data_476 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID 476 _Entry.Title ; 1H NMR Sequential Assignments and Secondary Structure Analysis of Human Fibrinogen gamma-Chain C-Terminal Residues 385-411 ; _Entry.Type macromolecule _Entry.Version_type update _Entry.Submission_date 1995-07-31 _Entry.Accession_date 1996-03-25 _Entry.Last_release_date . _Entry.Original_release_date . _Entry.Origination BMRB _Entry.NMR_STAR_version 3.1.1.61 _Entry.Original_NMR_STAR_version 2.1 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype . _Entry.Details . _Entry.BMRB_internal_directory_name . loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Middle_initials _Entry_author.Family_title _Entry_author.Entry_ID 1 Kevin Mayo . H. . 476 2 Carl Burke . . . 476 3 J. Lindon . N. . 476 4 Marek Kloczewiak . A. . 476 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID assigned_chemical_shifts 1 476 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 195 476 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 4 . . 2010-06-11 . revision BMRB 'Complete natural source information' 476 3 . . 1999-06-14 . revision BMRB 'Converted to BMRB NMR-STAR V 2.1 format' 476 2 . . 1996-03-25 . reformat BMRB 'Converted to the BMRB 1996-03-01 STAR flat-file format' 476 1 . . 1995-07-31 . original BMRB 'Last release in original BMRB flat-file format' 476 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID 476 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.CAS_abstract_code . _Citation.MEDLINE_UI_code . _Citation.DOI . _Citation.PubMed_ID . _Citation.Full_citation ; Mayo, Kevin H., Burke, Carl, Lindon, J.N., Kloczewiak, Marek A., "1H NMR Sequential Assignments and Secondary Structure Analysis of Human Fibrinogen gamma-Chain C-Terminal Residues 385-411," Biochemistry 29, 3277-3286 (1990). ; _Citation.Title ; 1H NMR Sequential Assignments and Secondary Structure Analysis of Human Fibrinogen gamma-Chain C-Terminal Residues 385-411 ; _Citation.Status published _Citation.Type journal _Citation.Journal_abbrev Biochemistry _Citation.Journal_name_full . _Citation.Journal_volume 29 _Citation.Journal_issue . _Citation.Journal_ASTM . _Citation.Journal_ISSN . _Citation.Journal_CSD . _Citation.Book_title . _Citation.Book_chapter_title . _Citation.Book_volume . _Citation.Book_series . _Citation.Book_publisher . _Citation.Book_publisher_city . _Citation.Book_ISBN . _Citation.Conference_title . _Citation.Conference_site . _Citation.Conference_state_province . _Citation.Conference_country . _Citation.Conference_start_date . _Citation.Conference_end_date . _Citation.Conference_abstract_number . _Citation.Thesis_institution . _Citation.Thesis_institution_city . _Citation.Thesis_institution_country . _Citation.WWW_URL . _Citation.Page_first 3277 _Citation.Page_last 3286 _Citation.Year 1990 _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 Kevin Mayo . H. . 476 1 2 Carl Burke . . . 476 1 3 J. Lindon . N. . 476 1 4 Marek Kloczewiak . A. . 476 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_system_fibrinogen _Assembly.Sf_category assembly _Assembly.Sf_framecode system_fibrinogen _Assembly.Entry_ID 476 _Assembly.ID 1 _Assembly.Name fibrinogen _Assembly.BMRB_code . _Assembly.Number_of_components . _Assembly.Organic_ligands . _Assembly.Metal_ions . _Assembly.Non_standard_bonds . _Assembly.Ambiguous_conformational_states . _Assembly.Ambiguous_chem_comp_sites . _Assembly.Molecules_in_chemical_exchange . _Assembly.Paramagnetic . _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 fibrinogen 1 $fibrinogen . . . . . . . . . 476 1 stop_ loop_ _Assembly_common_name.Name _Assembly_common_name.Type _Assembly_common_name.Entry_ID _Assembly_common_name.Assembly_ID fibrinogen system 476 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_fibrinogen _Entity.Sf_category entity _Entity.Sf_framecode fibrinogen _Entity.Entry_ID 476 _Entity.ID 1 _Entity.BMRB_code . _Entity.Name fibrinogen _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 ; KIIPFNRLTIGEGQQHHLGG AKQAGDV ; _Entity.Polymer_seq_one_letter_code ; KIIPFNRLTIGEGQQHHLGG AKQAGDV ; _Entity.Target_identifier . _Entity.Polymer_author_defined_seq . _Entity.Polymer_author_seq_details . _Entity.Ambiguous_conformational_states . _Entity.Ambiguous_chem_comp_sites . _Entity.Nstd_monomer . _Entity.Nstd_chirality . _Entity.Nstd_linkage . _Entity.Nonpolymer_comp_ID . _Entity.Nonpolymer_comp_label . _Entity.Number_of_monomers 27 _Entity.Number_of_nonpolymer_components . _Entity.Paramagnetic . _Entity.Thiol_state . _Entity.Src_method . _Entity.Parent_entity_ID 1 _Entity.Fragment . _Entity.Mutation . _Entity.EC_number . _Entity.Calc_isoelectric_point . _Entity.Formula_weight . _Entity.Formula_weight_exptl . _Entity.Formula_weight_exptl_meth . _Entity.Details . _Entity.DB_query_date . _Entity.DB_query_revised_last_date 2015-01-29 loop_ _Entity_db_link.Ordinal _Entity_db_link.Author_supplied _Entity_db_link.Database_code _Entity_db_link.Accession_code _Entity_db_link.Entry_mol_code _Entity_db_link.Entry_mol_name _Entity_db_link.Entry_experimental_method _Entity_db_link.Entry_structure_resolution _Entity_db_link.Entry_relation_type _Entity_db_link.Entry_details _Entity_db_link.Chimera_segment_ID _Entity_db_link.Seq_query_to_submitted_percent _Entity_db_link.Seq_subject_length _Entity_db_link.Seq_identity _Entity_db_link.Seq_positive _Entity_db_link.Seq_homology_expectation_val _Entity_db_link.Seq_align_begin _Entity_db_link.Seq_align_end _Entity_db_link.Seq_difference_details _Entity_db_link.Seq_alignment_details _Entity_db_link.Entry_ID _Entity_db_link.Entity_ID 1 no PDB 1DUG . "Structure Of The Fibrinogen G Chain Integrin Binding And Factor Xiiia Crosslinking Sites Obtained Through Carrier Protein Drive" . . . . . 51.85 234 100.00 100.00 2.16e+00 . . . . 476 1 2 no PDB 1FIB . "Recombinant Human Gamma-Fibrinogen Carboxyl Terminal Fragment (Residues 143-411) Bound To Calcium At Ph 6.0" . . . . . 100.00 269 100.00 100.00 6.24e-09 . . . . 476 1 3 no PDB 1FIC . "Structure Of Human Gamma Fibrinogen 30 Kd Carboxyl Terminal Fragment" . . . . . 100.00 269 100.00 100.00 6.24e-09 . . . . 476 1 4 no PDB 1FID . "Structure Of Human Gamma Fibrinogen 30 Kd Carboxyl Terminal Fragment" . . . . . 100.00 269 100.00 100.00 6.24e-09 . . . . 476 1 5 no PDB 1FZA . "Crystal Structure Of Fibrinogen Fragment D" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 6 no PDB 1FZB . "Crystal Structure Of Crosslinked Fragment D" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 7 no PDB 1FZC . "Crystal Structure Of Fragment Double-d From Human Fibrin With Two Different Bound Ligands" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 8 no PDB 1FZE . "Crystal Structure Of Fragment Double-D From Human Fibrin" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 9 no PDB 1FZF . "Crystal Structure Of Fragment Double-D From Human Fibrin With The Peptide Ligand Gly-His-Arg-Pro-Amide" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 10 no PDB 1FZG . "Crystal Structure Of Fragment D From Human Fibrinogen With The Peptide Ligand Gly-His-Arg-Pro-Amide" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 11 no PDB 1LSG . "Three-Dimensional Structure Of The Platelet Integrin Recognition Segment Of The Fibrinogen Gamma Chain Obtained By Carrier Prot" . . . . . 51.85 144 100.00 100.00 8.29e-01 . . . . 476 1 12 no PDB 1LT9 . "Crystal Structure Of Recombinant Human Fibrinogen Fragment D" . . . . . 81.48 311 100.00 100.00 1.22e-05 . . . . 476 1 13 no PDB 1LTJ . "Crystal Structure Of Recombinant Human Fibrinogen Fragment D With The Peptide Ligands Gly-Pro-Arg-Pro-Amide And Gly-His-Arg-Pro" . . . . . 81.48 311 100.00 100.00 1.22e-05 . . . . 476 1 14 no PDB 1N86 . "Crystal Structure Of Human D-Dimer From Cross-Linked Fibrin Complexed With Gpr And Ghrpldk Peptide Ligands." . . . . . 100.00 324 100.00 100.00 4.83e-09 . . . . 476 1 15 no PDB 1N8E . "Fragment Double-D From Human Fibrin" . . . . . 100.00 324 100.00 100.00 4.83e-09 . . . . 476 1 16 no PDB 1RE3 . "Crystal Structure Of Fragment D Of Bbetad398a Fibrinogen With The Peptide Ligand Gly-his-arg-pro-amide" . . . . . 81.48 311 100.00 100.00 1.22e-05 . . . . 476 1 17 no PDB 1RE4 . "Crystal Structure Of Fragment D Of Bbetad398a Fibrinogen" . . . . . 81.48 311 100.00 100.00 1.22e-05 . . . . 476 1 18 no PDB 1RF0 . "Crystal Structure Of Fragment D Of Gammae132a Fibrinogen" . . . . . 81.48 311 100.00 100.00 1.18e-05 . . . . 