data_A1IIH
# 
_chem_comp.id                                    A1IIH 
_chem_comp.name                                  "3-[2,2-bis(fluoranyl)-10,12-dimethyl-1$l^{4},3-diaza-2$l^{4}-boratricyclo[7.3.0.0^{3,7}]dodeca-1(12),4,6,8,10-pentaen-4-yl]-~{N}-[2-[2-[[2-[(6-oxidanylidene-7-oxa-2,5-diazaspiro[3.4]octan-2-yl)carbonyl]-2-azaspiro[3.3]heptan-6-yl]methyl]phenoxy]ethyl]propanamide" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C35 H41 B F2 N6 O5" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-07-17 
_chem_comp.pdbx_modified_date                    2025-06-06 
_chem_comp.pdbx_ambiguous_flag                   N 
_chem_comp.pdbx_release_status                   REL 
_chem_comp.pdbx_replaced_by                      ? 
_chem_comp.pdbx_replaces                         ? 
_chem_comp.formula_weight                        674.545 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1IIH 
_chem_comp.pdbx_model_coordinates_details        ? 
_chem_comp.pdbx_model_coordinates_missing_flag   N 
_chem_comp.pdbx_ideal_coordinates_details        Corina 
_chem_comp.pdbx_ideal_coordinates_missing_flag   N 
_chem_comp.pdbx_model_coordinates_db_code        9G4M 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  PDBE 
_chem_comp.pdbx_pcm                              ? 
# 
loop_
_chem_comp_atom.comp_id 
_chem_comp_atom.atom_id 
_chem_comp_atom.alt_atom_id 
_chem_comp_atom.type_symbol 
_chem_comp_atom.charge 
_chem_comp_atom.pdbx_align 
_chem_comp_atom.pdbx_aromatic_flag 
_chem_comp_atom.pdbx_leaving_atom_flag 
_chem_comp_atom.pdbx_stereo_config 
_chem_comp_atom.pdbx_n_terminal_atom_flag 
_chem_comp_atom.pdbx_backbone_atom_flag 
_chem_comp_atom.pdbx_c_terminal_atom_flag 
_chem_comp_atom.model_Cartn_x 
_chem_comp_atom.model_Cartn_y 
_chem_comp_atom.model_Cartn_z 
_chem_comp_atom.pdbx_model_Cartn_x_ideal 
_chem_comp_atom.pdbx_model_Cartn_y_ideal 
_chem_comp_atom.pdbx_model_Cartn_z_ideal 
_chem_comp_atom.pdbx_component_atom_id 
_chem_comp_atom.pdbx_component_comp_id 
_chem_comp_atom.pdbx_ordinal 
A1IIH N1  N1  N 0  1 N N N N N N 40.414 19.646 -9.605  -3.178 3.593  -0.862 N1  A1IIH 1  
A1IIH C7  C1  C 0  1 Y N N N N N 42.764 14.524 -12.793 -8.556 -0.377 0.610  C7  A1IIH 2  
A1IIH C8  C2  C 0  1 Y N N N N N 41.875 15.428 -12.238 -8.007 0.669  -0.126 C8  A1IIH 3  
A1IIH N2  N2  N 0  1 N N N N N N 34.034 20.515 -5.398  5.255  0.180  -0.988 N2  A1IIH 4  
A1IIH C9  C3  C 0  1 Y N N N N N 42.424 16.685 -12.363 -6.812 0.250  -0.625 C9  A1IIH 5  
A1IIH O1  O1  O 0  1 N N N N N N 40.330 20.353 -6.766  -0.529 4.407  -0.030 O1  A1IIH 6  
