data_U22 # _chem_comp.id U22 _chem_comp.name "uridine-5'-diphosphate-3-N-(R-3-hydroxylauroyl)-N-acetyl-D-glucosamine" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C29 H50 N4 O18 P2" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms ;(2R,3R,4R,5S,6R)-3-(acetylamino)-5-hydroxy-4-{[(3R)-3-hydroxydodecanoyl]amino}-6-(hydroxymethyl)tetrahydro-2H-pyran-2-y l [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl dihydrogen diphosphate ; _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2009-07-30 _chem_comp.pdbx_modified_date 2020-06-17 _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 804.671 _chem_comp.one_letter_code ? _chem_comp.three_letter_code U22 _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 3I3X _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 U22 C1 C1 C 0 1 N N R 63.928 -15.140 58.059 0.135 4.457 0.378 C1 U22 1 U22 O1 O1 O 0 1 N N N 63.422 -15.574 56.788 -0.595 3.302 -0.040 O1 U22 2 U22 C2 C2 C 0 1 N N R 63.400 -16.060 59.161 1.617 4.276 0.037 C2 U22 3 U22 N2 N2 N 0 1 N N N 63.799 -17.445 58.876 1.763 4.041 -1.401 N2 U22 4 U22 C3 C3 C 0 1 N N R 61.875 -15.978 59.260 2.167 3.073 0.811 C3 U22 5 U22 N3 N3 N 0 1 N N N 61.426 -16.659 60.483 3.602 2.937 0.549 N3 U22 6 U22 C4 C4 C 0 1 N N S 61.405 -14.523 59.284 1.938 3.295 2.309 C4 U22 7 U22 O4 O4 O 0 1 N N N 59.985 -14.477 59.121 2.383 2.148 3.035 O4 U22 8 U22 C5 C5 C 0 1 N N R 62.073 -13.712 58.173 0.444 3.515 2.562 C5 U22 9 U22 O5 O5 O 0 1 N N N 63.499 -13.794 58.311 -0.010 4.628 1.789 O5 U22 10 U22 C6 C6 C 0 1 N N N 61.634 -12.250 58.272 0.214 3.797 4.048 C6 U22 11 U22 O6 O6 O 0 1 N N N 60.591 -11.999 57.327 -1.189 3.886 4.304 O6 U22 12 U22 "C1'" "C1'" C 0 1 N N R 65.520 -16.869 50.321 -5.773 -3.861 -0.253 "C1'" U22 13 U22 "C2'" "C2'" C 0 1 N N R 64.251 -17.510 50.887 -6.596 -4.220 -1.510 "C2'" U22 14 U22 "O2'" "O2'" O 0 1 N N N 63.692 -18.399 49.917 -6.332 -5.565 -1.914 "O2'" U22 15 U22 "C3'" "C3'" C 0 1 N N S 63.306 -16.327 51.101 -6.098 -3.225 -2.582 "C3'" U22 16 U22 "O3'" "O3'" O 0 1 N N N 62.157 -16.477 50.263 -5.514 -3.924 -3.682 "O3'" U22 17 U22 "C4'" "C4'" C 0 1 N N R 64.121 -15.119 50.637 -5.034 -2.382 -1.846 "C4'" U22 18 U22 "O4'" "O4'" O 0 1 N N N 65.485 -15.527 50.825 -5.384 -2.484 -0.448 "O4'" U22 19 U22 "C5'" "C5'" C 0 1 N N N 63.817 -13.921 51.538 -5.097 -0.924 -2.306 "C5'" U22 20 U22 "O5'" "O5'" O 0 1 N N N 64.704 -13.884 52.659 -4.032 -0.187 -1.702 "O5'" U22 21 U22 CAM CAM C 0 1 N N N 59.968 -16.523 60.613 4.199 1.735 0.677 CAM U22 22 U22 OAN OAN O 0 1 N N N 64.943 -14.256 55.191 -2.593 1.907 -1.026 OAN U22 23 U22 PAO PAO P 0 1 N N N 64.422 -15.739 55.537 -2.136 3.359 -0.502 PAO U22 24 U22 CAP CAP C 0 1 N N N 62.993 -18.295 58.246 1.829 5.085 -2.251 CAP U22 25 U22 CAQ CAQ C 0 1 N N N 63.569 -19.696 58.033 1.980 4.844 -3.731 CAQ U22 26 U22 OAR OAR O 0 1 N N N 61.863 -18.009 57.852 1.768 6.219 -1.824 OAR U22 27 U22 OAS OAS O 0 1 N N N 65.525 -16.687 55.805 -3.055 3.792 0.748 OAS U22 28 U22 OAT OAT O 0 1 N N N 63.502 -16.186 54.293 -2.288 4.348 -1.592 OAT U22 29 U22 PAU PAU P 0 1 N N N 64.173 -13.369 54.089 -3.793 1.383 -1.963 PAU U22 30 U22 OAV OAV O 0 1 N N N 62.701 -13.446 54.217 -5.030 2.130 -1.644 OAV U22 31 U22 OAW OAW O 0 1 N N N 64.738 -11.871 54.256 -3.408 1.618 -3.509 OAW U22 32 U22 NAX NAX N 0 1 N N N 66.709 -17.568 50.858 -6.598 -3.992 0.951 NAX U22 33 U22 OAY OAY O 0 1 N N N 59.341 -16.918 59.391 3.548 0.767 1.009 OAY U22 34 U22 CBI CBI C 0 1 N N N 59.472 -17.414 61.754 5.675 1.595 0.408 CBI U22 35 U22 CBJ CBJ C 0 1 N N R 58.297 -18.263 61.264 6.097 0.140 0.624 CBJ U22 36 U22 CBK CBK C 0 1 N N N 67.561 -18.266 49.995 -7.694 -3.226 1.094 CBK U22 37 U22 CBL CBL C 0 1 N N N 58.819 -19.391 60.371 7.566 -0.028 0.231 CBL U22 38 U22 NBM NBM N 0 1 N N N 68.684 -18.925 50.508 -8.470 -3.326 2.190 NBM U22 39 U22 CBN CBN C 0 1 N N N 68.949 -18.884 51.882 -8.156 -4.201 3.166 CBN U22 40 U22 CBO CBO C 0 1 N N N 68.099 -18.190 52.736 -7.005 -5.014 3.028 CBO U22 41 U22 CBP CBP C 0 1 N N N 66.982 -17.533 52.231 -6.248 -4.896 1.916 CBP U22 42 U22 OBQ OBQ O 0 1 N N N 69.935 -19.463 52.335 -8.857 -4.292 4.158 OBQ U22 43 U22 CBR CBR C 0 1 N N N 57.830 -20.557 60.327 7.954 -1.505 0.329 CBR U22 44 U22 CBS CBS C 0 1 N N N 58.026 -21.395 59.062 9.423 -1.674 -0.064 CBS U22 45 U22 OBT OBT O 0 1 N N N 67.324 -18.299 48.788 -7.990 -2.432 0.221 OBT U22 46 U22 CBU CBU C 0 1 N N N 57.350 -20.735 57.858 9.810 -3.151 0.033 CBU U22 47 U22 CBV CBV C 0 1 N N N 57.462 -21.619 56.614 11.279 -3.319 -0.360 CBV U22 48 U22 CBW CBW C 0 1 N N N 57.015 -20.862 55.362 11.667 -4.796 -0.263 CBW U22 49 U22 CBX CBX C 0 1 N N N 57.356 -21.648 54.094 13.136 -4.965 -0.655 CBX U22 50 U22 CBY CBY C 0 1 N N N 56.939 -20.876 52.841 13.524 -6.442 -0.558 CBY U22 51 U22 CBZ CBZ C 0 1 N N N 56.853 -21.805 51.628 14.993 -6.611 -0.951 CBZ U22 52 U22 OCC OCC O 0 1 N N N 57.611 -18.822 62.387 5.929 -0.205 2.001 OCC U22 53 U22 H1 H1 H 0 1 N N N 65.027 -15.178 58.047 -0.250 5.338 -0.136 H1 U22 54 U22 H2 H2 H 0 1 N N N 63.829 -15.735 60.121 2.168 5.173 0.319 H2 U22 55 U22 HN2 HN2 H 0 1 N N N 64.704 -17.758 59.164 1.812 3.134 -1.742 HN2 U22 56 U22 H3 H3 H 0 1 N N N 61.442 -16.469 58.376 1.649 2.168 0.493 H3 U22 57 U22 HN3 HN3 H 0 1 N N N 62.021 -17.140 61.127 4.122 3.711 0.283 HN3 U22 58 U22 H4 H4 H 0 1 N N N 61.686 -14.083 60.252 2.496 4.172 2.636 H4 U22 59 U22 HO4 HO4 H 0 1 N N N 59.628 -15.353 59.204 2.267 2.219 3.993 HO4 U22 60 U22 H5 H5 H 0 1 N N N 61.776 -14.118 57.195 -0.109 2.621 2.272 H5 U22 61 U22 