data_4931 ####################### # Entry information # ####################### save_entry_information _Saveframe_category entry_information _Entry_title ; Solution structure of dynein light chain 8 (DLC8) and bim peptide complex ; _BMRB_accession_number 4931 _BMRB_flat_file_name bmr4931.str _Entry_type original _Submission_date 2000-12-21 _Accession_date 2000-12-21 _Entry_origination author _NMR_STAR_version 2.1.1 _Experimental_method NMR _Details . loop_ _Author_ordinal _Author_family_name _Author_given_name _Author_middle_initials _Author_family_title 1 Fan Jing-Song. . . 2 Zhang Qiang . . 3 Tochio Hidehito . . 4 Li Ming . . 5 Zhang Mingjie . . stop_ loop_ _Saveframe_category_type _Saveframe_category_type_count assigned_chemical_shifts 1 stop_ loop_ _Data_type _Data_type_count "1H chemical shifts" 516 "13C chemical shifts" 259 "15N chemical shifts" 89 stop_ loop_ _Revision_date _Revision_keyword _Revision_author _Revision_detail 2001-08-22 original author . stop_ _Original_release_date 2001-08-22 save_ ############################# # Citation for this entry # ############################# save_entry_citation _Saveframe_category entry_citation _Citation_full . _Citation_title ; Structural Basis of Diverse Sequence-dependent Target Recognition by the 8 kDa Dynein Light Chain ; _Citation_status published _Citation_type journal _CAS_abstract_code . _MEDLINE_UI_code 21103709 _PubMed_ID 11178896 loop_ _Author_ordinal _Author_family_name _Author_given_name _Author_middle_initials _Author_family_title 1 Fan Jing-song. . . 2 Zhang Qiang . . 3 Tochio Hidehito . . 4 Li Ming . . 5 Zhang Mingjie . . stop_ _Journal_abbreviation 'J. Mol. Biol.' _Journal_volume 306 _Journal_issue 1 _Journal_CSD . _Book_chapter_title . _Book_volume . _Book_series . _Book_ISBN . _Conference_state_province . _Conference_abstract_number . _Page_first 97 _Page_last 108 _Year 2001 _Details . loop_ _Keyword dynein 'light chain' DLC8 Bim stop_ save_ ################################## # Molecular system description # ################################## save_system_DLC8 _Saveframe_category molecular_system _Mol_system_name DYNEIN _Abbreviation_common DLC8 _Enzyme_commission_number . loop_ _Mol_system_component_name _Mol_label 'dynein unit 1' $DLC8 'dynein unit 2' $DLC8 'Bim unit 1' $Bim 'Bim unit 2' $Bim stop_ _System_molecular_weight . _System_physical_state native _System_oligomer_state dimer _System_paramagnetic no _System_thiol_state 'all free' loop_ _Magnetic_equivalence_ID _Magnetically_equivalent_system_component 1 'dynein unit 1' 1 'dynein unit 2' 2 'Bim unit 1' 2 'Bim unit 2' stop_ loop_ _Biological_function 'multifunctional regulatory protein' stop_ _Database_query_date . _Details . save_ ######################## # Monomeric polymers # ######################## save_DLC8 _Saveframe_category monomeric_polymer _Mol_type polymer _Mol_polymer_class protein _Name_common 'DYNEIN light chain 8' _Name_variant PIN _Abbreviation_common DLC8 _Molecular_mass 10300 _Mol_thiol_state 'all free' _Details 'it migrates to 8 kDa on SDS-PAGE.' ############################## # Polymer residue sequence # ############################## _Residue_count 89 _Mol_residue_sequence ; MCDRKAVIKNADMSEEMQQD SVECATQALEKYNIEKDIAA HIKKEFDKKYNPTWHCIVGR NFGSYVTHETKHFIYFYLGQ VAILLFKSG ; loop_ _Residue_seq_code _Residue_label 1 MET 2 CYS 3 ASP 4 ARG 5 LYS 6 ALA 7 VAL 8 ILE 9 LYS 10 ASN 11 ALA 12 ASP 13 MET 14 SER 15 GLU 16 GLU 17 MET 18 GLN 19 GLN 20 ASP 21 SER 22 VAL 23 GLU 24 CYS 25 ALA 26 THR 27 GLN 28 ALA 29 LEU 30 GLU 31 LYS 32 TYR 33 ASN 34 ILE 35 GLU 36 LYS 37 ASP 38 ILE 39 ALA 40 ALA 41 HIS 42 ILE 43 LYS 44 LYS 45 GLU 46 PHE 47 ASP 48 LYS 49 LYS 50 TYR 51 ASN 52 PRO 53 THR 54 TRP 55 HIS 56 CYS 57 ILE 58 VAL 59 GLY 60 ARG 61 ASN 62 PHE 63 GLY 64 SER 65 TYR 66 VAL 67 THR 68 HIS 69 GLU 70 THR 71 LYS 72 HIS 73 PHE 74 ILE 75 TYR 76 PHE 77 TYR 78 LEU 79 GLY 80 GLN 81 VAL 82 ALA 83 ILE 84 LEU 85 LEU 86 PHE 87 LYS 88 SER 89 GLY stop_ _Sequence_homology_query_date 2008-08-19 _Sequence_homology_query_revised_last_date 2008-08-19 loop_ _Database_name _Database_accession_code _Database_entry_mol_name _Sequence_query_to_submitted_percentage _Sequence_subject_length _Sequence_identity _Sequence_positive _Sequence_homology_expectation_value SWISS-PROT P63169 'Dynein light chain 1, cytoplasmic (Dynein light chain LC8-type 1) (8 kDa dynein light chain) (DLC8) (Protein inhibitor of neuronal nitric oxide synthase) (PIN)' 100.00 89 100.00 100.00 1.30e-46 SWISS-PROT P63168 'Dynein light chain 1, cytoplasmic (Dynein light chain LC8-type 1) (8 kDa dynein light chain) (DLC8) (Protein inhibitor of neuronal nitric oxide synthase) (PIN) (mPIN)' 100.00 89 100.00 100.00 1.30e-46 SWISS-PROT P63167 'Dynein light chain 1, cytoplasmic (Dynein light chain LC8-type 1) (8 kDa dynein light chain) (DLC8) (Protein inhibitor of neuronal nitric oxide synthase) (PIN)' 100.00 89 100.00 100.00 1.30e-46 SWISS-PROT P61285 'Dynein light chain 1, cytoplasmic (Dynein light chain LC8-type 1)' 100.00 89 100.00 100.00 1.30e-46 SWISS-PROT P61273 'Dynein light chain 1, cytoplasmic (Dynein light chain LC8-type 1)' 100.00 89 100.00 100.00 1.30e-46 REF NP_003737 'dynein light