 1 120 120 HIS CA C 13 55.638 . . 1 . . . . 119 H CA . 16500 1 564 . 1 1 120 120 HIS CB C 13 29.451 . . 1 . . . . 119 H CB . 16500 1 565 . 1 1 120 120 HIS N N 15 122.22 . . 1 . . . . 119 H N . 16500 1 stop_ save_