data_A1ARG
# 
_chem_comp.id                                    A1ARG 
_chem_comp.name                                  "O-tert-butyl-N-[(cyclopropylmethoxy)carbonyl]-L-threonyl-3-cyclohexyl-N-{(2R)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-alaninamide" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C29 H50 N4 O7" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-05-13 
_chem_comp.pdbx_modified_date                    2025-05-09 
_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                        566.730 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1ARG 
_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        9BQL 
_chem_comp.pdbx_subcomponent_list                ? 
_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 
A1ARG N    N1  N 0 1 N N N N N N -9.520  -15.486 -17.768 -0.096  -0.069 -1.014 N    A1ARG 1  
A1ARG C    C1  C 0 1 N N S N N N -10.166 -17.743 -18.081 -2.474  0.577  -0.793 C    A1ARG 2  
A1ARG O    O1  O 0 1 N N N N N N -10.710 -16.482 -16.130 -1.271  -0.755 0.739  O    A1ARG 3  
A1ARG C1   C2  C 0 1 N N N N N N -10.178 -16.509 -17.235 -1.238  -0.130 -0.300 C1   A1ARG 4  
A1ARG C10  C3  C 0 1 N N N N N N -14.711 -15.840 -14.707 6.870   0.088  1.851  C10  A1ARG 5  
A1ARG C11  C4  C 0 1 N N N N N N -8.848  -13.201 -18.141 1.069   -2.219 -0.983 C11  A1ARG 6  
A1ARG C12  C5  C 0 1 N N N N N N -7.477  -12.831 -17.572 -0.104  -2.932 -0.305 C12  A1ARG 7  
A1ARG C13  C6  C 0 1 N N R N N N -11.529 -18.373 -18.374 -2.190  2.077  -0.910 C13  A1ARG 8  
A1ARG C14  C7  C 0 1 N N N N N N -12.455 -17.329 -18.996 -3.478  2.811  -1.290 C14  A1ARG 9  
A1ARG C15  C8  C 0 1 N N N N N N -8.162  -18.953 -17.880 -4.849  0.437  -0.269 C15  A1ARG 10 
A1ARG C16  C9  C 0 1 N N N N N N -6.275  -20.463 -17.858 -7.208  0.336  0.076  C16  A1ARG 11 
A1ARG C17  C10 C 0 1 N N N N N N -11.928 -20.732 -18.997 -0.667  3.536  0.228  C17  A1ARG 12 
A1ARG C18  C11 C 0 1 N N N N N N -13.403 -20.604 -18.631 -1.124  4.676  -0.685 C18  A1ARG 13 
A1ARG C19  C12 C 0 1 N N N N N N -11.182 -21.400 -17.853 0.576   2.872  -0.368 C19  A1ARG 14 
A1ARG C2   C13 C 0 1 N N S N N N -9.658  -14.139 -17.246 1.105   -0.757 -0.534 C2   A1ARG 15 
A1ARG C20  C14 C 0 1 N N N N N N -11.843 -21.609 -20.239 -0.332  4.095  1.612  C20  A1ARG 16 
A1ARG C21  C15 C 0 1 N N N N N N -6.471  -12.718 -18.718 0.132   -2.978 1.206  C21  A1ARG 17 
A1ARG C22  C16 C 0 1 N N N N N N -5.088  -12.337 -18.197 -1.040  -3.690 1.883  C22  A1ARG 18 
A1ARG C23  C17 C 0 1 N N N N N N -4.634  -13.350 -17.159 -1.152  -5.116 1.341  C23  A1ARG 19 
A1ARG C24  C18 C 0 1 N N N N N N -5.615  -13.483 -16.002 -1.388  -5.070 -0.170 C24  A1ARG 20 
A1ARG C25  C19 C 0 1 N N N N N N -6.993  -13.845 -16.541 -0.216  -4.358 -0.848 C25  A1ARG 21 
A1ARG C26  C20 C 0 1 N N N N N N -5.322  -20.956 -16.796 -8.212  0.079  1.202  C26  A1ARG 22 
A1ARG C27  C21 C 0 1 N N N N N N -5.689  -20.401 -15.429 -9.117  -1.148 1.076  C27  A1ARG 23 
A1ARG C28  C22 C 0 1 N N N N N N -4.640  -19.693 -16.285 -9.697  0.254  0.878  C28  A1ARG 24 