chain 1 [Homo sapiens]' 100.00 89 100.00 100.00 1.30e-46 REF NP_001075487 'protein inhibitor of neuronal nitric oxide synthase [Oryctolagus cuniculus]' 100.00 89 100.00 100.00 1.30e-46 REF NP_001032584 'dynein light chain 1 [Homo sapiens]' 100.00 89 100.00 100.00 1.30e-46 REF NP_001032583 'dynein light chain 1 [Homo sapiens]' 100.00 89 100.00 100.00 1.30e-46 REF NP_001003901 'dynein, light chain, LC8-type 1 [Bos taurus]' 100.00 89 100.00 100.00 1.30e-46 GenBank AAD01643 'protein inhibitor of nitric oxide synthase [Mus musculus]' 100.00 89 100.00 100.00 1.30e-46 GenBank AAC32531 'protein inhibitor of neuronal nitric oxide synthase [Oryctolagus cuniculus]' 100.00 89 100.00 100.00 1.30e-46 GenBank AAC32530 'protein inhibitor of neuronal nitric oxide synthase [Oryctolagus cuniculus]' 100.00 89 100.00 100.00 1.30e-46 GenBank AAB38257 'protein inhibitor of neuronal nitric oxide synthase [Rattus norvegicus]' 100.00 89 100.00 100.00 1.30e-46 GenBank AAB04149 'cytoplasmic dynein light chain 1' 100.00 89 100.00 100.00 1.30e-46 EMBL CAG46925 'DNCL1 [Homo sapiens]' 100.00 89 100.00 100.00 1.30e-46 EMBL CAG28600 'DNCL1 [Homo sapiens]' 100.00 89 100.00 100.00 1.30e-46 DBJ BAB28973 'unnamed protein product [Mus musculus]' 100.00 89 98.88 98.88 4.45e-46 DBJ BAB28970 'unnamed protein product [Mus musculus]' 100.00 89 100.00 100.00 1.30e-46 DBJ BAB27117 'unnamed protein product [Mus musculus]' 100.00 89 100.00 100.00 1.30e-46 DBJ BAB27063 'unnamed protein product [Mus musculus]' 100.00 89 100.00 100.00 1.30e-46 DBJ BAB22160 'unnamed protein product [Mus musculus]' 100.00 89 100.00 100.00 1.30e-46 PDB 1F96 'Solution Structure Of Dynein Light Chain 8 (Dlc8) And Nnos Peptide Complex' 100.00 89 100.00 100.00 1.30e-46 PDB 1F95 'Solution Structure Of Dynein Light Chain 8 (Dlc8) And Bim Peptide Complex' 100.00 89 100.00 100.00 1.30e-46 PDB 1F3C 'Refined Solution Structure Of 8kda Dynein Light Chain (Dlc8)' 100.00 89 100.00 100.00 1.30e-46 PDB 1CMI 'Structure Of The Human PinLC8 DIMER WITH A BOUND PEPTIDE' 95.51 85 100.00 100.00 1.03e-43 BMRB 4912 'dynein light chain 8' 100.00 89 100.00 100.00 1.30e-46 BMRB 4911 'DYNEIN light chain 8' 100.00 89 100.00 100.00 1.30e-46 BMRB 4305 PIN 100.00 92 100.00 100.00 1.22e-46 stop_ save_ save_Bim _Saveframe_category monomeric_polymer _Mol_type polymer _Mol_polymer_class protein _Name_common Bcl-2 _Abbreviation_common Bim _Molecular_mass . _Mol_thiol_state 'all free' _Details . _Residue_count 9 _Mol_residue_sequence MSCDKSTQT loop_ _Residue_seq_code _Residue_label 1 MET 2 SER 3 CYS 4 ASP 5 LYS 6 SER 7 THR 8 GLN 9 THR stop_ _Sequence_homology_query_date . _Sequence_homology_query_revised_last_date . save_ #################### # Natural source # #################### save_natural_source _Saveframe_category natural_source loop_ _Mol_label _Organism_name_common _NCBI_taxonomy_ID _Superkingdom _Kingdom _Genus _Species $DLC8 Rat 10116 Eukaryota Metazoa Rattus norvegicus stop_ save_ ######################### # Experimental source # ######################### save_experimental_source _Saveframe_category experimental_source loop_ _Mol_label _Production_method _Host_organism_name_common _Genus _Species _Strain _Vector_name $DLC8 'recombinant technology' Bacteria Escherichia coli . PET14B stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Saveframe_category sample _Sample_type solution _Details . loop_ _Mol_label _Concentration_value _Concentration_value_units _Isotopic_labeling $DLC8 1.5 mM '[U-15N; U-13C]' $Bim 1.5 mM . stop_ save_ ############################ # Computer software used # ############################ save_VNMR _Saveframe_category software _Name VNMR _Version 6.1b loop_ _Task 'data collection' stop_ _Details varian save_ save_NMRPipe _Saveframe_category software _Name NMRPipe _Version 1.7 loop_ _Task 'data processing' stop_ _Details 'Delaglio, F' save_ save_X-PLOR _Saveframe_category software _Name X-PLOR _Version 3.8 loop_ _Task 'structure solution' stop_ _Details 'Brunger, A' save_ save_CNS _Saveframe_category software _Name CNS _Version 1.0 loop_ _Task refinement stop_ _Details 'Brunger, A' save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_NMR_spectrometer _Saveframe_category NMR_spectrometer _Manufacturer Varian _Model INOVA _Field_strength 750 _Details . save_ ############################# # NMR applied experiments # ############################# save_3D_15N-separated_NOESY_1 _Saveframe_category NMR_applied_experiment _Experiment_name '3D 15N-separated NOESY' _Sample_label . save_ save_3D_13C-separated_NOESY_2 _Saveframe_category NMR_applied_experiment _Experiment_name '3D 13C-separated NOESY' _Sample_label . save_ save_2D_NOESY_3 _Saveframe_category NMR_applied_experiment _Experiment_name '2D NOESY' _Sample_label . save_ save_NMR_spec_expt__0_1 _Saveframe_category NMR_applied_experiment _Experiment_name '3D 15N-separated NOESY' _BMRB_pulse_sequence_accession_number . _Details . save_ save_NMR_spec_expt__0_2 _Saveframe_category NMR_applied_experiment _Experiment_name '3D 13C-separated NOESY' _BMRB_pulse_sequence_accession_number . _Details . save_ save_NMR_spec_expt__0_3 _Saveframe_category NMR_applied_experiment _Experiment_name '2D NOESY' _BMRB_pulse_sequence_accession_number . _Details . save_ ####################### # Sample conditions # ####################### save_sample_cond_1 _Saveframe_category sample_conditions _Details . loop_ _Variable_type _Variable_value _Variable_value_error _Variable_value_units pH 7.0 0.2 n/a temperature 303 0.1 K pressure 1 . atm stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chemical_shift_reference _Saveframe_category chemical_shift_reference _Details . loop_ _Mol_common_name _Atom_type _Atom_isotope_number _Atom_group _Chem_shift_units _Chem_shift_value _Reference_method _Reference_type _External_reference_sample_geometry _External_reference_location _External_reference_axis _Indirect_shift_ratio DSS H 1 'methyl protons' ppm 0.0 internal direct . . . 1.0 DSS N 15 'methyl protons' ppm 0.0 . indirect . . . 0.101329118 DSS C 13 'methyl protons' ppm 0.0 . indirect . . . 0.251449530 stop_ save_ ################################### # Assigned chemical shift lists # ################################### ################################################################### # Chemical Shift Ambiguity Index Value Definitions # # # # The values other than 1 are used for those atoms with different # # chemical shifts that cannot be assigned to stereospecific atoms # # or to specific residues or chains. # # # # Index Value Definition # # # # 1 Unique (including isolated methyl protons, # # geminal atoms, and geminal methyl # # groups with identical chemical shifts) # # (e.g. ILE HD11, HD12, HD13 protons) # # 2 Ambiguity of geminal atoms or geminal methyl # # proton groups (e.g. ASP HB2 and HB3 # # protons, LEU CD1 and CD2 carbons, or # # LEU HD11, HD12, HD13 and HD21, HD22, # # HD23 methyl protons) # # 3 Aromatic atoms on opposite sides of # # symmetrical rings (e.g. TYR HE1 and HE2 # # protons) # # 4 Intraresidue ambiguities (e.g. LYS HG and # # HD protons or TRP HZ2 and HZ3 protons) # # 5 Interresidue ambiguities (LYS 12 vs. LYS 27) # # 6 Intermolecular ambiguities (e.g. ASP 31 CA # # in monomer 1 and ASP 31 CA in monomer 2 # # of an asymmetrical homodimer, duplex # # DNA assignments, or other assignments # # that may apply to atoms in one or more # # molecule in the molecular assembly) # # 9 Ambiguous, specific ambiguity not defined # # # ################################################################### save_chemical_shift_set_1 _Saveframe_category assigned_chemical_shifts _Details . loop_ _Sample_label $sample_1 stop_ _Sample_conditions_label $sample_cond_1 _Chem_shift_reference_set_label $chemical_shift_reference _Mol_system_component_name 'dynein unit 1' _Text_data_format . _Text_data . loop_ _Atom_shift_assign_ID _Residue_author_seq_code _Residue_seq_code _Residue_label _Atom_name _Atom_type _Chem_shift_value _Chem_shift_value_error _Chem_shift_ambiguity_code 1 . 1 MET N N 122.2400 0.05 1 2 . 1 MET H H 8.4700 0.02 1 3 . 1 MET CA C 56.2800 0.05 1 4 . 1 MET HA H 4.4200 0.02 1 5 . 1 MET CB C 33.0600 0.05 1 6 . 1 MET HB2 H 1.9800 0.02 1 7 . 1 MET HB3 H 2.0400 0.02 1 8 . 1 MET CG C 32.5600 0.05 1 9 . 1 MET HG2 H 2.4600 0.02 1 10 . 1 MET HG3 H 2.5300 0.02 1 11 . 1 MET CE C 17.5300 0.05 1 12 . 1 MET HE H 2.0600 0.02 1 13 . 2 CYS N N 120.4000 0.05 1 14 . 2 CYS H H 8.4300 0.02 1 15 . 2 CYS CA C 58.9600 0.05 1 16 . 2 CYS HA H 4.4570 0.02 1 17 . 2 CYS CB C 28.2800 0.05 1 18 . 2 CYS HB2 H 2.9200 0.02 1 19 . 2 CYS HB3 H 2.9200 0.02 1 20 . 3 ASP N N 123.5000 0.05 1 21 . 3 ASP H H 8.3400 0.02 1 22 . 3 ASP CA C 55.0000 0.05 1 23 . 3 ASP HA H 4.5760 0.02 1 24 . 3 ASP CB C 41.5100 0.05 1 25 . 3 ASP HB2 H 2.6900 0.02 1 26 . 3 ASP HB3 H 2.6900 0.02 1 27 . 4 ARG N N 121.7300 0.05 1 28 . 4 ARG H H 8.2000 0.02 1 29 . 4 ARG CA C 55.9200 0.05 1 30 . 4 ARG HA H 4.3000 0.02 1 31 . 4 ARG CB C 30.8000 0.05 1 32 . 4 ARG HB2 H 1.7300 0.02 1 33 . 4 ARG HB3 H 1.8490 0.02 1 34 . 4 ARG CG C 27.6600 0.05 1 35 . 4 ARG HG2 H 1.5860 0.02 1 36 . 4 ARG HG3 H 1.6390 0.02 1 37 . 4 ARG CD C 43.8500 0.05 1 38 . 4 ARG HD2 H 3.1220 0.02 1 39 . 4 ARG HD3 H 3.1220 0.02 1 40 . 5 LYS N N 122.1700 0.05 1 41 . 5 LYS H H 8.1000 0.02 1 42 . 5 LYS CA C 56.4200 0.05 1 43 . 5 LYS HA H 4.3000 0.02 1 44 . 5 LYS CB C 33.5600 0.05 1 45 . 5 LYS HB2 H 1.7850 0.02 1 46 . 5 LYS HB3 H 1.7850 0.02 1 47 . 5 LYS CG C 25.1100 0.05 1 48 . 5 LYS HG2 H 1.4000 0.02 1 49 . 5 LYS HG3 H 1.4000 0.02 1 50 . 5 LYS CD C 29.5600 0.05 1 51 . 5 LYS HD2 H 1.6750 0.02 1 52 . 5 LYS HD3 H 1.6750 0.02 1 53 . 5 LYS CE C 42.6900 0.05 1 54 . 5 LYS HE2 H 2.9840 0.02 1 55 . 5 LYS HE3 H 2.9840 0.02 1 56 . 6 ALA N N 127.5800 0.05 1 57 . 6 ALA H H 8.5300 0.02 1 58 . 6 ALA CA C 51.9500 0.05 1 59 . 6 ALA HA H 5.2000 0.02 1 60 . 6 ALA CB C 21.5400 0.05 1 61 . 6 ALA HB H 1.3300 0.02 1 62 . 7 VAL N N 123.6200 0.05 1 63 . 7 VAL H H 8.9300 0.02 1 64 . 7 VAL CA C 62.0100 0.05 1 65 . 7 VAL HA H 4.2400 0.02 1 66 . 7 VAL CB C 34.5500 0.05 1 67 . 7 VAL HB H 2.0400 0.02 1 68 . 7 VAL CG1 C 21.3600 0.05 1 69 . 7 VAL HG1 H 0.7360 0.02 1 70 . 7 VAL CG2 C 20.8200 0.05 1 71 . 7 VAL HG2 H 0.9200 0.02 1 72 . 8 ILE N N 129.6000 0.05 1 73 . 8 ILE H H 9.1700 0.02 1 74 . 8 ILE CA C 62.3800 0.05 1 75 . 8 ILE HA H 4.0300 0.02 1 76 . 8 ILE CB C 36.2400 0.05 1 77 . 8 ILE HB H 1.9600 0.02 1 78 . 8 ILE CG1 C 28.0700 0.05 1 79 . 8 ILE HG12 H 1.3200 0.02 1 80 . 8 ILE HG13 H 1.4700 0.02 1 81 . 8 ILE CG2 C 18.5800 0.05 1 82 . 8 ILE HG2 H 0.8500 0.02 1 83 . 8 ILE CD1 C 11.8800 0.05 1 84 . 8 ILE HD1 H 0.6800 0.02 1 85 . 9 LYS N N 129.8400 0.05 1 86 . 9 LYS H H 8.3700 0.02 1 87 . 9 LYS CA C 56.4200 0.05 1 88 . 9 LYS HA H 4.5200 0.02 1 89 . 9 LYS CB C 32.5600 0.05 1 90 . 9 LYS HB2 H 1.1700 0.02 1 91 . 9 LYS HB3 H 1.4800 0.02 1 92 . 9 LYS CG C 24.3700 0.05 1 93 . 9 LYS HG2 H 0.5530 0.02 1 94 . 9 LYS HG3 H 0.8200 0.02 1 95 . 9 LYS CD C 28.0800 0.05 1 96 . 9 LYS HD2 H 0.9570 0.02 1 97 . 9 LYS HD3 H 1.1000 0.02 1 98 . 9 LYS HE2 H 2.7800 0.02 1 99 . 9 LYS HE3 H 2.7800 0.02 1 100 . 10 ASN N N 116.6600 0.05 1 101 . 10 ASN H H 8.3100 0.02 1 102 . 10 ASN CA C 54.4600 0.05 1 103 . 10 ASN HA H 4.9700 0.02 1 104 . 10 ASN CB C 42.0000 0.05 1 105 . 10 ASN HB2 H 2.8900 0.02 1 106 . 10 ASN HB3 H 3.0600 0.02 1 107 . 11 ALA N N 126.1700 0.05 1 108 . 11 ALA H H 8.7700 0.02 1 109 . 11 ALA CA C 52.2300 0.05 1 110 . 11 ALA HA H 4.9700 0.02 1 111 . 11 ALA CB C 22.6200 0.05 1 112 . 11 ALA HB H 1.3600 0.02 1 113 . 12 ASP N N 123.5000 0.05 1 114 . 12 ASP H H 9.0100 0.02 1 115 . 12 ASP CA C 53.9300 0.05 1 116 . 12 ASP HA H 4.9100 0.02 1 117 . 12 ASP CB C 41.0900 0.05 1 118 . 12 ASP HB2 H 2.6900 0.02 1 119 . 12 ASP HB3 H 2.8200 0.02 1 120 . 13 MET N N 120.7900 0.05 1 121 . 13 MET H H 7.8800 0.02 1 122 . 13 MET CA C 56.4200 0.05 1 123 . 13 MET HA H 4.5800 0.02 1 124 . 13 MET CB C 38.9800 0.05 1 125 . 13 MET HB2 H 1.8370 0.02 1 126 . 13 MET HB3 H 2.0740 0.02 1 127 . 13 MET CG C 34.3500 0.05 1 128 . 13 MET HG3 H 2.8200 0.02 1 129 . 13 MET HG2 H 2.6000 0.02 1 130 . 13 MET CE C 18.0900 0.05 1 131 . 13 MET HE H 1.9800 0.02 1 132 . 14 SER N N 122.9700 0.05 1 133 . 14 SER H H 9.3000 0.02 1 134 . 14 SER CA C 58.9000 0.05 1 135 . 14 SER HA H 4.4300 0.02 1 136 . 14 SER CB C 64.8700 0.05 1 137 . 14 SER HB2 H 4.4300 0.02 1 138 . 14 SER HB3 H 4.1100 0.02 1 139 . 15 GLU N N 124.3100 0.05 1 140 . 15 GLU H H 9.2700 0.02 1 141 . 15 GLU CA C 60.8900 0.05 1 142 . 15 GLU HA H 3.7700 0.02 1 143 . 15 GLU CB C 29.5800 0.05 1 144 . 15 GLU HB2 H 2.0400 0.02 1 145 . 15 GLU HB3 H 2.0400 0.02 1 146 . 15 GLU CG C 37.0600 0.05 1 147 . 15 GLU HG2 H 2.3300 0.02 1 148 . 15 GLU HG3 H 2.3300 0.02 1 149 . 16 GLU N N 119.4500 0.05 1 150 . 16 GLU H H 9.1900 0.02 1 151 . 16 GLU CA C 60.8900 0.05 1 152 . 16 GLU HA H 4.0200 0.02 1 153 . 16 GLU CB C 29.0800 0.05 1 154 . 16 GLU HB2 H 2.0100 0.02 1 155 . 16 GLU HB3 H 2.0100 0.02 1 156 . 16 GLU CG C 37.1100 0.05 1 157 . 16 GLU HG2 H 2.3900 0.02 1 158 . 16 GLU HG3 H 2.3200 0.02 1 159 . 17 MET N N 121.2700 0.05 1 160 . 17 MET H H 7.6400 0.02 1 161 . 17 MET CA C 60.3900 0.05 1 162 . 17 MET HA H 3.9800 0.02 1 163 . 17 MET CB C 33.6600 0.05 1 164 . 17 MET HB2 H 2.0000 0.02 1 165 . 17 MET HB3 H 2.1300 0.02 1 166 . 17 MET CG C 33.7100 0.05 1 167 . 17 MET HG2 H 2.3500 0.02 1 168 . 17 MET HG3 H 2.3500 0.02 1 169 . 17 MET CE C 16.9700 0.05 1 170 . 17 MET HE H 1.6700 0.02 1 171 . 18 GLN N N 123.0900 0.05 1 172 . 18 GLN H H 8.5800 0.02 1 173 . 18 GLN CA C 60.3500 0.05 1 174 . 18 GLN HA H 3.7700 0.02 1 175 . 18 GLN CB C 29.0800 0.05 1 176 . 18 GLN HB3 H 2.0900 0.02 1 177 . 18 GLN HB2 H 2.0000 0.02 1 178 . 18 GLN CG C 34.7600 0.05 1 179 . 18 GLN HG2 H 2.4000 0.02 1 180 . 18 GLN HG3 H 2.4000 0.02 1 181 . 19 GLN N N 118.6800 0.05 1 182 . 19 GLN H H 7.9400 0.02 1 183 . 19 GLN CA C 59.4000 0.05 1 184 . 19 GLN HA H 3.8700 0.02 1 185 . 19 GLN CB C 28.0900 0.05 1 186 . 19 GLN HB2 H 2.1200 0.02 1 187 . 19 GLN HB3 H 2.1200 0.02 1 188 . 19 GLN CG C 34.0000 0.05 1 189 . 19 GLN HG2 H 2.4200 0.02 1 190 . 19 GLN HG3 H 2.4200 0.02 1 191 . 20 ASP N N 120.1700 0.05 1 192 . 20 ASP H H 7.9400 0.02 1 193 . 20 ASP CA C 57.9100 0.05 1 194 . 20 ASP HA H 4.5900 0.02 1 195 . 20 ASP CB C 41.0300 0.05 1 196 . 20 ASP HB2 H 2.7400 0.02 1 197 . 20 ASP HB3 H 2.8600 0.02 1 198 . 21 SER N N 118.9200 0.05 1 199 . 21 SER H H 8.4700 0.02 1 200 . 21 SER CA C 63.4100 0.05 1 201 . 21 SER HA H 3.9700 0.02 1 202 . 21 SER CB C 63.4100 0.05 1 203 . 21 SER HB3 H 3.8200 0.02 1 204 . 21 SER HB2 H 3.3900 0.02 1 205 . 22 VAL N N 121.8500 0.05 1 206 . 22 VAL H H 7.2900 0.02 1 207 . 22 VAL CA C 67.2300 0.05 1 208 . 22 VAL HA H 3.3800 0.02 1 209 . 22 VAL CB C 32.1900 0.05 1 210 . 22 VAL HB H 1.9500 0.02 1 211 . 22 VAL CG2 C 22.0700 0.05 1 212 . 22 VAL HG2 H 0.7800 0.02 1 213 . 22 VAL CG1 C 21.7100 0.05 1 214 . 22 VAL HG1 H 0.3900 0.02 1 215 . 23 GLU N N 124.3500 0.05 1 216 . 23 GLU H H 8.5300 0.02 1 217 . 23 GLU CA C 60.4100 0.05 1 218 . 23 GLU HA H 4.0600 0.02 1 219 . 23 GLU CB C 29.5800 0.05 1 220 . 23 GLU HB2 H 2.1600 0.02 1 221 . 23 GLU HB3 H 2.1600 0.02 1 222 . 23 GLU CG C 36.4800 0.05 1 223 . 23 GLU HG2 H 2.3500 0.02 1 224 . 23 GLU HG3 H 2.3500 0.02 1 225 . 24 CYS N N 120.7600 0.05 1 226 . 24 CYS H H 8.9200 0.02 1 227 . 24 CYS CA C 63.3200 0.05 1 228 . 24 CYS HA H 4.2500 0.02 1 229 . 24 CYS CB C 27.5900 0.05 1 230 . 24 CYS HB3 H 3.4100 0.02 1 231 . 24 CYS HB2 H 2.8200 0.02 1 232 . 25 ALA N N 120.7400 0.05 1 233 . 25 ALA H H 8.3200 0.02 1 234 . 25 ALA CA C 55.4200 0.05 1 235 . 25 ALA HA H 4.0000 0.02 1 236 . 