data_L4T # _chem_comp.id L4T _chem_comp.name "N-[(cyclopentyloxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(8-bromo-7-methoxy-2-{2-[(2-methylpropanoyl)amino]-1,3-thiazol-4-yl}quinolin-4-yl)oxy]-N-[(1R,2S)-1-carboxy-2-ethenylcyclopropyl]-L-prolinamide" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C40 H49 Br N6 O9 S" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms ? _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2010-10-20 _chem_comp.pdbx_modified_date 2012-10-01 _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 869.821 _chem_comp.one_letter_code ? _chem_comp.three_letter_code L4T _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 3P8N _chem_comp.pdbx_subcomponent_list "12W TBG 12X 0Y9" _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 L4T C25 C25 C 0 1 N N N 56.061 7.034 4.255 -4.237 3.498 -1.013 C25 12W 1 L4T O26 O26 O 0 1 N N N 56.067 5.929 4.799 -3.229 4.031 -0.592 O26 12W 2 L4T O27 O27 O 0 1 N N N 55.031 7.928 4.275 -5.334 4.237 -1.265 O27 12W 3 L4T C28 C28 C 0 1 N N N 53.848 7.545 5.040 -5.241 5.663 -1.010 C28 12W 4 L4T C29 C29 C 0 1 N N N 52.548 8.064 4.406 -5.730 5.978 0.419 C29 12W 5 L4T C30 C30 C 0 1 N N N 52.291 9.421 5.067 -6.473 7.330 0.277 C30 12W 6 L4T C31 C31 C 0 1 N N N 53.417 9.625 6.069 -7.185 7.187 -1.092 C31 12W 7 L4T C32 C32 C 0 1 N N N 53.844 8.213 6.404 -6.166 6.432 -1.970 C32 12W 8 L4T N24 N24 N 0 1 N N N 57.092 7.547 3.552 -4.255 2.169 -1.234 N TBG 9 L4T C19 C19 C 0 1 N N S 58.340 6.826 3.381 -3.061 1.365 -0.960 CA TBG 10 L4T C20 C20 C 0 1 N N N 59.001 6.940 1.962 -3.039 0.971 0.519 CB TBG 11 L4T C21 C21 C 0 1 N N N 60.351 6.176 1.934 -4.348 0.264 0.877 CG1 TBG 12 L4T C22 C22 C 0 1 N N N 59.273 8.402 1.521 -1.862 0.029 0.779 CG2 TBG 13 L4T C23 C23 C 0 1 N N N 58.086 6.260 0.932 -2.887 2.228 1.379 CG3 TBG 14 L4T C17 C17 C 0 1 N N N 59.233 7.355 4.531 -3.087 0.121 -1.810 C TBG 15 L4T O18 O18 O 0 1 N N N 59.453 8.557 4.629 -4.146 -0.401 -2.088 O TBG 16 L4T C10 C10 C 0 1 N N N 61.862 7.642 5.995 -2.342 -2.812 -2.183 C10 12X 17 L4T O11 O11 O 0 1 N N N 62.486 7.262 5.006 -2.802 -2.600 -1.082 O11 12X 18 L4T C12 C12 C 0 1 N N S 60.642 6.895 6.532 -1.806 -1.671 -3.008 C12 12X 19 L4T C13 C13 C 0 1 N N N 61.085 5.582 7.209 -0.304 -1.886 -3.289 C13 12X 20 L4T C14 C14 C 0 1 N N R 59.896 4.631 6.895 0.381 -1.025 -2.195 C14 12X 21 L4T C15 C15 C 0 1 N N N 59.647 4.975 5.447 -0.592 0.175 -2.090 C15 12X 22 L4T N16 N16 N 0 1 N N N 59.778 6.440 5.433 -1.934 -0.410 -2.262 N16 12X 23 L4T O33 O33 O 0 1 N N N 58.686 5.061 7.579 1.678 -0.597 -2.618 O33 12X 24 L4T C34 C34 C 0 1 Y N N 58.421 4.685 8.891 2.567 -0.276 -1.645 C34 12X 25 L4T C35 C35 C 0 1 Y N N 59.260 3.671 9.539 2.216 -0.340 -0.323 C35 12X 26 L4T C36 C36 C 0 1 Y N N 58.988 3.331 10.845 3.153 -0.003 0.663 C36 12X 27 L4T N37 N37 N 0 1 Y N N 57.922 3.931 11.495 4.379 0.380 0.350 N37 12X 28 L4T C38 C38 C 0 1 Y N N 57.065 4.862 10.960 4.779 0.461 -0.924 C38 12X 29 L4T C39 C39 C 0 1 Y N N 57.358 5.249 9.545 3.884 0.128 -1.970 C39 12X 30 L4T C40 C40 C 0 1 Y N N 56.474 6.258 8.860 4.308 0.210 -3.304 C40 12X 31 L4T C41 C41 C 0 1 Y N N 55.354 6.759 9.683 5.581 0.602 -3.588 C41 12X 32 L4T C42 C42 C 0 1 Y N N 55.122 6.366 10.967 6.475 0.927 -2.564 C42 12X 33 L4T C43 C43 C 0 1 Y N N 56.015 5.390 11.637 6.085 0.869 -1.244 C43 12X 34 L4T BR44 BR44 BR 0 0 N N N 55.663 4.870 13.444 7.307 1.313 0.129 BR44 12X 35 L4T O45 O45 O 0 1 N N N 54.067 6.824 11.772 7.739 1.315 -2.875 O45 12X 36 L4T C46 C46 C 0 1 N N N 53.136 7.782 11.208 8.080 1.367 -4.262 C46 12X 37 L4T C47 C47 C 0 1 Y N N 59.735 2.346 11.551 2.760 -0.076 2.089 C47 12X 38 L4T C48 C48 C 0 1 Y N N 59.459 1.950 12.850 3.609 0.233 3.088 C48 12X 39 L4T S49 S49 S 0 1 Y N N 60.555 0.724 13.309 2.763 0.018 4.618 S49 12X 40 L4T C50 C50 C 0 1 Y N N 61.308 0.812 11.773 1.313 -0.479 3.750 C50 12X 41 L4T N51 N51 N 0 1 Y N N 60.783 1.698 10.932 1.541 -0.448 2.475 N51 12X 42 L4T N52 N52 N 0 1 N N N 62.374 0.013 11.400 0.110 -0.843 4.341 N52 12X 43 L4T C53 C53 C 0 1 N N N 62.780 -1.136 12.054 -0.012 -0.831 5.683 C53 12X 44 L4T O54 O54 O 0 1 N N N 62.208 -1.539 13.051 0.928 -0.504 6.375 O54 12X 45 L4T C55 C55 C 0 1 N N N 64.030 -1.819 11.417 -1.317 -1.226 6.325 C55 12X 46 L4T C56 C56 C 0 1 N N N 63.767 -3.254 11.006 -1.189 -1.128 7.846 C56 12X 47 L4T C57 C57 C 0 1 N N N 65.269 -1.745 12.351 -2.426 -0.287 5.845 C57 12X 48 L4T N9 N9 N 0 1 N N N 62.148 8.778 6.708 -2.309 -4.069 -2.670 N20 0Y9 49 L4T C4 C4 C 0 1 N N R 62.968 9.824 6.137 -2.926 -5.162 -1.915 