A1ARG C3   C23 C 0 1 N N N N N N -11.104 -13.734 -17.290 2.329   -0.087 -1.104 C3   A1ARG 25 
A1ARG C4   C24 C 0 1 N N S N N N -13.023 -12.742 -16.281 4.746   0.099  -1.351 C4   A1ARG 26 
A1ARG C5   C25 C 0 1 N N N N N N -13.003 -11.251 -15.942 5.012   -0.437 -2.759 C5   A1ARG 27 
A1ARG C6   C26 C 0 1 N N N N N N -13.911 -13.527 -15.316 5.952   -0.196 -0.457 C6   A1ARG 28 
A1ARG C7   C27 C 0 1 N N S N N N -13.943 -15.007 -15.699 5.744   0.458  0.911  C7   A1ARG 29 
A1ARG C8   C28 C 0 1 N N N N N N -14.680 -15.258 -17.010 5.836   1.997  0.795  C8   A1ARG 30 
A1ARG C9   C29 C 0 1 N N N N N N -15.483 -16.532 -16.758 6.537   2.371  2.120  C9   A1ARG 31 
A1ARG N1   N2  N 0 1 N N N N N N -11.661 -13.251 -16.181 3.556   -0.552 -0.798 N1   A1ARG 32 
A1ARG N2   N3  N 0 1 N N N N N N -15.603 -16.613 -15.315 7.295   1.177  2.514  N2   A1ARG 33 
A1ARG N3   N4  N 0 1 N N N N N N -9.340  -18.672 -17.378 -3.571  0.360  0.152  N3   A1ARG 34 
A1ARG O1   O2  O 0 1 N N N N N N -11.753 -13.857 -18.318 2.210   0.871  -1.838 O1   A1ARG 35 
A1ARG O2   O3  O 0 1 N N N N N N -14.287 -10.639 -16.046 5.341   -1.826 -2.686 O2   A1ARG 36 
A1ARG O3   O4  O 0 1 N N N N N N -14.503 -15.803 -13.504 7.321   -1.030 1.989  O3   A1ARG 37 
A1ARG O4   O5  O 0 1 N N N N N N -11.324 -19.460 -19.297 -1.713  2.570  0.344  O4   A1ARG 38 
A1ARG O5   O6  O 0 1 N N N N N N -7.375  -19.909 -17.154 -5.858  0.237  0.600  O5   A1ARG 39 
A1ARG O6   O7  O 0 1 N N N N N N -7.710  -18.466 -18.909 -5.091  0.687  -1.434 O6   A1ARG 40 
A1ARG HN   H1  H 0 1 N N N N N N -8.915  -15.648 -18.548 -0.071  0.428  -1.847 HN   A1ARG 41 
A1ARG H0   H2  H 0 1 N N N N N N -9.694  -17.497 -19.044 -2.752  0.184  -1.771 H0   A1ARG 42 
A1ARG H111 H3  H 0 0 N N N N N N -8.698  -13.694 -19.113 2.002   -2.708 -0.703 H111 A1ARG 43 
A1ARG H112 H4  H 0 0 N N N N N N -9.425  -12.275 -18.284 0.945   -2.264 -2.065 H112 A1ARG 44 
A1ARG H12  H5  H 0 1 N N N N N N -7.558  -11.849 -17.083 -1.026  -2.390 -0.512 H12  A1ARG 45 
A1ARG H13  H6  H 0 1 N N N N N N -11.970 -18.740 -17.436 -1.436  2.245  -1.678 H13  A1ARG 46 
A1ARG H142 H7  H 0 0 N N N N N N -13.434 -17.785 -19.206 -4.230  2.650  -0.517 H142 A1ARG 47 
A1ARG H143 H8  H 0 0 N N N N N N -12.584 -16.490 -18.297 -3.274  3.878  -1.382 H143 A1ARG 48 
A1ARG H141 H9  H 0 0 N N N N N N -12.014 -16.960 -19.934 -3.847  2.428  -2.241 H141 A1ARG 49 
A1ARG H161 H10 H 0 0 N N N N N N -6.607  -21.297 -18.494 -7.348  -0.406 -0.711 H161 A1ARG 50 
A1ARG H162 H11 H 0 0 N N N N N N -5.792  -19.696 -18.481 -7.367  1.333  -0.333 H162 A1ARG 51 
A1ARG H182 H12 H 0 0 N N N N N N -13.815 -21.600 -18.412 -2.062  5.086  -0.312 H182 A1ARG 52 
A1ARG H183 H13 H 0 0 N N N N N N -13.506 -19.962 -17.744 -0.364  5.458  -0.698 H183 A1ARG 53 
A1ARG H181 H14 H 0 0 N N N N N N -13.952 -20.158 -19.473 -1.270  4.295  -1.696 H181 A1ARG 54 
A1ARG H192 H15 H 0 0 N N N N N N -11.648 -22.371 -17.628 0.338   2.475  -1.355 H192 A1ARG 55 
A1ARG H191 H16 H 0 0 N N N N N N -10.132 -21.555 -18.141 1.375   3.609  -0.457 H191 A1ARG 56 