25 ALA CB C 20.3600 0.05 1 237 . 25 ALA HB H 1.6100 0.02 1 238 . 26 THR N N 115.7500 0.05 1 239 . 26 THR H H 8.4000 0.02 1 240 . 26 THR CA C 68.3300 0.05 1 241 . 26 THR HA H 3.7400 0.02 1 242 . 26 THR CB C 69.1600 0.05 1 243 . 26 THR HB H 4.4500 0.02 1 244 . 26 THR CG2 C 21.4300 0.05 1 245 . 26 THR HG2 H 1.2300 0.02 1 246 . 27 GLN N N 121.0000 0.05 1 247 . 27 GLN H H 7.8600 0.02 1 248 . 27 GLN CA C 59.0400 0.05 1 249 . 27 GLN HA H 3.9800 0.02 1 250 . 27 GLN CB C 28.6000 0.05 1 251 . 27 GLN HB2 H 2.0500 0.02 1 252 . 27 GLN HB3 H 2.3100 0.02 1 253 . 27 GLN CG C 34.4300 0.05 1 254 . 27 GLN HG2 H 2.3500 0.02 1 255 . 27 GLN HG3 H 2.5600 0.02 1 256 . 28 ALA N N 122.6200 0.05 1 257 . 28 ALA H H 8.2400 0.02 1 258 . 28 ALA CA C 55.6800 0.05 1 259 . 28 ALA HA H 3.5200 0.02 1 260 . 28 ALA CB C 20.6200 0.05 1 261 . 28 ALA HB H 1.6900 0.02 1 262 . 29 LEU N N 118.1200 0.05 1 263 . 29 LEU H H 8.2500 0.02 1 264 . 29 LEU CA C 57.7200 0.05 1 265 . 29 LEU HA H 4.2100 0.02 1 266 . 29 LEU CB C 42.5200 0.05 1 267 . 29 LEU HB3 H 1.8200 0.02 1 268 . 29 LEU HB2 H 1.6200 0.02 1 269 . 29 LEU CG C 29.2100 0.05 1 270 . 29 LEU HG H 1.8300 0.02 1 271 . 29 LEU CD1 C 26.0100 0.05 1 272 . 29 LEU HD1 H 0.8400 0.02 1 273 . 29 LEU CD2 C 25.1400 0.05 1 274 . 29 LEU HD2 H 0.8800 0.02 1 275 . 30 GLU N N 116.7800 0.05 1 276 . 30 GLU H H 7.3300 0.02 1 277 . 30 GLU CA C 58.3000 0.05 1 278 . 30 GLU HA H 4.0600 0.02 1 279 . 30 GLU CB C 30.2900 0.05 1 280 . 30 GLU HB2 H 2.0150 0.02 1 281 . 30 GLU HB3 H 2.0150 0.02 1 282 . 30 GLU CG C 36.8300 0.05 1 283 . 30 GLU HG2 H 2.1970 0.02 1 284 . 30 GLU HG3 H 2.3900 0.02 1 285 . 31 LYS N N 118.0200 0.05 1 286 . 31 LYS H H 7.1700 0.02 1 287 . 31 LYS CA C 58.1000 0.05 1 288 . 31 LYS HA H 3.9200 0.02 1 289 . 31 LYS CB C 35.5300 0.05 1 290 . 31 LYS HB3 H 1.0500 0.02 1 291 . 31 LYS HB2 H 0.7800 0.02 1 292 . 31 LYS CG C 25.0600 0.05 1 293 . 31 LYS HG3 H 1.0400 0.02 1 294 . 31 LYS HG2 H 0.7200 0.02 1 295 . 31 LYS CD C 29.6300 0.05 1 296 . 31 LYS HD2 H 1.2100 0.02 1 297 . 31 LYS HD3 H 1.2100 0.02 1 298 . 31 LYS CE C 42.3600 0.05 1 299 . 31 LYS HE2 H 2.7800 0.02 1 300 . 31 LYS HE3 H 2.7800 0.02 1 301 . 32 TYR N N 118.0100 0.05 1 302 . 32 TYR H H 8.1400 0.02 1 303 . 32 TYR CA C 57.4100 0.05 1 304 . 32 TYR HA H 4.8900 0.02 1 305 . 32 TYR CB C 42.4000 0.05 1 306 . 32 TYR HB2 H 2.6200 0.02 1 307 . 32 TYR HB3 H 3.2400 0.02 1 308 . 33 ASN N N 114.8100 0.05 1 309 . 33 ASN H H 8.4000 0.02 1 310 . 33 ASN CA C 53.4400 0.05 1 311 . 33 ASN HA H 4.8700 0.02 1 312 . 33 ASN CB C 41.0100 0.05 1 313 . 33 ASN HB2 H 2.6200 0.02 1 314 . 33 ASN HB3 H 2.7900 0.02 1 315 . 34 ILE N N 121.8700 0.05 1 316 . 34 ILE H H 7.9000 0.02 1 317 . 34 ILE CA C 60.8900 0.05 1 318 . 34 ILE HA H 4.2300 0.02 1 319 . 34 ILE CB C 39.0900 0.05 1 320 . 34 ILE HB H 2.0000 0.02 1 321 . 34 ILE CG1 C 21.4200 0.05 1 322 . 34 ILE HG12 H 1.3100 0.02 1 323 . 34 ILE HG13 H 1.6100 0.02 1 324 . 34 ILE CG2 C 17.9900 0.05 1 325 . 34 ILE HG2 H 0.9700 0.02 1 326 . 34 ILE CD1 C 12.4700 0.05 1 327 . 34 ILE HD1 H 0.8900 0.02 1 328 . 35 GLU N N 131.3600 0.05 1 329 . 35 GLU H H 10.0600 0.02 1 330 . 35 GLU CA C 63.9300 0.05 1 331 . 35 GLU HA H 3.6800 0.02 1 332 . 35 GLU CB C 28.5900 0.05 1 333 . 35 GLU HB2 H 1.8800 0.02 1 334 . 35 GLU HB3 H 2.0000 0.02 1 335 . 35 GLU CG C 36.6000 0.05 1 336 . 35 GLU HG2 H 2.5700 0.02 1 337 . 35 GLU HG3 H 2.7400 0.02 1 338 . 36 LYS N N 116.4800 0.05 1 339 . 36 LYS H H 9.2000 0.02 1 340 . 36 LYS CA C 60.3900 0.05 1 341 . 36 LYS HA H 4.0400 0.02 1 342 . 36 LYS CB C 32.1000 0.05 1 343 . 36 LYS HB3 H 2.1100 0.02 1 344 . 36 LYS HB2 H 1.6900 0.02 1 345 . 36 LYS CG C 25.5100 0.05 1 346 . 36 LYS HG2 H 1.3700 0.02 1 347 . 36 LYS HG3 H 1.4500 0.02 1 348 . 36 LYS CD C 29.9200 0.05 1 349 . 36 LYS HD2 H 1.4500 0.02 1 350 . 36 LYS HD3 H 1.4500 0.02 1 351 . 36 LYS HE2 H 2.8100 0.02 1 352 . 36 LYS HE3 H 2.9200 0.02 1 353 . 37 ASP N N 123.7600 0.05 1 354 . 37 ASP H H 7.2000 0.02 1 355 . 37 ASP CA C 56.8700 0.05 1 356 . 37 ASP HA H 4.2400 0.02 1 357 . 37 ASP CB C 40.0200 0.05 1 358 . 37 ASP HB3 H 2.6500 0.02 1 359 . 37 ASP HB2 H 1.9400 0.02 1 360 . 38 ILE N N 124.1100 0.05 1 361 . 38 ILE H H 7.4400 0.02 1 362 . 38 ILE CA C 66.0300 0.05 1 363 . 38 ILE HA H 3.4600 0.02 1 364 . 38 ILE CB C 39.0200 0.05 1 365 . 38 ILE HB H 1.9200 0.02 1 366 . 38 ILE CG1 C 30.7500 0.05 1 367 . 38 ILE HG13 H 1.6200 0.02 1 368 . 38 ILE HG12 H 1.3100 0.02 1 369 . 38 ILE CG2 C 18.3600 0.05 1 370 . 38 ILE HG2 H 0.8500 0.02 1 371 . 38 ILE CD1 C 14.3900 0.05 1 372 . 38 ILE HD1 H 0.7200 0.02 1 373 . 39 ALA N N 119.9600 0.05 1 374 . 39 ALA H H 8.3400 0.02 1 375 . 39 ALA CA C 55.1200 0.05 1 376 . 39 ALA HA H 3.9400 0.02 1 377 . 39 ALA CB C 18.2400 0.05 1 378 . 39 ALA HB H 1.3000 0.02 1 379 . 40 ALA N N 119.3800 0.05 1 380 . 40 ALA H H 7.6700 0.02 1 381 . 40 ALA CA C 55.5700 0.05 1 382 . 40 ALA HA H 3.3000 0.02 1 383 . 40 ALA CB C 18.6500 0.05 1 384 . 40 ALA HB H 0.9200 0.02 1 385 . 41 HIS N N 116.6600 0.05 1 386 . 41 HIS H H 7.2800 0.02 1 387 . 41 HIS CA C 61.3900 0.05 1 388 . 41 HIS HA H 3.8900 0.02 1 389 . 41 HIS CB C 31.5700 0.05 1 390 . 41 HIS HB2 H 3.1200 0.02 1 391 . 41 HIS HB3 H 3.2800 0.02 1 392 . 41 HIS HD1 H 6.7400 0.02 1 393 . 