data_A1H1A
# 
_chem_comp.id                                    A1H1A 
_chem_comp.name                                  "Haemophilus influenzae type b (Hib) DP2 oligosaccharide" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C20 H40 O23 P2" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         "[(2~{R},3~{S},4~{R},5~{R})-2-(hydroxymethyl)-4,5-bis(oxidanyl)oxolan-3-yl] [(2~{R},3~{S},4~{S})-5-[(2~{R},3~{R},4~{S},5~{R})-5-(hydroxymethyl)-3-oxidanyl-4-[oxidanyl-[(2~{R},3~{S},4~{S})-2,3,4,5-tetrakis(oxidanyl)pentoxy]phosphoryl]oxy-oxolan-2-yl]oxy-2,3,4-tris(oxidanyl)pentyl] hydrogen phosphate" 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2023-12-21 
_chem_comp.pdbx_modified_date                    2024-05-10 
_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                        710.465 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1H1A 
_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        8RDA 
_chem_comp.pdbx_subcomponent_list                "BDR A1H0Z BDR A1H0Z" 
_chem_comp.pdbx_processing_site                  PDBE 
# 
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_n_terminal_atom_flag 
_chem_comp_atom.pdbx_backbone_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 
A1H1A C42 C16 C 0 1 N N R N N N -14.307 11.910 -35.807 -11.219 1.531  0.459  C4   BDR   1  
A1H1A O42 O16 O 0 1 N N N N N N -15.612 11.634 -36.366 -12.528 1.067  0.853  O4   BDR   2  
A1H1A C12 C14 C 0 1 N N R N N N -16.484 11.279 -35.298 -12.316 -0.252 1.401  C1   BDR   3  
A1H1A O11 O17 O 0 1 N N N N N N -16.600 9.910  -35.221 -13.534 -1.000 1.385  O1   BDR   4  
A1H1A C22 C10 C 0 1 N N R N N N -15.852 11.979 -34.093 -11.273 -0.905 0.467  C2   BDR   5  
A1H1A O22 O18 O 0 1 N N N N N N -15.909 13.389 -34.140 -10.366 -1.714 1.217  O2   BDR   6  
A1H1A C32 C15 C 0 1 N N S N N N -14.441 11.469 -34.351 -10.534 0.296  -0.167 C3   BDR   7  
A1H1A O32 O19 O 0 1 N N N N N N -13.451 12.046 -33.495 -9.146  0.266  0.172  O3   BDR   8  
A1H1A C52 C17 C 0 1 N N N N N N -13.208 11.263 -36.622 -11.337 2.654  -0.573 C5   BDR   9  
A1H1A O52 O20 O 0 1 N N N N N N -11.920 11.563 -36.102 -11.865 3.824  0.056  O5   BDR   10 
A1H1A O1  O5  O 0 1 N N N N N N -15.497 4.889  -29.770 0.730   -0.337 0.479  O1   A1H0Z 11 
A1H1A C1  C1  C 0 1 N N N N N N -15.265 6.214  -30.260 -0.352  -0.308 -0.454 C1   A1H0Z 12 
A1H1A O2  O6  O 0 1 N N N N N N -14.768 7.212  -28.141 -1.824  -1.541 1.014  O2   A1H0Z 13 
A1H1A C3  C3  C 0 1 N N S N N N -13.549 8.120  -30.029 -2.835  -0.152 -0.686 C3   A1H0Z 14 
A1H1A O3  O7  O 0 1 N N N N N N -12.507 8.556  -29.155 -2.691  1.081  -1.394 O3   A1H0Z 15 
A1H1A C4  C4  C 0 1 N N R N N N -14.462 9.316  -30.314 -4.163  -0.152 0.074  C4   A1H0Z 16 
A1H1A O4  O8  O 0 1 N N N N N N -15.498 8.953  -31.229 -4.306  -1.385 0.782  O4   A1H0Z 17 
A1H1A C5  C5  C 0 1 N N N N N N -13.693 10.472 -30.915 -5.317  0.004  -0.918 C5   A1H0Z 18 