A1IIH C1  C4  C 0  1 N N N N N N 47.204 15.579 -15.012 -6.509 -4.981 1.362  C1  A1IIH 7  
A1IIH C5  C5  C 0  1 N N N N N N 45.019 14.854 -13.930 -7.677 -2.723 1.085  C5  A1IIH 8  
A1IIH C6  C6  C 0  1 Y N N N N N 43.849 15.247 -13.254 -7.654 -1.439 0.545  C6  A1IIH 9  
A1IIH N3  N3  N 0  1 N N N N N N 31.869 20.486 -6.196  7.382  -0.677 -0.553 N3  A1IIH 10 
A1IIH C4  C7  C 0  1 N N N N N N 45.974 15.756 -14.328 -6.653 -3.651 0.897  C4  A1IIH 11 
A1IIH O4  O2  O 0  1 N N N N N N 27.542 20.173 -9.532  8.814  -5.644 -0.475 O4  A1IIH 12 
A1IIH C3  C8  C 0  1 N N N N N N 46.865 17.758 -14.593 -4.749 -4.392 0.141  C3  A1IIH 13 
A1IIH O3  O3  O 0  1 N N N N N N 28.930 21.895 -9.190  9.613  -4.161 1.011  O3  A1IIH 14 
A1IIH C2  C9  C 0  1 N N N N N N 47.736 16.830 -15.172 -5.313 -5.432 0.883  C2  A1IIH 15 
A1IIH N4  N4  N 0  1 N N N N N N 29.490 19.936 -8.337  8.151  -3.495 -0.562 N4  A1IIH 16 
A1IIH N   N5  N 1  1 N N N N N N 45.798 17.112 -14.073 -5.558 -3.358 0.166  N   A1IIH 17 
A1IIH C   C10 C 0  1 N N N N N N 47.791 14.260 -15.433 -7.483 -5.746 2.220  C   A1IIH 18 
A1IIH O   O4  O 0  1 N N N N N N 39.316 19.949 -11.539 -4.114 2.667  -2.648 O   A1IIH 19 
A1IIH B   B1  B -1 1 N N N N N N 44.609 17.736 -13.306 -5.452 -1.986 -0.474 B   A1IIH 20 
A1IIH C10 C11 C 0  1 N N N N N N 41.854 18.007 -11.950 -5.885 1.074  -1.481 C10 A1IIH 21 
A1IIH C11 C12 C 0  1 N N N N N N 40.517 17.905 -11.264 -4.990 1.932  -0.584 C11 A1IIH 22 
A1IIH C12 C13 C 0  1 N N N N N N 40.023 19.257 -10.815 -4.063 2.756  -1.439 C12 A1IIH 23 
A1IIH C13 C14 C 0  1 N N N N N N 40.022 20.926 -9.038  -2.282 4.399  -1.694 C13 A1IIH 24 
A1IIH C14 C15 C 0  1 N N N N N N 40.793 21.244 -7.791  -1.386 5.255  -0.797 C14 A1IIH 25 
A1IIH C15 C16 C 0  1 Y N N N N N 40.835 20.524 -5.507  0.336  5.014  0.825  C15 A1IIH 26 
A1IIH C16 C17 C 0  1 Y N N N N N 41.768 21.498 -5.186  0.360  6.397  0.923  C16 A1IIH 27 
A1IIH C17 C18 C 0  1 Y N N N N N 42.217 21.609 -3.881  1.241  7.011  1.792  C17 A1IIH 28 
A1IIH C18 C19 C 0  1 Y N N N N N 41.741 20.760 -2.908  2.097  6.249  2.564  C18 A1IIH 29 
A1IIH C19 C20 C 0  1 Y N N N N N 40.809 19.786 -3.231  2.076  4.870  2.468  C19 A1IIH 30 
A1IIH C20 C21 C 0  1 Y N N N N N 40.338 19.653 -4.533  1.193  4.250  1.605  C20 A1IIH 31 
A1IIH C21 C22 C 0  1 N N N N N N 39.271 18.638 -4.869  1.169  2.747  1.501  C21 A1IIH 32 
A1IIH C22 C23 C 0  1 N N N N N N 37.862 19.173 -4.588  2.053  2.303  0.333  C22 A1IIH 33 
A1IIH C23 C24 C 0  1 N N N N N N 36.629 18.296 -4.909  2.001  0.787  0.064  C23 A1IIH 34 
A1IIH C24 C25 C 0  1 N N N N N N 35.926 19.619 -5.268  3.510  0.865  -0.167 C24 A1IIH 35 
