data_1G1
# 
_chem_comp.id                                    1G1 
_chem_comp.name                                  "N3Phe-Leu-Leu-Phe(4-NH2CH2)-methyl vinyl sulfone, bound form" 
_chem_comp.type                                  peptide-like 
_chem_comp.pdbx_type                             ATOMP 
_chem_comp.formula                               "C33 H49 N7 O5 S" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2013-01-22 
_chem_comp.pdbx_modified_date                    2024-09-27 
_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                        655.851 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     1G1 
_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        4INR 
_chem_comp.pdbx_subcomponent_list                "1G2 LEU LEU 1G3" 
_chem_comp.pdbx_processing_site                  RCSB 
_chem_comp.pdbx_pcm                              Y 
# 
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 
1G1 C12 C12 C 0  1 N N N N N N 11.699 -138.017 21.124 -4.477  0.076  1.348  C12  1G2 1  
1G1 O13 O13 O 0  1 N N N N N N 12.333 -138.951 20.646 -4.379  0.695  2.387  O13  1G2 2  
1G1 C8  C8  C 0  1 N N S N N N 11.870 -137.736 22.593 -5.823  -0.085 0.690  C8   1G2 3  
1G1 N9  N9  N 0  1 N N N N N N 11.450 -138.996 23.173 -6.880  0.149  1.678  N9   1G2 4  
1G1 N10 N10 N 1  1 N N N N N N 10.353 -139.200 23.597 -7.957  -0.008 1.396  N10  1G2 5  
1G1 N11 N11 N -1 1 N N N N N N 9.239  -139.336 24.001 -9.033  -0.165 1.115  N11  1G2 6  
1G1 C7  C7  C 0  1 N N N N N N 13.336 -137.415 22.994 -5.958  0.926  -0.450 C7   1G2 7  
1G1 C3  C3  C 0  1 Y N N N N N 13.464 -137.209 24.515 -7.251  0.685  -1.186 C3   1G2 8  
1G1 C2  C2  C 0  1 Y N N N N N 13.460 -135.917 25.066 -8.405  1.332  -0.785 C2   1G2 9  
1G1 C1  C1  C 0  1 Y N N N N N 13.582 -135.737 26.452 -9.591  1.110  -1.459 C1   1G2 10 
1G1 C4  C4  C 0  1 Y N N N N N 13.601 -138.318 25.373 -7.282  -0.179 -2.264 C4   1G2 11 
1G1 C5  C5  C 0  1 Y N N N N N 13.720 -138.142 26.759 -8.468  -0.401 -2.939 C5   1G2 12 
1G1 C6  C6  C 0  1 Y N N N N N 13.712 -136.847 27.298 -9.623  0.242  -2.535 C6   1G2 13 
1G1 N14 N14 N 0  1 N N N N N N 10.858 -137.222 20.419 -3.380  -0.463 0.779  N    LEU 14 
1G1 C15 C15 C 0  1 N N S N N N 10.217 -137.706 19.195 -2.057  -0.214 1.358  CA   LEU 15 
1G1 C25 C25 C 0  1 N N N N N N 11.171 -137.586 18.045 -1.015  -0.267 0.270  C    LEU 16 
1G1 O26 O26 O 0  1 N N N N N N 11.755 -136.521 17.901 -1.253  -0.843 -0.770 O    LEU 17 
1G1 C16 C16 C 0  1 N N N N N N 8.901  -136.891 18.986 -1.752  -1.283 2.409  CB   LEU 18 
1G1 C17 C17 C 0  1 N N N N N N 7.580  -137.718 18.916 -0.424  -0.958 3.096  CG   LEU 19 