A1H1A C2  C2  C 0 1 N N S N N N -14.203 6.880  -29.411 -1.680  -0.308 0.306  C2   A1H0Z 19 
A1H1A O5  O9  O 0 1 N N N N N N -12.969 10.064 -32.082 -6.548  0.121  -0.201 O5   A1H0Z 20 
A1H1A P   P1  P 0 1 N N N N N N -12.217 11.166 -32.972 -7.973  0.299  -0.929 P    A1H0Z 21 
A1H1A O2P O10 O 0 1 N N N N N N -11.357 11.994 -32.076 -8.006  1.710  -1.705 O2P  A1H0Z 22 
A1H1A O1P O11 O 0 1 N N N N N N -11.549 10.479 -34.115 -8.174  -0.801 -1.898 O1P  A1H0Z 23 
A1H1A C41 C11 C 0 1 N N R N N N -15.314 2.597  -31.734 3.667   -1.689 -0.994 C4   BDR   24 
A1H1A O41 O12 O 0 1 N N N N N N -14.488 3.764  -31.509 2.234   -1.569 -0.857 O4   BDR   25 
A1H1A C11 C8  C 0 1 N N R N N N -14.456 4.040  -30.125 2.023   -0.339 -0.130 C1   BDR   26 
A1H1A C21 C9  C 0 1 N N R N N N -14.730 2.673  -29.497 3.127   -0.324 0.951  C2   BDR   27 
A1H1A O21 O13 O 0 1 N N N N N N -13.682 1.743  -29.672 3.617   1.003  1.147  O2   BDR   28 
A1H1A C31 C12 C 0 1 N N S N N N -15.923 2.311  -30.368 4.233   -1.233 0.369  C3   BDR   29 
A1H1A O31 O14 O 0 1 N N N N N N -16.285 0.944  -30.174 5.443   -0.494 0.187  O3   BDR   30 
A1H1A C51 C13 C 0 1 N N N N N N -16.310 2.823  -32.850 4.056   -3.142 -1.273 C5   BDR   31 
A1H1A O51 O15 O 0 1 N N N N N N -15.663 3.190  -34.060 3.559   -3.530 -2.555 O5   BDR   32 
A1H1A O6  O1  O 0 1 N N N N N N -10.620 -2.391 -27.779 14.809  2.477  -0.934 O1   A1H0Z 33 
A1H1A C6  C18 C 0 1 N N N N N N -11.560 -1.802 -26.884 14.032  1.500  -0.239 C1   A1H0Z 34 
A1H1A O7  O21 O 0 1 N N N N N N -12.427 -0.345 -28.592 12.205  3.034  0.147  O2   A1H0Z 35 
A1H1A C8  C19 C 0 1 N N S N N N -13.831 -0.725 -26.659 11.715  0.668  0.184  C3   A1H0Z 36 
A1H1A O8  O2  O 0 1 N N N N N N -14.199 -1.717 -25.700 12.054  -0.583 -0.418 O3   A1H0Z 37 
A1H1A C9  C7  C 0 1 N N R N N N -15.095 -0.198 -27.344 10.227  0.951  -0.032 C4   A1H0Z 38 
A1H1A O9  O22 O 0 1 N N N N N N -15.994 0.301  -26.352 9.888   2.202  0.570  O4   A1H0Z 39 
A1H1A C10 C20 C 0 1 N N N N N N -15.798 -1.245 -28.185 9.397   -0.164 0.607  C5   A1H0Z 40 
A1H1A C7  C6  C 0 1 N N S N N N -12.797 -1.320 -27.617 12.545  1.783  -0.455 C2   A1H0Z 41 
A1H1A O10 O23 O 0 1 N N N N N N -17.092 -0.936 -28.725 8.015   0.038  0.305  O5   A1H0Z 42 
A1H1A P1  P2  P 0 1 N N N N N N -17.466 0.565  -29.160 6.852   -0.950 0.819  P    A1H0Z 43 
A1H1A O13 O4  O 0 1 N N N N N N -17.432 1.466  -27.969 6.765   -0.887 2.425  O2P  A1H0Z 44 
A1H1A O12 O3  O 0 1 N N N N N N -18.755 0.542  -29.915 7.158   -2.335 0.396  O1P  A1H0Z 45 
A1H1A H28 H28 H 0 1 N N N N N N -14.140 12.997 -35.815 -10.660 1.873  1.330  H4   BDR   46 
A1H1A H26 H26 H 0 1 N N N N N N -17.472 11.730 -35.471 -11.927 -0.183 2.417  H1   BDR   47 
A1H1A H33 H33 H 0 1 N N N N N N -17.183 9.681  -34.507 -14.241 -0.610 1.917  HO1  BDR   48 
A1H1A H15 H15 H 0 1 N N N N N N -16.250 11.571 -33.152 -11.767 -1.498 -0.302 H2   BDR   49 
A1H1A H34 H34 H 0 1 N N N N N N -15.499 13.749 -33.362 -10.788 -2.449 1.684  HO2  BDR   50 
