data_HGG # _chem_comp.id HGG _chem_comp.name "(3R,5S,9R,21S)-1-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-3,5,9,21-tetrahydroxy-8,8-dimethyl-10,14,19-trioxo-2,4,6-trioxa-18-thia-11,15-diaza-3,5-diphosphatricosan-23-oic acid 3,5-dioxide" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C26 H42 N7 O20 P3 S" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms "3-Hydroxyl Glutaryl CoA" _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2010-04-29 _chem_comp.pdbx_modified_date 2021-03-01 _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 897.633 _chem_comp.one_letter_code ? _chem_comp.three_letter_code HGG _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 3MP3 _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 HGG N1 N1 N 0 1 Y N N 21.933 -32.280 -6.390 7.720 -7.381 2.102 N1 HGG 1 HGG C2 C2 C 0 1 Y N N 21.966 -31.927 -7.809 8.207 -6.287 2.657 C2 HGG 2 HGG N3 N3 N 0 1 Y N N 20.733 -31.222 -8.428 7.993 -5.087 2.160 N3 HGG 3 HGG C4 C4 C 0 1 Y N N 19.555 -30.936 -7.514 7.264 -4.929 1.060 C4 HGG 4 HGG C5 C5 C 0 1 Y N N 19.415 -31.267 -6.047 6.723 -6.063 0.431 C5 HGG 5 HGG C6 C6 C 0 1 Y N N 20.664 -31.955 -5.484 6.979 -7.323 1.000 C6 HGG 6 HGG N6 N6 N 0 1 N N N 20.697 -32.291 -4.229 6.473 -8.475 0.425 N6 HGG 7 HGG N7 N7 N 0 1 Y N N 18.212 -30.868 -5.535 6.034 -5.629 -0.651 N7 HGG 8 HGG C8 C8 C 0 1 Y N N 17.609 -30.328 -6.567 6.115 -4.333 -0.725 C8 HGG 9 HGG N9 N9 N 0 1 Y N N 18.370 -30.340 -7.792 6.864 -3.853 0.308 N9 HGG 10 HGG "C1'" "C1'" C 0 1 N N N 27.143 -21.518 2.409 -11.908 -1.500 -0.561 "C1'" HGG 11 HGG "O1'" "O1'" O 0 1 N N N 28.158 -21.395 1.678 -11.385 -2.056 0.383 "O1'" HGG 12 HGG C15 C15 C 0 1 N N R 18.100 -29.839 -9.170 7.182 -2.447 0.569 C15 HGG 13 HGG C16 C16 C 0 1 N N R 16.747 -30.220 -9.856 8.518 -2.064 -0.106 C16 HGG 14 HGG C17 C17 C 0 1 N N S 16.542 -28.956 -10.833 8.288 -0.618 -0.599 C17 HGG 15 HGG C18 C18 C 0 1 N N R 17.157 -27.753 -10.033 6.841 -0.299 -0.164 C18 HGG 16 HGG C19 C19 C 0 1 N N N 16.341 -26.999 -8.985 6.140 0.550 -1.227 C19 HGG 17 HGG "C2'" "C2'" C 0 1 N N N 26.980 -20.839 3.688 -13.160 -2.074 -1.174 "C2'" HGG 18 HGG O20 O20 O 0 1 N N N 16.733 -31.569 -10.469 9.588 -2.109 0.840 O20 HGG 19 HGG O21 O21 O 0 1 N N N 17.376 -29.042 -12.063 9.209 0.277 0.027 O21 HGG 20 HGG O22 O22 O 0 1 N N N 18.023 -28.380 -9.120 6.199 -1.587 -0.045 O22 HGG 21 HGG O23 O23 O 0 1 N N N 14.965 -27.396 -8.718 4.846 0.931 -0.755 O23 HGG 22 HGG "C3'" "C3'" C 0 1 N N S 27.517 -21.576 4.900 -13.557 -3.348 -0.425 "C3'" HGG 23 HGG "O3'" "O3'" O 0 1 N N N 28.868 -21.795 4.715 -13.911 -3.019 0.919 "O3'" HGG 24 HGG P31 P31 