data_7LP
# 
_chem_comp.id                                    7LP 
_chem_comp.name                                  "(5R,6S,7S)-5,6-dihydroxy-7-(octanoylamino)-N-(6-phenylhexyl)-8-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}octanamide" 
_chem_comp.type                                  NON-POLYMER 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C34 H58 N2 O10" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2016-11-14 
_chem_comp.pdbx_modified_date                    2017-09-15 
_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                        654.832 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     7LP 
_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        5TW2 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  RCSB 
# 
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.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 
7LP C2  C1  C 0 1 N N N -30.995 -3.935  -36.778 5.429   3.573  -0.515 C2  7LP 1   
7LP C1  C2  C 0 1 N N N -31.457 -5.167  -37.583 4.655   2.418  0.124  C1  7LP 2   
7LP O1  O1  O 0 1 N N N -33.686 -0.645  -35.543 -3.916  0.696  -0.930 O1  7LP 3   
7LP C7  C3  C 0 1 N N N -30.327 -0.325  -32.506 7.912   9.048  1.398  C7  7LP 4   
7LP C6  C4  C 0 1 N N N -29.724 -1.641  -32.930 7.600   7.993  0.334  C6  7LP 5   
7LP C5  C5  C 0 1 N N N -30.685 -2.201  -33.983 6.826   6.838  0.973  C5  7LP 6   
7LP C4  C6  C 0 1 N N N -29.834 -3.223  -34.723 6.515   5.783  -0.090 C4  7LP 7   
7LP C3  C7  C 0 1 N N N -30.670 -4.366  -35.336 5.741   4.628  0.549  C3  7LP 8   
7LP C20 C8  C 0 1 N N N -31.581 -4.838  -39.088 4.348   1.379  -0.923 C20 7LP 9   
7LP O   O2  O 0 1 N N N -30.570 -4.841  -39.783 4.713   1.546  -2.068 O   7LP 10  
7LP C27 C9  C 0 1 N N S -33.278 -4.391  -40.941 3.371   -0.746 -1.606 C27 7LP 11  
7LP C28 C10 C 0 1 N N N -32.751 -5.587  -41.855 4.563   -1.693 -1.750 C28 7LP 12  
7LP O4  O3  O 0 1 N N N -33.898 -6.402  -41.870 4.749   -2.413 -0.530 O4  7LP 13  
7LP C31 C11 C 0 1 N N S -33.862 -7.550  -42.718 5.844   -3.331 -0.557 C31 7LP 14  
7LP O9  O4  O 0 1 N N N -32.696 -8.390  -42.497 7.074   -2.604 -0.581 O9  7LP 15  
7LP C30 C12 C 0 1 N N R -32.541 -8.934  -41.148 7.258   -1.730 0.535  C30 7LP 16  
7LP C29 C13 C 0 1 N N N -31.367 -9.903  -41.166 8.587   -0.988 0.389  C29 7LP 17  
7LP O8  O5  O 0 1 N N N -30.243 -9.143  -41.635 8.533   -0.133 -0.755 O8  7LP 18  
7LP C34 C14 C 0 1 N N R -33.814 -9.678  -40.680 7.271   -2.551 1.827  C34 7LP 19  
7LP O7  O6  O 0 1 N N N -33.894 -10.962 -41.327 8.374   -3.459 1.805  O7  7LP 20  
7LP C33 C15 C 0 1 N N S -35.097 -8.850  -40.966 5.961   -3.338 1.936  C33 7LP 21  
7LP O6  O7  O 0 1 N N N -36.269 -9.645  -40.729 5.995   -4.164 3.102  O6  7LP 22  
7LP C32 C16 C 0 1 N N R -35.126 -8.343  -42.422 5.800   -4.216 0.691  C32 7LP 23  
7LP O5  O8  O 0 1 N N N -36.272 -7.496  -42.623 4.547   -4.900 0.748  O5  7LP 24  
