data_25680 ####################### # Entry information # ####################### save_entry_information _Saveframe_category entry_information _Entry_title ; FBP28 WW L453W ; _BMRB_accession_number 25680 _BMRB_flat_file_name bmr25680.str _Entry_type original _Submission_date 2015-07-01 _Accession_date 2015-07-01 _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 Medina Jordi . . 2 Macias Maria J. . 3 Martin-Malpartida Pau . . 4 Scheraga Harold A. . stop_ loop_ _Saveframe_category_type _Saveframe_category_type_count assigned_chemical_shifts 1 stop_ loop_ _Data_type _Data_type_count "1H chemical shifts" 207 stop_ loop_ _Revision_date _Revision_keyword _Revision_author _Revision_detail 2016-08-12 update BMRB 'update entry citation' 2015-10-19 original author 'original release' stop_ loop_ _Related_BMRB_accession_number _Relationship 25678 L453D 25679 L453E 25681 E454Y 25682 T456D 25683 T456Y stop_ _Original_release_date 2015-10-19 save_ ############################# # Citation for this entry # ############################# save_entry_citation _Saveframe_category entry_citation _Citation_full . _Citation_title ; Preventing fibril formation of a protein by selective mutation ; _Citation_status published _Citation_type journal _CAS_abstract_code . _MEDLINE_UI_code . _PubMed_ID 26483482 loop_ _Author_ordinal _Author_family_name _Author_given_name _Author_middle_initials _Author_family_title 1 Maisuradze Gia G. . 2 Medina Jordi . . 3 Kachlishvili Khatuna . . 4 Krupa Pawel . . 5 Mozolewska Magdalena . . 6 Martin-Malpartida Pau . . 7 Maisuradze Luka . . 8 Macias Maria J. . 9 Scheraga Harold A. . stop_ _Journal_abbreviation 'Proc. Natl. Acad. Sci. U.S.A.' _Journal_volume 112 _Journal_issue 44 _Journal_CSD . _Book_chapter_title . _Book_volume . _Book_series . _Book_ISBN . _Conference_state_province . _Conference_abstract_number . _Page_first 13549 _Page_last 13554 _Year 2015 _Details . save_ ################################## # Molecular system description # ################################## save_assembly _Saveframe_category molecular_system _Mol_system_name L453W _Enzyme_commission_number . loop_ _Mol_system_component_name _Mol_label entity $entity stop_ _System_molecular_weight . _System_physical_state native _System_oligomer_state ? _System_paramagnetic no _System_thiol_state . _Database_query_date . _Details . save_ ######################## # Monomeric polymers # ######################## save_entity _Saveframe_category monomeric_polymer _Mol_type polymer _Mol_polymer_class protein _Name_common entity _Molecular_mass 4437.812 _Mol_thiol_state 'not present' _Details . ############################## # Polymer residue sequence # ############################## _Residue_count 37 _Mol_residue_sequence ; GATAVSEWTEYKTADGKTYY YNNRTWESTWEKPQELK ; loop_ _Residue_seq_code _Residue_author_seq_code _Residue_label 1 428 GLY 2 429 ALA 3 430 THR 4 431 ALA 5 432 VAL 6 433 SER 7 434 GLU 8 435 TRP 9 436 THR 10 437 GLU 11 438 TYR 12 439 LYS 13 440 THR 14 441 ALA 15 442 ASP 16 443 GLY 17 444 LYS 18 445 THR 19 446 TYR 20 447 TYR 21 448 TYR 22 449 ASN 23 450 ASN 24 451 ARG 25 452 THR 26 453 TRP 27 454 GLU 28 455 SER 29 456 THR 30 457 TRP 31 458 GLU 32 459 LYS 33 460 PRO 34 461 GLN 35 462 GLU 36 463 LEU 37 464 LYS 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 $entity human 9606 Eukaryota Metazoa Homo sapiens 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 $entity 'recombinant technology' . Escherichia coli . pGAT2 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 _Concentration_min_value _Concentration_max_value _Isotopic_labeling $entity . uM 500 1000 'natural abundance' 'sodium phosphate' 25 mM . . 