A1ARG H193 H17 H 0 0 N N N N N N -11.226 -20.757 -16.962 0.902   2.061  0.282  H193 A1ARG 57 
A1ARG H2   H18 H 0 1 N N N N N N -9.282  -14.081 -16.214 1.140   -0.712 0.554  H2   A1ARG 58 
A1ARG H203 H19 H 0 0 N N N N N N -12.300 -22.587 -20.030 -0.007  3.283  2.263  H203 A1ARG 59 
A1ARG H202 H20 H 0 0 N N N N N N -12.379 -21.124 -21.068 0.466   4.832  1.524  H202 A1ARG 60 
A1ARG H201 H21 H 0 0 N N N N N N -10.788 -21.749 -20.517 -1.218  4.567  2.037  H201 A1ARG 61 
A1ARG H212 H22 H 0 0 N N N N N N -6.406  -13.686 -19.236 1.056   -3.519 1.413  H212 A1ARG 62 
A1ARG H211 H23 H 0 0 N N N N N N -6.815  -11.947 -19.423 0.213   -1.962 1.592  H211 A1ARG 63 
A1ARG H222 H24 H 0 0 N N N N N N -5.133  -11.338 -17.738 -0.872  -3.723 2.960  H222 A1ARG 64 
A1ARG H221 H25 H 0 0 N N N N N N -4.373  -12.325 -19.033 -1.963  -3.149 1.676  H221 A1ARG 65 
A1ARG H232 H26 H 0 0 N N N N N N -3.659  -13.033 -16.760 -0.229  -5.658 1.548  H232 A1ARG 66 
A1ARG H231 H27 H 0 0 N N N N N N -4.529  -14.331 -17.646 -1.987  -5.624 1.824  H231 A1ARG 67 
A1ARG H242 H28 H 0 0 N N N N N N -5.673  -12.528 -15.459 -1.468  -6.086 -0.556 H242 A1ARG 68 
A1ARG H241 H29 H 0 0 N N N N N N -5.270  -14.273 -15.318 -2.311  -4.529 -0.377 H241 A1ARG 69 
A1ARG H252 H30 H 0 0 N N N N N N -7.707  -13.873 -15.705 -0.384  -4.325 -1.924 H252 A1ARG 70 
A1ARG H251 H31 H 0 0 N N N N N N -6.942  -14.837 -17.013 0.707   -4.899 -0.640 H251 A1ARG 71 
A1ARG H26  H32 H 0 1 N N N N N N -4.772  -21.902 -16.905 -7.879  0.359  2.201  H26  A1ARG 72 
A1ARG H271 H33 H 0 0 N N N N N N -6.674  -19.937 -15.270 -8.998  -1.773 0.191  H271 A1ARG 73 
A1ARG H272 H34 H 0 0 N N N N N N -5.385  -20.937 -14.518 -9.379  -1.676 1.993  H272 A1ARG 74 
A1ARG H282 H35 H 0 0 N N N N N N -3.580  -19.720 -15.991 -10.341 0.649  1.664  H282 A1ARG 75 
A1ARG H281 H36 H 0 0 N N N N N N -4.869  -18.720 -16.743 -9.959  0.552  -0.138 H281 A1ARG 76 
A1ARG H4   H37 H 0 1 N N N N N N -13.401 -12.873 -17.306 4.582   1.176  -1.398 H4   A1ARG 77 
A1ARG H5   H38 H 0 1 N N N N N N -12.640 -11.131 -14.911 4.120   -0.307 -3.372 H5   A1ARG 78 
A1ARG H    H39 H 0 1 N N N N N N -12.315 -10.743 -16.634 5.843   0.110  -3.205 H    A1ARG 79 
A1ARG H62  H40 H 0 1 N N N N N N -13.514 -13.426 -14.295 6.057   -1.273 -0.333 H62  A1ARG 80 
A1ARG H61  H41 H 0 1 N N N N N N -14.933 -13.121 -15.353 6.853   0.207  -0.919 H61  A1ARG 81 
A1ARG H7   H42 H 0 1 N N N N N N -12.913 -15.385 -15.781 4.783   0.162  1.332  H7   A1ARG 82 
A1ARG H81  H43 H 0 1 N N N N N N -15.349 -14.417 -17.248 6.442   2.288  -0.063 H81  A1ARG 83 
A1ARG H82  H44 H 0 1 N N N N N N -13.967 -15.404 -17.835 4.844   2.444  0.739  H82  A1ARG 84 
A1ARG H92  H45 H 0 1 N N N N N N -14.951 -17.410 -17.153 7.210   3.214  1.966  H92  A1ARG 85 
A1ARG H91  H46 H 0 1 N N N N N N -16.476 -16.464 -17.226 5.798   2.612  2.883  H91  A1ARG 86 
A1ARG HN1  H47 H 0 1 N N N N N N -11.164 -13.238 -15.313 3.652   -1.318 -0.210 HN1  A1ARG 87 
A1ARG HN2  H48 H 0 1 N N N N N N -16.274 -17.180 -14.837 8.014   1.175  3.165  HN2  A1ARG 88 
A1ARG HN3  H49 H 0 1 N N N N N N -9.651  -19.096 -16.527 -3.378  0.160  1.082  HN3  A1ARG 89 