7LP C26 C17 C 0 1 N N S -34.346 -3.399  -41.457 2.134   -1.543 -1.186 C26 7LP 25  
7LP O3  O9  O 0 1 N N N -33.957 -2.599  -42.573 1.918   -2.610 -2.113 O3  7LP 26  
7LP C25 C18 C 0 1 N N R -34.910 -2.532  -40.318 0.912   -0.622 -1.176 C25 7LP 27  
7LP O2  O10 O 0 1 N N N -36.106 -1.909  -40.798 1.128   0.445  -0.250 O2  7LP 28  
7LP C24 C19 C 0 1 N N N -33.922 -1.477  -39.828 -0.324  -1.419 -0.757 C24 7LP 29  
7LP C23 C20 C 0 1 N N N -34.517 -1.125  -38.484 -1.565  -0.530 -0.866 C23 7LP 30  
7LP C22 C21 C 0 1 N N N -33.560 -0.139  -37.889 -2.802  -1.328 -0.446 C22 7LP 31  
7LP C21 C22 C 0 1 N N N -33.996 0.144   -36.434 -4.024  -0.453 -0.554 C21 7LP 32  
7LP N1  N1  N 0 1 N N N -34.630 1.314   -36.197 -5.236  -0.946 -0.233 N1  7LP 33  
7LP C19 C23 C 0 1 N N N -35.051 1.703   -34.836 -6.424  -0.095 -0.338 C19 7LP 34  
7LP C18 C24 C 0 1 N N N -35.218 3.193   -34.705 -7.661  -0.893 0.081  C18 7LP 35  
7LP C17 C25 C 0 1 N N N -36.607 3.501   -35.213 -8.902  -0.004 -0.028 C17 7LP 36  
7LP C16 C26 C 0 1 N N N -36.835 4.914   -34.755 -10.139 -0.802 0.391  C16 7LP 37  
7LP C15 C27 C 0 1 N N N -37.737 5.567   -35.775 -11.379 0.087  0.282  C15 7LP 38  
7LP C14 C28 C 0 1 N N N -38.180 6.861   -35.109 -12.616 -0.711 0.702  C14 7LP 39  
7LP C13 C29 C 0 1 Y N N -38.198 7.850   -36.096 -13.838 0.164  0.594  C13 7LP 40  
7LP C8  C30 C 0 1 Y N N -37.236 8.858   -36.139 -14.554 0.210  -0.588 C8  7LP 41  
7LP C9  C31 C 0 1 Y N N -37.298 9.825   -37.148 -15.675 1.013  -0.687 C9  7LP 42  
7LP C10 C32 C 0 1 Y N N -38.295 9.818   -38.111 -16.080 1.770  0.396  C10 7LP 43  
7LP C11 C33 C 0 1 Y N N -39.248 8.818   -38.065 -15.365 1.725  1.578  C11 7LP 44  
7LP C12 C34 C 0 1 Y N N -39.203 7.836   -37.068 -14.247 0.917  1.679  C12 7LP 45  
7LP N2  N2  N 0 1 N N N -32.823 -4.514  -39.535 3.669   0.265  -0.588 N2  7LP 46  
7LP H1  H1  H 0 1 N N N -30.096 -3.506  -37.245 6.361   3.197  -0.937 H1  7LP 47  
7LP H2  H2  H 0 1 N N N -31.797 -3.182  -36.765 4.827   4.021  -1.305 H2  7LP 48  
7LP H3  H3  H 0 1 N N N -32.437 -5.495  -37.206 5.257   1.971  0.915  H3  7LP 49  
7LP H4  H4  H 0 1 N N N -30.724 -5.977  -37.452 3.723   2.795  0.546  H4  7LP 50  
7LP H5  H5  H 0 1 N N N -29.688 0.143   -31.743 6.980   9.425  1.819  H5  7LP 51  
7LP H6  H6  H 0 1 N N N -30.404 0.341   -33.378 8.514   8.601  2.188  H6  7LP 52  
7LP H7  H7  H 0 1 N N N -31.329 -0.499  -32.088 8.463   9.871  0.942  H7  7LP 53  
7LP H8  H8  H 0 1 N N N -29.650 -2.326  -32.072 6.998   8.441  -0.456 H8  7LP 54  
7LP H9  H9  H 0 1 N N N -28.725 -1.486  -33.363 8.532   7.616  -0.088 H9  7LP 55  
7LP H10 H10 H 0 1 N N N -31.030 -1.408  -34.663 7.429   6.391  1.764  H10 7LP 56  
7LP H11 H11 H 0 1 N N N -31.554 -2.681  -33.509 5.895   7.215  1.395  H11 7LP 57  
7LP H12 H12 H 0 1 N N N -29.111 -3.656  -34.016 5.913   6.231  -0.881 H12 7LP 58  