'natural abundance' 'sodium chloride' 100 mM . . 'natural abundance' H2O 90 % . . 'natural abundance' D2O 10 % . . 'natural abundance' stop_ save_ ############################ # Computer software used # ############################ save_ARIA _Saveframe_category software _Name ARIA _Version . loop_ _Vendor _Address _Electronic_address "Linge, O'Donoghue and Nilges" . . stop_ loop_ _Task 'data analysis' stop_ _Details . save_ save_NMRPipe _Saveframe_category software _Name NMRPipe _Version . loop_ _Vendor _Address _Electronic_address 'Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax' . . stop_ loop_ _Task processing stop_ _Details . save_ save_TOPSPIN _Saveframe_category software _Name TOPSPIN _Version . loop_ _Vendor _Address _Electronic_address 'Bruker Biospin' . . stop_ loop_ _Task collection stop_ _Details . save_ save_CNSSOLVE _Saveframe_category software _Name CNSSOLVE _Version . loop_ _Vendor _Address _Electronic_address 'Brunger, Adams, Clore, Gros, Nilges and Read' . . stop_ loop_ _Task 'structure solution' stop_ _Details . save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_spectrometer_1 _Saveframe_category NMR_spectrometer _Manufacturer Bruker _Model Avance _Field_strength 600 _Details . save_ ############################# # NMR applied experiments # ############################# save_2D_1H-1H_TOCSY_1 _Saveframe_category NMR_applied_experiment _Experiment_name '2D 1H-1H TOCSY' _Sample_label $sample_1 save_ save_2D_1H-1H_NOESY_2 _Saveframe_category NMR_applied_experiment _Experiment_name '2D 1H-1H NOESY' _Sample_label $sample_1 save_ ####################### # Sample conditions # ####################### save_sample_conditions_1 _Saveframe_category sample_conditions _Details . loop_ _Variable_type _Variable_value _Variable_value_error _Variable_value_units pH 5.8 . pH pressure 1 . atm temperature 285 . K stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chemical_shift_reference_1 _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 0.00 internal direct . . . 1.000000000 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 _Saveframe_category assigned_chemical_shifts _Details . loop_ _Experiment_label '2D 1H-1H TOCSY' '2D 1H-1H NOESY' stop_ loop_ _Sample_label $sample_1 stop_ _Sample_conditions_label $sample_conditions_1 _Chem_shift_reference_set_label $chemical_shift_reference_1 _Mol_system_component_name entity _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 1 428 1 GLY HA3 H 3.736 0.010 2 2 428 1 GLY H H 8.285 0.001 1 3 429 2 ALA H H 8.092 0.010 1 4 429 2 ALA HA H 4.159 0.010 1 5 429 2 ALA HB H 1.176 0.010 1 6 430 3 THR H H 8.044 0.010 1 7 430 3 THR HA H 4.095 0.010 1 8 430 3 THR HB H 3.977 0.010 1 9 430 3 THR HG2 H 0.996 0.010 1 10 431 4 ALA H H 8.167 0.010 1 11 431 4 ALA HA H 4.155 0.003 1 12 431 4 ALA HB H 1.180 0.010 1 13 432 5 VAL H H 8.032 0.010 1 14 432 5 VAL HA H 3.900 0.010 1 15 432 5 VAL HB