1G1 C18 C18 C 0  1 N N N N N N 7.150  -138.355 20.278 -0.572  0.330  3.909  CD1  LEU 20 
1G1 C19 C19 C 0  1 N N N N N N 6.425  -136.783 18.442 -0.036  -2.108 4.027  CD2  LEU 21 
1G1 N27 N27 N 0  1 N N N N N N 11.327 -138.676 17.253 0.181   0.327  0.454  N    LEU 22 
1G1 C28 C28 C 0  1 N N S N N N 12.111 -138.608 16.028 1.154   0.367  -0.640 CA   LEU 23 
1G1 C33 C33 C 0  1 N N N N N N 11.240 -138.629 14.790 2.549   0.398  -0.071 C    LEU 24 
1G1 O34 O34 O 0  1 N N N N N N 10.058 -138.920 14.907 2.728   0.747  1.077  O    LEU 25 
1G1 C29 C29 C 0  1 N N N N N N 13.155 -139.759 15.966 0.920   1.621  -1.485 CB   LEU 26 
1G1 C30 C30 C 0  1 N N N N N N 14.353 -139.652 16.967 1.920   1.649  -2.643 CG   LEU 27 
1G1 C31 C31 C 0  1 N N N N N N 15.063 -141.037 17.058 1.648   0.470  -3.580 CD1  LEU 28 
1G1 C32 C32 C 0  1 N N N N N N 15.415 -138.570 16.592 1.767   2.960  -3.417 CD2  LEU 29 
1G1 O50 O50 O 0  1 N N N N N N 14.918 -140.582 10.684 5.396   4.491  -0.761 O50  1G3 30 
1G1 S48 S48 S 0  1 N N N N N N 14.172 -139.976 11.764 5.541   3.968  0.552  S48  1G3 31 
1G1 O49 O49 O 0  1 N N N N N N 14.902 -139.468 12.906 6.838   3.891  1.128  O49  1G3 32 
1G1 C51 C51 C 0  1 N N N N N N 12.982 -141.184 12.369 4.465   4.906  1.671  C51  1G3 33 
1G1 C47 C47 C 0  1 N N N N N N 13.193 -138.624 11.064 4.788   2.318  0.603  C47  1G3 34 
1G1 C46 C46 C 0  1 N N N N N N 11.650 -138.800 11.190 5.577   1.369  -0.300 C46  1G3 35 
1G1 C36 C36 C 0  1 N N S N N N 11.075 -137.989 12.411 4.942   -0.023 -0.257 C36  1G3 36 
1G1 C37 C37 C 0  1 N N N N N N 11.193 -136.476 12.051 5.801   -1.001 -1.061 C37  1G3 37 
1G1 C38 C38 C 0  1 Y N N N N N 10.153 -135.457 12.532 5.244   -2.394 -0.917 C38  1G3 38 
1G1 C43 C43 C 0  1 Y N N N N N 10.413 -134.112 12.219 5.678   -3.209 0.112  C43  1G3 39 
1G1 C42 C42 C 0  1 Y N N N N N 9.531  -133.105 12.612 5.166   -4.487 0.243  C42  1G3 40 
1G1 C41 C41 C 0  1 Y N N N N N 8.367  -133.419 13.328 4.221   -4.949 -0.654 C41  1G3 41 
1G1 C44 C44 C 0  1 N N N N N N 7.458  -132.237 13.716 3.664   -6.341 -0.510 C44  1G3 42 
1G1 N45 N45 N 0  1 N N N N N N 6.663  -132.389 14.955 2.473   -6.306 0.350  N45  1G3 43 
1G1 C40 C40 C 0  1 Y N N N N N 8.104  -134.765 13.642 3.787   -4.133 -1.681 C40  1G3 44 
1G1 C39 C39 C 0  1 Y N N N N N 8.989  -135.783 13.249 4.295   -2.854 -1.811 C39  1G3 45 
1G1 N35 N35 N 0  1 N N N N N N 11.842 -138.318 13.612 3.598   0.036  -0.836 N35  1G3 46 
1G1 H43 H43 H 0  1 N N N N N N 11.210 -136.913 22.906 -5.915  -1.095 0.292  H43  1G2 47 
1G1 H45 H45 H 0  1 N N N N N N 13.983 -138.251 22.689 -5.955  1.937  -0.042 H45  1G2 48 