7LP H13 H13 H 0 1 N N N -29.293 -2.710  -35.532 7.446   5.406  -0.512 H13 7LP 59  
7LP H14 H14 H 0 1 N N N -31.598 -4.510  -34.763 4.809   5.005  0.970  H14 7LP 60  
7LP H15 H15 H 0 1 N N N -30.092 -5.302  -35.339 6.343   4.181  1.339  H15 7LP 61  
7LP H16 H16 H 0 1 N N N -32.443 -3.732  -41.220 3.180   -0.255 -2.560 H16 7LP 62  
7LP H17 H17 H 0 1 N N N -31.891 -6.100  -41.401 4.374   -2.395 -2.561 H17 7LP 63  
7LP H18 H18 H 0 1 N N N -32.481 -5.242  -42.864 5.461   -1.115 -1.971 H18 7LP 64  
7LP H19 H19 H 0 1 N N N -33.888 -7.234  -43.771 5.773   -3.955 -1.448 H19 7LP 65  
7LP H20 H20 H 0 1 N N N -32.325 -8.121  -40.439 6.441   -1.010 0.570  H20 7LP 66  
7LP H21 H21 H 0 1 N N N -31.573 -10.743 -41.846 8.769   -0.389 1.281  H21 7LP 67  
7LP H22 H22 H 0 1 N N N -31.173 -10.290 -40.155 9.395   -1.710 0.265  H22 7LP 68  
7LP H23 H23 H 0 1 N N N -29.474 -9.701  -41.667 9.344   0.370  -0.910 H23 7LP 69  
7LP H24 H24 H 0 1 N N N -33.741 -9.823  -39.592 7.366   -1.883 2.682  H24 7LP 70  
7LP H25 H25 H 0 1 N N N -34.677 -11.415 -41.037 8.444   -4.013 2.595  H25 7LP 71  
7LP H26 H26 H 0 1 N N N -35.099 -7.978  -40.296 5.123   -2.644 2.005  H26 7LP 72  
7LP H27 H27 H 0 1 N N N -36.261 -9.963  -39.834 5.195   -4.691 3.234  H27 7LP 73  
7LP H28 H28 H 0 1 N N N -35.172 -9.210  -43.098 6.612   -4.943 0.651  H28 7LP 74  
7LP H29 H29 H 0 1 N N N -37.065 -7.986  -42.439 4.376   -5.472 -0.013 H29 7LP 75  
7LP H30 H30 H 0 1 N N N -35.186 -4.024  -41.794 2.288   -1.954 -0.189 H30 7LP 76  
7LP H31 H31 H 0 1 N N N -34.674 -2.025  -42.817 1.849   -2.323 -3.034 H31 7LP 77  
7LP H32 H32 H 0 1 N N N -35.154 -3.194  -39.474 0.759   -0.211 -2.174 H32 7LP 78  
7LP H33 H33 H 0 1 N N N -36.477 -1.365  -40.113 1.273   0.153  0.660  H33 7LP 79  
7LP H34 H34 H 0 1 N N N -32.908 -1.891  -39.725 -0.438  -2.284 -1.410 H34 7LP 80  
7LP H35 H35 H 0 1 N N N -33.896 -0.606  -40.499 -0.208  -1.755 0.274  H35 7LP 81  
7LP H36 H36 H 0 1 N N N -35.512 -0.673  -38.607 -1.451  0.335  -0.213 H36 7LP 82  
7LP H37 H37 H 0 1 N N N -34.596 -2.020  -37.849 -1.682  -0.194 -1.896 H37 7LP 83  
7LP H38 H38 H 0 1 N N N -32.542 -0.557  -37.898 -2.915  -2.193 -1.100 H38 7LP 84  
7LP H39 H39 H 0 1 N N N -33.578 0.794   -38.471 -2.685  -1.664 0.584  H39 7LP 85  
7LP H40 H40 H 0 1 N N N -34.818 1.931   -36.961 -5.322  -1.865 0.067  H40 7LP 86  
7LP H41 H41 H 0 1 N N N -36.011 1.216   -34.608 -6.311  0.770  0.315  H41 7LP 87  
7LP H42 H42 H 0 1 N N N -34.289 1.366   -34.118 -6.541  0.240  -1.368 H42 7LP 88  
7LP H43 H43 H 0 1 N N N -34.464 3.717   -35.311 -7.775  -1.758 -0.572 H43 7LP 89  
7LP H44 H44 H 0 1 N N N -35.119 3.498   -33.653 -7.544  -1.229 1.112  H44 7LP 90  
7LP H45 H45 H 0 1 N N N -37.349 2.819   -34.772 -8.788  0.861  0.625  H45 7LP 91  
7LP H46 H46 H 0 1 N N N -36.651 3.430   -36.310 -9.019  0.332  -1.058 H46 7LP 92  