476 1 19 no PDB 1RF1 . "Crystal Structure Of Fragment D Of Gammae132a Fibrinogen With The Peptide Ligand Gly-His-Arg-Pro-Amide" . . . . . 81.48 311 100.00 100.00 1.18e-05 . . . . 476 1 20 no PDB 2FFD . 'Fibrinogen Fragment D With "a" Knob Peptide Mimic Gprvve' . . . . . 81.48 311 100.00 100.00 1.22e-05 . . . . 476 1 21 no PDB 2FIB . "Recombinant Human Gamma-Fibrinogen Carboxyl Terminal Fragment (Residues 143-411) Complexed To The Peptide Gly- Pro-Arg-Pro At P" . . . . . 100.00 269 100.00 100.00 6.24e-09 . . . . 476 1 22 no PDB 2H43 . "Crystal Structure Of Human Fragment D Complexed With Ala-His-Arg-Pro- Amide" . . . . . 100.00 323 100.00 100.00 4.70e-09 . . . . 476 1 23 no PDB 2HLO . "Crystal Structure Of Fragment D-Dimer From Human Fibrin Complexed With Gly-Hydroxypro-Arg-Pro-Amide" . . . . . 100.00 324 100.00 100.00 4.83e-09 . . . . 476 1 24 no PDB 2HOD . "Crystal Structure Of Fragment D From Human Fibrinogen Complexed With Gly-hydroxypro-arg-pro-amide" . . . . . 100.00 323 100.00 100.00 4.70e-09 . . . . 476 1 25 no PDB 2HPC . "Crystal Structure Of Fragment D From Human Fibrinogen Complexed With Gly-Pro-Arg-Pro-Amide" . . . . . 100.00 323 100.00 100.00 4.70e-09 . . . . 476 1 26 no PDB 2OYH . "Crystal Structure Of Fragment D Of Gammad298,301a Fibrinogen With The Peptide Ligand Gly-His-Arg-Pro-Amide" . . . . . 81.48 311 100.00 100.00 1.30e-05 . . . . 476 1 27 no PDB 2OYI . "Crystal Structure Of Fragment D Of Gammad298,301a Fibrinogen With The Peptide Ligand Gly-Pro-Arg-Pro-Amide" . . . . . 81.48 311 100.00 100.00 1.30e-05 . . . . 476 1 28 no PDB 2Q9I . "Crystal Structure Of D-dimer From Human Fibrin Complexed With Met-his- Arg-pro-tyr-amide" . . . . . 100.00 324 100.00 100.00 4.83e-09 . . . . 476 1 29 no PDB 2XNX . "Bc1 Fragment Of Streptococcal M1 Protein In Complex With Human Fibrinogen" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 30 no PDB 2XNY . "A Fragment Of Streptococcal M1 Protein In Complex With Human Fibrinogen" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 31 no PDB 2Y7L . "Structure Of N-Terminal Domain Of Candida Albicans Als9-2 In Complex With Human Fibrinogen Gamma Peptide" . . . . . 62.96 17 100.00 100.00 2.17e-01 . . . . 476 1 32 no PDB 2Z4E . "Crystal Structure Of D-dimer From Human Fibrin Complexed With Gly-his- Arg-pro-tyr-amide" . . . . . 100.00 324 100.00 100.00 4.83e-09 . . . . 476 1 33 no PDB 3E1I . "Crystal Structure Of Bbetad432a Variant Fibrinogen Fragment D With The Peptide Ligand Gly-his-arg-pro-amide" . . . . . 81.48 319 100.00 100.00 1.16e-05 . . . . 476 1 34 no PDB 3GHG . "Crystal Structure Of Human Fibrinogen" . . . . . 100.00 411 100.00 100.00 1.75e-09 . . . . 476 1 35 no PDB 3H32 . "Crystal Structure Of D-Dimer From Human Fibrin Complexed With Gly-His- Arg-Pro-Tyr-Amide" . . . . . 100.00 317 100.00 100.00 5.30e-09 . . . . 476 1 36 no PDB 3HUS . "Crystal Structure Of Recombinant Gamma N308k Fibrinogen Fragment D With The Peptide Ligand Gly-Pro-Arg-Pro-Amide" . . . . . 81.48 311 100.00 100.00 1.26e-05 . . . . 476 1 37 no PDB 4B60 . "Structure Of Rfnbpa(189-505) In Complex With Fibrinogen Gamma Chain C-terminal Peptide" . . . . . 62.96 17 100.00 100.00 2.17e-01 . . . . 476 1 38 no DBJ BAF82111 . "unnamed protein product [Homo sapiens]" . . . . . 85.19 453 100.00 100.00 4.31e-07 . . . . 476 1 39 no DBJ BAF83513 . "unnamed protein product [Homo sapiens]" . . . . . 100.00 437 100.00 100.00 8.71e-10 . . . . 476 1 40 no DBJ BAI46090 . "fibrinogen gamma chain [synthetic construct]" . . . . . 85.19 453 100.00 100.00 4.31e-07 . . . . 476 1 41 no EMBL CAD98014 . "hypothetical protein [Homo sapiens]" . . . . . 100.00 399 100.00 100.00 4.16e-09 . . . . 476 1 42 no GB AAA52430 . "gamma fibrinogen type B (AA at 202), partial [Homo sapiens]" . . . . . 85.19 169 100.00 100.00 4.78e-07 . . . . 476 1 43 no GB AAA52431 . "gamma fibrinogen type A (AA at 202), partial [Homo sapiens]" . . . . . 100.00 153 100.00 100.00 2.82e-09 . . . . 476 1 44 no GB AAB59530 . "fibrinogen gamma-prime chain [Homo sapiens]" . . . . . 85.19 453 100.00 100.00 4.19e-07 . . . . 476 1 45 no GB AAB59531 . "fibrinogen gamma chain [Homo sapiens]" . . . . . 100.00 437 100.00 100.00 8.71e-10 . . . . 476 1 46 no GB AAF22036 . "PRO2061 [Homo sapiens]" . . . . . 100.00 437 100.00 100.00 8.71e-10 . . . . 