H 1.852 0.010 1 16 432 5 VAL HG1 H 1.005 0.010 2 17 432 5 VAL HG2 H 0.720 0.010 2 18 433 6 SER H H 8.223 0.010 1 19 433 6 SER HA H 4.289 0.010 1 20 433 6 SER HB2 H 3.802 0.010 2 21 433 6 SER HB3 H 3.691 0.010 2 22 434 7 GLU H H 8.644 0.010 1 23 434 7 GLU HA H 3.965 0.010 1 24 434 7 GLU HB2 H 1.789 0.010 2 25 434 7 GLU HB3 H 1.609 0.010 2 26 434 7 GLU HG2 H 1.692 0.010 2 27 434 7 GLU HG3 H 1.663 0.010 2 28 435 8 TRP H H 8.051 0.010 1 29 435 8 TRP HA H 5.139 0.010 1 30 435 8 TRP HB2 H 2.895 0.010 2 31 435 8 TRP HB3 H 2.733 0.010 2 32 435 8 TRP HD1 H 6.978 0.010 1 33 435 8 TRP HE1 H 10.051 0.010 1 34 435 8 TRP HE3 H 7.102 0.010 1 35 435 8 TRP HZ2 H 7.285 0.010 1 36 435 8 TRP HZ3 H 6.750 0.010 1 37 435 8 TRP HH2 H 6.871 0.010 1 38 436 9 THR H H 9.331 0.010 1 39 436 9 THR HA H 4.343 0.010 1 40 436 9 THR HB H 3.704 0.010 1 41 436 9 THR HG2 H 0.691 0.010 1 42 437 10 GLU H H 8.371 0.010 1 43 437 10 GLU HA H 4.187 0.010 1 44 437 10 GLU HB2 H 1.615 0.010 2 45 437 10 GLU HG2 H 1.608 0.010 2 46 438 11 TYR H H 8.463 0.010 1 47 438 11 TYR HA H 4.367 0.010 1 48 438 11 TYR HB2 H 2.313 0.010 2 49 438 11 TYR HB3 H 1.030 0.010 2 50 438 11 TYR HD1 H 6.617 0.010 3 51 438 11 TYR HE1 H 6.357 0.010 3 52 439 12 LYS H H 7.992 0.010 1 53 439 12 LYS HA H 5.253 0.001 1 54 439 12 LYS HB2 H 1.482 0.010 2 55 439 12 LYS HB3 H 1.419 0.010 2 56 439 12 LYS HG2 H 1.330 0.010 2 57 439 12 LYS HG3 H 1.148 0.010 2 58 439 12 LYS HD2 H 1.266 0.010 2 59 439 12 LYS HE2 H 2.657 0.010 2 60 440 13 THR H H 9.072 0.010 1 61 440 13 THR HA H 4.460 0.010 1 62 440 13 THR HB H 4.466 0.010 1 63 440 13 THR HG2 H 1.312 0.010 1 64 441 14 ALA H H 9.025 0.010 1 65 441 14 ALA HA H 3.950 0.010 1 66 441 14 ALA HB H 1.251 0.010 1 67 442 15 ASP H H 7.874 0.010 1 68 442 15 ASP HA H 4.459 0.010 1 69 442 15 ASP HB2 H 2.624 0.010 2 70 442 15 ASP HB3 H 2.440 0.010 2 71 443 16 GLY H H 7.818 0.010 1 72 443 16 GLY HA2 H 3.441 0.010 2 73 443 16 GLY HA3 H 3.982 0.010 2 74 444 17 LYS H H 7.716 0.010 1 75 444 17 LYS HA H 4.350 0.010 1 76 444 17 LYS HB2 H 2.111 0.010 2 77 444 17 LYS HB3 H 1.784 0.010 2 78 444 17 LYS HG2 H 1.139 0.010 2 79 444 17 LYS HG3 H 1.094 0.010 2 80 444 17 LYS HD2 H 1.888 0.010 2 81 444 17 LYS HE2 H 3.411 0.005 2 82 445 18 THR H H 8.526 0.010 1 83 445 18 THR HA H 4.781 0.003 1 84 445 18 THR HB H 3.714 0.010 1 85 445 18 THR HG2 H 0.679 0.001 1 86 446 19 TYR H H 8.551 0.002 1 87 446 19 TYR HA H 4.501 0.010 1 88 446 19 TYR HB2 H 2.138 0.010 2 89 446 19 TYR HB3 H 2.041 0.010 2 90 446 19 TYR HD2 H 6.515 0.010 3 91 446 19 TYR HE2 H 6.170 0.010 3 92 447 20 TYR H H 8.668 0.010 1 93 447 20 TYR HA H 4.970 0.010 1 94 447 20 TYR HB2 H 2.480 0.010 2 95 447 20 TYR HB3 H 2.441 0.010 2 96 447 20 TYR HD1 H 6.494 0.010 3 97 447 20 TYR HD2 H 6.490 0.010 3 98 447 20 TYR HE1 H 6.433 0.010 3 99 448 21 TYR H H 9.188 0.001 1 100 448 21 TYR HA H 5.408 0.010 1 101 448 21 TYR HB2 H 2.713 0.010 2 102 448 21 TYR HB3 H 2.696 0.010 2 103 448 21 TYR HD1 H 6.801 0.010 3 104 448 21 TYR HE1 H 6.456 0.010 3 105 449 22 ASN H H 8.112 0.001 1 106 449 22 ASN HA H 4.042 0.010 1 107 449 22 ASN HB2 H 2.154 0.010 2 108 449 22 ASN HB3 H 0.125 0.010 2 109 449 22 ASN HD21 H 6.975 0.010 2 110 449 22 ASN HD22 H 4.316 0.010 2 111 450 23 ASN H H 8.382 0.001 1 112 450 23 ASN HA H 3.968 0.010 1 113 450 23 ASN HB2 H 2.565 