7LP H47 H47 H 0 1 N N N -35.877 5.452   -34.698 -10.252 -1.667 -0.262 H47 7LP 93  
7LP H48 H48 H 0 1 N N N -37.317 4.918   -33.766 -10.022 -1.138 1.422  H48 7LP 94  
7LP H49 H49 H 0 1 N N N -38.603 4.926   -35.997 -11.266 0.952  0.936  H49 7LP 95  
7LP H50 H50 H 0 1 N N N -37.187 5.775   -36.705 -11.496 0.423  -0.748 H50 7LP 96  
7LP H51 H51 H 0 1 N N N -37.473 7.136   -34.313 -12.730 -1.576 0.048  H51 7LP 97  
7LP H52 H52 H 0 1 N N N -39.185 6.739   -34.680 -12.499 -1.046 1.732  H52 7LP 98  
7LP H53 H53 H 0 1 N N N -36.450 8.892   -35.400 -14.237 -0.382 -1.434 H53 7LP 99  
7LP H54 H54 H 0 1 N N N -36.547 10.600  -37.178 -16.233 1.049  -1.611 H54 7LP 100 
7LP H55 H55 H 0 1 N N N -38.326 10.576  -38.879 -16.953 2.401  0.317  H55 7LP 101 
7LP H56 H56 H 0 1 N N N -40.034 8.794   -38.805 -15.682 2.316  2.424  H56 7LP 102 
7LP H57 H57 H 0 1 N N N -39.953 7.059   -37.050 -13.689 0.882  2.602  H57 7LP 103 
7LP H58 H58 H 0 1 N N N -33.512 -4.338  -38.832 3.377   0.131  0.328  H58 7LP 104 
# 
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 
7LP C31 O9  SING N N 1   
7LP C31 C32 SING N N 2   
7LP C31 O4  SING N N 3   
7LP O5  C32 SING N N 4   
7LP O3  C26 SING N N 5   
7LP O9  C30 SING N N 6   
7LP C32 C33 SING N N 7   
7LP O4  C28 SING N N 8   
7LP C28 C27 SING N N 9   
7LP O8  C29 SING N N 10  
7LP C26 C27 SING N N 11  
7LP C26 C25 SING N N 12  
7LP O7  C34 SING N N 13  
7LP C29 C30 SING N N 14  
7LP C30 C34 SING N N 15  
7LP C33 O6  SING N N 16  
7LP C33 C34 SING N N 17  
7LP C27 N2  SING N N 18  
7LP O2  C25 SING N N 19  
7LP C25 C24 SING N N 20  
7LP C24 C23 SING N N 21  
7LP O   C20 DOUB N N 22  
7LP N2  C20 SING N N 23  
7LP C20 C1  SING N N 24  
7LP C23 C22 SING N N 25  
7LP C10 C11 DOUB Y N 26  
7LP C10 C9  SING Y N 27  
7LP C11 C12 SING Y N 28  
7LP C22 C21 SING N N 29  
7LP C1  C2  SING N N 30  
7LP C9  C8  DOUB Y N 31  
7LP C12 C13 DOUB Y N 32  
7LP C2  C3  SING N N 33  
7LP C21 N1  SING N N 34  
7LP C21 O1  DOUB N N 35  
7LP N1  C19 SING N N 36  
7LP C8  C13 SING Y N 37  
7LP C13 C14 SING N N 38  
7LP C15 C14 SING N N 39  
7LP C15 C16 SING N N 40  
7LP C3  C4  SING N N 41  
7LP C17 C16 SING N N 42  
7LP C17 C18 SING N N 43  
7LP C19 C18 SING N N 44  
7LP C4  C5  SING N N 45  
7LP C5  C6  SING N N 46  
7LP C6  C7  SING N N 47  
7LP C2  H1  SING N N 48  
7LP C2  H2  SING N N 49  
7LP C1  H3  SING N N 50  
7LP C1  H4  SING N N 51  
7LP C7  H5  SING N N 52  
7LP C7  H6  SING N N 53  
7LP C7  H7  SING N N 54  
7LP C6  H8  SING N N 55  
7LP C6  H9  SING N N 56  
7LP C5  H10 SING N N 57  
7LP C5  H11 SING N N 58  
7LP C4  H12 SING N N 59  
7LP C4  H13 SING N N 60  
7LP C3  H14 SING N N 61  
7LP C3  H15 SING N N 62  
7LP C27 H16 SING N N 63  
7LP C28 H17 SING N N 64  
7LP C28 H18 SING N N 65  
7LP C31 H19 SING N N 66  
7LP C30 H20 SING N N 67  
7LP C29 H21 SING N N 68  
7LP C29 H22 SING N N 69  
