data_1ZV
# 
_chem_comp.id                                    1ZV 
_chem_comp.name                                  "amino({3-[(3R,5R,14S,16S,21aR)-5,14-dihydroxy-1,4,17-trioxo-16-(2-phenylethyl)icosahydro-1H-pyrrolo[1,2-d][1,4,7,11]tetraazacyclononadecin-3-yl]propyl}amino)methaniminium" 
_chem_comp.type                                  peptide-like 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C30 H50 N7 O5" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    1 
_chem_comp.pdbx_initial_date                     2008-08-27 
_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                        588.762 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     1ZV 
_chem_comp.pdbx_model_coordinates_details        "not provided" 
_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        1ay6 
_chem_comp.pdbx_subcomponent_list                "HMF PRO 00W 8AC" 
_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_backbone_atom_flag 
_chem_comp_atom.pdbx_n_terminal_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 
1ZV N    N1  N 0 1 N N N N N N 17.319 -16.948 23.000 2.807  1.720  0.287  N    HMF 1  
1ZV CA   C1  C 0 1 N N R N N N 18.111 -15.809 23.640 2.769  0.257  0.410  CA   HMF 2  
1ZV C    C2  C 0 1 N N N N N N 17.746 -14.582 22.850 1.768  -0.303 -0.567 C    HMF 3  
1ZV O    O1  O 0 1 N N N N N N 16.602 -14.156 23.027 0.924  0.419  -1.054 O    HMF 4  
1ZV CB   C3  C 0 1 N N N N N N 17.642 -16.156 25.068 4.154  -0.317 0.107  CB   HMF 5  
1ZV CG   C4  C 0 1 N N N N N N 18.682 -16.036 26.102 5.183  0.307  1.052  CG   HMF 6  
1ZV C1   C5  C 0 1 Y N N N N N 20.119 -15.714 25.812 6.547  -0.258 0.753  C1   HMF 7  
1ZV C2   C6  C 0 1 Y N N N N N 21.020 -16.574 25.229 7.365  0.362  -0.173 C2   HMF 8  
1ZV C6   C7  C 0 1 Y N N N N N 20.646 -14.479 26.143 6.984  -1.394 1.409  C6   HMF 9  
1ZV C3   C8  C 0 1 Y N N N N N 22.347 -16.195 25.022 8.616  -0.156 -0.447 C3   HMF 10 
1ZV C5   C9  C 0 1 Y N N N N N 21.969 -14.096 25.984 8.236  -1.913 1.135  C5   HMF 11 
1ZV C4   C10 C 0 1 Y N N N N N 22.813 -14.999 25.389 9.051  -1.295 0.205  C4   HMF 12 
1ZV N1   N2  N 0 1 N N N N N N 18.583 -14.068 22.000 1.812  -1.611 -0.899 N    PRO 13 
1ZV CA1  C11 C 0 1 N N S N N N 18.220 -12.823 21.251 0.907  -2.276 -1.837 CA   PRO 14 
1ZV C7   C12 C 0 1 N N N N N N 16.877 -12.883 20.550 -0.522 -1.957 -1.476 C    PRO 15 
1ZV O1   O3  O 0 1 N N N N N N 16.539 -14.000 20.102 -0.941 -2.174 -0.358 O    PRO 16 
1ZV CB1  C13 C 0 1 N N N N N N 19.382 -12.566 20.336 1.142  -3.785 -1.736 CB   PRO 17 
1ZV CG1  C14 C 0 1 N N N N N N 20.395 -13.636 20.575 2.209  -3.985 -0.649 CG   PRO 18 
1ZV CD   C15 C 0 1 N N N N N N 19.891 -14.587 21.640 2.773  -2.583 -0.382 CD   PRO 19 
1ZV N2   N3  N 0 1 N N N N N N 16.070 -11.809 20.459 -1.336 -1.419 -2.434 N2   00W 20 
1ZV CA2  C16 C 0 1 N N S N N N 14.803 -11.692 19.760 -2.725 -1.149 -1.992 CA2  00W 21 
1ZV C8   C17 C 0 1 N N N N N N 14.752 -10.937 18.393 -2.935 0.343  -1.953 C8   00W 22 