P 0 1 N N N 13.747 -26.472 -8.195 3.829 1.832 -1.618 P31 HGG 25 HGG O32 O32 O 0 1 N N N 14.110 -25.028 -8.983 2.530 2.174 -0.730 O32 HGG 26 HGG O33 O33 O 0 1 N N N 12.466 -27.097 -8.709 4.499 3.090 -2.016 O33 HGG 27 HGG O34 O34 O 0 1 N N N 13.834 -26.246 -6.680 3.381 1.023 -2.935 O34 HGG 28 HGG P35 P35 P 0 1 N N N 15.010 -23.747 -8.393 1.331 3.240 -0.867 P35 HGG 29 HGG O36 O36 O 0 1 N N N 16.432 -23.919 -9.126 1.871 4.531 -1.347 O36 HGG 30 HGG O37 O37 O 0 1 N N N 14.497 -22.355 -8.833 0.241 2.690 -1.917 O37 HGG 31 HGG O38 O38 O 0 1 N N N 15.196 -23.697 -6.788 0.633 3.450 0.569 O38 HGG 32 HGG P39 P39 P 0 1 N N N 17.538 -29.273 -13.715 10.243 1.192 -0.800 P39 HGG 33 HGG "C4'" "C4'" C 0 1 N N N 27.264 -20.734 6.131 -14.752 -3.999 -1.124 "C4'" HGG 34 HGG "O4'" "O4'" O 0 1 N N N 27.086 -18.371 5.993 -14.402 -5.694 0.474 "O4'" HGG 35 HGG O40 O40 O 0 1 N N N 18.143 -30.711 -13.876 11.209 1.972 0.225 O40 HGG 36 HGG O41 O41 O 0 1 N N N 16.073 -29.128 -14.324 11.058 0.335 -1.690 O41 HGG 37 HGG O42 O42 O 0 1 N N N 18.504 -28.121 -14.168 9.425 2.260 -1.685 O42 HGG 38 HGG C43 C43 C 0 1 N N N 19.572 -24.592 -4.966 -3.058 5.164 1.528 C43 HGG 39 HGG C44 C44 C 0 1 N N R 18.248 -24.677 -4.176 -1.938 5.380 2.513 C44 HGG 40 HGG C45 C45 C 0 1 N N N 16.808 -24.915 -4.988 -0.834 4.350 2.265 C45 HGG 41 HGG C46 C46 C 0 1 N N N 16.416 -23.777 -5.967 -0.397 4.412 0.800 C46 HGG 42 HGG "C5'" "C5'" C 0 1 N N N 27.848 -19.444 6.275 -15.066 -5.315 -0.461 "C5'" HGG 43 HGG "O5'" "O5'" O 0 1 N N N 29.060 -19.319 6.644 -16.084 -6.066 -0.909 "O5'" HGG 44 HGG O51 O51 O 0 1 N N N 19.738 -24.944 -6.207 -3.201 5.927 0.596 O51 HGG 45 HGG O52 O52 O 0 1 N N N 18.515 -25.784 -3.277 -1.406 6.696 2.348 O52 HGG 46 HGG C53 C53 C 0 1 N N N 15.643 -24.953 -3.982 0.362 4.657 3.168 C53 HGG 47 HGG C57 C57 C 0 1 N N N 16.812 -26.219 -5.673 -1.364 2.949 2.580 C57 HGG 48 HGG C61 C61 C 0 1 N N N 22.851 -24.073 -3.421 -5.837 2.718 1.177 C61 HGG 49 HGG C62 C62 C 0 1 N N N 21.950 -23.885 -4.631 -5.051 3.973 0.789 C62 HGG 50 HGG N68 N68 N 0 1 N N N 20.626 -24.080 -4.196 -3.899 4.122 1.682 N68 HGG 51 HGG C69 C69 C 0 1 N N N 23.743 -22.906 -2.864 -7.022 2.565 0.259 C69 HGG 52 HGG N71 N71 N 0 1 N N N 24.535 -23.321 -1.700 -7.863 1.523 0.413 N71 HGG 53 HGG O72 O72 O 0 1 N N N 23.703 -21.740 -3.467 -7.219 3.379 -0.619 O72 HGG 54 HGG C73 C73 C 0 1 N N N 26.229 -23.437 0.153 -9.801 0.120 -0.093 C73 HGG 55 HGG C74 C74 C 0 1 N N N 25.661 -22.762 -0.951 -9.016 1.374 -0.480 C74 HGG 56 HGG S81 S81 S 0 1 N N N 25.918 -22.613 1.759 -11.225 -0.065 -1.195 S81 HGG 57 HGG H2 H2 H 0 1 N N N 22.832 -32.153 -8.413 8.804 -6.379 