A1IIH C25 C26 C 0  1 N N N N N N 37.309 20.220 -5.585  3.531  2.111  0.718  C25 A1IIH 36 
A1IIH C26 C27 C 0  1 N N N N N N 34.782 19.640 -6.305  4.421  -0.329 0.121  C26 A1IIH 37 
A1IIH C27 C28 C 0  1 N N N N N N 34.969 20.332 -4.287  4.098  0.884  -1.579 C27 A1IIH 38 
A1IIH C28 C29 C 0  1 N N N N N N 32.705 20.650 -5.149  6.555  0.057  -1.322 C28 A1IIH 39 
A1IIH C29 C30 C 0  1 N N N N N N 30.476 20.942 -6.209  8.810  -1.040 -0.580 C29 A1IIH 40 
A1IIH C30 C31 C 0  1 N N N N N N 30.500 20.819 -7.754  8.444  -2.290 0.207  C30 A1IIH 41 
A1IIH C31 C32 C 0  1 N N N N N N 30.214 22.102 -8.548  9.439  -2.736 1.280  C31 A1IIH 42 
A1IIH C32 C33 C 0  1 N N N N N N 28.578 20.591 -9.067  8.857  -4.512 -0.038 C32 A1IIH 43 
A1IIH C33 C34 C 0  1 N N N N N N 31.988 20.403 -7.657  7.256  -1.463 0.687  C33 A1IIH 44 
A1IIH C34 C35 C 0  1 N N N N N N 47.025 19.247 -14.527 -3.424 -4.448 -0.574 C34 A1IIH 45 
A1IIH F   F1  F 0  1 N N N N N N 45.063 18.315 -12.133 -4.298 -1.400 -0.024 F   A1IIH 46 
A1IIH F1  F2  F 0  1 N N N N N N 43.977 18.697 -14.085 -5.329 -2.161 -1.827 F1  A1IIH 47 
A1IIH N5  N6  N 0  1 Y N N N N N 43.630 16.583 -12.973 -6.590 -1.017 -0.231 N5  A1IIH 48 
A1IIH O2  O5  O 0  1 N N N N N N 32.284 20.899 -4.032  6.981  0.609  -2.318 O2  A1IIH 49 
A1IIH H11 H1  H 0  1 N N N N N N 40.997 19.038 -9.067  -3.138 3.664  0.105  H11 A1IIH 50 
A1IIH H5  H2  H 0  1 N N N N N N 42.635 13.454 -12.855 -9.500 -0.367 1.135  H5  A1IIH 51 
A1IIH H6  H3  H 0  1 N N N N N N 40.922 15.191 -11.788 -8.451 1.642  -0.275 H6  A1IIH 52 
A1IIH H4  H4  H 0  1 N N N N N N 45.171 13.806 -14.143 -8.531 -3.014 1.679  H4  A1IIH 53 
A1IIH H3  H5  H 0  1 N N N N N N 48.670 17.061 -15.662 -4.884 -6.410 1.046  H3  A1IIH 54 
A1IIH H35 H6  H 0  1 N N N N N N 29.481 18.945 -8.204  7.549  -3.552 -1.321 H35 A1IIH 55 
A1IIH H2  H7  H 0  1 N N N N N N 47.105 13.447 -15.154 -7.091 -6.745 2.412  H2  A1IIH 56 
A1IIH H   H8  H 0  1 N N N N N N 47.940 14.256 -16.523 -7.624 -5.223 3.166  H   A1IIH 57 
A1IIH H1  H9  H 0  1 N N N N N N 48.758 14.112 -14.930 -8.439 -5.825 1.702  H1  A1IIH 58 
A1IIH H7  H10 H 0  1 N N N N N N 42.562 18.490 -11.260 -5.265 0.413  -2.086 H7  A1IIH 59 
A1IIH H8  H11 H 0  1 N N N N N N 41.736 18.630 -12.849 -6.472 1.721  -2.133 H8  A1IIH 60 
A1IIH H10 H12 H 0  1 N N N N N N 39.788 17.472 -11.965 -5.610 2.593  0.022  H10 A1IIH 61 
A1IIH H9  H13 H 0  1 N N N N N N 40.615 17.250 -10.386 -4.403 1.285  0.069  H9  A1IIH 62 
A1IIH H12 H14 H 0  1 N N N N N N 40.206 21.716 -9.781  -1.662 3.740  -2.303 H12 A1IIH 63 
A1IIH H13 H15 H 0  1 N N N N N N 38.950 20.894 -8.795  -2.872 5.046  -2.342 H13 A1IIH 64 