1ZV O2   O5  O 0 1 N N N N N N 13.641 -11.000 17.586 -2.047 1.087  -2.292 O2   00W 23 
1ZV CB2  C18 C 0 1 N N N N N N 13.730 -11.074 20.639 -2.944 -1.736 -0.596 CB2  00W 24 
1ZV CG2  C19 C 0 1 N N N N N N 13.081 -11.986 21.608 -4.437 -1.718 -0.264 CG2  00W 25 
1ZV CD1  C20 C 0 1 N N N N N N 12.155 -11.285 22.535 -4.646 -2.197 1.174  CD1  00W 26 
1ZV NE   N4  N 0 1 N N N N N N 11.503 -12.307 23.298 -6.075 -2.180 1.492  NE   00W 27 
1ZV CZ   C21 C 0 1 N N N N N N 10.723 -12.181 24.301 -6.505 -2.571 2.731  CZ   00W 28 
1ZV NH1  N5  N 0 1 N N N N N N 10.496 -10.886 24.684 -5.623 -2.967 3.647  NH1  00W 29 
1ZV NH2  N6  N 1 1 N N N N N N 10.080 -13.174 24.927 -7.805 -2.555 3.020  NH2  00W 30 
1ZV C9   C22 C 0 1 N N R N N N 15.993 -11.521 17.538 -4.254 0.905  -1.489 C9   00W 31 
1ZV O3   O7  O 0 1 N N N N N N 16.576 -10.487 17.780 -5.319 0.272  -2.201 O3   00W 32 
1ZV N3   N7  N 0 1 N N N N N N 16.900 -12.362 16.717 -4.286 2.352  -1.744 N3   8AC 33 
1ZV C11  C23 C 0 1 N N N N N N 16.506 -13.762 16.555 -4.224 3.109  -0.487 C11  8AC 34 
1ZV C21  C24 C 0 1 N N N N N N 16.601 -14.709 17.758 -3.378 4.368  -0.692 C21  8AC 35 
1ZV C31  C25 C 0 1 N N N N N N 15.647 -15.875 18.091 -2.603 4.675  0.591  C31  8AC 36 
1ZV C41  C26 C 0 1 N N N N N N 16.248 -17.304 18.343 -1.237 5.265  0.232  C41  8AC 37 
1ZV C51  C27 C 0 1 N N N N N N 15.679 -18.249 19.462 -0.192 4.779  1.238  C51  8AC 38 
1ZV C61  C28 C 0 1 N N N N N N 16.667 -19.000 20.369 0.813  3.868  0.530  C61  8AC 39 
1ZV C71  C29 C 0 1 N N N N N N 16.921 -18.986 21.869 2.113  3.822  1.335  C71  8AC 40 
1ZV C81  C30 C 0 1 N N R N N N 17.869 -18.084 22.506 2.513  2.365  1.574  C81  8AC 41 
1ZV O8   O8  O 0 1 N N N N N N 19.113 -18.288 22.552 1.439  1.675  2.217  O8   8AC 42 
1ZV H    H1  H 0 1 N N N N N N 16.696 -17.259 23.718 3.695  2.029  -0.078 H    HMF 43 
1ZV HA   H3  H 0 1 N N N N N N 19.199 -15.651 23.659 2.477  -0.014 1.425  HA   HMF 44 
1ZV HB2  H5  H 0 1 N N N N N N 16.826 -15.466 25.330 4.139  -1.398 0.248  HB2  HMF 45 
1ZV HB3  H6  H 0 1 N N N N N N 17.293 -17.199 25.063 4.424  -0.089 -0.925 HB3  HMF 46 
1ZV HG2  H7  H 0 1 N N N N N N 18.337 -15.223 26.758 5.198  1.388  0.911  HG2  HMF 47 
1ZV HG3  H8  H 0 1 N N N N N N 18.706 -17.019 26.594 4.913  0.079  2.083  HG3  HMF 48 
1ZV HC2  H9  H 0 1 N N N N N N 20.695 -17.559 24.926 7.025  1.252  -0.682 HC2  HMF 49 
1ZV H6   H10 H 0 1 N N N N N N 19.968 -13.750 26.562 6.347  -1.877 2.136  H6   HMF 50 
1ZV H3   H11 H 0 1 N N N N N N 23.021 -16.894 24.548 9.255  0.329  -1.171 H3   HMF 51 
1ZV H5   H12 H 0 1 N N N N N N 22.320 -13.129 26.314 8.577  -2.800 1.647  H5   HMF 52 
1ZV H4   H13 H 0 1 N N N N N N 23.848 -14.744 25.218 10.029 -1.700 -0.009 H4   HMF 53 
1ZV HA1  H15 H 0 1 N N N N N N 18.063 -11.980 21.940 1.112  -1.935 -2.853 HA   PRO 54 
1ZV HB21 H16 H 0 0 N N N N N N 19.049 -12.589 19.288 0.218  -4.290 -1.452 HB2  PRO 55 
1ZV HB31 H17 H 0 0 N N N N N N 19.819 -11.579 20.549 1.501  -4.173 -2.689 HB3  PRO 56 