41 HIS HE1 H 7.8700 0.02 1 394 . 42 ILE N N 117.0800 0.05 1 395 . 42 ILE H H 7.5000 0.02 1 396 . 42 ILE CA C 65.8600 0.05 1 397 . 42 ILE HA H 3.6500 0.02 1 398 . 42 ILE CB C 38.9500 0.05 1 399 . 42 ILE HB H 1.9020 0.02 1 400 . 42 ILE HG12 H 2.0980 0.02 1 401 . 42 ILE HG13 H 2.0980 0.02 1 402 . 42 ILE CG2 C 19.7000 0.05 1 403 . 42 ILE HG2 H 0.6700 0.02 1 404 . 42 ILE CD1 C 15.6200 0.05 1 405 . 42 ILE HD1 H 0.7800 0.02 1 406 . 43 LYS N N 119.1800 0.05 1 407 . 43 LYS H H 8.2500 0.02 1 408 . 43 LYS CA C 61.3900 0.05 1 409 . 43 LYS HA H 3.4100 0.02 1 410 . 43 LYS CB C 36.0400 0.05 1 411 . 43 LYS HB2 H 1.9000 0.02 1 412 . 43 LYS HB3 H 2.1100 0.02 1 413 . 44 LYS N N 117.6700 0.05 1 414 . 44 LYS H H 8.2400 0.02 1 415 . 44 LYS CA C 60.8900 0.05 1 416 . 44 LYS HA H 3.8200 0.02 1 417 . 44 LYS CB C 32.5600 0.05 1 418 . 44 LYS HB2 H 1.6400 0.02 1 419 . 44 LYS HB3 H 1.7500 0.02 1 420 . 44 LYS CG C 29.7700 0.05 1 421 . 44 LYS HG2 H 1.4000 0.02 1 422 . 44 LYS HG3 H 1.4900 0.02 1 423 . 44 LYS CE C 42.2500 0.05 1 424 . 44 LYS HE2 H 2.6300 0.02 1 425 . 44 LYS HE3 H 2.6300 0.02 1 426 . 45 GLU N N 120.3700 0.05 1 427 . 45 GLU H H 7.7700 0.02 1 428 . 45 GLU CA C 59.4000 0.05 1 429 . 45 GLU HA H 3.8800 0.02 1 430 . 45 GLU CB C 30.0800 0.05 1 431 . 45 GLU HB2 H 1.7600 0.02 1 432 . 45 GLU HB3 H 1.9700 0.02 1 433 . 45 GLU CG C 34.0000 0.05 1 434 . 45 GLU HG2 H 2.4200 0.02 1 435 . 45 GLU HG3 H 2.9800 0.02 1 436 . 46 PHE N N 123.8600 0.05 1 437 . 46 PHE H H 8.4400 0.02 1 438 . 46 PHE CA C 63.8700 0.05 1 439 . 46 PHE HA H 3.6100 0.02 1 440 . 46 PHE CB C 36.3500 0.05 1 441 . 46 PHE HB2 H 0.6500 0.02 1 442 . 46 PHE HB3 H 2.5700 0.02 1 443 . 46 PHE HD1 H 5.8000 0.02 1 444 . 46 PHE HD2 H 5.8000 0.02 1 445 . 46 PHE HE1 H 6.6000 0.02 1 446 . 46 PHE HE2 H 6.6000 0.02 1 447 . 46 PHE HZ H 7.1700 0.02 1 448 . 47 ASP N N 120.7500 0.05 1 449 . 47 ASP H H 8.4700 0.02 1 450 . 47 ASP CA C 57.9100 0.05 1 451 . 47 ASP HA H 4.2800 0.02 1 452 . 47 ASP CB C 40.5200 0.05 1 453 . 47 ASP HB3 H 2.7400 0.02 1 454 . 47 ASP HB2 H 2.5400 0.02 1 455 . 48 LYS N N 118.0200 0.05 1 456 . 48 LYS H H 7.1600 0.02 1 457 . 48 LYS CA C 59.9000 0.05 1 458 . 48 LYS HA H 3.9200 0.02 1 459 . 48 LYS CB C 33.0600 0.05 1 460 . 48 LYS HB2 H 1.7600 0.02 1 461 . 48 LYS HB3 H 1.7600 0.02 1 462 . 48 LYS CG C 25.2900 0.05 1 463 . 48 LYS HG3 H 1.4500 0.02 1 464 . 48 LYS HG2 H 1.2400 0.02 1 465 . 48 LYS CD C 29.8200 0.05 1 466 . 48 LYS HD2 H 1.5900 0.02 1 467 . 48 LYS CE C 42.2100 0.05 1 468 . 48 LYS HE2 H 2.8200 0.02 1 469 . 49 LYS N N 118.2900 0.05 1 470 . 49 LYS H H 7.9500 0.02 1 471 . 49 LYS CA C 59.3500 0.05 1 472 . 49 LYS HA H 3.7300 0.02 1 473 . 49 LYS CB C 34.5300 0.05 1 474 . 49 LYS HB3 H 1.0700 0.02 1 475 . 49 LYS HB2 H 0.6900 0.02 1 476 . 49 LYS CG C 25.5100 0.05 1 477 . 49 LYS HG3 H 0.8900 0.02 1 478 . 49 LYS HG2 H 0.2500 0.02 1 479 . 49 LYS CD C 29.8100 0.05 1 480 . 49 LYS HD2 H 1.1000 0.02 1 481 . 49 LYS HD3 H 1.1800 0.02 1 482 . 49 LYS CE C 42.1000 0.05 1 483 . 49 LYS HE2 H 2.5100 0.02 1 484 . 49 LYS HE3 H 2.6000 0.02 1 485 . 50 TYR N N 115.9400 0.05 1 486 . 50 TYR H H 8.4400 0.02 1 487 . 50 TYR CA C 58.9000 0.05 1 488 . 50 TYR HA H 4.8500 0.02 1 489 . 50 TYR CB C 40.0100 0.05 1 490 . 50 TYR HB3 H 3.9000 0.02 1 491 . 50 TYR HB2 H 2.7900 0.02 1 492 . 50 TYR HD1 H 6.4800 0.02 1 493 . 50 TYR HD2 H 6.4800 0.02 1 494 . 50 TYR HE1 H 6.1900 0.02 1 495 . 50 TYR HE2 H 6.1900 0.02 1 496 . 51 ASN N N 113.5100 0.05 1 497 . 51 ASN H H 6.9500 0.02 1 498 . 51 ASN CA C 55.7900 0.05 1 499 . 51 ASN HA H 4.8960 0.02 1 500 . 51 ASN CB C 36.9100 0.05 1 501 . 51 ASN HB2 H 2.8600 0.02 1 502 . 51 ASN HB3 H 3.7200 0.02 1 503 . 52 PRO CA C 61.0400 0.05 1 504 . 52 PRO HA H 5.1900 0.02 1 505 . 52 PRO CB C 32.6900 0.05 1 506 . 52 PRO HB2 H 2.0130 0.02 1 507 . 52 PRO HB3 H 2.2050 0.02 1 508 . 52 PRO CG C 28.4500 0.05 1 509 . 52 PRO HG2 H 1.8500 0.02 1 510 . 52 PRO HG3 H 2.0100 0.02 1 511 . 52 PRO CD C 50.8000 0.05 1 512 . 52 PRO HD2 H 3.5500 0.02 1 513 . 52 PRO HD3 H 3.8700 0.02 1 514 . 53 THR N N 121.0300 0.05 1 515 . 53 THR H H 7.8100 0.02 1 516 . 53 THR CA C 65.8500 0.05 1 517 . 53 THR HA H 3.7600 0.02 1 518 . 53 THR CB C 69.8400 0.05 1 519 . 53 THR HB H 3.7900 0.02 1 520 . 53 THR CG2 C 23.3200 0.05 1 521 . 53 THR HG2 H 0.9600 0.02 1 522 . 54 TRP N N 128.1200 0.05 1 523 . 54 TRP H H 9.3600 0.02 1 524 . 54 TRP CA C 55.9200 0.05 1 525 . 54 TRP HA H 4.8600 0.02 1 526 . 54 TRP CB C 30.0800 0.05 1 527 . 54 TRP HB3 H 3.0200 0.02 1 528 . 54 TRP HB2 H 2.8800 0.02 1 529 . 54 TRP HD1 H 8.1300 0.02 1 530 . 54 TRP HE3 H 7.2400 0.02 1 531 . 54 TRP HZ2 H 7.4300 0.02 1 532 . 54 TRP HZ3 H 6.6100 0.02 1 533 . 54 TRP HH2 H 7.3100 0.02 1 534 . 54 TRP NE1 N 130.7500 0.05 1 535 . 54 TRP HE1 H 9.1700 0.02 1 536 . 55 HIS N N 119.0700 0.05 1 537 . 55 HIS H H 8.4600 0.02 1 538 . 55 HIS CA C 55.4200 0.05 1 539 . 55 HIS HA H 4.8500 0.02 1 540 . 55 HIS CB C 35.0700 0.05 1 541 . 55 HIS HB3 H 2.5900 0.02 1 542 . 55 HIS HB2 H 1.6200 0.02 1 543 . 55 HIS HD1 H 7.2600 0.02 1 544 . 55 HIS HE1 H 8.4700 0.02 1 545 . 56 CYS N N 121.2500 0.05 1 546 . 56 CYS H H 8.5000 0.02 1 547 . 56 CYS CA C 57.4100 0.05 1 548 . 56 CYS HA H 5.8700 0.02 1 549 . 56 CYS CB C 31.0700 0.05 1 550 . 56 CYS HB2 H 2.5720 0.02 1 551 . 