A1IIH H14 H16 H 0  1 N N N N N N 41.869 21.092 -7.964  -2.006 5.849  -0.125 H14 A1IIH 65 
A1IIH H15 H17 H 0  1 N N N N N N 40.613 22.287 -7.493  -0.781 5.919  -1.415 H15 A1IIH 66 
A1IIH H16 H18 H 0  1 N N N N N N 42.142 22.165 -5.948  -0.309 6.993  0.320  H16 A1IIH 67 
A1IIH H17 H19 H 0  1 N N N N N N 42.944 22.365 -3.625  1.260  8.089  1.869  H17 A1IIH 68 
A1IIH H18 H20 H 0  1 N N N N N N 42.094 20.853 -1.892  2.785  6.731  3.243  H18 A1IIH 69 
A1IIH H19 H21 H 0  1 N N N N N N 40.444 19.122 -2.462  2.746  4.276  3.072  H19 A1IIH 70 
A1IIH H20 H22 H 0  1 N N N N N N 39.348 18.382 -5.936  1.546  2.313  2.427  H20 A1IIH 71 
A1IIH H21 H23 H 0  1 N N N N N N 39.436 17.735 -4.263  0.147  2.410  1.331  H21 A1IIH 72 
A1IIH H22 H24 H 0  1 N N N N N N 37.797 19.557 -3.559  1.909  2.909  -0.561 H22 A1IIH 73 
A1IIH H23 H25 H 0  1 N N N N N N 36.761 17.596 -5.748  1.722  0.197  0.937  H23 A1IIH 74 
A1IIH H24 H26 H 0  1 N N N N N N 36.202 17.760 -4.048  1.435  0.521  -0.828 H24 A1IIH 75 
A1IIH H26 H27 H 0  1 N N N N N N 37.644 20.095 -6.625  4.186  2.900  0.348  H26 A1IIH 76 
A1IIH H25 H28 H 0  1 N N N N N N 37.442 21.269 -5.281  3.684  1.894  1.776  H25 A1IIH 77 
A1IIH H27 H29 H 0  1 N N N N N N 35.048 20.102 -7.267  3.958  -1.295 -0.084 H27 A1IIH 78 
A1IIH H28 H30 H 0  1 N N N N N N 34.312 18.662 -6.485  4.908  -0.287 1.095  H28 A1IIH 79 
A1IIH H29 H31 H 0  1 N N N N N N 35.364 21.268 -3.865  4.331  1.883  -1.946 H29 A1IIH 80 
A1IIH H30 H32 H 0  1 N N N N N N 34.591 19.694 -3.474  3.538  0.284  -2.296 H30 A1IIH 81 
A1IIH H32 H33 H 0  1 N N N N N N 29.769 20.263 -5.709  9.186  -1.250 -1.582 H32 A1IIH 82 
A1IIH H31 H34 H 0  1 N N N N N N 30.328 21.966 -5.835  9.445  -0.348 -0.027 H31 A1IIH 83 
A1IIH H34 H35 H 0  1 N N N N N N 30.168 22.968 -7.872  9.024  -2.581 2.276  H34 A1IIH 84 
A1IIH H33 H36 H 0  1 N N N N N N 30.997 22.267 -9.303  10.385 -2.206 1.171  H33 A1IIH 85 
A1IIH H37 H37 H 0  1 N N N N N N 32.206 19.395 -8.040  7.461  -0.891 1.592  H37 A1IIH 86 
A1IIH H36 H38 H 0  1 N N N N N N 32.692 21.123 -8.099  6.327  -2.030 0.746  H36 A1IIH 87 
A1IIH H40 H39 H 0  1 N N N N N N 46.163 19.686 -14.004 -2.634 -4.115 0.098  H40 A1IIH 88 
A1IIH H39 H40 H 0  1 N N N N N N 47.948 19.493 -13.982 -3.224 -5.472 -0.890 H39 A1IIH 89 
A1IIH H38 H41 H 0  1 N N N N N N 47.081 19.655 -15.547 -3.455 -3.798 -1.449 H38 A1IIH 90 
# 
loop_
_chem_comp_bond.comp_id 
_chem_comp_bond.atom_id_1 
_chem_comp_bond.atom_id_2 
_chem_comp_bond.value_order 
_chem_comp_bond.pdbx_aromatic_flag 
_chem_comp_bond.pdbx_stereo_config 
_chem_comp_bond.pdbx_ordinal 
A1IIH C   C1  SING N N 1  
A1IIH C1  C2  DOUB N N 2  
A1IIH C2  C3  SING N N 3  