7LP O8  H23 SING N N 70  
7LP C34 H24 SING N N 71  
7LP O7  H25 SING N N 72  
7LP C33 H26 SING N N 73  
7LP O6  H27 SING N N 74  
7LP C32 H28 SING N N 75  
7LP O5  H29 SING N N 76  
7LP C26 H30 SING N N 77  
7LP O3  H31 SING N N 78  
7LP C25 H32 SING N N 79  
7LP O2  H33 SING N N 80  
7LP C24 H34 SING N N 81  
7LP C24 H35 SING N N 82  
7LP C23 H36 SING N N 83  
7LP C23 H37 SING N N 84  
7LP C22 H38 SING N N 85  
7LP C22 H39 SING N N 86  
7LP N1  H40 SING N N 87  
7LP C19 H41 SING N N 88  
7LP C19 H42 SING N N 89  
7LP C18 H43 SING N N 90  
7LP C18 H44 SING N N 91  
7LP C17 H45 SING N N 92  
7LP C17 H46 SING N N 93  
7LP C16 H47 SING N N 94  
7LP C16 H48 SING N N 95  
7LP C15 H49 SING N N 96  
7LP C15 H50 SING N N 97  
7LP C14 H51 SING N N 98  
7LP C14 H52 SING N N 99  
7LP C8  H53 SING N N 100 
7LP C9  H54 SING N N 101 
7LP C10 H55 SING N N 102 
7LP C11 H56 SING N N 103 
7LP C12 H57 SING N N 104 
7LP N2  H58 SING N N 105 
# 
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 
7LP SMILES           ACDLabs              12.01 "C(CCCCC)CC(=O)NC(COC1OC(C(O)C(O)C1O)CO)C(C(CCCC(=O)NCCCCCCc2ccccc2)O)O" 
7LP InChI            InChI                1.03  
;InChI=1S/C34H58N2O10/c1-2-3-4-5-12-19-29(40)36-25(23-45-34-33(44)32(43)31(42)27(22-37)46-34)30(41)26(38)18-14-20-28(39)35-21-13-7-6-9-15-24-16-10-8-11-17-24/h8,10-11,16-17,25-27,30-34,37-38,41-44H,2-7,9,12-15,18-23H2,1H3,(H,35,39)(H,36,40)/t25-,26+,27+,30-,31-,32-,33+,34-/m0/s1
;
7LP InChIKey         InChI                1.03  GAPCJLRKOKSZTA-RMRXMYJTSA-N 
7LP SMILES_CANONICAL CACTVS               3.385 "CCCCCCCC(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCC(=O)NCCCCCCc2ccccc2" 
7LP SMILES           CACTVS               3.385 "CCCCCCCC(=O)N[CH](CO[CH]1O[CH](CO)[CH](O)[CH](O)[CH]1O)[CH](O)[CH](O)CCCC(=O)NCCCCCCc2ccccc2" 
7LP SMILES_CANONICAL "OpenEye OEToolkits" 2.0.6 "CCCCCCCC(=O)NC(CO[C@@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O)[C@@H]([C@@H](CCCC(=O)NCCCCCCc2ccccc2)O)O" 
7LP SMILES           "OpenEye OEToolkits" 2.0.6 "CCCCCCCC(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCC(=O)NCCCCCCc2ccccc2)O)O" 
# 
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 
7LP "SYSTEMATIC NAME" ACDLabs              12.01 "(5R,6S,7S)-5,6-dihydroxy-7-(octanoylamino)-N-(6-phenylhexyl)-8-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}octanamide (non-preferred name)" 
7LP "SYSTEMATIC NAME" "OpenEye OEToolkits" 2.0.6 "(5~{R},6~{S})-8-[(2~{S},3~{R},4~{S},5~{R},6~{R})-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-7-(octanoylamino)-5,6-bis(oxidanyl)-~{N}-(6-phenylhexyl)octanamide"          
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loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
7LP "Create component" 2016-11-14 RCSB 
7LP "Initial release"  2017-09-20 RCSB 
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