476 1 47 no PRF 0602239A . "fibrinogen gamma" . . . . . 100.00 410 100.00 100.00 2.08e-09 . . . . 476 1 48 no REF NP_000500 . "fibrinogen gamma chain isoform gamma-A precursor [Homo sapiens]" . . . . . 100.00 437 100.00 100.00 8.71e-10 . . . . 476 1 49 no REF NP_068656 . "fibrinogen gamma chain isoform gamma-B precursor [Homo sapiens]" . . . . . 85.19 453 100.00 100.00 4.31e-07 . . . . 476 1 50 no REF XP_001089651 . "PREDICTED: fibrinogen gamma chain isoform 2 [Macaca mulatta]" . . . . . 85.19 453 100.00 100.00 4.31e-07 . . . . 476 1 51 no REF XP_001090810 . "PREDICTED: fibrinogen gamma chain isoform 9 [Macaca mulatta]" . . . . . 100.00 437 100.00 100.00 8.54e-10 . . . . 476 1 52 no REF XP_001138780 . "PREDICTED: fibrinogen gamma chain isoform X2 [Pan troglodytes]" . . . . . 100.00 437 100.00 100.00 8.97e-10 . . . . 476 1 53 no SP P02679 . "RecName: Full=Fibrinogen gamma chain; Flags: Precursor [Homo sapiens]" . . . . . 85.19 453 100.00 100.00 4.31e-07 . . . . 476 1 stop_ loop_ _Entity_common_name.Name _Entity_common_name.Type _Entity_common_name.Entry_ID _Entity_common_name.Entity_ID fibrinogen common 476 1 'gamma-chain C-terminal residues 384-411' variant 476 1 stop_ loop_ _Entity_comp_index.ID _Entity_comp_index.Auth_seq_ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 . LYS . 476 1 2 . ILE . 476 1 3 . ILE . 476 1 4 . PRO . 476 1 5 . PHE . 476 1 6 . ASN . 476 1 7 . ARG . 476 1 8 . LEU . 476 1 9 . THR . 476 1 10 . ILE . 476 1 11 . GLY . 476 1 12 . GLU . 476 1 13 . GLY . 476 1 14 . GLN . 476 1 15 . GLN . 476 1 16 . HIS . 476 1 17 . HIS . 476 1 18 . LEU . 476 1 19 . GLY . 476 1 20 . GLY . 476 1 21 . ALA . 476 1 22 . LYS . 476 1 23 . GLN . 476 1 24 . ALA . 476 1 25 . GLY . 476 1 26 . ASP . 476 1 27 . VAL . 476 1 stop_ loop_ _Entity_poly_seq.Hetero _Entity_poly_seq.Mon_ID _Entity_poly_seq.Num _Entity_poly_seq.Comp_index_ID _Entity_poly_seq.Entry_ID _Entity_poly_seq.Entity_ID . LYS 1 1 476 1 . ILE 2 2 476 1 . ILE 3 3 476 1 . PRO 4 4 476 1 . PHE 5 5 476 1 . ASN 6 6 476 1 . ARG 7 7 476 1 . LEU 8 8 476 1 . THR 9 9 476 1 . ILE 10 10 476 1 . GLY 11 11 476 1 . GLU 12 12 476 1 . GLY 13 13 476 1 . GLN 14 14 476 1 . GLN 15 15 476 1 . HIS 16 16 476 1 . HIS 17 17 476 1 . LEU 18 18 476 1 . GLY 19 19 476 1 . GLY 20 20 476 1 . ALA 21 21 476 1 . LYS 22 22 476 1 . GLN 23 23 476 1 . ALA 24 24 476 1 . GLY 25 25 476 1 . ASP 26 26 476 1 . VAL 27 27 476 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 476 _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 $fibrinogen . 9606 organism . 'Homo sapiens' human . . Eukaryota Metazoa Homo sapiens generic . . . . . . . . . . . . . . . . . . . . 476 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 476 _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 $fibrinogen . 'not available' . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 476 1 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_one _Sample.Sf_category sample _Sample.Sf_framecode sample_one _Sample.Entry_ID 476 _Sample.ID 1 _Sample.Type solution _Sample.Sub_type . _Sample.Details . _Sample.Aggregate_sample_number . _Sample.Solvent_system . _Sample.Preparation_date . _Sample.Preparation_expiration_date . _Sample.Polycrystallization_protocol . _Sample.Single_crystal_protocol . _Sample.Crystal_grow_apparatus . _Sample.Crystal_grow_atmosphere . _Sample.Crystal_grow_details . _Sample.Crystal_grow_method . _Sample.Crystal_grow_method_cit_ID . _Sample.Crystal_grow_pH . _Sample.Crystal_grow_pH_range . _Sample.Crystal_grow_pressure . _Sample.Crystal_grow_pressure_esd . _Sample.Crystal_grow_seeding . _Sample.Crystal_grow_seeding_cit_ID . _Sample.Crystal_grow_temp . _Sample.Crystal_grow_temp_details . _Sample.Crystal_grow_temp_esd . _Sample.Crystal_grow_time . _Sample.Oriented_sample_prep_protocol . _Sample.Lyophilization_cryo_protectant . _Sample.Storage_protocol . save_ ####################### # Sample conditions # ####################### save_sample_condition_set_one _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_condition_set_one _Sample_condition_list.Entry_ID 476 _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 3 . na 476 1 temperature 303 . K 476 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_spectrometer_list _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode spectrometer_list _NMR_spectrometer.Entry_ID 476 _NMR_spectrometer.ID 1 _NMR_spectrometer.Details 'spectrometer information not available' _NMR_spectrometer.Manufacturer unknown _NMR_spectrometer.Model unknown _NMR_spectrometer.Serial_number . _NMR_spectrometer.Field_strength 0 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 476 _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 unknown unknown . 