1ZV HG21 H18 H 0 0 N N N N N N 20.567 -14.191 19.641 1.755  -4.389 0.256  HG2  PRO 57 
1ZV HG31 H19 H 0 0 N N N N N N 21.338 -13.178 20.910 2.996  -4.648 -1.009 HG3  PRO 58 
1ZV HD2  H20 H 0 1 N N N N N N 20.565 -14.604 22.509 3.729  -2.466 -0.892 HD2  PRO 59 
1ZV HD3  H21 H 0 1 N N N N N N 19.818 -15.614 21.253 2.907  -2.437 0.690  HD3  PRO 60 
1ZV H1   H23 H 0 1 N N N N N N 16.384 -10.987 20.934 -1.028 -1.228 -3.333 H1   00W 61 
1ZV HA2  H25 H 0 1 N N N N N N 14.628 -12.751 19.518 -3.427 -1.599 -2.695 HA2  00W 62 
1ZV HB22 H26 H 0 0 N N N N N N 14.203 -10.266 21.215 -2.579 -2.763 -0.573 HB22 00W 63 
1ZV HB32 H27 H 0 0 N N N N N N 12.943 -10.688 19.974 -2.401 -1.140 0.137  HB32 00W 64 
1ZV HG22 H28 H 0 0 N N N N N N 12.505 -12.735 21.045 -4.820 -0.703 -0.367 HG22 00W 65 
1ZV HG32 H29 H 0 0 N N N N N N 13.867 -12.471 22.206 -4.970 -2.379 -0.948 HG32 00W 66 
1ZV HD21 H30 H 0 0 N N N N N N 12.712 -10.605 23.196 -4.262 -3.213 1.277  HD21 00W 67 
1ZV HD31 H31 H 0 0 N N N N N N 11.418 -10.694 21.971 -4.113 -1.537 1.858  HD31 00W 68 
1ZV HE   H32 H 0 1 N N N N N N 11.683 -13.246 23.006 -6.717 -1.892 0.825  HE   00W 69 
1ZV HH11 H33 H 0 0 N N N N N N 9.855  -10.689 25.425 -4.677 -2.979 3.437  HH11 00W 70 
1ZV HH12 H34 H 0 0 N N N N N N 10.972 -10.137 24.222 -5.928 -3.244 4.526  HH12 00W 71 
1ZV HH21 H35 H 0 0 N N N N N N 9.440  -12.967 25.667 -8.447 -2.267 2.353  HH21 00W 72 
1ZV HH22 H36 H 0 0 N N N N N N 10.239 -14.123 24.654 -8.110 -2.832 3.899  HH22 00W 73 
1ZV H11  H39 H 0 1 N N N N N N 15.515 -12.477 17.279 -4.372 0.722  -0.421 H11  00W 74 
1ZV HO   H41 H 0 1 N N N N N N 15.944 -9.791  17.914 -6.199 0.586  -1.953 HO   00W 75 
1ZV HN   H38 H 0 1 N N N N N N 16.938 -11.956 15.804 -3.543 2.625  -2.369 HN   8AC 76 
1ZV H111 H42 H 0 0 N N N N N N 15.449 -13.753 16.250 -5.232 3.394  -0.184 H111 8AC 77 
1ZV H12  H43 H 0 1 N N N N N N 17.163 -14.181 15.778 -3.773 2.490  0.288  H12  8AC 78 
1ZV H21  H44 H 0 1 N N N N N N 17.583 -15.191 17.642 -2.677 4.205  -1.510 H21  8AC 79 
1ZV H22  H45 H 0 1 N N N N N N 16.524 -14.043 18.630 -4.030 5.208  -0.933 H22  8AC 80 
1ZV H31  H46 H 0 1 N N N N N N 15.121 -15.592 19.015 -3.163 5.393  1.190  H31  8AC 81 
1ZV H32  H47 H 0 1 N N N N N N 14.964 -15.972 17.234 -2.464 3.756  1.160  H32  8AC 82 
1ZV H41  H48 H 0 1 N N N N N N 16.117 -17.851 17.398 -0.955 4.943  -0.770 H41  8AC 83 
1ZV H42  H49 H 0 1 N N N N N N 17.304 -17.140 18.602 -1.292 6.353  0.262  H42  8AC 84 
1ZV H51  H50 H 0 1 N N N N N N 15.067 -17.617 20.123 0.330  5.636  1.662  H51  8AC 85 
1ZV H52  H51 H 0 1 N N N N N N 15.082 -19.017 18.948 -0.686 4.224  2.036  H52  8AC 86 
1ZV H61  H52 H 0 1 N N N N N N 16.396 -20.051 20.189 0.399  2.863  0.450  H61  8AC 87 
1ZV H62  H53 H 0 1 N N N N N N 17.640 -18.683 19.965 1.016  4.258  -0.467 H62  8AC 88 
1ZV H71  H54 H 0 1 N N N N N N 15.948 -18.748 22.323 2.902  4.329  0.780  H71  8AC 89 
1ZV H72  H55 H 0 1 N N N N N N 17.280 -19.998 22.109 1.966  4.320  2.293  H72  8AC 90 