A1H1A H27 H27 H 0 1 N N N N N N -14.425 10.371 -34.292 -10.663 0.295  -1.250 H3   BDR   51 
A1H1A H29 H29 H 0 1 N N N N N N -13.269 11.630 -37.657 -10.352 2.875  -0.984 H51  BDR   52 
A1H1A H30 H30 H 0 1 N N N N N N -13.351 10.172 -36.611 -12.004 2.341  -1.376 H52  BDR   53 
A1H1A H35 H35 H 0 1 N N N N N N -11.794 11.102 -35.281 -11.967 4.579  -0.541 HO5  BDR   54 
A1H1A H2  H2  H 0 1 N N N N N N -16.197 6.795  -30.205 -0.282  0.593  -1.063 H12  A1H0Z 55 
A1H1A H1  H1  H 0 1 N N N N N N -14.924 6.165  -31.305 -0.301  -1.187 -1.097 H11  A1H0Z 56 
A1H1A H16 H16 H 0 1 N N N N N N -14.109 7.631  -27.600 -1.820  -2.324 0.446  HO2  A1H0Z 57 
A1H1A H4  H4  H 0 1 N N N N N N -13.101 7.813  -30.986 -2.820  -0.981 -1.393 HC3  A1H0Z 58 
A1H1A H17 H17 H 0 1 N N N N N N -11.927 7.828  -28.965 -2.695  1.863  -0.826 HO3  A1H0Z 59 
A1H1A H5  H5  H 0 1 N N N N N N -14.906 9.647  -29.363 -4.177  0.677  0.781  HC4  A1H0Z 60 
A1H1A H18 H18 H 0 1 N N N N N N -15.996 8.227  -30.872 -4.302  -2.168 0.213  HO4  A1H0Z 61 
A1H1A H6  H6  H 0 1 N N N N N N -12.982 10.857 -30.169 -5.161  0.899  -1.520 H51  A1H0Z 62 
A1H1A H7  H7  H 0 1 N N N N N N -14.400 11.268 -31.192 -5.358  -0.869 -1.569 H52  A1H0Z 63 
A1H1A H3  H3  H 0 1 N N N N N N -13.404 6.141  -29.250 -1.694  0.521  1.013  HC2  A1H0Z 64 
A1H1A H19 H19 H 0 1 N N N N N N -10.458 11.962 -32.381 -7.880  2.478  -1.131 HOP2 A1H0Z 65 
A1H1A H20 H20 H 0 1 N N N N N N -14.672 1.747  -32.009 4.028   -1.039 -1.791 H4   BDR   66 
A1H1A H12 H12 H 0 1 N N N N N N -13.475 4.419  -29.801 2.129   0.518  -0.795 H1   BDR   67 
A1H1A H14 H14 H 0 1 N N N N N N -15.030 2.780  -28.444 2.750   -0.734 1.888  H2   BDR   68 
A1H1A H21 H21 H 0 1 N N N N N N -12.947 1.986  -29.121 2.947   1.629  1.455  HO2  BDR   69 
A1H1A H22 H22 H 0 1 N N N N N N -16.765 2.991  -30.171 4.405   -2.092 1.018  H3   BDR   70 
A1H1A H23 H23 H 0 1 N N N N N N -17.000 3.628  -32.556 5.142   -3.237 -1.259 H51  BDR   71 
A1H1A H24 H24 H 0 1 N N N N N N -16.878 1.895  -33.016 3.626   -3.787 -0.506 H52  BDR   72 
A1H1A H25 H25 H 0 1 N N N N N N -16.313 3.324  -34.739 3.769   -4.442 -2.798 HO5  BDR   73 
A1H1A H8  H8  H 0 1 N N N N N N -9.858  -2.682 -27.292 15.765  2.359  -0.841 HO1  A1H0Z 74 
A1H1A H32 H32 H 0 1 N N N N N N -11.087 -0.946 -26.380 14.272  0.507  -0.619 H12  A1H0Z 75 
A1H1A H31 H31 H 0 1 N N N N N N -11.857 -2.550 -26.134 14.260  1.545  0.826  H11  A1H0Z 76 
A1H1A H36 H36 H 0 1 N N N N N N -13.203 -0.044 -29.050 12.367  3.068  1.100  HO2  A1H0Z 77 
A1H1A H37 H37 H 0 1 N N N N N N -13.357 0.119  -26.137 11.925  0.625  1.253  HC3  A1H0Z 78 
A1H1A H10 H10 H 0 1 N N N N N N -14.841 -1.356 -25.101 11.893  -0.617 -1.371 HO3  A1H0Z 79 
A1H1A H11 H11 H 0 1 N N N N N N -14.798 0.627  -28.008 10.017  0.993  -1.101 HC4  A1H0Z 80 
A1H1A H38 H38 H 0 1 N N N N N N -15.553 0.957  -25.825 10.049  2.236  1.523  HO4  A1H0Z 81 