C21 0Y9 50 L4T C6 C6 C 0 1 N N S 62.315 10.715 5.043 -4.444 -5.322 -2.014 C22 0Y9 51 L4T C5 C5 C 0 1 N N N 62.544 11.285 6.419 -3.522 -6.324 -2.713 C23 0Y9 52 L4T C7 C7 C 0 1 N N N 63.039 11.242 3.866 -5.177 -5.792 -0.784 C24 0Y9 53 L4T C8 C8 C 0 1 N N N 62.740 10.940 2.598 -6.103 -5.038 -0.245 C25 0Y9 54 L4T C2 C2 C 0 1 N N N 64.470 9.469 6.152 -2.277 -5.486 -0.594 C26 0Y9 55 L4T O3 O3 O 0 1 N N N 65.336 10.271 5.667 -2.567 -6.505 -0.012 O27 0Y9 56 L4T O1 O1 O 0 1 N N N 64.832 8.338 6.688 -1.378 -4.643 -0.063 OXT 0Y9 57 L4T H26 H26 H 0 1 N N N 53.794 6.452 5.156 -4.211 5.998 -1.136 H26 12W 58 L4T H27 H27 H 0 1 N N N 52.669 8.182 3.319 -6.412 5.203 0.768 H27 12W 59 L4T H28 H28 H 0 1 N N N 51.717 7.373 4.610 -4.884 6.077 1.098 H28 12W 60 L4T H29 H29 H 0 1 N N N 52.303 10.221 4.312 -7.200 7.457 1.079 H29 12W 61 L4T H30 H30 H 0 1 N N N 51.319 9.416 5.582 -5.766 8.159 0.260 H30 12W 62 L4T H31 H31 H 0 1 N N N 54.246 10.192 5.620 -8.101 6.606 -0.986 H31 12W 63 L4T H32 H32 H 0 1 N N N 53.056 10.151 6.965 -7.400 8.168 -1.514 H32 12W 64 L4T H33 H33 H 0 1 N N N 53.125 7.730 7.082 -5.585 7.141 -2.561 H33 12W 65 L4T H34 H34 H 0 1 N N N 54.846 8.197 6.859 -6.685 5.734 -2.628 H34 12W 66 L4T H25 H25 H 0 1 N N N 56.993 8.451 3.136 -5.058 1.744 -1.574 H TBG 67 L4T H15 H15 H 0 1 N N N 58.158 5.758 3.570 -2.170 1.947 -1.194 HA TBG 68 L4T H16 H16 H 0 1 N N N 61.044 6.628 2.659 -4.456 -0.631 0.265 HG11 TBG 69 L4T H17 H17 H 0 1 N N N 60.181 5.122 2.198 -4.332 -0.017 1.931 HG12 TBG 70 L4T H18 H18 H 0 1 N N N 60.785 6.236 0.925 -5.187 0.935 0.692 HG13 TBG 71 L4T H19 H19 H 0 1 N N N 59.928 8.892 2.257 -0.927 0.561 0.607 HG21 TBG 72 L4T H20 H20 H 0 1 N N N 59.763 8.403 0.536 -1.897 -0.320 1.811 HG22 TBG 73 L4T H21 H21 H 0 1 N N N 58.321 8.949 1.457 -1.924 -0.824 0.104 HG23 TBG 74 L4T H22 H22 H 0 1 N N N 57.891 5.223 1.242 -3.726 2.899 1.194 HG31 TBG 75 L4T H23 H23 H 0 1 N N N 57.135 6.808 0.868 -2.872 1.947 2.432 HG32 TBG 76 L4T H24 H24 H 0 1 N N N 58.577 6.262 -0.052 -1.955 2.732 1.123 HG33 TBG 77 L4T H9 H9 H 0 1 N N N 60.087 7.524 7.244 -2.353 -1.604 -3.949 H9 12X 78 L4T H10 H10 H 0 1 N N N 62.022 5.205 6.773 -0.037 -2.937 -3.176 H10 12X 79 L4T H11 H11 H 0 1 N N N 61.213 5.716 8.293 -0.042 -1.529 -4.285 H11 12X 80 