A1ARG HO2  H50 H 0 1 N N N N N N -14.218 -9.717  -15.826 5.523   -2.233 -3.544 HO2  A1ARG 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 
A1ARG O6  C15  DOUB N N 1  
A1ARG O5  C15  SING N N 2  
A1ARG C15 N3   SING N N 3  
A1ARG C16 O5   SING N N 4  
A1ARG C26 C16  SING N N 5  
A1ARG C26 C28  SING N N 6  
A1ARG C27 C26  SING N N 7  
A1ARG C28 C27  SING N N 8  
A1ARG N3  C    SING N N 9  
A1ARG C13 C    SING N N 10 
A1ARG C   C1   SING N N 11 
A1ARG O4  C13  SING N N 12 
A1ARG C14 C13  SING N N 13 
A1ARG C17 O4   SING N N 14 
A1ARG C20 C17  SING N N 15 
A1ARG C19 C17  SING N N 16 
A1ARG C18 C17  SING N N 17 
A1ARG O   C1   DOUB N N 18 
A1ARG C1  N    SING N N 19 
A1ARG N   C2   SING N N 20 
A1ARG C11 C2   SING N N 21 
A1ARG C2  C3   SING N N 22 
A1ARG C12 C11  SING N N 23 
A1ARG C12 C25  SING N N 24 
A1ARG C21 C12  SING N N 25 
A1ARG C25 C24  SING N N 26 
A1ARG C24 C23  SING N N 27 
A1ARG C23 C22  SING N N 28 
A1ARG C22 C21  SING N N 29 
A1ARG O1  C3   DOUB N N 30 
A1ARG C3  N1   SING N N 31 
A1ARG N1  C4   SING N N 32 
A1ARG C5  C4   SING N N 33 
A1ARG C4  C6   SING N N 34 
A1ARG O2  C5   SING N N 35 
A1ARG C6  C7   SING N N 36 
A1ARG C7  C10  SING N N 37 
A1ARG C7  C8   SING N N 38 
A1ARG C10 O3   DOUB N N 39 
A1ARG N2  C10  SING N N 40 
A1ARG C9  N2   SING N N 41 
A1ARG C8  C9   SING N N 42 
A1ARG N   HN   SING N N 43 
A1ARG C   H0   SING N N 44 
A1ARG C11 H111 SING N N 45 
A1ARG C11 H112 SING N N 46 
A1ARG C12 H12  SING N N 47 
A1ARG C13 H13  SING N N 48 
A1ARG C14 H142 SING N N 49 
A1ARG C14 H143 SING N N 50 
A1ARG C14 H141 SING N N 51 
A1ARG C16 H161 SING N N 52 
A1ARG C16 H162 SING N N 53 
A1ARG C18 H182 SING N N 54 
A1ARG C18 H183 SING N N 55 
A1ARG C18 H181 SING N N 56 
A1ARG C19 H192 SING N N 57 
A1ARG C19 H191 SING N N 58 
A1ARG C19 H193 SING N N 59 
A1ARG C2  H2   SING N N 60 
A1ARG C20 H203 SING N N 61 
A1ARG C20 H202 SING N N 62 
A1ARG C20 H201 SING N N 63 
A1ARG C21 H212 SING N N 64 
A1ARG C21 H211 SING N N 65 
A1ARG C22 H222 SING N N 66 
A1ARG C22 H221 SING N N 67 
A1ARG C23 H232 SING N N 68 
A1ARG C23 H231 SING N N 69 
A1ARG C24 H242 SING N N 70 
A1ARG C24 H241 SING N N 71 
A1ARG C25 H252 SING N N 72 
A1ARG C25 H251 SING N N 73 
A1ARG C26 H26  SING N N 74 
A1ARG C27 H271 SING N N 75 
A1ARG C27 H272 SING N N 76 
A1ARG C28 H282 SING N N 77 
A1ARG C28 H281 SING N N 78 
A1ARG C4  H4   SING N N 79 
A1ARG C5  H5   SING N N 80 
A1ARG C5  H    SING N N 81 
A1ARG C6  H62  SING N N 82 
A1ARG C6  H61  SING N N 83 
A1ARG C7  H7   SING N N 84 
A1ARG C8  H81  SING N N 85 
A1ARG C8  H82  SING N N 86 
A1ARG C9  H92  SING N N 87 
A1ARG C9  H91  SING N N 88 
A1ARG N1  HN1  SING N N 89 
A1ARG N2  HN2  SING N N 90 
A1ARG N3  HN3  SING N N 91 
A1ARG O2  HO2  SING N N 92 
# 
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 
A1ARG SMILES           ACDLabs              12.01 "CC(C)(C)OC(C)C(NC(=O)OCC1CC1)C(=O)NC(CC1CCCCC1)C(=O)NC(CC1CCNC1=O)CO"                                                                                                                                                                 