1ZV H81  H56 H 0 1 N N N N N N 18.666 -18.720 22.919 3.398  2.330  2.208  H81  8AC 91 
1ZV HO8  H58 H 0 1 N N N N N N 19.535 -17.573 23.014 1.241  1.998  3.107  HO8  8AC 92 
# 
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 
1ZV N   CA   SING N N 1  
1ZV N   H    SING N N 2  
1ZV CA  C    SING N N 3  
1ZV CA  CB   SING N N 4  
1ZV CA  HA   SING N N 5  
1ZV C   O    DOUB N N 6  
1ZV CB  CG   SING N N 7  
1ZV CB  HB2  SING N N 8  
1ZV CB  HB3  SING N N 9  
1ZV CG  C1   SING N N 10 
1ZV CG  HG2  SING N N 11 
1ZV CG  HG3  SING N N 12 
1ZV C1  C2   DOUB Y N 13 
1ZV C1  C6   SING Y N 14 
1ZV C2  C3   SING Y N 15 
1ZV C2  HC2  SING N N 16 
1ZV C6  C5   DOUB Y N 17 
1ZV C6  H6   SING N N 18 
1ZV C3  C4   DOUB Y N 19 
1ZV C3  H3   SING N N 20 
1ZV C5  C4   SING Y N 21 
1ZV C5  H5   SING N N 22 
1ZV C4  H4   SING N N 23 
1ZV N1  CA1  SING N N 24 
1ZV N1  CD   SING N N 25 
1ZV CA1 C7   SING N N 26 
1ZV CA1 CB1  SING N N 27 
1ZV CA1 HA1  SING N N 28 
1ZV C7  O1   DOUB N N 29 
1ZV CB1 CG1  SING N N 30 
1ZV CB1 HB21 SING N N 31 
1ZV CB1 HB31 SING N N 32 
1ZV CG1 CD   SING N N 33 
1ZV CG1 HG21 SING N N 34 
1ZV CG1 HG31 SING N N 35 
1ZV CD  HD2  SING N N 36 
1ZV CD  HD3  SING N N 37 
1ZV N2  CA2  SING N N 38 
1ZV N2  H1   SING N N 39 
1ZV CA2 C8   SING N N 40 
1ZV CA2 CB2  SING N N 41 
1ZV CA2 HA2  SING N N 42 
1ZV C8  O2   DOUB N N 43 
1ZV CB2 CG2  SING N N 44 
1ZV CB2 HB22 SING N N 45 
1ZV CB2 HB32 SING N N 46 
1ZV CG2 CD1  SING N N 47 
1ZV CG2 HG22 SING N N 48 
1ZV CG2 HG32 SING N N 49 
1ZV CD1 NE   SING N N 50 
1ZV CD1 HD21 SING N N 51 
1ZV CD1 HD31 SING N N 52 
1ZV NE  CZ   SING N N 53 
1ZV NE  HE   SING N N 54 
1ZV CZ  NH1  SING N N 55 
1ZV CZ  NH2  DOUB N N 56 
1ZV NH1 HH11 SING N N 57 
1ZV NH1 HH12 SING N N 58 
1ZV NH2 HH21 SING N N 59 
1ZV NH2 HH22 SING N N 60 
1ZV N3  C9   SING N N 61 
1ZV N3  C11  SING N N 62 
1ZV N3  HN   SING N N 63 
1ZV C9  O3   SING N N 64 
1ZV C9  H11  SING N N 65 
1ZV O3  HO   SING N N 66 
1ZV C11 C21  SING N N 67 
1ZV C11 H111 SING N N 68 
1ZV C11 H12  SING N N 69 
1ZV C21 C31  SING N N 70 
1ZV C21 H21  SING N N 71 
1ZV C21 H22  SING N N 72 
1ZV C31 C41  SING N N 73 
1ZV C31 H31  SING N N 74 
1ZV C31 H32  SING N N 75 
1ZV C41 C51  SING N N 76 
1ZV C41 H41  SING N N 77 
1ZV C41 H42  SING N N 78 
1ZV C51 C61  SING N N 79 
1ZV C51 H51  SING N N 80 
1ZV C51 H52  SING N N 81 
1ZV C61 C71  SING N N 82 
1ZV C61 H61  SING N N 83 
1ZV C61 H62  SING N N 84 
1ZV C71 C81  SING N N 85 
1ZV C71 H71  SING N N 86 
1ZV C71 H72  SING N N 87 
1ZV C81 O8   SING N N 88 
1ZV C81 H81  SING N N 89 
1ZV O8  HO8  SING N N 90 
1ZV C   N1   SING N N 91 
1ZV C7  N2   SING N N 92 
1ZV C8  C9   SING N N 93 
1ZV C81 N    SING N N 94 
# 
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 
1ZV SMILES           ACDLabs              12.01 "O=C1N3C(C(=O)NC(C(=O)C(O)NCCCCCCCC(O)NC1CCc2ccccc2)CCCNC(=[NH2+])\\N)CCC3"                                                                                                                                                                                  