1G1 H46 H46 H 0  1 N N N N N N 13.656 -136.497 22.479 -5.121  0.811  -1.139 H46  1G2 49 
1G1 H47 H47 H 0  1 N N N N N N 13.362 -135.058 24.419 -8.380  2.010  0.055  H47  1G2 50 
1G1 H48 H48 H 0  1 N N N N N N 13.576 -134.740 26.868 -10.493 1.615  -1.146 H48  1G2 51 
1G1 H49 H49 H 0  1 N N N N N N 13.615 -139.315 24.958 -6.379  -0.681 -2.580 H49  1G2 52 
1G1 H50 H50 H 0  1 N N N N N N 13.817 -138.999 27.408 -8.492  -1.075 -3.782 H50  1G2 53 
1G1 H51 H51 H 0  1 N N N N N N 13.806 -136.705 28.365 -10.550 0.069  -3.062 H51  1G2 54 
1G1 H42 H42 H 0  1 N N N N N N 10.673 -136.293 20.739 -3.467  -1.015 -0.014 H    LEU 55 
1G1 H32 H32 H 0  1 N N N N N N 9.945  -138.764 19.321 -2.045  0.770  1.826  HA   LEU 56 
1G1 H33 H33 H 0  1 N N N N N N 8.998  -136.334 18.043 -2.550  -1.301 3.151  HB2  LEU 57 
1G1 H34 H34 H 0  1 N N N N N N 8.809  -136.183 19.822 -1.683  -2.258 1.927  HB3  LEU 58 
1G1 H35 H35 H 0  1 N N N N N N 7.707  -138.523 18.177 0.352   -0.823 2.342  HG   LEU 59 
1G1 H39 H39 H 0  1 N N N N N N 7.947  -139.022 20.639 0.393   0.603  4.335  HD11 LEU 60 
1G1 H40 H40 H 0  1 N N N N N N 6.976  -137.558 21.016 -0.923  1.132  3.260  HD12 LEU 61 
1G1 H41 H41 H 0  1 N N N N N N 6.225  -138.933 20.137 -1.292  0.171  4.713  HD13 LEU 62 
1G1 H36 H36 H 0  1 N N N N N N 5.487  -137.356 18.389 0.069   -3.025 3.447  HD21 LEU 63 
1G1 H37 H37 H 0  1 N N N N N N 6.308  -135.954 19.156 0.910   -1.876 4.516  HD22 LEU 64 
1G1 H38 H38 H 0  1 N N N N N N 6.665  -136.379 17.447 -0.812  -2.242 4.781  HD23 LEU 65 
1G1 H31 H31 H 0  1 N N N N N N 10.897 -139.540 17.515 0.397   0.728  1.310  H    LEU 66 
1G1 H21 H21 H 0  1 N N N N N N 12.671 -137.661 16.026 1.036   -0.519 -1.264 HA   LEU 67 
1G1 H22 H22 H 0  1 N N N N N N 12.628 -140.703 16.171 -0.095  1.608  -1.882 HB2  LEU 68 
1G1 H23 H23 H 0  1 N N N N N N 13.569 -139.784 14.947 1.057   2.507  -0.865 HB3  LEU 69 
1G1 H24 H24 H 0  1 N N N N N N 13.949 -139.407 17.960 2.934   1.575  -2.250 HG   LEU 70 
1G1 H28 H28 H 0  1 N N N N N N 15.907 -140.971 17.760 0.655   0.574  -4.016 HD11 LEU 71 
1G1 H29 H29 H 0  1 N N N N N N 14.348 -141.793 17.415 2.395   0.458  -4.374 HD12 LEU 72 
1G1 H30 H30 H 0  1 N N N N N N 15.435 -141.324 16.063 1.702   -0.461 -3.016 HD13 LEU 73 
1G1 H25 H25 H 0  1 N N N N N N 16.216 -138.565 17.346 1.961   3.800  -2.750 HD21 LEU 74 
1G1 H26 H26 H 0  1 N N N N N N 15.842 -138.802 15.605 2.479   2.980  -4.242 HD22 LEU 75 
1G1 H27 H27 H 0  1 N N N N N N 14.935 -137.581 16.560 0.753   3.034  -3.810 HD23 LEU 76 
1G1 H1  H1  H 0  1 N N N N N N 12.401 -140.746 13.193 3.444   4.890  1.291  H1   1G3 77 