L4T H12 H12 H 0 1 N N N 60.150 3.572 7.052 0.439 -1.566 -1.251 H12 12X 81 L4T H13 H13 H 0 1 N N N 58.639 4.664 5.134 -0.507 0.648 -1.111 H13 12X 82 L4T H14 H14 H 0 1 N N N 60.396 4.504 4.793 -0.388 0.900 -2.878 H14 12X 83 L4T H35 H35 H 0 1 N N N 60.072 3.202 9.004 1.221 -0.649 -0.041 H35 12X 84 L4T H36 H36 H 0 1 N N N 56.645 6.589 7.846 3.627 -0.039 -4.104 H36 12X 85 L4T H37 H37 H 0 1 N N N 54.680 7.478 9.241 5.903 0.663 -4.617 H37 12X 86 L4T H38 H38 H 0 1 N N N 52.374 8.039 11.959 7.961 0.377 -4.702 H38 12X 87 L4T H39 H39 H 0 1 N N N 53.680 8.691 10.912 7.424 2.073 -4.771 H39 12X 88 L4T H40 H40 H 0 1 N N N 52.648 7.343 10.326 9.115 1.691 -4.370 H40 12X 89 L4T H41 H41 H 0 1 N N N 58.675 2.353 13.473 4.633 0.557 2.971 H41 12X 90 L4T H42 H42 H 0 1 N N N 62.894 0.289 10.591 -0.642 -1.105 3.788 H42 12X 91 L4T H43 H43 H 0 1 N N N 64.277 -1.253 10.506 -1.564 -2.251 6.046 H43 12X 92 L4T H44 H44 H 0 1 N N N 64.679 -3.683 10.565 -0.943 -0.103 8.124 H44 12X 93 L4T H45 H45 H 0 1 N N N 63.476 -3.841 11.890 -2.133 -1.413 8.310 H45 12X 94 L4T H46 H46 H 0 1 N N N 62.955 -3.280 10.265 -0.399 -1.797 8.188 H46 12X 95 L4T H47 H47 H 0 1 N N N 65.448 -0.699 12.641 -3.370 -0.573 6.308 H47 12X 96 L4T H48 H48 H 0 1 N N N 65.086 -2.349 13.252 -2.180 0.738 6.123 H48 12X 97 L4T H49 H49 H 0 1 N N N 66.151 -2.135 11.822 -2.518 -0.357 4.761 H49 12X 98 L4T H8 H8 H 0 1 N N N 61.785 8.885 7.634 -1.878 -4.249 -3.520 H12 0Y9 99 L4T H4 H4 H 0 1 N N N 61.266 10.449 4.844 -4.985 -4.614 -2.641 H13 0Y9 100 L4T H2 H2 H 0 1 N N N 63.312 12.058 6.570 -3.456 -6.273 -3.800 H14 0Y9 101 L4T H3 H3 H 0 1 N N N 61.686 11.488 7.076 -3.445 -7.322 -2.282 H15 0Y9 102 L4T H5 H5 H 0 1 N N N 63.864 11.916 4.042 -4.938 -6.750 -0.346 H16 0Y9 103 L4T H6 H6 H 0 1 N N N 63.317 11.366 1.791 -6.628 -5.375 0.636 H17 0Y9 104 L4T H7 H7 H 0 1 N N N 61.921 10.270 2.381 -6.342 -4.081 -0.683 H18 0Y9 105 L4T H1 H1 H 0 1 N N N 65.777 8.254 6.642 -0.989 -4.894 0.786 HXT 0Y9 106 # 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 L4T C23 C20 SING N N 1 L4T C22 C20 SING N N 2 L4T C21 C20 SING N N 3 L4T C20 C19 SING N N 4 L4T C8 C7 DOUB N N 5 L4T C19 N24 SING N N 6 L4T C19 C17 SING N N 7 L4T N24 C25 SING N N 8 L4T C7 C6 SING N N 9 L4T C25 O27 SING N N 10 L4T C25 