0.010 2 114 450 23 ASN HB3 H 2.517 0.010 2 115 450 23 ASN HD21 H 7.149 0.010 2 116 450 23 ASN HD22 H 7.061 0.010 2 117 451 24 ARG H H 8.316 0.010 1 118 451 24 ARG HA H 3.975 0.010 1 119 451 24 ARG HB2 H 1.601 0.010 2 120 451 24 ARG HB3 H 1.333 0.010 2 121 451 24 ARG HG2 H 1.154 0.010 2 122 451 24 ARG HG3 H 0.961 0.010 2 123 451 24 ARG HD2 H 2.948 0.010 2 124 451 24 ARG HD3 H 2.727 0.010 2 125 451 24 ARG HE H 7.702 0.010 1 126 451 24 ARG HH21 H 6.521 0.010 2 127 452 25 THR H H 7.579 0.010 1 128 452 25 THR HA H 3.464 0.010 1 129 452 25 THR HB H 3.897 0.010 1 130 452 25 THR HG2 H 0.608 0.010 1 131 453 26 TRP H H 7.654 0.010 1 132 453 26 TRP HA H 4.065 0.001 1 133 453 26 TRP HB2 H 3.458 0.010 2 134 453 26 TRP HB3 H 3.276 0.010 2 135 453 26 TRP HD1 H 6.714 0.010 1 136 453 26 TRP HE1 H 9.435 0.004 1 137 453 26 TRP HE3 H 7.271 0.010 1 138 453 26 TRP HZ2 H 7.132 0.001 1 139 453 26 TRP HZ3 H 6.787 0.033 1 140 454 27 GLU H H 7.109 0.010 1 141 454 27 GLU HA H 4.170 0.010 1 142 454 27 GLU HB2 H 2.058 0.010 2 143 454 27 GLU HB3 H 1.923 0.010 2 144 454 27 GLU HG2 H 1.708 0.010 2 145 454 27 GLU HG3 H 1.564 0.010 2 146 455 28 SER H H 8.288 0.010 1 147 455 28 SER HA H 5.831 0.010 1 148 455 28 SER HB2 H 3.409 0.010 2 149 456 29 THR H H 9.146 0.010 1 150 456 29 THR HA H 4.624 0.010 1 151 456 29 THR HB H 4.069 0.010 1 152 456 29 THR HG2 H 0.958 0.010 1 153 457 30 TRP H H 8.307 0.010 1 154 457 30 TRP HA H 4.796 0.010 1 155 457 30 TRP HB2 H 3.428 0.010 2 156 457 30 TRP HB3 H 2.977 0.010 2 157 457 30 TRP HD1 H 7.164 0.010 1 158 457 30 TRP HE1 H 9.831 0.010 1 159 457 30 TRP HE3 H 7.845 0.010 1 160 457 30 TRP HZ2 H 7.042 0.010 1 161 457 30 TRP HZ3 H 6.706 0.010 1 162 457 30 TRP HH2 H 6.810 0.001 1 163 458 31 GLU H H 8.001 0.010 1 164 458 31 GLU HA H 4.174 0.010 1 165 458 31 GLU HB2 H 1.589 0.010 2 166 458 31 GLU HB3 H 1.514 0.010 2 167 458 31 GLU HG2 H 1.885 0.010 2 168 459 32 LYS H H 8.203 0.010 1 169 459 32 LYS HA H 2.523 0.010 1 170 459 32 LYS HB2 H 1.241 0.010 2 171 459 32 LYS HB3 H 1.156 0.010 2 172 459 32 LYS HG2 H 0.829 0.010 2 173 459 32 LYS HG3 H 0.367 0.010 2 174 459 32 LYS HE2 H 2.606 0.010 2 175 460 33 PRO HA H 3.703 0.010 1 176 460 33 PRO HB2 H 1.177 0.010 2 177 460 33 PRO HB3 H 0.842 0.010 2 178 460 33 PRO HG2 H -0.061 0.010 2 179 460 33 PRO HG3 H -0.117 0.010 2 180 460 33 PRO HD2 H 2.435 0.010 2 181 460 33 PRO HD3 H 1.894 0.010 2 182 461 34 GLN H H 8.340 0.010 1 183 461 34 GLN HA H 3.575 0.010 1 184 461 34 GLN HB2 H 1.800 0.010 2 185 461 34 GLN HB3 H 1.739 0.010 2 186 461 34 GLN HG2 H 2.139 0.010 2 187 461 34 GLN HE21 H 7.398 0.010 2 188 461 34 GLN HE22 H 6.696 0.010 2 189 462 35 GLU H H 8.860 0.010 1 190 462 35 GLU HA H 3.936 0.010 1 191 462 35 GLU HB2 H 1.843 0.010 2 192 462 35 GLU HB3 H 1.779 0.010 2 193 462 35 GLU HG2 H 2.086 0.010 2 194 463 36 LEU H H 7.395 0.010 1 195 463 36 LEU HA H 4.196 0.010 1 196 463 36 LEU HB2 H 1.137 0.010 2 197 463 36 LEU HB3 H 1.072 0.010 2 198 463 36 LEU HG H 1.383 0.010 1 199 463 36 LEU HD1 H 0.653 0.010 2 200 463 36 LEU HD2 H 0.561 0.010 2 201 464 37 LYS H H 7.444 0.010 1 202 464 37 LYS HA H 3.756 0.010 1 203 464 37 LYS HB2 H 1.584 0.010 2 204 464 37 LYS HB3 H 1.491 0.010 2 205 464 37 LYS HG2 H 1.168 0.010 2 206 464 37 LYS HG3 H 1.030 0.003 2 207 464 37 LYS HD2 H 1.370 0.006 2 stop_ save_