0 'spectrometer information not available' . . 476 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 476 _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 . . . . . . . . . . . . 1 $sample_one . . . 1 $sample_condition_set_one . . . 1 $spectrometer_list . . . . . . . . . . . . . . . . 476 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_reference_par_set_one _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference_par_set_one _Chem_shift_reference.Entry_ID 476 _Chem_shift_reference.ID 1 _Chem_shift_reference.Details . loop_ _Chem_shift_ref.Atom_type _Chem_shift_ref.Atom_isotope_number _Chem_shift_ref.Mol_common_name _Chem_shift_ref.Atom_group _Chem_shift_ref.Concentration_val _Chem_shift_ref.Concentration_units _Chem_shift_ref.Solvent _Chem_shift_ref.Rank _Chem_shift_ref.Chem_shift_units _Chem_shift_ref.Chem_shift_val _Chem_shift_ref.Ref_method _Chem_shift_ref.Ref_type _Chem_shift_ref.Indirect_shift_ratio _Chem_shift_ref.External_ref_loc _Chem_shift_ref.External_ref_sample_geometry _Chem_shift_ref.External_ref_axis _Chem_shift_ref.Indirect_shift_ratio_cit_ID _Chem_shift_ref.Indirect_shift_ratio_cit_label _Chem_shift_ref.Ref_correction_type _Chem_shift_ref.Correction_val _Chem_shift_ref.Correction_val_cit_ID _Chem_shift_ref.Correction_val_cit_label _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H . TSP . . . . . ppm 0 . . . . . . 1 $entry_citation . . 1 $entry_citation 476 1 stop_ save_ ################################### # Assigned chemical shift lists # ################################### ################################################################### # Chemical Shift Ambiguity Index Value Definitions # # # # The values other than 1 are used for those atoms with different # # chemical shifts that cannot be assigned to stereospecific atoms # # or to specific residues or chains. # # # # Index Value Definition # # # # 1 Unique (including isolated methyl protons, # # geminal atoms, and geminal methyl # # groups with identical chemical shifts) # # (e.g. ILE HD11, HD12, HD13 protons) # # 2 Ambiguity of geminal atoms or geminal methyl # # proton groups (e.g. ASP HB2 and HB3 # # protons, LEU CD1 and CD2 carbons, or # # LEU HD11, HD12, HD13 and HD21, HD22, # # HD23 methyl protons) # # 3 Aromatic atoms on opposite sides of # # symmetrical rings (e.g. TYR HE1 and HE2 # # protons) # # 4 Intraresidue ambiguities (e.g. LYS HG and # # HD protons or TRP HZ2 and HZ3 protons) # # 5 Interresidue ambiguities (LYS 12 vs. LYS 27) # # 6 Intermolecular ambiguities (e.g. ASP 31 CA # # in monomer 1 and ASP 31 CA in monomer 2 # # of an asymmetrical homodimer, duplex # # DNA assignments, or other assignments # # that may apply to atoms in one or more # # molecule in the molecular assembly) # # 9 Ambiguous, specific ambiguity not defined # # # ################################################################### save_chemical_shift_assignment_data_set_one _Assigned_chem_shift_list.Sf_category assigned_chemical_shifts _Assigned_chem_shift_list.Sf_framecode 'chemical_shift_assignment_data_set_one' _Assigned_chem_shift_list.Entry_ID 476 _Assigned_chem_shift_list.ID 1 _Assigned_chem_shift_list.Sample_condition_list_ID 1 _Assigned_chem_shift_list.Sample_condition_list_label $sample_condition_set_one _Assigned_chem_shift_list.Chem_shift_reference_ID 1 _Assigned_chem_shift_list.Chem_shift_reference_label $chem_shift_reference_par_set_one _Assigned_chem_shift_list.Chem_shift_1H_err . _Assigned_chem_shift_list.Chem_shift_13C_err . _Assigned_chem_shift_list.Chem_shift_15N_err . _Assigned_chem_shift_list.Chem_shift_31P_err . _Assigned_chem_shift_list.Chem_shift_2H_err . _Assigned_chem_shift_list.Chem_shift_19F_err . _Assigned_chem_shift_list.Error_derivation_method . _Assigned_chem_shift_list.Details . _Assigned_chem_shift_list.Text_data_format . _Assigned_chem_shift_list.Text_data . loop_ _Chem_shift_experiment.Experiment_ID _Chem_shift_experiment.Experiment_name _Chem_shift_experiment.Sample_ID _Chem_shift_experiment.Sample_label _Chem_shift_experiment.Sample_state _Chem_shift_experiment.Entry_ID _Chem_shift_experiment.Assigned_chem_shift_list_ID . . 