O26 DOUB N N 11 L4T O27 C28 SING N N 12 L4T C29 C28 SING N N 13 L4T C29 C30 SING N N 14 L4T C17 O18 DOUB N N 15 L4T C17 N16 SING N N 16 L4T O11 C10 DOUB N N 17 L4T C28 C32 SING N N 18 L4T C6 C4 SING N N 19 L4T C6 C5 SING N N 20 L4T C30 C31 SING N N 21 L4T N16 C15 SING N N 22 L4T N16 C12 SING N N 23 L4T C15 C14 SING N N 24 L4T O3 C2 DOUB N N 25 L4T C10 C12 SING N N 26 L4T C10 N9 SING N N 27 L4T C31 C32 SING N N 28 L4T C4 C2 SING N N 29 L4T C4 C5 SING N N 30 L4T C4 N9 SING N N 31 L4T C2 O1 SING N N 32 L4T C12 C13 SING N N 33 L4T C14 C13 SING N N 34 L4T C14 O33 SING N N 35 L4T O33 C34 SING N N 36 L4T C40 C39 DOUB Y N 37 L4T C40 C41 SING Y N 38 L4T C34 C35 DOUB Y N 39 L4T C34 C39 SING Y N 40 L4T C35 C36 SING Y N 41 L4T C39 C38 SING Y N 42 L4T C41 C42 DOUB Y N 43 L4T C36 N37 DOUB Y N 44 L4T C36 C47 SING N N 45 L4T N51 C47 SING Y N 46 L4T N51 C50 DOUB Y N 47 L4T C38 N37 SING Y N 48 L4T C38 C43 DOUB Y N 49 L4T C42 C43 SING Y N 50 L4T C42 O45 SING N N 51 L4T C56 C55 SING N N 52 L4T C46 O45 SING N N 53 L4T N52 C50 SING N N 54 L4T N52 C53 SING N N 55 L4T C55 C53 SING N N 56 L4T C55 C57 SING N N 57 L4T C47 C48 DOUB Y N 58 L4T C43 BR44 SING N N 59 L4T C50 S49 SING Y N 60 L4T C53 O54 DOUB N N 61 L4T C48 S49 SING Y N 62 L4T O1 H1 SING N N 63 L4T C5 H2 SING N N 64 L4T C5 H3 SING N N 65 L4T C6 H4 SING N N 66 L4T C7 H5 SING N N 67 L4T C8 H6 SING N N 68 L4T C8 H7 SING N N 69 L4T N9 H8 SING N N 70 L4T C12 H9 SING N N 71 L4T C13 H10 SING N N 72 L4T C13 H11 SING N N 73 L4T C14 H12 SING N N 74 L4T C15 H13 SING N N 75 L4T C15 H14 SING N N 76 L4T C19 H15 SING N N 77 L4T C21 H16 SING N N 78 L4T C21 H17 SING N N 79 L4T C21 H18 SING N N 80 L4T C22 H19 SING N N 81 L4T C22 H20 SING N N 82 L4T C22 H21 SING N N 83 L4T C23 H22 SING N N 84 L4T C23 H23 SING N N 85 L4T C23 H24 SING N N 86 L4T N24 H25 SING N N 87 L4T C28 H26 SING N N 88 L4T C29 H27 SING N N 89 L4T C29 H28 SING N N 90 L4T C30 H29 SING N N 91 L4T C30 H30 SING N N 92 L4T C31 H31 SING N N 93 L4T C31 H32 SING N N 94 L4T C32 H33 SING N N 95 L4T C32 H34 SING N N 96 L4T C35 H35 SING N N 97 L4T C40 H36 SING N N 98 L4T C41 H37 SING N N 99 L4T C46 H38 SING N N 100 L4T C46 H39 SING N N 101 L4T C46 H40 SING N N 102 L4T C48 H41 SING N N 103 L4T N52 H42 SING N N 104 L4T C55 H43 