1G1 H2  H2  H 0  1 N N N N N N 12.302 -141.470 11.553 4.491   4.455  2.663  H2   1G3 78 
1G1 H3  H3  H 0  1 N N N N N N 13.516 -142.075 12.731 4.815   5.937  1.732  H3   1G3 79 
1G1 H4  H4  H 0  1 N N N N N N 13.441 -138.539 9.996  4.804   1.943  1.627  H4   1G3 80 
1G1 H5  H5  H 0  1 N N N N N N 13.475 -137.695 11.581 3.757   2.378  0.255  H5   1G3 81 
1G1 H6  H6  H 0  1 N N N N N N 11.173 -138.442 10.266 5.561   1.744  -1.324 H6   1G3 82 
1G1 H7  H7  H 0  1 N N N N N N 11.422 -139.867 11.330 6.608   1.308  0.048  H7   1G3 83 
1G1 H8  H8  H 0  1 N N N N N N 10.014 -138.248 12.547 4.877   -0.360 0.777  H8   1G3 84 
1G1 H9  H9  H 0  1 N N N N N N 12.164 -136.138 12.443 5.793   -0.713 -2.112 H9   1G3 85 
1G1 H10 H10 H 0  1 N N N N N N 11.201 -136.418 10.953 6.824   -0.978 -0.685 H10  1G3 86 
1G1 H11 H11 H 0  1 N N N N N N 11.306 -133.855 11.668 6.416   -2.848 0.812  H11  1G3 87 
1G1 H12 H12 H 0  1 N N N N N N 9.746  -132.076 12.363 5.506   -5.124 1.046  H12  1G3 88 
1G1 H13 H13 H 0  1 N N N N N N 8.098  -131.350 13.837 3.391   -6.727 -1.492 H13  1G3 89 
1G1 H14 H14 H 0  1 N N N N N N 6.755  -132.071 12.887 4.417   -6.990 -0.062 H14  1G3 90 
1G1 H15 H15 H 0  1 N N N N N N 6.116  -131.565 15.104 2.081   -7.229 0.462  H15  1G3 91 
1G1 H16 H16 H 0  1 N N N N N N 6.058  -133.180 14.867 2.686   -5.893 1.245  H16  1G3 92 
1G1 H18 H18 H 0  1 N N N N N N 7.210  -135.019 14.192 3.048   -4.494 -2.382 H18  1G3 93 
1G1 H19 H19 H 0  1 N N N N N N 8.776  -136.812 13.497 3.953   -2.215 -2.611 H19  1G3 94 
1G1 H20 H20 H 0  1 N N N N N N 12.841 -138.314 13.565 3.462   -0.185 -1.771 H20  1G3 95 
# 
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 
1G1 O50 S48 DOUB N N 1  
1G1 C47 C46 SING N N 2  
1G1 C47 S48 SING N N 3  
1G1 C46 C36 SING N N 4  
1G1 S48 C51 SING N N 5  
1G1 S48 O49 DOUB N N 6  
1G1 C37 C36 SING N N 7  
1G1 C37 C38 SING N N 8  
1G1 C43 C38 DOUB Y N 9  
1G1 C43 C42 SING Y N 10 
1G1 C36 N35 SING N N 11 
1G1 C38 C39 SING Y N 12 
1G1 C42 C41 DOUB Y N 13 
1G1 C39 C40 DOUB Y N 14 
1G1 C41 C40 SING Y N 15 
1G1 C41 C44 SING N N 16 
1G1 N35 C33 SING N N 17 
1G1 C44 N45 SING N N 18 
1G1 C33 O34 DOUB N N 19 
1G1 C33 C28 SING N N 20 
1G1 C29 C28 SING N N 21 
1G1 C29 C30 SING N N 22 
1G1 C28 N27 SING N N 23 
1G1 C32 C30 SING N N 24 
1G1 C30 C31 SING N N 25 
1G1 N27 C25 SING N N 26 
1G1 O26 C25 DOUB N N 27 
1G1 C25 C15 SING N N 28 
1G1 C19 C17 SING N N 29 
1G1 C17 C16 SING N N 30 
1G1 C17 C18 SING N N 31 
1G1 C16 C15 SING N N 32 
1G1 C15 N14 SING N N 33 
1G1 N14 C12 SING N N 34 
1G1 O13 C12 DOUB N N 35 
1G1 C12 C8  SING N N 36 
1G1 C8  C7  SING N N 37 
1G1 C8  N9  SING N N 38 
1G1 C7  C3  SING N N 39 
1G1 N9  N10 DOUB N N 40 