1ZV InChI            InChI                1.03  "InChI=1S/C30H49N7O5/c31-30(32)34-19-9-13-22-26(39)28(41)33-18-8-3-1-2-7-15-25(38)35-23(17-16-21-11-5-4-6-12-21)29(42)37-20-10-14-24(37)27(40)36-22/h4-6,11-12,22-25,28,33,35,38,41H,1-3,7-10,13-20H2,(H,36,40)(H4,31,32,34)/p+1/t22-,23+,24-,25+,28?/m0/s1" 
1ZV InChIKey         InChI                1.03  SNOALCJXRGNTNQ-VDKCFFHZSA-O                                                                                                                                                                                                                                  
1ZV SMILES_CANONICAL CACTVS               3.385 "NC(=[NH2+])NCCC[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H](CCc3ccccc3)N[C@H](O)CCCCCCCN[C@H](O)C1=O"                                                                                                                                                               
1ZV SMILES           CACTVS               3.385 "NC(=[NH2+])NCCC[CH]1NC(=O)[CH]2CCCN2C(=O)[CH](CCc3ccccc3)N[CH](O)CCCCCCCN[CH](O)C1=O"                                                                                                                                                                       
1ZV SMILES_CANONICAL "OpenEye OEToolkits" 1.7.5 "c1ccc(cc1)CC[C@@H]2C(=O)N3CCC[C@H]3C(=O)N[C@H](C(=O)[C@H](NCCCCCCC[C@H](N2)O)O)CCCNC(=[NH2+])N"                                                                                                                                                             
1ZV SMILES           "OpenEye OEToolkits" 1.7.5 "c1ccc(cc1)CCC2C(=O)N3CCCC3C(=O)NC(C(=O)C(NCCCCCCCC(N2)O)O)CCCNC(=[NH2+])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 
1ZV "SYSTEMATIC NAME" ACDLabs              12.01 "amino({3-[(3S,5R,14R,16R,21aS)-5,14-dihydroxy-1,4,17-trioxo-16-(2-phenylethyl)icosahydro-1H-pyrrolo[1,2-d][1,4,7,11]tetraazacyclononadecin-3-yl]propyl}amino)methaniminium" 
1ZV "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.7.0 "[azanyl-[3-[(3R,5R,14R,16S,19S)-5,14-dihydroxy-2,15,18-trioxo-3-phenethyl-1,4,13,17-tetrazabicyclo[17.3.0]docosan-16-yl]propylamino]methylidene]azanium"                    
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
1ZV "Create component"         2008-08-27 RCSB 
1ZV "Modify subcomponent list" 2011-02-08 RCSB 
1ZV "Modify aromatic_flag"     2011-06-04 RCSB 
1ZV "Modify descriptor"        2011-06-04 RCSB 
1ZV "Modify descriptor"        2012-01-05 RCSB 
1ZV "Modify PCM"               2024-09-27 PDBE 
# 
_pdbx_chem_comp_pcm.pcm_id                             1 
_pdbx_chem_comp_pcm.comp_id                            1ZV 
_pdbx_chem_comp_pcm.modified_residue_id                SER 
_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               C8 
_pdbx_chem_comp_pcm.modified_residue_id_linking_atom   OG 
_pdbx_chem_comp_pcm.uniprot_specific_ptm_accession     ? 
_pdbx_chem_comp_pcm.uniprot_generic_ptm_accession      ? 
# 