1 $sample_one . 476 1 stop_ loop_ _Atom_chem_shift.ID _Atom_chem_shift.Assembly_atom_ID _Atom_chem_shift.Entity_assembly_ID _Atom_chem_shift.Entity_ID _Atom_chem_shift.Comp_index_ID _Atom_chem_shift.Seq_ID _Atom_chem_shift.Comp_ID _Atom_chem_shift.Atom_ID _Atom_chem_shift.Atom_type _Atom_chem_shift.Atom_isotope_number _Atom_chem_shift.Val _Atom_chem_shift.Val_err _Atom_chem_shift.Assign_fig_of_merit _Atom_chem_shift.Ambiguity_code _Atom_chem_shift.Occupancy _Atom_chem_shift.Resonance_ID _Atom_chem_shift.Auth_entity_assembly_ID _Atom_chem_shift.Auth_asym_ID _Atom_chem_shift.Auth_seq_ID _Atom_chem_shift.Auth_comp_ID _Atom_chem_shift.Auth_atom_ID _Atom_chem_shift.Details _Atom_chem_shift.Entry_ID _Atom_chem_shift.Assigned_chem_shift_list_ID 1 . 1 1 1 1 LYS HA H 1 4.1 . . 1 . . . . . . . . 476 1 2 . 1 1 1 1 LYS HB2 H 1 1.91 . . 1 . . . . . . . . 476 1 3 . 1 1 1 1 LYS HB3 H 1 1.91 . . 1 . . . . . . . . 476 1 4 . 1 1 1 1 LYS HG2 H 1 1.43 . . 1 . . . . . . . . 476 1 5 . 1 1 1 1 LYS HG3 H 1 1.43 . . 1 . . . . . . . . 476 1 6 . 1 1 1 1 LYS HD2 H 1 1.72 . . 1 . . . . . . . . 476 1 7 . 1 1 1 1 LYS HD3 H 1 1.72 . . 1 . . . . . . . . 476 1 8 . 1 1 1 1 LYS HE2 H 1 3.03 . . 1 . . . . . . . . 476 1 9 . 1 1 1 1 LYS HE3 H 1 3.03 . . 1 . . . . . . . . 476 1 10 . 1 1 1 1 LYS HZ1 H 1 7.62 . . 1 . . . . . . . . 476 1 11 . 1 1 1 1 LYS HZ2 H 1 7.62 . . 1 . . . . . . . . 476 1 12 . 1 1 1 1 LYS HZ3 H 1 7.62 . . 1 . . . . . . . . 476 1 13 . 1 1 2 2 ILE H H 1 8.62 . . 1 . . . . . . . . 476 1 14 . 1 1 2 2 ILE HA H 1 4.22 . . 1 . . . . . . . . 476 1 15 . 1 1 2 2 ILE HB H 1 1.82 . . 1 . . . . . . . . 476 1 16 . 1 1 2 2 ILE HG12 H 1 1.42 . . 2 . . . . . . . . 476 1 17 . 1 1 2 2 ILE HG13 H 1 1.15 . . 2 . . . . . . . . 476 1 18 . 1 1 2 2 ILE HG21 H 1 .95 . . 1 . . . . . . . . 476 1 19 . 1 1 2 2 ILE HG22 H 1 .95 . . 1 . . . . . . . . 476 1 20 . 1 1 2 2 ILE HG23 H 1 .95 . . 1 . . . . . . . . 476 1 21 . 1 1 2 2 ILE HD11 H 1 .84 . . 1 . . . . . . . . 476 1 22 . 1 1 2 2 ILE HD12 H 1 .84 . . 1 . . . . . . . . 476 1 23 . 1 1 2 2 ILE HD13 H 1 .84 . . 1 . . . . . . . . 476 1 24 . 1 1 3 3 ILE H H 1 8.46 . . 1 . . . . . . . . 476 1 25 . 1 1 3 3 ILE HA H 1 4.51 . . 1 . . . . . . . . 476 1 26 . 1 1 3 3 ILE HB H 1 1.87 . . 1 . . . . . . . . 476 1 27 . 1 1 3 3 ILE HG12 H 1 1.5 . . 2 . . . . . . . . 476 1 28 . 1 1 3 3 ILE HG13 H 1 1.18 . . 2 . . . . . . . . 476 1 29 . 1 1 3 3 ILE HG21 H 1 .9 . . 1 . . . . . . . . 476 1 30 . 1 1 3 3 ILE HG22 H 1 .9 . . 1 . . . . . . . . 476 1 31 . 1 1 3 3 ILE HG23 H 1 .9 . . 1 . . . . . . . . 476 1 32 . 1 1 3 3 ILE HD11 H 1 .85 . . 1 . . . . . . . . 476 1 33 . 1 1 3 3 ILE HD12 H 1 .85 . . 1 . . . . . . . . 476 1 34 . 1 1 3 3 ILE HD13 H 1 .85 . . 1 . . . . . . . . 476 1 35 . 1 1 4 4 PRO HA H 1 4.4 . . 1 . . . . . . . . 476 1 36 . 1 1 4 4 PRO HB2 H 1 2.26 . . 2 . . . . . . . . 476 1 37 . 1 1 4 4 PRO HB3 H 1 1.88 . . 2 . . . . . . . . 476 1 38 . 1 1 4 4 PRO HG2 H 1 2.03 . . 1 . . . . . . . . 476 1 39 . 1 1 4 4 PRO HG3 H 1 2.03 . . 1 . . . . . . . . 476 1 40 . 1 1 4 4 PRO HD2 H 1 3.92 . . 2 . . . . . . . . 476 1 41 . 1 1 4 4 PRO HD3 H 1 3.71 . . 2 . . . . . . . . 476 1 42 . 1 1 5 5 PHE H H 1 8.21 . . 1 . . . . . . . . 476 1 43 . 1 1 5 5 PHE HA H 1 4.54 . . 1 . . . . . . . . 476 1 44 . 1 1 5 5 PHE HB2 H 1 3.11 . . 2 . . . . . . . . 476 1 45 . 1 1 5 5 PHE HB3 H 1 3.07 . . 2 . . . . . . . . 476 1 46 . 1 1 5 5 PHE HD1 H 1 7.24 . . 1 . . . . . . . . 476 1 47 . 1 1 5 5 PHE HD2 H 1 7.24 . . 1 . . . . . . . . 476 1 48 . 1 1 5 5 PHE HE1 H 1 7.33 . . 1 . . . . . . . . 476 1 49 . 1 1 5 5 PHE HE2 H 1 7.33 . . 1 . . . . . . . . 476 1 50 . 1 1 5 5 PHE HZ H 1 7.29 . . 1 . . . . . . . . 476 1 51 . 1 1 6 6 ASN H H 1 8.24 . . 1 . . . . . . . . 476 1 52 . 1 1 6 6 ASN HA H 1 4.64 . . 1 . . . . . . . . 476 1 53 . 1 1 6 6 ASN HB2 H 1 2.77 . . 2 . . . . . . . . 476 1 54 . 1 1 6 6 ASN HB3 H 1 2.7 . . 2 . . . . . . . . 476 1 55 . 