3.553 H2 HGG 58 HGG HN6 HN6 H 0 1 N N N 21.573 -32.728 -4.023 6.657 -9.339 0.827 HN6 HGG 59 HGG HN6A HN6A H 0 0 N N N 20.591 -31.474 -3.662 5.934 -8.420 -0.380 HN6A HGG 60 HGG H8 H8 H 0 1 N N N 16.617 -29.906 -6.504 5.658 -3.726 -1.492 H8 HGG 61 HGG H15 H15 H 0 1 N N N 18.915 -30.302 -9.745 7.231 -2.263 1.642 H15 HGG 62 HGG H16 H16 H 0 1 N N N 15.894 -30.358 -9.175 8.725 -2.727 -0.947 H16 HGG 63 HGG H17 H17 H 0 1 N N N 15.482 -28.881 -11.118 8.381 -0.566 -1.684 H17 HGG 64 HGG H18 H18 H 0 1 N N N 17.457 -27.058 -10.832 6.839 0.217 0.796 H18 HGG 65 HGG H19 H19 H 0 1 N N N 16.883 -27.113 -8.034 6.732 1.443 -1.427 H19 HGG 66 HGG H19A H19A H 0 0 N N N 16.298 -25.953 -9.324 6.036 -0.030 -2.144 H19A HGG 67 HGG "H2'" "H2'" H 0 1 N N N 27.515 -19.880 3.622 -13.967 -1.345 -1.103 "H2'" HGG 68 HGG "H2'A" "H2'A" H 0 0 N N N 25.902 -20.688 3.846 -12.975 -2.311 -2.222 "H2'A" HGG 69 HGG HO20 HO20 H 0 0 N N N 15.884 -31.729 -10.864 9.736 -2.984 1.225 HO20 HGG 70 HGG "H3'" "H3'" H 0 1 N N N 27.015 -22.546 5.031 -12.717 -4.043 -0.420 "H3'" HGG 71 HGG "HO3'" "HO3'" H 0 0 N N N 29.220 -22.257 5.467 -14.653 -2.403 0.991 "HO3'" HGG 72 HGG HO34 HO34 H 0 0 N N N 13.032 -26.546 -6.268 2.933 0.186 -2.750 HO34 HGG 73 HGG HO37 HO37 H 0 0 N N N 15.132 -21.952 -9.414 -0.155 1.845 -1.666 HO37 HGG 74 HGG "H4'" "H4'" H 0 1 N N N 26.176 -20.574 6.165 -15.618 -3.340 -1.051 "H4'" HGG 75 HGG "H4'A" "H4'A" H 0 0 N N N 27.637 -21.327 6.979 -14.512 -4.168 -2.173 "H4'A" HGG 76 HGG HO40 HO40 H 0 0 N N N 17.518 -31.270 -14.322 11.859 2.544 -0.205 HO40 HGG 77 HGG HO42 HO42 H 0 0 N N N 18.038 -27.523 -14.740 8.868 2.857 -1.166 HO42 HGG 78 HGG H44 H44 H 0 1 N N N 18.040 -23.690 -3.737 -2.320 5.267 3.528 H44 HGG 79 HGG H46 H46 H 0 1 N N N 17.234 -23.765 -6.703 -0.020 5.410 0.576 H46 HGG 80 HGG H46A H46A H 0 0 N N N 16.367 -22.882 -5.329 -1.250 4.194 0.157 H46A HGG 81 HGG "HO5'" "HO5'" H 0 0 N N N 29.289 -18.397 6.675 -16.247 -6.903 -0.452 "HO5'" HGG 82 HGG HO52 HO52 H 0 0 N N N 17.756 -25.936 -2.727 -1.048 6.868 1.467 HO52 HGG 83 HGG H53 H53 H 0 1 N N N 14.697 -25.110 -4.521 0.032 4.704 4.206 H53 HGG 84 HGG H53A H53A H 0 0 N N N 15.800 -25.777 -3.270 1.110 3.871 3.061 H53A HGG 85 HGG H53B H53B H 0 0 N N N 15.599 -23.999 -3.435 0.797 5.614 2.882 H53B HGG 86 HGG H57 H57 H 0 1 N N N 15.858 -26.359 -6.202 -2.148 2.689 1.868 H57 HGG 87 HGG H57A H57A H 0 0 N N N 17.640 -26.250 -6.397 -0.551 2.228 2.504 H57A HGG 88 HGG H57B H57B H 0 0 N N N 16.942 -27.022 -4.932 -1.772 2.933 3.591 H57B HGG 89 HGG H61 H61 H 0 1 N N N 22.181 -24.352 -2.595 -5.192 1.844 1.087 H61 HGG 90 HGG H61A H61A H 0 0 N N N 23.552 -24.874 -3.697 -6.184 2.810 2.206 H61A HGG 91 HGG H62 H62 H 0 1 N N N 22.071 -22.872 -5.042 -4.704 3.881 -0.240 H62 HGG 92 HGG H62A H62A H 0 0 N N N 22.205 -24.615 -5.413 -5.695 4.847 0.879 H62A HGG 93 HGG HN68 HN68 H 0 0 N N N 20.418 -23.830 -3.250 -3.741 3.471 2.384 HN68 HGG 94 HGG H73 H73 H 0 1 N N N 25.794 -24.446 0.197 -9.157 -0.755 -0.182 H73 HGG 95 HGG H73A H73A H 0 0 N N N 27.317 -23.487 -0.000 -10.149 0.212 0.937 H73A HGG 96 HGG H74 H74 H 0 1 N N N 26.476 -22.653 -1.681 -9.660 2.249 -0.391 H74 HGG 97 HGG H74A H74A H 0 0 N N N 25.304 -21.799 -0.556 -8.668 1.282 -1.509 H74A HGG 98 HGG HN71 HN71 H 0 0 N N N 24.232 -24.199 -1.329 -7.706 0.873 1.115 HN71 HGG 99 # # 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 HGG C2 N1 DOUB Y N 1 HGG N1 C6 SING Y N 2 HGG N3 C2 SING Y N 3 HGG C2 H2 SING N N 4 HGG N3 C4 DOUB Y N 5 HGG N9 C4 SING Y N 6 HGG C4 C5 SING Y N 7 HGG C5 N7 SING Y N 8 HGG C5 C6 DOUB Y N 9 HGG C6 N6 SING N N 10 HGG N6 HN6 SING N N 11 HGG N6 HN6A SING N N 12 HGG C8 N7 DOUB Y N 13 HGG N9 C8 SING Y N 14 HGG C8 H8 SING N N 15 HGG C15 N9 SING N N 16 HGG "O1'" "C1'" DOUB N N 17 HGG S81 "C1'" SING N N 18 HGG "C1'" "C2'" SING N N 19 HGG C16 C15 SING N N 20 HGG C15 O22 SING N N 21 HGG C15 H15 SING N N 22 HGG C17 C16 SING N N 23 HGG O20 C16 SING N N 24 HGG C16 H16 SING N N 25 HGG O21 C17 SING N N 26 HGG C17 C18 SING N N 27 HGG C17 H17 SING N N 28 HGG C18 O22 SING N N 29 HGG C18 C19 SING N N 30 HGG C18 H18 SING N N 31 HGG C19 O23 SING N N 32 HGG C19 H19 SING N N 33 HGG C19 H19A SING N N 34 HGG "C2'" "C3'" SING N N 35 HGG "C2'" "H2'" SING N N 36 HGG "C2'" "H2'A" SING N N 37 HGG O20 HO20 SING N N 38 HGG P39 O21 SING N N 39 HGG O23 P31 SING N N 40 HGG "O3'" "C3'" SING N N 41 HGG "C3'" "C4'" SING N N 42 HGG "C3'" "H3'" SING N N 43 HGG "O3'" "HO3'" SING N N 44 HGG O32 P31 SING N N 45 HGG O33 P31 DOUB N N 46 HGG P31 O34 SING N N 47 HGG O32 P35 SING N N 48 HGG O34 HO34 SING N N 49 HGG O36 P35 DOUB N N 50 HGG O37 P35 SING N N 51 HGG P35 O38 SING N N 52 HGG O37 HO37 SING N N 53 HGG O38 C46 SING N N 54 HGG O41 P39 DOUB N N 55 HGG O42 P39 SING N N 56 HGG O40 P39 SING N N 57 HGG "C4'" "C5'" SING N N 58 HGG "C4'" "H4'" SING N N 59 HGG "C4'" "H4'A" SING N N 60 HGG "O4'" "C5'" DOUB N N 61 HGG O40 HO40 SING N N 62 HGG O42 HO42 SING N N 63 HGG O51 C43 DOUB N N 64 HGG C43 N68 SING N N 65 HGG C43 C44 SING N N 66 HGG C45 C44 SING N N 67 HGG C44 O52 SING N N 68 HGG C44 H44 SING N N 69 HGG C46 C45 SING N N 70 HGG C57 C45 SING N N 71 HGG C45 C53 SING N N 72 HGG C46 H46 SING N N 73 HGG C46 H46A SING N N 74 HGG "C5'" "O5'" SING N N 75 HGG "O5'" "HO5'" SING N N 76 