1G1 N10 N11 DOUB N N 41 
1G1 C3  C2  DOUB Y N 42 
1G1 C3  C4  SING Y N 43 
1G1 C2  C1  SING Y N 44 
1G1 C4  C5  DOUB Y N 45 
1G1 C1  C6  DOUB Y N 46 
1G1 C5  C6  SING Y N 47 
1G1 C51 H1  SING N N 48 
1G1 C51 H2  SING N N 49 
1G1 C51 H3  SING N N 50 
1G1 C47 H4  SING N N 51 
1G1 C47 H5  SING N N 52 
1G1 C46 H6  SING N N 53 
1G1 C46 H7  SING N N 54 
1G1 C36 H8  SING N N 55 
1G1 C37 H9  SING N N 56 
1G1 C37 H10 SING N N 57 
1G1 C43 H11 SING N N 58 
1G1 C42 H12 SING N N 59 
1G1 C44 H13 SING N N 60 
1G1 C44 H14 SING N N 61 
1G1 N45 H15 SING N N 62 
1G1 N45 H16 SING N N 63 
1G1 C40 H18 SING N N 64 
1G1 C39 H19 SING N N 65 
1G1 N35 H20 SING N N 66 
1G1 C28 H21 SING N N 67 
1G1 C29 H22 SING N N 68 
1G1 C29 H23 SING N N 69 
1G1 C30 H24 SING N N 70 
1G1 C32 H25 SING N N 71 
1G1 C32 H26 SING N N 72 
1G1 C32 H27 SING N N 73 
1G1 C31 H28 SING N N 74 
1G1 C31 H29 SING N N 75 
1G1 C31 H30 SING N N 76 
1G1 N27 H31 SING N N 77 
1G1 C15 H32 SING N N 78 
1G1 C16 H33 SING N N 79 
1G1 C16 H34 SING N N 80 
1G1 C17 H35 SING N N 81 
1G1 C19 H36 SING N N 82 
1G1 C19 H37 SING N N 83 
1G1 C19 H38 SING N N 84 
1G1 C18 H39 SING N N 85 
1G1 C18 H40 SING N N 86 
1G1 C18 H41 SING N N 87 
1G1 N14 H42 SING N N 88 
1G1 C8  H43 SING N N 89 
1G1 C7  H45 SING N N 90 
1G1 C7  H46 SING N N 91 
1G1 C2  H47 SING N N 92 
1G1 C1  H48 SING N N 93 
1G1 C4  H49 SING N N 94 
1G1 C5  H50 SING N N 95 
1G1 C6  H51 SING N N 96 
# 
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 
1G1 SMILES           ACDLabs              12.01 "NCc1ccc(CC(CCS(C)(=O)=O)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(Cc2ccccc2)/N=[N+]=[N-])cc1"                                                                                                                                                            
1G1 InChI            InChI                1.06  "InChI=1S/C33H49N7O5S/c1-22(2)17-28(31(41)36-27(15-16-46(5,44)45)19-25-11-13-26(21-34)14-12-25)37-32(42)29(18-23(3)4)38-33(43)30(39-40-35)20-24-9-7-6-8-10-24/h6-14,22-23,27-30H,15-21,34H2,1-5H3,(H,36,41)(H,37,42)(H,38,43)/t27-,28+,29+,30+/m1/s1" 
1G1 InChIKey         InChI                1.06  JORBDDYVSOOLMV-RYTSNQFKSA-N                                                                                                                                                                                                                           
1G1 SMILES_CANONICAL CACTVS               3.385 "CC(C)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)N=[N+]=[N-])C(=O)N[C@H](CC[S](C)(=O)=O)Cc2ccc(CN)cc2"                                                                                                                                           