SING N N 105 L4T C56 H44 SING N N 106 L4T C56 H45 SING N N 107 L4T C56 H46 SING N N 108 L4T C57 H47 SING N N 109 L4T C57 H48 SING N N 110 L4T C57 H49 SING N N 111 # 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 L4T SMILES ACDLabs 12.01 "O=C(Nc6nc(c4nc5c(c(OC3CC(C(=O)NC1(C(=O)O)CC1/C=C)N(C(=O)C(NC(=O)OC2CCCC2)C(C)(C)C)C3)c4)ccc(OC)c5Br)cs6)C(C)C" L4T InChI InChI 1.03 ;InChI=1S/C40H49BrN6O9S/c1-8-21-17-40(21,36(51)52)46-34(49)27-15-23(18-47(27)35(50)32(39(4,5)6)44-38(53)56-22-11-9-10-12-22)55-29-16-25(26-19-57-37(43-26)45-33(48)20(2)3)42-31-24(29)13-14-28(54-7)30(31)41/h8,13-14,16,19-23,27,32H,1,9-12,15,17-18H2,2-7H3,(H,44,53)(H,46,49)(H,51,52)(H,43,45,48)/t21-,23-,27+,32-,40-/m1/s1 ; L4T InChIKey InChI 1.03 LLGDPTDZOVKFDU-XUHJSTDZSA-N L4T SMILES_CANONICAL CACTVS 3.370 "COc1ccc2c(O[C@@H]3C[C@H](N(C3)C(=O)[C@@H](NC(=O)OC4CCCC4)C(C)(C)C)C(=O)N[C@@]5(C[C@H]5C=C)C(O)=O)cc(nc2c1Br)c6csc(NC(=O)C(C)C)n6" L4T SMILES CACTVS 3.370 "COc1ccc2c(O[CH]3C[CH](N(C3)C(=O)[CH](NC(=O)OC4CCCC4)C(C)(C)C)C(=O)N[C]5(C[CH]5C=C)C(O)=O)cc(nc2c1Br)c6csc(NC(=O)C(C)C)n6" L4T SMILES_CANONICAL "OpenEye OEToolkits" 1.7.6 "CC(C)C(=O)Nc1nc(cs1)c2cc(c3ccc(c(c3n2)Br)OC)O[C@@H]4C[C@H](N(C4)C(=O)[C@H](C(C)(C)C)NC(=O)OC5CCCC5)C(=O)N[C@@]6(C[C@H]6C=C)C(=O)O" L4T SMILES "OpenEye OEToolkits" 1.7.6 "CC(C)C(=O)Nc1nc(cs1)c2cc(c3ccc(c(c3n2)Br)OC)OC4CC(N(C4)C(=O)C(C(C)(C)C)NC(=O)OC5CCCC5)C(=O)NC6(CC6C=C)C(=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 L4T "SYSTEMATIC NAME" ACDLabs 12.01 "N-[(cyclopentyloxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(8-bromo-7-methoxy-2-{2-[(2-methylpropanoyl)amino]-1,3-thiazol-4-yl}quinolin-4-yl)oxy]-N-[(1R,2S)-1-carboxy-2-ethenylcyclopropyl]-L-prolinamide" L4T "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.7.6 "(1R,2S)-1-[[(2S,4R)-4-[8-bromanyl-7-methoxy-2-[2-(2-methylpropanoylamino)-1,3-thiazol-4-yl]quinolin-4-yl]oxy-1-[(2S)-2-(cyclopentyloxycarbonylamino)-3,3-dimethyl-butanoyl]pyrrolidin-2-yl]carbonylamino]-2-ethenyl-cyclopropane-1-carboxylic acid" # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site L4T "Create component" 2010-10-20 RCSB L4T "Modify aromatic_flag" 2011-06-04 RCSB L4T "Modify descriptor" 2011-06-04 RCSB L4T "Modify subcomponent list" 2011-06-04 RCSB #