1 1 7 7 ARG H H 1 8.27 . . 1 . . . . . . . . 476 1 56 . 1 1 7 7 ARG HA H 1 4.24 . . 1 . . . . . . . . 476 1 57 . 1 1 7 7 ARG HB2 H 1 1.87 . . 2 . . . . . . . . 476 1 58 . 1 1 7 7 ARG HB3 H 1 1.77 . . 2 . . . . . . . . 476 1 59 . 1 1 7 7 ARG HG2 H 1 1.62 . . 1 . . . . . . . . 476 1 60 . 1 1 7 7 ARG HG3 H 1 1.62 . . 1 . . . . . . . . 476 1 61 . 1 1 7 7 ARG HD2 H 1 3.22 . . 1 . . . . . . . . 476 1 62 . 1 1 7 7 ARG HD3 H 1 3.22 . . 1 . . . . . . . . 476 1 63 . 1 1 7 7 ARG HE H 1 7.25 . . 1 . . . . . . . . 476 1 64 . 1 1 8 8 LEU H H 1 8.19 . . 1 . . . . . . . . 476 1 65 . 1 1 8 8 LEU HA H 1 4.4 . . 1 . . . . . . . . 476 1 66 . 1 1 8 8 LEU HB2 H 1 1.69 . . 2 . . . . . . . . 476 1 67 . 1 1 8 8 LEU HB3 H 1 1.59 . . 2 . . . . . . . . 476 1 68 . 1 1 8 8 LEU HG H 1 1.69 . . 1 . . . . . . . . 476 1 69 . 1 1 8 8 LEU HD11 H 1 .92 . . 2 . . . . . . . . 476 1 70 . 1 1 8 8 LEU HD12 H 1 .92 . . 2 . . . . . . . . 476 1 71 . 1 1 8 8 LEU HD13 H 1 .92 . . 2 . . . . . . . . 476 1 72 . 1 1 8 8 LEU HD21 H 1 .85 . . 2 . . . . . . . . 476 1 73 . 1 1 8 8 LEU HD22 H 1 .85 . . 2 . . . . . . . . 476 1 74 . 1 1 8 8 LEU HD23 H 1 .85 . . 2 . . . . . . . . 476 1 75 . 1 1 9 9 THR H H 1 8 . . 1 . . . . . . . . 476 1 76 . 1 1 9 9 THR HA H 1 4.33 . . 1 . . . . . . . . 476 1 77 . 1 1 9 9 THR HB H 1 4.24 . . 1 . . . . . . . . 476 1 78 . 1 1 9 9 THR HG21 H 1 1.17 . . 1 . . . . . . . . 476 1 79 . 1 1 9 9 THR HG22 H 1 1.17 . . 1 . . . . . . . . 476 1 80 . 1 1 9 9 THR HG23 H 1 1.17 . . 1 . . . . . . . . 476 1 81 . 1 1 10 10 ILE H H 1 8.01 . . 1 . . . . . . . . 476 1 82 . 1 1 10 10 ILE HA H 1 4.15 . . 1 . . . . . . . . 476 1 83 . 1 1 10 10 ILE HB H 1 1.59 . . 1 . . . . . . . . 476 1 84 . 1 1 10 10 ILE HG12 H 1 1.47 . . 2 . . . . . . . . 476 1 85 . 1 1 10 10 ILE HG13 H 1 1.2 . . 2 . . . . . . . . 476 1 86 . 1 1 10 10 ILE HG21 H 1 .99 . . 1 . . . . . . . . 476 1 87 . 1 1 10 10 ILE HG22 H 1 .99 . . 1 . . . . . . . . 476 1 88 . 1 1 10 10 ILE HG23 H 1 .99 . . 1 . . . . . . . . 476 1 89 . 1 1 10 10 ILE HD11 H 1 .94 . . 1 . . . . . . . . 476 1 90 . 1 1 10 10 ILE HD12 H 1 .94 . . 1 . . . . . . . . 476 1 91 . 1 1 10 10 ILE HD13 H 1 .94 . . 1 . . . . . . . . 476 1 92 . 1 1 11 11 GLY H H 1 8.47 . . 1 . . . . . . . . 476 1 93 . 1 1 11 11 GLY HA2 H 1 3.96 . . 1 . . . . . . . . 476 1 94 . 1 1 11 11 GLY HA3 H 1 3.96 . . 1 . . . . . . . . 476 1 95 . 1 1 12 12 GLU H H 1 8.25 . . 1 . . . . . . . . 476 1 96 . 1 1 12 12 GLU HA H 1 4.37 . . 1 . . . . . . . . 476 1 97 . 1 1 12 12 GLU HB2 H 1 2.16 . . 2 . . . . . . . . 476 1 98 . 1 1 12 12 GLU HB3 H 1 2.01 . . 2 . . . . . . . . 476 1 99 . 1 1 12 12 GLU HG2 H 1 2.47 . . 1 . . . . . . . . 476 1 100 . 1 1 12 12 GLU HG3 H 1 2.47 . . 1 . . . . . . . . 476 1 101 . 1 1 13 13 GLY H H 1 8.55 . . 1 . . . . . . . . 476 1 102 . 1 1 13 13 GLY HA2 H 1 3.97 . . 1 . . . . . . . . 476 1 103 . 1 1 13 13 GLY HA3 H 1 3.97 . . 1 . . . . . . . . 476 1 104 . 1 1 14 14 GLN H H 1 8.21 . . 1 . . . . . . . . 476 1 105 . 1 1 14 14 GLN HA H 1 4.3 . . 1 . . . . . . . . 476 1 106 . 1 1 14 14 GLN HB2 H 1 2.1 . . 2 . . . . . . . . 476 1 107 . 1 1 14 14 GLN HB3 H 1 1.95 . . 2 . . . . . . . . 476 1 108 . 1 1 14 14 GLN HG2 H 1 2.33 . . 1 . . . . . . . . 476 1 109 . 1 1 14 14 GLN HG3 H 1 2.33 . . 1 . . . . . . . . 476 1 110 . 1 1 14 14 GLN HE21 H 1 7.45 . . 2 . . . . . . . . 476 1 111 . 1 1 14 14 GLN HE22 H 1 6.83 . . 2 . . . . . . . . 476 1 112 . 1 1 15 15 GLN H H 1 8.37 . . 1 . . . . . . . . 476 1 113 . 1 1 15 15 GLN HA H 1 4.23 . . 1 . . . . . . . . 476 1 114 . 1 1 15 15 GLN HB2 H 1 1.9 . . 1 . . . . . . . . 476 1 115 . 1 1 15 15 GLN HB3 H 1 1.9 . . 1 . . . . . . . . 476 1 116 . 1 1 15 15 GLN HG2 H 1 2.31 . . 1 . . . . . . . . 476 1 117 . 1 1 15 15 GLN HG3 H 1 2.31 . . 1 . . . . . . . . 476 1 118 . 1 1 15 15 GLN HE21 H 1 7.51 . . 2 . . . . . . . . 476 1 119 . 1 1 15 15 GLN HE22 H 1 6.83 . . 2 . . . . . . . . 476 1 120 . 1 1 16 16 HIS H H 1 8.5 . . 1 . . . . . . . . 476 1 121 . 1 1 16 16 HIS HA H 1 4.62 . . 1 . . . . . . . . 476 1 122 . 1 1 16 16 HIS HB2 H 1 3.26 . . 2 . . . . . . . . 476 1 123 . 1 1 16 16 HIS HB3 H 1 3.15 . . 2 . . . . . . . . 476 1 124 . 1 1 16 16 HIS HD2 H 1 7.32 . . 1 . . . . . . . . 476 1 125 . 1 1 16 16 HIS HE1 H 1 8.67 . . 1 . . . . . . . . 476 1 126 . 