H6 H6 H 0 1 N N N 61.265 -12.046 59.288 0.641 2.989 4.641 H6 U22 62 U22 H6A H6A H 0 1 N N N 62.491 -11.595 58.055 0.694 4.738 4.317 H6A U22 63 U22 HO6 HO6 H 0 1 N N N 60.319 -11.091 57.389 -1.409 4.064 5.229 HO6 U22 64 U22 "H1'" "H1'" H 0 1 N N N 65.571 -16.914 49.223 -4.892 -4.498 -0.180 "H1'" U22 65 U22 "H2'" "H2'" H 0 1 N N N 64.433 -18.087 51.806 -7.661 -4.079 -1.323 "H2'" U22 66 U22 "HO2'" "HO2'" H 0 0 N N N 62.904 -18.797 50.268 -6.822 -5.843 -2.700 "HO2'" U22 67 U22 "H3'" "H3'" H 0 1 N N N 62.955 -16.238 52.140 -6.917 -2.591 -2.925 "H3'" U22 68 U22 "HO3'" "HO3'" H 0 0 N N N 61.570 -15.742 50.396 -6.126 -4.514 -4.143 "HO3'" U22 69 U22 "H4'" "H4'" H 0 1 N N N 63.900 -14.825 49.600 -4.039 -2.792 -2.019 "H4'" U22 70 U22 "H5'" "H5'" H 0 1 N N N 63.939 -12.996 50.955 -4.999 -0.880 -3.390 "H5'" U22 71 U22 "H5'A" "H5'A" H 0 0 N N N 62.783 -14.002 51.903 -6.052 -0.491 -2.009 "H5'A" U22 72 U22 HAQ HAQ H 0 1 N N N 62.831 -20.321 57.508 0.994 4.769 -4.189 HAQ U22 73 U22 HAQA HAQA H 0 0 N N N 64.486 -19.627 57.430 2.527 5.673 -4.180 HAQA U22 74 U22 HAQB HAQB H 0 0 N N N 63.804 -20.148 59.008 2.528 3.916 -3.894 HAQB U22 75 U22 HOAS HOAS H 0 0 N N N 65.488 -17.402 55.180 -3.005 3.188 1.501 HOAS U22 76 U22 HOAW HOAW H 0 0 N N N 64.015 -11.275 54.412 -2.606 1.157 -3.789 HOAW U22 77 U22 HBI HBI H 0 1 N N N 60.288 -18.073 62.086 5.886 1.885 -0.621 HBI U22 78 U22 HBIA HBIA H 0 0 N N N 59.144 -16.785 62.595 6.231 2.240 1.089 HBIA U22 79 U22 HBJ HBJ H 0 1 N N N 57.604 -17.632 60.689 5.479 -0.513 0.008 HBJ U22 80 U22 HBL HBL H 0 1 N N N 58.960 -19.003 59.351 7.711 0.319 -0.792 HBL U22 81 U22 HBLA HBLA H 0 0 N N N 59.778 -19.750 60.773 8.192 0.557 0.906 HBLA U22 82 U22 HNBM HNBM H 0 0 N N N 69.296 -19.424 49.894 -9.257 -2.766 2.277 HNBM U22 83 U22 HBO HBO H 0 1 N N N 68.307 -18.161 53.795 -6.738 -5.720 3.800 HBO U22 84 U22 HBP HBP H 0 1 N N N 66.325 -16.995 52.898 -5.368 -5.510 1.792 HBP U22 85 U22 HBR HBR H 0 1 N N N 57.991 -21.196 61.208 7.809 -1.852 1.352 HBR U22 86 U22 HBRA HBRA H 0 0 N N N 56.805 -20.157 60.336 7.328 -2.090 -0.346 HBRA U22 87 U22 HBS HBS H 0 1 N N N 59.103 -21.491 58.860 9.568 -1.327 -1.087 HBS U22 88 U22 HBSA HBSA H 0 0 N N N 57.584 -22.390 59.220 10.048 -1.089 0.610 HBSA U22 89 U22 HBU HBU H 0 1 N N N 56.286 -20.575 58.088 9.665 -3.498 1.056 HBU U22 90 U22 HBUA HBUA H 0 0 N N N 57.840 -19.771 57.657 9.184 -3.736 -0.641 HBUA U22 91 U22 HBV HBV H 0 1 N N N 58.510 -21.929 56.489 11.424 -2.972 -1.383 HBV U22 92 U22 HBVA HBVA H 0 0 N N N 56.821 -22.503 56.745 11.905 -2.735 0.315 HBVA U22 93 U22 HBW HBW H 0 1 N N N 55.926 -20.710 55.406 11.522 -5.143 0.760 HBW U22 94 U22 HBWA HBWA H 0 0 N N N 57.529 -19.890 55.329 11.041 -5.381 -0.937 HBWA U22 95 U22 HBX HBX H 0 1 N N N 58.442 -21.821 54.062 13.281 -4.618 -1.678 HBX U22 96 U22 HBXA HBXA H 0 0 N N N 56.822 -22.610 54.115 13.762 -4.380 0.019 HBXA U22 97 U22 HBY HBY H 0 1 N N N 55.953 -20.421 53.013 13.379 -6.789 0.465 HBY U22 98 U22 HBYA HBYA H 0 0 N N N 57.684 -20.093 52.639 12.898 -7.027 -1.232 HBYA U22 99 U22 HBZ HBZ H 0 1 N N N 56.552 -21.226 50.743 15.137 -6.263 -1.974 HBZ U22 100 U22 HBZA HBZA H 0 0 N N N 57.836 -22.265 51.448 15.618 -6.026 -0.277 HBZA U22 101 U22 HBZB HBZB H 0 0 N N N 56.109 -22.592 51.821 15.269 -7.663 -0.882 HBZB U22 102 U22 HOCC HOCC H 0 0 N N N 56.882 -19.349 62.083 6.451 0.337 2.608 HOCC U22 103 # # 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 U22 C1 O5 SING N N 1 U22 C1 C2 SING N N 2 U22 O1 C1 SING N N 3 U22 C2 C3 SING N N 4 U22 N2 C2 SING N N 5 U22 C3 C4 SING N N 6 U22 C3 N3 SING N N 7 U22 N3 CAM SING N N 8 U22 O4 C4 SING N N 9 U22 C5 C4 SING N N 10 U22 C5 C6 SING N N 11 U22 C5 O5 SING N N 12 U22 O6 C6 SING N N 13 U22 "C1'" "O4'" SING N N 14 U22 "C1'" NAX SING N N 15 U22 "C1'" "C2'" SING N N 16 U22 "C2'" "C3'" SING N N 17 U22 "O2'" "C2'" SING N N 18 U22 "O3'" "C3'" SING N N 19 U22 "C4'" "C3'" SING N N 20 U22 "C4'" "O4'" SING N N 21 U22 "C4'" "C5'" SING N N 22 U22 "C5'" "O5'" SING N N 23 U22 "O5'" PAU SING N N 24 U22 CAM CBI SING N N 25 U22 OAN PAO SING N N 26 U22 PAO O1 SING N N 27 U22 PAO OAS SING N N 28 U22 CAP N2 SING N N 29 U22 CAQ CAP SING N N 30 U22 OAR CAP DOUB N N 31 U22 OAT PAO DOUB N N 32 U22 PAU OAN SING N N 33 U22 PAU OAV DOUB N N 34 U22 PAU OAW SING N N 35 U22 NAX CBP SING N N 36 U22 OAY CAM DOUB N N 37 U22 CBJ CBI SING N N 38 U22 CBJ OCC SING N N 39 U22 CBK NAX SING N N 40 U22 CBK NBM SING N N 41 U22 CBL CBJ SING N N 42 U22 NBM CBN SING N N 43 U22 CBN OBQ DOUB N N 44 U22 CBN CBO SING N N 45 U22 CBP CBO DOUB N N 46 U22 CBR CBL SING N N 47 U22 CBS CBR SING N N 48 U22 OBT CBK DOUB N N 49 U22 CBU CBS SING N N 50 U22 CBV CBU SING N N 51 U22 CBW CBV SING N N 52 U22 CBX CBW SING N N 53 U22 CBY CBX SING N N 54 U22 CBZ CBY SING N N 55 U22 C1 H1 SING N N 56 U22 C2 H2 SING N N 57 U22 N2 HN2 SING N N 58 U22 C3 H3 SING N N 59 U22 N3 HN3 SING N N 60 U22 C4 H4 SING N N 61 U22 O4 HO4 SING N N 62 U22 C5 H5 SING N N 63 U22 C6 H6 SING N N 64 U22 C6 H6A SING N N 65 U22 O6 HO6 SING N N 66 U22 "C1'" "H1'" SING N N 67 U22 "C2'" "H2'" SING N N 68 U22 "O2'" "HO2'" SING N N 69 U22 "C3'" "H3'" SING N N 70 U22 "O3'" "HO3'" SING N N 71 U22 "C4'" "H4'" SING N N 72 U22 "C5'" "H5'" SING N N 73 U22 "C5'" "H5'A" SING N N 74 U22 CAQ HAQ SING N N 75 U22 CAQ HAQA SING N N 76 U22 CAQ HAQB SING N N 77 U22 OAS HOAS SING N N 78 U22 OAW HOAW SING N N 79 U22 CBI HBI SING N N 80 U22 CBI HBIA SING N N 81 U22 CBJ HBJ SING N N 82 U22 CBL HBL SING N N 83 U22 CBL HBLA SING N N 84 U22 NBM HNBM SING