A1IIH C3  N   DOUB N N 4  
A1IIH N   C4  SING N N 5  
A1IIH C1  C4  SING N N 6  
A1IIH C4  C5  DOUB N N 7  
A1IIH C5  C6  SING N N 8  
A1IIH C6  C7  DOUB Y N 9  
A1IIH C7  C8  SING Y N 10 
A1IIH C8  C9  DOUB Y N 11 
A1IIH C10 C9  SING N N 12 
A1IIH C11 C10 SING N N 13 
A1IIH C12 C11 SING N N 14 
A1IIH O   C12 DOUB N N 15 
A1IIH N1  C12 SING N N 16 
A1IIH C13 N1  SING N N 17 
A1IIH C14 C13 SING N N 18 
A1IIH O1  C14 SING N N 19 
A1IIH C15 O1  SING N N 20 
A1IIH C15 C16 DOUB Y N 21 
A1IIH C16 C17 SING Y N 22 
A1IIH C17 C18 DOUB Y N 23 
A1IIH C18 C19 SING Y N 24 
A1IIH C19 C20 DOUB Y N 25 
A1IIH C20 C15 SING Y N 26 
A1IIH C21 C20 SING N N 27 
A1IIH C22 C21 SING N N 28 
A1IIH C22 C23 SING N N 29 
A1IIH C23 C24 SING N N 30 
A1IIH C24 C25 SING N N 31 
A1IIH C25 C22 SING N N 32 
A1IIH C24 C26 SING N N 33 
A1IIH C26 N2  SING N N 34 
A1IIH N2  C27 SING N N 35 
A1IIH C27 C24 SING N N 36 
A1IIH C28 N2  SING N N 37 
A1IIH O2  C28 DOUB N N 38 
A1IIH N3  C28 SING N N 39 
A1IIH N3  C29 SING N N 40 
A1IIH C29 C30 SING N N 41 
A1IIH C30 C31 SING N N 42 
A1IIH C31 O3  SING N N 43 
A1IIH O3  C32 SING N N 44 
A1IIH O4  C32 DOUB N N 45 
A1IIH C32 N4  SING N N 46 
A1IIH N4  C30 SING N N 47 
A1IIH C30 C33 SING N N 48 
A1IIH C33 N3  SING N N 49 
A1IIH C9  N5  SING Y N 50 
A1IIH C6  N5  SING Y N 51 
A1IIH N5  B   SING N N 52 
A1IIH N   B   SING N N 53 
A1IIH F   B   SING N N 54 
A1IIH B   F1  SING N N 55 
A1IIH C34 C3  SING N N 56 
A1IIH N1  H11 SING N N 57 
A1IIH C7  H5  SING N N 58 
A1IIH C8  H6  SING N N 59 
A1IIH C5  H4  SING N N 60 
A1IIH C2  H3  SING N N 61 
A1IIH N4  H35 SING N N 62 
A1IIH C   H2  SING N N 63 
A1IIH C   H   SING N N 64 
A1IIH C   H1  SING N N 65 
A1IIH C10 H7  SING N N 66 
A1IIH C10 H8  SING N N 67 
A1IIH C11 H10 SING N N 68 
A1IIH C11 H9  SING N N 69 
A1IIH C13 H12 SING N N 70 
A1IIH C13 H13 SING N N 71 
A1IIH C14 H14 SING N N 72 
A1IIH C14 H15 SING N N 73 
A1IIH C16 H16 SING N N 74 
A1IIH C17 H17 SING N N 75 
A1IIH C18 H18 SING N N 76 
A1IIH C19 H19 SING N N 77 
A1IIH C21 H20 SING N N 78 
A1IIH C21 H21 SING N N 79 
A1IIH C22 H22 SING N N 80 
A1IIH C23 H23 SING N N 81 
A1IIH C23 H24 SING N N 82 
A1IIH C25 H26 SING N N 83 
A1IIH C25 H25 SING N N 84 
A1IIH C26 H27 SING N N 85 
A1IIH C26 H28 SING N N 86 
A1IIH C27 H29 SING N N 87 
A1IIH C27 H30 SING N N 88 
A1IIH C29 H32 SING N N 89 
A1IIH C29 H31 SING N N 90 
A1IIH C31 H34 SING N N 91 
A1IIH C31 H33 SING N N 92 
A1IIH C33 H37 SING N N 93 
A1IIH C33 H36 SING N N 94 
A1IIH C34 H40 SING N N 95 
A1IIH C34 H39 SING N N 96 
A1IIH C34 H38 SING N N 97 
# 
loop_
_pdbx_chem_comp_descriptor.comp_id 
_pdbx_chem_comp_descriptor.type 