HGG O52 HO52 SING N N 77 HGG C53 H53 SING N N 78 HGG C53 H53A SING N N 79 HGG C53 H53B SING N N 80 HGG C57 H57 SING N N 81 HGG C57 H57A SING N N 82 HGG C57 H57B SING N N 83 HGG C62 C61 SING N N 84 HGG C61 C69 SING N N 85 HGG C61 H61 SING N N 86 HGG C61 H61A SING N N 87 HGG C62 N68 SING N N 88 HGG C62 H62 SING N N 89 HGG C62 H62A SING N N 90 HGG N68 HN68 SING N N 91 HGG O72 C69 DOUB N N 92 HGG C69 N71 SING N N 93 HGG N71 C74 SING N N 94 HGG C74 C73 SING N N 95 HGG C73 S81 SING N N 96 HGG C73 H73 SING N N 97 HGG C73 H73A SING N N 98 HGG C74 H74 SING N N 99 HGG C74 H74A SING N N 100 HGG N71 HN71 SING N N 101 # # 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 HGG SMILES ACDLabs 12.01 "O=C(O)CC(O)CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O" HGG SMILES_CANONICAL CACTVS 3.370 "CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C[C@@H](O)CC(O)=O" HGG SMILES CACTVS 3.370 "CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCSC(=O)C[CH](O)CC(O)=O" HGG SMILES_CANONICAL "OpenEye OEToolkits" 1.7.0 "CC(C)(CO[P@](=O)(O)O[P@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)C[C@H](CC(=O)O)O)O" HGG SMILES "OpenEye OEToolkits" 1.7.0 "CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)CC(CC(=O)O)O)O" HGG InChI InChI 1.03 "InChI=1S/C26H42N7O20P3S/c1-26(2,21(40)24(41)29-4-3-15(35)28-5-6-57-17(38)8-13(34)7-16(36)37)10-50-56(47,48)53-55(45,46)49-9-14-20(52-54(42,43)44)19(39)25(51-14)33-12-32-18-22(27)30-11-31-23(18)33/h11-14,19-21,25,34,39-40H,3-10H2,1-2H3,(H,28,35)(H,29,41)(H,36,37)(H,45,46)(H,47,48)(H2,27,30,31)(H2,42,43,44)/t13-,14+,19+,20+,21-,25+/m0/s1" HGG InChIKey InChI 1.03 IIYZSYKTQRIPRG-UPWLPGGHSA-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 HGG "SYSTEMATIC NAME" ACDLabs 12.01 "(3R,5S,9R,21S)-1-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-3,5,9,21-tetrahydroxy-8,8-dimethyl-10,14,19-trioxo-2,4,6-trioxa-18-thia-11,15-diaza-3,5-diphosphatricosan-23-oic acid 3,5-dioxide (non-preferred name)" HGG "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.7.0 "(3S)-5-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-2-hydroxy-3,3-dimethyl-butanoyl]amino]propanoylamino]ethylsulfanyl]-3-hydroxy-5-oxo-pentanoic 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 HGG "Create component" 2010-04-29 RCSB HGG "Modify aromatic_flag" 2011-06-04 RCSB HGG "Modify descriptor" 2011-06-04 RCSB HGG "Modify synonyms" 2021-03-01 PDBE # _pdbx_chem_comp_synonyms.ordinal 1 _pdbx_chem_comp_synonyms.comp_id HGG _pdbx_chem_comp_synonyms.name "3-Hydroxyl Glutaryl CoA" _pdbx_chem_comp_synonyms.provenance ? _pdbx_chem_comp_synonyms.type ? ##