56 CYS HB3 H 2.8000 0.02 1 552 . 57 ILE N N 132.7000 0.05 1 553 . 57 ILE H H 9.4000 0.02 1 554 . 57 ILE CA C 60.7700 0.05 1 555 . 57 ILE HA H 4.6300 0.02 1 556 . 57 ILE CB C 40.5400 0.05 1 557 . 57 ILE HB H 1.6900 0.02 1 558 . 57 ILE CG1 C 30.2800 0.05 1 559 . 57 ILE HG12 H 1.2800 0.02 1 560 . 57 ILE HG13 H 1.3500 0.02 1 561 . 57 ILE CG2 C 19.5800 0.05 1 562 . 57 ILE HG2 H -0.0980 0.02 1 563 . 57 ILE CD1 C 14.2800 0.05 1 564 . 57 ILE HD1 H 0.8500 0.02 1 565 . 58 VAL N N 126.3700 0.05 1 566 . 58 VAL H H 8.6100 0.02 1 567 . 58 VAL CA C 59.9000 0.05 1 568 . 58 VAL HA H 5.2500 0.02 1 569 . 58 VAL CB C 36.5400 0.05 1 570 . 58 VAL HB H 1.7100 0.02 1 571 . 58 VAL CG2 C 22.5800 0.05 1 572 . 58 VAL HG2 H 0.9000 0.02 1 573 . 58 VAL CG1 C 21.4700 0.05 1 574 . 58 VAL HG1 H 0.8400 0.02 1 575 . 59 GLY N N 112.9700 0.05 1 576 . 59 GLY H H 9.7800 0.02 1 577 . 59 GLY CA C 47.4700 0.05 1 578 . 59 GLY HA2 H 4.4800 0.02 1 579 . 59 GLY HA3 H 4.7500 0.02 1 580 . 60 ARG N N 116.5800 0.05 1 581 . 60 ARG H H 8.2200 0.02 1 582 . 60 ARG CA C 57.4100 0.05 1 583 . 60 ARG HA H 4.9500 0.02 1 584 . 60 ARG CB C 34.0700 0.05 1 585 . 60 ARG HB2 H 1.5720 0.02 1 586 . 60 ARG HB3 H 1.7500 0.02 1 587 . 60 ARG HG2 H 2.1000 0.02 1 588 . 60 ARG HG3 H 2.1000 0.02 1 589 . 60 ARG HD2 H 3.2600 0.02 1 590 . 60 ARG HD3 H 3.2600 0.02 1 591 . 61 ASN N N 118.1300 0.05 1 592 . 61 ASN H H 8.9900 0.02 1 593 . 61 ASN CA C 54.7300 0.05 1 594 . 61 ASN HA H 5.6800 0.02 1 595 . 61 ASN CB C 41.9700 0.05 1 596 . 61 ASN HB2 H 2.8500 0.02 1 597 . 62 PHE N N 122.2400 0.05 1 598 . 62 PHE H H 8.8800 0.02 1 599 . 62 PHE CA C 57.9600 0.05 1 600 . 62 PHE HA H 5.2700 0.02 1 601 . 62 PHE CB C 39.4800 0.05 1 602 . 62 PHE HB3 H 3.3900 0.02 1 603 . 62 PHE HB2 H 2.2400 0.02 1 604 . 62 PHE HD1 H 6.5900 0.02 1 605 . 62 PHE HD2 H 6.5900 0.02 1 606 . 62 PHE HE1 H 7.0100 0.02 1 607 . 62 PHE HE2 H 7.0100 0.02 1 608 . 62 PHE HZ H 6.8900 0.02 1 609 . 63 GLY N N 110.8400 0.05 1 610 . 63 GLY H H 9.6100 0.02 1 611 . 63 GLY CA C 44.3300 0.05 1 612 . 63 GLY HA3 H 4.8300 0.02 1 613 . 63 GLY HA2 H 3.5100 0.02 1 614 . 64 SER N N 115.6900 0.05 1 615 . 64 SER H H 9.1800 0.02 1 616 . 64 SER CA C 57.3400 0.05 1 617 . 64 SER HA H 5.4300 0.02 1 618 . 64 SER CB C 68.3900 0.05 1 619 . 64 SER HB2 H 3.6700 0.02 1 620 . 65 TYR N N 122.2200 0.05 1 621 . 65 TYR H H 8.6600 0.02 1 622 . 65 TYR CA C 60.8900 0.05 1 623 . 65 TYR HA H 4.9100 0.02 1 624 . 65 TYR CB C 41.0100 0.05 1 625 . 65 TYR HB2 H 2.6300 0.02 1 626 . 65 TYR HB3 H 2.7900 0.02 1 627 . 65 TYR HD1 H 6.7500 0.02 1 628 . 65 TYR HD2 H 6.7500 0.02 1 629 . 66 VAL N N 120.0000 0.05 1 630 . 66 VAL H H 8.4200 0.02 1 631 . 66 VAL CA C 57.9100 0.05 1 632 . 66 VAL HA H 5.1100 0.02 1 633 . 66 VAL CB C 34.9400 0.05 1 634 . 66 VAL HB H 2.1500 0.02 1 635 . 66 VAL CG2 C 20.8100 0.05 1 636 . 66 VAL HG2 H 0.6900 0.02 1 637 . 66 VAL CG1 C 16.5200 0.05 1 638 . 66 VAL HG1 H -0.0570 0.02 1 639 . 67 THR N N 119.0800 0.05 1 640 . 67 THR H H 8.8000 0.02 1 641 . 67 THR CA C 61.8900 0.05 1 642 . 67 THR HA H 5.1100 0.02 1 643 . 67 THR CB C 71.3300 0.05 1 644 . 67 THR HB H 3.4200 0.02 1 645 . 67 THR CG2 C 23.4000 0.05 1 646 . 67 THR HG2 H 1.1200 0.02 1 647 . 68 HIS N N 119.7700 0.05 1 648 . 68 HIS H H 8.9700 0.02 1 649 . 68 HIS CA C 52.9400 0.05 1 650 . 68 HIS HA H 5.7800 0.02 1 651 . 68 HIS CB C 35.0500 0.05 1 652 . 68 HIS HB3 H 3.6230 0.02 1 653 . 68 HIS HB2 H 3.0350 0.02 1 654 . 69 GLU N N 122.0400 0.05 1 655 . 69 GLU H H 8.6400 0.02 1 656 . 69 GLU CA C 56.9200 0.05 1 657 . 69 GLU HA H 4.6000 0.02 1 658 . 69 GLU CB C 30.5800 0.05 1 659 . 69 GLU HB2 H 1.5500 0.02 1 660 . 69 GLU HB3 H 1.9300 0.02 1 661 . 69 GLU CG C 36.2100 0.05 1 662 . 69 GLU HG2 H 2.2500 0.02 1 663 . 69 GLU HG3 H 2.2500 0.02 1 664 . 70 THR N N 127.6600 0.05 1 665 . 70 THR H H 9.1200 0.02 1 666 . 70 THR CA C 65.3600 0.05 1 667 . 70 THR HA H 4.1200 0.02 1 668 . 70 THR CB C 69.3400 0.05 1 669 . 70 THR HB H 4.2700 0.02 1 670 . 70 THR CG2 C 23.3100 0.05 1 671 . 70 THR HG2 H 1.3400 0.02 1 672 . 71 LYS N N 123.4400 0.05 1 673 . 71 LYS H H 9.5500 0.02 1 674 . 71 LYS CA C 59.4200 0.05 1 675 . 71 LYS HA H 3.7200 0.02 1 676 . 71 LYS CB C 30.5800 0.05 1 677 . 71 LYS HB2 H 1.9900 0.02 1 678 . 71 LYS HB3 H 2.1800 0.02 1 679 . 71 LYS CG C 25.5200 0.05 1 680 . 71 LYS HG3 H 1.4500 0.02 1 681 . 71 LYS HG2 H 1.7400 0.02 1 682 . 71 LYS CD C 29.5800 0.05 1 683 . 71 LYS HD2 H 1.1600 0.02 1 684 . 71 LYS HD3 H 1.1600 0.02 1 685 . 71 LYS HE2 H 2.9800 0.02 1 686 . 71 LYS HE3 H 2.9800 0.02 1 687 . 72 HIS N N 116.2200 0.05 1 688 . 72 HIS H H 7.9600 0.02 1 689 . 72 HIS CA C 55.9200 0.05 1 690 . 72 HIS HA H 5.0700 0.02 1 691 . 72 HIS CB C 30.5600 0.05 1 692 . 72 HIS HB3 H 3.0300 0.02 1 693 . 72 HIS HB2 H 2.8820 0.02 1 694 . 72 HIS HD1 H 7.5700 0.02 1 695 . 73 PHE N N 122.0400 0.05 1 696 . 73 PHE H H 8.0900 0.02 1 697 . 73 PHE CA C 58.9000 0.05 1 698 . 73 PHE HA H 5.0700 0.02 1 699 . 73 PHE CB C 42.5000 0.05 1 700 . 73 PHE HB3 H 2.3400 0.02 1 701 . 73 PHE HB2 H 1.8800 0.02 1 702 . 73 PHE HD1 H 6.8000 0.02 1 703 . 73 PHE HD2 H 6.8000 0.02 1 704 . 73 PHE HE1 H 6.5700 0.02 1 705 . 73 PHE HE2 H 6.5700 0.02 1 706 . 73 PHE HZ H 6.7000 0.02 1 707 . 74 ILE N N 129.6200 0.05 1 708 . 