N N 85 U22 CBO HBO SING N N 86 U22 CBP HBP SING N N 87 U22 CBR HBR SING N N 88 U22 CBR HBRA SING N N 89 U22 CBS HBS SING N N 90 U22 CBS HBSA SING N N 91 U22 CBU HBU SING N N 92 U22 CBU HBUA SING N N 93 U22 CBV HBV SING N N 94 U22 CBV HBVA SING N N 95 U22 CBW HBW SING N N 96 U22 CBW HBWA SING N N 97 U22 CBX HBX SING N N 98 U22 CBX HBXA SING N N 99 U22 CBY HBY SING N N 100 U22 CBY HBYA SING N N 101 U22 CBZ HBZ SING N N 102 U22 CBZ HBZA SING N N 103 U22 CBZ HBZB SING N N 104 U22 OCC HOCC 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 U22 SMILES ACDLabs 11.02 "O=C1C=CN(C(=O)N1)C2OC(C(O)C2O)COP(=O)(OP(=O)(OC3OC(C(O)C(NC(=O)CC(O)CCCCCCCCC)C3NC(=O)C)CO)O)O" U22 SMILES_CANONICAL CACTVS 3.352 "CCCCCCCCC[C@@H](O)CC(=O)N[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[P](O)(=O)O[P](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O)[C@@H]1NC(C)=O" U22 SMILES CACTVS 3.352 "CCCCCCCCC[CH](O)CC(=O)N[CH]1[CH](O)[CH](CO)O[CH](O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O)[CH]1NC(C)=O" U22 SMILES_CANONICAL "OpenEye OEToolkits" 1.7.0 "CCCCCCCCC[C@H](CC(=O)N[C@@H]1[C@H]([C@H](O[C@@H]([C@H]1O)CO)O[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)NC(=O)C)O" U22 SMILES "OpenEye OEToolkits" 1.7.0 "CCCCCCCCCC(CC(=O)NC1C(C(OC(C1O)CO)OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)NC(=O)C)O" U22 InChI InChI 1.03 "InChI=1S/C29H50N4O18P2/c1-3-4-5-6-7-8-9-10-17(36)13-21(38)31-22-23(30-16(2)35)28(49-18(14-34)24(22)39)50-53(45,46)51-52(43,44)47-15-19-25(40)26(41)27(48-19)33-12-11-20(37)32-29(33)42/h11-12,17-19,22-28,34,36,39-41H,3-10,13-15H2,1-2H3,(H,30,35)(H,31,38)(H,43,44)(H,45,46)(H,32,37,42)/t17-,18-,19-,22-,23-,24-,25-,26-,27-,28-/m1/s1" U22 InChIKey InChI 1.03 AGYVEKOUTSGPCD-SSVOXRMNSA-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 U22 "SYSTEMATIC NAME" ACDLabs 11.02 "(2R,3R,4R,5S,6R)-3-(acetylamino)-5-hydroxy-4-{[(3R)-3-hydroxydodecanoyl]amino}-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl dihydrogen diphosphate (non-preferred name)" U22 "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.6.1 "[(2R,3R,4R,5S,6R)-3-acetamido-5-hydroxy-4-[[(3R)-3-hydroxydodecanoyl]amino]-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl] hydrogen phosphate" # # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site U22 "Create component" 2009-07-30 RCSB U22 "Modify descriptor" 2011-06-04 RCSB U22 "Modify synonyms" 2020-06-05 PDBE # _pdbx_chem_comp_synonyms.ordinal 1 _pdbx_chem_comp_synonyms.comp_id U22 _pdbx_chem_comp_synonyms.name "(2R,3R,4R,5S,6R)-3-(acetylamino)-5-hydroxy-4-{[(3R)-3-hydroxydodecanoyl]amino}-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl dihydrogen diphosphate" _pdbx_chem_comp_synonyms.provenance ? _pdbx_chem_comp_synonyms.type ? ##