A1H1A H39 H39 H 0 1 N N N N N N -15.914 -2.141 -27.558 9.718   -1.128 0.211  H51  A1H0Z 82 
A1H1A H40 H40 H 0 1 N N N N N N -15.138 -1.475 -29.035 9.540   -0.150 1.687  H52  A1H0Z 83 
A1H1A H9  H9  H 0 1 N N N N N N -13.256 -2.183 -28.120 12.334  1.826  -1.524 HC2  A1H0Z 84 
A1H1A H13 H13 H 0 1 N N N N N N -18.272 1.901  -27.876 6.567   -0.007 2.774  HOP2 A1H0Z 85 
# 
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 
A1H1A C52 O52 SING N N 1  
A1H1A C52 C42 SING N N 2  
A1H1A O42 C42 SING N N 3  
A1H1A O42 C12 SING N N 4  
A1H1A C42 C32 SING N N 5  
A1H1A C12 O11 SING N N 6  
A1H1A C12 C22 SING N N 7  
A1H1A C32 C22 SING N N 8  
A1H1A C32 O32 SING N N 9  
A1H1A O22 C22 SING N N 10 
A1H1A O1P P   DOUB N N 11 
A1H1A O51 C51 SING N N 12 
A1H1A O32 P   SING N N 13 
A1H1A P   O5  SING N N 14 
A1H1A P   O2P SING N N 15 
A1H1A C51 C41 SING N N 16 
A1H1A O5  C5  SING N N 17 
A1H1A C41 O41 SING N N 18 
A1H1A C41 C31 SING N N 19 
A1H1A O41 C11 SING N N 20 
A1H1A O4  C4  SING N N 21 
A1H1A C5  C4  SING N N 22 
A1H1A C31 O31 SING N N 23 
A1H1A C31 C21 SING N N 24 
A1H1A C4  C3  SING N N 25 
A1H1A C1  O1  SING N N 26 
A1H1A C1  C2  SING N N 27 
A1H1A O31 P1  SING N N 28 
A1H1A C11 O1  SING N N 29 
A1H1A C11 C21 SING N N 30 
A1H1A C3  C2  SING N N 31 
A1H1A C3  O3  SING N N 32 
A1H1A O12 P1  DOUB N N 33 
A1H1A O21 C21 SING N N 34 
A1H1A C2  O2  SING N N 35 
A1H1A P1  O10 SING N N 36 
A1H1A P1  O13 SING N N 37 
A1H1A O10 C10 SING N N 38 
A1H1A O7  C7  SING N N 39 
A1H1A C10 C9  SING N N 40 
A1H1A O6  C6  SING N N 41 
A1H1A C7  C6  SING N N 42 
A1H1A C7  C8  SING N N 43 
A1H1A C9  C8  SING N N 44 
A1H1A C9  O9  SING N N 45 
A1H1A C8  O8  SING N N 46 
A1H1A C1  H1  SING N N 47 
A1H1A C1  H2  SING N N 48 
A1H1A C2  H3  SING N N 49 
A1H1A C3  H4  SING N N 50 
A1H1A C4  H5  SING N N 51 
A1H1A C5  H6  SING N N 52 
A1H1A C5  H7  SING N N 53 
A1H1A O6  H8  SING N N 54 
A1H1A C7  H9  SING N N 55 
A1H1A O8  H10 SING N N 56 
A1H1A C9  H11 SING N N 57 
A1H1A C11 H12 SING N N 58 
A1H1A O13 H13 SING N N 59 
A1H1A C21 H14 SING N N 60 
A1H1A C22 H15 SING N N 61 
A1H1A O2  H16 SING N N 62 
A1H1A O3  H17 SING N N 63 
A1H1A O4  H18 SING N N 64 
A1H1A O2P H19 SING N N 65 
A1H1A C41 H20 SING N N 66 
A1H1A O21 H21 SING N N 67 
A1H1A C31 H22 SING N N 68 
A1H1A C51 H23 SING N N 69 
A1H1A C51 H24 SING N N 70 
A1H1A O51 H25 SING N N 71 
A1H1A C12 H26 SING N N 72 
A1H1A C32 H27 SING N N 73 
A1H1A C42 H28 SING N N 74 
A1H1A C52 H29 SING N N 75 
A1H1A C52 H30 SING N N 76 
A1H1A C6  H31 SING N N 77 
A1H1A C6  H32 SING N N 78 
A1H1A O11 H33 SING N N 79 
A1H1A O22 H34 SING N N 80 
A1H1A O52 H35 SING N N 81 
A1H1A O7  H36 SING N N 82 
A1H1A C8  H37 SING N N 83 
A1H1A O9  H38 SING N N 84 
A1H1A C10 H39 SING N N 85 
A1H1A C10 H40 SING N N 86 
# 
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 
A1H1A InChI            InChI                1.06  "InChI=1S/C20H40O23P2/c21-1-7(24)13(28)9(26)5-38-45(35,36)43-18-12(3-23)41-20(16(18)31)37-4-8(25)14(29)10(27)6-39-44(33,34)42-17-11(2-22)40-19(32)15(17)30/h7-32H,1-6H2,(H,33,34)(H,35,36)/t7-,8-,9+,10+,11+,12+,13-,14-,15+,16+,17+,18+,19+,20+/m0/s1" 