1G1 SMILES           CACTVS               3.385 "CC(C)C[CH](NC(=O)[CH](CC(C)C)NC(=O)[CH](Cc1ccccc1)N=[N+]=[N-])C(=O)N[CH](CC[S](C)(=O)=O)Cc2ccc(CN)cc2"                                                                                                                                               
1G1 SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "CC(C)C[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCS(=O)(=O)C)Cc1ccc(cc1)CN)NC(=O)[C@H](Cc2ccccc2)N=[N+]=[N-]"                                                                                                                                           
1G1 SMILES           "OpenEye OEToolkits" 2.0.7 "CC(C)CC(C(=O)NC(CC(C)C)C(=O)NC(CCS(=O)(=O)C)Cc1ccc(cc1)CN)NC(=O)C(Cc2ccccc2)N=[N+]=[N-]"                                                                                                                                                             
# 
loop_
_pdbx_chem_comp_identifier.comp_id 
_pdbx_chem_comp_identifier.type 
_pdbx_chem_comp_identifier.program 
_pdbx_chem_comp_identifier.program_version 
_pdbx_chem_comp_identifier.identifier 
1G1 "SYSTEMATIC NAME" ACDLabs              12.01 "N-[(2S)-2-azido-3-phenylpropanoyl]-L-leucyl-N-[(2S)-1-[4-(aminomethyl)phenyl]-4-(methanesulfonyl)butan-2-yl]-L-leucinamide"                                                                              
1G1 "SYSTEMATIC NAME" "OpenEye OEToolkits" 2.0.7 "(2~{S})-~{N}-[(2~{S})-1-[[(2~{S})-1-[4-(aminomethyl)phenyl]-4-methylsulfonyl-butan-2-yl]amino]-4-methyl-1-oxidanylidene-pentan-2-yl]-2-[[(2~{S})-2-azido-3-phenyl-propanoyl]amino]-4-methyl-pentanamide" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
1G1 "Create component"   2013-01-22 RCSB 
1G1 "Initial release"    2013-01-25 RCSB 
1G1 "Other modification" 2024-05-08 RCSB 
1G1 "Modify PCM"         2024-09-27 PDBE 
# 
_pdbx_chem_comp_pcm.pcm_id                             1 
_pdbx_chem_comp_pcm.comp_id                            1G1 
_pdbx_chem_comp_pcm.modified_residue_id                THR 
_pdbx_chem_comp_pcm.type                               None 
_pdbx_chem_comp_pcm.category                           "Covalent chemical modification" 
_pdbx_chem_comp_pcm.position                           "Amino-acid side chain" 
_pdbx_chem_comp_pcm.polypeptide_position               "Any position" 
_pdbx_chem_comp_pcm.comp_id_linking_atom               C46 
_pdbx_chem_comp_pcm.modified_residue_id_linking_atom   OG1 
_pdbx_chem_comp_pcm.uniprot_specific_ptm_accession     ? 
_pdbx_chem_comp_pcm.uniprot_generic_ptm_accession      ? 
# 