_pdbx_chem_comp_descriptor.program 
_pdbx_chem_comp_descriptor.program_version 
_pdbx_chem_comp_descriptor.descriptor 
A1IIH InChI            InChI                1.06  "InChI=1S/C35H41BF2N6O5/c1-23-13-24(2)43-29(23)15-28-8-7-27(44(28)36(43,37)38)9-10-31(45)39-11-12-48-30-6-4-3-5-26(30)14-25-16-34(17-25)18-41(19-34)33(47)42-20-35(21-42)22-49-32(46)40-35/h3-8,13,15,25H,9-12,14,16-22H2,1-2H3,(H,39,45)(H,40,46)" 
A1IIH InChIKey         InChI                1.06  IREDGWRMCRGHGX-UHFFFAOYSA-N                                                                                                                                                                                                                         
A1IIH SMILES_CANONICAL CACTVS               3.385 "CC1=CC(=[N+]2C1=Cc3ccc(CCC(=O)NCCOc4ccccc4CC5CC6(C5)CN(C6)C(=O)N7CC8(COC(=O)N8)C7)n3[B-]2(F)F)C"                                                                                                                                                   
A1IIH SMILES           CACTVS               3.385 "CC1=CC(=[N+]2C1=Cc3ccc(CCC(=O)NCCOc4ccccc4CC5CC6(C5)CN(C6)C(=O)N7CC8(COC(=O)N8)C7)n3[B-]2(F)F)C"                                                                                                                                                   
A1IIH SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "[B-]1(n2c(ccc2CCC(=O)NCCOc3ccccc3CC4CC5(C4)CN(C5)C(=O)N6CC7(C6)COC(=O)N7)C=C8[N+]1=C(C=C8C)C)(F)F"                                                                                                                                                 
A1IIH SMILES           "OpenEye OEToolkits" 2.0.7 "[B-]1(n2c(ccc2CCC(=O)NCCOc3ccccc3CC4CC5(C4)CN(C5)C(=O)N6CC7(C6)COC(=O)N7)C=C8[N+]1=C(C=C8C)C)(F)F"                                                                                                                                                 
# 
_pdbx_chem_comp_identifier.comp_id           A1IIH 
_pdbx_chem_comp_identifier.type              "SYSTEMATIC NAME" 
_pdbx_chem_comp_identifier.program           "OpenEye OEToolkits" 
_pdbx_chem_comp_identifier.program_version   2.0.7 
_pdbx_chem_comp_identifier.identifier        "3-[2,2-bis(fluoranyl)-10,12-dimethyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.0^{3,7}]dodeca-1(12),4,6,8,10-pentaen-4-yl]-~{N}-[2-[2-[[2-[(6-oxidanylidene-7-oxa-2,5-diazaspiro[3.4]octan-2-yl)carbonyl]-2-azaspiro[3.3]heptan-6-yl]methyl]phenoxy]ethyl]propanamide" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1IIH "Create component" 2024-07-17 PDBE 
A1IIH "Initial release"  2025-06-11 RCSB 
# 