A1H1A InChIKey         InChI                1.06  HIDLWJXKOHQXBH-VBFGRUPISA-N                                                                                                                                                                                                                             
A1H1A SMILES_CANONICAL CACTVS               3.385 "OC[C@H](O)[C@H](O)[C@H](O)CO[P](O)(=O)O[C@H]1[C@@H](O)[C@H](OC[C@H](O)[C@H](O)[C@H](O)CO[P](O)(=O)O[C@H]2[C@@H](O)[C@H](O)O[C@@H]2CO)O[C@@H]1CO"                                                                                                       
A1H1A SMILES           CACTVS               3.385 "OC[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[CH]1[CH](O)[CH](OC[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[CH]2[CH](O)[CH](O)O[CH]2CO)O[CH]1CO"                                                                                                                         
A1H1A SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C([C@@H]1[C@H]([C@H]([C@@H](O1)O)O)OP(=O)(O)OC[C@H]([C@H]([C@H](CO[C@H]2[C@@H]([C@@H]([C@H](O2)CO)OP(=O)(O)OC[C@H]([C@H]([C@H](CO)O)O)O)O)O)O)O)O"                                                                                                     
A1H1A SMILES           "OpenEye OEToolkits" 2.0.7 "C(C1C(C(C(O1)O)O)OP(=O)(O)OCC(C(C(COC2C(C(C(O2)CO)OP(=O)(O)OCC(C(C(CO)O)O)O)O)O)O)O)O"                                                                                                                                                                 
# 
_pdbx_chem_comp_identifier.comp_id           A1H1A 
_pdbx_chem_comp_identifier.type              "SYSTEMATIC NAME" 
_pdbx_chem_comp_identifier.program           "OpenEye OEToolkits" 
_pdbx_chem_comp_identifier.program_version   2.0.7 
_pdbx_chem_comp_identifier.identifier        "[(2~{R},3~{S},4~{R},5~{R})-2-(hydroxymethyl)-4,5-bis(oxidanyl)oxolan-3-yl] [(2~{R},3~{S},4~{S})-5-[(2~{R},3~{R},4~{S},5~{R})-5-(hydroxymethyl)-3-oxidanyl-4-[oxidanyl-[(2~{R},3~{S},4~{S})-2,3,4,5-tetrakis(oxidanyl)pentoxy]phosphoryl]oxy-oxolan-2-yl]oxy-2,3,4-tris(oxidanyl)pentyl] 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 
A1H1A "Create component" 2023-12-21 PDBE 
A1H1A "Initial release"  2024-05-15 RCSB 
# 
_pdbx_chem_comp_synonyms.ordinal      1 
_pdbx_chem_comp_synonyms.comp_id      A1H1A 
_pdbx_chem_comp_synonyms.name         "[(2~{R},3~{S},4~{R},5~{R})-2-(hydroxymethyl)-4,5-bis(oxidanyl)oxolan-3-yl] [(2~{R},3~{S},4~{S})-5-[(2~{R},3~{R},4~{S},5~{R})-5-(hydroxymethyl)-3-oxidanyl-4-[oxidanyl-[(2~{R},3~{S},4~{S})-2,3,4,5-tetrakis(oxidanyl)pentoxy]phosphoryl]oxy-oxolan-2-yl]oxy-2,3,4-tris(oxidanyl)pentyl] hydrogen phosphate" 
_pdbx_chem_comp_synonyms.provenance   PDB 
_pdbx_chem_comp_synonyms.type         ? 
# 