1 1 17 17 HIS H H 1 8.6 . . 1 . . . . . . . . 476 1 127 . 1 1 17 17 HIS HA H 1 4.69 . . 1 . . . . . . . . 476 1 128 . 1 1 17 17 HIS HB2 H 1 3.27 . . 2 . . . . . . . . 476 1 129 . 1 1 17 17 HIS HB3 H 1 3.22 . . 2 . . . . . . . . 476 1 130 . 1 1 17 17 HIS HD2 H 1 7.31 . . 1 . . . . . . . . 476 1 131 . 1 1 17 17 HIS HE1 H 1 8.66 . . 1 . . . . . . . . 476 1 132 . 1 1 18 18 LEU H H 1 8.49 . . 1 . . . . . . . . 476 1 133 . 1 1 18 18 LEU HA H 1 4.39 . . 1 . . . . . . . . 476 1 134 . 1 1 18 18 LEU HB2 H 1 1.66 . . 2 . . . . . . . . 476 1 135 . 1 1 18 18 LEU HB3 H 1 1.6 . . 2 . . . . . . . . 476 1 136 . 1 1 18 18 LEU HG H 1 1.66 . . 1 . . . . . . . . 476 1 137 . 1 1 18 18 LEU HD11 H 1 .92 . . 2 . . . . . . . . 476 1 138 . 1 1 18 18 LEU HD12 H 1 .92 . . 2 . . . . . . . . 476 1 139 . 1 1 18 18 LEU HD13 H 1 .92 . . 2 . . . . . . . . 476 1 140 . 1 1 18 18 LEU HD21 H 1 .88 . . 2 . . . . . . . . 476 1 141 . 1 1 18 18 LEU HD22 H 1 .88 . . 2 . . . . . . . . 476 1 142 . 1 1 18 18 LEU HD23 H 1 .88 . . 2 . . . . . . . . 476 1 143 . 1 1 19 19 GLY H H 1 8.5 . . 1 . . . . . . . . 476 1 144 . 1 1 19 19 GLY HA2 H 1 3.98 . . 1 . . . . . . . . 476 1 145 . 1 1 19 19 GLY HA3 H 1 3.98 . . 1 . . . . . . . . 476 1 146 . 1 1 20 20 GLY H H 1 8.28 . . 1 . . . . . . . . 476 1 147 . 1 1 20 20 GLY HA2 H 1 4 . . 2 . . . . . . . . 476 1 148 . 1 1 20 20 GLY HA3 H 1 3.97 . . 2 . . . . . . . . 476 1 149 . 1 1 21 21 ALA H H 1 8.23 . . 1 . . . . . . . . 476 1 150 . 1 1 21 21 ALA HA H 1 4.33 . . 1 . . . . . . . . 476 1 151 . 1 1 21 21 ALA HB1 H 1 1.37 . . 1 . . . . . . . . 476 1 152 . 1 1 21 21 ALA HB2 H 1 1.37 . . 1 . . . . . . . . 476 1 153 . 1 1 21 21 ALA HB3 H 1 1.37 . . 1 . . . . . . . . 476 1 154 . 1 1 22 22 LYS H H 1 8.35 . . 1 . . . . . . . . 476 1 155 . 1 1 22 22 LYS HA H 1 4.3 . . 1 . . . . . . . . 476 1 156 . 1 1 22 22 LYS HB2 H 1 1.86 . . 1 . . . . . . . . 476 1 157 . 1 1 22 22 LYS HB3 H 1 1.86 . . 1 . . . . . . . . 476 1 158 . 1 1 22 22 LYS HG2 H 1 1.42 . . 1 . . . . . . . . 476 1 159 . 1 1 22 22 LYS HG3 H 1 1.42 . . 1 . . . . . . . . 476 1 160 . 1 1 22 22 LYS HD2 H 1 1.69 . . 1 . . . . . . . . 476 1 161 . 1 1 22 22 LYS HD3 H 1 1.69 . . 1 . . . . . . . . 476 1 162 . 1 1 22 22 LYS HE2 H 1 3.03 . . 1 . . . . . . . . 476 1 163 . 1 1 22 22 LYS HE3 H 1 3.03 . . 1 . . . . . . . . 476 1 164 . 1 1 22 22 LYS HZ1 H 1 7.62 . . 1 . . . . . . . . 476 1 165 . 1 1 22 22 LYS HZ2 H 1 7.62 . . 1 . . . . . . . . 476 1 166 . 1 1 22 22 LYS HZ3 H 1 7.62 . . 1 . . . . . . . . 476 1 167 . 1 1 23 23 GLN H H 1 8.36 . . 1 . . . . . . . . 476 1 168 . 1 1 23 23 GLN HA H 1 4.34 . . 1 . . . . . . . . 476 1 169 . 1 1 23 23 GLN HB2 H 1 2.09 . . 2 . . . . . . . . 476 1 170 . 1 1 23 23 GLN HB3 H 1 1.98 . . 2 . . . . . . . . 476 1 171 . 1 1 23 23 GLN HG2 H 1 2.36 . . 1 . . . . . . . . 476 1 172 . 1 1 23 23 GLN HG3 H 1 2.36 . . 1 . . . . . . . . 476 1 173 . 1 1 23 23 GLN HE21 H 1 7.55 . . 2 . . . . . . . . 476 1 174 . 1 1 23 23 GLN HE22 H 1 6.83 . . 2 . . . . . . . . 476 1 175 . 1 1 24 24 ALA H H 1 8.4 . . 1 . . . . . . . . 476 1 176 . 1 1 24 24 ALA HA H 1 4.32 . . 1 . . . . . . . . 476 1 177 . 1 1 24 24 ALA HB1 H 1 1.4 . . 1 . . . . . . . . 476 1 178 . 1 1 24 24 ALA HB2 H 1 1.4 . . 1 . . . . . . . . 476 1 179 . 1 1 24 24 ALA HB3 H 1 1.4 . . 1 . . . . . . . . 476 1 180 . 1 1 25 25 GLY H H 1 8.38 . . 1 . . . . . . . . 476 1 181 . 1 1 25 25 GLY HA2 H 1 3.97 . . 2 . . . . . . . . 476 1 182 . 1 1 25 25 GLY HA3 H 1 3.93 . . 2 . . . . . . . . 476 1 183 . 1 1 26 26 ASP H H 1 8.25 . . 1 . . . . . . . . 476 1 184 . 1 1 26 26 ASP HA H 1 4.8 . . 1 . . . . . . . . 476 1 185 . 1 1 26 26 ASP HB2 H 1 2.92 . . 2 . . . . . . . . 476 1 186 . 1 1 26 26 ASP HB3 H 1 2.82 . . 2 . . . . . . . . 476 1 187 . 1 1 27 27 VAL H H 1 7.93 . . 1 . . . . . . . . 476 1 188 . 1 1 27 27 VAL HA H 1 4.18 . . 1 . . . . . . . . 476 1 189 . 1 1 27 27 VAL HB H 1 2.13 . . 1 . . . . . . . . 476 1 190 . 1 1 27 27 VAL HG11 H 1 .93 . . 1 . . . . . . . . 476 1 191 . 1 1 27 27 VAL HG12 H 1 .93 . . 1 . . . . . . . . 476 1 192 . 1 1 27 27 VAL HG13 H 1 .93 . . 1 . . . . . . . . 476 1 193 . 1 1 27 27 VAL HG21 H 1 .93 . . 1 . . . . . . . . 476 1 194 . 1 1 27 27 VAL HG22 H 1 .93 . . 1 . . . . . . . . 476 1 195 . 1 1 27 27 VAL HG23 H 1 .93 . . 1 . . . . . . . . 476 1 stop_ save_