74 ILE H H 8.7300 0.02 1 709 . 74 ILE CA C 62.8800 0.05 1 710 . 74 ILE HA H 4.3300 0.02 1 711 . 74 ILE CB C 41.5100 0.05 1 712 . 74 ILE HB H 2.2600 0.02 1 713 . 74 ILE CG1 C 30.7500 0.05 1 714 . 74 ILE HG12 H 1.3400 0.02 1 715 . 74 ILE HG13 H 1.5800 0.02 1 716 . 74 ILE CG2 C 16.0300 0.05 1 717 . 74 ILE HG2 H 1.0000 0.02 1 718 . 74 ILE CD1 C 14.4700 0.05 1 719 . 74 ILE HD1 H 0.6500 0.02 1 720 . 75 TYR N N 126.1800 0.05 1 721 . 75 TYR H H 8.2600 0.02 1 722 . 75 TYR CA C 54.4300 0.05 1 723 . 75 TYR HA H 5.9600 0.02 1 724 . 75 TYR CB C 41.5100 0.05 1 725 . 75 TYR HB2 H 2.8900 0.02 1 726 . 75 TYR HB3 H 2.8900 0.02 1 727 . 76 PHE N N 125.6100 0.05 1 728 . 76 PHE H H 9.2000 0.02 1 729 . 76 PHE CA C 55.4200 0.05 1 730 . 76 PHE HA H 5.1200 0.02 1 731 . 76 PHE CB C 43.5000 0.05 1 732 . 76 PHE HB2 H 2.8900 0.02 1 733 . 76 PHE HB3 H 3.1300 0.02 1 734 . 76 PHE HD1 H 6.6100 0.02 1 735 . 76 PHE HD2 H 6.6100 0.02 1 736 . 76 PHE HE1 H 6.9700 0.02 1 737 . 76 PHE HE2 H 6.9700 0.02 1 738 . 76 PHE HZ H 7.0800 0.02 1 739 . 77 TYR N N 119.0500 0.05 1 740 . 77 TYR H H 9.1300 0.02 1 741 . 77 TYR CA C 54.4300 0.05 1 742 . 77 TYR HA H 5.3500 0.02 1 743 . 77 TYR CB C 40.4900 0.05 1 744 . 77 TYR HB3 H 2.9200 0.02 1 745 . 77 TYR HB2 H 2.7800 0.02 1 746 . 77 TYR HD1 H 6.9200 0.02 1 747 . 77 TYR HD2 H 6.9200 0.02 1 748 . 77 TYR HE1 H 6.7800 0.02 1 749 . 77 TYR HE2 H 6.7800 0.02 1 750 . 78 LEU N N 122.6300 0.05 1 751 . 78 LEU H H 8.6100 0.02 1 752 . 78 LEU CA C 54.4200 0.05 1 753 . 78 LEU HA H 4.6400 0.02 1 754 . 78 LEU CB C 45.0100 0.05 1 755 . 78 LEU HB2 H 1.4400 0.02 1 756 . 78 LEU HB3 H 1.4400 0.02 1 757 . 78 LEU HG H 1.5600 0.02 1 758 . 78 LEU CD1 C 27.7500 0.05 1 759 . 78 LEU HD1 H 0.8400 0.02 1 760 . 78 LEU CD2 C 24.5200 0.05 1 761 . 78 LEU HD2 H 0.9000 0.02 1 762 . 79 GLY N N 114.7500 0.05 1 763 . 79 GLY H H 8.8000 0.02 1 764 . 79 GLY CA C 47.4800 0.05 1 765 . 79 GLY HA3 H 4.0200 0.02 1 766 . 79 GLY HA2 H 3.6900 0.02 1 767 . 80 GLN N N 124.9500 0.05 1 768 . 80 GLN H H 8.9500 0.02 1 769 . 80 GLN CA C 56.3700 0.05 1 770 . 80 GLN HA H 4.4400 0.02 1 771 . 80 GLN CB C 29.8000 0.05 1 772 . 80 GLN HB2 H 2.0000 0.02 1 773 . 80 GLN CG C 34.4100 0.05 1 774 . 80 GLN HG2 H 2.4400 0.02 1 775 . 80 GLN HG3 H 2.4400 0.02 1 776 . 81 VAL N N 117.8800 0.05 1 777 . 81 VAL H H 7.6800 0.02 1 778 . 81 VAL CA C 60.5600 0.05 1 779 . 81 VAL HA H 3.9500 0.02 1 780 . 81 VAL CB C 36.2000 0.05 1 781 . 81 VAL HB H 2.0900 0.02 1 782 . 81 VAL CG1 C 22.3800 0.05 1 783 . 81 VAL HG1 H 0.9000 0.02 1 784 . 81 VAL CG2 C 19.5800 0.05 1 785 . 81 VAL HG2 H 0.8100 0.02 1 786 . 82 ALA N N 129.3400 0.05 1 787 . 82 ALA H H 8.3200 0.02 1 788 . 82 ALA CA C 51.0600 0.05 1 789 . 82 ALA HA H 4.0400 0.02 1 790 . 82 ALA CB C 23.6200 0.05 1 791 . 82 ALA HB H 0.8400 0.02 1 792 . 83 ILE N N 120.9400 0.05 1 793 . 83 ILE H H 8.8000 0.02 1 794 . 83 ILE CA C 61.8900 0.05 1 795 . 83 ILE HA H 4.6300 0.02 1 796 . 83 ILE CB C 40.0200 0.05 1 797 . 83 ILE HB H 0.1600 0.02 1 798 . 83 ILE CG1 C 29.2100 0.05 1 799 . 83 ILE HG13 H 1.1100 0.02 1 800 . 83 ILE HG12 H 0.6400 0.02 1 801 . 83 ILE CG2 C 19.2100 0.05 1 802 . 83 ILE HG2 H 0.3300 0.02 1 803 . 83 ILE CD1 C 15.3900 0.05 1 804 . 83 ILE HD1 H 0.4300 0.02 1 805 . 84 LEU N N 129.1800 0.05 1 806 . 84 LEU H H 9.3800 0.02 1 807 . 84 LEU CA C 53.9800 0.05 1 808 . 84 LEU HA H 5.2400 0.02 1 809 . 84 LEU CB C 45.9800 0.05 1 810 . 84 LEU HB2 H 1.5000 0.02 1 811 . 84 LEU HB3 H 2.1900 0.02 1 812 . 84 LEU HG H 1.7100 0.02 1 813 . 84 LEU CD1 C 26.1400 0.05 1 814 . 84 LEU HD1 H 0.8500 0.02 1 815 . 84 LEU CD2 C 27.0300 0.05 1 816 . 84 LEU HD2 H 0.9600 0.02 1 817 . 85 LEU N N 130.7000 0.05 1 818 . 85 LEU H H 8.7900 0.02 1 819 . 85 LEU CA C 54.4300 0.05 1 820 . 85 LEU HA H 5.6400 0.02 1 821 . 85 LEU CB C 46.9800 0.05 1 822 . 85 LEU HB2 H 1.2000 0.02 1 823 . 85 LEU HB3 H 1.8500 0.02 1 824 . 85 LEU CG C 27.7200 0.05 1 825 . 85 LEU HG H 1.3700 0.02 1 826 . 85 LEU CD1 C 23.0600 0.05 1 827 . 85 LEU HD1 H 0.6800 0.02 1 828 . 85 LEU CD2 C 24.1200 0.05 1 829 . 85 LEU HD2 H -0.4400 0.02 1 830 . 86 PHE N N 121.0000 0.05 1 831 . 86 PHE H H 8.6900 0.02 1 832 . 86 PHE CA C 56.4200 0.05 1 833 . 86 PHE HA H 5.6400 0.02 1 834 . 86 PHE CB C 42.5000 0.05 1 835 . 86 PHE HB2 H 3.3000 0.02 1 836 . 86 PHE HB3 H 3.4200 0.02 1 837 . 86 PHE HD1 H 6.5700 0.02 1 838 . 86 PHE HD2 H 6.5700 0.02 1 839 . 86 PHE HE1 H 6.9700 0.02 1 840 . 86 PHE HE2 H 6.9700 0.02 1 841 . 86 PHE HZ H 7.2200 0.02 1 842 . 87 LYS N N 123.2200 0.05 1 843 . 87 LYS H H 7.5700 0.02 1 844 . 87 LYS CA C 54.4300 0.05 1 845 . 87 LYS HA H 4.6000 0.02 1 846 . 87 LYS CB C 37.4100 0.05 1 847 . 87 LYS HB3 H 0.9500 0.02 1 848 . 87 LYS HB2 H -0.7500 0.02 1 849 . 87 LYS HG2 H 0.2000 0.02 1 850 . 87 LYS HD2 H 0.7200 0.02 1 851 . 87 LYS HE2 H 3.7500 0.02 1 852 . 87 LYS HE3 H 3.7500 0.02 1 853 . 88 SER N N 118.9700 0.05 1 854 . 88 SER H H 8.3200 0.02 1 855 . 88 SER CA C 60.3900 0.05 1 856 . 88 SER HA H 4.6100 0.02 1 857 . 88 SER CB C 65.3600 0.05 1 858 . 88 SER HB2 H 3.7500 0.02 1 859 . 88 SER HB3 H 3.7500 0.02 1 860 . 89 GLY N N 125.5400 0.05 1 861 . 89 GLY H H 8.7400 0.02 1 862 . 89 GLY CA C 46.5200 0.05 1 863 . 89 GLY HA3 H 3.8100 0.02 1 864 . 89 GLY HA2 H 3.6600 0.02 1 stop_ save_