A1ARG InChI            InChI                1.06  "InChI=1S/C29H50N4O7/c1-18(40-29(2,3)4)24(33-28(38)39-17-20-10-11-20)27(37)32-23(14-19-8-6-5-7-9-19)26(36)31-22(16-34)15-21-12-13-30-25(21)35/h18-24,34H,5-17H2,1-4H3,(H,30,35)(H,31,36)(H,32,37)(H,33,38)/t18-,21+,22-,23+,24?/m1/s1" 
A1ARG InChIKey         InChI                1.06  HGHJOBJIAMXYGG-HATMDWNPSA-N                                                                                                                                                                                                            
A1ARG SMILES_CANONICAL CACTVS               3.385 "C[C@@H](OC(C)(C)C)[C@H](NC(=O)OCC1CC1)C(=O)N[C@@H](CC2CCCCC2)C(=O)N[C@H](CO)C[C@@H]3CCNC3=O"                                                                                                                                          
A1ARG SMILES           CACTVS               3.385 "C[CH](OC(C)(C)C)[CH](NC(=O)OCC1CC1)C(=O)N[CH](CC2CCCCC2)C(=O)N[CH](CO)C[CH]3CCNC3=O"                                                                                                                                                  
A1ARG SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C[C@H]([C@@H](C(=O)N[C@@H](CC1CCCCC1)C(=O)N[C@@H](C[C@@H]2CCNC2=O)CO)NC(=O)OCC3CC3)OC(C)(C)C"                                                                                                                                         
A1ARG SMILES           "OpenEye OEToolkits" 2.0.7 "CC(C(C(=O)NC(CC1CCCCC1)C(=O)NC(CC2CCNC2=O)CO)NC(=O)OCC3CC3)OC(C)(C)C"                                                                                                                                                                 
# 
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 
A1ARG "SYSTEMATIC NAME" ACDLabs              12.01 "O-tert-butyl-N-[(cyclopropylmethoxy)carbonyl]-L-threonyl-3-cyclohexyl-N-{(2R)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-L-alaninamide"                                                                                                        
A1ARG "SYSTEMATIC NAME" "OpenEye OEToolkits" 2.0.7 "cyclopropylmethyl ~{N}-[(2~{S},3~{R})-1-[[(2~{S})-3-cyclohexyl-1-oxidanylidene-1-[[(2~{S})-1-oxidanyl-3-[(3~{S})-2-oxidanylidenepyrrolidin-3-yl]propan-2-yl]amino]propan-2-yl]amino]-3-[(2-methylpropan-2-yl)oxy]-1-oxidanylidene-butan-2-yl]carbamate" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1ARG "Create component" 2024-05-13 RCSB 
A1ARG "Modify PCM"       2024-09-27 PDBE 
A1ARG "Initial release"  2025-05-14 RCSB 
# 
_pdbx_chem_comp_pcm.pcm_id                             1 
_pdbx_chem_comp_pcm.comp_id                            A1ARG 
_pdbx_chem_comp_pcm.modified_residue_id                CYS 
_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               C5 
_pdbx_chem_comp_pcm.modified_residue_id_linking_atom   SG 
_pdbx_chem_comp_pcm.uniprot_specific_ptm_accession     ? 
_pdbx_chem_comp_pcm.uniprot_generic_ptm_accession      ? 
# 
